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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Noncovalent assembly of reduced graphene oxide and alkyl-grafted mesoporous silica: an effective drug carrier for near-infrared light-responsive controlled drug release
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Noncovalent assembly of reduced graphene oxide and alkyl-grafted mesoporous silica: an effective drug carrier for near-infrared light-responsive controlled drug release

机译:氧化石墨烯和烷基接枝的介孔二氧化硅的非共价组装:有效的药物载体,用于近红外光响应性受控药物释放

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摘要

In this paper, we report the assembly of reduced graphene oxide (RGO) and mesoporous silica grafted with alkyl chains (MSN-C-18) to develop a new class of drug carriers which are able to deliver the loaded drug molecules into living cells upon exposure to near-infrared (NIR) light. This novel drug carrier consists of a structure formed by the noncovalent interaction of RGO caps and alkyl chains on the surface of MSN-C-18. The capping of RGO sheets on mesoporous silica effectively blocks the pore mouths in the absence of NIR light. Conversely, and very importantly, the photothermal heating effect of RGO leads to a rapid increase in the local temperature upon exposure to NIR light, resulting in the weakening of the RGO sheet/alkyl chain noncovalent interaction. The RGO sheets will then be removed from the MSN surface, and the pores are uncapped. This uncapping mechanism makes it possible to release the loaded drug molecules upon irradiation with NIR light. In the present study, such a noncovalent assembly was examined by the use of doxorubicin as a model drug for NIR light-responsive intracellular controlled release studies. We believe that this noncovalent assembly will prove to be a promising drug delivery system for cancer therapy in the near future.
机译:在本文中,我们报道了还原型氧化石墨烯(RGO)和接枝有烷基链的中孔二氧化硅(MSN-C-18)的组装,从而开发出新型的药物载体,能够将负载的药物分子递送至活细胞。暴露于近红外(NIR)光下。这种新型药物载体由RGO帽和MSN-C-18表面上的烷基链的非共价相互作用形成的结构组成。在没有近红外光的情况下,RGO薄片在中孔二氧化硅上的覆盖有效地堵塞了孔口。相反,非常重要的是,RGO的光热加热作用会导致其在暴露于NIR光线后局部温度迅速升高,从而导致RGO片/烷基链非共价相互作用减弱。然后将RGO薄板从MSN表面去除,并打开毛孔。这种解封机制使得在用NIR光照射时可以释放负载的药物分子。在本研究中,通过使用阿霉素作为近红外光反应性细胞内控释研究的模型药物来检查这种非共价装配体。我们相信,这种非共价装配体将在不久的将来被证明是用于癌症治疗的有希望的药物输送系统。

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