A bio‐based reactive diluent (BRD) was synthesized from succinic acid and glycerol, and successfully copolymerized with epoxy acrylate (EA). Chemical structure of BRD was studied by nuclear magnetic resonance and Fourier transform infrared. The performance of vinyl ester resin compositions has been examined through differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical analysis, as well as tensile and flexural tests. Results demonstrated good compatibility between EA and the BRD. Compared to styrene, the BRD contribution of 50 wt% enhanced the elastic modulus (~40%). Samples copolymerized with BRD or styrene, have shown a similar thermal stability. Mechanical properties of cured blends, containing up to 25 wt% of BRD, found to be superior than styrene‐diluted compartments. Viscosities of EA–BRD blends were in range of 3.25–0.43 Pa/s at 30°C. Inexpensive bio‐based source, good thermomechanical and rheological properties, and great compatibility with EA are of advantages of these BRD‐containing formulations.

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