In vitro Endothelialization and Platelet Adhesion on Titaniferous Upgraded Polyether and Polycarbonate Polyurethanes

Materials

Jing Li¹  Karla Lehle¹  Christof Schmid¹  Thomas Schmid²  Daniel Wehner²  Björn Hartmann³  Hanngörg Zimmermann³ 

[1] Department of Cardiothoracic Surgery, University Medical Centre Regensburg, Franz-Josef-Strauss-Allee 11, 93042 Regensburg, Germany;Dualis Medtech GmbH, Am Technologiepark 8+10, 82229 Seefeld, Germany;PFM medical titanium, Höfener Str. 45, 90431 Nürnberg, Germany;

关键词: endothelial cell seeding;    cytocompatibility;    haemocompatibility;    platelet adhesion;    cardiovascular tissue engineering;    titanium;   

DOI  :  10.3390/ma7020623

来源: DOAJ

【 摘 要 】

Polycarbonateurethanes (PCU) and polyetherurethanes (PEU) are used for medical devices, however their bio- and haemocompatibility is limited. In this study, the effect of titaniferous upgrading of different polyurethanes on the bio- and haemocompatibility was investigated by endothelial cell (EC) adhesion/proliferation and platelet adhesion (scanning electron microscopy), respectively. There was no EC adhesion/proliferation and only minor platelet adhesion on upgraded and pure PCU (Desmopan). PEUs (Texin 985, Tecothane 1085, Elastollan 1180A) differed in theircyto- and haemocompatibility. While EC adhesion depended on the type of PEU, any proliferative activity was inhibited. Additional titaniferous upgrading of PEU induced EC proliferation and increased metabolic activity. However, adherent ECs were significantly activated. While Texin was highly thrombotic, only small amounts of platelets adhered onto Tecothane and Elastollan. Additional titaniferous upgrading reduced thrombogenicity of Texin, preserved haemocompatibility of Elastollan, and increased platelet activation/aggregation on Tecothane. In conclusion, none of the PUs was cytocompatible; only titaniferous upgrading allowed EC proliferation and metabolism on PEUs. Haemocompatibility depended on the type of PU.

【 授权许可】

Unknown