Oh Joo Han, Kim Woo, Park Kyoung Un, Roh Young Hak
Department of Orthopaedic Surgery, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Orthopedic Surgery, Nalgae Hospital, Seoul, Korea.
Am J Sports Med. 2015 Dec;43(12):3062-70. doi: 10.1177/0363546515608481. Epub 2015 Oct 15.
Variations in formulations used to prepare platelet-rich plasmas (PRPs) result in differences in the cellular composition and biomolecular characteristics.
To evaluate the cellular composition and the cytokine-release kinetics of PRP according to differences in the preparation protocols.
Controlled laboratory study.
Five preparation procedures were performed for 14 healthy subjects, including 2 manual procedures (single-spin [SS] at 900 g for 5 minutes; double-spin [DS] at 900 g for 5 minutes and then 1500 g for 15 minutes) and 3 methods with commercial kits (Arthrex ACP, Biomet GPS, and Prodizen Prosys). After evaluation of cellular composition, each preparation was divided into 4 aliquots and incubated for 1 hour, 24 hours, 72 hours, and 7 days for the assessment of cytokine release over time. The cytokine-release kinetics were evaluated by assessing platelet-derived growth factor (PDGF), transforming growth factor (TGF), vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF), interleukin-1 (IL-1), and matrix metalloproteinase-9 (MMP-9) concentrations of each aliquot with bead-based sandwich immunoassay.
The DS PRP had a higher concentration of platelets and leukocytes than did the SS PRP. Every PRP preparation exhibited an increase in PDGF, TGF, VEGF, and FGF release when compared with whole blood samples. The FGF and TGF release occurred quickly and decreased over time, while the PDGF and VEGF release was constant and sustained over 7 days. The PDGF and VEGF concentrations were higher in the DS PRP than in the SS PRP, whereas the TGF and FGF concentrations were higher in the SS PRP than in the DS PRP. Biomet GPS had the highest VEGF and MMP-9 concentrations but the lowest TGF concentration. Arthrex ACP had the highest FGF concentration but the lowest PDGF concentration. Prodizen Prosys had the highest IL-1 concentration and higher PDGF concentration than Arthrex ACP.
The DS method generally led to a higher concentration of platelet relative to the SS method. However, the cytokine content was not necessarily proportional to the cellular composition of the PRPs, as the greater content could be different between the SS or DS method depending on the type of cytokine.
Physicians should select proper PRP preparations after considering their biomolecular characteristics and patient indications.
用于制备富血小板血浆(PRP)的配方差异会导致细胞组成和生物分子特性的不同。
根据制备方案的差异评估PRP的细胞组成和细胞因子释放动力学。
对照实验室研究。
对14名健康受试者进行了5种制备程序,包括2种手动程序(900g单采5分钟;900g双采5分钟,然后1500g双采15分钟)和3种使用商业试剂盒的方法(Arthrex ACP、Biomet GPS和Prodizen Prosys)。在评估细胞组成后,将每种制备物分成4份等分试样,并分别孵育1小时、24小时、72小时和7天,以评估随时间的细胞因子释放情况。通过基于磁珠的夹心免疫测定法评估每份等分试样的血小板衍生生长因子(PDGF)、转化生长因子(TGF)、血管内皮生长因子(VEGF)、成纤维细胞生长因子(FGF)、白细胞介素-1(IL-1)和基质金属蛋白酶-9(MMP-9)浓度,从而评估细胞因子释放动力学。
双采PRP的血小板和白细胞浓度高于单采PRP。与全血样本相比,每种PRP制备物的PDGF、TGF、VEGF和FGF释放均有所增加。FGF和TGF的释放在短时间内迅速发生并随时间下降,而PDGF和VEGF的释放在7天内保持恒定且持续释放。双采PRP中的PDGF和VEGF浓度高于单采PRP,而单采PRP中的TGF和FGF浓度高于双采PRP。Biomet GPS的VEGF和MMP-9浓度最高,但TGF浓度最低。Arthrex ACP的FGF浓度最高,但PDGF浓度最低。Prodizen Prosys的IL-1浓度最高,且PDGF浓度高于Arthrex ACP。
与单采方法相比,双采方法通常会产生更高浓度的血小板。然而,细胞因子含量不一定与PRP的细胞组成成正比,因为根据细胞因子的类型,单采或双采方法之间的含量差异可能会有所不同。
医生在考虑PRP的生物分子特性和患者适应症后,应选择合适的PRP制备方法。