Interactions between circulating nanoengineered polymer particles and extracellular matrix components in vitro

被引:10
作者
Braunger, Julia A. [1 ,2 ]
Bjornmalm, Mattias [1 ,2 ]
Isles, Nathan A. [1 ,2 ]
Cui, Jiwei [1 ,2 ]
Henderson, Timothy M. A. [2 ]
O'Connor, Andrea J. [2 ]
Caruso, Frank [1 ,2 ]
机构
[1] Univ Melbourne, ARC Ctr Excellence Convergent Bionano Sci & Techn, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Dept Chem & Biomol Engn, Parkville, Vic 3010, Australia
基金
澳大利亚研究理事会;
关键词
ORGANS-ON-CHIPS; DRUG-DELIVERY; BASEMENT-MEMBRANE; TUMOR MICROENVIRONMENT; NANOPARTICLE DELIVERY; BIOLOGICAL-ACTIVITY; GOLD NANOPARTICLES; HYDROGEL PARTICLES; HYALURONIC-ACID; BLOOD-VESSELS;
D O I
10.1039/c6bm00726k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The extracellular matrix (ECM) that surrounds cells in vivo represents a biological barrier for nanomaterials in biomedicine. Herein, we present a system for investigating the interactions between circulating polymer particles and ECM components in vitro using a commercially available flow-based device. We use this system to show how material-dependent interactions of two different particle types-one assembled using poly(ethylene glycol) (PEG) and one prepared using poly(methacrylic acid) (PMA)-affect their interactions with basement membrane extracts during in vitro circulation, with PEG particles remaining in circulation longer than PMA particles. Further, by comparing macroporous hyaluronic acid gel constructs (typically used for tissue engineering) with basement membrane extracts, we show that scaffoldeffects (porosity and surface chemistry) impact on circulation time in vitro. The presented system is simple and modular, and can be used to rapidly screen fundamental interactions of engineered particles with biologically relevant microenvironments under flow-conditions.
引用
收藏
页码:267 / 273
页数:7
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