Muramatsu N, Kondo T
J Biomed Mater Res. 1983 Nov;17(6):959-71. doi: 10.1002/jbm.820170607.
Microcapsules having different numbers of sulfonic acid groups on their surfaces were prepared by the interfacial polycondensation method. Platelets adhered to these capsules, and the rate and degree of platelet adhesion were found to be remarkable on those microcapsules that had high surface charge compared to those with low surface charge. This trend was strengthened by the coating of the capsules with plasma, while the electrophoretic mobilities of the plasma-coated capsules showed a considerable reduction and no appreciable difference between the respective mobilities could be observed. This trend suggest that the adsorption of plasma components on microcapsules, and not their surface negative charge, affected platelet adhesiveness directly. In connection with the glycosyl transferase hypothesis, the adsorption pattern and its effect on platelet adhesion of albumin, gamma-globulin, and fibrinogen were examined. The protein adsorption pattern varied depending on both the type of protein and the magnitude of negative charge on the microcapsule surface, but its effect on platelet adhesion was not fully consistent with the glycosyl transferase hypothesis. It was concluded from the findings that the surface negative charge of the capsules strongly affected the composition, molecular orientation, and/or configuration of the adsorbed plasma components, which probably induced the differences in platelet adhesiveness depending on the magnitude of surface negative charge of the microcapsules.
通过界面缩聚法制备了表面具有不同磺酸基团数量的微胶囊。血小板黏附于这些微胶囊,并且发现与低表面电荷的微胶囊相比,血小板在高表面电荷的微胶囊上的黏附速率和程度更为显著。用血浆包被微胶囊后这种趋势得到增强,而血浆包被的微胶囊的电泳迁移率显著降低,且各迁移率之间未观察到明显差异。这种趋势表明,微胶囊上血浆成分的吸附而非其表面负电荷直接影响血小板黏附性。结合糖基转移酶假说,研究了白蛋白、γ球蛋白和纤维蛋白原的吸附模式及其对血小板黏附的影响。蛋白质吸附模式因蛋白质类型和微胶囊表面负电荷大小而异,但其对血小板黏附的影响并不完全符合糖基转移酶假说。从这些发现得出的结论是,微胶囊的表面负电荷强烈影响吸附的血浆成分的组成、分子取向和/或构象,这可能导致了血小板黏附性因微胶囊表面负电荷大小不同而产生差异。