前药
胞嘧啶脱氨酶
癌症研究
结直肠癌
免疫疗法
肿瘤微环境
免疫系统
药理学
医学
化疗
癌症
化学
免疫学
生物化学
遗传增强
内科学
基因
作者
You‐Teng Qin,Xinhua Liu,Jiaxin An,Zhu Chen,Mei‐Ting Niu,Xiao Yan,Qianru Li,Zhi‐Yong Rao,Xian‐Zheng Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-08-15
卷期号:18 (34): 23497-23507
被引量:5
标识
DOI:10.1021/acsnano.4c07115
摘要
Colorectal cancer (CRC) is a major global health concern, and the development of effective treatment strategies is crucial. Enzyme prodrug therapy (EPT) shows promise in combating tumors but faces challenges in achieving sustained expression of therapeutic enzymes and optimal biological distribution. To address these issues, a fungi-triggered in situ chemotherapeutics generator (named as SC@CS@5-FC) was constructed via oral delivery of a prodrug (5-fluorocytosine, 5-FC) for the treatment of orthotopic colorectal tumor. When SC@CS@5-FC targets the tumor through tropism by
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