A Potential Breakthrough in the Enhancement of Glimepiride Solubility and Dissolution Rate by Binary and Ternary Solid Dispersion Technique and In Vitro Comparison with Marketed Formulation-Reference-Cited by-同舟云学术

A Potential Breakthrough in the Enhancement of Glimepiride Solubility and Dissolution Rate by Binary and Ternary Solid Dispersion Technique and In Vitro Comparison with Marketed Formulation

Published:2023-08-25 Issue:4 Volume:18 Page:1981-1991
ISSN:1872-5120
Container-title:Journal of Pharmaceutical Innovation
language:en
Short-container-title:J Pharm Innov

Author:

Chakraborty Rideb^ORCID,Afrose Naureen^ORCID,Kuotsu Ketousetuo^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmaceutical Science

Link

https://link.springer.com/content/pdf/10.1007/s12247-023-09761-2.pdf

Reference29 articles.

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2. Akhter S, Hossen MS, Salahuddin M, Sunny MA, Sathi FA, Islam MS. In vitro dissolution study of glimepiride from binary and ternary solid dispersion formulation. Univers J Pharm Res. 2019;4(5):7–12.

3. Malkawi R, Malkawi WI, Al-Mahmoud Y, Tawalbeh J. Current trends on solid dispersions: past, present, and future. Adv Pharmacol Pharm Sci. 2022;2022.

4. Gurunath S, Kumar SP, Basavaraj NK, Patil PA. Amorphous solid dispersion method for improving oral bioavailability of poorly water-soluble drugs. J Pharm Res. 2013;6(4):476–80.

5. Sareen S, Mathew G, Joseph L. Improvement in solubility of poor water-soluble drugs by solid dispersion. Int J Pharm Investig. 2012;2(1):12.

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