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将肝素作为分子间隔物固定在微球上,以提高血液灌流中的血液相容性。

Heparin as a molecular spacer immobilized on microspheres to improve blood compatibility in hemoperfusion.

机构信息

Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400030, PR China.

Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400030, PR China.

出版信息

Carbohydr Polym. 2019 Feb 1;205:89-97. doi: 10.1016/j.carbpol.2018.08.067. Epub 2018 Sep 1.

Abstract

Heparin, a highly sulfated linear polysaccharide, with anticoagulation function and blood compatibility is widely used as a biomaterials in medical application, but the most importance of heparin is its structure function as the macromolecular space arm. In this study, heparin as a spacer was covalently immobilized on the chloromethylated polystyrene microspheres (Ps) and then connected with l-phenylalanine forming the Ps-Hep-Phe structure, which was developed for endotoxin adsorption in hemoperfusion. The grafting density of heparin reach the maximum when the initial concentration of heparin solution was 5 mg/mL. The adsorbents with the heparin as a spacer showed the prolonged clotting times, low protein adsorption, and reduced the hemolysis rate, indicating that heparin-modified adsorbents have great blood compatibility. The adsorption capacity of Ps-Hep-Phe for endotoxin was 25.15 EU/g in dynamic adsorption, higher than that of Ps. Therefore, this study imply that heparin would be promising for modification of adsorbents in hemoperfusion.

摘要

肝素是一种高度硫酸化的线性多糖,具有抗凝和血液相容性,被广泛用作医学应用中的生物材料,但肝素最重要的是其作为大分子空间臂的结构功能。在这项研究中,肝素作为间隔臂被共价固定在氯甲基化聚苯乙烯微球(Ps)上,然后与 L-苯丙氨酸连接形成 Ps-Hep-Phe 结构,用于血液灌流中的内毒素吸附。当肝素溶液的初始浓度为 5mg/mL 时,肝素的接枝密度达到最大值。具有间隔臂的肝素修饰吸附剂表现出延长的凝血时间、低蛋白质吸附和降低的溶血率,表明肝素修饰的吸附剂具有良好的血液相容性。Ps-Hep-Phe 对内毒素的动态吸附容量为 25.15EU/g,高于 Ps。因此,本研究表明肝素有望用于血液灌流中吸附剂的修饰。

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