化学
纳米载体
体内
共轭体系
纳米颗粒
低密度脂蛋白受体
配体(生物化学)
临床前影像学
生物物理学
生物相容性材料
脂蛋白
低密度脂蛋白
药物输送
纳米技术
生物医学工程
生物化学
胆固醇
受体
有机化学
聚合物
生物
生物技术
医学
材料科学
作者
Juan Chen,Ian R. Corbin,Hui Li,Weiguo Cao,Jerry D. Glickson,Gang Zheng
摘要
LDL particles are high-capacity nanocarriers with precisely controlled size and are naturally biocompatible, biodegradable, and nonimmunogenic. However, their utilities as drug carriers are limited by the narrow purview of LDL receptor-positive tumors. Here, we synthsized a ligand-conjugated, NIR-labeled LDL that enables the first in vivo demonstration of rerouting LDL from LDL receptors to selected alternate receptors, thus drastically expanding the range of using LDL particles as nanocarriers for in vivo cancer imaging and treatment.
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