A New Liposomal-Drug-in-Adhesive Patch for Transdermal Delivery of Sodium Diclofenac

DOI: 10.4236/jbnb.2011.225069   PDF   HTML     8,428 Downloads   15,459 Views   Citations


Liposomes are known to have considerable potential as drug carriers such as liposomal suspension, freeze dried and cream-based systems among many other liposomal formulations. In this study a new drug-in-adhesive patch was fabricated using liposome-based nanocarrier. Transfersomes as ultra-deformable liposomes are based on phosphatidylcholin 95% (phospholipon 90G) and phosphatidylcholin 50% (phosal 50PG) were prepared and further optimized in a final acrylic patch system for effective adhesion. The prepared liposomes were added to an acrylic adhesive to obtain a new hybrid transdermal patch termed as “lipo-drug-in-adhesive” patch system. The sodium diclofenac was selected as a model drug and the permeation of the drug across rat skin was evaluated (P > 0.05), using the lipo-drug-in-adhesive patch system with various percentages of transfersomes (4% - 8%w/w) and constant concentration of the drug (2% w/w). The peel strength and tack value of samples were also examined and quantified. The maximum flux of sodium diclofenac was observed in samples containing 8% (w/w) phosphatidylcholin 50%. The peel strength and tack value in samples containing phosphatidylcholin 50% were lower than those samples containing phosphatidylcholin 95%. It was observed that with increased amount of liposome in drug-in-adhesive patch system, the rate of skin permeation of the drug was also increased. It can be concluded that the developed lipo-drug-in-adhesive patch system enhances the drug release potential of transdermal delivering systems.

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Taghizadeh, S. and Bajgholi, S. (2011) A New Liposomal-Drug-in-Adhesive Patch for Transdermal Delivery of Sodium Diclofenac. Journal of Biomaterials and Nanobiotechnology, 2, 576-581. doi: 10.4236/jbnb.2011.225069.

Conflicts of Interest

The authors declare no conflicts of interest.


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