Tumor-targeted biocatalyst with self-accelerated cascade reactions for enhanced synergistic starvation and photodynamic therapy

化学 光动力疗法 催化作用 乙二醇 体内 过氧化氢 生物物理学 激进的 肿瘤微环境 组合化学 光化学 癌症研究 生物化学 肿瘤细胞 有机化学 生物技术 生物
作者
Xuan Gao,Jing Feng,Shuyan Song,Kai Liu,Kaimin Du,Yifei Zhou,Kehong Lv,Hongjie Zhang
出处
期刊:Nano Today [Elsevier BV]
卷期号:43: 101433-101433 被引量:54
标识
DOI:10.1016/j.nantod.2022.101433
摘要

• A multifunctional nanosystem (USCGP) is constructed to elicit enhanced enzyme catalytic and photocatalytic effects. • USCGP biocatalyst making the best use of each component amplifies the starvation and photodynamic antitumor effects. • USCGP biocatalyst could well-metabolized from mice and have negligible toxicity or side effect in vivo . An intelligent biocatalyst based on engineered upconversion nanoparticles, mesoporous silica, and CeO 2 nanoparticles has been developed for synergistic starvation and photodynamic therapy, which greatly suppresses tumor growth by the addictive cascade enzyme reactions and photocatalytic reactions upon NIR laser irradiation. Combination therapy has been considered as an attractive strategy in complementary anticancer treatment. However, its therapeutic outcomes could be inhibited by the tumor microenvironment (TME) such as hypoxia and insufficient endogenous hydrogen peroxide concentration. Herein, we typically design a multilayered porous biocatalyst (USCGP) realizing cascade reactions-enhanced synergistic cancer therapy. Glucose oxidase (GOD) loaded on USCGP catalyzes glucose decomposition accompanied by regulating TME, which activates double enzyme-like catalysis of USCGP. Concurrently, the cascade reactions between GOD and cerium oxide (CeO 2 ) not only promote nutrition consumption but also enhance the generation of hydroxyl radicals (•OH). In addition, under near-infrared (NIR) laser excitation, upconversion nanoparticles (UCNPs) in the core could convert NIR light to UV emission to trigger photocatalysis reactions of CeO 2 , achieving efficient spatio-temporal controllable photodynamic therapy. In particular, the modification of poly(ethylene glycol)-cyclo (Arg-Gly-Asp- d -Phe-Lys) (NH 2 -PEG 1000 -cRGDfK, abbreviated as PEG-cRGDfK) facilitates the accumulation of USCGP into tumor cells. Furthermore, USCGP could also be served as excellent contrast agent for computed tomography (CT) imaging in tumor diagnosis. Taken together, USCGP exhibits high-performance in tumor suppression with minimal side effects in vitro and in vivo , realizing additive cooperation of long-term starvation and robust photodynamic treatment strategy.
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