FORMULATION AND CHARACTERIZATION OF TRANSDERMAL FILMS OF TORASEMIDE

Journal Title: Indo American Journal of Pharmaceutical Research - Year 2011, Vol 1, Issue 5

Abstract

The purpose of this research was to develop a matrix-type transdermal therapeutic system containing drug Aceclofenac with different ratios of hydrophilic (hydroxyl propyl cellulose) and hydrophobic (ethyl cellulose) polymeric systems by the solvent evaporation technique by using 15 % w/w of dibutyl phthalate to the polymer weight, incorporated as plasticizer. Different concentrations of oleic acid and isopropyl myristate were used to enhance the transdermal permeation of Torasemide. Formulated transdermal films were physically evaluated with regard to thickness, weight variation, drug content, flatness, tensile strength, folding endurance, percentage of moisture content and water vapour transmission rate. All prepared formulations indicated good physical stability. In-vitro permeation studies of formulations were performed by using Franz diffusion cells. Formulation prepared with hydrophilic polymer containing permeation enhancer showed best in-vitro skin permeation through rat skin (Wistar albino rat) as compared to all other formulations. The results followed the release profile of Aceclofenac followed mixed zero-order and first-order kinetics in different formulation. However, the release profile of the optimized formulation F4 (r2 = 0.9935 for Higuchi) indicated that the permeation of the drug from the patches was governed by a diffusion mechanism. These results indicate that the formulation containing the F4 [CAP: PVP (6:1)] has shown optimum release in concentration independent manner.

Authors and Affiliations

. D. L Jayachandran, Krishnamoorthy M. Rao, S. Jeganath, V. Ashlin Viji, K. Sheeja Devi

Keywords

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  • EP ID EP221940
  • DOI -
  • Views 114
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How To Cite

. D. L Jayachandran, Krishnamoorthy M. Rao, S. Jeganath, V. Ashlin Viji, K. Sheeja Devi (2011). FORMULATION AND CHARACTERIZATION OF TRANSDERMAL FILMS OF TORASEMIDE. Indo American Journal of Pharmaceutical Research, 1(5), 289-304. https://europub.co.uk/articles/-A-221940