\\n\\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\\n\\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\\n"}]',published:!0,mainMedia:{caption:"Highly Cited",originalUrl:"/media/original/117"}},components:[{type:"htmlEditorComponent",content:'IntechOpen is proud to announce that 191 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\nThroughout the years, the list has named a total of 261 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\nReleased this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\nWe wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
Note: Edited in March 2021
\n'}],latestNews:[{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"},{slug:"intechopen-identified-as-one-of-the-most-significant-contributor-to-oa-book-growth-in-doab-20210809",title:"IntechOpen Identified as One of the Most Significant Contributors to OA Book Growth in DOAB"}]},book:{item:{type:"book",id:"6406",leadTitle:null,fullTitle:"Parkinson's Disease - Understanding Pathophysiology and Developing Therapeutic Strategies",title:"Parkinson's Disease",subtitle:"Understanding Pathophysiology and Developing Therapeutic Strategies",reviewType:"peer-reviewed",abstract:'Parkinson\'s disease (PD) is the second most common neurodegenerative disorder results due to loss of dopamine producing brain cells. Knowledge relating to PD condition has been known since 5000BC, however no effective therapeutic strategies are available till today. Therefore it is important for neurobiologists to work further by taking advantage of modern scientific methods and develop appropriate therapeutic strategies. Efforts in this direction are worthy as they will reduce the burden of PD among elderly, who are already burdened with age related systemic degenerative processes. This book is a humble effort in that progressive direction. It has chapters covering multiple aspects relating to etiology, pathophysiology of PD, available and futuristic therapeutics strategies. Therefore it will be of interest to common man, biomedical researchers and clinicians. This is one small step in a direction "to reduce the burden of neurological disease."',isbn:"978-1-78923-153-3",printIsbn:"978-1-78923-152-6",pdfIsbn:"978-1-83881-459-5",doi:"10.5772/intechopen.70111",price:119,priceEur:129,priceUsd:155,slug:"parkinson-s-disease-understanding-pathophysiology-and-developing-therapeutic-strategies",numberOfPages:126,isOpenForSubmission:!1,isInWos:1,isInBkci:!1,hash:"0038453d1272466535c41e37d94ee52f",bookSignature:"Sarat Chandra Yenisetti",publishedDate:"May 30th 2018",coverURL:"https://cdn.intechopen.com/books/images_new/6406.jpg",numberOfDownloads:9688,numberOfWosCitations:2,numberOfCrossrefCitations:5,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:12,numberOfDimensionsCitationsByBook:0,hasAltmetrics:1,numberOfTotalCitations:19,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"June 13th 2017",dateEndSecondStepPublish:"July 4th 2017",dateEndThirdStepPublish:"October 28th 2017",dateEndFourthStepPublish:"December 29th 2017",dateEndFifthStepPublish:"February 28th 2018",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"181774",title:"Prof.",name:"Sarat Chandra",middleName:null,surname:"Yenisetti",slug:"sarat-chandra-yenisetti",fullName:"Sarat Chandra Yenisetti",profilePictureURL:"https://mts.intechopen.com/storage/users/181774/images/system/181774.jpeg",biography:"Dr. Sarat Chandra Yenisetti is an Associate Professor and Head of Drosophila Neurobiology Laboratory in Department of Zoology, Nagaland University (Central), Nagaland, India. He completed M.Sc. from Bangaluru University, India and was awarded a Ph.D. from Kuvempu University, India. Dr. Sarat obtained post-doctoral training in 'modelling Parkinson’s disease using Drosophila” from Neurogenetics, National Institute of Neurological Disorders and Stroke (NINDS) of National Institutes of Health (NIH), Bethesda, USA and University of Regensburg, Germany. His laboratory, funded through multiple research grants from Department of Biotechnology (DBT), India, University of Grants Commission (UGC), India and Department of Science and Technology (DST), India, focuses on Drosophila approach to understand Parkinson's Disease associated neurodegeneration as well as identification of novel therapeutic targets which may help to reduce the burden of PD in human.",institutionString:"Nagaland University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"3",totalChapterViews:"0",totalEditedBooks:"2",institution:{name:"Nagaland University",institutionURL:null,country:{name:"India"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"1056",title:"Neurology",slug:"neurology"}],chapters:[{id:"59923",title:"Sleep Disorders in Parkinson’s Disease",doi:"10.5772/intechopen.73520",slug:"sleep-disorders-in-parkinson-s-disease",totalDownloads:1144,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,abstract:"Sleep disorders in Parkinson’s disease (PD) are common. They can develop due to many factors. PD symptoms like rigidity or tremor, some PD medications, restless legs syndrome, depression, nocturia, and degenerative changes in the brainstem can cause sleep disorders in PD. Sleep disorders in PD may occur during the day or at night. Sleep disorders can occur before or during the disease. Sleep disorders can impair patients’ quality of life and worsen their symptoms. For this reason, it is very important to recognize these disorders and treat them appropriately. This chapter discusses the clinical features, diagnosis, comorbidities, management, and pathogenesis of sleep disorders in PD under the literature light. At the same time, it describes the most appropriate treatment considerations.",signatures:"Dursun Aygun",downloadPdfUrl:"/chapter/pdf-download/59923",previewPdfUrl:"/chapter/pdf-preview/59923",authors:[{id:"211345",title:"Prof.",name:"Dursun",surname:"Aygun",slug:"dursun-aygun",fullName:"Dursun Aygun"}],corrections:null},{id:"59466",title:"A Description of Parkinson’s Disease in People of African Origin",doi:"10.5772/intechopen.73519",slug:"a-description-of-parkinson-s-disease-in-people-of-african-origin",totalDownloads:847,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"With the increase in life expectancy of African populations, the burden of degenerative diseases such as Parkinson’s disease (PD) has grown. Neurologists are noticing trends in the differences reported in the phenotype of PD among African populations compared to Caucasian counterparts. These differences are chiefly in age of onset and clinical presentation. This chapter focuses on different aspects of the presentation of Parkinson’s disease, as they apply to African populations and those of African origin.",signatures:"Marcelle Smith",downloadPdfUrl:"/chapter/pdf-download/59466",previewPdfUrl:"/chapter/pdf-preview/59466",authors:[{id:"221768",title:"Dr.",name:"Marcelle",surname:"Smith",slug:"marcelle-smith",fullName:"Marcelle Smith"}],corrections:null},{id:"59811",title:"Effects of Genetic Variability in Dopaminergic Pathway on Treatment Response in Parkinson’s Disease",doi:"10.5772/intechopen.75051",slug:"effects-of-genetic-variability-in-dopaminergic-pathway-on-treatment-response-in-parkinson-s-disease",totalDownloads:957,totalCrossrefCites:0,totalDimensionsCites:4,hasAltmetrics:1,abstract:"Parkinson’s disease (PD) is a chronic progressive neurodegenerative brain disorder presenting with motor signs and symptoms, such as akinesia, rest tremor, rigidity, and later in disease progression postural instability. However, nonmotor symptoms may harm patients’ quality of life even more than the motor ones. The etiopathogenesis is not clear yet. PD may develop due to a combination of genetic and environmental factors. It is treated symptomatically with dopaminergic drugs. The gold standard of PD management is L-Dopa, however also other drugs are frequently used, such as dopamine agonists, MAOB inhibitors, COMT inhibitors, and occasionally amantadine and anticholinergic drugs. Many patients experience several adverse events of L-Dopa treatment, such as different motor complications. Furthermore, nonmotor adverse events of dopaminergic treatment may occur. The efficacy of drugs varies between patients as well. Several polymorphic genes have already been associated with treatment outcome in PD, such as metabolic enzymes, transport and receptor genes, and might serve as treatment outcome prediction factors. As gene-environment interactions were also shown to contribute to PD development, they might also be able to predict treatment response. Such genetic biomarkers could be helpful in personalized care of PD patients to prevent adverse events and inefficacy of a certain drug.",signatures:"Sara Redenšek, Maja Trošt and Vita Dolžan",downloadPdfUrl:"/chapter/pdf-download/59811",previewPdfUrl:"/chapter/pdf-preview/59811",authors:[{id:"60449",title:"Prof.",name:"Vita",surname:"Dolžan",slug:"vita-dolzan",fullName:"Vita Dolžan"},{id:"201284",title:"MSc.",name:"Sara",surname:"Redenšek",slug:"sara-redensek",fullName:"Sara Redenšek"},{id:"216258",title:"Dr.",name:"Maja",surname:"Trošt",slug:"maja-trost",fullName:"Maja Trošt"}],corrections:null},{id:"59956",title:"Non-Invasive Neuromodulation Therapies for Parkinson’s Disease",doi:"10.5772/intechopen.75052",slug:"non-invasive-neuromodulation-therapies-for-parkinson-s-disease",totalDownloads:1154,totalCrossrefCites:3,totalDimensionsCites:4,hasAltmetrics:0,abstract:"Noninvasive brain stimulation (NIBS) technologies have been applied to study brain physiology and, more recently, have been recognized for their therapeutic potential as an adjunctive treatment for various neurologic and psychiatric disorders. Transcranial magnetic stimulation (TMS) and transcranial electric stimulation (tES) are two of the most studied NIBS modalities in Parkinson’s disease. They are non-systemic and relatively safe. Most therapeutic trials have been conducted to ameliorate motor symptoms of Parkinson’s disease (PD) with overall positive results using various stimulation modalities and methods. Notwithstanding significant results, evidence has not yet been compelling mainly due to small-size studies, lack of standardization of methodologies and other study design limitations. NIBS hold promise for treatment of PD symptoms and PD related complications. Large, well designed clinical trials are needed to corroborate these positive findings and inform its durability and the overall clinical relevance for the treatment of PD.",signatures:"Milton C. Biagioni, Kush Sharma, Hamzeh A. Migdadi and Alberto\nCucca",downloadPdfUrl:"/chapter/pdf-download/59956",previewPdfUrl:"/chapter/pdf-preview/59956",authors:[{id:"216856",title:"Dr.",name:"Milton",surname:"Biagioni",slug:"milton-biagioni",fullName:"Milton Biagioni"},{id:"218126",title:"Dr.",name:"Alberto",surname:"Cucca",slug:"alberto-cucca",fullName:"Alberto Cucca"},{id:"218127",title:"Dr.",name:"Hamzeh",surname:"Migdadi",slug:"hamzeh-migdadi",fullName:"Hamzeh Migdadi"},{id:"218128",title:"Dr.",name:"Kush",surname:"Sharma",slug:"kush-sharma",fullName:"Kush Sharma"}],corrections:null},{id:"59296",title:"Development of Neural Stem Cell-Based Therapies for Parkinson’s Disease",doi:"10.5772/intechopen.73870",slug:"development-of-neural-stem-cell-based-therapies-for-parkinson-s-disease",totalDownloads:1052,totalCrossrefCites:0,totalDimensionsCites:2,hasAltmetrics:0,abstract:"Neural stem cell (NSC)-based therapies, such as cell transplantation, are an emerging strategy for restoring neuronal function in Parkinson’s disease (PD), which is characterized by a profound and selective loss of nigrostriatal dopaminergic (DA) neurons. Advanced researches on the microenvironment of grafted cells will promote clinical applications of NSCs for neurological disorders. A novel cell culture model of the neurovascular network was therefore devised to investigate autocrine, paracrine, and juxtacrine signaling in the neurovascular unit generated by NSCs and vascular endothelial cells. Preclinical studies using cutting-edge technologies, including cellular reprogramming, advancement in scaffolds for brain tissue engineering, image-guided injection, and noninvasive monitoring of tissue regeneration will pave the way for successful clinical trials of NSC-based therapies for PD. Once the implanted or regenerated DA neurons are integrated into the existing nigrostriatal DA pathway, the symptoms of PD can potentially be alleviated by reversing characteristic neurodegeneration.",signatures:"Jiunn-Tay Lee, Chia-Kuang Tsai and Chung-Hsing Chou",downloadPdfUrl:"/chapter/pdf-download/59296",previewPdfUrl:"/chapter/pdf-preview/59296",authors:[{id:"214630",title:"Dr.",name:"Chung-Hsing",surname:"Chou",slug:"chung-hsing-chou",fullName:"Chung-Hsing Chou"},{id:"234165",title:"Dr.",name:"Jiunn-Tay",surname:"Lee",slug:"jiunn-tay-lee",fullName:"Jiunn-Tay Lee"},{id:"234166",title:"Dr.",name:"Chia-Kuang",surname:"Tsai",slug:"chia-kuang-tsai",fullName:"Chia-Kuang Tsai"}],corrections:null},{id:"60608",title:"Mucuna and Parkinson’s Disease: Treatment with Natural Levodopa",doi:"10.5772/intechopen.74062",slug:"mucuna-and-parkinson-s-disease-treatment-with-natural-levodopa",totalDownloads:4538,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:1,abstract:"Mucuna pruriens is a tropical bean containing large amounts of levodopa and is the most important natural remedy for Parkinson’s disease. Famous neurologists have patented methods of extraction for its advantages over the synthetic forms, Sinemet and Madopar. This natural levodopa is less toxic and has a faster and more lasting effect and can delay the need for pharmaceuticals and combination therapies. Currently, there are many patients with Parkinson’s disease who take Mucuna and spontaneously reduce the dose of conventional drugs and do so behind their doctors’ backs. Mucuna should always be taken under medical supervision.",signatures:"Rafael González Maldonado",downloadPdfUrl:"/chapter/pdf-download/60608",previewPdfUrl:"/chapter/pdf-preview/60608",authors:[{id:"214658",title:"Dr.",name:"Rafael",surname:"Gonzalez-Maldonado",slug:"rafael-gonzalez-maldonado",fullName:"Rafael Gonzalez-Maldonado"}],corrections:null}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},subseries:null,tags:null},relatedBooks:[{type:"book",id:"7256",title:"Dopamine",subtitle:"Health and Disease",isOpenForSubmission:!1,hash:"e46d08f526c35d787be15bcb17126fb8",slug:"dopamine-health-and-disease",bookSignature:"Sarat Chandra Yenisetti",coverURL:"https://cdn.intechopen.com/books/images_new/7256.jpg",editedByType:"Edited by",editors:[{id:"181774",title:"Prof.",name:"Sarat Chandra",surname:"Yenisetti",slug:"sarat-chandra-yenisetti",fullName:"Sarat Chandra Yenisetti"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"1191",title:"Neuromuscular Disorders",subtitle:null,isOpenForSubmission:!1,hash:"6f634511340dcd5fe321e13e83a62531",slug:"neuromuscular-disorders",bookSignature:"Ashraf Zaher",coverURL:"https://cdn.intechopen.com/books/images_new/1191.jpg",editedByType:"Edited by",editors:[{id:"66392",title:"Prof.",name:"Ashraf",surname:"Zaher",slug:"ashraf-zaher",fullName:"Ashraf Zaher"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"745",title:"Neurodegenerative Diseases",subtitle:"Processes, Prevention, Protection and Monitoring",isOpenForSubmission:!1,hash:"3d5795dad33257368f0b7848c22d5dd4",slug:"neurodegenerative-diseases-processes-prevention-protection-and-monitoring",bookSignature:"Raymond Chuen-Chung Chang",coverURL:"https://cdn.intechopen.com/books/images_new/745.jpg",editedByType:"Edited by",editors:[{id:"33396",title:"Dr.",name:"Raymond Chuen-Chung",surname:"Chang",slug:"raymond-chuen-chung-chang",fullName:"Raymond Chuen-Chung Chang"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3278",title:"Neurodegenerative Diseases",subtitle:null,isOpenForSubmission:!1,hash:"aa717c2801cf98db641d48414cef8ced",slug:"neurodegenerative-diseases",bookSignature:"Uday Kishore",coverURL:"https://cdn.intechopen.com/books/images_new/3278.jpg",editedByType:"Edited by",editors:[{id:"155691",title:"Dr.",name:"Uday",surname:"Kishore",slug:"uday-kishore",fullName:"Uday Kishore"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"434",title:"Alzheimer's Disease Pathogenesis",subtitle:"Core Concepts, Shifting Paradigms and Therapeutic Targets",isOpenForSubmission:!1,hash:"49f4c7dbf69e8a9eaf780e37f4aae1ab",slug:"alzheimer-s-disease-pathogenesis-core-concepts-shifting-paradigms-and-therapeutic-targets",bookSignature:"Suzanne De La Monte",coverURL:"https://cdn.intechopen.com/books/images_new/434.jpg",editedByType:"Edited by",editors:[{id:"29111",title:"Dr.",name:"Suzanne",surname:"De La Monte",slug:"suzanne-de-la-monte",fullName:"Suzanne De La Monte"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3296",title:"Understanding Alzheimer's Disease",subtitle:null,isOpenForSubmission:!1,hash:"b040d696d429a2a6dc90cd236f160778",slug:"understanding-alzheimer-s-disease",bookSignature:"Inga Zerr",coverURL:"https://cdn.intechopen.com/books/images_new/3296.jpg",editedByType:"Edited by",editors:[{id:"26013",title:"Prof.",name:"Inga",surname:"Zerr",slug:"inga-zerr",fullName:"Inga Zerr"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"3437",title:"Mood Disorders",subtitle:null,isOpenForSubmission:!1,hash:"62c54b70da87ce48e712c07601105311",slug:"mood-disorders",bookSignature:"Nese Kocabasoglu",coverURL:"https://cdn.intechopen.com/books/images_new/3437.jpg",editedByType:"Edited by",editors:[{id:"91417",title:"Prof.",name:"Nese",surname:"Kocabasoglu",slug:"nese-kocabasoglu",fullName:"Nese Kocabasoglu"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"1062",title:"Dystonia",subtitle:"The Many Facets",isOpenForSubmission:!1,hash:"81069e5ab5b7c4bb52cf7bd16d0c4cb2",slug:"dystonia-the-many-facets",bookSignature:"Raymond L. 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The ultimate goal of pharmacovigilance is to accurately characterize and optimize the benefit/risk ratio of a health product throughout its life cycle which will be highlighted in this book. The Pharmacovigilance Risk Assessment Committee (PRAC) is responsible for assessing and monitoring safety issues for human medicines. PRAC provides the safety recommendations to CHMP. A dedicated chapter will be included for this. It will describe the main tools for the passive and active surveillance of adverse effects associated with drugs. It will provide examples of diseases in various contexts related to clinical studies and the analysis of adverse drug reactions, and offer case studies that illustrate real-life clinical situations.
\r\n\r\n\tThe book will discuss important concepts related to pharmacoepidemiology and pharmacovigilance, describe the importance of signal detection, its method, and approach, and outline how the discipline of Pharmacoepidemiology fits into and can be applied within the drug development process.
\r\n\tThis book is intended for Pharmaceutical industry personnel (especially those working in drug safety), clinical investigators, medical evaluators, those seeking regulatory approval, students, and professors in Clinical Pharmacology, Epidemiology, and Pharmacovigilance.
Tropane alkaloids (Figure 1) are among the oldest medicines known to men. A secondary metabolites containing the tropane nucleus constitute one of the largest and most important group of naturally occurring compounds [1]. Secondary metabolites of Solanaceae plant, sharing tropane skeleton (1) as a common structural feature can be divided into two classes: tropine (2) and ecgonine (3) derivatives [2]. The first group is represented by atropine from
Some tropane alkaloids.
Over 600 naturally occurring alkaloids of tropane can be found in plants such as
Alkaloids possess quite complex structures, and the study of biosynthesis of these alkaloids has a long history. It is generally thought that the tropane moiety arises from complex enzymatic processes involving phytochemical precursors. Incorporation of radioactive labeled precursors has eased monitoring pathway on which the tropane derivatives are formed [10]. Recent studies making use of labeled ornithine (7),
3Alpha-senecioyloxy-6beta-hydroxytropane.
Amino acids precursors in the biosynthesis of tropane skeeton.
It has been found that oxidation of tropane ring can be achieved by molecular oxygen in the presence of ferrous ions. Also, it has been found that these keto forms of tropane can be catalyzed by an enzyme called reductase [12]. For instance, the biosynthesis pathway to tropane alkaloids, tropinone (10), is reduced by reductase to tropine (2), as it can be seen in Figure 4.
Bio-synthesis of tropane
Structural assignments of tropane molecules have exhibited difficult problems, and, as a result, progress in their endeavors has been closely associated with development of modern analytical techniques of spectroscopy, of which mass spectroscopy deserves particular mention such as ESI MS, GC-MS, HPLC-MS, and MALDI MS.
Concerning the pharmacological effects, these compounds are so important because of their pharmacological properties [13]. Alkaloids such as atropine (4), scopolamine (5), and cocaine (6) and their derivatives are best recognized to have pharmacological actions related in the body to the function of neurotransmitter acetylcholine [14]. Some tropane alkaloids can act as anticholinergic effects or stimulants [15]. Pharmaceuticals of tropane derivatives are economically important. Over 20 active pharmaceutical ingredients containing tropane moiety in their structures are manufactured and used as antispasmodics, anesthetic, and mydriatics (see Figure 5) [16].
Some pharmaceutical ingredients containing tropane moiety.
Tropane does not occur naturally in free forms. The favored forms of tropane in plant species are the esters forms. These esters are generally secondary metabolites of the plant species. Tropane esters were isolated from different plant families like Proteaceae, Rhizophoraceae, Euphorbiaceae, and Convolvulaceae, and they are well known to occur in Solanaceae. Most tropane alkaloids in the Solanaceae family arises from the esterification of acids, such as acetic acid, propanoic acid, isobutyric acid, isovaleric acid, 2-methylbutyric acid, tifilic acid (+)-α-hydroxyl-β-phenylpropionic acid, tropic acid, and atropic acid with various hydroxytropanes (α-tropane-diol or α-tropane-triol) [5]. Almost all of the tropane-based pharmaceuticals are natural or semisynthetic esters [5, 17, 18]. There are also alkylated or arylated tropane compounds known as phenyltropane (Figure 6).
Some phenyl tropane compounds.
Although there are many synthetic routes, Robinsons one-pot synthesis of tropane and its derivatives designed in 1917 [19] is still the best choice for the synthesis of such compounds. The parameters have been changed from time to time in order to increase yield to synthesize a specific derivative (Figure 7).
Robinson’s one pot synthesis of tropinone (10).
The naturally occurring alkaloid, cocaine (6), possesses a functional group at C-2 in the tropane ring system, which has been modified to give various 2-aminotropanes. Willstatter [20], in his work devoted to the elucidation of the structure of ecgonine (3), obtained the amide (11) which it degraded by Hofmann reaction to 2α-aminotropane (12) (the α-configurations retained throughout this sequence can be assigned for later work) (Figure 8) [21].
Hoffmann of the amide (11) to the (12).
Willstatter also obtained (12) by Curtius reaction of the ester (13), and this reaction has been used earlier by Fodor [22] to obtain the amino alcohols (14) and (15), although, again, the configurations at C-2 and C-3 were not known when the work was carried out (Figure 9).
Curtius reduction of ecgonine to amino alcohols (14) and (15).
Apart from these isolated examples, the most consistent interest in 2-substituted tropanes was shown in connection with the alkaloid dioscorine (16), which was for some time thought to have structure (17) and therefore to be related to tropan-2-one (18). This ketone is an optically active form, which was first prepared by Bell and Archer from ecgonine (3) (Figure 10) [23].
Some 2-substituted tropane alkaloids.
The action of phosphoryl chloride on ecgonine (3) was shown by Einborn to give the acid chloride of anhydroecgonine (19) [24]. Bell and Archer converted the crude acid chloride directly to the corresponding amide (20), from which L-(+)-tropan-2-one (18) was obtained in fair yield by Hofmann reaction (Figure 11).
Synthesis of tropane-2-one.
When this material was compared with the ketone obtained by degradation of dioscorine (16), the two could not be distinguished [25], and it was left to Pinder and his co-workers to prove that dioscorine was not in fact a tropane derivative [26]. Pinder found that tropidine (21) reacts with the more usual peracid oxidizing agents to give the N-oxide (22), and in acid solution no reaction took place [27]. However, the action of trifluoroperacetic acid on tropidine trifluoroacetate salt (23) gave the 2β,3β-epoxide (24). Reduction of the epoxide with lithium aluminum hydride yielded tropan-3-β-o1 (25), but it was found impossible to oxidize this amino alcohol to tropan-2-one (18) (Figure 12).
Synthesis of tropane-beta-ol (25).
A synthesis of the desired ketone was eventually achieved by a larger route. Treatment of 2-ethoxycarbonyl-pyrrole (26) with phosphoryl chloride and dimethylformide yielded the two isomeric aldehydes, (27) and (28), which were separated fairly easily by fractional distillation in vacuum. Thereafter the crucial stage, a Dieckmann cyclization, led to the β-ketoester (29), which hydrolyzed and was decarboxylated to tropan-2-one (18), outlined in Figure 13 [26].
Synthesis of tropane-2-one (18).
Pinder resolved the racemic product into its optically active components and discovered that (+)-tropan-2-one (18) was quite different from the ketone derived from the alkaloid dioscorine (16). With this demonstration that dioscorine (16) was not a tropane derivative, the interest in 2-substituted tropanes diminished, and few papers concerned with these compounds have appeared since 1962.
Tropane-2-one (18) is a convenient source of both tropan-2-αβ-ols. Reduction of the ketone with lithium aluminum hydride yields tropan-2α-ol (25), which is the expected, equatorial product [23, 26]. Reduction of a cyclic ketone with sodium alcohol mixtures also usually gives the thermodynamically more stable, equatorial alcohol [28], but with sodium in propan-2-ol, pentan-3-ol, tropan-2-one gave mixtures of tropan-2β-ol (30) and tropan-2α-ol (25) [23] (Figures 13 and 14). Moreover, when the ratio of alcohol to alkoxide ion at the end of the reaction was increased, the product was found to contain increasing amounts up to 90% of tropan-2β-ol (30). These facts suggested that the axial alcohol (25) is more stable thermodynamically, and this was confirmed by subjecting the pure equatorial isomer (25) to equilibration by means of sodium 2-pentoxide in pentan-3-ol containing 10% fluorenone: the equilibrium mixture contained 85% of the axial isomer (25) [23].
Synthesis of tropane-2-ol (30).
This reversal of the usual axial equatorial stability relationship may be attributed to the presence of strong, intramolecular hydrogen bonding between the axial hydroxyl group and the nitrogen bridge (31). When the possibility of hydrogen bond formation is removed, as in the anions (32) and (33), the equatorial configuration becomes more stable. When the ratio of free alcohol to alkoxide ion at the end of the sodium alcohol reduction is large, the equilibrium will be mainly between the two alcohols (25) and (30); in these conditions, the product will contain a high proportion of the more stable, axial alcohol. Conversely, when the final proportion of alkoxide ion in the reaction mixture is high, a significant equilibrium between anions (32) and (33) will exist, and the product will contain a higher proportion of the equatorial alcohol (30), arising from the more stable anion (32) (Figure 15). These stability relationships enable a useful control of the product ratio to be exercised.
The stability relationship of the products (25) and (30).
Two further preparations, of 2-halotropanes, are worthy of note. Nickon found that the addition of 1 molar equivalent of bromine to a methanolic solution of tropinone (10) yielded a granular complex, which rearranged to 2β-bromotropinone (34), by spontaneous transition under ether or by acid catalysis [29]. Earlier, Hobson and Riddell obtained 2β-chlorotropane (36) by decomposition of the
Synthesis of 2-bromo-3-tropinone (34) and the 2-chlorotropane (36).
Although tropan-2-one (18) appeared to be a very convenient synthetic precursor of both tropan-2α-ol (30) and tropan-2β-ol (25), the ketone itself was not easy to prepare. The ketone may be obtained in good yield from ecgonine (3) or cocaine (6), but these alkaloids are expensive. The alternative starting material used by Pinder and co-workers, 2-ethoxycarbonyl-pyrrole (26), is also expensive, and the subsequent synthesis was too long for it to be useful for the preparation of large amount of tropan-2-one.
Tropinone (10) was available in reasonable quantities and was chosen as a convenient source of tropane derivatives. Reduction of this ketone with borohydride gave a mixture of the epimeric tropan-3-ols (38), which were dehydrated to tropidine (21) by Landenburg’s method [31] as it can be seen in Figure 17.
Synthesis of tropidine (21) from Tropane-3-one.
An allylic oxidation of tropidine (21) with selenium dioxide [32] to yield a β-unsaturated ketone (39) was an attractive prospect, but this could not be realized: there was no apparent reaction in aqueous dioxin after 50 hours on a boiling water bath. Other allylic reagents, such as
Synthesis of the compound (40).
Goering and Mayer [34] have reported that optically pure bicyclo[3.2.1]oct-2-ene (41) reacts with tert-butyl perbenzoate, in the presence of cuprous ion, to give racemic of (42) presumably via a symmetrical allyl radical (Figure 19).
Synthesis of the racemic mixture of (42).
Epoxidation of unreactive olefins with trifluoroperacetic acid is usually carried out in dichloromethane with phosphate present to buffer the trifluoroacetic acid that is a product of the reaction [35]. The epoxidation of
Synthesis of the epoxides of (40).
Synthesis of peroxycarboximidic acid.
For example, the epoxidations of (44) and (45) proceeded smoothly with benzonitrile and hydrogen peroxide to (46) and (47), respectively (Figure 22), whereas (44) was found to undergo Baeyer-Villiger cleavage with peracetic acid [41]. The reaction of
Oxidation of some unreactive olefines.
As mentioned earlier, molecules that contained tropane structure, for example, tropane (1), ecgonine (2), tropinone (3), and cocaine (4) or one of its fragments, show central stimulating effects [40, 41, 42, 43, 44, 45], using them as anticholinergic agents [46, 47].
Much of the modification designs involved isomeric studies [48]. Most of the modifications came to the tropane moiety, the bridge nitrogen (N8) [49], or modification at the C2 position [50]. Many processes for synthesizing anhydroecgonine derivatives without using cocaine as a starting material have been reported in literature. For example, it was shown by Grundmann and Ottman [51] as well as Okano and Osamu [52] that the reaction of ethyl cycloheptatriene-7-carboxylate (49) with methylamine gave anhydroecgonine ethyl ester (50) (Figure 23). Conversion of the corresponding carboxylic acid to tropane-2-one has been accomplished by Bell and Archer [53] in a four-step sequence involving conversion to the carboxamide and Hofmann degradation with sodium hypochlorite.
Synthesis of anhydroecgonine ethyl ester (50).
Because (49) was not readily available, Hobson et al. [54] as well as Okano and Itoh [55] developed a relatively inexpensive route starting with corresponding cyano-derivatives which is readily accessible by reaction of tropylium fluoroborate (51) with sodium cyanide to give (52). The nitrile (52) was reacted with methylamine in t-butanol to give the 2-cyano tropidine (53) in high yield (see Figure 24).
Synthesis of the acetonitrile (52) and it’s conversion to (18).
In our work on the 1,3,5-cycloheptatriene-2-ylphosphorus derivatives (54) and (55) (Figure 25), little success was achieved in obtaining isolable products from reactions with nitrogen nucleophiles, except in those cases, for example, pyrrole2-aldehyde, where the presence of aldehyde group enabled the intermediate ylide to be trapped [56].
7-phosphonium and phosphine oxide of cycloheptatriene.
Investigation of the behavior of the 2-(
Synthesis of 2-(
Its mass spectrum showed a molecular ion peak at m/e 277, and the IR spectrum showed a band at 1600 cm−1 characterizing the double bond. Identification of this compound was confirmed by the 1H-NMR spectrum, which showed signals at δ 3.15 and 3.45 due to the bridgehead protons, H1 and H5; a 1-H multiplet at 6.82 as well as upfield protons between 1.2 and 2.8 ppm (see Structure 57, a = Me).
Similarly the sulfone (56a) was refluxed with an excess of
The diastereomers (58) and (59).
In the case of the reaction of (56a) with benzylamine, a slightly different result was obtained. The product was obtained as needles, mp 172°C, and elemental analysis, mass spectroscopy, and spectral data confirmed the structure (60) (Figure 28).
Synthesis of compound (60).
The mechanism for the formation of compounds (57a–d) and (60) presumably involves in the first step of the Michael addition of the amine to C1 of the sulfone (56a) to give intermediate compound (61). Further base-catalyzed isomerization gives the compound (62), followed by intramolecular Michael addition which would lead to the compounds (63a–d) and (60) (Figure 29). In the case of the compound (63a–d), further isomerization to the conjugated sulfone took place which was presumably facilitated by the presence of the strong bases, methylamine (pKa 10.659),
Synthesis of 2-(
The total absence of 2-(
Show the formation of compound (64) and absence of compound (65).
Attempts to react the sulfone (56a) with ammonia were unsuccessful; a solution of the sulfone (58a) in dry acetonitrile was refluxed and ammonia bubbled through for 24 hours. The only product to be isolated was a small quantity of what appeared to be, from its spectral properties, a pure toluene-
The tropane alkaloids made a great contribution to the history of medicine. Intensive research on chemistry and pharmacology of tropane alkaloids led to a fast development of pharmaceutical industries, particularly drugs that have anticholinergic effects. Since the first one-pot synthesis of tropane-3-one by Robinsons in 1917, several routes for synthesizing semisynthetic and synthetic tropane derivatives were published in literature. Chemical synthetic routes from different disciplines and field of research combined in this chapter, in an attempt to illustrate how through continual research, facilitate and develop synthetic chemistry of tropane derivatives. However, the synthesis of the famous tropane derivative, anhydroecgonine from 7-(
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His studies in robotics lead him not only to a PhD degree but also inspired him to co-found and build the International Journal of Advanced Robotic Systems - world's first Open Access journal in the field of robotics.",institutionString:null,institution:{name:"TU Wien",country:{name:"Austria"}}},{id:"441",title:"Ph.D.",name:"Jaekyu",middleName:null,surname:"Park",slug:"jaekyu-park",fullName:"Jaekyu Park",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/441/images/1881_n.jpg",biography:null,institutionString:null,institution:{name:"LG Corporation (South Korea)",country:{name:"Korea, South"}}},{id:"465",title:"Dr",name:"Christian",middleName:null,surname:"Martens",slug:"christian-martens",fullName:"Christian Martens",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:null},{id:"479",title:"Dr.",name:"Valentina",middleName:null,surname:"Colla",slug:"valentina-colla",fullName:"Valentina Colla",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/479/images/358_n.jpg",biography:null,institutionString:null,institution:{name:"Sant'Anna School of Advanced Studies",country:{name:"Italy"}}},{id:"494",title:"PhD",name:"Loris",middleName:null,surname:"Nanni",slug:"loris-nanni",fullName:"Loris Nanni",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/494/images/system/494.jpg",biography:"Loris Nanni received his Master Degree cum laude on June-2002 from the University of Bologna, and the April 26th 2006 he received his Ph.D. in Computer Engineering at DEIS, University of Bologna. On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. 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Delac received his B.Sc.E.E. degree in 2003 and is currentlypursuing a Ph.D. degree at the University of Zagreb, Faculty of Electrical Engineering andComputing. His current research interests are digital image analysis, pattern recognition andbiometrics.",institutionString:null,institution:{name:"University of Zagreb",country:{name:"Croatia"}}},{id:"557",title:"Dr.",name:"Andon",middleName:"Venelinov",surname:"Topalov",slug:"andon-topalov",fullName:"Andon Topalov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/557/images/1927_n.jpg",biography:"Dr. Andon V. Topalov received the MSc degree in Control Engineering from the Faculty of Information Systems, Technologies, and Automation at Moscow State University of Civil Engineering (MGGU) in 1979. He then received his PhD degree in Control Engineering from the Department of Automation and Remote Control at Moscow State Mining University (MGSU), Moscow, in 1984. From 1985 to 1986, he was a Research Fellow in the Research Institute for Electronic Equipment, ZZU AD, Plovdiv, Bulgaria. In 1986, he joined the Department of Control Systems, Technical University of Sofia at the Plovdiv campus, where he is presently a Full Professor. He has held long-term visiting Professor/Scholar positions at various institutions in South Korea, Turkey, Mexico, Greece, Belgium, UK, and Germany. And he has coauthored one book and authored or coauthored more than 80 research papers in conference proceedings and journals. 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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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Vázquez-Olmos, Enrique Acosta-Gío and Marco Antonio Álvarez-Pérez",authors:[{id:"272164",title:"Dr.",name:"Alejandro",middleName:"Luis",surname:"Vega-Jiménez",slug:"alejandro-vega-jimenez",fullName:"Alejandro Vega-Jiménez"},{id:"273073",title:"Dr.",name:"América",middleName:null,surname:"Vázquez-Olmos",slug:"america-vazquez-olmos",fullName:"América Vázquez-Olmos"},{id:"273075",title:"Dr.",name:"Enrique",middleName:null,surname:"Acosta-Gío",slug:"enrique-acosta-gio",fullName:"Enrique Acosta-Gío"},{id:"273078",title:"Dr.",name:"Marco Antonio",middleName:null,surname:"Alvarez-Pérez",slug:"marco-antonio-alvarez-perez",fullName:"Marco Antonio Alvarez-Pérez"}]},{id:"66445",doi:"10.5772/intechopen.84442",title:"An Update on Nanoemulsions Using Nanosized Liquid in Liquid Colloidal Systems",slug:"an-update-on-nanoemulsions-using-nanosized-liquid-in-liquid-colloidal-systems",totalDownloads:1404,totalCrossrefCites:5,totalDimensionsCites:11,abstract:"Nanoemulsions, kinetically stable and thermodynamically unstable colloidal liquid-in-liquid dispersions with droplet sizes in the order of 20–500 nm mainly consist of oil, surfactants, co surfactants and an aqueous phase. There are various methods for the fabrication of Nano-emulsions which can be divided based on the energy required—High energy emulsification methods and Low energy emulsification methods. High energy emulsification includes methods like Ultra sonication, high pressure homogenization using either microfluidizers or high-pressure homogenizers. Low energy emulsification has drawn attention since they are soft, nondestructive and cause no damage to encapsulated molecules and includes methods like phase inversion temperature, solvent displacement, phase inversion composition method. Nanoemulsions are best suited for drug delivery systems because of their lipophilic nature, optical clarity and surface area. Owing to their nature to prevent flocculation and inherent creaming, nanoemulsions find an important place in the cosmetic industry also. This chapter provides an insight into the use of nanogels, emulsion based wet wipes and PEG free nanoemulsions in cosmetics. In the food industry, nanoemulsions are utilized for the production of functional foods. Some of the patented nanoemulsions and their commercial applications have also been mentioned.",book:{id:"8440",slug:"nanoemulsions-properties-fabrications-and-applications",title:"Nanoemulsions",fullTitle:"Nanoemulsions - Properties, Fabrications and Applications"},signatures:"Praveen Kumar Gupta, Nividha Bhandari, Hardik N. Shah, Vartika Khanchandani, R. Keerthana, Vidhyavathy Nagarajan and Lingayya Hiremath",authors:[{id:"271775",title:"Dr.",name:"Praveen Kumar",middleName:null,surname:"Gupta",slug:"praveen-kumar-gupta",fullName:"Praveen Kumar Gupta"},{id:"288900",title:"Ms.",name:"Nividha",middleName:null,surname:"Bhandari",slug:"nividha-bhandari",fullName:"Nividha Bhandari"},{id:"288901",title:"Mr.",name:"Hardik",middleName:null,surname:"N Shah",slug:"hardik-n-shah",fullName:"Hardik N Shah"},{id:"288902",title:"Ms.",name:"Vartika",middleName:null,surname:"Khanchandani",slug:"vartika-khanchandani",fullName:"Vartika Khanchandani"},{id:"288903",title:"Ms.",name:"Keerthana",middleName:null,surname:"R",slug:"keerthana-r",fullName:"Keerthana R"},{id:"288904",title:"Ms.",name:"Vidhyavathy",middleName:null,surname:"Nagarajan",slug:"vidhyavathy-nagarajan",fullName:"Vidhyavathy Nagarajan"},{id:"288954",title:"Dr.",name:"Lingayya",middleName:null,surname:"Hiremath",slug:"lingayya-hiremath",fullName:"Lingayya Hiremath"}]},{id:"66762",doi:"10.5772/intechopen.84201",title:"Importance of Surface Energy in Nanoemulsion",slug:"importance-of-surface-energy-in-nanoemulsion",totalDownloads:1118,totalCrossrefCites:5,totalDimensionsCites:9,abstract:"The emerging prospects of nanoscience and nanotechnology have an enormous promise to revolutionize various aspects of human life. In this context, the application of nanoemulsion stands at the vanguard of introducing newer dimensions to the way we see the everyday world. Naturally, the preparation and stability of nanoemulsion demand a precise understanding of the underlying forces of interaction toward achieving a greater control over their functionality and regulating them. The stability of nanoemulsion is primarily governed by the conjugate and complex interplay of van der Waals forces and steric interactions. The present chapter will be dedicated to the discussion of the regulatory roles of these forces in dictating the stability of nanoemulsion with particular emphasis on the origin of these fundamental forces from a molecular-level viewpoint.",book:{id:"8440",slug:"nanoemulsions-properties-fabrications-and-applications",title:"Nanoemulsions",fullTitle:"Nanoemulsions - Properties, Fabrications and Applications"},signatures:"Kaustav Bhattacharjee",authors:[{id:"280003",title:"Dr.",name:"Kaustav",middleName:null,surname:"Bhattacharjee",slug:"kaustav-bhattacharjee",fullName:"Kaustav Bhattacharjee"}]},{id:"54331",doi:"10.5772/67700",title:"Chiral Solvation Induced Supramolecular Chiral Assembly of Achiral Polymers",slug:"chiral-solvation-induced-supramolecular-chiral-assembly-of-achiral-polymers",totalDownloads:1537,totalCrossrefCites:1,totalDimensionsCites:2,abstract:"To date, liquid crystal chirality, mechanophysical chirality, circularly polarized photon chirality, gelation and chiral solvation are all feasible candidates to generate optically active polymers and supramolecular chirality when employing achiral molecules as starting substances. Among this, chiral‐solvation‐induced chirality is one of the dominant methods for construction of chirality from achiral sources, such as achiral poly(n‐hexyl isocyanate) (PHIC), π‐conjugated polymers, oligo(p‐phenylenevinylene), polyacetylenes, σ‐conjugated polysilanes and side‐chain polymers. Supramolecular chirality is well established through their intra‐ or inter‐molecular noncovalent interactions, such as van der Waals, CH/π, dipole‐dipole interactions, hydrogen bonding and metal‐ligand coordinating interactions. Compared with the traditional methods, this strategy avoids the use of expensive chiral reagents and also expands the scope towards challenging substrates. This chapter highlights a series of studies that include: (i) the development‐historical background of chiral solvent induction strategy; (ii) the chiral‐solvation‐induced chirality in small molecules and oligomers; and (iii) recent developments in polymers, especially in π‐conjugated polymers and σ‐conjugated polymers.",book:{id:"5849",slug:"molecular-self-assembly-in-nanoscience-and-nanotechnology",title:"Molecular Self-assembly in Nanoscience and Nanotechnology",fullTitle:"Molecular Self-assembly in Nanoscience and Nanotechnology"},signatures:"Wei Zhang, Yin Zhao and Lu Yin",authors:[{id:"197834",title:"Prof.",name:"Wei",middleName:null,surname:"Zhang",slug:"wei-zhang",fullName:"Wei Zhang"},{id:"199289",title:"Dr.",name:"Yin",middleName:null,surname:"Zhao",slug:"yin-zhao",fullName:"Yin Zhao"},{id:"199292",title:"Dr.",name:"Lu",middleName:null,surname:"Yin",slug:"lu-yin",fullName:"Lu Yin"}]},{id:"67779",doi:"10.5772/intechopen.87104",title:"Introductory Chapter: From Microemulsions to Nanoemulsions",slug:"introductory-chapter-from-microemulsions-to-nanoemulsions",totalDownloads:1040,totalCrossrefCites:1,totalDimensionsCites:2,abstract:null,book:{id:"8440",slug:"nanoemulsions-properties-fabrications-and-applications",title:"Nanoemulsions",fullTitle:"Nanoemulsions - Properties, Fabrications and Applications"},signatures:"Koh Kai Seng and Wong Voon Loong",authors:[{id:"222878",title:"Dr.",name:"Kai Seng",middleName:null,surname:"Koh",slug:"kai-seng-koh",fullName:"Kai Seng Koh"},{id:"224066",title:"Dr.",name:"Voon Loong",middleName:null,surname:"Wong",slug:"voon-loong-wong",fullName:"Voon Loong Wong"}]}],mostDownloadedChaptersLast30Days:[{id:"67779",title:"Introductory Chapter: From Microemulsions to Nanoemulsions",slug:"introductory-chapter-from-microemulsions-to-nanoemulsions",totalDownloads:1040,totalCrossrefCites:1,totalDimensionsCites:2,abstract:null,book:{id:"8440",slug:"nanoemulsions-properties-fabrications-and-applications",title:"Nanoemulsions",fullTitle:"Nanoemulsions - Properties, Fabrications and Applications"},signatures:"Koh Kai Seng and Wong Voon Loong",authors:[{id:"222878",title:"Dr.",name:"Kai Seng",middleName:null,surname:"Koh",slug:"kai-seng-koh",fullName:"Kai Seng Koh"},{id:"224066",title:"Dr.",name:"Voon Loong",middleName:null,surname:"Wong",slug:"voon-loong-wong",fullName:"Voon Loong Wong"}]},{id:"55094",title:"Nanostructured Morphologies by Self-Assembly of Diblock Copolymers: A Review",slug:"nanostructured-morphologies-by-self-assembly-of-diblock-copolymers-a-review",totalDownloads:1962,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Due to the thermodynamic incompatibility between blocks, diblock copolymers can self‐assemble in a wide variety of nanostructures, covalent linkage among blocks preventing the phase separation at macroscopic scale. Those nanostructures depend on copolymer composition (f), Flory‐Huggins interaction parameter among both blocks (χ), and polymerization degree of the copolymer (N). Thin films of block copolymers can show different equilibrium morphologies such as spheres, cylinders, gyroids, and lamellas. Besides mentioned parameters, film preparation process (substrate, annealing process if any) and used solvent will determine self‐assembled morphology. In the present review, the most important morphologies or microstructures obtained for different diblock copolymer films are presented, as well as the most important phase transitions among them. Different microstructures and the way in which they can be obtained become of great importance, as they could be used as templates for nanoparticle deposition, nanolithography, or nanopatterned materials with several potential applications in different fields such as nanoelectronics or nanomedicine.",book:{id:"5849",slug:"molecular-self-assembly-in-nanoscience-and-nanotechnology",title:"Molecular Self-assembly in Nanoscience and Nanotechnology",fullTitle:"Molecular Self-assembly in Nanoscience and Nanotechnology"},signatures:"Galder Kortaberria",authors:[{id:"102097",title:"Dr.",name:"Galder",middleName:null,surname:"Kortaberria",slug:"galder-kortaberria",fullName:"Galder Kortaberria"}]},{id:"67020",title:"Nanoformulated Delivery Systems of Essential Nutraceuticals and Their Applications",slug:"nanoformulated-delivery-systems-of-essential-nutraceuticals-and-their-applications",totalDownloads:992,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"Malnutrition and poor diet constitute the number one driver of the global burden of disease. Undernutrition is responsible for up to 50% of all deaths in children under the age of 5. In South Africa, 25% of the country’s children suffer from undernutrition. This increases the risk of child mortality as well as contracting infectious diseases. It also affects the physical and intellectual development of the children. The greatest drawback in malnutrition is the deficiency of essential nutraceuticals involved in important biological functions. Innovative technologies such as nanoformulated products are needed for food and agriculture in order to enhance the children’s health. The evaluation and application of various nanoformulated delivery systems will be explored for improving the stability and bioavailability of essential nutraceuticals for consumers.",book:{id:"8440",slug:"nanoemulsions-properties-fabrications-and-applications",title:"Nanoemulsions",fullTitle:"Nanoemulsions - Properties, Fabrications and Applications"},signatures:"Lebogang Katata-Seru, Bathabile Ramalapa and Lesego Tshweu",authors:[{id:"275575",title:"Prof.",name:"Lebogang",middleName:null,surname:"Katata-Seru",slug:"lebogang-katata-seru",fullName:"Lebogang Katata-Seru"},{id:"300636",title:"Dr.",name:"Bathabile",middleName:null,surname:"Ramalapa",slug:"bathabile-ramalapa",fullName:"Bathabile Ramalapa"},{id:"300637",title:"Mr.",name:"Lesego",middleName:null,surname:"Tshweu",slug:"lesego-tshweu",fullName:"Lesego Tshweu"}]},{id:"65648",title:"In vitro Antimicrobial Activity Evaluation of Metal Oxide Nanoparticles",slug:"-em-in-vitro-em-antimicrobial-activity-evaluation-of-metal-oxide-nanoparticles",totalDownloads:1725,totalCrossrefCites:10,totalDimensionsCites:23,abstract:"In recent years, infectious diseases, specifically those that are caused by pathogens, have seen a dramatic proliferation due to resistance to multiple antibiotics, opening the colony by opportunistic pathogens. Nanotechnology and tissue engineering have been applied in the development of new antimicrobial therapies, capable of fighting opportunistic infections. In the medical field, research on antimicrobial properties of metal oxide nanoparticles have emerged to find new antimicrobial agents as an alternative against resistant bacteria. The metal oxides, particularly those formed by transition metals are compounds with electronic properties, and most magnetic phenomena involve this type of oxides. Nanoparticles-based metal oxide properties such as shape, size, roughness, zeta potential and their large surface area, make oxides ideal candidates to interact with bacteria and able to have an antimicrobial effectiveness. The aim of this chapter is to offer an updated panorama about the relationships between the use of metal oxide nanoparticles in the medical field, with an emphasis on their role as antimicrobial agents and the properties that influence their antimicrobial response. In addition, the mechanism of nano-antimicrobial action is described and the importance of using in vitro test methods, adopted by leading international regulatory agencies, that can be used to determine the antimicrobial activity of the metal oxide nanoparticles.",book:{id:"8440",slug:"nanoemulsions-properties-fabrications-and-applications",title:"Nanoemulsions",fullTitle:"Nanoemulsions - Properties, Fabrications and Applications"},signatures:"Alejandro L. Vega-Jiménez, América R. Vázquez-Olmos, Enrique Acosta-Gío and Marco Antonio Álvarez-Pérez",authors:[{id:"272164",title:"Dr.",name:"Alejandro",middleName:"Luis",surname:"Vega-Jiménez",slug:"alejandro-vega-jimenez",fullName:"Alejandro Vega-Jiménez"},{id:"273073",title:"Dr.",name:"América",middleName:null,surname:"Vázquez-Olmos",slug:"america-vazquez-olmos",fullName:"América Vázquez-Olmos"},{id:"273075",title:"Dr.",name:"Enrique",middleName:null,surname:"Acosta-Gío",slug:"enrique-acosta-gio",fullName:"Enrique Acosta-Gío"},{id:"273078",title:"Dr.",name:"Marco Antonio",middleName:null,surname:"Alvarez-Pérez",slug:"marco-antonio-alvarez-perez",fullName:"Marco Antonio Alvarez-Pérez"}]},{id:"65728",title:"Development of Nano-Emulsions of Essential Citrus Oil Stabilized with Mesquite Gum",slug:"development-of-nano-emulsions-of-essential-citrus-oil-stabilized-with-mesquite-gum",totalDownloads:1172,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"The use of nano-emulsions has great advantages over conventional macro-emulsions since the small droplet size allows to expand the options of applications besides presenting a greater surface area. This chapter focuses on the formulation of nano-emulsions of citrus essential oils in water, stabilized with a natural gum (mesquite gum), using a high pressure microfluidic homogenizer to obtain appropriate physicochemical characteristics and kinetic stability. When establishing the general conditions of the methods for obtaining nano-emulsions by high pressure homogenization, several formulations presented stability and size corresponding to nano-emulsions, and these were monitored during 4 months in order to study their stability as a function of time. Taking into account the results of size and stability, the best nano-emulsion obtained had a composition of Persian lemon oil (9.86%), mesquite gum (4.93%) Tween 80 (4.89%), Span 20 (1.45%), and deionized water (78.86%) with an average droplet size of 40 nm. In addition, the antibacterial activity studies also showed that this formulation had the best performance against common bacteria such as Staphylococcus aureus and Escherichia coli. The analysis of the minimum inhibitory concentration (MIC) shows that it is possible to prevent the growth of these particular bacteria using 6.25% of the best nano-emulsion formulations.",book:{id:"8440",slug:"nanoemulsions-properties-fabrications-and-applications",title:"Nanoemulsions",fullTitle:"Nanoemulsions - Properties, Fabrications and Applications"},signatures:"Maira Berenice Moreno-Trejo, Arturo Adrián Rodríguez-Rodríguez, Ángela Suarez-Jacobo and Margarita Sánchez-Domínguez",authors:[{id:"93593",title:"Dr.",name:"Margarita",middleName:null,surname:"Sanchez-Dominguez",slug:"margarita-sanchez-dominguez",fullName:"Margarita Sanchez-Dominguez"},{id:"284208",title:"Dr.",name:"Maira B.",middleName:null,surname:"Moreno-Trejo",slug:"maira-b.-moreno-trejo",fullName:"Maira B. Moreno-Trejo"},{id:"284211",title:"Dr.",name:"Angela",middleName:null,surname:"Suarez-Jacobo",slug:"angela-suarez-jacobo",fullName:"Angela Suarez-Jacobo"},{id:"290287",title:"Dr.",name:"Arturo A.",middleName:null,surname:"Rodríguez-Rodríguez",slug:"arturo-a.-rodriguez-rodriguez",fullName:"Arturo A. Rodríguez-Rodríguez"}]}],onlineFirstChaptersFilter:{topicId:"508",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},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:8,numberOfPublishedChapters:87,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:98,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:27,numberOfPublishedChapters:286,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:9,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:139,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:129,numberOfOpenTopics:0,numberOfUpcomingTopics:2,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!1},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:105,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:9,numberOfPublishedChapters:101,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:11,numberOfOpenTopics:2,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:0,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!1},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:9,numberOfOpenTopics:4,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{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"}}}},{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. 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