光敏剂
光动力疗法
喜树碱
谷胱甘肽
药品
化学
亚甲蓝
药理学
化疗
癌症研究
连接器
医学
光化学
生物化学
酶
有机化学
内科学
光催化
催化作用
操作系统
计算机科学
作者
Yanjun Yang,Yifeng Zhang,Ran Wang,Rong Xiang,Ting Liu,Xiang Xia,Jiangli Fan,Wen Sun,Xiaojun Peng
标识
DOI:10.1016/j.cclet.2022.03.040
摘要
During cancer treatment, chemotherapeutic drugs always result in severe side-effects and drug resistance. Therefore, combining cheomtherapy with other therapeutic modalities, such as photodynamic therapy (PDT) and designing an activable platform is promising for precise and efficient anticancer treatment. Herein, we report a “pro-drug-photosensitizer” agent, LMB-S-CPT, bearing a disulfide bond as the glutathione (GSH)-activatable linker. LMB-S-CPT can be selectively activated by GSH to release activated drug, camptothecin (CPT), for chemotherapy and activated photosensitizer, methylene blue (MB), for PDT. LMB-S-CPT exhibits excellent tumor-activatable performance when injected into tumor-bearing mice, as well as specific cancer therapy with negligible toxic side effects. The activatable pro-drug-photosensitizer offers a new strategy for chemo-photodynamic therapy and displays precise, selective and excellent antitumor effect.
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