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首页> 外文期刊>International Journal of Nanomedicine >Amphiphilic poly{[α-maleic anhydride-ω-methoxypoly(ethylene glycol)]-co-(ethyl cyanoacrylate)} graft copolymer nanoparticles as carriers for transdermal drug delivery
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Amphiphilic poly{[α-maleic anhydride-ω-methoxypoly(ethylene glycol)]-co-(ethyl cyanoacrylate)} graft copolymer nanoparticles as carriers for transdermal drug delivery

机译:两亲性聚{[α-马来酸酐-ω-甲氧基聚(乙二醇)]-共-(氰基丙烯酸乙酯)}接枝共聚物纳米粒子作为载体进行透皮给药

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Abstract: In this study, the transdermal drug delivery properties of D,L-tetrahydropalmatine (THP)-loaded amphiphilic poly{[α-maleic anhydride-ω-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.
机译:摘要:本研究研究了负载D,L-四氢巴马汀(THP)的两亲性聚{[α-马来酸酐-ω-甲氧基-聚(乙二醇)]-共-(氰基丙烯酸乙酯)}的透皮给药特性( PEGECA)接枝共聚物纳米颗粒(PEGECAT NPs)通过体外皮肤渗透实验进行了评估。体外透皮渗透实验是在Franz扩散池中进行的,使用的是THP负载的PEGECAT NP作为供体系统。透射电子显微镜和傅立叶变换红外光谱用于表征受体液。结果表明,THP负载的PEGECAT NP能够穿透大鼠皮肤。荧光显微镜测量表明,THP负载的PEGECAT NPs不仅可以通过附肢途径而且可以通过表皮途径渗透皮肤。该纳米技术在透皮药物递送中具有潜在的应用。

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