Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/600649
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dc.date.accessioned2024-11-12T08:05:40Z-
dc.date.available2024-11-12T08:05:40Z-
dc.identifier.urihttp://hdl.handle.net/10603/600649-
dc.description.abstractAbstract: newlineDifferent antifungal loaded novel emulgels containing several permeation enhancers were formulated for transungualdrug deliveryfor the management of onychomycosis, which affects the nails. The physicochemical properties like droplet size, zeta potential, pH, viscosity, spreadability, extrudability, oil binding capacity, drug content, and microscopic study were evaluated. The Pseudo-ternary phase diagram was constructed for the development of novel emulsions and characterized for clarity, mean droplet size, zeta potential, viscosity, pH, transmittance, refractive index, and stability. The mean droplet size determined for LCZ, KCZ and AmB loaded novel emulsions and found in the range 38.78-171.4, 47.62-192.10 and 172.16-284.12 nm, respectively. Determined zeta potential for LCZ, KCZ and AmB novel emulsions was in the range of 0.00 to -6.6, -0.6 to -6.1 and - 0.41 to -4.2 mV. Prepared emulsions were converted into novel emulgels by adding different concentration of the gelling agent in the external phase, and a drug release study was conducted. Formulation with better drug release was chosen as control formulation. Different penetration enhancers were added separately in the optimized novelemulgels and further evaluated for pH, viscosity, spreadability, extrudability, oil binding capacity, drug content, microscopic study, Compatibility study, XRD, DSC and stability. Encouraging docking scores of Luliconazole and Ketoconazole was observed against Lanosterol 14-alpha-demethylase, In-vitrodrug release study suggested that the novel emulgels containing sodium sulfide as penetration enhancer, showed better drug release, which was almost double than the control formulations. Ex-vivo transungual permeation studies were conducted with LCZ, KCZ and AmB emulgels through cutting nail clippings and drug uptake were found to be in the range of 28.18 - 36.52, 108.42-119.43and 32.24 - 46.91 and#956;g/mm2, respectively. All the optimized newline2 newlinenovel emulgels showed significant zone of inhibition against fungus strains as compared t
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dc.languageEnglish
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dc.rightsuniversity
dc.titleDesign And Development Of Novel Drug Delivery System For The Topical Treatment Of Onychomycosis
dc.title.alternative
dc.creator.researcherGiri, Yashwant
dc.subject.keywordImmunology
dc.subject.keywordLife Sciences
dc.subject.keywordOnychomycosis
dc.subject.keywordPharmacology and Pharmacy
dc.description.note: Transungual Drug Delivery, Onychomycosis, Microemulsions, Microemulgel, Nanoemulsions, Nanoemulgel
dc.contributor.guideBehera, Amulyaratna and Mohanty, Biswaranjan
dc.publisher.placeGajapati
dc.publisher.universityCenturion University of Technology and Management
dc.publisher.institutionDEPARTMENT OF PHARMACY
dc.date.registered2020
dc.date.completed2024
dc.date.awarded2024
dc.format.dimensions
dc.format.accompanyingmaterialDVD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:DEPARTMENT OF PHARMACY

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01. title.pdfAttached File35.48 kBAdobe PDFView/Open
02. priliminary pages.pdf506.88 kBAdobe PDFView/Open
03. table of contents.pdf64.04 kBAdobe PDFView/Open
04. abstract.pdf163.27 kBAdobe PDFView/Open
05. chapter 1.pdf1.19 MBAdobe PDFView/Open
06. chapter 2.pdf315.77 kBAdobe PDFView/Open
07. chapter 3.pdf174.89 kBAdobe PDFView/Open
08. chapter 4.pdf248.85 kBAdobe PDFView/Open
09. chapter 5.pdf339.46 kBAdobe PDFView/Open
10. chapter 6.pdf391.58 kBAdobe PDFView/Open
11. chapter 7.pdf782.96 kBAdobe PDFView/Open
12. chapter 8.pdf4.59 MBAdobe PDFView/Open
13.chapter 9.pdf301.52 kBAdobe PDFView/Open
14. annexxure.pdf574.15 kBAdobe PDFView/Open
80_recommendation.pdf4.93 MBAdobe PDFView/Open


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