透明质酸
化学
药物输送
阿霉素
肿瘤微环境
介孔二氧化硅
药品
谷胱甘肽
多重耐药
抗药性
癌症研究
生物化学
化疗
药理学
介孔材料
有机化学
肿瘤细胞
酶
医学
微生物学
生物
遗传学
外科
抗生素
催化作用
作者
Yi Liu,Man Zhu,Minsi Meng,Qiao Wang,Yun Wang,Lei Yu,Yanmin Zhang,Lin Weng,Xin Chen
标识
DOI:10.1016/j.cclet.2022.06.006
摘要
Chemotherapy is restricted by efficient drug outflow due to the multiple drug resistance (MDR) in heterogenous nature of tumor. Herein, we present a dual-responsive hyaluronic acid (HA) nanocomposite hydrogel that can not only response to the tumor microenvironment but also enhance chemotherapy. This HA hydrogel consists of a core-shell SiO2 ([email protected]2-Arg) and mesoporous silica nanoparticles (MSNs) with doxorubicin (DOX) as the cargo ([email protected]). It could rapidly release the [email protected]2-Arg nanoparticles at the low pH tumor-specific environment due to the cleavage of imine bond. [email protected]2-Arg activated by over-expressed glutathione (GSH) in tumor cells releases GOD due to the cleavage of disulfide bonds, which could oxidize glucose to produce hydrogen peroxide (H2O2) for in situ NO generation via reaction between Arg and H2O2. The validity of this study might provide a method to modulate the tumor microenvironment for enhancing chemotherapy.
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