Hemocompatibility evaluation of different silver nanoparticle concentrations employing a modified Chandler-loop in vitro assay on human blood

Due to their antibacterial effects, the use of silver nanoparticles (AgNPs) in a great variety of medical applications like coatings of medical devices has increased markedly in the last few years. However, blood in contact with AgNPs may induce adverse effects, thereby altering hemostatic functions...

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Veröffentlicht in:Acta biomaterialia 2013-07, Vol.9 (7), p.7460-7468
Hauptverfasser: Krajewski, Stefanie, Prucek, Robert, Panacek, Ales, Avci-Adali, Meltem, Nolte, Andrea, Straub, Andreas, Zboril, Radek, Wendel, Hans P., Kvitek, Libor
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container_end_page 7468
container_issue 7
container_start_page 7460
container_title Acta biomaterialia
container_volume 9
creator Krajewski, Stefanie
Prucek, Robert
Panacek, Ales
Avci-Adali, Meltem
Nolte, Andrea
Straub, Andreas
Zboril, Radek
Wendel, Hans P.
Kvitek, Libor
description Due to their antibacterial effects, the use of silver nanoparticles (AgNPs) in a great variety of medical applications like coatings of medical devices has increased markedly in the last few years. However, blood in contact with AgNPs may induce adverse effects, thereby altering hemostatic functions. The objective of this study was to investigate the hemocompatibility of AgNPs in whole blood. Human whole blood (n=6) was treated with different AgNPs concentrations (1, 3 and 30mgl−1) or with saline/blank solutions as controls before being circulated in an in vitro Chandler-loop model for 60min at 37°C. Before and after circulation, various hematologic markers were investigated. Based on the hematologic parameters measured, no profound changes were observed in the groups treated with AgNP concentrations of 1 or 3mgl−1. AgNP concentrations of 30mgl−1 induced hemolysis of erythrocytes and α-granule secretion in platelets, increased CD11b expression on granulocytes, increased coagulation markers thrombin–antithrombin-III complex, kallikrein-like and FXIIa-like activities as well as complementing cascade activation. Overall, we provide for the first time a comprehensive evaluation including all hematologic parameters required to reliably assess the hemocompatibility of AgNPs. We strongly recommend integrating these hemocompatibility tests to preclinical test procedures prior to in vivo application of new AgNP-based therapies.
doi_str_mv 10.1016/j.actbio.2013.03.016
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However, blood in contact with AgNPs may induce adverse effects, thereby altering hemostatic functions. The objective of this study was to investigate the hemocompatibility of AgNPs in whole blood. Human whole blood (n=6) was treated with different AgNPs concentrations (1, 3 and 30mgl−1) or with saline/blank solutions as controls before being circulated in an in vitro Chandler-loop model for 60min at 37°C. Before and after circulation, various hematologic markers were investigated. Based on the hematologic parameters measured, no profound changes were observed in the groups treated with AgNP concentrations of 1 or 3mgl−1. AgNP concentrations of 30mgl−1 induced hemolysis of erythrocytes and α-granule secretion in platelets, increased CD11b expression on granulocytes, increased coagulation markers thrombin–antithrombin-III complex, kallikrein-like and FXIIa-like activities as well as complementing cascade activation. 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subjects adverse effects
antibacterial properties
Biological Assay - instrumentation
Biological Assay - methods
Blood Coagulation - drug effects
Blood Coagulation - physiology
Blood Physiological Phenomena - drug effects
Cells, Cultured
Coagulation
coatings
Equipment Design
Equipment Failure Analysis
erythrocytes
granulocytes
Hemocompatibility
hemolysis
Humans
in vitro studies
Inflammation
Materials Testing - instrumentation
Materials Testing - methods
medical equipment
Metal Nanoparticles - administration & dosage
nanosilver
secretion
Silver - pharmacology
Silver nanoparticles
title Hemocompatibility evaluation of different silver nanoparticle concentrations employing a modified Chandler-loop in vitro assay on human blood
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