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Surface Modification and In Vitro Blood Compatibilities of Polyurethanes Containing α-Amino Acids in the Main Chain

机译:在主链中含有α-氨基酸的聚氨酯的表面改性和体外血液相容性

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Polyurethanes containing γ-benzyl L-glutamate segments (PUBLG) were synthesized using 4,4'-diphenylmethane diisocyanate, poly(tetramethylene glycol), and amino-terminated γ-benzyl L-glutamate oligomer as the chain extender. Heparin-immobilized PUBLG (PUBLG-H) was prepared by hydrolysis reaction of PUBLG with an alkaline aqueous solution, followed by a coupling reaction with heparin. The activation of plasma proteins, platelets and peripheral blood mononuclear cells were significantly suppressed on PUBLG-H, suggesting good in vitro blood compatibility.
机译:使用4,4'-二苯基甲烷二异氰酸酯,聚(四亚甲基二醇)和氨基封端的γ-苄基L-谷氨酸低聚物作为链增量剂合成含γ-苄基L-谷氨酸区段(PUPPG)的聚氨酯。通过用碱性水溶液的PUPLICLE的水解反应制备肝素 - 固定化公文(PUPPG-H),然后用肝素偶联反应。在publg-h上显着抑制了血浆蛋白,血小板和外周血单核细胞的激活,表明良好的体外血液相容性。

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