Complications associated with current bladder treatment.
\\n\\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\\n\\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\\n"}]',published:!0,mainMedia:{caption:"Highly Cited",originalUrl:"/media/original/117"}},components:[{type:"htmlEditorComponent",content:'IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\nThroughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\nReleased this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\n'}],latestNews:[{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"},{slug:"intechopen-identified-as-one-of-the-most-significant-contributor-to-oa-book-growth-in-doab-20210809",title:"IntechOpen Identified as One of the Most Significant Contributors to OA Book Growth in DOAB"}]},book:{item:{type:"book",id:"9086",leadTitle:null,fullTitle:"Drug Repurposing - Hypothesis, Molecular Aspects and Therapeutic Applications",title:"Drug Repurposing",subtitle:"Hypothesis, Molecular Aspects and Therapeutic Applications",reviewType:"peer-reviewed",abstract:"Drug repurposing or drug repositioning is a new approach to presenting new indications for common commercial and clinically approved existing drugs. For example, chloroquine, an old antimalarial drug, showed promising results for treating COVID-19, interfering with MDR in several types of cancer, and chemosensitizing human leukemic cells.This book focuses on the hypothesis, risk/benefits, and economic impacts of drug repurposing on drug discovery in dermatology, infectious diseases, neurological disorders, cancer, and orphan diseases. It brings together up-to-date research to provide readers with an informative, illustrative, and easy-to-read book useful for students, clinicians, and the pharmaceutical industry.",isbn:"978-1-83968-521-7",printIsbn:"978-1-83968-520-0",pdfIsbn:"978-1-83968-522-4",doi:"10.5772/intechopen.83082",price:119,priceEur:129,priceUsd:155,slug:"drug-repurposing-hypothesis-molecular-aspects-and-therapeutic-applications",numberOfPages:234,isOpenForSubmission:!1,isInWos:1,isInBkci:!1,hash:"5b13e06123db7a16dcdae682eb47ac66",bookSignature:"Farid A. Badria",publishedDate:"December 2nd 2020",coverURL:"https://cdn.intechopen.com/books/images_new/9086.jpg",numberOfDownloads:8964,numberOfWosCitations:20,numberOfCrossrefCitations:21,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:39,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:80,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"December 6th 2019",dateEndSecondStepPublish:"March 13th 2020",dateEndThirdStepPublish:"May 12th 2020",dateEndFourthStepPublish:"July 31st 2020",dateEndFifthStepPublish:"September 29th 2020",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"41865",title:"Prof.",name:"Farid A.",middleName:null,surname:"Badria",slug:"farid-a.-badria",fullName:"Farid A. Badria",profilePictureURL:"https://mts.intechopen.com/storage/users/41865/images/system/41865.jpg",biography:"Farid A. Badria, Ph.D., is a scholar of the Arab Development Fund, Kuwait; ICRO-UNESCO, Chile; and UNESCO Biotechnology France. He has submitted 47 patents, 20 of which have been granted final certificates. He has more than 250 publications, 12 books, and several marketed pharmaceutical products to his credit. He continues to lead research projects on developing new therapies for liver disease, skin disorders, and cancer. Dr. Badria was listed among the top 2% of most-cited scientists in medical and biomolecular chemistry by Stanford University in 2019 and 2020. He has received several awards including the TWAS Prize for “Public Understanding and Popularization of Science”; WIPO Gold Medal (Best Inventor); State Outstanding Award in Medicine; Outstanding Arab Scholar, Kuwait; and Khawrazmi International Award, Iran.",institutionString:"Mansoura University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"5",totalChapterViews:"0",totalEditedBooks:"7",institution:{name:"Mansoura University",institutionURL:null,country:{name:"Egypt"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"1197",title:"Pharmaceutical Drug",slug:"pharmaceutical-drug"}],chapters:[{id:"72744",title:"Drug Repurposing (DR): An Emerging Approach in Drug Discovery",doi:"10.5772/intechopen.93193",slug:"drug-repurposing-dr-an-emerging-approach-in-drug-discovery",totalDownloads:2711,totalCrossrefCites:17,totalDimensionsCites:29,hasAltmetrics:1,abstract:"Drug repurposing (DR) (also known as drug repositioning) is a process of identifying new therapeutic use(s) for old/existing/available drugs. It is an effective strategy in discovering or developing drug molecules with new pharmacological/therapeutic indications. In recent years, many pharmaceutical companies are developing new drugs with the discovery of novel biological targets by applying the drug repositioning strategy in drug discovery and development program. This strategy is highly efficient, time saving, low-cost and minimum risk of failure. It maximizes the therapeutic value of a drug and consequently increases the success rate. Thus, drug repositioning is an effective alternative approach to traditional drug discovery process. Finding new molecular entities (NME) by traditional or de novo approach of drug discovery is a lengthy, time consuming and expensive venture. Drug repositioning utilizes the combined efforts of activity-based or experimental and in silico-based or computational approaches to develop/identify the new uses of drug molecules on a rational basis. It is, therefore, believed to be an emerging strategy where existing medicines, having already been tested safe in humans, are redirected based on a valid target molecule to combat particularly, rare, difficult-to-treat diseases and neglected diseases.",signatures:"Mithun Rudrapal, Shubham J. Khairnar and Anil G. Jadhav",downloadPdfUrl:"/chapter/pdf-download/72744",previewPdfUrl:"/chapter/pdf-preview/72744",authors:[{id:"314279",title:"Dr.",name:"Mithun",surname:"Rudrapal",slug:"mithun-rudrapal",fullName:"Mithun Rudrapal"}],corrections:null},{id:"72930",title:"Risk-Benefit Events Associated with the Use of Aspirin for Primary Prevention of Cardiovascular Disorders",doi:"10.5772/intechopen.93286",slug:"risk-benefit-events-associated-with-the-use-of-aspirin-for-primary-prevention-of-cardiovascular-diso",totalDownloads:469,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Aspirin had been introduced as a nonsteroidal anti-inflammatory molecule. As further research on aspirin started, other therapeutic effects have been revealed. Now, this molecule has become the polychrest in medical science. Aspirin has served as a drug of choice for the primary prevention of cardiovascular disease (CVD) for the last few decades. However, recent trials have raised questions on the use of aspirin for CVD prevention due to some life-threatening adverse drug events. In spite of that, outcomes of trials will surely assist to frame a guideline for anoxic administration regimen of aspirin in order to prevent CVD.",signatures:"Deepak Kumar Dash, Vishal Jain, Anil Kumar Sahu, Rajnikant Panik and Vaibhav Tripathi",downloadPdfUrl:"/chapter/pdf-download/72930",previewPdfUrl:"/chapter/pdf-preview/72930",authors:[{id:"204256",title:"Dr.",name:"Anil",surname:"Kumar Sahu",slug:"anil-kumar-sahu",fullName:"Anil Kumar Sahu"},{id:"280860",title:"Dr.",name:"Vishal",surname:"Jain",slug:"vishal-jain",fullName:"Vishal Jain"},{id:"280861",title:"Prof.",name:"Deepak Kumar",surname:"Dash",slug:"deepak-kumar-dash",fullName:"Deepak Kumar Dash"},{id:"314683",title:"Dr.",name:"Rajnikant",surname:"Panik",slug:"rajnikant-panik",fullName:"Rajnikant Panik"},{id:"316679",title:"Dr.",name:"Vaibhav",surname:"Tripathi",slug:"vaibhav-tripathi",fullName:"Vaibhav Tripathi"}],corrections:null},{id:"72957",title:"Drug Repurposing in Dermatology: Molecular Biology and Omics Approach",doi:"10.5772/intechopen.93344",slug:"drug-repurposing-in-dermatology-molecular-biology-and-omics-approach",totalDownloads:521,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"The withdrawal of several blockbuster drugs due to severe adverse effects and the failure of several developed drugs in clinical trials raised questions about the efficacy of current approaches of drug discovery. Moreover, the limitation of resources and the long and costive process of drug discovery made a lot of pharmaceutical companies to employ drug repurposing strategies to get new insights about activities that were not considered during their initial discovery. The development of therapeutics for treatment of dermatological condition is not considered as priority although it affects the lifestyle of thousands of people around the world. Serendipity and observations have contributed significantly in this field but immerse efforts have been exerted to find systematic methods to identify new indications for drugs, especially with the unprecedented progress in molecular biology and omics. So, in this chapter, we will emphasize on different approaches used for drug repositioning and how it was applied to find new therapeutics for different dermatoses.",signatures:"Farid A. Badria and Abdullah A. Elgazar",downloadPdfUrl:"/chapter/pdf-download/72957",previewPdfUrl:"/chapter/pdf-preview/72957",authors:[{id:"41865",title:"Prof.",name:"Farid A.",surname:"Badria",slug:"farid-a.-badria",fullName:"Farid A. Badria"},{id:"275570",title:"Ph.D. Student",name:"Abdullah A.",surname:"Elgazar",slug:"abdullah-a.-elgazar",fullName:"Abdullah A. Elgazar"}],corrections:null},{id:"71901",title:"Drug Repurposing and Orphan Disease Therapeutics",doi:"10.5772/intechopen.91941",slug:"drug-repurposing-and-orphan-disease-therapeutics",totalDownloads:1023,totalCrossrefCites:1,totalDimensionsCites:2,hasAltmetrics:1,abstract:"Drug repurposing (or drug repositioning) is an innovative way to find out the new indications of a drug that already exists in the market with known therapeutic indications. It offers an effective way to drug developers or the pharmaceutical companies to identify new targets for FDA-approved drugs. Less time consumption, low cost and low risk of failure are some of the advantages being offered with drug repurposing. Sildenafil (Viagra), a landmark example of a repurposed drug, was introduced into the market as an antianginal drug. But at present, its use is repurposed as drug for erectile dysfunction. In a similar way, numerous drugs are there that have been successfully repurposed in managing the clinical conditions. The chapter would be highlighting the various drug repurposing strategies, drugs repurposed in the past and the current status of repurposed drugs in the orphan disease therapeutics along with regulatory guidelines for drug repurposing.",signatures:"Neha Dhir, Ashish Jain, Dhruv Mahendru, Ajay Prakash and Bikash Medhi",downloadPdfUrl:"/chapter/pdf-download/71901",previewPdfUrl:"/chapter/pdf-preview/71901",authors:[{id:"209466",title:"Prof.",name:"Bikash",surname:"Medhi",slug:"bikash-medhi",fullName:"Bikash Medhi"},{id:"319119",title:"Dr.",name:"Ajay",surname:"Prakash",slug:"ajay-prakash",fullName:"Ajay Prakash"},{id:"319120",title:"Ms.",name:"Neha",surname:"Dhir",slug:"neha-dhir",fullName:"Neha Dhir"},{id:"319121",title:"Mr.",name:"Ashish",surname:"Jain",slug:"ashish-jain",fullName:"Ashish Jain"},{id:"319122",title:"Dr.",name:"Dhruv",surname:"Mahendru",slug:"dhruv-mahendru",fullName:"Dhruv Mahendru"}],corrections:null},{id:"72622",title:"Drug Repurposing in Neurological Diseases: Opportunities and Challenges",doi:"10.5772/intechopen.93093",slug:"drug-repurposing-in-neurological-diseases-opportunities-and-challenges",totalDownloads:650,totalCrossrefCites:1,totalDimensionsCites:2,hasAltmetrics:0,abstract:"Drug repurposing or repositioning refers to “studying of clinically approved drugs in one disease to see if they have therapeutic value and do not trigger side effects in other diseases.” Nowadays, it is a vital drug discovery approach to explore new therapeutic benefits of existing drugs or drug candidates in various human diseases including neurological disorders. This approach overcomes the shortage faced during traditional drug development in grounds of financial support and timeline. It is especially hopeful in some refractory diseases including neurological diseases. The feature that structure complexity of the nervous system and influence of blood–brain barrier permeability often becomes more difficult to develop new drugs in neuropathological conditions than diseases in other organs; therefore, drug repurposing is particularly of utmost importance. In this chapter, we discuss the role of drug repurposing in neurological diseases and make a summarization of repurposing candidates currently in clinical trials for neurological diseases and potential mechanisms as well as preliminary results. Subsequently we also outline drug repurposing approaches and limitations and challenges in the future investigations.",signatures:"Xiao-Yuan Mao",downloadPdfUrl:"/chapter/pdf-download/72622",previewPdfUrl:"/chapter/pdf-preview/72622",authors:[{id:"317713",title:"Dr.",name:"Xiao-Yuan",surname:"Mao",slug:"xiao-yuan-mao",fullName:"Xiao-Yuan Mao"}],corrections:null},{id:"73248",title:"Drugs Repurposing for Multi-Drug Resistant Bacterial Infections",doi:"10.5772/intechopen.93635",slug:"drugs-repurposing-for-multi-drug-resistant-bacterial-infections",totalDownloads:563,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"Different institutions recognized that antimicrobial resistance is a global health threat that has compounded by the reduction in the discovery and development of new antimicrobial agents. Therefore, the development of new antimicrobial therapeutic strategies requires immediate attention to avoid the 10 million deaths predicted to occur by 2050 as a result of multidrug-resistant (MDR) bacteria. Despite the great interest in the development of repurposing drugs, only few repurposing drugs are under clinical development against Gram-negative critical-priority pathogens. In this chapter, we aim: (i) to discuss the therapeutic potential of the repurposing drugs for treating MDR bacterial infections, (ii) to summarize their mechanism of action, and (iii) to provide an overview for their preclinical and clinical development against these critical-priority pathogens.",signatures:"Andrea Vila Domínguez, Manuel Enrique Jiménez Mejías and Younes Smani",downloadPdfUrl:"/chapter/pdf-download/73248",previewPdfUrl:"/chapter/pdf-preview/73248",authors:[{id:"319022",title:"Dr.",name:"Younes",surname:"Smani",slug:"younes-smani",fullName:"Younes Smani"},{id:"328013",title:"Ms.",name:"Andrea",surname:"Vila Domínguez",slug:"andrea-vila-dominguez",fullName:"Andrea Vila Domínguez"},{id:"328014",title:"Dr.",name:"Manuel Enrique",surname:"Jiménez Mejías",slug:"manuel-enrique-jimenez-mejias",fullName:"Manuel Enrique Jiménez Mejías"}],corrections:null},{id:"72049",title:"Drug Repurposing in Oncotherapeutics",doi:"10.5772/intechopen.92302",slug:"drug-repurposing-in-oncotherapeutics",totalDownloads:381,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Repurposing or repositioning means validating and application of previously approved drugs in the treatment of another disease that might be relevant or irrelevant to existing use in disease based on the principle of polypharmacology. Repurposed drugs are already well documented for pharmacokinetic, pharmacodynamic, drug interaction, and toxicity parameters. In 1962, thalidomide treatment in pregnant women led to phocomelia in their newborn but while repurposed based on anti-angiogenesis property, it showed efficacy in hematologic malignancies like multiple myeloma. The repurposing is becoming an essential tool in the anti-cancer drug development due to existing drugs are not effective, high cost of treatment, therapy may degrade the quality of life, improvement of survival after treatment is not guaranteed, relapse may occur, and drug resistance may develop due to tumor heterogeneity. Repurposing can be addressed well with the help of literature-based discovery, high throughput technology, bioinformatics multi-omics approaches, side effects, and phenotypes. Many regulatory bodies like EML, NIH, and FDA promote repurposing programs that support the identification of alternative uses of existing medicines. Cancer becomes the major health issue, and the need to discover promising anti-cancer drugs through repurposing remains very high due to decline in FDA approval since 1990, huge expenses incurred in the drug development and prediction of dangerous future burden.",signatures:"Alkeshkumar Patel",downloadPdfUrl:"/chapter/pdf-download/72049",previewPdfUrl:"/chapter/pdf-preview/72049",authors:[{id:"317034",title:"Dr.",name:"Alkeshkumar",surname:"Patel",slug:"alkeshkumar-patel",fullName:"Alkeshkumar Patel"}],corrections:null},{id:"72600",title:"Drug Repositioning for the Treatment of Glioma: Current State and Future Perspective",doi:"10.5772/intechopen.92803",slug:"drug-repositioning-for-the-treatment-of-glioma-current-state-and-future-perspective",totalDownloads:586,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:1,abstract:"Gliomas are the most common primary brain tumors. Among them, glioblastoma (GBM) possesses the most malignant phenotype. Despite the current standard therapy using an alkylating anticancer agent, temozolomide, most patients with GBM die within 2 years. Novel chemotherapeutic agents are urgently needed to improve the prognosis of GBM. One of the solutions, drug repositioning, which broadens the indications of existing drugs, has gained attention. Herein, we categorize candidate agents, which are newly identified as therapeutic drugs for malignant glioma into 10 classifications based on these original identifications. Some drugs are in clinical trials with hope. Additionally, the obstacles, which should be overcome in order to accomplish drug repositioning as an application for GBM and the future perspectives, have been discussed.",signatures:"Sho Tamai, Nozomi Hirai, Shabierjiang Jiapaer, Takuya Furuta and Mitsutoshi Nakada",downloadPdfUrl:"/chapter/pdf-download/72600",previewPdfUrl:"/chapter/pdf-preview/72600",authors:[{id:"43162",title:"Prof.",name:"Mitsutoshi",surname:"Nakada",slug:"mitsutoshi-nakada",fullName:"Mitsutoshi Nakada"},{id:"321063",title:"Dr.",name:"Sho",surname:"Tamai",slug:"sho-tamai",fullName:"Sho Tamai"},{id:"321064",title:"Dr.",name:"Nozomi",surname:"Hirai",slug:"nozomi-hirai",fullName:"Nozomi Hirai"},{id:"321065",title:"Dr.",name:"Shabierjiang",surname:"Jiapaer",slug:"shabierjiang-jiapaer",fullName:"Shabierjiang Jiapaer"},{id:"321066",title:"Dr.",name:"Takuya",surname:"Furuta",slug:"takuya-furuta",fullName:"Takuya Furuta"}],corrections:null},{id:"72447",title:"Repurposing Infectious Pathogen Vaccines in Cancer Immunotherapy",doi:"10.5772/intechopen.92780",slug:"repurposing-infectious-pathogen-vaccines-in-cancer-immunotherapy",totalDownloads:651,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Reports in the literature show that certain vaccines against infectious pathogens, can be effective in eliciting antitumor immune response when injected intratumorally. In mouse tumor models, intratumoral delivery of rotavirus, yellow fever, and influenza vaccines have been shown to also synergize with checkpoint inhibitors, in the leading immunotherapy in the clinical practice today. The combined approach can thus become a very promising novel strategy for anticancer immunotherapy. In humans, an attenuated poliomyelitis virus vaccine, a peptide-based vaccines against papilloma and one based on detoxified diphtheria protein have already been tested as intratumoral treatments readily. In those studies, the role of available anti-pathogen immunity appears an important element in mediating the activity of the repurposed vaccines against cancer. We therefore suggest how evaluating or eventually developing anti-pathogen immunity before intratumoral delivery could be helpful in repurposing infectious pathogen vaccines in cancer immunotherapy.",signatures:"Matteo Conti",downloadPdfUrl:"/chapter/pdf-download/72447",previewPdfUrl:"/chapter/pdf-preview/72447",authors:[{id:"319456",title:"Ph.D.",name:"Matteo",surname:"Conti",slug:"matteo-conti",fullName:"Matteo Conti"}],corrections:null},{id:"71495",title:"Salicylic Acid Sans Aspirin in Animals and Man",doi:"10.5772/intechopen.91706",slug:"salicylic-acid-sans-aspirin-in-animals-and-man",totalDownloads:658,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Analyses in non-aspirin takers finding salicylic acid (SA) and hydroxylated metabolites in serum also SA and salicyluric acid (SU) in urine led to a re-evaluation of dietary sources of salicylates. Fruit and vegetable sources explained higher levels found in drug-free vegetarians, which overlapped with those from patients on low dose aspirin. That drug’s chemo-protective action in cancer is, at least partially, attributable to its principal metabolite, SA—which we believe contributes to the benefits of a vegetarian diet. However, diet is unlikely to be the sole source of the circulating salicylate found in aspirin-free animals and man. We adduced evidence for its persistence in prolonged fasting and biosynthesis in vivo from labelled benzoic acid. We review the roles, defined and potential, of SA in the biosphere. Emphasis on the antiplatelet effect of aspirin in man has detracted from the likely pivotal role of SA in many potential areas of bioregulation—probably as important in animals as in plants. In this expanding field, some aspirin effects, mediated by apparently conserved receptors responding to SA, are discussed. The perspectives revealed may lead to re-evaluation of the place of salicylates in therapeutics and potentially improve formulations and drug delivery systems.",signatures:"James Ronald Lawrence, Gwendoline Joan Baxter and John Robert Paterson",downloadPdfUrl:"/chapter/pdf-download/71495",previewPdfUrl:"/chapter/pdf-preview/71495",authors:[{id:"314403",title:"Dr.",name:"Jim",surname:"Lawrence",slug:"jim-lawrence",fullName:"Jim Lawrence"},{id:"316821",title:"Dr.",name:"Gwendoline J.",surname:"Baxter",slug:"gwendoline-j.-baxter",fullName:"Gwendoline J. Baxter"}],corrections:null},{id:"71631",title:"Repurposing Fumaric Acid Esters to Treat Conditions of Oxidative Stress and Inflammation: A Promising Emerging Approach with Broad Potential",doi:"10.5772/intechopen.91915",slug:"repurposing-fumaric-acid-esters-to-treat-conditions-of-oxidative-stress-and-inflammation-a-promising",totalDownloads:756,totalCrossrefCites:2,totalDimensionsCites:4,hasAltmetrics:0,abstract:"The medicinal benefit of salts of fumaric acid and its esters (FAE), known as fumarates (mono and dimethyl fumarate), was realized many years ago. Early on, FAE were derived from plants and mushrooms (e.g., Fumaria officinalis, Boletus fomentarius var. pseudo-igniarius). The FAE containing formulation Fumaderm® was licensed in Germany for the treatment of psoriasis in 1994. Recently, a clinical formulation of dimethyl fumarate known as BG12 (Tecfidera) was approved for use in the United States, New Zealand, Australia, European Union, Switzerland, and Canada for the treatment of multiple sclerosis. Others and we have assessed the potential benefit of FAE in a number of disease conditions that are diverse with respect to etiology but unified with regard to the involvement of inflammation and oxidative stress. Hence, a FAE-based drug with robust anti-oxidative and anti-inflammatory effects that is already US-FDA approved is a perfect contender for repurposing and rapid clinical implementation for their management. There is a burgeoning literature on the use of FAE in the prevention and treatment of diseases, other than psoriasis and MS, in which oxidative stress and/or inflammation are prominent. This chapter highlights critical information gleaned from these studies, exposes lacunae of potential importance, and provides related perspectives.",signatures:"Ravirajsinh N. Jadeja, Folami L. Powell and Pamela M. Martin",downloadPdfUrl:"/chapter/pdf-download/71631",previewPdfUrl:"/chapter/pdf-preview/71631",authors:[{id:"265689",title:"Dr.",name:"Ravirajsinh",surname:"Jadeja",slug:"ravirajsinh-jadeja",fullName:"Ravirajsinh Jadeja"},{id:"316978",title:"Prof.",name:"Pamela",surname:"Martin",slug:"pamela-martin",fullName:"Pamela Martin"},{id:"316979",title:"Dr.",name:"Folami",surname:"Powell",slug:"folami-powell",fullName:"Folami Powell"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"5767",title:"Natural Products and Cancer Drug Discovery",subtitle:null,isOpenForSubmission:!1,hash:"6d12d5b2fe98bfc2a6411f1b26d8f028",slug:"natural-products-and-cancer-drug-discovery",bookSignature:"Farid A. 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Indeed activities of each organs lead to the cellular production of metabolites. These metabolic products are discharged into the blood system to be supported by the urinary apparatus. The purification of the blood is essential to preserve the homeostasis of the organism and the blood pressure. The upper urinary tract is composed of kidneys which filter the blood to evacuate the excessive water, ions and toxic metabolic products. Then, this mixture called terminal urine is transported in the lower urinary tract by the ureters. The lower urinary tract consists of the bladder which stocks the urine until its evacuation by the urethra. The terminal urine is cytotoxic because of its composition of nitrogenous and potential carcinogenic elements, also its pH which varies between 4.5 and 8.3 [1, 2]. Therefore, the storage of urine need to be safe, this is why the bladder possesses two specific characteristics.
Firstly, the bladder wall is watertight in order to prevent the urine from seeping through the different tissue layers and damage their structure. Secondly, the bladder is compliant in order to keep a low pressure during the urine filling, and prevent reflux towards the upper urinary tract which could lead to kidneys failure. Thereby, the bladder is able to adapt its capacity to the volume of the accumulated urine. These properties are entirely related to the nature and the structure of different tissues which compose the bladder wall (Figure 1). As shown in the figure 1, the tissue directly in contact with urine is the urothelium. This is an epithelium highly specialized regarding the watertight function and adaptation to large changes in urine volume. This distensible property is assumed by the pseudo-stratified character of the urothelium, while the water tightness is provided by the most differentiated urothelial cells known as umbrella cells. These cells are endowed with very tight junctions in the apicolateral side, while a well-organized protein barrier, called uroplakin plaque, covers the luminal surface [3, 4]. The urothelium rest upon the lamina propria: an extracellular matrix which serves of nutritive and informative support for cells. The lamina propria is mostly made of collagen of type I and III [5, 6]. Another type of extracellular matrix is found at the lower level. It contains three organized smooth muscle cells bundles responsible for urine emptying because of their contractile property. This extracellular matrix is characterized by the presence of an elastic fibres network which allows the distension of the bladder and a low pressure during filing.
Scheme of bladder wall.
Every year 400 million person of all ages suffers from urinary disorders. Several congenital disorders such as bladder exstrophy or neurogenic bladder can affect the function of this organ. But there are also acquired bladder problems like traumatisms, inflammations, chronic interstitial cystitis and cancer which is the sixth most detected. All of these pathologies may require surgical augmentation or reconstruction of bladder wall to restore the storage capacity. The first application of a free tissue graft for bladder replacement was reported by Neuhof in 1917 [7], when fascia was used to augment bladders in dogs. Since that first report, diverse methods have been proposed for this type of surgical intervention, but actually the gold standard is the bladder replacement/repair with autologous segment of the gastrointestinal tract, also named Enterocystoplasty [8, 9]. It has the advantage of being highly vascularized, promoting the survival of the graft. Unfortunately, this technique is associated with multiple short and long-term complications well documented (Table 1). The most frequent is metabolic disturbance, but mucus secretion, stone formation, bladder perforation and malignancy have also been found many years after enterocystoplasty [10-13]. These complications predominantly result from the difference between the absorption property of intestinal mucosa and the watertight function of the bladder epithelium, concerning the contact with urine.
\n\t\t\t | \n\t\t\t\t BLADDER | \n\t\t
Pathologies | \n\t\t\tCongenital malformations | \n\t\t
Common treatment | \n\t\t\tSurgical bladder repair or reconstruction with intestinal segment. The choice of the segment depend mainly on age and medical history. | \n\t\t
Associated complications | \n\t\t\tIntestinal dysfunctions | \n\t\t
Complications associated with current bladder treatment.
The lack of autologous tissue with similar properties to the native bladder is a limitation which led numerous research groups to develop alternative approaches. These last years, many fundamental knowledge concerning bladder cells and matrix have emerged, and have constituted an essential aid to the in vitro elaboration of various bladder models. This chapter will explain the different sources of cells used, the different type of engineered matrices, and the advanced concerning the techniques of in vitro culture. The emphasis will be placed on qualities and inconveniences of each approach, as well as the clinical potential of the engineered models.
Although the bladder is composed of many type of cells, the most harvested for vesical tissue-engineering is urothelial and smooth muscle cells. Urothelial cells are organized into three layers which are anchored to the basal lamina. Basal cells, reside in the lower layer [14]. These progenitor cells develop themselves into intermediate cells, and differentiate into umbrella cells which are the most mature urothelial cells. The degree of urothelial differentiation is defined by the expression of specific proteins, such as keratins, claudins and uroplakins (Table 2) [15]. Smooth muscle cells have a fusiform shape and are assembled into bundles also organised into three layers. In the outer and inner layers, the smooth muscle bundles are oriented longitudinally, while those of the middle layer circularly. In each bundle, a single smooth muscle cell is innervated and action potential can propagated to neighboring cells in order to causes a coordinated contraction. The proliferation and differentiation of urothelial and smooth muscle cells are interdependent, because of factors released from these cells [16].
\n\t\t\t | \n\t\t\t\t UROTHELIAL CELLS | \n\t\t||||
\n\t\t\t\t Markers | \n\t\t\tbasal | \n\t\t\tlower | \n\t\t\tupper | \n\t\t\tsuperficial | \n\t\t|
\n\t\t\t\t K5 - 10 - 17 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t | |
\n\t\t\t\t K13 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t | |
\n\t\t\t\t K14 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t | |
\n\t\t\t\t K7 - 8 - 18 - 19 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t | |
\n\t\t\t\t K20 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t | |
\n\t\t\t\t ZO1 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t\t\t Intercellular junctions | \n\t\t|
\n\t\t\t\t Cldn3 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t\t\t Intercellular junctions | \n\t\t|
\n\t\t\t\t Cldn4 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t\t\t Intercellular junctions | \n\t\t|
\n\t\t\t\t Cldn5 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t\t\t Intercellular junctions | \n\t\t|
\n\t\t\t\t Cldn7 | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t\t Intercellular junctions | \n\t\t\t\n\t\t | |
\n\t\t\t\t Occldn | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t\t Intercellular junctions | \n\t\t\t\n\t\t | |
\n\t\t\t\t UPIa/Ib/II/IIIa | \n\t\t\t\n\t\t\t | \n\t\t\t | \n\t\t\t | \n\t\t |
Markers of urothelial cells (white = no presence, light-blue = low presence, dark-blue = strong presence).
The importance to associate cells to a urological substitute was described by numerous studies [17-19]. These works showed that bladder substitute seeded with cells led to better in vivo regeneration, than the use of scaffold only. Cells help the graft integration; this is why the latest bladder substitutes are generally constituted by a combination of scaffold and cells.
Urothelial cells culture dates back to more than 30 years [20], and two major methods are developed for their extraction. The most former method is the explant technique. It consists to put a fragment of biopsy in nutritive medium, and let cells to migrate. Then, sequential action of trypsin will permit to harvest different cells with distinct adhesion properties. The other way is the enzymatic technique which consists to detach the urothelium from basal lamina, undergoing matrix extracellular protease action (thermolysin, dispase, collagenase IV) [21, 22]. This last method is faster, led to a suitable yield and a good purity. Finally to obtain enough cells, an amplification stage must be engaged. Generally, epithelial medium is used and supplemented with serum or/and specific growth factor (e.g. epithelial growth factor).
Smooth muscle cells were first described in 1913. In the same manner of urothelial cells, the two approaches could be used for extraction [23]. In the case of enzymatic treatment, the collagenase will be used to digest the extracellular matrix, made of collagen I principally, to liberate these cells. In the amplification stage, it is important to know that the serum percentage could modify the phenotype (contractile or secretory) and the functional property (electrophysiological) of these cells [24-26].
Endothelial cells are more and more frequently extracted and used for bladder reconstruction. Indeed, after transplantation the graft need to be rapidly vascularized to survive in vivo. Endothelial cells could organize themselves into capillary or secrete angiogenic factors which could improve a certain inosculation between the substitute and the host vasculature [27]. Some teams harvest endothelial cells from human umbilical vein (HUVEC), what asks ethical question, and other achieve these cells extraction from bladder microcapillaries which appeared more physiological for the elaboration of the vesical substitute. In this last case, enzymatic treatment could be used and the harvested cells must be purified with beads coupled with a specific endothelial marker (e.g. PECAM-1) [21].
In some situation the bladder is too affected and no healthy cells could be harvested to elaborate a tissue-engineering substitute. So, stem cells could represent a serious alternative and major avenue in the regenerative medicine. These cells are characterised by their capacity to maintain themselves by symmetrical division. But in a second phase, asymmetrical division occurs and leads to a daughter stem cell and a daughter differentiated cell. This last event makes difficult the in vitro preservation of stem cells and the constitution of an usable stock.
Embryonic stem cells are pluripotent and therefore can evolve into cells of all three embryonic layers (ectoderm, mesoderm and endoderm). The method of culture to enable specific differentiation pathways are not yet discovered, but the in vivo benefits have already been shown [28-29]. Unfortunately, their aptitudes to initiate teratoma, the need of genetic donor-host match to avoid immune-rejection and their potential illegal and non-ethical character compromise their clinical use.
Autologous stem cells could resolve these limitations. They present a low possibility of tumor malignancy and an exact histocompatibility. These cells niche within many adult tissues, in order to maintain homeostasis during tissue turnover and repair. However, they present lower proliferation capacity and plasticity which restricted their use.
Induced pluripotent stem cells appeared in 2006 and consist of reversion of differentiated cells into stem cells [30]. The reprogramming of adult cells requires the introduction of specific transcription factors (Oct4, Sox2, Klf4 and Myc), which allow to acquire differentiation potential comparable to the embryonic stem cells [31, 32]. This ethical approach provides an easy and important cell sources for clinical application. However, even if a major risk of cancer has been corrected [33], epigenetic changes not yet entirely documented.
Once the cells have been obtained, they must be seeded onto a support (Table 3). The scaffolds are not only a physical support, but also supplier of biochemical information. It is difficult to encourage an appropriate in vitro cellular behaviour because spatial and temporal evolutions occurred during organogenesis. The complexity of extracellular matrix sequentially increases from morula to blastocyst stage [34, 35], and the signalisation between cells and extracellular matrix proteins change in a dynamic way [36]. In the present state of our knowledge, laminin is firstly synthetized to allow cellular adherence, while collagen IV and fibronectin appear more latter to initiate the cellular migration [37]. In a second phase, these extracellular matrix proteins form an organized matrix, the basal lamina, which is essential for the development of specialized tissue like epithelium [38]. Thus, tissue engineering must tend to create a controlled cellular microenvironment, taking into account the physiological process, to reach the experimental organogenesis goal. In another hand, scaffolds must offer comparable physical properties and have the capacity to confront the same mechanical strain. In the case of vesical repair, the substitute must combine resistance with elasticity to adapt itself to cyclic pressure caused by bladder filling and emptying. The scaffold biocompatibility is the starting point of material choice, and many products have been experimented with a clinical application point of view.
\n\t\t\t\t STEPS | \n\t\t\t\n\t\t\t\t DESCRIPTION | \n\t\t
Harvesting bladder cells | \n\t\t\tVery small biopsy is taken. | \n\t\t
Cells amplification | \n\t\t\tProtocols exempt of biological risks. | \n\t\t
Assessing cells into a support | \n\t\t\tSeeded cells must be functional and located at their physiological area. | \n\t\t
Surgical implantation | \n\t\t\tThe substitute must be functional before the bladder repair. | \n\t\t
General procedure in bladder reconstruction field.
Autologous tissues have been tested for bladder repair before the standard use of intestinal segment in the beginning of the eighties [1]. The skin, the omentum, the stomach, the pericardium have been used with very limited success [39-42]. Indeed, the epithelium of these tissues is not specialized in watertight function. So, the direct contact between the non-urological tissues and the toxic urine leads mainly to the formation of fibrosis and the contraction of the graft [43, 44].
Acellular tissue matrices represent a growing interest in the urological regenerative medicine. They are prepared from native tissue with a decellularisation and sterilisation process [45]. The purpose is to abolish immunological potential by discarding cells with physical, enzymatic or chemical protocols [46]. This materials offer the advantages of mechanical and biochemical environment ideal for the cellular recognition. Their matrix architecture is relatively preserved and the physiological organization of extracellular proteins can generate appropriate signalling to induce a suitable cellular behaviour [47]. Unfortunately, the decellularisation and sterilisation protocols include offensive biophysical and biochemical elements (temperature, pH, ionic detergents) which can denature extracellular matrix proteins and damage the physiological environment [48]. Compared to other scaffolds, the ability to provide a nutritive supply by neovascularization after the graft, and therefore to promote the graft survival constitutes an attractive advantage which justifies the choice of acellular matrices [49, 50]. Small intestinal submucosa (SIS) [51] and bladder acellular matrix graft (BAMG) [52, 53] are the most tested for bladder reconstruction in animal models. Microscopic analyses generally show a relative cellular organization, probably due to the presence of growth factors [54]. But functional tests such as watertightness or compliance are very seldom evaluated.
Concerning SIS, studies are conflicting. Some experiments describe the benefit to use SIS with contractility testing and immunostaining analysis [18], while other report fibrotic scarring observations and contraction during in vivo bladder augmentation in canine model [55]. Histologically, the urothelial and smooth muscle cells seeding led to a suitable adherence but without cellular maturation. This lack of regenerative potential could be caused by an absence of the appropriate extracellular proteins-cells communications, due to the fact that intestinal and bladder matrices are not similar [56]. It is known that extracellular matrix composition and structure presented by the bladder basal lamina have an impact on urothelial cells behaviour [57]. This is why bladder acellular matrix graft (BAMG) has been also tested. However, porcine bladder augmentation with a seeded BAMG demonstrated a local cells infiltration which remained limited in the periphery [58]. The insufficient cellular organization resulted in calcification process within the graft and its shrinkage. This incomplete cellular migration within the BAMG could be attributed to the decellularisation treatment, because it was reported that laminin and fibronectin are not preserved [59]. Thus, even if urological cells are placed into a familiar environment, the alteration of matrix proteins and the removal of intrinsic growth factors do not permit an optimal cellular signalisation [60]. Moreover, the disruption of the extracellular matrix compromises the specific architecture and leads to the loss of mechanicals properties, such as elasticity or resistance [61]. Optimization of these protocols is in progress and the damages caused by the preparation of decellularised tissue tend to be corrected [62, 63].
Intestinal segment and bladder wall are richly vascularized tissues, and this specificity is not negligible for the survival of the graft. However some parameters limit the clinical use of BAMG and SIS such as their xenogeneic origin and the associated risks of contamination by pathogens. Generally, the matrix proteins are highly conserved between the different species and seem to be non-immunogenic but an epitope, which is present in many species except human and a category of monkeys, was found in marketed SIS extracellular matrix [64]. Numerous postoperative inflammations have been reported [65] and in vitro DNA residues have been detected [66]. Because of their biological nature, the acellular tissues constitute a great potential for bladder reconstruction but the protocols of preparation must be improve to better preserve the extracellular matrix composition/architecture and to remove effectively any cellular fragments [67].
Synthetic polymers are made of chemically assembled macromolecules and could have different physical properties (thermoplastics, thermo-hardenings and elastomers). The use of synthetic scaffolds, supported by the capacity to deliver any three-dimensional shape at low-price, would allow to overcome the lack of native tissue available for transplantation. Each characteristic of this type of material can be controlled. The hydrolysis degradation of synthetic substitutes is important in the context of organ repair. The material used for bladder reconstruction must remain stable until the organization of seeded cells and the migration of surrounding cells. But during the terminal tissue remodelling, the substitute degradation must follow the tissue regeneration. The degradation rate of synthetic materials can be determinate by the molecular weight and the nature of biopolymer used for copolymerisation. Then the degraded fragments can be treated by the metabolic pathways [68-70]. The size of pores can also be modulated in order to influence the cellular migration, vascular invasion, and diffusion of nutrients, waste and oxygen [71, 72]. The cell adherence and growth can be enhanced by synthetic support, as shown for the reconstruction of different damaged tissues [73]. But in the case of bladder substitute, the in vitro evolution of seeded urologic cells into a mature cellular tissue has not yet demonstrated. There are fundamental differences between synthetic and biological molecules. The size range of fibers, their biophysical and biochemical properties are not comparable, and the challenge for these supports is to enhance a suitable interaction between cells and synthetic microenvironment, in spite of the dissimilarities existing with the physiological context.
Silicone, polyvinyl sponge and teflon, have been firstly tested for bladder reconstruction with the help of synthetic materials [74-78]. The advantage was to construct neobladders in a reproducible way, but the poor cytocompatibility, the lack of vascularization and their immunological potential led to significant complications. Because of the absence of cellular development, and urothelial cells particularly, the direct contact with urine caused the formation of fibrosis and contraction of the alloplastic graft.
The more recent synthetic polymers including poly(ethylene glycol) (PEG), poly l-lactic acid (PLLA), poly(lactic-co- glycolic acid) (PLGA), poly(ε-caprolactone) (PCL), and polyurethane (PU), are used to pursue the bladder tissue-engineering research [79]. Few successes have been reported, but like in the case of acellular tissue matrices, it has been shown that the cell seeding play an important role concerning the graft integration [19]. This experience of canine bladder reconstruction have been led at mid-term with PGA scaffold coated with PLGA, and contrarily to the seeded synthetic substitute, contracture and inflammatory response have been observed with free scaffold one month post-transplantation. In spite of association of urothelial cells with a high proliferative capacity when urothelium is damaged [80], the surrounding cells of the host do not migrate in the whole surface of tissue-engineered bladder. The only one microscopic result demonstrated a well development of an urothelial tissue onto the seeded scaffold, with the presence of muscle bundles, but no analysis was led to assess the degree of urothelial maturation or the contractility function of smooth muscle cells. The potential of synthetic materials to support urothelial differentiation have not been proven yet. The same team have combined collagen with their PGA scaffold to lead bladder augmentation in patients with end-stage bladder disease [81]. The strategy is to supply a three-dimensional shape and mechanical resistance with the help of PGA, and to induce a cellular signal with the help of the collagen. It was shown that the biological activity provided by collagen improve the cellular propagation and development of seeded urothelial and smooth muscle cells. Additionally, omentum was used as a vascularization bed to support the graft survival [82]. Even if significant improvement of vesical capacity has been shown for only one of the seven patients, great strategic progresses have been made to initiate the elaboration of a composite scaffold able to communicate with cells and enhance their appropriate and terminal development. The scale of cellular environment and signalisation induced by specific protein sequences have been taking into account with the advent of biotechnologies.
The nanotechnologies, which emerged in the last decade of the twentieth century, are defined by specific functions induced by the nanoscale dimension or the nanoscale organization of a material [83]. This characteristic could permit to overcome the problems encountered with the classic synthetic substitutes made of micrometer scale elements. The interest to include nanometer elements in the composition of synthetic scaffolds is to reproduce the scale of the size of native extracellular matrix proteins, and better manage cellular behaviour [84]. Recent researches demonstrated the effect of roughness surface, comparable with the roughness of the native bladder, on smooth muscle cells adhesion and urothelial cells development [85-87]. On another hand, the surface of synthetic materials could be modified with different chemistry, topography or roughness parameters, to improve the interaction with proteins. Thus, extracellular matrix proteins could be added to the scaffold in order to enhance the cellular interaction and to tend toward natural signalisation. Recent publication reported that vitronectin adsorption is improved by 20% if the roughness of synthetic surface is augmented with nanotechnology process, compared to nanosmooth surface [88]. A concrete example is illustrated by the increase of fibronectin adsorption onto synthetic material, because of the augmentation of roughness surface by adding carbon nanotubes and without changing the chemical properties.
Smooth muscle cells phenotype is affected by the nanometer topography of synthetic surfaces. This phenomenon was illustrated by recent works. One of them reported the elaboration of PLGA/PU materials with different feature dimensions. It is appeared that more the features size is comparable to the nanometer scale, like the extracellular matrix proteins, more the adhesion of bladder smooth muscle cells is improved [85]. A new chemically etching technique, which breaks ester and ether bonds via NaOH and HNO3 treatments, was tested by the same team to convert synthetic surface from micrometer to nanometer scale [89]. It was shown that this chemical treatment can generate nanoscale features on various synthetic surfaces (PLGA, PCL, PU), and then enhances the functions of bladder smooth muscle cells, compared to the conventional nanosmooth polymers. It is noted that micron, submicron and nanostructured polymers was generated with this same chemical protocol, and the development of bladder smooth muscle cells have been improved on the nanostructured surface, independently of a chemical action. So, any type of synthetic scaffold could be nano-engineered and promote bladder smooth muscle cell functions, such as elastin and collagen secretion [86]. Further studies demonstrated that the direct action of nanometer and submicron scale surface features is to promote the adsorption of proteins from serum present in culture media. Therefore it seems that the bladder smooth muscle cells behaviour is more directly improved by this serum proteins coating rather than the synthetic nanostructured environment [90, 91]. These observations lead us to believe that the next generation of synthetic substitute could be grafted with soluble proteins in order to ameliorate the cellular signalisation.
Urothelial cells growth is also affected by the roughness of synthetic surfaces [87]. With nanometer rough synthetic surface, results show the improvement of adhesion and proliferation of urothelial cells, and also the reduction of calcium stones, often noticed with conventional synthetic materials. In vivo studies were performed in rodent model and confirmed the benefits showed with bladder smooth muscle cells. But nanostructured synthetic scaffold did not resist the contact with urine, leading to post-graft bladder leaks [92]. Further optimizations must be proposed to induce cellular differentiation. Fibronectin is recognized to induce cell migration, laminin for its adherence potential, therefore synthetic scaffolds will be completed with bioactive nano-elements. Protein sequences implicated in cellular signalisation will be used such as RGD peptide, a cell adhesive integrin-binding peptide found in most of extracellular matrix protein [93]. The development and maturation of seeded cells must be evaluated at longer term, while in vivo testing will occurred throughout animal models more comparable to human (the porcine urologic system is the nearest of human [94]).
The natural and synthetic materials have their own characteristics (Table 4), specific bioactive elements for the first and processing reproducibility for the second. The advances deserve a particular attention even if these experimental scaffolds could not be recommended at that time for clinical application. Acellular matrices present the risk of incomplete decellularisation and variability of biological activity. While synthetic materials are too far from the composition and architecture of physiological extracellular matrix. But one of the common disadvantages of these two models is the possibility of immunological response in vivo and therefore a graft rejection.
\n\t\t\t\t BIOMATERIALS | \n\t\t\t\n\t\t\t\t CHARACTERISTICS | \n\t\t
Non autologous natural matrices | \n\t\t\t+ Biologically organized tissue. | \n\t\t
Synthetic matrices | \n\t\t\t+ Control of physical properties. | \n\t\t
Autologous matrix | \n\t\t\t+ Limitation of immunoreaction. | \n\t\t
Types of engineered bladder substitute.
Autologous and functional substitute represents the ideal alternative to avoid immunosuppressive therapy and to enhance the in vivo regeneration. The tissue-engineering field proposes a new approach to attain these objectives: the self-assembly method [95]. This technique is based on the use of the own cells of patient and their capacity to differentiate in vitro in order to form a mature tissue. At the Laboratoire d’organogénèse expérimentale (LOEX) many autologous substitutes are elaborated with controlled culture conditions and without the help of exogenous biomaterials. Human cornea [96], psoriatic skin model [97], microvascularized tissue-engineered skin substitute [98] has been developed for clinical repair or pharmacological investigations. Based on this method, an autologous vesical tissue was elaborated with a view to future clinical bladder repair/augmentation.
A minimally invasive preoperative technique was developed to extract the bladder cells from the same small biopsy. Enzymatic method allows the harvesting of bladder cells with high purity [21]. Fibroblast, urothelial, endothelial and smooth muscle cells can be grown in the laboratory setting. Appropriate growth factors (e.g. epidermal growth factor for urothelial proliferation or vascular endothelial growth factor for endothelial cells) permit a good cellular expansion and the constitution of sufficient cellular bank.
The preparation of engineered vesical tissue begins with the elaboration of matrix support [99]. In presence of ascorbic acid [100, 101], fibroblasts have the ability to synthesize and assemble their own collagen fibers, and form an extracellular matrix layer which could be manipulated. The autologous matrix layers are superimposed to provide a sufficient mechanical resistance and to create a three-dimensional biological environment. It is known that mesenchymal-epithelial interactions play critical role in tissue development [102-105]. In the urological tract, mesenchyme regulates epithelial maturation and functional activities, while epithelium also contributes to the mesenchymal cells differentiation [106]. This is why the self-assembled scaffold is made of a specifically organized extracellular matrix where cells can develop themselves with appropriate biological signalling. Urothelial cells are seeded on the top of fused matrix layers and cultivated until they have proliferated on the whole surface, then we induced epithelial maturation with the use of the culture at air/liquid interface (Figure 2).
The self-assembly method (A) used to elaborate the engineered bladder tissue (B).
Masson’s trichrome staining displayed a homogenous distribution of collagen I and the covering of stratified urothelium was roughly similar to a native vesical mucosa. Cytokeratin 8/18 staining confirmed the well widespread of a stratified urothelium, and claudine-4 staining demonstrated the presence of tight junctions which are important to avoid urine infiltration. More interestingly, the permeability evaluation at urea was performed on the reconstructed vesical tissues and their watertightness profile is comparable to the native bladder. Conversely, the permeability test realized on self-assembled matrix, devoid of reconstructed urothelium, showed a fast diffusion of urea. This result supports the necessity to have a mature urothelium, in order to avoid urine extravasation, followed by in vivo necrosis and fibrosis of tissues. An attention was paid to the endothelialization of the substitute in order to encourage the post-graft survival. LOEX laboratory obtained a rapid inosculation between a capillary-like network of reconstructed skin and the host vasculature [6]. Thus endothelial cells, harvested from bladder microcapillaries, can be added before the seeding of urothelial cells, and cultured in order to form microcapillary-like network within the self-assembled substitute. The endothelialized vesical substitute displayed an also good watertightness profile than the native bladder, and mechanical properties were acceptable to allow suturing. The potential limit of this method is the incertitude to dispose of healthy bladder cells, especially in a case of end-stage disease. This is why the question concerning the getting of an appropriate source of cells remains in reflection, but in some case, urological cells could be harvested from upper segment of urethra because of its sharing of the same embryologic origin with the bladder [107]. The self-assembled vesical model still must to be completed and tested in vivo, but its autologous character and its efficiency as a barrier to urea are essential properties to tend toward an ideal substitute for bladder augmentation.
In regenerative medicine domain, the goal of tissue engineering is to deliver a functional substitute. It consists in obtaining specific cells with sufficient purity and quantity, and inducing their differentiation in order to ensure their biological role. Self-assembled extracellular matrix provides both a physical and informative support for urological cells, but the control of cellular proliferation/differentiation balance deserve to be better taking into account. Several studies reported an altered maturation of urothelial cells in vitro, particularly a defect of uroplakins synthesis [108] and their incomplete assembly at the apical surface of urothelial cells [109, 110]. The pathway of differentiation is induced by defined intracellular signals. Transcription factors such as Fox-A1, PPARγ and RXR, have been identified as being involved in the expression of proteins implicated in the urothelial functions [111]. The bladder is subjected to different pressure during the emptying/filling cycle, and the cells are constantly exposed to mechanical stresses (e.g. hydrodynamic strength) [112]. It was shown that mechanical stress acts on survival, migration and proliferation of bladder cells [113-115]. More accurately, cyclic hydrostatic pressure seems to promote uroplakin trafficking/maturation [116-118], and to influence the growth of bladder smooth muscle cells by activating Rac1 signaling pathway [119], or their proliferation via the PI3K activation [120]. Even if the molecular mechanism acting under cyclic pressure remains not elucidated, the conviction that physiological stimulations would be required for the differentiation of bladder cells cultured in vitro is more and more evocated in the literature [121-123].
In the beginning, mechanical stimuli were included in cellular culture protocols and interactions between cells or between cells and extracellular matrix proteins were analyzed [124, 125], but physiological conditions were not yet investigated. In 2008, the mimic of bladder filling and emptying was tested through a bioreactor which applies hydrostatic pressure waves in a cyclic way [126]. Porcine BAMG was used and the expression of extracellular matrix proteins was more elevated under dynamic condition. This result is encouraging for acellular matrix application. Indeed, acellularisation treatment deteriorates the matrix architecture and the obtained tissue after treatment had a too high porosity [127]. Because of its property to support cell proliferation and migration, hyaluronic acid could be used in static regime to decrease the porosity observed after the acellularisation process [128], but this step could be replaced by placing the reconstructed substitute under physical stress. The urothelial cells were also influenced since mechanical stimulations induced the increasing of uroplakin II expression. The effects of physical strain must be studied in more details because gene expression does not constitute sufficient information, since the protein functionality depends on its complete synthesis, its good folding and its appropriate localization. But these preliminary results encourage the integration of mechanical phase in the process of engineered bladder. This is why we designed a bioreactor which is scheduled to reproduce the physiological intravesical pressures at the fetal stage, and replace the air/liquid phase used for our self-assembled model. Briefly, our self-assembled vesical tissue is placed between two chambers, with urothelial side face to the pressure chamber. To mimic the low pressure maintained during filling phase, 5 cm H2O is applied during few hours. In the last hour the pressure slowly increase until 15 cm H2O, and then decline quickly to zero in a few seconds in order to simulate the voiding and complete the urination cycle. Compared to static condition, short-term dynamic culture significantly improves the urothelial development and the watertightness profile of the self-assembled substitute [129]. These results are in conformity with outcomes related in our dynamical engineered urethra which displayed an increase of uroplakins immunostaining at urothelial cells surface [130]. Whatever the substitute model, the mechanical stimulations must take more importance within protocols of in vitro bladder reconstruction. When must the dynamic phase intervene? How long time must it intervene? Should the pressure cycle follow a constant scheme or must it evolved during the process? Better understanding of bladder cells mechanotransduction may ameliorate the setting up of a dynamical environment appropriate to the reconstruction of a mature and functional vesical tissue.
Bladder exposition to diverse pathologies could jeopardize its function of elastic and watertight reservoir. To date, the clinical technique for bladder repair is associated to a high level of morbidity. Based on the well documented post-operative complications, it is appear that the ideal bladder substitute must combine the compliance conferred by the nature and architecture of the matrix support, with a urinary barrier provided by the differentiation degree of urothelium. Natural and synthetic scaffolds were investigated to reproduce the bladder abilities and some successes were furthered the urological tissue-engineering domain. But due to their poor mechanical stability, immune responses, and incomplete cellular maturation, these models remain insufficiently developed to be used in clinical application. At present, teams which support the acellularised or polymeric substitute are working on the next generation of engineered bladder model. For example, nanodimensional surface features would be included in order to imitate the nanometer topography of native tissue, and therefore, to enhance interactions between bladder cells and the proposed environment. Among all biotechnologies, the self-assembly method proves to be a promising approach to elaborate a vesical substitute comparable to the structure and function of native tissue. The good watertightness of reconstructed mucosa and its autologous character will permit a suitable integration in vivo, and promote the cellular expansion. The application of appropriate culture method, such as dynamical regime, will lead to the maturation of the reconstructed connective tissue and its urothelium. The capacity of the self-assembled tissue to be pre-endothelialized might avoid the necrosis of the graft attributed to the lack of synchronized neovascularization. Another aspect which is rarely taking into account is the capacity for a graft to growth with pediatric patient. The self-assembled tissue is made of autologous cells only, and constitutes a serious alternative in the urological tissue-engineering field. Research continues its efforts to optimize the different reconstructed substitutes, and agree the necessity to evaluate them at long-term through bladder with specific dysfunctions.
The authors thank Kenza Bouhout for her useful discussions and her participation in the illustration of this chapter.
The biometrics is a Greek word divided in to two parts “bio” means life and “metrics” means measurements. Biometric science is an old science concerning the documentation of the features or bio measurements or identification characteristics of the targets which could be human, animals and even fossils. It has been used to describe and record the measurement and biological data for, both animal and human (tracking of the similarities of life forms). It is based on anatomic uniqueness of an individual and specificity of physiological and behavior characteristics. Biometrics approach based on behavior characteristics is less expensive and less dangerous for the user; while physiological approach offers highly exact of identification. However, both kinds provide high level of identification than others like passwords and cards.
In general, biometrics were applied in different platforms [1] as follows.
Criminalistics (using of biometric identifiers to recognize victims, unknown body and prevent kidnapping for identified children).
Marketing (using of biometrics to identify owners of loyal cards)
Time accounting systems at work, schools, etc.
Security systems (to control the access to the rooms and the internet resources)
Voting system (to identify/authenticate a person who takes a part in voting during the functionality of voting system).
It used as apart in passport informations as an international required by various organizations such as demands ICAO standards which involve biometrics in passport.
Biometrics identifiers are used also for registration of immigrants and foreign workers among immigration Affairs. It allows identifying people even without documents.
In animal, a biometric identifier or measurable could be found as robust and distinctive physical, anatomical or molecular trait that can be used to uniquely identify or verify the claimed identity of an animal [2]. Among the advantages of biometrics usage, it does not cause pain or change in the appearance of organisms. For this reason and others, this chapter focuses on the biometrics in animals particularly aquatic organisms. Their analysis can be considered as a first step to investigate the stock structure with large population sizes. The morphological differentiation of partially-isolated stocks due to environmental differences in the habitats could be known as phenotypic markers [3]. The interactive effects of environment produce morphometric differences within a species, variability in growth, development, and maturation creating a variety of body shapes within a species [4, 5, 6]. Hence, it is necessary to identify specimens correctly and investigate other biological traits as growth, mortality, fecundity, trophic relation, parasite relationship, historical and paleontological events [7]. The biometric measurements could be applied on different aquatic organisms as sharks, Rays, Mollusca, Crustaceans, Protozoa, etc. and even for different organs like teeth, otolith and appendages.
It is well known that morphology is directly related to species life history and habitat use. Thus, fish morphometric analysis represents an important tool to determine their systematic, growth variation, population parameters and environmental relationships [8, 9, 10]. It also, covers several fields of research such as: ecomorphology evaluating the role of environmental pressures on shaping species diet, feeding behavior, ecological strategies, niche partitioning, habitat use and trophic structure population ecology and metapopulations studies, investigating differences in body shape among populations spatially isolated [9, 10, 11, 12]. In addition to that, males and females of the same species may be identified as different species because the intraspecific characteristics, therefore information about morphological sexual variation is important to avoid species misleading identification [13, 14, 15, 16]. Moreover, the sexual dimorphism is an important evolutionary adaptation mechanism, and to diminishing intraspecific competition by increasing niche portioning [16, 17]. It establishes the relationship between morphology and behavior, elucidating possible ontogenetic niche shifts and the evolutionary plasticity of an organism [18].
Many biologists and taxonomists are still studying the external biometrics (morphometric and meristics) of the organisms in various research fields, even with the presence of molecular biology techniques, giving faster, and low-cost results [19, 20, 21, 22, 23].
From another view, the species identification and population discrimination are important in the biodiversity conservation, natural resources, and fisheries management. In certain cases, particularly when we lost some biometric characters for species identification due to sampling and handling processes, we need intensive measurements. So, the modern morphometric technique needed to be applied; as truss network technique (Figure 1); it is applied to provide supplementary taxonomic information to enhance the species identification. It could be used also in case of unclear diagnostic characters available for the identification of species as in ariids species which have overlapped characteristics among several species. This technique was provided by Turan et al. [24] and Abdurahman et al. [25]. In addition, the implementation of biometrics could be applied on the internal parasite and used as species identification of host and as a sexual dimorphism indicator [26], the later author studied the impact of Sacculina sp. parasites, Rhizocephalans (Sacculinidae) on two host crabs
Truss network distances of ariids family. A: snout to first dorsal fin; B: snout to pectoral fin; C: pectoral fin to F. dorsal fin; D: origin of dorsal fin to pelvic fin; E: pectoral fin to end of dorsal fin; F: origin of dorsal fin to E. dorsal fin; G: pectoral fin to pelvic fin; H: end of dorsal fin to pelvic fin; I: end of dorsal fin to F. anal fin; J: pelvic fin to F. adipose fin; K: end of dorsal fin to F. adipose fin; L: pelvic fin to F. anal fin; M: first of adipose fin to F. anal fin; N: first of adipose fin to E. anal fin; O: anal fin to E. adipose fin; P: length of adipose fin; Q: length of anal fin; R: end of adipose fin to E. anal fin; S: end of adipose fin to caudal fin; and T: end of anal fin to caudal fin.
Sexual dimorphism is an important to distinguish males and females. Paiva et al. [30] studied the ontogenetic sexual dimorphism of
a. Photographs showing
In this example, it is another application of biometrics on other category of biota “cephalopoda,” the morphometric characters of male and female
The different morphometric measurements of
The another biometric differentiation was used also for sexual dimorphism of three carangid species (
Schematic illustration of measurements taken on the body of the Three Carangidae Specie considered from the southern Red Sea, Hurghada, Egypt. 1. total length (TL); 2. fork length (FL); 3. standard length (SL); 4. body depth (BD); 5. head length (HL); 6. eye diameter (EyD); 7. snout length (SnL); 8. postorbital length (POL); 9. upper jaw length (UJL); 10. curved lateral line segment length (CLL);11. straight lateral line segment length (SLL); 12. soft dorsal fin base length (SDFL); 13. soft anal fin base length (SAFL); 14. soft dorsal fin height (SDFH); 15. soft anal fin height (SAFH); 16. pectoral fin length (PFL); 17. distance between the first soft dorsal fin ray and the first soft anal fin ray (SDSAFL); 18. distance between anal and dorsal fin insertions (ADFEL); 19. distance between the first spine of the dorsal fin and the first soft anal fin ray (SpDASFL); 20. distance between the first soft dorsal fin ray and ventral fin origin (SDVOFL); 21. distance between the first soft dorsal fin ray and the insertion of anal fin (SDEAFL); 22. distance between the insertion of dorsal fin and the first soft anal fin ray (EDSAFL); 23. predorsal fin length (PRDFL).
The biometric investigations play a role in the field of parasitology and micro examinations. Golemansky and Todorov [34], studied the morphology and biometry of eight marine interstitial testate protozoa, amoebae (
Another example for using the biometrics, is its application for certain parts like fish scales, since its morphology and ultrastructure characteristics are important for fish identification, taxonomy and phylogeny. The biometrics were applied on the scale morphologically and also on the electron scanning picture of
Schematic drawing scale of
(a and b): Scanning electron micrographs show scales of
Jawad et al. [36] applied the biometric characteristics on another part such as otolith of two species of parrotfish, family Scaridae, from the Red Sea coast of Egypt. It was applied to identify the most appropriate taxonomic characters that compare or separate these species. Ontogenetic changes in the otoliths of the two scarid fishes become evident. In the otoliths of
a. Mesial surface of the left otolith of
The understanding of normal morphology of larvae is very important in aquaculture especially in hatcheries, to evaluate culture conditions for the juveniles and adults. The morphology is an indicator of the abnormalities in the larval morphology in relation to water quality, for production the high-quality individuals [37]. The later author described the allometric growth of Sea bream larvae reared under intensive and extensive conditions, and examined the effect of these conditions on their morphometric proportions; they stated that the intensive marine hatcheries may face many rearing conditions that may reduce the quality of the reared fish, compared to that of the wild ones. These may result in the absence of a swim bladder [38]; osteological and morphological malformations [39], and extra……. The abnormalities in aquatic animals can influence the biometric features, from the modern methods is x-ray utilization, it was applied on three fish species collected from Jubail Vicinity, Saudi Arabia, Arabian Gulf [40] and presented in (Figure 9).
The biometrics were used as comparative tools for species from different habitats and evaluate the effect of environmental conditions. Farrag et al. [20] investigated the biometrics and meristics of puffer fish species
Using hard parts as spines; the spines are also used in comparison and identification depending on its biometrics and structure. Jawad et al. [13] described structure of the pectoral fins spine of 4 catfish species
Left and right pectoral fin spine of
The enlarged left pectoral-fin spine of
Biometric methods have therefore been developed to recognize animals based on physical characteristics or behavioral signs. Some of these methods have been used for some time for reliable identification of humans. An animal biometric identifier is any measurable, robust and distinctive physical, anatomical or molecular trait that can be used to uniquely identify or verify the claimed identity of an animal [2].
Sharawy et al. [32] have identified some Penaeid shrimps from Mediterranean, Egypt by different methods. Among them, the authors have applied the biometrics firstly to be correct way to advanced methods or following one. Three penaeid species
a. Carapace of green tiger prawn
The Photographic identification is among biometric methods, it has been used since the 1970s to identify aquatic animals such as dolphins and whales [41]. Individual bottlenose dolphins can be identified by comparing photographs of their fins, which display curves, notches, nicks and tears (Figure 14). Whales can be distinguished by the callosity patterns on their heads [42].
Dorsal fins of bottlenose dolphins displaying unique permanent characteristics used for their identification (© 2007 Dolphin Research Center, 58901 Overseas Highway, Grassy Key, FL 33050-6019, USA.
The photographing and its treatments using technology used in wide range particularly for wild animals. The most obvious biometric marker is the coat pattern of animals which often appears on major body parts as colourations of either fur, feathers, skin or scales. For example, zebras and tigers can be identified from their stripes; cheetahs and African penguins carry unique spot patterns and snakes have colored rings [28]. From another side, the photographing may face some problem. Problems may occur in the field in different light settings or surroundings, but new techniques including digital photography and video filming have reduced these difficulties. Digital images can also be manipulated to make recognition easier. The method is cheap and at its simplest needs no more than paper and pencil. In addition, observations can be made at a distance, reducing the risk of stress and altered behavior.
This is another application for morphometric characteristics used to evaluate the growth of species. This was applied on blue swimming crab
The morphometric measurements in
The application of the morphology and morphometric was also used to characterize the parasites. It was applied on
Line diagram of adult
The biometrics now play an important role in computer analysis of the pictures. The retinal vascular pattern is another biometric trait in animals. The retinal vessels seem to like branching patterns, which are present from birth and do not change during the animal’s life. The blood vessels in the eye of each individual can be detected using a retinal scanner. This pattern can be recorded with a hand-held device about the size of a video camera. Some devices can also measure GPS coordinates that used when marking cattle and can be compared to nose-prints. The method is also relatively cheap. Retinal imaging and nose-prints of sheep and cattle were compared by Rusk et al. [45]. However, the nose-prints are a quicker method than retinal scanning, but retinal scans are easy to analyze for inexperienced operators [46]. Computer software for the analysis of digital pictures from both retinal scana and nose-prints makes analysis faster, cheaper and more reliable.
The movement pattern is sometimes used as identifier for aquatic animals by analyzing their movement patterns using a tri-axial accelerometry device [47]. By measuring the movements of animals in three dimensions, their movement patterns can be stored and these can be used to diagnose aberrant behavioral patterns, such as those associated with infections. Accelometery may have the potential to be a powerful tool to produce maps for conservation purposes, where animal movements can be plotted.
This trend was mentioned by Kumar et al. [48] through recognition systems and this contains different points. For example, the low-Cost Cattle Recognition System Using Multimedia Wireless Network, this system is proposed for verification of individual cattle based on its muzzle point image pattern using wireless multimedia networks. The images are captured using a 20-megapixel camera (system configuration: 14.48 centimeters (5.7-inch) IPS capacitive touchscreen with 1440 × 720 pixels resolution and 283 ppi pixel density, 4GB RAM) and transferred them to the server of cattle recognition using Wi-Fi communication technology. The system performs the image pre-processing on the captured muzzle point image of individual cattle. It mitigates and filter the noise from the captured images and increases the quality [48]. This system could be applied also on the aquatic animals.
The system takes the visual biometric feature characteristics such as coat pattern, body coat pattern, and spot point pattern, and other visual features of species or individual animal. The major issue and challenges of visual animal biometrics-based recognition systems are demonstrated as follows.
How do species or individual animal gets its body coat pattern? [27].
What type of suitable algorithms and animal biometrics recognition systems or frameworks is available to compute the visual features from the body coat pattern of species? [27, 28].
Can detection and representation of visual feature of body pattern of species be possible in their habitats? [28].
How visual animal biometrics-based recognition and framework can monitor animal population? [28].
How visual animal biometrics-based recognition system generates unique templates from stored visual biometric feature of species? [27].
Knowing the variations between different organisms and different shapes, therefore should have measurements according to kind of organisms, (Shark, rays, bony fish, crabs, etc).
It will be better to take the biometric measurements for fresh samples to avoid any error due to preservation or damage in samples. In case of formalin preservation, some changes may happen especially in coloration. So, the more measurements are preferred to be considered.
In case of comparative study between different habitats, it is preferred to fix the measurements and inputs like length range to avoid bias due to changes in ecological conditions.
In case of applying biometrics on the internal parts or using scanning techniques, the accuracy, resolution and magnification should be considered.
In case of using some tools like sensors, it should be easily presented to a sensor and converted into a quantifiable format, should not subjected to changes over time and should differ in the patterns among the general population, the higher the degree of distinctiveness, the more unique is an identifier.
Biometric methods should not cause pain and do not alter the appearance of the animal, having no effect on the behavior and survivability of the animals, except in some necessary as repeated capture and/or handling.
In case of visual patterns methods, some species have external characteristics as color, spots, rings, that are easy to recognize and that are specific for each individual. These patterns can be used by photographing using high resolution of digital camera to avoid the problems that may occur in the field in different light settings or surroundings.
Many common marking procedures also involve tissue damage and therefore cause pain, such as branding (heat, cold or chemicals), tattooing, toe clipping, ear notching and tagging.
Wearing a mark may alter the animal’s appearance, social interaction, other behaviors and ultimately its survival.
In visual animal biometrics for computer treatment purposes, various issues and challenges lie in coping with unconstrained environment such as variable lighting, partial occlusion of animal body, and extr…. the captured data sets, images, videos are required to train various computer vision models, framework, and methods.
The followings are summarized guide for general outer measurements and descriptions that could be taken for various forms and examples of some aquatic organisms including crustaceans, fishes, reptiles and some marine mammals (Figures 17–24).
General morphometric measurement and description of the common form of crabs.
General morphometric measurement and description of the common form of bony fish.
General morphometric measurement and description of the common form of cartilaginous fish.
General morphometric measurement and description of the other form of cartilaginous fish (skates).
Top-down and profile diagrams of entire crocodile (a) and head (b) illustrating measurements taken using Method A (A) and Method B (B). DCL = dorsal cranial length; SEL = snout–eye length; MHW = maximum head width; MCW = maximum cranial width; IOW = inter-orbital width; CH = cranial height; SPL = snout–pelvis length; TaL = tail length; TaL1 = anterior tail length; TaL2 = posterior tail length; SPL + TaL1 = snout–scute junction (SSJ); SPL + TaL1 + TaL2 = total length (TL) [
General morphometric measurement and description of some sea turtles.
Measurement points for the body proportions of Bryde’s whales. Measurement points were selected based on the study by Mackintosh and Wheeler [
General morphometric measurement and description of other marine mammals.
In conclusion, the biometrics in organisms (Morphometric, meristics and description) have widely importance used in various fields’ “taxonomy, species identifications, monitoring of pollution, species abnormalities, comparison, indicator of environmental changes, growth variation, feeding behavior, ecological strategies, population parameters and water quality of aquaculture operations. The scientists are still applying these measurements even with the presence of advanced techniques because it is the principal knowledge and first guide, low cost, faster and more available tools used. The considerations for the biometric implementation should be taken during the analysis considering the specificity of the quality, preservation status, kind, form of organism and main target of analysis. Its recommended to give more attention to care the biometrics outer/ inner organisms in scientific studies using the advanced techniques, this will be more beneficially together with other modern techniques which required in certain cases for the same purposes.
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This will pose serious problems with food, water and energy supply, particularly in less-developed countries. Considering that the human pressure over natural resources has already reached critical levels, international agencies such as the World Bank and UN Food and Agriculture Organization (FAO) are soliciting scientific research in order to identify innovative solutions to support the primary sector. Nanotechnology is a rapidly evolving field with the potential to take forward the agriculture and food industry with new tools which promise to increase food production in a sustainable manner and to protect crops from pests. Such expectations are coupled with some uncertainties about the fate of nanomaterials in the agro-environment. 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Miscellaneous neglected and underutilized grain legumes (MNUGLs) are crops primarily characterized by inherent features and capabilities to withstand the effects of abiotic stress and climate change, significantly replenish the soil, as well as boost food and protein security. This chapter provides insight into the benefits of MNUGLs as food and nutritional security climate smart crops, capable of growing on marginal lands. Exploring and improving MNUGLs depend on a number of factors among which are concerted research efforts, cultivation and production, as well as utilization awareness across global populace geared toward reawakening the interest on the abandoned legumes. The emergence of the clustered regularly interspaced short palindromic repeat (CRISPR/cas9) technology combined with marker-assisted selection (MAS) offers great opportunities to improve MNUGLs for sustainable utilization. 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To develop a transgenic plant, parameters such as vector constructions, transformation methods, transgene integration, and inheritance of transgene need to be carefully considered to ensure the success of the transformation event. 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Therefore, a full understanding of plant-NP interaction and phytotoxicological mechanism is required for accurate risk assessment to ensure the safe use of nanoparticle. A range of analytical techniques have been developed to detect and characterize the uptake, translocation, cellular internalization and intracellular biotransformation of nanoparticles in plants. Imaging methodologies, including various electron microscopy, spectrometry-based techniques, together with ICP-based techniques such as ICP-OES, ICP-MS and SP-ICP-MS, have been widely used to obtain information about NPs size, morphology, size distribution, cellular localization, elemental speciation, mass concentration and so on. Due to the complexity of biological samples to be analyzed, these techniques are often combined accordingly to provide complementary information regarding plant-NP interaction. This review provides an introduction to the most widely used techniques in the study of interactions between plants and nanoparticles. 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His research interests include computer/machine vision, machine learning, pattern recognition, computational intelligence. \nDr. Papakostas served as a reviewer in numerous journals, as a program\ncommittee member in international conferences and he is a member of the IAENG, MIR Labs, EUCogIII, INSTICC and the Technical Chamber of Greece (TEE).",institutionString:null,institution:{name:"International Hellenic University",institutionURL:null,country:{name:"Greece"}}},editorTwo:null,editorThree:null},{id:"25",title:"Evolutionary Computation",coverUrl:"https://cdn.intechopen.com/series_topics/covers/25.jpg",isOpenForSubmission:!0,editor:{id:"136112",title:"Dr.",name:"Sebastian",middleName:null,surname:"Ventura Soto",slug:"sebastian-ventura-soto",fullName:"Sebastian Ventura Soto",profilePictureURL:"https://mts.intechopen.com/storage/users/136112/images/system/136112.png",biography:"Sebastian Ventura is a Spanish researcher, a full professor with the Department of Computer Science and Numerical Analysis, University of Córdoba. 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He received a Ph.D. (Magna Cum Laude) in Electrical Engineering in 2002. Since 2017, Dr. Gaiceanu has been a Ph.D. supervisor for students in Electrical Engineering. He has been employed at Dunarea de Jos University of Galati since 1996, where he is currently a professor. Dr. Gaiceanu is a member of the National Council for Attesting Titles, Diplomas and Certificates, an expert of the Executive Agency for Higher Education, Research Funding, and a member of the Senate of the Dunarea de Jos University of Galati. He has been the head of the Integrated Energy Conversion Systems and Advanced Control of Complex Processes Research Center, Romania, since 2016. He has conducted several projects in power converter systems for electrical drives, power quality, PEM and SOFC fuel cell power converters for utilities, electric vehicles, and marine applications with the Department of Regulation and Control, SIEI S.pA. (2002–2004) and the Polytechnic University of Turin, Italy (2002–2004, 2006–2007). He is a member of the Institute of Electrical and Electronics Engineers (IEEE) and cofounder-member of the IEEE Power Electronics Romanian Chapter. He is a guest editor at Energies and an academic book editor for IntechOpen. He is also a member of the editorial boards of the Journal of Electrical Engineering, Electronics, Control and Computer Science and Sustainability. 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He has more than 200 publications in reputed international journals, refereed conference proceedings, and 20 book chapters in books published by internationally renowned publishing houses, such as Springer, CRC press, IGI Global, etc. Currently, he is serving on the editorial board of the prestigious journal Frontiers in Communications and Networks and in the technical program committees of a number of high-ranked international conferences organized by the IEEE, USA, and the ACM, USA. 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Ms. Mehtab has published seven papers in international conferences and one of her papers has been accepted for publication in a reputable international journal. She has won the best paper awards in two prestigious international conferences – BAICONF 2019, and ICADCML 2021, organized in the Indian Institute of Management, Bangalore, India in December 2019, and SOA University, Bhubaneswar, India in January 2021. Besides, Ms. Mehtab has also published two book chapters in two books. Seven of her book chapters will be published in a volume shortly in 2021 by Cambridge Scholars’ Press, UK. Currently, she is working as the joint editor of two edited volumes on Time Series Analysis and Forecasting to be published in the first half of 2021 by an international house. Currently, she is working as a Data Scientist with an MNC in Delhi, India.",institutionString:"NSHM College of Management and Technology",institution:null},{id:"226240",title:"Dr.",name:"Andri Irfan",middleName:null,surname:"Rifai",slug:"andri-irfan-rifai",fullName:"Andri Irfan Rifai",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/226240/images/7412_n.jpg",biography:"Andri IRFAN is a Senior Lecturer of Civil Engineering and Planning. He completed the PhD at the Universitas Indonesia & Universidade do Minho with Sandwich Program Scholarship from the Directorate General of Higher Education and LPDP scholarship. He has been teaching for more than 19 years and much active to applied his knowledge in the project construction in Indonesia. His research interest ranges from pavement management system to advanced data mining techniques for transportation engineering. He has published more than 50 papers in journals and 2 books.",institutionString:null,institution:{name:"Universitas Internasional Batam",country:{name:"Indonesia"}}},{id:"314576",title:"Dr.",name:"Ibai",middleName:null,surname:"Laña",slug:"ibai-lana",fullName:"Ibai Laña",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/314576/images/system/314576.jpg",biography:"Dr. Ibai Laña works at TECNALIA as a data analyst. He received his Ph.D. in Artificial Intelligence from the University of the Basque Country (UPV/EHU), Spain, in 2018. He is currently a senior researcher at TECNALIA. His research interests fall within the intersection of intelligent transportation systems, machine learning, traffic data analysis, and data science. He has dealt with urban traffic forecasting problems, applying machine learning models and evolutionary algorithms. He has experience in origin-destination matrix estimation or point of interest and trajectory detection. Working with large volumes of data has given him a good command of big data processing tools and NoSQL databases. He has also been a visiting scholar at the Knowledge Engineering and Discovery Research Institute, Auckland University of Technology.",institutionString:"TECNALIA Research & Innovation",institution:{name:"Tecnalia",country:{name:"Spain"}}},{id:"314575",title:"Dr.",name:"Jesus",middleName:null,surname:"L. Lobo",slug:"jesus-l.-lobo",fullName:"Jesus L. Lobo",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/314575/images/system/314575.png",biography:"Dr. Jesús López is currently based in Bilbao (Spain) working at TECNALIA as Artificial Intelligence Research Scientist. In most cases, a project idea or a new research line needs to be investigated to see if it is good enough to take into production or to focus on it. That is exactly what he does, diving into Machine Learning algorithms and technologies to help TECNALIA to decide whether something is great in theory or will actually impact on the product or processes of its projects. So, he is expert at framing experiments, developing hypotheses, and proving whether they’re true or not, in order to investigate fundamental problems with a longer time horizon. He is also able to design and develop PoCs and system prototypes in simulation. He has participated in several national and internacional R&D projects.\n\nAs another relevant part of his everyday research work, he usually publishes his findings in reputed scientific refereed journals and international conferences, occasionally acting as reviewer and Programme Commitee member. Concretely, since 2018 he has published 9 JCR (8 Q1) journal papers, 9 conference papers (e.g. ECML PKDD 2021), and he has co-edited a book. He is also active in popular science writing data science stories for reputed blogs (KDNuggets, TowardsDataScience, Naukas). Besides, he has recently embarked on mentoring programmes as mentor, and has also worked as data science trainer.",institutionString:"TECNALIA Research & Innovation",institution:{name:"Tecnalia",country:{name:"Spain"}}},{id:"339677",title:"Dr.",name:"Mrinmoy",middleName:null,surname:"Roy",slug:"mrinmoy-roy",fullName:"Mrinmoy Roy",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/339677/images/16768_n.jpg",biography:"An accomplished Sales & Marketing professional with 12 years of cross-functional experience in well-known organisations such as CIPLA, LUPIN, GLENMARK, ASTRAZENECA across different segment of Sales & Marketing, International Business, Institutional Business, Product Management, Strategic Marketing of HIV, Oncology, Derma, Respiratory, Anti-Diabetic, Nutraceutical & Stomatological Product Portfolio and Generic as well as Chronic Critical Care Portfolio. A First Class MBA in International Business & Strategic Marketing, B.Pharm, D.Pharm, Google Certified Digital Marketing Professional. Qualified PhD Candidate in Operations and Management with special focus on Artificial Intelligence and Machine Learning adoption, analysis and use in Healthcare, Hospital & Pharma Domain. Seasoned with diverse therapy area of Pharmaceutical Sales & Marketing ranging from generating revenue through generating prescriptions, launching new products, and making them big brands with continuous strategy execution at the Physician and Patients level. Moved from Sales to Marketing and Business Development for 3.5 years in South East Asian Market operating from Manila, Philippines. Came back to India and handled and developed Brands such as Gluconorm, Lupisulin, Supracal, Absolut Woman, Hemozink, Fabiflu (For COVID 19), and many more. In my previous assignment I used to develop and execute strategies on Sales & Marketing, Commercialization & Business Development for Institution and Corporate Hospital Business portfolio of Oncology Therapy Area for AstraZeneca Pharma India Ltd. Being a Research Scholar and Student of ‘Operations Research & Management: Artificial Intelligence’ I published several pioneer research papers and book chapters on the same in Internationally reputed journals and Books indexed in Scopus, Springer and Ei Compendex, Google Scholar etc. Currently, I am launching PGDM Pharmaceutical Management Program in IIHMR Bangalore and spearheading the course curriculum and structure of the same. I am interested in Collaboration for Healthcare Innovation, Pharma AI Innovation, Future trend in Marketing and Management with incubation on Healthcare, Healthcare IT startups, AI-ML Modelling and Healthcare Algorithm based training module development. I am also an affiliated member of the Institute of Management Consultant of India, looking forward to Healthcare, Healthcare IT and Innovation, Pharma and Hospital Management Consulting works.",institutionString:null,institution:{name:"Lovely Professional University",country:{name:"India"}}},{id:"1063",title:"Prof.",name:"Constantin",middleName:null,surname:"Volosencu",slug:"constantin-volosencu",fullName:"Constantin Volosencu",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/1063/images/system/1063.png",biography:"Prof. Dr. Constantin Voloşencu graduated as an engineer from\nPolitehnica University of Timișoara, Romania, where he also\nobtained a doctorate degree. He is currently a full professor in\nthe Department of Automation and Applied Informatics at the\nsame university. Dr. Voloşencu is the author of ten books, seven\nbook chapters, and more than 160 papers published in journals\nand conference proceedings. He has also edited twelve books and\nhas twenty-seven patents to his name. He is a manager of research grants, editor in\nchief and member of international journal editorial boards, a former plenary speaker, a member of scientific committees, and chair at international conferences. His\nresearch is in the fields of control systems, control of electric drives, fuzzy control\nsystems, neural network applications, fault detection and diagnosis, sensor network\napplications, monitoring of distributed parameter systems, and power ultrasound\napplications. He has developed automation equipment for machine tools, spooling\nmachines, high-power ultrasound processes, and more.",institutionString:"Polytechnic University of Timişoara",institution:{name:"Polytechnic University of Timişoara",country:{name:"Romania"}}},{id:"221364",title:"Dr.",name:"Eneko",middleName:null,surname:"Osaba",slug:"eneko-osaba",fullName:"Eneko Osaba",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/221364/images/system/221364.jpg",biography:"Dr. Eneko Osaba works at TECNALIA as a senior researcher. He obtained his Ph.D. in Artificial Intelligence in 2015. He has participated in more than twenty-five local and European research projects, and in the publication of more than 130 papers. He has performed several stays at universities in the United Kingdom, Italy, and Malta. Dr. Osaba has served as a program committee member in more than forty international conferences and participated in organizing activities in more than ten international conferences. He is a member of the editorial board of the International Journal of Artificial Intelligence, Data in Brief, and Journal of Advanced Transportation. He is also a guest editor for the Journal of Computational Science, Neurocomputing, Swarm, and Evolutionary Computation and IEEE ITS Magazine.",institutionString:"TECNALIA Research & Innovation",institution:{name:"Tecnalia",country:{name:"Spain"}}},{id:"275829",title:"Dr.",name:"Esther",middleName:null,surname:"Villar-Rodriguez",slug:"esther-villar-rodriguez",fullName:"Esther Villar-Rodriguez",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/275829/images/system/275829.jpg",biography:"Dr. Esther Villar obtained a Ph.D. in Information and Communication Technologies from the University of Alcalá, Spain, in 2015. She obtained a degree in Computer Science from the University of Deusto, Spain, in 2010, and an MSc in Computer Languages and Systems from the National University of Distance Education, Spain, in 2012. Her areas of interest and knowledge include natural language processing (NLP), detection of impersonation in social networks, semantic web, and machine learning. Dr. Esther Villar made several contributions at conferences and publishing in various journals in those fields. Currently, she is working within the OPTIMA (Optimization Modeling & Analytics) business of TECNALIA’s ICT Division as a data scientist in projects related to the prediction and optimization of management and industrial processes (resource planning, energy efficiency, etc).",institutionString:"TECNALIA Research & Innovation",institution:{name:"Tecnalia",country:{name:"Spain"}}},{id:"49813",title:"Dr.",name:"Javier",middleName:null,surname:"Del Ser",slug:"javier-del-ser",fullName:"Javier Del Ser",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/49813/images/system/49813.png",biography:"Prof. Dr. Javier Del Ser received his first PhD in Telecommunication Engineering (Cum Laude) from the University of Navarra, Spain, in 2006, and a second PhD in Computational Intelligence (Summa Cum Laude) from the University of Alcala, Spain, in 2013. He is currently a principal researcher in data analytics and optimisation at TECNALIA (Spain), a visiting fellow at the Basque Center for Applied Mathematics (BCAM) and a part-time lecturer at the University of the Basque Country (UPV/EHU). His research interests gravitate on the use of descriptive, prescriptive and predictive algorithms for data mining and optimization in a diverse range of application fields such as Energy, Transport, Telecommunications, Health and Industry, among others. In these fields he has published more than 240 articles, co-supervised 8 Ph.D. theses, edited 6 books, coauthored 7 patents and participated/led more than 40 research projects. He is a Senior Member of the IEEE, and a recipient of the Biscay Talent prize for his academic career.",institutionString:"Tecnalia Research & Innovation",institution:null},{id:"278948",title:"Dr.",name:"Carlos Pedro",middleName:null,surname:"Gonçalves",slug:"carlos-pedro-goncalves",fullName:"Carlos Pedro Gonçalves",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRcmyQAC/Profile_Picture_1564224512145",biography:'Carlos Pedro Gonçalves (PhD) is an Associate Professor at Lusophone University of Humanities and Technologies and a researcher on Complexity Sciences, Quantum Technologies, Artificial Intelligence, Strategic Studies, Studies in Intelligence and Security, FinTech and Financial Risk Modeling. He is also a progammer with programming experience in:\n\nA) Quantum Computing using Qiskit Python module and IBM Quantum Experience Platform, with software developed on the simulation of Quantum Artificial Neural Networks and Quantum Cybersecurity;\n\nB) Artificial Intelligence and Machine learning programming in Python;\n\nC) Artificial Intelligence, Multiagent Systems Modeling and System Dynamics Modeling in Netlogo, with models developed in the areas of Chaos Theory, Econophysics, Artificial Intelligence, Classical and Quantum Complex Systems Science, with the Econophysics models having been cited worldwide and incorporated in PhD programs by different Universities.\n\nReceived an Arctic Code Vault Contributor status by GitHub, due to having developed open source software preserved in the \\"Arctic Code Vault\\" for future generations (https://archiveprogram.github.com/arctic-vault/), with the Strategy Analyzer A.I. module for decision making support (based on his PhD thesis, used in his Classes on Decision Making and in Strategic Intelligence Consulting Activities) and QNeural Python Quantum Neural Network simulator also preserved in the \\"Arctic Code Vault\\", for access to these software modules see: https://github.com/cpgoncalves. He is also a peer reviewer with outsanding review status from Elsevier journals, including Physica A, Neurocomputing and Engineering Applications of Artificial Intelligence. Science CV available at: https://www.cienciavitae.pt//pt/8E1C-A8B3-78C5 and ORCID: https://orcid.org/0000-0002-0298-3974',institutionString:"University of Lisbon",institution:{name:"Universidade Lusófona",country:{name:"Portugal"}}},{id:"241400",title:"Prof.",name:"Mohammed",middleName:null,surname:"Bsiss",slug:"mohammed-bsiss",fullName:"Mohammed Bsiss",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/241400/images/8062_n.jpg",biography:null,institutionString:null,institution:null},{id:"276128",title:"Dr.",name:"Hira",middleName:null,surname:"Fatima",slug:"hira-fatima",fullName:"Hira Fatima",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/276128/images/14420_n.jpg",biography:"Dr. Hira Fatima\nAssistant Professor\nDepartment of Mathematics\nInstitute of Applied Science\nMangalayatan University, Aligarh\nMobile: no : 8532041179\nhirafatima2014@gmal.com\n\nDr. Hira Fatima has received his Ph.D. degree in pure Mathematics from Aligarh Muslim University, Aligarh India. Currently working as an Assistant Professor in the Department of Mathematics, Institute of Applied Science, Mangalayatan University, Aligarh. She taught so many courses of Mathematics of UG and PG level. Her research Area of Expertise is Functional Analysis & Sequence Spaces. She has been working on Ideal Convergence of double sequence. She has published 17 research papers in National and International Journals including Cogent Mathematics, Filomat, Journal of Intelligent and Fuzzy Systems, Advances in Difference Equations, Journal of Mathematical Analysis, Journal of Mathematical & Computer Science etc. She has also reviewed few research papers for the and international journals. She is a member of Indian Mathematical Society.",institutionString:null,institution:null},{id:"302698",title:"Dr.",name:"Yao",middleName:null,surname:"Shan",slug:"yao-shan",fullName:"Yao Shan",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Dalian University of Technology",country:{name:"China"}}},{id:"125911",title:"Prof.",name:"Jia-Ching",middleName:null,surname:"Wang",slug:"jia-ching-wang",fullName:"Jia-Ching Wang",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"National Central University",country:{name:"Taiwan"}}},{id:"357085",title:"Mr.",name:"P. Mohan",middleName:null,surname:"Anand",slug:"p.-mohan-anand",fullName:"P. Mohan Anand",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Indian Institute of Technology Kanpur",country:{name:"India"}}},{id:"356696",title:"Ph.D. Student",name:"P.V.",middleName:null,surname:"Sai Charan",slug:"p.v.-sai-charan",fullName:"P.V. Sai Charan",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Indian Institute of Technology Kanpur",country:{name:"India"}}},{id:"357086",title:"Prof.",name:"Sandeep K.",middleName:null,surname:"Shukla",slug:"sandeep-k.-shukla",fullName:"Sandeep K. Shukla",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Indian Institute of Technology Kanpur",country:{name:"India"}}},{id:"356823",title:"MSc.",name:"Seonghee",middleName:null,surname:"Min",slug:"seonghee-min",fullName:"Seonghee Min",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Daegu University",country:{name:"Korea, South"}}},{id:"353307",title:"Prof.",name:"Yoosoo",middleName:null,surname:"Oh",slug:"yoosoo-oh",fullName:"Yoosoo Oh",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:"Yoosoo Oh received his Bachelor's degree in the Department of Electronics and Engineering from Kyungpook National University in 2002. He obtained his Master’s degree in the Department of Information and Communications from Gwangju Institute of Science and Technology (GIST) in 2003. In 2010, he received his Ph.D. degree in the School of Information and Mechatronics from GIST. In the meantime, he was an executed team leader at Culture Technology Institute, GIST, 2010-2012. In 2011, he worked at Lancaster University, the UK as a visiting scholar. In September 2012, he joined Daegu University, where he is currently an associate professor in the School of ICT Conver, Daegu University. Also, he served as the Board of Directors of KSIIS since 2019, and HCI Korea since 2016. From 2017~2019, he worked as a center director of the Mixed Reality Convergence Research Center at Daegu University. From 2015-2017, He worked as a director in the Enterprise Supporting Office of LINC Project Group, Daegu University. His research interests include Activity Fusion & Reasoning, Machine Learning, Context-aware Middleware, Human-Computer Interaction, etc.",institutionString:null,institution:{name:"Daegu Gyeongbuk Institute of Science and Technology",country:{name:"Korea, South"}}},{id:"262719",title:"Dr.",name:"Esma",middleName:null,surname:"Ergüner Özkoç",slug:"esma-erguner-ozkoc",fullName:"Esma Ergüner Özkoç",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Başkent University",country:{name:"Turkey"}}},{id:"419199",title:"Dr.",name:"Qun",middleName:null,surname:"Yang",slug:"qun-yang",fullName:"Qun Yang",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Auckland",country:{name:"New Zealand"}}},{id:"351158",title:"Prof.",name:"David W.",middleName:null,surname:"Anderson",slug:"david-w.-anderson",fullName:"David W. Anderson",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Calgary",country:{name:"Canada"}}},{id:"351159",title:"BSc.",name:"Kalum J.",middleName:null,surname:"Ost",slug:"kalum-j.-ost",fullName:"Kalum J. Ost",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Calgary",country:{name:"Canada"}}},{id:"325029",title:"Dr.",name:"Prem Chand",middleName:null,surname:"Jain",slug:"prem-chand-jain",fullName:"Prem Chand Jain",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Shiv Nadar University",country:{name:"India"}}},{id:"357275",title:"Dr.",name:"Thomas",middleName:null,surname:"Mih",slug:"thomas-mih",fullName:"Thomas Mih",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Buea",country:{name:"Cameroon"}}},{id:"305305",title:"Dr.",name:"Arturo Yosimar",middleName:null,surname:"Jaen-Cuellar",slug:"arturo-yosimar-jaen-cuellar",fullName:"Arturo Yosimar Jaen-Cuellar",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Autonomous University of Queretaro",country:{name:"Mexico"}}},{id:"305315",title:"Dr.",name:"David Alejandro",middleName:null,surname:"Elvira-Ortiz",slug:"david-alejandro-elvira-ortiz",fullName:"David Alejandro Elvira-Ortiz",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Autonomous University of Queretaro",country:{name:"Mexico"}}},{id:"344374",title:"Dr.",name:"Manuel",middleName:null,surname:"Toledano-Ayala",slug:"manuel-toledano-ayala",fullName:"Manuel Toledano-Ayala",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Autonomous University of Queretaro",country:{name:"Mexico"}}}]}},subseries:{item:{id:"18",type:"subseries",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",hasOnlineFirst:!0,hasPublishedBooks:!0,annualVolume:11414,editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",slug:"paolo-iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",biography:"Paolo Iadarola graduated with a degree in Chemistry from the University of Pavia (Italy) in July 1972. He then worked as an Assistant Professor at the Faculty of Science of the same University until 1984. In 1985, Prof. Iadarola became Associate Professor at the Department of Biology and Biotechnologies of the University of Pavia and retired in October 2017. Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. He is a Consultant Reviewer for several journals, including the Journal of Chromatography A, Journal of Chromatography B, Plos ONE, Proteomes, International Journal of Molecular Science, Biotech, Electrophoresis, and others. He is also Associate Editor of Biotech.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",slug:"simona-viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",biography:"Simona Viglio is an Associate Professor of Biochemistry at the Department of Molecular Medicine at the University of Pavia. She has been working since 1995 on the determination of proteolytic enzymes involved in the degradation process of connective tissue matrix and on the identification of biological markers of lung diseases. She gained considerable experience in developing and validating new methodologies whose applications allowed her to determine both the amount of biomarkers (Desmosine and Isodesmosine) in the urine of patients affected by COPD, and the activity of proteolytic enzymes (HNE, Cathepsin G, Pseudomonas aeruginosa elastase) in the sputa of these patients. Simona Viglio was also involved in research dealing with the supplementation of amino acids in patients with brain injury and chronic heart failure. She is presently engaged in the development of 2-DE and LC-MS techniques for the study of proteomics in biological fluids. The aim of this research is the identification of potential biomarkers of lung diseases. She is an author of about 90 publications (According to Scopus: H-Index: 23; According to WOS: H-Index: 20) on peer-reviewed journals, a member of the “Società Italiana di Biochimica e Biologia Molecolare,“ and a Consultant Reviewer for International Journal of Molecular Science, Journal of Chromatography A, COPD, Plos ONE and Nutritional Neuroscience.",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,series:{id:"11",title:"Biochemistry",doi:"10.5772/intechopen.72877",issn:"2632-0983"},editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",slug:"arli-aditya-parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",slug:"cesar-lopez-camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",slug:"shymaa-enany",fullName:"Shymaa Enany",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRqB9QAK/Profile_Picture_1626163237970",institutionString:null,institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]},onlineFirstChapters:{paginationCount:7,paginationItems:[{id:"79909",title:"Cryopreservation Methods and Frontiers in the Art of Freezing Life in Animal Models",doi:"10.5772/intechopen.101750",signatures:"Feda S. 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Main aspects of the topic are: Applying bioinformatics in drug discovery and development; Bioinformatics in clinical diagnostics (genetic variants that act as markers for a condition or a disease); Blockchain and Artificial Intelligence/Machine Learning in personalized medicine; Customize disease-prevention strategies in personalized medicine; Big data analysis in personalized medicine; Translating stratification algorithms into clinical practice of personalized medicine.",annualVolume:11403,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/7.jpg",editor:{id:"351533",title:"Dr.",name:"Slawomir",middleName:null,surname:"Wilczynski",fullName:"Slawomir Wilczynski",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000035U1loQAC/Profile_Picture_1630074514792",institutionString:null,institution:{name:"Medical University of Silesia",institutionURL:null,country:{name:"Poland"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"5886",title:"Dr.",name:"Alexandros",middleName:"T.",surname:"Tzallas",fullName:"Alexandros Tzallas",profilePictureURL:"https://mts.intechopen.com/storage/users/5886/images/system/5886.png",institutionString:"University of Ioannina, Greece & Imperial College London",institution:{name:"University of Ioannina",institutionURL:null,country:{name:"Greece"}}},{id:"257388",title:"Distinguished Prof.",name:"Lulu",middleName:null,surname:"Wang",fullName:"Lulu Wang",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRX6kQAG/Profile_Picture_1630329584194",institutionString:null,institution:{name:"Shenzhen Technology University",institutionURL:null,country:{name:"China"}}},{id:"225387",title:"Prof.",name:"Reda",middleName:"R.",surname:"Gharieb",fullName:"Reda Gharieb",profilePictureURL:"https://mts.intechopen.com/storage/users/225387/images/system/225387.jpg",institutionString:"Assiut University",institution:{name:"Assiut University",institutionURL:null,country:{name:"Egypt"}}}]},{id:"8",title:"Bioinspired Technology and Biomechanics",keywords:"Bioinspired Systems, Biomechanics, Assistive Technology, Rehabilitation",scope:'Bioinspired technologies take advantage of understanding the actual biological system to provide solutions to problems in several areas. Recently, bioinspired systems have been successfully employing biomechanics to develop and improve assistive technology and rehabilitation devices. The research topic "Bioinspired Technology and Biomechanics" welcomes studies reporting recent advances in bioinspired technologies that contribute to individuals\' health, inclusion, and rehabilitation. Possible contributions can address (but are not limited to) the following research topics: Bioinspired design and control of exoskeletons, orthoses, and prostheses; Experimental evaluation of the effect of assistive devices (e.g., influence on gait, balance, and neuromuscular system); Bioinspired technologies for rehabilitation, including clinical studies reporting evaluations; Application of neuromuscular and biomechanical models to the development of bioinspired technology.',annualVolume:11404,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/8.jpg",editor:{id:"144937",title:"Prof.",name:"Adriano",middleName:"De Oliveira",surname:"Andrade",fullName:"Adriano Andrade",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRC8QQAW/Profile_Picture_1625219101815",institutionString:null,institution:{name:"Federal University of Uberlândia",institutionURL:null,country:{name:"Brazil"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"49517",title:"Prof.",name:"Hitoshi",middleName:null,surname:"Tsunashima",fullName:"Hitoshi Tsunashima",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYTP4QAO/Profile_Picture_1625819726528",institutionString:null,institution:{name:"Nihon University",institutionURL:null,country:{name:"Japan"}}},{id:"425354",title:"Dr.",name:"Marcus",middleName:"Fraga",surname:"Vieira",fullName:"Marcus Vieira",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003BJSgIQAX/Profile_Picture_1627904687309",institutionString:null,institution:{name:"Universidade Federal de Goiás",institutionURL:null,country:{name:"Brazil"}}},{id:"196746",title:"Dr.",name:"Ramana",middleName:null,surname:"Vinjamuri",fullName:"Ramana Vinjamuri",profilePictureURL:"https://mts.intechopen.com/storage/users/196746/images/system/196746.jpeg",institutionString:"University of Maryland, Baltimore County",institution:{name:"University of Maryland, Baltimore County",institutionURL:null,country:{name:"United States of America"}}}]},{id:"9",title:"Biotechnology - Biosensors, Biomaterials and Tissue Engineering",keywords:"Biotechnology, Biosensors, Biomaterials, Tissue Engineering",scope:"The Biotechnology - Biosensors, Biomaterials and Tissue Engineering topic within the Biomedical Engineering Series aims to rapidly publish contributions on all aspects of biotechnology, biosensors, biomaterial and tissue engineering. We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics can include but are not limited to: Biotechnology such as biotechnological products and process engineering; Biotechnologically relevant enzymes and proteins; Bioenergy and biofuels; Applied genetics and molecular biotechnology; Genomics, transcriptomics, proteomics; Applied microbial and cell physiology; Environmental biotechnology; Methods and protocols. Moreover, topics in biosensor technology, like sensors that incorporate enzymes, antibodies, nucleic acids, whole cells, tissues and organelles, and other biological or biologically inspired components will be considered, and topics exploring transducers, including those based on electrochemical and optical piezoelectric, thermal, magnetic, and micromechanical elements. Chapters exploring biomaterial approaches such as polymer synthesis and characterization, drug and gene vector design, biocompatibility, immunology and toxicology, and self-assembly at the nanoscale, are welcome. Finally, the tissue engineering subcategory will support topics such as the fundamentals of stem cells and progenitor cells and their proliferation, differentiation, bioreactors for three-dimensional culture and studies of phenotypic changes, stem and progenitor cells, both short and long term, ex vivo and in vivo implantation both in preclinical models and also in clinical trials.",annualVolume:11405,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/9.jpg",editor:{id:"126286",title:"Dr.",name:"Luis",middleName:"Jesús",surname:"Villarreal-Gómez",fullName:"Luis Villarreal-Gómez",profilePictureURL:"https://mts.intechopen.com/storage/users/126286/images/system/126286.jpg",institutionString:null,institution:{name:"Autonomous University of Baja California",institutionURL:null,country:{name:"Mexico"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"35539",title:"Dr.",name:"Cecilia",middleName:null,surname:"Cristea",fullName:"Cecilia Cristea",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYQ65QAG/Profile_Picture_1621007741527",institutionString:null,institution:{name:"Iuliu Hațieganu University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"40735",title:"Dr.",name:"Gil",middleName:"Alberto Batista",surname:"Gonçalves",fullName:"Gil Gonçalves",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYRLGQA4/Profile_Picture_1628492612759",institutionString:null,institution:{name:"University of Aveiro",institutionURL:null,country:{name:"Portugal"}}},{id:"211725",title:"Associate Prof.",name:"Johann F.",middleName:null,surname:"Osma",fullName:"Johann F. Osma",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSDv7QAG/Profile_Picture_1626602531691",institutionString:null,institution:{name:"Universidad de Los Andes",institutionURL:null,country:{name:"Colombia"}}},{id:"69697",title:"Dr.",name:"Mani T.",middleName:null,surname:"Valarmathi",fullName:"Mani T. Valarmathi",profilePictureURL:"https://mts.intechopen.com/storage/users/69697/images/system/69697.jpg",institutionString:"Religen Inc. | A Life Science Company, United States of America",institution:null},{id:"205081",title:"Dr.",name:"Marco",middleName:"Vinícius",surname:"Chaud",fullName:"Marco Chaud",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSDGeQAO/Profile_Picture_1622624307737",institutionString:null,institution:{name:"Universidade de Sorocaba",institutionURL:null,country:{name:"Brazil"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"onlineFirst.detail",path:"/online-first/81260",hash:"",query:{},params:{id:"81260"},fullPath:"/online-first/81260",meta:{},from:{name:null,path:"/",hash:"",query:{},params:{},fullPath:"/",meta:{}}}},function(){var e;(e=document.currentScript||document.scripts[document.scripts.length-1]).parentNode.removeChild(e)}()