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M.Mudasir1*, N.Tabassum1, J.Ali2, R.Jan3
1Department of Pharmaceutical sciences, University of
Kashmir, Srinagar-190006 (INDIA)
2Department of Pharmaceutics, Faculty of Pharmacy, Jamia
Hamdard University,
New Delhi-110062 (INDIA)
3Department of Clinical Biochemistry, Sher-i- Kashmir
Institute of Medical Sciences,
Soura, Srinagar-190009 (INDIA) |
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In vitro percutaneous
absorption of Aceclofenac was done in order to assess its feasibility
for transdermal development across wistar rat skin and formulating into
a sustained release transdermal gels containing penetration enhancers
like dimethyl sulfoxide (DMSO). Transdermal gels were prepared using
different polymers like carbopol-934, PVA (hot), HPMC-K4M,
HPC-M and SCMC. The formulated gels were subjected to physicochemical
studies, in-vitro release studies and in-vitro skin permeations
studies. The in-vitro release studies of prepared gels were
performed using specially designed Fites cell and in-vitro skin
permeation studies were performed using keshary-chien diffusion cell
through rat skin. The optimized gel which showed best in-vitro
skin permeation of aceclofenac was compared with the marketed
formulation and it was found that optimized one (carbapol 934) produced
better results in comparison to marketed one. |