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纳米尺度的二乙基二硫代氨基甲酸盐配位聚合物作为一种药物自传递系统,用于高效、特异的癌症治疗。

Nanoscale Copper(II)-Diethyldithiocarbamate Coordination Polymer as a Drug Self-Delivery System for Highly Robust and Specific Cancer Therapy.

机构信息

Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan 410013, China.

Department of Nuclear Medicine, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.

出版信息

Mol Pharm. 2020 Aug 3;17(8):2864-2873. doi: 10.1021/acs.molpharmaceut.0c00284. Epub 2020 Jul 1.

DOI:10.1021/acs.molpharmaceut.0c00284
PMID:32551674
Abstract

Disulfiram (DSF), an old alcohol-aversion drug, has been repurposed for cancer therapy, and mechanistic studies reveal that it needs to be metabolized to diethyldithiocarbamate (DTC) and subsequently coordinates with copper(II) to form the DTC-copper complex (CuET) for anticancer activation. Here, we utilized this mechanism to construct a CuET self-delivery nanosystem based on the metal coordination polymer for highly robust and selective cancer therapy. In our design, the nanoparticles were facilely prepared under mild conditions by virtue of the strong coordination between Cu and DTC, yielding 100% CuET loading capacity and allowing for further hyaluronic acid (HA) modification (CuET@HA NPs). The CuET@HA NPs could selectively deliver into cancer cells and release the active component of CuET in response to both endo/lysosome acidic pH and intracellular abundant GSH, which induces strong cytotoxicity toward cancer cells over normal cells taking advantage of the p97 pathway interference mechanism. Upon intravenous injection, the self-assembled system could passively accumulate into a tumor and elicit potent tumor growth inhibition at a dose of 1 mg/kg without any noticeable side effects. Given the cost-effective and easily scaled-up preparation, our designed nanosystem provides a promising strategy to pave the way for clinical translation of DSF-based cancer chemotherapy.

摘要

双硫仑(DSF)是一种古老的戒酒药物,已被重新用于癌症治疗,机制研究表明它需要代谢成二乙基二硫代氨基甲酸盐(DTC),然后与铜(II)配位形成 DTC-铜配合物(CuET)以实现抗癌激活。在这里,我们利用该机制构建了基于金属配位聚合物的 CuET 自递药纳米系统,用于高度稳健和选择性的癌症治疗。在我们的设计中,纳米粒子可以通过 Cu 和 DTC 之间的强配位,在温和的条件下轻易制备,从而实现 100%的 CuET 负载能力,并允许进一步进行透明质酸(HA)修饰(CuET@HA NPs)。CuET@HA NPs 可以选择性地递送至癌细胞,并响应内体/溶酶体酸性 pH 和细胞内丰富的 GSH 释放活性成分 CuET,从而利用 p97 途径干扰机制诱导对癌细胞的强烈细胞毒性,而对正常细胞的毒性较小。静脉注射后,自组装系统可以被动地积累到肿瘤中,并以 1mg/kg 的剂量引起强烈的肿瘤生长抑制,而没有任何明显的副作用。鉴于其具有成本效益且易于规模化制备,我们设计的纳米系统为基于 DSF 的癌症化疗的临床转化提供了一种有前途的策略。

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