脂质体
跨细胞
纳米医学
材料科学
渗透(战争)
纳米载体
肿瘤微环境
前药
吉西他滨
纳米技术
药物输送
内吞作用
纳米颗粒
癌症研究
药理学
化学
医学
肿瘤细胞
化疗
受体
生物化学
内科学
工程类
运筹学
作者
Guowei Wang,Chao Zhang,Yifan Jiang,Yue Song,Jifan Chen,Yu Sun,Qunying Li,Zhuxian Zhou,Youqing Shen,Pintong Huang
标识
DOI:10.1002/adfm.202102786
摘要
Abstract Active tumor penetration has been recently recognized as a promising strategy to resolve the limitation of nanomedicine in terms of tumor penetration, but it is challenging to develop active transporting nanocarriers. Here, an ultrasonic cavitation‐assisted and acid‐activatable active transporting liposome for a broad range of tumors is reported. The active transporting liposome (size and charge dual‐conversional gemcitabine prodrug‐integrated liposomal nanodroplet (SCGLN)) overcomes the tight blood vessel walls with the aid of ultrasonic cavitation. The SCGLN subsequently transforms from micro‐size to nano‐size under prolonged ultrasound radiation. Once in the acidic tumor microenvironment, the nanosized SCGLN undergoes negative‐to‐positive charge‐reversal and triggers the cationization‐initiated transcytosis to penetrate deep into tumor parenchyma. The gemcitabine‐loaded SCGLN exhibits potent antitumor activity in multiple poorly permeable tumor models, which completely erases subcutaneous U251 glioma and stops the progression of orthotopic BxPC3 pancreatic ductal adenocarcinoma. This study presents a promising and universal strategy to develop active penetrating nanomedicines for efficient drug delivery in the low permeable tumor.
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