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动态羧甲基壳聚糖基纳米前药精确调节强大的协同化疗。

Dynamic carboxymethyl chitosan-based nano-prodrugs precisely mediate robust synergistic chemotherapy.

机构信息

Engineering Research Center for Biomedical Materials, Anhui Key Laboratory of Modern Biomanufacturing, School of Life Sciences, Anhui University, 111 Jiulong Road, Hefei, Anhui Province 230601, PR China.

Engineering Research Center for Biomedical Materials, Anhui Key Laboratory of Modern Biomanufacturing, School of Life Sciences, Anhui University, 111 Jiulong Road, Hefei, Anhui Province 230601, PR China.

出版信息

Carbohydr Polym. 2022 Sep 1;291:119671. doi: 10.1016/j.carbpol.2022.119671. Epub 2022 May 28.

Abstract

Currently, the polysaccharide-based nano-prodrug crosslinked by stimuli-responsive synergetic prodrug is of great demand, owing to its excellent stability, synergetic effect and tumor selectivity, and circumventing the dilemma of dose-limiting toxicity and immunogenicity induced by that crosslinked or grafted via a single drug. Herein, the dynamic carboxymethyl chitosan (CMCS)-based nano-prodrugs with precise structure were facilely fabricated, via crosslinking reaction between CMCS and water-soluble synergistic small molecule prodrug (cisplatin-demethylcantharidin conjugate) and further stabilization by glutaraldehyde. The pH/glutathione (GSH)-responsive double-crosslinked structure endowed the nano-prodrugs with long-term storge and circulation stability at physiological pH, and dynamic transitions at tumor sites including extracellular surface amino protonation and intracellular efficient drug release, which promoted selective tumor accumulation and synergistic cytotoxicity, therefore achieving robust tumor suppression while decreasing side effects. Thus, the dynamic precise CMCS-based nano-prodrugs crosslinked by water-soluble synergistic prodrug have great potential for highly selective robust chemotherapy attractive for clinical translation.

摘要

目前,刺激响应协同前药交联的基于多糖的纳米前药由于其优异的稳定性、协同作用和肿瘤选择性,以及避免了单一药物交联或接枝引起的剂量限制毒性和免疫原性的困境,因此需求很大。本文通过羧甲基壳聚糖(CMCS)与水溶性协同小分子前药(顺铂去甲基斑蝥素缀合物)的交联反应,进一步用戊二醛稳定,简便地制备了具有精确结构的动态羧甲基壳聚糖(CMCS)基纳米前药。pH/谷胱甘肽(GSH)响应的双重交联结构使纳米前药在生理 pH 值下具有长期的储存和循环稳定性,并在肿瘤部位发生动态转变,包括细胞外表面质子化和细胞内有效药物释放,从而促进选择性肿瘤积累和协同细胞毒性,从而实现强大的肿瘤抑制作用,同时减少副作用。因此,基于水溶性协同前药交联的动态精确 CMCS 基纳米前药具有很高的选择性和强大的化学治疗潜力,非常适合临床转化。

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