首页> 外文期刊>Knee surgery, sports traumatology, arthroscopy: official journal of the ESSKA >Platelet-rich plasma activation in combination with biphasic osteochondral scaffolds-conditions for maximal growth factor production.
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Platelet-rich plasma activation in combination with biphasic osteochondral scaffolds-conditions for maximal growth factor production.

机译:富血小板血浆激活与双相骨软骨支架相结合,可产生最大的生长因子。

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PURPOSE: The combination of scaffolds and biological factors may enhance articular cartilage repair. Little is known regarding the activation and subsequent growth factor release of platelet-rich plasma (PRP) in contact with biosynthetic scaffolds. The purpose of this study was i) to identify whether the addition of thrombin was required to activate PRP in the presence of a collagen osteochondral scaffold and ii) to compare the activity of PRP when applied to both collagen- and polylactide-based osteochondral scaffolds. METHODS: Equal combined volumes of test substances were used (n = 3): 500 mul PRP alone or on scaffolds; 375 mul PRP + 125 mul autologous thrombin on scaffolds; 455 mul PRP + 45 mul bovine thrombin on scaffolds. Scaffolds and/or PRP were cultured in vitro in DMEM/F12 medium for 10 days. TGF-beta1, PDGF-AB and bFGF were measured using ELISA. RESULTS: A similar cumulative release profile in all growth factors was found over the 10-day period i.e. a burst release and further physiological prolonged release. A significantly higher release of PDGF-AB was seen in the PRP + collagen scaffold groups at all time points, compared to scaffold + PRP + thrombins (P < 0.001). A significantly increased cumulative volume of PDGF-AB was released from the collagen scaffold compared to the polylactide scaffold (P < 0.001). CONCLUSION: This study shows that polylactide and particularly collagen osteochondral scaffolds activate PRP in vitro. If PRP is combined with these scaffolds clinically, no exogenous activation with thrombin is required to achieve growth factor release, which may be of benefit for articular cartilage repair applications.
机译:目的:脚手架和生物学因素的结合可以增强关节软骨的修复。关于与生物合成支架接触的富含血小板的血浆(PRP)的激活和随后的生长因子释放知之甚少。这项研究的目的是:i)确定在胶原骨软骨支架存在下是否需要添加凝血酶来激活PRP,以及ii)比较当同时应用于基于胶原和聚乳酸的骨软骨支架时PRP的活性。方法:使用相等体积的被测物质(n = 3):单独或在支架上使用500 mul PRP;在试验台上使用PRP。支架上375 mul PRP + 125 mul自体凝血酶;支架上455 mul PRP + 45 mul牛凝血酶。支架和/或PRP在DMEM / F12培养基中体外培养10天。使用ELISA测量TGF-β1,PDGF-AB和bFGF。结果:在10天的时间内发现所有生长因子的累积释放曲线相似,即爆发释放和进一步的生理延长释放。与支架+ PRP +凝血酶相比,在所有时间点,PRP +胶原支架组中PDGF-AB的释放均显着较高(P <0.001)。与聚乳酸支架相比,PDGF-AB的累积累积体积显着增加(P <0.001)。结论:这项研究表明聚乳酸,尤其是胶原骨软骨支架在体外可以激活PRP。如果临床上将PRP与这些支架结合使用,则不需要用凝血酶进行外源性激活即可实现生长因子的释放,这可能有益于关节软骨修复应用。

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