dc.contributor.advisor | Chowdhury, Rezwana Nasrin | |
dc.contributor.author | Habiba, Nur Aktar | |
dc.date.accessioned | 2015-11-29T07:19:31Z | |
dc.date.available | 2015-11-29T07:19:31Z | |
dc.date.copyright | 2015 | |
dc.date.issued | 2015-08-20 | |
dc.identifier.other | ID 11346005 | |
dc.identifier.uri | http://hdl.handle.net/10361/4660 | |
dc.description | This project report is submitted in a partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2015 | en_US |
dc.description | Cataloged from PDF version of Internship report. | |
dc.description | Includes bibliographical references (page 51-53). | |
dc.description.abstract | The solid dispersion has become a momentous solubilization technology for poorly water
soluble drugs.It is usually two component system of drug polymer, which interacts between
the drug design and its performance. Solid dispersion in water-soluble carriers have
interacted a means of developing the dissolution rate and bioavailability of the hydrophobic
drugs. The aim of this present study is to compare the solubility of different drugs with the
increased polymer concentration. The solid dispersion is stable under accelerated storage
conditions.PVP K30 brings out a way to enhance the solubility and dissolution rate of the
certain drug. Solid dispersions have attracted considerable interest as an important means of
mounting dissolution rate with various methodologies. The main focus of this article is on
advantages, disadvantages, developing various methods and categorization of the solid
dispersion. There are various carriers which have been used in the solid dispersion
technology and this has been focused in this article. | en_US |
dc.description.statementofresponsibility | Nur Aktar Habiba | |
dc.format.extent | 53 pages | |
dc.language.iso | en | en_US |
dc.publisher | BRAC University | en_US |
dc.rights | BRAC University project report are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. | |
dc.subject | Pharmacy | en_US |
dc.subject | Solid dispersion | en_US |
dc.title | A review on solid dispersion : a substitute approach for poorly water soluble drug | en_US |
dc.type | Project report | en_US |
dc.contributor.department | Department of Pharmacy, BRAC University | |
dc.description.degree | B. Pharmacy | |