Improved in vitro blood compatibility of polycaprolactone nanowire surfaces.
Improved in vitro blood compatibility of polycaprolactone nanowire surfaces.
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DOI:
10.1021/am503508r
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发表时间:
2014-09-24
影响因子:
9.5
通讯作者:
Popat, Ketul C.
中科院分区:
文献类型:
--
作者:
Leszczak, Victoria;Popat, Ketul C.
关键词:
There are a multitude of polymeric materials currently utilized to prepare a variety of blood-contacting implantable medical devices. These devices include tissue grafts, coronary artery and vascular stents, and orthopedic implants. The thrombogenic nature of such materials can cause serious complications in patients, and ultimately lead to functional failure. To date, there is no truly hemocompatible biomaterial surface. Nanostructured surfaces improve cellular interactions but there is a limited amount of information regarding their blood compatibility. In this study, the in vitro blood compatibility of four different surfaces (control, PCL; nanowire, NW; collagen immobilized control, cPCL; collagen immobilized nanowire, cNW) were investigated for their use as interfaces for blood-contacting implants. The results presented here indicate enhanced in vitro blood compatibility of nanowire surfaces compared control surfaces. Although there were no significant differences in leukocyte adhesion, there was a decrease in platelet adhesion on NW surfaces. Scanning electron microscopy images showed a decrease in platelet/leukocyte complexes on cNW surfaces and no apparent complexes were formed on NW surfaces compared to PCL and cPCL surfaces. The increase in these complexes likely contributed to a higher expression of specific markers for platelet and leukocyte activation on PCL and cPCL surfaces. No significant differences were found in contact and complement activation on any surface. Further, thrombin antithrombin complexes were significantly reduced on NW surfaces. A significant increase in hemolysis and fibrinogen adsorption was identified on PCL surfaces likely caused by its hydrophobic surface. This work shows the improved blood-compatibility of nanostructured surfaces, identifying this specific nanoarchitecture as a potential interface for promoting the long-term success of blood-contacting biomaterials.
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影响因子:
4.8
作者:
Leszczak V;Baskett DA;Popat KC
通讯作者:
Popat KC
DOI:
10.1039/df9480300011
发表时间:
1948-01-01
期刊:
DISCUSSIONS OF THE FARADAY SOCIETY
影响因子:
--
作者:
CASSIE, ABD
通讯作者:
CASSIE, ABD
影响因子:
14
作者:
Hoshi, Ryan A.;Van Lith, Robert;Jen, Michele C.;Allen, Josephine B.;Lapidos, Karen A.;Ameer, Guillermo
通讯作者:
Ameer, Guillermo
影响因子:
14
作者:
Karlsson, M;Pålsgård, E;Di Silvio, L
通讯作者:
Di Silvio, L
影响因子:
6.7
作者:
Blezer, R;Willems, GM;Lindhout, T
通讯作者:
Lindhout, T