Polycation-siRNA nanoparticles can disassemble at the kidney glomerular basement membrane

被引:310
作者
Zuckerman, Jonathan E. [1 ]
Choi, Chung Hang J. [1 ]
Han, Han [1 ]
Davis, Mark E. [1 ]
机构
[1] CALTECH, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
pharmacokinetics; glomerulus; IN-VIVO; TARGETED NANOPARTICLES; GENE DELIVERY; THERAPEUTICS; VITRO; PHARMACOKINETICS; BIODISTRIBUTION; LOCALIZATION; STABILITY; COMPLEXES;
D O I
10.1073/pnas.1200718109
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
Despite being engineered to avoid renal clearance, many cationic polymer (polycation)-based siRNA nanoparticles that are used for systemic delivery are rapidly eliminated from the circulation. Here, we show that a component of the renal filtration barrier-the glomerular basement membrane (GBM)-can disassemble cationic cyclodextrin-containing polymer (CDP)-based siRNA nanoparticles and, thereby, facilitate their rapid elimination from circulation. Using confocal and electron microscopies, positron emission tomography, and compartment modeling, we demonstrate that siRNA nanoparticles, but not free siRNA, accumulate and disassemble in the GBM. We also confirm that the siRNA nanoparticles do not disassemble in blood plasma in vitro and in vivo. This clearance mechanism may affect any nanoparticles that assemble primarily by electrostatic interactions between cationic delivery components and anionic nucleic acids (or other therapeutic entities).
引用
收藏
页码:3137 / 3142
页数:6
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