胶束
化学
药品
药理学
药物输送
靶向给药
蛋白酵素
化疗
细胞凋亡
心脏毒性
癌症
生物利用度
癌细胞
细胞内
肽
癌症治疗
癌症研究
蛋白酶
两亲性
阿霉素
前药
组织蛋白酶D
作用机理
内化
毒品携带者
丝氨酸蛋白酶
细胞毒性
细胞穿透肽
酶
作者
Yonghui Liu,Jinwang Tan,Mengyuan Zhang,Zijian Li,Dong Wan,Jie Pan
标识
DOI:10.1021/acsabm.6c00009
摘要
Cancer, as a global health crisis, continues to threaten human life and health. Chemotherapy occupies a central position in cancer treatment, but conventional chemotherapeutic agents have some limitations, such as low solubility, lack of specific targeting, insufficient bioavailability and high toxicity to normal tissues. However, the use of DOX is associated with serious adverse effects, including cardiotoxicity and myelosuppression, which limit its effectiveness in antitumor therapy. To overcome these challenges, drug delivery systems (DDSs) have been developed, with polymeric micelles emerging as a highly promising option. In this study, we designed and synthesized a multistage enzyme-responsive amphiphilic molecule, mPEG-GFLGRGDEVD-DOX, for targeted cancer therapy through self-assembly into micelles. Upon cleavage of the GFLG by Cathepsin B, the micelles shed the mPEG crown, thereby exposing the active targeting peptide sequence RGD, which enhances micelle uptake by tumor cells. Concurrently, the DOX loaded in the micelles partially leaks out, inducing apoptosis and activating the apoptotic protease Caspase-3. Caspase-3 then cleaves the DEVD tail, facilitating the rapid intracellular release of the drug. This approach specifically highlights the innovative use of a dual-enzyme cascade (Cathepsin B and Caspase-3) to sequentially trigger tumor-specific drug release, overcoming the limitations of current clinical applications. The synergistic action of these enzymes enhances both drug release and selectivity, offering a promising strategy for improved cancer therapy.
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