Spectral conditions of elements determination.
\\n\\n
IntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\\n\\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\\n\\nLaunching 2021
\\n\\nArtificial Intelligence, ISSN 2633-1403
\\n\\nVeterinary Medicine and Science, ISSN 2632-0517
\\n\\nBiochemistry, ISSN 2632-0983
\\n\\nBiomedical Engineering, ISSN 2631-5343
\\n\\nInfectious Diseases, ISSN 2631-6188
\\n\\nPhysiology (Coming Soon)
\\n\\nDentistry (Coming Soon)
\\n\\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\\n\\nNote: Edited in October 2021
\\n"}]',published:!0,mainMedia:{caption:"",originalUrl:"/media/original/132"}},components:[{type:"htmlEditorComponent",content:'With the desire to make book publishing more relevant for the digital age and offer innovative Open Access publishing options, we are thrilled to announce the launch of our new publishing format: IntechOpen Book Series.
\n\nDesigned to cover fast-moving research fields in rapidly expanding areas, our Book Series feature a Topic structure allowing us to present the most relevant sub-disciplines. Book Series are headed by Series Editors, and a team of Topic Editors supported by international Editorial Board members. Topics are always open for submissions, with an Annual Volume published each calendar year.
\n\nAfter a robust peer-review process, accepted works are published quickly, thanks to Online First, ensuring research is made available to the scientific community without delay.
\n\nOur innovative Book Series format brings you:
\n\nIntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\n\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\n\nLaunching 2021
\n\nArtificial Intelligence, ISSN 2633-1403
\n\nVeterinary Medicine and Science, ISSN 2632-0517
\n\nBiochemistry, ISSN 2632-0983
\n\nBiomedical Engineering, ISSN 2631-5343
\n\nInfectious Diseases, ISSN 2631-6188
\n\nPhysiology (Coming Soon)
\n\nDentistry (Coming Soon)
\n\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\n\nNote: Edited in October 2021
\n'}],latestNews:[{slug:"intechopen-supports-asapbio-s-new-initiative-publish-your-reviews-20220729",title:"IntechOpen Supports ASAPbio’s New Initiative Publish Your Reviews"},{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{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"}]},book:{item:{type:"book",id:"9665",leadTitle:null,fullTitle:"Pseudomonas aeruginosa - Biofilm Formation, Infections and Treatments",title:"Pseudomonas aeruginosa",subtitle:"Biofilm Formation, Infections and Treatments",reviewType:"peer-reviewed",abstract:"Emerging antibiotic resistance of bacteria is driving us to catastrophic failure of the healthcare system. Pseudomonas aeruginosa is one such pathogen that is responsible for causing nosocomial infections, urinary tract infections, cystic fibrosis, otitis media, and infections of wounds and burns. P. aeruginosa is a critical pathogen as defined by the World Health Organization (WHO) due to its intrinsic and adaptive competence to defy antibiotics and persist as a superbug. This book covers a wide array of subjects relevant to bacterial biofilms specifically focusing on P. aeruginosa and associated infections. It provides readers with a clear and comprehensive overview of biofilm formation and associated detrimental impacts. In addition, this book also examines topics related to biosynthesis virulence factors by P. aeruginosa to facilitate biofilm formation, antibiotic resistance mechanisms, and infections.",isbn:"978-1-83968-648-1",printIsbn:"978-1-83968-647-4",pdfIsbn:"978-1-83968-649-8",doi:"10.5772/intechopen.87468",price:119,priceEur:129,priceUsd:155,slug:"pseudomonas-aeruginosa-biofilm-formation-infections-and-treatments",numberOfPages:114,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"00e9f0f41cf8cd97ff33fac3bcea14cb",bookSignature:"Theerthankar Das",publishedDate:"June 9th 2021",coverURL:"https://cdn.intechopen.com/books/images_new/9665.jpg",numberOfDownloads:1799,numberOfWosCitations:1,numberOfCrossrefCitations:2,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:5,numberOfDimensionsCitationsByBook:0,hasAltmetrics:0,numberOfTotalCitations:8,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"September 1st 2020",dateEndSecondStepPublish:"September 29th 2020",dateEndThirdStepPublish:"November 28th 2020",dateEndFourthStepPublish:"February 16th 2021",dateEndFifthStepPublish:"April 17th 2021",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"179493",title:"Dr.",name:"Theerthankar",middleName:null,surname:"Das",slug:"theerthankar-das",fullName:"Theerthankar Das",profilePictureURL:"https://mts.intechopen.com/storage/users/179493/images/system/179493.png",biography:"Dr. Theerthankar Das (Department of Infectious Diseases and Immunology, School of Medical Sciences, University of Sydney, Australia) is an experienced microbiologist. He joined the University of Sydney after being awarded the prestigious University of Sydney Fellowship in 2015. His primary research focuses on the development of novel strategies to disrupt bacterial biofilms. In recent years, he has won various research funding/grants from Sydney University, Industry, and the Australian Government valued at more than $4.5 million. To date, Dr. Das has authored/co-authored thirty publications, and six book chapters in eminent journals and books and have edited a book and guest editor for Scientific Journal. He is also a reviewer for many high-impact scientific journals. Dr. Das currently supervises Ph.D. students and teaches first-year Medical and Advanced Medical Bacteriology students.",institutionString:"University of Sydney",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"4",totalChapterViews:"0",totalEditedBooks:"1",institution:{name:"University of Sydney",institutionURL:null,country:{name:"Australia"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"906",title:"Bacteriology",slug:"pure-microbiology-bacteriology"}],chapters:[{id:"76707",title:"Introductory Chapter: Understanding Infections Caused by Opportunistic Bacterial Pathogens",doi:"10.5772/intechopen.97831",slug:"introductory-chapter-understanding-infections-caused-by-opportunistic-bacterial-pathogens",totalDownloads:197,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:null,signatures:"Theerthankar Das",downloadPdfUrl:"/chapter/pdf-download/76707",previewPdfUrl:"/chapter/pdf-preview/76707",authors:[{id:"179493",title:"Dr.",name:"Theerthankar",surname:"Das",slug:"theerthankar-das",fullName:"Theerthankar Das"}],corrections:null},{id:"74413",title:"Pseudomonas aeruginosa: Diseases, Biofilm and Antibiotic Resistance",doi:"10.5772/intechopen.95251",slug:"-em-pseudomonas-aeruginosa-em-diseases-biofilm-and-antibiotic-resistance",totalDownloads:487,totalCrossrefCites:0,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Pseudomonas aeruginosa is Gram negative bacteria that can adapt to extreme environmental conditions and withstand to different antibacterial agents. It si responsible for arrays of infections both community and hospital acquired especially ICU infections. Respiratory tract infection, blood stream infection, wound infection, burn infection, and urinary tract infections ware top five P. aeruginosa infections. Additionally as an opportunistic bacteria, it may be associated with healthcare infections in intensive care units (ICUs), ventilator-associated pneumonia (VAP), central line-associated blood stream infections, surgical site infections, otitis media, and keratitis. P. aeruginosa can form biofilms as self-produced extracellular matrix to protects the cells from antibiotics and the host immune response. Antibiotic resistance was an prominent feature of this pathogen and can donate it one of the three resistance patterns: Multidrug (MDR), extensive drug (XDR) and pan drug resistance. It exploit many resistance mechanisms ranged from overexpression of drug efflux systems protein, modifying enzyme production, reducing the permeability and using shelters like biofilms.",signatures:"Hussein Al-Dahmoshi, Raad D. Al-Obaidi and Noor Al-Khafaji",downloadPdfUrl:"/chapter/pdf-download/74413",previewPdfUrl:"/chapter/pdf-preview/74413",authors:[{id:"250698",title:"Dr.",name:"Hussein",surname:"O. M. Al-Dahmoshi",slug:"hussein-o.-m.-al-dahmoshi",fullName:"Hussein O. M. Al-Dahmoshi"},{id:"272591",title:"Dr.",name:"Noor S.K",surname:"Al-Khafaji",slug:"noor-s.k-al-khafaji",fullName:"Noor S.K Al-Khafaji"},{id:"338694",title:"MSc.",name:"Raad D.",surname:"Al-Obaidi",slug:"raad-d.-al-obaidi",fullName:"Raad D. Al-Obaidi"}],corrections:null},{id:"75039",title:"Pseudomonas aeruginosa as a Cause of Nosocomial Infections",doi:"10.5772/intechopen.95908",slug:"-em-pseudomonas-aeruginosa-em-as-a-cause-of-nosocomial-infections",totalDownloads:280,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Pseudomonas aeruginosa, as a gram-negative aerobic rod, is still one of the most resistant agents of nosocomial infections. It is used for the development of respiratory, urinary and wound infections. It causes bacteremia, especially in patients who are hospitalized for anesthesiology and resuscitation department or ICU, who often have respiratory insufficiency and hemodynamic instability and require artificial lung ventilation. Mechanical ventilation itself is a significant risk factor for the development of pseudomonad pneumonia. Pseudomonas aeruginosa has enzymes that are encoded on both chromosomes and plasmids, often in combination with other mechanisms of resistance, such as reducing the permeability of the outer or cytoplasmic membrane. Due to carbapenemases, Pseudomonas aeruginosa loses sensitivity to carbapenem and becomes resistant to this antibiotic. It also becomes resistant to aminoglycosides, cephalosporins and ureidopenicillins. It is also resistant to Quaternary disinfectants. The reservoir of pseudomonas nosocomial infection is hospital water, taps, shower roses, swimming pools, healing waters and others. The intervention of anti-epidemic measures in the case of infections caused by pseudomonad strains has not yet reached such sophistication as in the case of MRSA for time, personnel and economic reasons. In the absence of an epidemic, intervention in sporadic cases consists of informing nursing staff of the occurrence of a multidrug-resistant agent, including providing all patient demographics and relieving careful adherence to the barrier treatment, cleansing, disinfection and isolation regimen.",signatures:"Silvia Labovská",downloadPdfUrl:"/chapter/pdf-download/75039",previewPdfUrl:"/chapter/pdf-preview/75039",authors:[{id:"311482",title:"Ph.D.",name:"Silvia",surname:"Labovská",slug:"silvia-labovska",fullName:"Silvia Labovská"}],corrections:null},{id:"74799",title:"Pseudomonas aeruginosa Biofilm Lung Infection in Cystic Fibrosis: The Challenge of Persisters",doi:"10.5772/intechopen.95590",slug:"-em-pseudomonas-aeruginosa-em-biofilm-lung-infection-in-cystic-fibrosis-the-challenge-of-persisters",totalDownloads:330,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Pseudomonas aeruginosa lung infection is difficult to eradicate due to the multiple (intrinsic and acquired) antibiotic resistance of bacteria and to their ability to produce a thick biofilm. Antibiotic treatment is hampered by poor antibiotic diffusion, efflux pump overexpression and the development of a persistent subpopulation with low metabolic activity. This is a cause for special concern in Cystic Fibrosis (CF) patients, where P. aeruginosa lung infection is the chief cause of morbidity and mortality. Combined tobramycin-ciprofloxacin treatment is routinely adopted due to the low frequency of resistant strains and its ostensible ability to control the infection. Nevertheless, symptoms usually recur, mainly due to the antibiotic persisters, which are difficult to detect in routine cultural microbiological assays. This chapter describes the issues involved in the microbiological diagnosis of P. aeruginosa lung infection in CF patients and the possible role of subinhibitory antibiotic concentrations in persister development and infection recurrence.",signatures:"Gianmarco Mangiaterra, Mehdi Amiri, Nicholas Cedraro and Francesca Biavasco",downloadPdfUrl:"/chapter/pdf-download/74799",previewPdfUrl:"/chapter/pdf-preview/74799",authors:[{id:"334557",title:"Ph.D.",name:"Gianmarco",surname:"Mangiaterra",slug:"gianmarco-mangiaterra",fullName:"Gianmarco Mangiaterra"},{id:"335142",title:"BSc.",name:"Nicholas",surname:"Cedraro",slug:"nicholas-cedraro",fullName:"Nicholas Cedraro"},{id:"335143",title:"Prof.",name:"Francesca",surname:"Biavasco",slug:"francesca-biavasco",fullName:"Francesca Biavasco"},{id:"344065",title:"Dr.",name:"Mehdi",surname:"Amiri",slug:"mehdi-amiri",fullName:"Mehdi Amiri"}],corrections:null},{id:"75844",title:"Pseudomonas aeruginosa Secreted Biomolecules and Their Diverse Functions in Biofilm Formation and Virulence",doi:"10.5772/intechopen.96866",slug:"-em-pseudomonas-aeruginosa-em-secreted-biomolecules-and-their-diverse-functions-in-biofilm-formation",totalDownloads:312,totalCrossrefCites:0,totalDimensionsCites:2,hasAltmetrics:0,abstract:"Pseudomonas aeruginosa is an opportunistic Gram-negative bacterium accountable for causing life-threatening infections in humans. According to the World Health Organization, P. aeruginosa classified as a critical pathogen. Specifically, P. aeruginosa in its colonized or biofilm state presents a major infection threat to immunocompromised (HIV) patients, Cystic fibrosis, burns, wounds and surgery associated infection. It is also a common pathogen responsible for causing hospital acquired/nosocomial infection and Urinary tract infections. P. aeruginosa biofilm is made up of bacterial self-synthesized biomolecules includes extracellular DNA, polysaccharides, proteins, RNA, siderophores and metabolites such as pyocyanin. This chapter will elaborate the manifold functions of P. aeruginosa secreted biomolecules in establishing and stabilizing biofilms, triggering virulence and pathogenicity in host, and resisting antibiotics and antibacterial agents.",signatures:"Theerthankar Das",downloadPdfUrl:"/chapter/pdf-download/75844",previewPdfUrl:"/chapter/pdf-preview/75844",authors:[{id:"179493",title:"Dr.",name:"Theerthankar",surname:"Das",slug:"theerthankar-das",fullName:"Theerthankar Das"}],corrections:null},{id:"75457",title:"Chemotherapy and Mechanisms of Action of Antimicrobial Agent",doi:"10.5772/intechopen.95476",slug:"chemotherapy-and-mechanisms-of-action-of-antimicrobial-agent",totalDownloads:193,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"Pseudomonas aeruginosa is a widespread opportunistic pathogen that causes bloodstream, urinary tract, burn wounds infections and is one of the largest pathogens that infect cystic fibrosis patients’ airways and can be life-threatening for P. aeruginosa infections. In addition, P. aeruginosa remains one of the most significant and difficult nosocomial pathogens to handle. Increasingly, multi-drug resistance (MDR) strains are identified and the option of therapy is often very limited in these cases, particularly when searching for antimicrobial combinations to treat serious infections. The fact that no new antimicrobial agents are active against the MDR strains of P. aeruginosa is an additional matter of concern. In recent decades, bacterial drug resistance has increased, but the rate of discovery of new antibiotics has decreased steadily. The fight for new, powerful antibacterial agents has therefore become a top priority. This chapter illustrates and explores the current state of several innovative therapeutic methods that can be further discussed in clinical practice in the treatment of P. aeruginosa infections.",signatures:"Rahman Laibi Chelab",downloadPdfUrl:"/chapter/pdf-download/75457",previewPdfUrl:"/chapter/pdf-preview/75457",authors:[{id:"334102",title:"Prof.",name:"Rahman",surname:"Chelab",slug:"rahman-chelab",fullName:"Rahman Chelab"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"5471",title:"Frontiers in Staphylococcus aureus",subtitle:null,isOpenForSubmission:!1,hash:"514afc8c2d4eb28ddca22c032ad96d9e",slug:"frontiers-in-i-staphylococcus-aureus-i-",bookSignature:"Shymaa Enany and Laura E. 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The objective of the book will be to highlight the importance of sex education and explain normal human sexuality. With the growing number of males and females reporting sexual dysfunction the need for a ready reckoner of sexual dysfunction may be relevant and necessary.
\r\n\r\n\tThe book will have chapters on normal human sexuality, sexual health, Sexual dysfunction in the male and female, sexual dysfunction disorders related to libido, orgasm, ejaculation, erection, and genetic or hormonal or developmental or sexuo-erotic orientation defects.
\r\n\r\n\tThe book will also highlight the importance of sex counselors and therapists.
\r\n\tThere will be a chapter on secondary causes of sexual dysfunction disorders related to diabetes, cardiovascular disease, and obesity. A chapter on remedial measures to enhance sexual activity and maintain human relationships will be discussed. As there is a growing number of cancer survivors a chapter on cancer-related sexual dysfunction will be welcomed for including it.
This review was designed to highlight the available evidence that suggests drinking water and possible survival in water as a probable transmission mode for
Although the natural niche for
It has been over a century since Walery Jaworski at Cracow University detected a spiral bacteria named
The answer to this question hangs within the realm of conjecture, because - so far - no dominant route of infection by
The different mode of transmission of
Data for the confirmation of oral - oral transmission is based on various observations that are related to, among others, research on infection within the family. Research showed that if one person in the family was found to be infected with
An important argument for transmission of
An important factor in the acquisition of
Major epidemiologic risk factors for acquisition of
In view of the widespread use of the gastroscopy as a means for diagnosing the upper gastrointestinal tract disorders, the iatrogenic transmission of
Literature evidence that water may serve as a potential source and reservoir of
The breakthrough discovery that water can be a source and route of the
The following methods are used in order to detect the presence of
Culturable methods – that utilize the specialized media bacterial growth, and
The methods of molecular assessment of
We found only a few studies that report successful isolation of
In the second case,
In another study [50] drinking water samples (n= 600) were collected from ground-drilled water supplied by water and sanitation agencies in different localities within the Lahore metropolitan area, Pakistan, and were used within six hours for culturing of
Survival studies in water samples demonstrate that
Fluorescent in situ hybridization (FISH) with rRNA oligonucleotide probes has been used for detection and identification of VBNC forms of bacteria [62]. In addition to PCR, FISH was validated as a quick and sensitive method for detection of
In the United States, actively respiring
This method allows the identification of DNA which is specific for
Despite the numerous research findings identifying
Janzon et al [71] developed tested and optimized two complementary
Since
To evaluate the possibility that the absence of
To further determine the presence of inhibitory factors in the field study water and biofilm samples from Dhaka, the real-time PCR analysis was repeated on all field samples but spiked with 1,000 genomes of
Possible degradation of
It is well known that waterborne bacteria can attach to surfaces by aggregating in a hydrated exopolymer known as a biofilm [72, 73]. The association of bacteria, particularly pathogens, with biofilm communities within a water distribution system may offer vulnerable and susceptible bacteria protection from disinfection and protozoan predation [74]. In fact microorganisms in drinking water are predominantly associated with biofilms rather than in the planktonic state [72, 73, 75]. There is evidence that biofilms in water distribution systems may harbor
Adams et al. [81] have shown that in pure culture
The evidence based medicine regarding
In the U.S. the problem of drinking water pollution is handled by the Environmental Protection Agency (EPA). On the basis of a survey which was carried out, the Agency has developed and issued a list of microbiological contaminants of water, which are likely to significantly affect the public health of consumers of drinking water. The list includes three species of bacteria:
The water contamination of bacteria was documented specially in suburban areas because the number of systems for discharging sewage to sewage treatment plants is inadequate. The reason of these bacterial contaminations is not fully understood but some mechanisms were already proposed. Moreover, many farms and households either have their own small wastewater treatment plants, which do not always function properly, or in worse cases, waste is disposed of by releasing pollutants into nearby rivers, streams or roadside ditches. Some farms have leaky septic tanks often built near wells from which they derive all their household water.
Recent advances in the role of the particular ionic concentrations and the possible correlation between the presence or absence of contamination of water samples tested for
Determining the concentrations of the suggested ions and the possible correlation between the presence and absence of contamination of water samples tested for
The samples were collected, cooled and stored in polyethylene containers prior to analyses. Before quantitative elemental analysis, if appropriate the samples were filtered and diluted adequately to fit the analytical signal to the linear range of calibration curve.
Quantitative determinations of sodium and potassium were made using flame photometry method in air acetylene flame in standard conditions (Perkin Elmer AAS spectrometer Model 3110, USA).
Determinations of Fe, Mg and Zn were performed by means of atomic absorption spectrometry, flame technique (air acetylene flame) using Perkin Elmer AAS spectrometer Model 3110, USA. In both methods, analyses were preceded by thorough optimization of measurement conditions (flame characteristic, burner position, and nebulizer performance). Spectral conditions are given in Table 1.
\n\t\t\t\t | \n\t\t\t\n\t\t\t\t | \n\t\t\t\n\t\t\t\t | \n\t\t\t\n\t\t\t\t | \n\t\t\t\n\t\t\t\t | \n\t\t
K | \n\t\t\tAES | \n\t\t\t\n\t\t\t | 766.5 | \n\t\t\t0.7 | \n\t\t
Na | \n\t\t\tAES | \n\t\t\t\n\t\t\t | 589.0 | \n\t\t\t0.2 | \n\t\t
Fe | \n\t\t\tF AAS | \n\t\t\tHCL | \n\t\t\t248.3 | \n\t\t\t0.2 | \n\t\t
Mg | \n\t\t\tF AAS | \n\t\t\tHCL | \n\t\t\t285.2 | \n\t\t\t0.7 | \n\t\t
Zn | \n\t\t\tF AAS | \n\t\t\tHCL | \n\t\t\t213.9 | \n\t\t\t0.7 | \n\t\t
Spectral conditions of elements determination.
All measurements were made using the calibration curve technique. In case of Mg measurements, the samples characterized by high Na concentration were quantified using the method of standard additions calibration. Measurements were made in triplicate.
We have collected 150 water samples from different municipal water distribution systems (n=49), rivers (n=48), water reservoirs (n=39) and drinking water tanks and wells (n=14) and they were analyzed between June and December 2012. Samples of 1000 ml water were poured into smaller tubes water and were processed to remove organic matter by centrifugation at 121xg for 5 min. The supernatant was concentrated by centrifugation at 7740xg for 15 min. The resultant pellet was dissolve in 1 ml of PBS, followed by centrifugation at 10 000Xg for 5 min. Finally the pellet was stored at -20°C. Total DNA from concentrated samples for PCR was purified using Genomic Mini or Genomic Mini AX Bacteria (A & A Biotechnology, Gdynia, Poland). DNA was stored at -20°C. All PCR amplifications were performed using the GoTaq DNA Polymerase (Promega, WI, USA) in Thermo cycler T3 (Biometra, Gottingen, Germany).
A negative control with sterile water and positive control with
PCR with primers specific for
First, samples were analyzed for
For DNA visualization, electrophoresis or PCR products was performed through 2% agarose gel containing ethidium bromide and gels were photographed under UV light. A 100 bp and 50 bp ladder were used as a molecular weight marker.
GlmM-forward | \n\t\t\tphosphoglucosamine mutase gene | \n\t\t\tAGG CTT TTA GGG GTG TTA GGG GTT T | \n\t\t\t[85] | \n\t\t
GlmM-reverse | \n\t\t\tAAG CTT ACT TTC TAA CAC TAA CGC | \n\t\t||
Cluster2 | \n\t\t\t16S rRNA hyper variable flanking region of | \n\t\t\tGGC GTT ATC AAC AGA ATG GC | \n\t\t\t[86] | \n\t\t
B1J99 | \n\t\t\tCTC AGT TCG GAT TGT AGG CTG C | \n\t\t||
HelGen-forward | \n\t\t\t23S rRNA | \n\t\t\tAAC GGG GCT AAG ATA GAC | \n\t\t\t[87] | \n\t\t
HelGen-reverse | \n\t\t\tTCT CAT CTA CCT GTG TCG | \n\t\t
PCR primer used in this study.
*References
On the basis of a chemometric analysis that involved the use of multidimensional data analysis known as multivariate data analysis it was possible to distinguish water samples containing DNA
In analyzing the results of water sampling conducted in the framework of the project “Detection of Helicobacter pylori in drinking water samples. In what way is the water contaminated and what is the source of contamination?” we have reached the conclusion that we cannot yet say with certainty whether water can be considered as a source of
As the results of our study confirmed the presence of the bacteria in tap water only (i.e., after the process of purification/water treatment), but was not found in rivers, reservoirs and in wells where the water is completely untreated, the first question concerns the existence of a link between the amount of bacteria and the degree and process of the water treatment. The link between the amount of bacteria present in tap water and the distance from the point of chlorination can also be taken into consideration (the farther from the treatment, the smaller the concentration of bactericidal chlorine).
On the basis of these results it can be concluded that the presence of
This raises the question - if the bacteria can survive for so long in distilled water, does this mean that the physiologically important endogenous pool of metals is enough for them?
If so we can expect that the metals in the water around them will be important for their survival? On the other hand, there is no doubt about the effects of toxic metals, but these levels are continuously monitored in water - as is the bacterial cell toxicity of heavy metals. And do the levels of acceptable standards for drinking water have anything to do with this.
Determination of
Understanding the effects of dissolved organic carbon in the survival of bacteria during water treatment.
Taking into account the differences in the composition and concentration studied seasonal elements for the possible coexistence of
These relationships can be used to develop a better method of treating water in order to minimize the exposure of humans to infection
The study was a part of the project of National Center of Science in Poland entitled "Detection of
Extensive research in the chemical synthetic approaches has led to a huge increment in the poorly water-soluble drug’s development [1]. In the present scenario, statistical reports suggest that there are approximately 70% of poor water-soluble new chemical entities (NCEs) [2]. These newly developed drugs possess lipophilic characteristic and are challenging to deliver through the oral route. They have poor oral bioavailability, show variation in intra- as well as intersubject pharmacokinetics, have poor dose proportionality, and have erratic absorption [3]. Researchers have made many strategies to overcome the limitation of poor solubility and bioavailability. Different delivery system formulation development and chemical and/or physical modification of drug moiety can be used to solve the poor solubility issue of drugs. Though there are many drug delivery system approaches, lipid-based drug delivery system has gained much interest in lipophilic drug delivery. It includes macroemulsion, nanoemulsion, niosomes, self-emulsifying formulation, liposomes, solid-lipid nanoparticle, etc. Among all these formulation approaches, emulsion-based preparation can be considered an industrially feasible approach to overcome the limitation of poor bioavailability [4]. Nanoemulsion is capable of improving the topical drug absorption thereby increasing the bioavailability and permeability of lipophilic drug; thus, it can be a good alternative option for drug delivery [5]. Nanoemulsion is further incorporated into gel matrix to prepare nanoemulgel which has even better permeation and stability. So far, there is no review article reported on the promising future of nanoemulgel applications as a delivery system in the treatment of various diseases. This article is a complete package of nanoemulgel comprising information of potent selected formulation component, formulation procedure, advantages over other delivery system, and widespread possible application of nanoemulgel in the treatment therapy. In this article, we have mentioned only reported applications, and there are many to still go in the upcoming future.
Though oral route offers better patient compliance, it has various limitations like gastric irritation, unavoidable side effects, systemic toxicity, and hepatic first-pass metabolism [6]. To avoid all these issues, a nonirritating, non-painful, and a noninvasive topical drug delivery system can be a suitable alternative. It has several advantages over oral route such as targeted site-specific delivery of drug with least systemic toxicity, no gastric irritation, first-pass metabolism bypass, and improved bioavailability of a drug [7, 8]. Apart from many advantages, traditional topical formulations, namely lotions, creams, and ointments suffer from sticky nature, stability issue, low spreadability, etc. which affect the patient’s compliance. Whereas, modern transdermal preparations like transparent gel, nanogel, and (micro/nano) emulgel not only have shown improved patient compliance but also improves the formulation efficacy, stability, and safety. Several studies have reported that topical drug delivery system improves the bioavailability of the drug [9, 10]. Bioavailability of lacidipine given through transdermal route was found to be increased by 3.5-fold than the oral route. It may be due to the avoidance of the first-pass metabolism of the drug [9]. In another study conducted by Bhaskar and team, it was found that the topical nanoemulsion of flurbiprofen exhibits 4.4 times more bioavailability than oral delivery [10]. Thus, the bioavailability of a lipophilic drug can be enhanced by the topical drug delivery system. Topical delivery not only reduces the drug metabolism but also improves the permeation across the skin by maintaining longer steady-state delivery of the drug [9].
Delivery of a lipophilic drug is a big obstacle for the conventional transdermal delivery system due to low therapeutic potential and poor skin permeability capability. Researches propose that nanoscale-sized transdermal preparation can increase the drug permeability by disrupting the skin bilayer of lipid [11] and extending the drug retention time at the site of action [12, 13]. Nanoemulsion can be a promising carrier delivery of hydrophobic drug, since it has greater thermodynamic stability and higher capability of drug solubilization over emulsion and other dispersion systems. It also has longer shelf life and requires a small amount of external energy for manufacturing [14]. Nanoemulsion is a dispersed system which consists of nanoscale-sized (20–200 nm diameter) droplets solvent composed of an oil phase and water phase and stabilized by the suitable surfactant. Drug is entrapped in the core which is surrounded by emulsifier layer as shown in Figure 1. Generally, permeation enhancers are not required when nanoemulsion is used as a carrier for delivery of the lipophilic drug [15]. It has less tendency of phase separation than other ordinary emulsions which makes it more stable [16]. Different studies have reported better permeation of drug into the skin through nanoemulsion delivery system than conventional ointment [17], cream [18], gel [19], and emulsion [20]. Depending on the type of nanoemulsion, viz. oil-in-water or water-in-oil, it can solubilize both hydrophobic and hydrophilic drug in its structure [21].
Structure of nanoemulsion.
In spite of lots of advantages, nanoemulsion suffers from low spreadability, low viscosity, and poor skin retention issue [22]. Due to these, the clinical application of topical nanoemulsion is restrained [23]. Researchers converted nanoemulsion into nanoemulgel by incorporating it into the gel matrix and solved this problem.
Nanoemulgel is the fusion of two systems: nanoemulsion system and hydrogel system. Both the systems have some limitations, such as nanoemulsion that suffers low spreadability and poor retention, whereas hydrogels are incapable of incorporating lipophilic molecule [24, 25]. Nanoemulgel has different types of polymeric materials, surfactants, and fatty substances of natural, synthetic, and semisynthetic nature with a droplet size range from 5 to 500 nm [26]. Nanoemulgel has the capability to overcome the limitation of both the systems. The lipophilic drug is dissolved in the oil phase of nanoemulsion which is then added to hydrogel base to form nanoemulgel [27] which enables the incorporation of lipophilic drug into a hydrogel, simultaneously improving the viscosity of nanoemulsion. In transdermal drug delivery, nanoemulgel acts as a reservoir of the drug. The drug is first to release from the inner phase to the outer phase and from there into the skin surface. When applied on skin, oily droplets were released from the gel matrix of nanoemulgel, which then penetrate deep into the skin via stratum corneum, and there they directly deliver the drug moiety [23]. The mechanism of drug release depends on the crosslink density as well as the composition of a network of polymer chains [28].
Nanoemulgel is a fusion of two separate systems, viz. the nanoemulsion and a gel system. Nanoemulsion acting as a vehicle for drug delivery can be either water-in-oil or oil-in-water type. In both cases, it consists of an oil phase, aqueous phase, surfactant, and sometime cosurfactant. Overview of commonly used major components of nanoemulgel formulation has been apprehended in this section (Figure 2).
Potent formulation component of nanoemulgel.
Oil is an important component of the nanoemulgel formulation that should be selected appropriately based on the solubility, stability, permeability, and viscosity of the formulation. Vegetable oils/edible oils are not frequently used in nanoemulgel formulation, since they had shown poor emulsification properties and drug solubility [29, 30, 31]. Thus, chemically modified oils such as mono or diglyceride or medium-chain triglycerides are commonly used as an oil phase in the nanoemulgel formulation for lipophilic drug delivery [15]. A medium-chain triglyceride, Labrafac, has been used by Syamala and his group to prepare butenafine nanoemulgel [32]. Capryol 90 is another example used as an oil phase in the preparation of nanoemulsion, which has shown better stability of the nanoemulsion formulation of leflunomide and paclitaxel [3, 33].
On the other hand, scientists are focusing on utilizing the supplementary benefit of natural oil in therapeutic effect. Antimicrobial activity of tea tree oil was combined with an antifungal agent itraconazole for a synergistic effect of nanoemulgel preparation against vaginal candidiasis [34]. Another nanoemulgel of curcumin has been reported by Jeengar and team with emu oil. Emu oil obtained from emu bird has analgesic, antipruritic, anesthetic, antioxidants, and anti-inflammatory properties, and it has shown the improvement in permeability of drug in the treatment of joint synovial [35]. Various oils used by different researchers in nanoemulgel preparation are listed in Table 1.
Oil | Surfactant | Cosurfactant | Gelling agents | Reference | |
---|---|---|---|---|---|
Caprylic acid, isopropyl myristate, and tea tree oil | Tween 20 | PEG 400 | Carbopol 940 | [36] | |
Emu oil | Cremophor RH40 | Labrafil M2125CS | Carbopol | [35] | |
Linseed oil, isopropyl myristate and triacetin | Tween 80 | Ethanol + PEG 400 + propylene glycol | Carbopol 940 | [37] | |
Labrafac™ LipophileWL1349 | Tween 80 | PEG 400 | Carbopol | [38] | |
Oleic acid | Tween 80 | Transcutol P | Guar gum | [24] | |
Isosteryl isostearate | Labrasol | Plurol isostearique | Carbopol 940 | [39] | |
Capryol 90 | Tween 20 | Carbitol | Carbopol 934 | [15] | |
Labrafac | Cremophore RH40 | Ethanol | Carbopol | [32] | |
Oleic acid | Tween 80 | Transcutol P | Carbopol 940 | [40] | |
Oleic acid | Tween 80 | Ethanol | Carbopol 934 | [41] | |
Sefsol-218 | Tween 80 | Transcutol-P | Carbopol | [42] | |
Olive oil and miglyol | Polysorbate 80 | Transcutol | Propylene glycol | [43] | |
Liquid paraffin | Polysorbate 80 | Glycerin | Carbopol 940 | [44] | |
Labrafac and triacetin | Tween 80 | Diethylene glycol monorthyl ether | Carbopol 934 | [45] | |
Oleic acid and IPM | Tween 20 | Carbitol | Carbopol 934 | [46] | |
Labrafil | Acrysol | Carbitol | Carbopol | [47] |
Various components used in different nanoemulgel formulations.
Surfactant reduces the interfacial tension between the mixtures of two immiscible liquids and changes the dispersion entropy, thus stabilizing thermodynamically unstable emulsion system. Selection of appropriate surfactant for nanoemulgel is based on the safety, stability, high drug loading capacity as well as good emulsification properties [31]. Also, the surfactant should be selected based on the solubility with oil like Tween 20 that was used on the basis of solubility of Capryol 90 and oleic acid [15, 40].
Cosurfactant may combine with surfactant and help in the emulsification process by disrupting the interfacial film. It may also help in solubilization of oil [15]. Depending on the physicochemical properties, most frequently used cosurfactants in nanoemulsion and nanoemulgel preparation are propylene glycol, PEG 400, ethanol, transcutol P, carbitol, etc. [35, 40]. Studies suggest that with the increase in the concentration of cosurfactant, the area of nanoemulsion in phase diagram decreases [48, 49].
Aqueous solvents act as the aqueous phase in emulsion preparation. Worldwide widely used aqueous solvents are ethanol and water.
Carbapol 934, Carbapol 940, and hydroxy propyl methyl cellulose (HPMC) are widely used gelling agent for nanoemulgel. They increased the thickness of the formulation and may interact with the surfactant to modify the viscosity of the formulation [41]. It is added to the nanoemulsion preparation to change the physical state of nanoemulsion formulation from liquid to gel, thus solving the problem of low spreadability, low viscosity, and poor skin retention issue of nanoemulsion.
To protect the formulation from microbial attack and increase the shelf life of formulation, preservatives are added in the preparation. Most commonly used preservatives are methylparaben, benzoic acid, propylparaben, benzalkonium chloride, etc. Antioxidants like butylate hydroxyl toluene, butylate hydroxyl anisole, and ascorbyl palmitate are used to prevent oxidative degradation of formulation components and to prevent loss of moisture, glycerin and propylene glycol are used as humectants [50]. Hence, the stability of the nanoemulsion and nanoemulgel preparation increased.
Two steps are involved in the manufacturing of nanoemulgel. The first step is nanoemulsion formulation which is then incorporated into a gelling agent in the second step to form nanoemulgel. Figure 3 schematically represents the procedure of preparation of nanoemulgel.
Procedure of nanoemulgel preparation.
Methods used for the preparation of nanoemulsion can be high-energy emulsification methods or low-energy emulsification methods [49, 51]. In high-energy emulsification methods, external energy is applied which rupture the oil phase to form nanosized droplets in the aqueous phase. It includes ultrasonic emulsification and high-pressure homogenization. Solvent displacement method, phase inversion composition method, and phase inversion temperature method are low-energy emulsification in which low energy is required for prepared nanoemulsion [21].
The selected surfactant is dissolved in either the aqueous phase or the oil phase. Based on the solubility, the drug is then added and solubilized in the oil phase or aqueous phase followed by heating. Then one phase is gradually added into another with continuous stirring till the temperature of the mixture reaches to room temperature.
The appropriate gelling agent is dissolved in distilled water with continuous stirring to prepare gel base. The pH of prepared gel is adjusted, then the nanoemulsion system is incorporated slowly into the prepared gel at a particular ratio with continuous stirring to get nanoemulgel preparation.
Nanoemulgel preparations have various advantages over other topical as well as conventional preparation. Some of the advantages are listed as follows (Figure 4).
Advantages of nanoemulgel preparation.
The lipophilic drug moieties base show improper drug release mechanism in the gel due to its insolubility in aqueous base. Fusion of the hydrogel system with emulsion system enables the incorporation of lipophilic drug into the aqueous base, thus improving the release mechanism of the drug. Lipophilic drug is dissolved in the oil phase of emulsion which is then incorporated into hydrogel system [52].
Better loading capacity has been observed by nanoemulgel as compared to than other novel drug delivery systems. Due to its nanoscale size, it has a larger surface area and better entrapment efficiency which enable it to load more amount of drugs in its network-like system [52].
Nanoemulgel system is more stable than other transdermal drug delivery system, because it decreases the interfacial as well as the surface tension of the formulation, which make it superior from a conventional transdermal delivery system [53].
Nanoemulgel acts as a drug reservoir and has shown prolong residence time leading to sustain release of the drug. Thus, it is beneficial for the drugs having shorter half-life [52].
Nanoemulgel formulation gives higher Tmax and peak plasma concentration of lipophilic drugs than the conventional gel as well as oral formulation. Thereby, nanoemulgel preparation improves the bioavailability of lipophilic drug many folds than the other lipophilic drug formulations [53].
Major issue with the transdermal preparation is the sticky nature and low spreading coefficient which require rubbing mechanism. Nanoemulgel being nonsticky and easily spreadable preparation results in better patient compliance than other transdermal preparations [28].
Nanoemulgel has shown significant enhancement in the permeability of the drug through skin than other formulation since from nanoemulgel preparation, the drug can permeate the skin layer through both paracellular and transcellular route, whereas, in nanoemulsion, only transcellular permeation route is seen [53]. Comparison of cumulative drug permeability through the skin from different formulation is represented in Figure 5 [24].
Comparative representation of cumulative cyclosporine permeated through the skin of albino rat from different formulations. Regenerated from [
Nanoemulgel bypasses the first-pass metabolism, thus solving one of the major problems of drug, that is, the oral side effect. It does not cause skin irritation or any toxicity on the application [53].
A significant number of the nanoemulgel formulation of drugs has been carried out and reported by various researchers to show its application as a more potent and effective drug delivery system. Some of the studies have shown outstanding result over the conventional oral drug delivery system, suggesting a promising future of nanoemulgel application.
Thymol nanoemulgel formulation for acne vulgaris, a common chronic skin disease, was prepared by Ahmad and team. The preparation showed better efficacy [36].
It is the skin condition in which skin cells build up and form itchy, dry patches, and scales. A nanoemulgel formulation of leflunomide by Pund and team showed considerably higher anti-psoriatic and anti-melanoma activity in human keratinocyte cell line due to improved permeability of drug. Amount of drug deposited in the skin after 12 hours by nanoemulgel was found to be sixfold more than ordinary gel [33]. In another study by Somagoni and team, nanoemulgel showed 3.22- and 2.01-fold more reduction of ear swelling than drug solution and marketed product, respectively, in psoriatic-like model [43].
High skin permeability of nanoemulgel has made it a better alternative for the faster treatment of fungal infection. Syamala has reported that it took only 12 days to Butenafine nanoemulgel to cure fungus-infected rat skin, whereas cream took 16 days [32]. Nanoemulgel has also shown a notable increase in antifungal activity of the drug. Higher area of inhibition zone was observed with Ketoconazole nanoemulgel than drug solution when incubated for 48 hours [38]. Nanoemulgel of Amphotericin B can overcome formulation limitation of Amphotericin B making it a better alternative to painful intravenous administration. It could be used as a stable, effective, and safe carrier for sustained and enhanced localized delivery of Amphotericin B against fungal infection [42].
Nanoemulgel is a better alternative for poor water-soluble anti-inflammatory drugs, and it also bypasses the related oral side effects of drugs like gastrointestinal irritation, renal, and cardiovascular problems, etc. Many researchers have reported remarkably higher activity of anti-inflammatory drugs in nanoemulgel formulation than other drug carrier system [35, 40, 54, 55, 56, 57]. Nanoemulgel of ketoprofen, an extensively utilized non steroidal anti inflammatory drugs (NSAIDs) for rheumatoid arthritis and osteoarthritis treatment, was developed by Arora and team. Along with enhancing the skin permeability and solubility of ketoprofen, it also bypasses the problems related to chronic oral delivery of ketoprofen. Comparison of the optimized formulation with the marketed product and drug solution showed 1.5- and 2-fold higher permeability, respectively [40].
Another common drug used in osteoarthritis and rheumatoid arthritis is piroxicam. It is also used in the treatment of the musculoskeletal and joint disorder. It also possesses the problem of poor solubility along with undesirable side effect on stomach and kidney. Dhawan and team reported that piroxicam nanoemulgel can be used as a feasible alternative [41].
Apart from these, attempt has also made to establish the stability, efficacy, and safety of certain drugs with anti-inflammatory activity which has poor solubility and permeability profile and/or oral side effect like curcumin [35], Swietenia macrophylla [27], Lornoxicam [54], Nimesulide [55], mangosteen [56], and diclofenac diethylamine [57]. Figure 6 represents the comparison of anti-inflammatory effect of flurbiprofen nanoemulgel by Radhika and Guruprasad with marketed preparation [37].
Graphical representation of improvement in anti-inflammatory effect of nanoemulgel of flurbiprofen. Regenerated from [
Dental nanoemulgel preparation is intended for periodontal delivery of drug to treat chronic bacterial infection of the gum and bone supporting teeth. Periodontal disease causes inflammation of gum forming pockets which may lead to gum tissue and bone damage. Srivastava and team formulated syringeable ketoprofen nanoemulgel for intra-pocket delivery and found satisfied pharmaceutical characterization offering sustained release of ketoprofen into the pocket. Significant reduction was observed in alveolar bone loss, gingival index, and tooth motility by ketoprofen nanoemulgel due to decreased cytokine levels [58]. Whereas, the study of Nayak and team suggested that controlled released delivery of Quercetin nanoemulgel can be used successfully in periodontitis [59].
Ocular nanoemulgel can be better alternative drug delivery system to the conventional eye drops to cure corneal fungal infection. Permeation of fluconazole from nanoemulgel preparation was found four times that of commercial fluconazole eye drop due to high permeation, sustained release of drug, and prolongation in the precorneal residence time. Prolong release was achieved by in situ gelation of Gellan gum due to its crosslinking with tear fluid. Fluconazole nanoemulgel formulation showed no sign of any ocular irritation and tissue damage [60]. Whereas, Tayel used a rabbit model to successfully control the release rate of terbinafine-HCL nanoemulgel, which can be an effective alternative to conventional eye drop for ocular fungal infection, into the rabbit aqueous humor [61].
A thermo-sensitive nanoemulgel of itraconazole with tea tree oil was prepared for patients suffering from periodic vaginal candidiasis. Antimicrobial activity of itraconazole and tea tree oil combined to give synergistic effect covering cure for wide range microbial infection [34].
Minoxidil is the commonly used drug for the treatment of hair loss also known as alopecia. Nanoemulgel is capable of increasing solubility and permeability of drug through the skin; hence, nanoemulgel preparation of minoxidil will be more effective and safer than conventional preparation present in the market for the treatment of alopecia areata [62].
Nasal nanoemulgel of zaleplon was formulated by Hosny and Banjar for the treatment of insomnia. The main objective was to solve the problem with marketed zaleplon tablet. Zaleplon tablet suffers from poor bioavailability due to extensive first-pass metabolism and delayed onset of action due to poor aqueous solubility. Nasal zaleplon nanoemulgel showed eight times more bioavailability than the marketed zaleplon tablet [63].
Selegiline HCL-loaded nanoemulgel possess better sustains release effect of the drug and higher bioavailability than the conventional gel and a marketed tablet. Bioavailability was reported to be 5.53 and 6.56 times that of normal gel and tablet [64]. Microemulgel loaded with rotigotine has also shown significantly higher bioavailability than marketed patch of rotigotine in the treatment of Parkinson’s disease [65].
Use of nanotechnology in cosmetics is very common. Fullerenes, solid-lipid nanoparticle, liposomes, nanosomes, etc., are already nourishing in cosmetic industries. Ferulic acid nanoemulgel was developed by Harwansh and team to protect the skin damage from harmful UV radiation. Ferulic acid strongly absorbs the UV radiation. Its incorporation into nanoemulgel system made it effective for more than 4 hours on the UV-exposed skin [39].
Currently available marketed emulgel products for the treatment of acne and pimple, inflammation, and pain caused by osteoarthritis and rheumatoid arthritis and skin infection have been listed in Table 2.
Product brand name | Active pharmaceutical ingredient(s) | Manufacturers | Application |
---|---|---|---|
Benzolait AZ emulgel | Benzoylperoxide | Roydermal | Pimple and blacks on skin |
Coolnac Gel emulgel 1% | Diclofenac diethyl ammonium | Chumchon | Inflammation and pain due to trauma |
Diclobar emulgel | Diclofenac diethyl amine | Barakat Pharma | Inflammation due to trauma and rheumatic diseases |
Levorage emulgel | Liquorice, hibiscus, and natural extract | THD Ltd | Anal fissures |
Meloxic emulgel | Meloxicum | Laboratories Provet | Musculoskeletal pain management and inflammation |
Miconaz-H-emulgel | Miconazole nitrate, hydrocortisone | Medical Union Pharmaceutics | Skin infection by candida |
Reumadep emulgel | Ashwagandha, myrrh, arnica, rosemary, mint, and cloves | Erbozeta | Inflammation and pain due to trauma |
Voltaren emulgel | Diclofenac diethyl ammonium | Novartis Pharma | Osteoarthritis joint pain |
Voveron emulgel | Diclofenac diethyl amine | Novartis Pharma | Osteoarthritis joint pain |
Available marketed emulgel preparations.
The skin permeability as well as bioavailability of nanoemulgel may be enhanced by various mechanisms. Some of the studied mechanisms with types of nanoemulgel are listed in Table 3.
Types of nanoemulgel | Mechanism of permeability/bioavailability | References |
---|---|---|
Conjugate of curcumin | Induced apoptosis in cancer cells, suppressing the expression of NF-κB, TNF-α, and COX-2 cellular targets | [66] |
Clove essential oil | Dispersion of the nanoemulsion in the polymeric matrices of the prepared nanoemulgel | [67] |
Snakehead fish (pphiocephalus striatus) | Ex vivo transdermal permeation value | [68] |
Methotrexate | Change in temperature experienced by the nanogel | [69] |
Terbinafine | Ex vivo drug permeation and in vivo antifungal activity | [70] |
Paclitaxel | Nanogel exerts high cytotoxicity to cancer cells and reverses multidrug resistance effectively | [71] |
Diphenhydramine | First-order kinetics and Fickian diffusion | [72] |
Raloxifene hydrochloride | Ex vivo permeation, histopathology, SEM, DSC, and CLSM studies | [73] |
Desonide | DES, Franz diffusion cell system, CLSM | [74] |
Ketoconazole | Ex vivo permeation | [75] |
Telmisartan | Ex vivo permeation, first-order reaction, and Higuchi model with non-Fickian diffusion | [76] |
Ibuprofen | Drug diffusion, however, drug partition, and matrix erosion | [77] |
Piroxicam | Franz diffusion cell | [78] |
Mechanism involved in enhancing permeability and bioavailability of some nanoemulgel preparations.
NF: nuclear factor, TNF: tumor necrosis factor, SEM: scanning electron microscopy, DSC: differential scan calorimetry, DES: dielectric spectroscopy, CLSM: confocal laser scanning microscopy.
Nanoemulgel has been found to be extraordinarily good vehicle system for hydrophobic drug delivery. High drug loading due to better solubilizing efficacy, improved bioavailability due to better permeability, and capability to control the release of drug make it a potent alternative delivery system in the treatment of various diseases. Application of nanoemulgel preparation in the treatment of acne, pimple, psoriasis, fungal infection, and inflammation due to osteoarthritis as well as rheumatoid arthritis has shown significantly higher efficacy. Besides transdermal application, it can also be applied for ocular, vaginal, dental, and nose to brain delivery of drug for the treatment of diverse local and systemic ailments such as alopecia, periodontitis, and Parkinson’s disease. Nanoemulgel has also shown its application in the cosmetic industries as a UV absorber nanoemulgel to protect skin from sunburn. Precisely, the nanoemulgel system has a marvelous ability to be applied in various local and systemic ailments. Some preparations are already present in the market, whereas others need a further clinical study to launch the product in the market.
This is a brief overview of the main steps involved in publishing with IntechOpen Compacts, Monographs and Edited Books. Once you submit your proposal you will be appointed a Author Service Manager who will be your single point of contact and lead you through all the described steps below.
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\n\n2. SUBMIT YOUR MANUSCRIPT
\n\nAfter approval, you will proceed in submitting your full-length manuscript. 50-130 pages for compacts, 130-500 for Monographs & Edited Books.Your full-length manuscript must follow IntechOpen's Author Guidelines and comply with our publishing rules. Once the manuscript is submitted, but before it is forwarded for peer review, it will be screened for plagiarism.
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Aalborg University has Two Satellite Campuses, one in Copenhagen (Aalborg University Copenhagen) and the other in Esbjerg (Aalborg University Esbjerg).\n· He is a member of prestigious IEEE (Institute of Electrical and Electronics Engineers), and IAENG (International Association of Engineers) organizations. \n· He is the chief Editor of the Journal of Software Engineering.\n· He is the member of the Editorial Board of International Journal of Computer Science and Software Technology (IJCSST) and International Journal of Computer Engineering and Information Technology. \n· He is also the Editor of Communication in Computer and Information Science CCIS-20 by Springer.\n· Reviewer For Many Conferences\nHe is the lead person in making collaboration agreements between Aalborg University and many universities of Pakistan, for which the MOU’s (Memorandum of Understanding) have been signed.\nProfessor Akbar is working in Academia since 1990, he started his career as a Lab demonstrator/TA at the University of Sussex. After finishing his P. hD degree in 1992, he served in the Industry as a Scientific Officer and continued his academic career as a visiting scholar for a number of educational institutions. In 1996 he joined National University of Science & Technology Pakistan (NUST) as an Associate Professor; NUST is one of the top few universities in Pakistan. In 1999 he joined an International Company Lineo Inc, Canada as Manager Compiler Group, where he headed the group for developing Compiler Tool Chain and Porting of Operating Systems for the BLACKfin processor. The processor development was a joint venture by Intel and Analog Devices. In 2002 Lineo Inc., was taken over by another company, so he joined Aalborg University Denmark as an Assistant Professor.\nProfessor Akbar has truly a multi-disciplined career and he continued his legacy and making progress in many areas of his interests both in teaching and research. 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Watt",authors:[{id:"145620",title:"Dr.",name:"Gina",middleName:null,surname:"Forster",slug:"gina-forster",fullName:"Gina Forster"},{id:"146553",title:"BSc.",name:"Andrew",middleName:null,surname:"Novick",slug:"andrew-novick",fullName:"Andrew Novick"},{id:"146554",title:"MSc.",name:"Jamie",middleName:null,surname:"Scholl",slug:"jamie-scholl",fullName:"Jamie Scholl"},{id:"146555",title:"Dr.",name:"Michael",middleName:null,surname:"Watt",slug:"michael-watt",fullName:"Michael Watt"}]},{id:"26258",doi:"10.5772/28300",title:"Excitotoxicity and Oxidative Stress in Acute Ischemic Stroke",slug:"excitotoxicity-and-oxidative-stress-in-acute-ischemic-stroke",totalDownloads:7206,totalCrossrefCites:6,totalDimensionsCites:27,abstract:null,book:{id:"931",slug:"acute-ischemic-stroke",title:"Acute Ischemic Stroke",fullTitle:"Acute Ischemic Stroke"},signatures:"Ramón Rama Bretón and Julio César García Rodríguez",authors:[{id:"73430",title:"Prof.",name:"Ramon",middleName:null,surname:"Rama",slug:"ramon-rama",fullName:"Ramon Rama"},{id:"124643",title:"Prof.",name:"Julio Cesar",middleName:null,surname:"García",slug:"julio-cesar-garcia",fullName:"Julio Cesar García"}]},{id:"62072",doi:"10.5772/intechopen.78695",title:"Brain-Computer Interface and Motor Imagery Training: The Role of Visual Feedback and Embodiment",slug:"brain-computer-interface-and-motor-imagery-training-the-role-of-visual-feedback-and-embodiment",totalDownloads:1473,totalCrossrefCites:13,totalDimensionsCites:25,abstract:"Controlling a brain-computer interface (BCI) is a difficult task that requires extensive training. Particularly in the case of motor imagery BCIs, users may need several training sessions before they learn how to generate desired brain activity and reach an acceptable performance. A typical training protocol for such BCIs includes execution of a motor imagery task by the user, followed by presentation of an extending bar or a moving object on a computer screen. In this chapter, we discuss the importance of a visual feedback that resembles human actions, the effect of human factors such as confidence and motivation, and the role of embodiment in the learning process of a motor imagery task. Our results from a series of experiments in which users BCI-operated a humanlike android robot confirm that realistic visual feedback can induce a sense of embodiment, which promotes a significant learning of the motor imagery task in a short amount of time. We review the impact of humanlike visual feedback in optimized modulation of brain activity by the BCI users.",book:{id:"6610",slug:"evolving-bci-therapy-engaging-brain-state-dynamics",title:"Evolving BCI Therapy",fullTitle:"Evolving BCI Therapy - Engaging Brain State Dynamics"},signatures:"Maryam Alimardani, Shuichi Nishio and Hiroshi Ishiguro",authors:[{id:"11981",title:"Prof.",name:"Hiroshi",middleName:null,surname:"Ishiguro",slug:"hiroshi-ishiguro",fullName:"Hiroshi Ishiguro"},{id:"231131",title:"Dr.",name:"Maryam",middleName:null,surname:"Alimardani",slug:"maryam-alimardani",fullName:"Maryam Alimardani"},{id:"231134",title:"Dr.",name:"Shuichi",middleName:null,surname:"Nishio",slug:"shuichi-nishio",fullName:"Shuichi Nishio"}]}],mostDownloadedChaptersLast30Days:[{id:"29764",title:"Underlying Causes of Paresthesia",slug:"underlying-causes-of-paresthesia",totalDownloads:193348,totalCrossrefCites:3,totalDimensionsCites:7,abstract:null,book:{id:"1069",slug:"paresthesia",title:"Paresthesia",fullTitle:"Paresthesia"},signatures:"Mahdi Sharif-Alhoseini, Vafa Rahimi-Movaghar and Alexander R. Vaccaro",authors:[{id:"91165",title:"Prof.",name:"Vafa",middleName:null,surname:"Rahimi-Movaghar",slug:"vafa-rahimi-movaghar",fullName:"Vafa Rahimi-Movaghar"}]},{id:"63258",title:"Anatomy and Function of the Hypothalamus",slug:"anatomy-and-function-of-the-hypothalamus",totalDownloads:4632,totalCrossrefCites:6,totalDimensionsCites:12,abstract:"The hypothalamus is a small but important area of the brain formed by various nucleus and nervous fibers. Through its neuronal connections, it is involved in many complex functions of the organism such as vegetative system control, homeostasis of the organism, thermoregulation, and also in adjusting the emotional behavior. The hypothalamus is involved in different daily activities like eating or drinking, in the control of the body’s temperature and energy maintenance, and in the process of memorizing. It also modulates the endocrine system through its connections with the pituitary gland. Precise anatomical description along with a correct characterization of the component structures is essential for understanding its functions.",book:{id:"6331",slug:"hypothalamus-in-health-and-diseases",title:"Hypothalamus in Health and Diseases",fullTitle:"Hypothalamus in Health and Diseases"},signatures:"Miana Gabriela Pop, Carmen Crivii and Iulian Opincariu",authors:null},{id:"57103",title:"GABA and Glutamate: Their Transmitter Role in the CNS and Pancreatic Islets",slug:"gaba-and-glutamate-their-transmitter-role-in-the-cns-and-pancreatic-islets",totalDownloads:3565,totalCrossrefCites:4,totalDimensionsCites:10,abstract:"Glutamate and gamma-aminobutyric acid (GABA) are the major neurotransmitters in the mammalian brain. Inhibitory GABA and excitatory glutamate work together to control many processes, including the brain’s overall level of excitation. The contributions of GABA and glutamate in extra-neuronal signaling are by far less widely recognized. In this chapter, we first discuss the role of both neurotransmitters during development, emphasizing the importance of the shift from excitatory to inhibitory GABAergic neurotransmission. The second part summarizes the biosynthesis and role of GABA and glutamate in neurotransmission in the mature brain, and major neurological disorders associated with glutamate and GABA receptors and GABA release mechanisms. The final part focuses on extra-neuronal glutamatergic and GABAergic signaling in pancreatic islets of Langerhans, and possible associations with type 1 diabetes mellitus.",book:{id:"6237",slug:"gaba-and-glutamate-new-developments-in-neurotransmission-research",title:"GABA And Glutamate",fullTitle:"GABA And Glutamate - New Developments In Neurotransmission Research"},signatures:"Christiane S. Hampe, Hiroshi Mitoma and Mario Manto",authors:[{id:"210220",title:"Prof.",name:"Christiane",middleName:null,surname:"Hampe",slug:"christiane-hampe",fullName:"Christiane Hampe"},{id:"210485",title:"Prof.",name:"Mario",middleName:null,surname:"Manto",slug:"mario-manto",fullName:"Mario Manto"},{id:"210486",title:"Prof.",name:"Hiroshi",middleName:null,surname:"Mitoma",slug:"hiroshi-mitoma",fullName:"Hiroshi Mitoma"}]},{id:"35802",title:"Cross-Cultural/Linguistic Differences in the Prevalence of Developmental Dyslexia and the Hypothesis of Granularity and Transparency",slug:"cross-cultural-linguistic-differences-in-the-prevalence-of-developmental-dyslexia-and-the-hypothesis",totalDownloads:3622,totalCrossrefCites:2,totalDimensionsCites:7,abstract:null,book:{id:"673",slug:"dyslexia-a-comprehensive-and-international-approach",title:"Dyslexia",fullTitle:"Dyslexia - A Comprehensive and International Approach"},signatures:"Taeko N. Wydell",authors:[{id:"87489",title:"Prof.",name:"Taeko",middleName:"N.",surname:"Wydell",slug:"taeko-wydell",fullName:"Taeko Wydell"}]},{id:"58597",title:"Testosterone and Erectile Function: A Review of Evidence from Basic Research",slug:"testosterone-and-erectile-function-a-review-of-evidence-from-basic-research",totalDownloads:1370,totalCrossrefCites:2,totalDimensionsCites:3,abstract:"Androgens are essential for male physical activity and normal erectile function. Hence, age-related testosterone deficiency, known as late-onset hypogonadism (LOH), is considered a risk factor for erectile dysfunction (ED). This chapter summarizes relevant basic research reports examining the effects of testosterone on erectile function. Testosterone affects several organs and is especially active on the erectile tissue. The mechanism of testosterone deficiency effects on erectile function and the results of testosterone replacement therapy (TRT) have been well studied. Testosterone affects nitric oxide (NO) production and phosphodiesterase type 5 (PDE-5) expression in the corpus cavernosum through molecular pathways, preserves smooth muscle contractility by regulating both contraction and relaxation, and maintains the structure of the corpus cavernosum. Interestingly, testosterone deficiency has relationship to neurological diseases, which leads to ED. Testosterone replacement therapy is widely used to treat patients with testosterone deficiency; however, this treatment might also induce some problems. Basic research suggests that PDE-5 inhibitors, L-citrulline, and/or resveratrol therapy might be effective therapeutic options for testosterone deficiency-induced ED. Future research should confirm these findings through more specific experiments using molecular tools and may shed more light on endocrine-related ED and its possible treatments.",book:{id:"5994",slug:"sex-hormones-in-neurodegenerative-processes-and-diseases",title:"Sex Hormones in Neurodegenerative Processes and Diseases",fullTitle:"Sex Hormones in Neurodegenerative Processes and Diseases"},signatures:"Tomoya Kataoka and Kazunori Kimura",authors:[{id:"219042",title:"Ph.D.",name:"Tomoya",middleName:null,surname:"Kataoka",slug:"tomoya-kataoka",fullName:"Tomoya Kataoka"},{id:"229066",title:"Prof.",name:"Kazunori",middleName:null,surname:"Kimura",slug:"kazunori-kimura",fullName:"Kazunori Kimura"}]}],onlineFirstChaptersFilter:{topicId:"18",limit:6,offset:0},onlineFirstChaptersCollection:[{id:"82953",title:"Early Visual Areas are Activated during Object Recognition in Emerging Images",slug:"early-visual-areas-are-activated-during-object-recognition-in-emerging-images",totalDownloads:1,totalDimensionsCites:0,doi:"10.5772/intechopen.105756",abstract:"Human observers can reliably segment visual input and recognise objects. However, the underlying processes happen so quickly that they normally cannot be captured with fMRI. We used Emerging Images (EI), which contains a hidden object and extends the process of recognition, to investigate the involvement of early visual areas (V1, V2 and V3) and lateral occipital complex (LOC) in object recognition. The early visual areas were located with a retinotopy scan and the LOC with a localiser. The participants (N=8) then viewed an EI, followed by the hidden object’s silhouette (disambiguation), and then, the EI was repeated. BOLD responses before and after disambiguation were compared. The retinotopy parameters were used to back-project the BOLD response onto the visual field, creating spatially detailed maps of the activity change. V1 and V2 (but not V3) showed stronger response after disambiguation, while there was no difference in the LOC. The back-projections revealed no distinct pattern or changes in activity on object location, indicating that the activity in V1 and V2 is not specific for voxels corresponding to the object location. We found no difference before and after disambiguation in the LOC, which may be repetition suppression counteracting the effect of recognition.",book:{id:"11374",title:"Sensory Nervous System - Computational Neuroimaging Investigations of Topographical Organization in Human Sensory Cortex",coverURL:"https://cdn.intechopen.com/books/images_new/11374.jpg"},signatures:"Marleen Bakker, Hinke N. Halbertsma, Nicolás Gravel, Remco Renken, Frans W. Cornelissen and Barbara Nordhjem"},{id:"82931",title:"Neuroinflammation in Traumatic Brain Injury",slug:"neuroinflammation-in-traumatic-brain-injury",totalDownloads:3,totalDimensionsCites:0,doi:"10.5772/intechopen.105178",abstract:"Neuroinflammation following traumatic brain injury (TBI) is an important cause of secondary brain injury that perpetuates the duration and scope of disease after initial impact. This chapter discusses the pathophysiology of acute and chronic neuroinflammation, providing insight into factors that influence the acute clinical course and later functional outcomes. Secondary injury due to neuroinflammation is described by mechanisms of action such as ischemia, neuroexcitotoxicity, oxidative stress, and glymphatic and lymphatic dysfunction. Neurodegenerative sequelae of inflammation, including chronic traumatic encephalopathy, which are important to understand for clinical practice, are detailed by disease type. Prominent research topics of TBI animal models and biomarkers of traumatic neuroinflammation are outlined to provide insight into the advances in TBI research. We then discuss current clinical treatments in TBI and their implications in preventing inflammation. To complete the chapter, recent research models, novel biomarkers, and future research directions aimed at mitigating TBI will be described and will highlight novel therapeutic targets. Understanding the pathophysiology and contributors of neuroinflammation after TBI will aid in future development of prophylaxis strategies, as well as more tailored management and treatment algorithms. This topic chapter is important to both clinicians and basic and translational scientists, with the goal of improving patient outcomes in this common disease.",book:{id:"11367",title:"Traumatic Brain Injury",coverURL:"https://cdn.intechopen.com/books/images_new/11367.jpg"},signatures:"Grace Y. Kuo, Fawaz Philip Tarzi, Stan Louie and Roy A. Poblete"},{id:"82876",title:"Oxygen Tissue Levels as an Effectively Modifiable Factor in Alzheimer’s Disease Improvement",slug:"oxygen-tissue-levels-as-an-effectively-modifiable-factor-in-alzheimer-s-disease-improvement",totalDownloads:8,totalDimensionsCites:0,doi:"10.5772/intechopen.106331",abstract:"Despite the advance in biochemistry, there are two substantial errors that have remained for at least two centuries. One is that oxygen from the atmosphere passes through the lungs and reaches the bloodstream, which distributes it throughout the body. Another major mistake is the belief that such oxygen is used by the cell to obtain energy, by combining it with glucose. Since the late nineteenth century, it began to be published that the gas exchange in the lungs cannot be explained by diffusion. Even Christian Bohr suggested that it looked like a cellular secretion. But despite experimental evidence to the contrary and based only on theoretical models, the dogma that our body takes the oxygen it contains inside from the air around it has been perpetuated to this day. The oxygen levels contained in the human body are high, close to 99%, and the atmosphere only contains between 19 and 21%. The hypothesis that there is a supposed oxygen concentrating mechanism has not been experimentally proven to date, after almost two centuries. The mistaken belief, even among neurologists, that our body takes oxygen from the atmosphere is widespread, even though there is no experimental basis to support it, just theoretical models. Our finding that the human body can take oxygen from the water it contains, not from the air around it, like plants, comes to mark a before and after in biology in general, and the CNS is no exception. Therefore, establishing the true origin of the oxygen present within our body and brain will allow us to better understand the physio pathogenesis of neurodegenerative diseases.",book:{id:"11637",title:"Neuropsychology of Dementia",coverURL:"https://cdn.intechopen.com/books/images_new/11637.jpg"},signatures:"Arturo Solís Herrera"},{id:"82859",title:"Impact of Hypoxia on Astrocyte Induced Pathogenesis",slug:"impact-of-hypoxia-on-astrocyte-induced-pathogenesis",totalDownloads:6,totalDimensionsCites:0,doi:"10.5772/intechopen.106263",abstract:"Astrocytes are the most abundant cells of the central nervous system. These cells are of diverse types based on their function and structure. Astrocyte activation is linked mainly with microbial infections, but long-term activation can lead to neurological impairment. Astrocytes play a significant role in neuro-inflammation by activating pro-inflammatory pathways. Activation of interleukins and cytokines causes neuroinflammation resulting in many neurodegenerative disorders such as stroke, growth of tumours, and Alzheimer’s. Inflammation of the brain hinders neural circulation and compromises blood flow by affecting the blood–brain barrier. So the oxygen concentration is lowered, causing brain hypoxia. Hypoxia leads to the activation of nuclear factor kappa B (NFkB) and hypoxia-inducible factors (HIF), which aggravates the inflammatory state of the brain. Hypoxia evoked changes in the blood–brain barrier, further complicating astrocyte-induced pathogenesis.",book:{id:"10744",title:"Astrocytes in Brain Communication and Disease",coverURL:"https://cdn.intechopen.com/books/images_new/10744.jpg"},signatures:"Farwa Munir, Nida Islam, Muhammad Hassan Nasir, Zainab Anis, Shahar Bano, Shahzaib Naeem, Atif Amin Baig and Zaineb Sohail"},{id:"82839",title:"Neurophysiology of Emotions",slug:"neurophysiology-of-emotions",totalDownloads:2,totalDimensionsCites:0,doi:"10.5772/intechopen.106043",abstract:"Emotions are automatic and primary patterns of purposeful cognitive-behavioral organizations. They have three main functions: coordination, signaling, and information. First, emotions coordinate organs and tissues, thus predisposing the body to peculiar responses. Scholars have not reached a consensus on the plausibility of emotion-specific response patterns yet. Despite the limitations, data support the hypothesis of specific response patterns for distinct subtypes of emotions. Second, emotional episodes signal the current state of the individual. Humans display their state with verbal behaviors, nonverbal actions (e.g., facial movements), and neurovegetative signals. Third, emotions inform the brain for interpretative and evaluative purposes. Emotional experiences include mental representations of arousal, relations, and situations. Every emotional episode begins with exposure to stimuli with distinctive features (i.e., elicitor). These inputs can arise from learning, expressions, empathy, and be inherited, or rely on limited aspects of the environment (i.e., sign stimuli). The existence of the latter ones in humans is unclear; however, emotions influence several processes, such as perception, attention, learning, memory, decision-making, attitudes, and mental schemes. Overall, the literature suggests the nonlinearity of the emotional process. Each section outlines the neurophysiological basis of elements of emotion.",book:{id:"11742",title:"Neurophysiology",coverURL:"https://cdn.intechopen.com/books/images_new/11742.jpg"},signatures:"Maurizio Oggiano"},{id:"82172",title:"Neuroimaging in Common Neurological Diseases Treated by Anticoagulants",slug:"neuroimaging-in-common-neurological-diseases-treated-by-anticoagulants",totalDownloads:7,totalDimensionsCites:0,doi:"10.5772/intechopen.105128",abstract:"Stroke imaging/Cerebral Venous sinus thrombosis/Arterial dissecting disease in Head and Neck regions/Neurocomplication of anticoagulation therapy. Nowsday, anticoagulant drugs are common drugs used in daily practice for patients in neurology clinic. Anticoagulant treatment used for treated symptomatic patients as well as for prophylaxis therapy in asymptomatic patients. The purpose of this chapter based on the review of essential neuroimaging in the most common neurological conditions that benefit from treatment with anticoagulant drugs such as ischemic stroke, cerebral venous sinus thrombosis, and arterial dissecting disease of head and neck arteries and will be enclosed with neuroimaging in case of neurocomplication by anticoagulant therapy.",book:{id:"11742",title:"Neurophysiology",coverURL:"https://cdn.intechopen.com/books/images_new/11742.jpg"},signatures:"Pipat Chiewvit"}],onlineFirstChaptersTotal:12},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:90,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:107,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:33,numberOfPublishedChapters:330,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:14,numberOfPublishedChapters:145,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:9,numberOfPublishedChapters:139,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!0},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:122,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:112,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:21,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:10,numberOfOpenTopics:1,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!0},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:1,numberOfPublishedChapters:19,numberOfOpenTopics:5,numberOfUpcomingTopics:0,issn:"2753-6580",doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}},{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}}]},series:{item:{id:"14",title:"Artificial Intelligence",doi:"10.5772/intechopen.79920",issn:"2633-1403",scope:"Artificial Intelligence (AI) is a rapidly developing multidisciplinary research area that aims to solve increasingly complex problems. In today's highly integrated world, AI promises to become a robust and powerful means for obtaining solutions to previously unsolvable problems. This Series is intended for researchers and students alike interested in this fascinating field and its many applications.",coverUrl:"https://cdn.intechopen.com/series/covers/14.jpg",latestPublicationDate:"July 5th, 2022",hasOnlineFirst:!0,numberOfPublishedBooks:9,editor:{id:"218714",title:"Prof.",name:"Andries",middleName:null,surname:"Engelbrecht",slug:"andries-engelbrecht",fullName:"Andries Engelbrecht",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRNR8QAO/Profile_Picture_1622640468300",biography:"Andries Engelbrecht received the Masters and PhD degrees in Computer Science from the University of Stellenbosch, South Africa, in 1994 and 1999 respectively. He is currently appointed as the Voigt Chair in Data Science in the Department of Industrial Engineering, with a joint appointment as Professor in the Computer Science Division, Stellenbosch University. Prior to his appointment at Stellenbosch University, he has been at the University of Pretoria, Department of Computer Science (1998-2018), where he was appointed as South Africa Research Chair in Artifical Intelligence (2007-2018), the head of the Department of Computer Science (2008-2017), and Director of the Institute for Big Data and Data Science (2017-2018). In addition to a number of research articles, he has written two books, Computational Intelligence: An Introduction and Fundamentals of Computational Swarm Intelligence.",institutionString:null,institution:{name:"Stellenbosch University",institutionURL:null,country:{name:"South Africa"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:6,paginationItems:[{id:"22",title:"Applied Intelligence",coverUrl:"https://cdn.intechopen.com/series_topics/covers/22.jpg",isOpenForSubmission:!0,editor:{id:"27170",title:"Prof.",name:"Carlos",middleName:"M.",surname:"Travieso-Gonzalez",slug:"carlos-travieso-gonzalez",fullName:"Carlos Travieso-Gonzalez",profilePictureURL:"https://mts.intechopen.com/storage/users/27170/images/system/27170.jpeg",biography:"Carlos M. Travieso-González received his MSc degree in Telecommunication Engineering at Polytechnic University of Catalonia (UPC), Spain in 1997, and his Ph.D. degree in 2002 at the University of Las Palmas de Gran Canaria (ULPGC-Spain). He is a full professor of signal processing and pattern recognition and is head of the Signals and Communications Department at ULPGC, teaching from 2001 on subjects on signal processing and learning theory. His research lines are biometrics, biomedical signals and images, data mining, classification system, signal and image processing, machine learning, and environmental intelligence. He has researched in 52 international and Spanish research projects, some of them as head researcher. He is co-author of 4 books, co-editor of 27 proceedings books, guest editor for 8 JCR-ISI international journals, and up to 24 book chapters. He has over 450 papers published in international journals and conferences (81 of them indexed on JCR – ISI - Web of Science). He has published seven patents in the Spanish Patent and Trademark Office. He has been a supervisor on 8 Ph.D. theses (11 more are under supervision), and 130 master theses. He is the founder of The IEEE IWOBI conference series and the president of its Steering Committee, as well as the founder of both the InnoEducaTIC and APPIS conference series. He is an evaluator of project proposals for the European Union (H2020), Medical Research Council (MRC, UK), Spanish Government (ANECA, Spain), Research National Agency (ANR, France), DAAD (Germany), Argentinian Government, and the Colombian Institutions. He has been a reviewer in different indexed international journals (<70) and conferences (<250) since 2001. He has been a member of the IASTED Technical Committee on Image Processing from 2007 and a member of the IASTED Technical Committee on Artificial Intelligence and Expert Systems from 2011. \n\nHe has held the general chair position for the following: ACM-APPIS (2020, 2021), IEEE-IWOBI (2019, 2020 and 2020), A PPIS (2018, 2019), IEEE-IWOBI (2014, 2015, 2017, 2018), InnoEducaTIC (2014, 2017), IEEE-INES (2013), NoLISP (2011), JRBP (2012), and IEEE-ICCST (2005)\n\nHe is an associate editor of the Computational Intelligence and Neuroscience Journal (Hindawi – Q2 JCR-ISI). He was vice dean from 2004 to 2010 in the Higher Technical School of Telecommunication Engineers at ULPGC and the vice dean of Graduate and Postgraduate Studies from March 2013 to November 2017. He won the “Catedra Telefonica” Awards in Modality of Knowledge Transfer, 2017, 2018, and 2019 editions, and awards in Modality of COVID Research in 2020.\n\nPublic References:\nResearcher ID http://www.researcherid.com/rid/N-5967-2014\nORCID https://orcid.org/0000-0002-4621-2768 \nScopus Author ID https://www.scopus.com/authid/detail.uri?authorId=6602376272\nScholar Google https://scholar.google.es/citations?user=G1ks9nIAAAAJ&hl=en \nResearchGate https://www.researchgate.net/profile/Carlos_Travieso",institutionString:null,institution:{name:"University of Las Palmas de Gran Canaria",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null},{id:"23",title:"Computational Neuroscience",coverUrl:"https://cdn.intechopen.com/series_topics/covers/23.jpg",isOpenForSubmission:!0,editor:{id:"14004",title:"Dr.",name:"Magnus",middleName:null,surname:"Johnsson",slug:"magnus-johnsson",fullName:"Magnus Johnsson",profilePictureURL:"https://mts.intechopen.com/storage/users/14004/images/system/14004.png",biography:"Dr Magnus Johnsson is a cross-disciplinary scientist, lecturer, scientific editor and AI/machine learning consultant from Sweden. \n\nHe is currently at Malmö University in Sweden, but also held positions at Lund University in Sweden and at Moscow Engineering Physics Institute. \nHe holds editorial positions at several international scientific journals and has served as a scientific editor for books and special journal issues. \nHis research interests are wide and include, but are not limited to, autonomous systems, computer modeling, artificial neural networks, artificial intelligence, cognitive neuroscience, cognitive robotics, cognitive architectures, cognitive aids and the philosophy of mind. \n\nDr. Johnsson has experience from working in the industry and he has a keen interest in the application of neural networks and artificial intelligence to fields like industry, finance, and medicine. \n\nWeb page: www.magnusjohnsson.se",institutionString:null,institution:{name:"Malmö University",institutionURL:null,country:{name:"Sweden"}}},editorTwo:null,editorThree:null},{id:"24",title:"Computer Vision",coverUrl:"https://cdn.intechopen.com/series_topics/covers/24.jpg",isOpenForSubmission:!0,editor:{id:"294154",title:"Prof.",name:"George",middleName:null,surname:"Papakostas",slug:"george-papakostas",fullName:"George Papakostas",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002hYaGbQAK/Profile_Picture_1624519712088",biography:"George A. Papakostas has received a diploma in Electrical and Computer Engineering in 1999 and the M.Sc. and Ph.D. degrees in Electrical and Computer Engineering in 2002 and 2007, respectively, from the Democritus University of Thrace (DUTH), Greece. Dr. Papakostas serves as a Tenured Full Professor at the Department of Computer Science, International Hellenic University, Greece. Dr. Papakostas has 10 years of experience in large-scale systems design as a senior software engineer and technical manager, and 20 years of research experience in the field of Artificial Intelligence. Currently, he is the Head of the “Visual Computing” division of HUman-MAchines INteraction Laboratory (HUMAIN-Lab) and the Director of the MPhil program “Advanced Technologies in Informatics and Computers” hosted by the Department of Computer Science, International Hellenic University. He has (co)authored more than 150 publications in indexed journals, international conferences and book chapters, 1 book (in Greek), 3 edited books, and 5 journal special issues. His publications have more than 2100 citations with h-index 27 (GoogleScholar). 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. Dr Ventura also holds the positions of Affiliated Professor at Virginia Commonwealth University (Richmond, USA) and Distinguished Adjunct Professor at King Abdulaziz University (Jeddah, Saudi Arabia). Additionally, he is deputy director of the Andalusian Research Institute in Data Science and Computational Intelligence (DaSCI) and heads the Knowledge Discovery and Intelligent Systems Research Laboratory. He has published more than ten books and over 300 articles in journals and scientific conferences. Currently, his work has received over 18,000 citations according to Google Scholar, including more than 2200 citations in 2020. In the last five years, he has published more than 60 papers in international journals indexed in the JCR (around 70% of them belonging to first quartile journals) and he has edited some Springer books “Supervised Descriptive Pattern Mining” (2018), “Multiple Instance Learning - Foundations and Algorithms” (2016), and “Pattern Mining with Evolutionary Algorithms” (2016). He has also been involved in more than 20 research projects supported by the Spanish and Andalusian governments and the European Union. He currently belongs to the editorial board of PeerJ Computer Science, Information Fusion and Engineering Applications of Artificial Intelligence journals, being also associate editor of Applied Computational Intelligence and Soft Computing and IEEE Transactions on Cybernetics. Finally, he is editor-in-chief of Progress in Artificial Intelligence. He is a Senior Member of the IEEE Computer, the IEEE Computational Intelligence, and the IEEE Systems, Man, and Cybernetics Societies, and the Association of Computing Machinery (ACM). Finally, his main research interests include data science, computational intelligence, and their applications.",institutionString:null,institution:{name:"University of Córdoba",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null},{id:"26",title:"Machine Learning and Data Mining",coverUrl:"https://cdn.intechopen.com/series_topics/covers/26.jpg",isOpenForSubmission:!0,editor:{id:"24555",title:"Dr.",name:"Marco Antonio",middleName:null,surname:"Aceves Fernandez",slug:"marco-antonio-aceves-fernandez",fullName:"Marco Antonio Aceves Fernandez",profilePictureURL:"https://mts.intechopen.com/storage/users/24555/images/system/24555.jpg",biography:"Dr. Marco Antonio Aceves Fernandez obtained his B.Sc. (Eng.) in Telematics from the Universidad de Colima, Mexico. 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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. 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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. 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