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Optimization of pure platelet-rich plasma preparation: A comparative study of pure platelet-rich plasma obtained using different centrifugal conditions in a single-donor model

机译:纯血小板富含血浆制剂的优化:使用不同离心条件在单举者模型中获得的纯血小板富血浆的对比研究

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While it has been proved that centrifugal conditions for pure platelet-rich plasma (P-PRP) preparation influence the cellular composition of P-PRP obtained, the optimal centrifugal conditions to prepare P-PRP have not yet been identified. In the present study, platelet-containing plasma (PCP) was prepared with the first-spin of different double-spin methods and P-PRP was prepared with different double-spin methods. Whole-blood analysis was performed to evaluate the cellular composition of PCP and P-PRP. The basal and ADP-induced CD62P expression rates of platelets were assessed by flow cytometry to evaluate the function of platelets in PCP and P-PRP. Enzyme-linked immune sorbent assay was performed to quantify interleukin-1 beta, tumor necrosis factor -alpha, platelet-derived growth factor AB and transforming growth factor (31 concentrations of PCP and P-PRP. Correlations between the cellular characteristics and cytokine concentrations of P-PRP were analyzed by Pearson correlation analysis. Effects of P-PRP on the proliferation, survival and migration of human bone marrow-derived mesenchymal stem cells and human articular chondrocytes were evaluated by a Cell Counting Kit-8 assay, live/dead staining and Transwell assay, respectively. The results showed that centrifugation at 160 x g for 10 min and 250 x g for 15 min successively captured and concentrated platelets and growth factors significantly more efficiently with preservation of platelet function compared with other conditions (P 0.05) and the maximization of platelet concentration, platelet enrichment factor, platelet capture efficiency and platelet function resulted in the maximization of growth factor concentrations in P-PRP obtained using the optimal conditions (P 0.05). Therefore, centrifugation at 160 x g for 10 min and 250 x g for 15 min successively with removal of the buffy coat as a crucial step may provide an optimal preparation system of P-PRP for clinical application.
机译:虽然已经证明,富血小板富含血浆的离心条件(P-PRP)制剂影响了所得p-PRP的细胞组成,但尚未确定制备P-PRP的最佳离心条件。在本研究中,用含血小板的等离子体(PCP)用不同的双旋旋用双旋旋制备,并用不同的双自旋方法制备P-PRP。进行全血分析以评估PCP和P-PRP的细胞组成。通过流式细胞术评估基底和ADP诱导的血小板CD62P表达速率,以评估PCP和P-PRP中血小板的功能。进行酶联免疫吸附剂测定以定量白细胞介素-1β,肿瘤坏死因子 - α,血小板衍生的生长因子AB和转化生长因子(31种浓度的PCP和P-PRP。细胞特征与细胞因子浓度之间的相关性通过Pearson相关分析分析P-PRP。P-PRP对人骨髓间充质干细胞和人关节软骨细胞的增殖,存活和迁移的影响是通过计数试剂盒-8测定,活/染色来评估人骨髓间充质干细胞和人关节软骨细胞的影响分别分别分别测定。结果表明,在与其他条件相比(P 0.05)相比(P 0.05)和最大化相比血小板浓度,血小板富集因子,血小板捕获效率和血小板函数导致M使用最佳条件获得的P-PRP中生长因子浓度的同学(P 0.05)。因此,以160×g以160×g离心10分钟,依次连续15分钟,以除去Buffy涂层作为关键步骤,可以提供临床应用的P-PRP的最佳制剂系统。

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