Bauer James W, Xu Li-Chong, Vogler Erwin A, Siedlecki Christopher A
Department of Bioengineering, Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033.
Department of Surgery, Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033.
Biointerphases. 2017 May 17;12(2):02D410. doi: 10.1116/1.4983634.
Studies of the activation of FXII in both platelet poor plasma and in neat buffer solutions were undertaken for a series of mixed thiol self-assembled monolayers spanning a broad range of water wettability. A wide spectrum of carboxyl/methyl-, hydroxyl/methyl-, and amine/methyl-thiol modified surfaces were prepared, characterized, and then utilized as the procoagulant materials in a series of FXII activation studies. X-ray photoelectron spectroscopy was utilized to verify the sample surface's thiol composition and contact angles measured to determine the sample surface's wettability. These samples were then used in in vitro coagulation assays using a 50% mixture of recalcified plasma in phosphate buffered saline. Alternatively, the samples were placed into purified FXII solutions for 30 min to assess FXII activation in neat buffer solution. Plasma coagulation studies supported a strong role for anionic surfaces in contact activation, in line with the traditional models of coagulation, while the activation results in neat buffer solution demonstrated that FXIIa production is related to surface wettability with minimum levels of enzyme activation observed at midrange wettabilities, and no statistically distinguishable differences in FXII activation seen between highly wettable and highly nonwettable surfaces. Results demonstrated that the composition of the solution and the surface properties of the material all contribute to the observation of contact activation, and the activation of FXII is not specific to anionic surfaces as has been long believed.
针对一系列具有广泛水润湿性的混合硫醇自组装单分子层,开展了在乏血小板血浆和纯缓冲溶液中FXII激活的研究。制备了多种羧基/甲基、羟基/甲基和胺/甲基硫醇修饰的表面,进行了表征,然后在一系列FXII激活研究中用作促凝材料。利用X射线光电子能谱验证样品表面的硫醇组成,并测量接触角以确定样品表面的润湿性。然后将这些样品用于体外凝血试验,使用磷酸盐缓冲盐水中50%的重新钙化血浆混合物。或者,将样品置于纯化的FXII溶液中30分钟,以评估纯缓冲溶液中的FXII激活情况。血浆凝血研究支持了阴离子表面在接触激活中的重要作用,这与传统的凝血模型一致,而在纯缓冲溶液中的激活结果表明,FXIIa的产生与表面润湿性有关,在中等润湿性下观察到最低水平的酶激活,在高润湿性和高非润湿性表面之间未观察到FXII激活的统计学显著差异。结果表明,溶液的组成和材料的表面性质都有助于观察到接触激活,并且FXII的激活并不像长期以来所认为的那样特定于阴离子表面。