纳米医学
两亲性
胶束
药物输送
前药
纳米技术
体内
化学
小泡
组合化学
纳米颗粒
生物物理学
材料科学
生物化学
水溶液
有机化学
共聚物
膜
生物
生物技术
聚合物
作者
Shasha He,Chan Li,Qingfei Zhang,Jianxun Ding,Xing‐Jie Liang,Xuesi Chen,Haihua Xiao,Xiaoyuan Chen,Dongfang Zhou,Yubin Huang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-06-15
卷期号:12 (7): 7272-7281
被引量:116
标识
DOI:10.1021/acsnano.8b03476
摘要
Drug, targeting ligand, and imaging agent are the three essential components in a nanoparticle-based drug delivery system. However, tremendous batch-to-batch variation of composition and drug content typically accompany the current approaches of building these components together. Herein, we report the design of photoactivatable platinum(IV) (Pt(IV)) amphiphiles containing one or two hydrophilic lactose targeting ligands per hydrophobic Pt(IV) prodrug for an all-in-one precise nanomedicine. Self-assembly of these Pt(IV) amphiphiles results in either micelle or vesicle formation with a fixed Pt/targeting moiety ratio and a constantly high content of Pt. The micelles and vesicles are capable of hepatoma cell-targeting, fluorescence/Pt-based CT imaging and have shown effective anticancer efficacy under laser irradiation in vitro and in vivo. This photoactivatable, active self-targeting, and multimodal theranostic amphiphile strategy shows great potential in constructing precise nanomedicine.
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