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基于定向石墨烯的纳米平台用于热疗:克服多药耐药性。

Directed Graphene-Based Nanoplatforms for Hyperthermia: Overcoming Multiple Drug Resistance.

机构信息

Institut für Organische Chemie und Biochemie, Freie Universität Berlin, Takustrasse 3, 14195, Berlin, Germany.

Department of Pharmaceutical Engineering, School of Engineering, China Pharmaceutical University, Nanjing, 210009, China.

出版信息

Angew Chem Int Ed Engl. 2018 Aug 27;57(35):11198-11202. doi: 10.1002/anie.201804291. Epub 2018 Aug 3.

Abstract

Multidrug resistance (MDR), which leads tumors resistance to traditional anticancer drugs, can cause the failure of chemotherapy treatments. Herein, we present a new way to overcome this problem using smart multifunctional graphene-based drug delivery systems which can target subcellular organelles and show synergistic hyperthermia and chemotherapy. Mitochondria-targeting ligands are conjugated onto the doxorubicin-loaded, polyglycerol-covered nanographene sheets to actively accumulate them inside the mitochondria after charge-mediated cellular internalization. Upon near-infrared (NIR) irradiation, adenosine triphosphate (ATP) synthesis and mitochondrial function were inhibited and doxorubicin released into the cellular interior. The hyperthermia-accelerated drug release led to a highly selective anticancer efficiency, confirmed by in vitro and in vivo experiments.

摘要

多药耐药性(MDR)会导致肿瘤对传统抗癌药物产生耐药性,从而使化疗治疗失败。在此,我们提出了一种使用智能多功能基于石墨烯的药物输送系统来克服这一问题的新方法,该系统可以靶向亚细胞细胞器,并表现出协同的热疗和化疗作用。线粒体靶向配体被连接到负载多柔比星的、聚甘油覆盖的纳米石墨烯片上,以便在带电荷的细胞内吞作用后主动将其聚集到线粒体内部。近红外(NIR)照射后,三磷酸腺苷(ATP)合成和线粒体功能受到抑制,多柔比星释放到细胞内部。热疗加速了药物释放,通过体外和体内实验证实了其具有高度的选择性抗癌效率。

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