Modified Solubility of Etodolac through Solid Dispersion and Complexation

Author:

Gulabrao Bhamare Vaibhav1,Keshavrao Kamble Ravindra2

Affiliation:

1. Department of Pharmaceutics, K. K. Wagh College of Pharmacy, Panchavati, Nashik, 422003, Maharashtra, India.

2. Department of Pharmaceutics, Faculty of Pharmacy, Bhupal Nobles’ University, Old Station Road, Udaipur- 313001. Rajasthan, India.

Abstract

Solubility and dissolution is an essential requirement for any drug to perform well in vivo. The present research was undertaken to enhance the dissolution rate of poor water soluble drug Etodolac through solid dispersion and complexation technique. Fusion method and kneading methods were employed for solubility enhancement by Solid Dispersion technique and complexation technique respectively. PEG-6000, HPMC K4M, β-Cyclodextrin and PVPK-30 are used as carriers. Physical mixtures were prepared in different ratio of drug and carriers. The prepared blends were evaluated for solubility, drug content, percent yield and drug release. Solubility enhancement was observed for all the experimental mixtures having maximum attainment for polymers PEG 6000 and PVPK-30. Pre and post enhancement Etodolac solubility values confirm the successful modification in solubility of drug through solid dispersion technique and complexation technique with slight edge toward complexation technique.

Publisher

A and V Publications

Subject

Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Reference24 articles.

1. Verma S, et al. Solid Dispersion: A Strategy for Solubility Enhancement. International Journal of Pharmacy and Technology. 2011; 3: 1062-1099.

2. Brahmankar DM, Jaiswal SB. Biopharmaceutics and Pharmacokinetics a Treatise. Vallabh Prakashan, Delhi. 2006.

3. Giri TK, et al. Carriers used for the development of solid dispersion for poorly water soluble drugs. Research Journal of Pharmacy and Technology. 2011; 4(3): 356-366.

4. Venkatesh N, et al. Solid dispersions, a unique technique to improve the aqueous solubility of poorly soluble drugs- A review. International Journal of Pharmaceutical Research. 2008; 1: 5-12.

5. Chiou, WL, Riegelman S. Preparation and dissolution characteristics of several fast-release solid dispersions of griseofulvin. Journal of Pharmaceutical Sciences.1969; 58: 1505-1509.

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