Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/363038
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dc.date.accessioned2022-02-16T10:25:29Z-
dc.date.available2022-02-16T10:25:29Z-
dc.identifier.urihttp://hdl.handle.net/10603/363038-
dc.description.abstractFixed dose combination of Pioglitazone plus Glimepiride immediate release and Metformin sustained release provide loading and maintenance dose and have proven to be very effective in the management of Type 2 Diabetes mellitus (T2DM). Multiparticulate systems have the advantage of providing minimal fluctuations in plasma drug concentrations and enhancing the patient convenience and compliances in comparison to single unit dosage forms. However, till date no multiunit system containing the combination of these drugs has been commercialised. The objective of this study was to develop and compare fixed dose combination of Metformin (500 mg) as sustained release and Pioglitazone (15 mg) and Glimepiride (1 mg) as immediate release pellets with the innovator products, Glucophage Tablet 500 mg (for Metformin), Actos Tablet 15 mg (for Pioglitazone) and Amaryl Tablet 1 mg (for Glimepride). Metformin hydrochloride pellets were prepared using Carbopol 971 as hydrophilic control release polymer and microcrystalline cellulose as an extrusion spheronization aid whereas Glimepiride and Pioglitazone hydrochloride immediate release pellets were formulated using lactose monohydrate (solubilizer), microcrystalline cellulose (disintegrant) and Tween 80 (surfactant). Both, sustained as well as immediate release pellets, prepared by extrusion-spheronization technique, were found to possess drug content within 90% to 110% range of the label claimed dose. The SEM images confirmed the spherical shape of the pellets. Development involves design of experiment approach (DoE,IV-Design, Three factorial design) , where studied factors and ranges demonstrated comparable results as that of final composition, which confirms that within studied design space product showed no significant impact with respect to product quality. Dissolution of immediate release pellets exhibited of more than 80 % at 15 minutes for Glimepride and complete release at 30 minutes for Pioglitazone, which was comparable to the release provided by Amaryl and Actos release. newline
dc.format.extent139p
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleDevelopment and Evaluation of Multiparticulate Delivery System for the treatment of Type II Diabetes
dc.title.alternative
dc.creator.researcherDhanorkar Vandana
dc.subject.keywordClinical and Health
dc.subject.keywordClinical care - Medicine Diabetes
dc.subject.keywordPharmaceutics
dc.description.note
dc.contributor.guideShah Pranav J
dc.publisher.placeBarodli
dc.publisher.universityUka Tarsadia University
dc.publisher.institutionFaculty of Pharmacy
dc.date.registered2014
dc.date.completed2022
dc.date.awarded2022
dc.format.dimensions
dc.format.accompanyingmaterialCD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Faculty of Pharmacy

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01_title.pdfAttached File110.81 kBAdobe PDFView/Open
02_certificates.pdf816.33 kBAdobe PDFView/Open
03_preliminary pages.pdf506.14 kBAdobe PDFView/Open
04_chapter_1.pdf411.92 kBAdobe PDFView/Open
05_chapter_2.pdf119.51 kBAdobe PDFView/Open
06_chapter_3.pdf205.65 kBAdobe PDFView/Open
07_chapter_4.pdf240.24 kBAdobe PDFView/Open
08_chapter_5.pdf238.91 kBAdobe PDFView/Open
09_chapter_6.pdf1.46 MBAdobe PDFView/Open
10_chapter_7.pdf97.91 kBAdobe PDFView/Open
11_ references.pdf173.87 kBAdobe PDFView/Open
12_publications.pdf871.58 kBAdobe PDFView/Open
13_plagiarism report.pdf48.84 kBAdobe PDFView/Open
80_recommendation.pdf278.81 kBAdobe PDFView/Open


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