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Comparison of different procedures to prepare platelet-rich plasma for studies of platelet aggregation by light transmission aggregometry

机译:制备富血小板血浆的不同程序的比较,用于通过光聚集法测定血小板聚集

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摘要

Light transmission aggregometry (LTA), the gold standard for the study of patients with defects of platelet function, is a poorly standardized technique. The guidelines that have been produced so far are largely based on consensus of experts, due to the absence of studies directly comparing different procedures. Therefore, ad hoc studies are needed to gather scientific evidence on how to choose the most appropriate procedures for LTA measurement. In this study, we aimed at evaluating the most appropriate conditions for preparing samples of platelet-rich plasma (PRP) for studies of platelet aggregation by LTA. Citrate-anticoagulated blood from 32 individuals was centrifuged at 150, 200, 250 or 300×g at room temperature for 10min. Red blood cells contamination was highest in PRP prepared at 150×g; mean platelet volume (MPV) was lowest in PRP prepared at 300×g. The extent of platelet aggregation measured by LTA was lower and more variable in PRP prepared at 300×g. Therefore, centrifugation of blood at 200×g or 250×g for 10min appears to be the best condition for preparing PRP for LTA studies.
机译:透光聚集法(LTA)是研究血小板功能缺陷患者的黄金标准,是一项标准化程度较低的技术。到目前为止,由于缺乏直接比较不同程序的研究,因此已制定的指南很大程度上基于专家的共识。因此,需要进行专项研究以收集有关如何选择最合适的LTA测量程序的科学证据。在这项研究中,我们旨在评估最合适的条件,以制备用于通过LTA研究血小板聚集的富血小板血浆(PRP)样品。将来自32个个体的柠檬酸盐抗凝血液在室温下分别以150、200、250或300×g离心10分钟。在150×g制备的PRP中,红细胞污染最高。在300×g制备的PRP中,平均血小板体积(MPV)最低。在300×g制备的PRP中,通过LTA测得的血小板聚集程度较低且变化较大。因此,将血液以200×g或250×g离心10分钟似乎是制备用于LTA研究的PRP的最佳条件。

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