Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/590120
Full metadata record
DC FieldValueLanguage
dc.coverage.spatial
dc.date.accessioned2024-09-19T07:04:39Z-
dc.date.available2024-09-19T07:04:39Z-
dc.identifier.urihttp://hdl.handle.net/10603/590120-
dc.description.abstractDiabetes mellitus, a pervasive metabolic disorder, imposes a substantial global health burden, with Type 2 Diabetes (T2D) being a prevalent form characterized by insulin resistance and impaired glucose metabolism. The conventional treatment often involves oral anti-diabetic medications, such as Pioglitazone (PGZ). However, the challenges of poor water solubility inherent in PGZ necessitate innovative solutions. Nanoparticle-based drug delivery systems present a promising avenue for enhancing solubility and bioavailability. newlineThis research focuses on encapsulating PGZ within nanoparticles to achieve controlled drug release, targeted delivery, and improved therapeutic outcomes. The study outlines primary objectives, including the formulation and optimization of PGZ-loaded nanoparticles and the evaluation of enhanced bioavailability. By leveraging nanotechnology and building upon established research in diabetes management, this study explores the potential implications for T2D treatment. newlineThe experimental approach involves nanogrinding PGZ using a nanosuspension precipitation method. Stabilizing effects of Tween 80 Emulsifier surface active agents are investigated, with formulation factors and process parameters meticulously examined. The study evaluates the ratio of polymer to drug, milling time, and concentration of PGZ beads, while different concentrations of surfactants, such as Tween 80 and ethanol: distilled water, are explored for nanosuspension preparation. Responses measured include particle size, zeta potential, and Yield Percentage. newlineThe outcomes of this research hold promise for revolutionizing PGZ therapy, offering a pathway to enhance solubility and bioavailability. The potential benefits include improved therapeutic efficacy, dose reduction, enhanced patient compliance, and targeted drug delivery. This study contributes to the broader landscape of diabetes research, striving towards enhancing patient outcomes and quality of life in the management of Type 2 Diabetes. newline
dc.format.extent168
dc.languageEnglish
dc.relation259
dc.rightsuniversity
dc.titleFormulation and Evaluation of Nanoparticles of Poorly Soluble Anti Diabetic Drug
dc.title.alternative
dc.creator.researcherZanke, Ashwini Arun
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordDiabetes mellitus
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.subject.keywordType 2 Diabetes
dc.description.note
dc.contributor.guideGhule, Santosh
dc.publisher.placeIndore
dc.publisher.universityOriental University
dc.publisher.institutionPharmacy
dc.date.registered2021
dc.date.completed2024
dc.date.awarded2024
dc.format.dimensions
dc.format.accompanyingmaterialDVD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Pharmacy

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File394.63 kBAdobe PDFView/Open
02_preliminary pages.pdf1.16 MBAdobe PDFView/Open
03-contents.pdf492.37 kBAdobe PDFView/Open
04_abstract.pdf382.64 kBAdobe PDFView/Open
05_chapter 1.pdf1.17 MBAdobe PDFView/Open
06_chapter 2.pdf1.14 MBAdobe PDFView/Open
07_chapter 3.pdf730.37 kBAdobe PDFView/Open
09_chapter 5.pdf2.47 MBAdobe PDFView/Open
10_anexures.pdf1.11 MBAdobe PDFView/Open
11_chapter 6.pdf1.04 MBAdobe PDFView/Open
12_chapter 7.pdf1.11 MBAdobe PDFView/Open
80_recommendation.pdf394.63 kBAdobe PDFView/Open


Items in Shodhganga are licensed under Creative Commons Licence Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0).

Altmetric Badge: