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
  • [1] [Anonymous], GUID VAL LIM AM LYS
  • [2] CHANDLER AB, 1958, LAB INVEST, V7, P110
  • [3] Surgery combined with controlled-release doxorubicin silk films as a treatment strategy in an orthotopic neuroblastoma mouse model
    Chiu, B.
    Coburn, J.
    Pilichowska, M.
    Holcroft, C.
    Seib, F. P.
    Charest, A.
    Kaplan, D. L.
    [J]. BRITISH JOURNAL OF CANCER, 2014, 111 (04) : 708 - 715
  • [4] CHOULY C, 1994, CLIN MATER, V15, P293, DOI 10.1016/0267-6605(94)90061-2
  • [5] Interaction between polymeric multilayer capsules and immune cells
    Dierendonck, Marijke
    De Koker, Stefaan
    Vervaet, Chris
    Remon, Jean Paul
    De Geest, Bruno G.
    [J]. JOURNAL OF CONTROLLED RELEASE, 2012, 161 (02) : 592 - 599
  • [6] Nanomedicine(s) under the Microscope
    Duncan, Ruth
    Gaspar, Rogerio
    [J]. MOLECULAR PHARMACEUTICS, 2011, 8 (06) : 2101 - 2141
  • [7] Functionalized Spider Silk Spheres As Drug Carriers for Targeted Cancer Therapy
    Florczak, Anna
    Mackiewicz, Andrzej
    Dams-Kozlowska, Hanna
    [J]. BIOMACROMOLECULES, 2014, 15 (08) : 2971 - 2981
  • [8] Therapeutic Inflammatory Monocyte Modulation Using Immune-Modifying Microparticles
    Getts, Daniel R.
    Terry, Rachael L.
    Getts, Meghann Teague
    Deffrasnes, Celine
    Mueller, Marcus
    van Vreden, Caryn
    Ashhurst, Thomas M.
    Chami, Belal
    McCarthy, Derrick
    Wu, Huiling
    Ma, Jin
    Martin, Aaron
    Shae, Lonnie D.
    Witting, Paul
    Kansas, Geoffrey S.
    Kuehn, Joachim
    Hafezi, Wali
    Campbell, Iain L.
    Reilly, David
    Say, Jana
    Brown, Louise
    White, Melanie Y.
    Cordwell, Stuart J.
    Chadban, Steven J.
    Thorp, Edward B.
    Bao, Shisan
    Miller, Stephen D.
    King, Nicholas J. C.
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (219)
  • [9] Nanoparticles induce platelet activation in vitro through stimulation of canonical signalling pathways
    Guidetti, Gianni F.
    Consonni, Alessandra
    Cipolla, Lina
    Mustarelli, Piercarlo
    Balduini, Cesare
    Torti, Mauro
    [J]. NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2012, 8 (08) : 1329 - 1336
  • [10] Gupta V, 2009, INT J NANOMED, V4, P115