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具有高度多孔碳基质的花状纳米酶引发针对耐药癌症的强大氧化风暴。

Flower-like Nanozyme with Highly Porous Carbon Matrix Induces Robust Oxidative Storm against Drug-Resistant Cancer.

作者信息

Xing Yuxin, Li Lin, Chen Yuhua, Wang Lu, Tang Shuqi, Xie Xiyue, Wang Shuai, Huang Jixi, Cai Kaiyong, Zhang Jixi

机构信息

Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, No. 174 Shazheng Road, Chongqing 400044, China.

出版信息

ACS Nano. 2023 Apr 11;17(7):6731-6744. doi: 10.1021/acsnano.2c12698. Epub 2023 Mar 22.

Abstract

Reactive oxygen species (ROS) generators are sparking breakthroughs in sensitization and treatment of therapy-resistant tumors, yet the efficacy is drastically compromised by limited substrate concentrations, short lifetimes of free radicals, and restricted oxidative damage. Herein, a flower-like nanozyme with highly permeable leaflets accommodating catalytic metal sites was developed to address the challenges by boosting substrate and product accessibility. In the formation of a zeolite imidazole framework, cobalt ions promoted catalytic polymerization and deposition of polydopamine. The polymers acted as a stiffener for preventing framework collapse and maneuvering pore reopening during carbonization. The cobalt single-atom/cluster sites in the highly porous matrix generated peroxidase/oxidase-like activities with high catalytic efficiency (/) up to 6 orders of magnitude greater than that of conventional nano-/biozymes. Thereby, a robust ROS storm induced by selective catalysis led to rapid accumulation of oxidative damage and failure of antioxidant and antiapoptotic defense synchronization in drug-resistant cancer cells. By synergy of a redox homeostasis disrupter co-delivered, a significantly high antitumor efficiency was realized . This work offers a route to kinetically favorable ROS generators for advancing the treatment of therapy-resistant tumors.

摘要

活性氧(ROS)发生器正在引发治疗难治性肿瘤的敏化和治疗方面的突破,然而,有限的底物浓度、自由基的短寿命以及受限的氧化损伤严重损害了其疗效。在此,开发了一种具有容纳催化金属位点的高渗透性小叶的花状纳米酶,以通过提高底物和产物的可及性来应对这些挑战。在沸石咪唑框架的形成过程中,钴离子促进了聚多巴胺的催化聚合和沉积。这些聚合物充当增强剂,用于防止框架坍塌并在碳化过程中控制孔的重新开放。高度多孔基质中的钴单原子/簇位点产生过氧化物酶/氧化酶样活性,其催化效率(/)比传统的纳米/生物酶高6个数量级。因此,由选择性催化诱导的强烈ROS风暴导致氧化损伤的快速积累以及耐药癌细胞中抗氧化和抗凋亡防御同步的失效。通过共同递送的氧化还原稳态破坏剂的协同作用,实现了显著高的抗肿瘤效率。这项工作为动力学上有利的ROS发生器提供了一条途径,以推进治疗难治性肿瘤的治疗。

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