Tanasait Ngawhirunpat ,
Supinya Thipwichai,
Praneet Opanasopit,
Theerasak Rojanarata,
Suwannee Panomsuk
Faculty of Pharmacy, Silpakorn University, Nakhon Pathom 73000, Thailand;
For correspondence:- Tanasait Ngawhirunpat
Email: tanasait@su.ac.th Tel:+6634255800
Received: 29 December 2011
Accepted: 18 June 2012
Published: 16 August 2012
Citation:
Ngawhirunpat T, Thipwichai S, Opanasopit P, Rojanarata T, Panomsuk S.
Development and Evaluation of Ketoprofen Acrylic Transdermal Patches. Trop J Pharm Res 2012; 11(4):553-560
doi:
10.4314/tjpr.v11i4.5
© 2012 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Abstract
Purpose: To fabricate ketoprofen transdermal patches (KTPs) using an acrylic pressure-sensitive adhesive (PSA) polymer.
Methods: KTPs were prepared using solvent casting method. The influence of the amount of PSA, drug content, and terpenes as penetration enhancers on the characteristics of the patch, namely, thickness, W/A ratio, and adhesiveness and in vitro skin permeation, were investigated. Scanning electron microscope (SEM) and differential scanning calorimetry (DSC) studies were also performed on the patches. The physical and chemical stability of KTPs after storage at 40 oC, and 75 %RH for 1 month was also evaluated.
Results: DSC thermograms demonstrate that the drug was dispersed molecularly in the polymer in all the formulations. Increase in PSA content increased the W/A ratio and adhesiveness of KTPs. Ketoprofen release from the transdermal patches followed the Higuchi diffusion model. Ketoprofen flux increased with increase in the ketoprofen content of the adhesive matrix. Inclusion of terpenes in the patch formulations significantly increased the permeation of ketoprofen through the skin, with enhancement ratio (ER) ranging from 1.4 to 2.6.
Conclusion: KTPs formulated with acrylic pressure-sensitive adhesive and incorporating terpenes as permeation enhancers demonstrated suitable characteristics for transdermal delivery of ketoprofen.
Keywords: Ketoprofen, Transdermal patch, Skin permeation, Acrylic matrix, Terpenes, Pressure-sensitive adhesive