光响应纳米颗粒用于触发组织穿透和药物递送。

Photoswitchable nanoparticles for triggered tissue penetration and drug delivery.

机构信息

Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.

出版信息

J Am Chem Soc. 2012 May 30;134(21):8848-55. doi: 10.1021/ja211888a. Epub 2012 Mar 16.

Abstract

We report a novel nanoparticulate drug delivery system that undergoes reversible volume change from 150 to 40 nm upon phototriggering with UV light. The volume change of these monodisperse nanoparticles comprising spiropyran, which undergoes reversible photoisomerization, and PEGylated lipid enables repetitive dosing from a single administration and enhances tissue penetration. The photoswitching allows particles to fluoresce and release drugs inside cells when illuminated with UV light. The mechanism of the light-induced size switching and triggered-release is studied. These particles provide spatiotemporal control of drug release and enhanced tissue penetration, useful properties in many disease states including cancer.

摘要

我们报告了一种新型的纳米颗粒药物输送系统,该系统在紫外光光触发下可发生可逆的体积变化,从 150nm 变为 40nm。这些单分散纳米颗粒由螺吡喃组成,螺吡喃可发生可逆光致异构化,并且含有聚乙二醇化脂质,这使得它们能够在单次给药后进行重复给药,并且增强组织穿透性。光开关使粒子在受到紫外光照射时发出荧光并在细胞内释放药物。研究了光诱导的尺寸切换和触发释放的机制。这些粒子提供了药物释放的时空控制和增强的组织穿透性,在许多疾病状态下都具有有用的性质,包括癌症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea0/3363369/8043041e9d2b/ja-2011-11888a_0010.jpg

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