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载有秋水仙素的脂质双层涂层 50nm 介孔纳米粒子在被细胞摄取后能有效诱导微管解聚。

Colchicine-loaded lipid bilayer-coated 50 nm mesoporous nanoparticles efficiently induce microtubule depolymerization upon cell uptake.

机构信息

Department of Chemistry, University of Munich (LMU), Munich, Germany.

出版信息

Nano Lett. 2010 Jul 14;10(7):2484-92. doi: 10.1021/nl100991w.

Abstract

We report on a one-step assembly route where supported lipid bilayers (SLB) are deposited on functionalized colloidal mesoporous silica (CMS) nanoparticles, resulting in a core-shell hybrid system (SLB@CMS). The supported membrane acts as an intact barrier against the escape of encapsulated dye molecules. These stable SLB@CMS particles loaded with the anticancer drug colchicine are readily taken up by cells and lead to the depolymerization of microtubules with remarkably enhanced efficiency as compared to the same dose of drug in solution.

摘要

我们报告了一种一步组装途径,其中在功能化胶体介孔硅 (CMS) 纳米粒子上沉积支撑脂质双层 (SLB),从而形成核壳混合系统 (SLB@CMS)。支撑膜充当完整的屏障,防止封装的染料分子逸出。这些负载有抗癌药物秋水仙素的稳定 SLB@CMS 颗粒很容易被细胞摄取,并导致微管解聚,与相同剂量的药物溶液相比,效率显著提高。

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