Arora Priyanka, Mukherjee Biswajit
University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh 160 014, India.
J Pharm Sci. 2002 Sep;91(9):2076-89. doi: 10.1002/jps.10200.
In this study, matrix-type transdermal patches containing diclofenac diethylamine were prepared using different ratios of polyvinylpyrrolidone (PVP) and ethylcellulose (EC) by solvent evaporation technique. The drug matrix film of PVP and EC was casted on a polyvinylalcohol backing membrane. All the prepared formulations were subjected to physical studies (moisture content, moisture uptake, and flatness), in vitro release studies and in vitro skin permeation studies. In vitro permeation studies were performed across cadaver skin using a modified diffusion cell. Variations in drug release profiles among the formulations studied were observed. Based on a physicochemical and in vitro skin permeation study, formulation PA4 (PVP/EC, 1:2) and PA5 (PVP/EC, 1:5) were chosen for further in vivo experiments. The antiinflammatory effect and a sustaining action of diclofenac diethylamine from the two transdermal patches selected were studied by inducing paw edema in rats with 1% w/v carrageenan solution. When the patches were applied half an hour before the subplantar injection of carrageenan in the hind paw of male Wistar rats, it was observed that formulation PA4 produced 100% inhibition of paw edema in rats 12 h after carrageenan insult, whereas in the case of formulation PA5, 4% mean paw edema was obtained half an hour after the carrageenan injection and the value became 19.23% 12 h after the carrageenan insult. The efficacy of transdermal patches was also compared with the marketed Voveran gel and it was found that PA4 transdermal patches produced a better result as compared with the Voveran gel. Hence, it can be reasonably concluded that diclofenac diethylamine can be formulated into the transdermal matrix type patches to sustain its release characteristics and the polymeric composition (PVP/EC, 1:2) was found to be the best choice for manufacturing transdermal patches of diclofenac diethylamine among the formulations studied.
在本研究中,采用溶剂蒸发技术,使用不同比例的聚乙烯吡咯烷酮(PVP)和乙基纤维素(EC)制备了含双氯芬酸二乙胺的基质型透皮贴剂。将PVP和EC的药物基质膜浇铸在聚乙烯醇背衬膜上。对所有制备的制剂进行了物理研究(水分含量、吸湿量和平整度)、体外释放研究和体外皮肤渗透研究。使用改良的扩散池在尸体皮肤上进行体外渗透研究。观察到所研究制剂之间药物释放曲线的差异。基于物理化学和体外皮肤渗透研究,选择制剂PA4(PVP/EC,1:2)和PA5(PVP/EC,1:5)进行进一步的体内实验。通过用1% w/v角叉菜胶溶液诱导大鼠爪肿胀,研究了所选两种透皮贴剂中双氯芬酸二乙胺的抗炎作用和持续作用。当在雄性Wistar大鼠后爪足底注射角叉菜胶前半小时应用贴剂时,观察到制剂PA4在角叉菜胶刺激后12小时对大鼠爪肿胀产生了100%的抑制作用,而对于制剂PA5,在角叉菜胶注射后半小时平均爪肿胀率为4%,在角叉菜胶刺激后12小时该值变为19.23%。还将透皮贴剂的疗效与市售的扶他林凝胶进行了比较,发现与扶他林凝胶相比,PA4透皮贴剂产生了更好的效果。因此,可以合理地得出结论,双氯芬酸二乙胺可以制成透皮基质型贴剂以维持其释放特性,在所研究的制剂中,聚合物组合物(PVP/EC,1:2)被发现是制造双氯芬酸二乙胺透皮贴剂的最佳选择。