Erythrocyte membrane-camouflaged polymeric nanoparticles as a biomimetic delivery platform

被引:1868
作者
Hu, Che-Ming J.
Zhang, Li
Aryal, Santosh
Cheung, Connie
Fang, Ronnie H.
Zhang, Liangfang [1 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
biomimetic nanoparticle; drug delivery; long circulation; red blood cell membrane; RED-BLOOD-CELLS; DRUG-DELIVERY; HYBRID NANOPARTICLES; SELF; BIODISTRIBUTION; PARTICLES; CANCER; MICROPARTICLES; SURFACE; SYSTEM;
D O I
10.1073/pnas.1106634108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Efforts to extend nanoparticle residence time in vivo have inspired many strategies in particle surface modifications to bypass macrophage uptake and systemic clearance. Here we report a top-down biomimetic approach in particle functionalization by coating biodegradable polymeric nanoparticles with natural erythrocyte membranes, including both membrane lipids and associated membrane proteins for long-circulating cargo delivery. The structure, size and surface zeta potential, and protein contents of the erythrocyte membrane-coated nanoparticles were verified using transmission electron microscopy, dynamic light scattering, and gel electrophoresis, respectively. Mice injections with fluorophore-loaded nanoparticles revealed superior circulation half-life by the erythrocyte-mimicking nanoparticles as compared to control particles coated with the state-of-the-art synthetic stealth materials. Biodistribution study revealed significant particle retention in the blood 72 h following the particle injection. The translocation of natural cellular membranes, their associated proteins, and the corresponding functionalities to the surface of synthetic particles represents a unique approach in nanoparticle functionalization.
引用
收藏
页码:10980 / 10985
页数:6
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