Department of Chemical Engineering, National Taiwan University of Science and Technology, No. 43, Sec. 4, Keelung Rd, Taipei 106, Taiwan.
Department of Life Science, Fu-Jen Catholic University, New Taipei City 242, Taiwan.
Int J Pharm. 2019 Jul 20;566:708-716. doi: 10.1016/j.ijpharm.2019.06.029. Epub 2019 Jun 15.
In this study, a facile, economically feasible, and scalable approach to fabricate macroporous poly(vinyl alcohol)-GO (PVA-GO) nanocomposite films with varying filler loadings was demonstrated. The nanocomposite films were prepared using a solvent casting process and employed as a diffusion layer for modulating the transdermal delivery of an anti-inflammatory drug (i.e., ketoprofen). The diffusion membrane was assembled in a three-layer structure with PVA/PVA-GO films between ketoprofen-loaded cellulose and cellulose acetate to mimic skin barrier. Through the incorporation of GO sheets into PVA matrix, the mass diffusion and drug release rate of ketoprofen could be modulated to attain a controlled-release system within period in comparison to that of neat PVA film, which showed more rapid release. It was observed that the dispersion level of GO sheets in the polymer matrix played a crucial role to slow the diffusion rate and drug release, where 3 wt% filler loading gave the slowest rate of release. The results from the present study shed light on the mechanism of and may provide guidelines for modulating drug release rates of NSAID in film-based delivery vehicles for transdermal delivery applications.
在这项研究中,展示了一种简便、经济可行且可扩展的方法,用于制造具有不同填充负载的大孔聚(乙烯醇)-GO(PVA-GO)纳米复合材料薄膜。纳米复合材料薄膜是通过溶剂浇铸工艺制备的,并用作调节抗炎药物(即酮洛芬)经皮传递的扩散层。扩散膜采用三层结构组装,在载有酮洛芬的纤维素和醋酸纤维素之间夹有 PVA/PVA-GO 薄膜,以模拟皮肤屏障。通过将 GO 片掺入 PVA 基质中,可以调节酮洛芬的质量扩散和药物释放率,与纯 PVA 薄膜相比,实现了一段时间内的控制释放系统,后者显示出更快的释放速度。观察到 GO 片在聚合物基质中的分散水平对减缓扩散速率和药物释放起着至关重要的作用,其中 3wt%的填充负载给出了最慢的释放速率。本研究的结果阐明了机制,并可能为调节基于薄膜的传递载体中 NSAID 的药物释放速率提供指导,以用于经皮传递应用。