Effect of penetration enhancers on the transdermal delivery of bupranolol through rat skin

36Citations
Citations of this article
28Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Bupranolol (BPL) is a suitable drug candidate for transdermal drug delivery system development based on its favorable physicochemical and pharmacokinetic properties. The effect of different penetration enhancers on the permeation of BPL across rat skin was studied using side-by-side diffusion cells. 2-pyrrolidone (PY), 1-methyl-2-pyrrolidone (MPY), and propylene glycol (PG) at various concentrations were used as penetration enhancers along with 0.4% w/v aqueous suspension of BPL. Menthol at different concentrations in isopropanol-water (6:4) mixture also was used as an enhancer wherein BPL at 0.4% w/v was completely solubilized. Skin pretreatment studies were carried out with all the above enhancers to understand their role in the penetration enhancement effect. PY and MPY at 5% w/v concentrations increased the permeation of BPL by 3.8- and 2.4-fold, respectively, versus control (p

Cite

CITATION STYLE

APA

Babu, R. J., & Pandit, J. K. (2005). Effect of penetration enhancers on the transdermal delivery of bupranolol through rat skin. Drug Delivery: Journal of Delivery and Targeting of Therapeutic Agents, 12(3), 165–169. https://doi.org/10.1080/10717540590931936

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