Lactate-driving Pt nanoflower with positive chemotaxis for deep intratumoral penetration

渗透(战争) 趋化性 体内 体外 化学 生物物理学 生物医学工程 纳米技术 癌症研究 材料科学 生物化学 生物 医学 生物技术 受体 工程类 运筹学
作者
Zhentao Zhang,Haiqing Zhong,Yi Zhou,Ke Peng,Qi Dai,Yiying Lu,Xincheng Zhong,Qiyao Yang,Yiyi Xia,Xiaoyan Bao,Lin-Jie Wu,Min Han,Jianqing Gao
出处
期刊:Nano Today [Elsevier]
卷期号:45: 101542-101542 被引量:15
标识
DOI:10.1016/j.nantod.2022.101542
摘要

The deep penetration in response to specific intratumoral conditions holds considerable potential in achieving a more effective therapy. Lactate is mainly produced by exuberant-metabolism tumor cells growing in the deep center of solid tumor, which would form the characteristic of higher-level lactate deep inside tumor in distance with blood vessels. Herein, inspired by the in vitro directional chemotaxis of enzyme-powered nanomotor driven by substrate gradient, a novel lactate oxidase (LOX)-powered Pt Nanoflowers (Pt NFs) was developed to achieve deep intratumoral penetration triggered by the lactate-driving positive chemotaxis that was confirmed both in vitro and in vivo for the first time. Besides, LOX-powered Pt NFs with self-oxygenation could achieve a more thorough effect on hypoxic relief via the cascading catalysis: (1) the orthotopic extra H2O2 production from lactate catalyzed by LOX, and (2) the effective conversion of both extra-supplement and endogenous H2O2 into O2 catalyzed by Pt NFs, further overcoming the hypoxia-induced radioresistance. Meanwhile, the X-ray radiation deposited inside Pt NFs could improve low-dose radiotherapy effect with increasing ROS level and enhancing nuclear DNA damage. Collectively, this work would provide a blueprint for developing substrate gradient-driving "smart" delivery systems and radiosensitization strategy.
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