FORMULATION AND EVALUATION OF GLICLAZIDE LOADED ALGINATE BEADS FOR CONTROLLED RELEASE

RAO T.V.1, BHADRAMMA N.2, IMMANUELU I.3, RADHIKA M.4, SRINIJA5, SYAMALA K.6
1Bapatla College of Pharmacy, Bapatla- 522 101, AP, India.
2Bapatla College of Pharmacy, Bapatla- 522 101, AP, India.
3Bapatla College of Pharmacy, Bapatla- 522 101, AP, India.
4Bapatla College of Pharmacy, Bapatla- 522 101, AP, India.
5Bapatla College of Pharmacy, Bapatla- 522 101, AP, India.
6Bapatla College of Pharmacy, Bapatla- 522 101, AP, India.

Received : 14-11-2013     Accepted : 12-12-2013     Published : 26-12-2013
Volume : 1     Issue : 2       Pages : 33 - 37
World Res J Pharmaceut Res 1.2 (2013):33-37

Cite - MLA : RAO T.V., et al "FORMULATION AND EVALUATION OF GLICLAZIDE LOADED ALGINATE BEADS FOR CONTROLLED RELEASE." World Research Journal of Pharmaceutical Research 1.2 (2013):33-37.

Cite - APA : RAO T.V., BHADRAMMA N., IMMANUELU I., RADHIKA M., SRINIJA, SYAMALA K. (2013). FORMULATION AND EVALUATION OF GLICLAZIDE LOADED ALGINATE BEADS FOR CONTROLLED RELEASE. World Research Journal of Pharmaceutical Research, 1 (2), 33-37.

Cite - Chicago : RAO T.V., BHADRAMMA N., IMMANUELU I., RADHIKA M., SRINIJA, and SYAMALA K. "FORMULATION AND EVALUATION OF GLICLAZIDE LOADED ALGINATE BEADS FOR CONTROLLED RELEASE." World Research Journal of Pharmaceutical Research 1, no. 2 (2013):33-37.

Copyright : © 2013, RAO T.V., et al, Published by Bioinfo Publications. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.

Abstract

Microencapsulation by emulsification-ionic gelation technique is an approach to achieve controlled release of drug, gliclazide beads were designed to improve the absorption and bioavailability of the drug. Gliclazide beads were formulated with sodium alginate and by combination of sodium alginate with hydrophilic polymer such as Na CMC in the ratio of (core:coat) 1:1,1:2, 1:3, 2:1 and 3:1. The prepared beads were characterized such as particle size of beads, angle of repose by fixed funnel method, compressibility index, Hausner’s ratios, wall thickness, drug content,entrapment efficiency. The shape of beads were found to be spherical by SEM analysis. In-vitro dissolution data revealed that formulations exhibited the zero order kinetics and followed peppas transport mechanism.