Department of Polymer Science and Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, People's Republic of China.
Int J Nanomedicine. 2009;4:227-32. doi: 10.2147/ijn.s7814. Epub 2009 Oct 19.
In this study, the transdermal drug delivery properties of D,L-tetrahydropalmatine (THP)-loaded amphiphilic poly{[alpha-maleic anhydride-omega-methoxy-poly(ethylene glycol)]-co-(ethyl cyanoacrylate)} (PEGECA) graft copolymer nanoparticles (PEGECAT NPs) were evaluated by skin penetration experiments in vitro. The transdermal permeation experiments in vitro were carried out in Franz diffusion cells using THP-loaded PEGECAT NPs as the donor system. Transmission electron microscopy and Fourier transform infrared spectroscopy were used to characterize the receptor fluid. The results indicate that the THP-loaded PEGECAT NPs are able to penetrate the rat skin. Fluorescent microscopy measurements demonstrate that THP-loaded PEGECAT NPs can penetrate the skin not only via appendage routes but also via epidermal routes. This nanotechnology has potential application in transdermal drug delivery.
本研究通过体外皮肤渗透实验评估了 D,L-四氢巴马汀(THP)负载的两亲性聚{[α-马来酸酐-ω-甲氧基-聚(乙二醇)]-共-(乙基氰基丙烯酸酯)}(PEGECA)接枝共聚物纳米粒子(PEGECAT NPs)的透皮给药特性。体外透皮渗透实验采用Franz 扩散池,以 THP 负载的 PEGECAT NPs 作为供体系统。透射电子显微镜和傅里叶变换红外光谱用于表征接收液。结果表明,THP 负载的 PEGECAT NPs 能够穿透大鼠皮肤。荧光显微镜测量表明,THP 负载的 PEGECAT NPs 不仅可以通过附属途径,还可以通过表皮途径穿透皮肤。这项纳米技术在透皮给药方面具有潜在的应用前景。