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创建血液相容表面:一种通过含有活性氧物质清除基团的氮氧自由基聚合物来抑制血液激活和凝血的新策略。

Creation of a blood-compatible surface: a novel strategy for suppressing blood activation and coagulation using a nitroxide radical-containing polymer with reactive oxygen species scavenging activity.

机构信息

Department of Materials Sciences, Graduate School of Pure and Applied Sciences, University of Tsukuba, Tennoudai 1-1-1, Tsukuba, Ibaraki 305-8573, Japan.

出版信息

Acta Biomater. 2012 Mar;8(3):1323-9. doi: 10.1016/j.actbio.2011.11.029. Epub 2011 Dec 2.

Abstract

Various polymeric materials have been used in medical devices, including blood-contacting artificial organs. Contact between blood and foreign materials causes blood cell activation and adhesion, followed by blood coagulation. Concurrently, the activated blood cells release inflammatory cytokines together with reactive oxygen species (ROS). We have hypothesized that the suppression of ROS generation plays a crucial role in blood activation and coagulation. To confirm this hypothesis, surface-coated polymers containing nitroxide radical compounds (nitroxide radical-containing polymers (NRP)) were designed and developed. The NRP was composed of a hydrophobic poly(chloromethylstyrene) (PCMS) chain to which 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) moieties were conjugated via condensation reaction of the chloromethyl groups in PCMS with the sodium alcoholate group of 4-hydroxy-TEMPO. Blood compatibility was investigated by placing NRP-coated beads in contact with rat whole blood. The amount of ROS generated on PCMS-coated beads used as a control increased significantly with time, while NRP-coated beads suppressed ROS generation. It is interesting to note that the suppression of inflammatory cytokine generation by NRP-coated beads was shown to be significantly higher than that by PCMS-coated beads. Both platelet and leukocyte adhesion to the beads were suppressed with increasing TEMPO incorporation in the polymer. These results confirm that the suppression of ROS by NRP prevents inflammatory cytokine generation, which in turn results in the suppression of blood activation and coagulation on the beads.

摘要

各种聚合材料已被应用于医疗器械,包括与血液接触的人工器官。血液与异物接触会引起血细胞的激活和黏附,随后引发血液凝固。同时,被激活的血细胞会释放炎症细胞因子和活性氧(ROS)。我们假设 ROS 的生成抑制在血液激活和凝血中起着至关重要的作用。为了验证这一假说,我们设计并开发了含有氮氧自由基化合物的表面涂层聚合物(氮氧自由基聚合物(NRP))。NRP 由疏水性聚(氯甲基苯乙烯)(PCMS)链组成,通过 PCMS 中的氯甲基与 4-羟基-TEMPO 的醇盐基团的缩合反应,将 2,2,6,6-四甲基哌啶-N-氧自由基(TEMPO)基团连接到 PCMS 上。通过将 NRP 涂层珠粒与大鼠全血接触来研究血液相容性。用作对照的 PCMS 涂层珠粒上生成的 ROS 量随时间显著增加,而 NRP 涂层珠粒则抑制了 ROS 的生成。有趣的是,NRP 涂层珠粒对炎症细胞因子生成的抑制作用明显高于 PCMS 涂层珠粒。随着聚合物中 TEMPO 含量的增加,血小板和白细胞对珠粒的黏附也被抑制。这些结果证实,NRP 对 ROS 的抑制作用阻止了炎症细胞因子的生成,进而抑制了珠粒上的血液激活和凝血。

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