Biocompatibility assessment of silk nanoparticles: hemocompatibility and internalization by human blood cells

被引:63
作者
Maitz, Manfred F. [1 ]
Sperling, Claudia [1 ]
Wongpinyochit, Thidarat [2 ]
Herklotz, Manuela [1 ]
Werner, Carsten [1 ]
Seib, F. Philipp [1 ,2 ]
机构
[1] Max Bergmann Ctr Biomat Dresden, Leibniz Inst Polymer Res Dresden, D-01069 Dresden, Germany
[2] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow G4 0RE, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
Silk; Fibroin; Silica; Blood compatibility; IN-VITRO; FIBROIN NANOPARTICLES; DRUG CARRIERS; COAGULATION; FILMS; SURFACE; NANOMEDICINE; PEGYLATION; CURVATURE; DELIVERY;
D O I
10.1016/j.nano.2017.07.012
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Many nanoparticles are designed for use as potential nanomedicines for parenteral administration. However, emerging evidence suggests that hemocompatibility is important, but is highly particle-and test-bed dependent. Thus, knowledge of bulk material properties does not predict the hemocompatibility of uncharacterized nanoparticles, including silk nanoparticles. This study compares the hemocompatibility of silk versus silica nanoparticles, using whole human blood under quasi-static and flow conditions. Substantial hemocompatibility differences are noted for some nanoparticles in quasi-static versus dynamic studies; i.e., the inflammatory response to silk nanoparticles is significantly lower under flow versus quasi-static conditions. Silk nanoparticles also have very low coagulant properties - an observation that scales from the macro-to the nano-level. These nanoparticle hemocompatibility studies are complemented by preliminary live cell measurements to evaluate the endocytosis and trafficking of nanoparticles in human blood cells. Overall, this study demonstrates that nanoparticle hemocompatibility is affected by several factors, including the test bed design. (C) 2017 The Authors. Published by Elsevier Inc.
引用
收藏
页码:2633 / 2642
页数:10
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