Institute of Biomaterial Science and Berlin-Brandenburg Centre for Regenerative Therapies, Helmholtz-Zentrum Geesthacht, Kantstrasse 55, Teltow, Germany.
Clin Hemorheol Microcirc. 2013 Jan 1;54(3):235-48. doi: 10.3233/CH-131729.
Linear, side-chain methylated oligoglycerols (OGMe) were recently reported as potential surface passivating molecules for improving the protein resistance of cardiovascular application relevant poly(ether imide) (PEI) membranes. A previously reported in vitro screening under static test conditions allowed an end-point evaluation of the adhesion and activation of adherent thrombocytes performed on the material surfaces and revealed similar levels of thrombogenicity on PEI membranes, functionalized with OGMe and oligo(ethylene glycol) (OEG) of similar molecular weight (Mn = 1,300 g·mol-1 - 1,800 g·mol-1). In the present study, we investigated the hemocompatibility of these materials in a dynamic closed loop system, in order to study time-dependent thrombocyte material interactions also of the circulating thrombocytes by mimicking in vivo relevant flow conditions in a dynamic test system with multiple material contacts. Activation and aggregation of circulating thrombocytes as well as complement activation and plasmatic coagulation were evaluated after 40 circulations of thrombocyte rich plasma in the closed loop system. The results of the dynamic tests revealed no differences between the OGMe and OEG functionalized PEI membranes. Furthermore, no differences were observed between the latter and a PEI membrane treated under the conditions of functionalization at pH 11 (PEI-pH11) without an oligoether being present. Blood plasma protein adsorption, as well as activation, and adherence of circulating thrombocytes occurred in a comparable, but minor manner on all investigated PEI membranes. From this we conclude that the OGMe and OEG surface functionalization did not lead to an improvement of the already good hemocompatibility of the PEI-pH11 membrane.
线性、侧链甲基化低聚糖(OGMe)最近被报道为一种潜在的表面钝化分子,可提高心血管应用相关聚醚酰亚胺(PEI)膜的蛋白质抗性。以前在静态测试条件下进行的体外筛选允许对材料表面上的附着和激活的粘着血小板进行终点评估,并揭示了在具有类似分子量(Mn=1300g·mol-1-1800g·mol-1)的 OGMe 和聚乙二醇(OEG)官能化的 PEI 膜上相似的血栓形成水平。在本研究中,我们在动态闭环系统中研究了这些材料的血液相容性,以便通过模拟体内相关的流动条件在动态测试系统中研究时间依赖性血小板与材料的相互作用,并进行多次材料接触。在闭环系统中循环富血小板血浆 40 次后,评估了循环血小板的激活和聚集以及补体激活和血浆凝固。动态测试的结果表明,OGMe 和 OEG 官能化的 PEI 膜之间没有差异。此外,在不存在低聚醚的情况下,在 pH11 下(PEI-pH11)进行官能化处理的 PEI 膜与后者之间也没有观察到差异。在所有研究的 PEI 膜上,血浆蛋白吸附以及循环血小板的激活和附着以类似但较小的方式发生。由此我们得出结论,OGMe 和 OEG 表面官能化并未导致已经具有良好血液相容性的 PEI-pH11 膜得到改善。