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
相关论文
共 60 条
  • [51] Design and evaluation of novel blood incubation systems for in vitro hemocompatibility assessment of planar solid surfaces
    Streller, U
    Sperling, C
    Hübner, J
    Hanke, R
    Werner, C
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2003, 66B (01) : 379 - 390
  • [52] In vivo bioresponses to silk proteins
    Thurber, Amy E.
    Omenetto, Fiorenzo G.
    Kaplan, David L.
    [J]. BIOMATERIALS, 2015, 71 : 145 - 157
  • [53] Doxorubicin-Loaded Magnetic Silk Fibroin Nanoparticles for Targeted Therapy of Multidrug-Resistant Cancer
    Tian, Ye
    Jiang, Xuejiao
    Chen, Xin
    Shao, Zhengzhong
    Yang, Wuli
    [J]. ADVANCED MATERIALS, 2014, 26 (43) : 7393 - 7398
  • [54] Protein ultrastructure and the nanoscience of complement activation
    Vorup-Jensen, Thomas
    Boesen, Thomas
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2011, 63 (12) : 1008 - 1019
  • [55] Wang ZJ, 2014, NAT NANOTECHNOL, V9, P204, DOI [10.1038/NNANO.2014.17, 10.1038/nnano.2014.17]
  • [56] Wongpinyochit T, 2016, JOVE-J VIS EXP, DOI [10.3791/54669(2016), 10.3791/54669]
  • [57] PEGylated Silk Nanoparticles for Anticancer Drug Delivery
    Wongpinyochit, Thidarat
    Uhlmann, Petra
    Urquhart, Andrew J.
    Seib, F. Philipp
    [J]. BIOMACROMOLECULES, 2015, 16 (11) : 3712 - 3722
  • [58] Cancer nanomedicine: from targeted delivery to combination therapy
    Xu, Xiaoyang
    Ho, William
    Zhang, Xueqing
    Bertrand, Nicolas
    Farokhzad, Omid
    [J]. TRENDS IN MOLECULAR MEDICINE, 2015, 21 (04) : 223 - 232
  • [59] Formation of silk fibroin nanoparticles in water-miscible organic solvent and their characterization
    Zhang, Yu-Qing
    Shen, Wei-De
    Xiang, Ru-Li
    Zhuge, Lan-Jian
    Gao, Wei-Jian
    Wang, Wen-Bao
    [J]. JOURNAL OF NANOPARTICLE RESEARCH, 2007, 9 (05) : 885 - 900
  • [60] Silk Fibroin-Based Nanoparticles for Drug Delivery
    Zhao, Zheng
    Li, Yi
    Xie, Mao-Bin
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2015, 16 (03): : 4880 - 4903