Graiet Hajer, Lokchine Anna, Francois Pauline, Velier Melanie, Grimaud Fanny, Loyens Maxime, Berda-Haddad Yael, Veran Julie, Dignat-George Francoise, Sabatier Florence, Magalon Jeremy
Cell Therapy Laboratory, CBT-1409, INSERM, Assistance Publique Hôpitaux de Marseille, Marseille, France.
INSERM, INRA, C2VN, Aix-Marseille University, Marseille, France.
BMJ Open Sport Exerc Med. 2018 Nov 13;4(1):e000442. doi: 10.1136/bmjsem-2018-000442. eCollection 2018.
BACKGROUND/AIMS: Platelet-rich plasma (PRP) injections are used in sports medicine and have been the subject of increased clinical interest. However, there have been very few reports of the composition of initial whole blood and the final PRP product. The objective of this study was to provide technical tools to perform a correct characterisation of platelets, leucocytes and red blood cells (RBCs) from whole blood and PRP.
Blood and PRP were obtained from 26 healthy volunteers and prepared according to the varying parameters encountered within PRP process preparation and quantification (harvesting method, anticoagulant used, sampling method, counting method). Concentrations were measured at t=0, t=1, t=6 and t=24 hours.
Sampling of blood in Eppendorf tubes significantly decreased platelet concentration over time, whereas sampling in Microvette EDTA-coated tube kept platelet concentration stable until 24 hours. A non-significant difference was observed in platelet counts in PRP with impedance (median (IQR): 521.8 G/L (505.3-524.7)) and fluorescence (591.5 G/L (581.5-595.8)) methods. Other studied parameters did not influence platelet concentrations in blood or PRP samples. Leucocytes and RBC counts were similar whatever the anticoagulant, sampling, harvesting and counting methods used for both blood and PRP samples.
Systematic sampling of blood and PRP in EDTA-coated tubes for quality control is recommended. The use of a validated counter for PRP sample should also be taken into account.
背景/目的:富含血小板血浆(PRP)注射已应用于运动医学领域,并且越来越受到临床关注。然而,关于初始全血和最终PRP产品成分的报道非常少。本研究的目的是提供技术工具,以正确表征全血和PRP中的血小板、白细胞和红细胞(RBC)。
从26名健康志愿者身上采集血液和PRP,并根据PRP制备和定量过程中遇到的不同参数(采集方法、使用的抗凝剂、采样方法、计数方法)进行制备。在t = 0、t = 1、t = 6和t = 24小时测量浓度。
在Eppendorf管中采集血液会使血小板浓度随时间显著降低,而在涂有EDTA的Microvette管中采样可使血小板浓度在24小时内保持稳定。采用阻抗法(中位数(IQR):521.8 G/L(505.3 - 524.7))和荧光法(591.5 G/L(581.5 - 595.8))检测PRP中的血小板计数,差异无统计学意义。其他研究参数对血液或PRP样本中的血小板浓度没有影响。无论用于血液和PRP样本的抗凝剂、采样、采集和计数方法如何,白细胞和红细胞计数均相似。
建议在涂有EDTA的试管中对血液和PRP进行系统采样以进行质量控制。还应考虑使用经过验证的计数器对PRP样本进行计数。