前药
纳米载体
阿霉素
体内
化学
右旋糖酐
体外
药理学
药品
多糖
药物输送
靶向给药
化疗
生物化学
医学
生物
内科学
有机化学
生物技术
作者
Di Li,Weiguo Xu,Pengqiang Li,Jianxun Ding,Zhiliang Cheng,Li Chen,Lesan Yan,Xuesi Chen
标识
DOI:10.1021/acs.molpharmaceut.6b00747
摘要
Self-targetability is an emerging targeting strategy for polymer nanocarriers with facile preparation and high targeting efficiency. An acid-sensitive dextran-doxorubicin prodrug (Dex-g-DOX) has been synthesized and used as a self-targeted drug delivery system for the treatment of orthotopic hepatoma. The polysaccharide prodrug exhibits ultraselective accumulation in cancerous liver tissue, acid-sensitive DOX release within cells, and high antitumor efficacy in vitro and in vivo. Therefore, Dex-g-DOX demonstrates great potential for chemotherapy of orthotopic hepatoma.
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