外渗
跨细胞
化学
效力
膜
药理学
结合
药物输送
体外
内吞作用
细胞
药品
癌症研究
生物化学
医学
免疫学
数学分析
数学
有机化学
作者
Siqin Chen,Yin Zhong,Wufa Fan,Jiajia Xiang,Guowei Wang,Quan Zhou,Jinqiang Wang,Yu Geng,Rui Sun,Zhen Zhang,Ying Piao,Jianguo Wang,Jianyong Zhuo,Hailin Cong,Haiping Jiang,Jun Ling,Zi‐Chen Li,Dong Yang,Xin Yao,Xiao Xu,Zhuxian Zhou,Jianbin Tang,Youqing Shen
标识
DOI:10.1038/s41551-021-00701-4
摘要
Effective anticancer nanomedicines need to exhibit prolonged circulation in blood, to extravasate and accumulate in tumours, and to be taken up by tumour cells. These contrasting criteria for persistent circulation and cell-membrane affinity have often led to complex nanoparticle designs with hampered clinical translatability. Here, we show that conjugates of small-molecule anticancer drugs with the polyzwitterion poly(2-(N-oxide-N,N-diethylamino)ethyl methacrylate) have long blood-circulation half-lives and bind reversibly to cell membranes, owing to the negligible interaction of the polyzwitterion with proteins and its weak interaction with phospholipids. Adsorption of the polyzwitterion-drug conjugates to tumour endothelial cells and then to cancer cells favoured their transcytosis-mediated extravasation into tumour interstitium and infiltration into tumours, and led to the eradication of large tumours and patient-derived tumour xenografts in mice. The simplicity and potency of the polyzwitterion-drug conjugates should facilitate the design of translational anticancer nanomedicines.
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