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具有磷脂极性基团的聚合物的血栓形成性降低。

Reduced thrombogenicity of polymers having phospholipid polar groups.

作者信息

Ishihara K, Aragaki R, Ueda T, Watenabe A, Nakabayashi N

机构信息

Institute for Medical and Dental Engineering, Tokyo Medical and Dental University, Japan.

出版信息

J Biomed Mater Res. 1990 Aug;24(8):1069-77. doi: 10.1002/jbm.820240809.

Abstract

The thrombogenicity of polymers having a phospholipid polar group, poly(2-methacryloyloxyethyl phosphorylcholine (MPC)-co-n-butyl methacrylate (BMA)), was evaluated by a microsphere-column method with attention to the activation and adhesion of platelets on the polymer surface. When citrated platelet-rich plasma (PRP) contacted with the polymers, a large number of platelets adhered and aggregated on poly(BMA). The number of adherent platelets decreased and deformation and aggregation were suppressed with increasing MPC composition. The same tendency was noted when Ca2(+)-re-added PRP came in contact with the polymers. In the case of poly(MPC-co-BMA) with 0.320 mole fraction of MPC, activation of platelets and formation of fibrin were completely suppressed. Therefore, MPC moieties in the polymer play an important role in the reduction of thrombogenicity of the polymer.

摘要

通过微球柱法评估了具有磷脂极性基团的聚合物聚(2-甲基丙烯酰氧基乙基磷酰胆碱(MPC)-共-甲基丙烯酸正丁酯(BMA))的血栓形成性,重点关注血小板在聚合物表面的活化和黏附情况。当枸橼酸化富血小板血浆(PRP)与聚合物接触时,大量血小板黏附并聚集在聚(BMA)上。随着MPC组成的增加,黏附血小板的数量减少,变形和聚集受到抑制。当重新添加Ca2+的PRP与聚合物接触时,也观察到相同的趋势。在MPC摩尔分数为0.320的聚(MPC-共-BMA)的情况下,血小板的活化和纤维蛋白的形成被完全抑制。因此,聚合物中的MPC部分在降低聚合物血栓形成性方面起着重要作用。

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