Sustained release solid dispersion of a BCS class II Drug

dc.contributor.advisorKabir, Eva Rahman
dc.contributor.authorAhmed, Fairuza
dc.date.accessioned2021-06-07T07:55:36Z
dc.date.available2021-06-07T07:55:36Z
dc.date.issued2020-03
dc.descriptionCataloged from PDF version of thesis report.
dc.descriptionIncludes bibliographical references (pages 32-36).
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2020.
dc.description.abstractThe present study aims to develop a sustained-release solid dispersion (SRSD) of a Biopharmaceutical Classification System (BCS) Class II drug by employing a blend of polymers. The SRSD was prepared by kneading technique, followed by solvent evaporation using rotary evaporator. After conducting an equilibrium solubility study, SRSD (F5) was found to be the optimal formulation. The dissolution profiles of SRSD (F5) were examined at different pH values. Since Carvedilol exhibits pH dependent solubility, the drug release from SRSD (F5) was limited at pH 6.8 and increased at pH 1.2. The structural characteristic of SRSD (F5) was examined by using powder X-ray diffraction (PXRD), which shows a change in drug crystallinity to an amorphous form. The results obtained from the dissolution study suggest that SRSD (F5) could be a promising approach for developing sustained-release oral dosage form of Carvedilol, thereby reducing the dosing frequency and improving the oral bioavailability.
dc.identifier.otherID: 16146002
dc.identifier.otherhttps://dspace.bracu.ac.bd/server/api/core/items/439b3c68-c8ae-4b53-ad22-914772af2e6c
dc.identifier.urihttp://hdl.handle.net/10361/14492
dc.language.isoen_US
dc.publisherBRAC University
dc.sourceBRAC University Institutional Repository
dc.subjectSustained release solid dispersion (SRSD)
dc.subjectDissolution
dc.subjectBCS Class II drug
dc.subjectOral bioavailability
dc.titleSustained release solid dispersion of a BCS class II Drug
dc.typeThesis

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