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纳米拓扑结构通过整合素依赖性机制促进体内高分子量治疗药物的透皮递送。

Nanotopography facilitates in vivo transdermal delivery of high molecular weight therapeutics through an integrin-dependent mechanism.

作者信息

Walsh Laura, Ryu Jubin, Bock Suzanne, Koval Michael, Mauro Theodora, Ross Russell, Desai Tejal

机构信息

†Department of Bioengineering and Therapeutic Sciences, University of California-San Francisco, 1700 Fourth Street, Room 204, San Francisco, California 94158-2330, United States.

‡Department of Dermatology, University of California-San Francisco, 1701 Divisadero Street, San Francisco, California 94115, United States.

出版信息

Nano Lett. 2015 Apr 8;15(4):2434-41. doi: 10.1021/nl504829f. Epub 2015 Mar 27.

Abstract

Transdermal delivery of therapeutics is restricted by narrow limitations on size and hydrophobicity. Nanotopography has been shown to significantly enhance high molecular weight paracellular transport in vitro. Herein, we demonstrate for the first time that nanotopography applied to microneedles significantly enhances transdermal delivery of etanercept, a 150 kD therapeutic, in both rats and rabbits. We further show that this effect is mediated by remodeling of the tight junction proteins initiated via integrin binding to the nanotopography, followed by phosphorylation of myosin light chain (MLC) and activation of the actomyosin complex, which in turn increase paracellular permeability.

摘要

治疗药物的经皮递送受到大小和疏水性方面的严格限制。纳米拓扑结构已被证明在体外能显著增强高分子量药物的细胞旁转运。在此,我们首次证明,应用于微针的纳米拓扑结构能显著增强大鼠和兔子体内150kD治疗药物依那西普的经皮递送。我们进一步表明,这种作用是由紧密连接蛋白的重塑介导的,该重塑过程通过整合素与纳米拓扑结构结合启动,随后是肌球蛋白轻链(MLC)的磷酸化和肌动球蛋白复合物的激活,进而增加细胞旁通透性。

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