化学
葡萄糖氧化酶
谷胱甘肽
丁硫胺
生物化学
体内
微泡
生物物理学
癌症研究
酶
小RNA
生物
基因
生物技术
作者
Yang Luo,Peng Yan,Xinyang Li,Jianwen Hou,Yi Wang,Shaobing Zhou
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2021-09-17
卷期号:22 (10): 4383-4394
被引量:32
标识
DOI:10.1021/acs.biomac.1c00960
摘要
Typical glucose oxidase (GOx)-based starvation therapy is a promising strategy for tumor treatment; however, it is still difficult to achieve an effective therapeutic effect via a single starvation therapy. Herein, we designed a pH-sensitive polymeric vesicle (PV) self-assembled by histamine-modified chondroitin sulfate (CS-his) for codelivery of GOx and l-buthionine sulfoximine (BSO). GOx can consume glucose to induce the starvation therapy after the PVs reach cancer cell. Moreover, the product H2O2 will be reduced by a high concentration of glutathione (GSH) in the tumor cell, resulting in a reduction of the GSH content. The released BSO finally further reduced the GSH level. As a result, the signaling pathway of the ferroptosis will be activated. The in vivo results demonstrated that GOx/BSO@CS PVs exhibit a good inhibitory effect on the growth of 4T1 tumors in mice. Thus, this work provides a facile strategy to prepare pH-sensitive nanomedicine for synergistic starvation-ferroptosis therapy of tumor.
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