Solubility Enhancement of Poorly Soluble Drug Simvastatin by Solid Dispersion Technique
DOI:
https://doi.org/10.53555/bp.v2i1.147Keywords:
Simvastatin,, kneading, solid dispersions,, SSG, carrierAbstract
The objective of the present study was to formulate solid dispersions (SDs) of Simvastatin (SIM) to improve the aqueous solubility, dissolution rate & to facilitate faster onset of action. Simvastatin is a BCS class II drug having low solubility & therefore low oral bioavailability. In the present study, SDs of Simvastatin different drug-carrier ratios was prepared by kneading method. The results showed that Simvastatin solubility & dissolution rate was enhanced with polymer SSG in the ratio 1:7 due to increase in wetting property (or) may be due to change in crystallinity of the drug.
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References
T. Kai, et. al, oral absorption improvement of poorly soluble drug using Solid dispersion technique, Chemical and pharma Bulletin. , 1996, 44, 568-571.
Hamsaraj Karanth, et. al,”Industrially Feasible Alternative Approaches in the Manufacture of Solid Dispersions: A Technical Report”, American Association of pharmaceutical Scientist .,2006; 7(4) Article 37.
L. H. Emara, et. al, “Improving the dissolution & bioavailability of Nifedipine using Solid dispersions & Solubilizens,”Drug development and industrial pharmacy, 2002, 28, 795-807.
A, M. Juppo, et. al,”Evaluation of Solid dispersion particles prepared by SEDS”, International journal of pharmaceutics. , 2003, 250, 385-401.

