Programmed delivery of verapamil hydrochloride from tablet in a capsule device

3Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

The aim of the present work was to develop a programmed drug delivery system which would be able to release the drug after 6 h of lag time by use of hydrophilic polymers. The capsule body was made impermeable by use of formaldehyde vapor treatment, while the cap was untreated. The capsule was filled with two layered tablets (tablet-in-capsule), followed by a sodium bicarbonate:citric acid mixture (SBCM) and lactose as bulking agent. Sodium alginate, chitosan, HPMC K15 and chitosan:sodium alginate complex (CSAC) were used as the rate modulating layer. Through combined use of HPMC K15 and adjusting the ratio of CSAC, the desired lag time of 6 h was obtained. The effect of the bulking agents on the lag time were also studied and it was found that the lag time was decreased with higher amounts of lactose, and delayed dissolution and decreased lag time was observed at higher amount of effervescent mixture.

Cite

CITATION STYLE

APA

Sah, M. L., & Juyal, V. (2012). Programmed delivery of verapamil hydrochloride from tablet in a capsule device. Brazilian Journal of Pharmaceutical Sciences, 48(2), 237–242. https://doi.org/10.1590/S1984-82502012000200007

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free