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双可点击介孔二氧化硅纳米颗粒:用于具有主动靶向的可控药物递送的光驱动纳米机器的简便制备

Bis-clickable Mesoporous Silica Nanoparticles: Straightforward Preparation of Light-Actuated Nanomachines for Controlled Drug Delivery with Active Targeting.

作者信息

Noureddine Achraf, Gary-Bobo Magali, Lichon Laure, Garcia Marcel, Zink Jeffrey I, Wong Chi Man Michel, Cattoën Xavier

机构信息

Institut Charles Gerhardt Montpellier, UMR 5253 CNRS, Université de Montpellier-ENSCM, 8, rue de l'école normale, 34296, Montpellier, France.

Institut des Biomolécules Max Mousseron, UMR 5247 CNRS, Faculté de Pharmacie, Université de Montpellier, 15 Avenue Charles Flahault, 34093, Montpellier cedex 05, France.

出版信息

Chemistry. 2016 Jul 4;22(28):9624-30. doi: 10.1002/chem.201600870. Epub 2016 Jun 3.

Abstract

Bis(clickable) mesoporous silica nanospheres (ca. 100 nm) were obtained by the co-condensation of TEOS with variable amounts (2-5 % each) of two clickable organosilanes in the presence of CTAB. Such nanoparticles could be easily functionalized with two independent functions using the copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction to transform them into nanomachines bearing cancer cell targeting ligands with the ability to deliver drugs on-demand. The active targeting was made possible after anchoring folic acid by CuAAC click reaction, whereas the controlled delivery was performed by clicked azobenzene fragments. Indeed, the azobenzene groups are able to obstruct the pores of the nanoparticles in the dark whereas upon irradiation in the UV or in the blue range, their trans-to-cis photoisomerization provokes disorder in the pores, enabling the delivery of the cargo molecules. The on-command delivery was proven in solution by dye release experiments, and in vitro by doxorubicin delivery. The added value of the folic acid ligand was clearly evidenced by the difference of cell killing induced by doxorubicin-loaded nanoparticles under blue irradiation, depending on whether the particles featured the clicked folic acid ligand or not.

摘要

通过在十六烷基三甲基溴化铵(CTAB)存在下,将正硅酸乙酯(TEOS)与两种可点击有机硅烷(各2 - 5%)的不同量进行共缩合,获得了双(可点击)介孔二氧化硅纳米球(约100纳米)。使用铜催化的炔烃 - 叠氮环加成(CuAAC)反应,这种纳米颗粒可以很容易地用两种独立的功能进行功能化,将它们转化为带有癌细胞靶向配体且能够按需递送药物的纳米机器。通过CuAAC点击反应锚定叶酸后实现主动靶向,而通过点击的偶氮苯片段进行可控递送。实际上,偶氮苯基团在黑暗中能够阻塞纳米颗粒的孔隙,而在紫外或蓝光范围内照射时,它们从反式到顺式的光异构化会引发孔隙中的无序,从而使货物分子得以递送。通过染料释放实验在溶液中以及通过阿霉素递送在体外证明了按需递送。负载阿霉素的纳米颗粒在蓝光照射下诱导的细胞杀伤差异,清楚地证明了叶酸配体的附加值,这取决于颗粒是否带有点击的叶酸配体。

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