Weibrich Gernot, Kleis Wilfried K G, Hitzler Walter E, Hafner Gerd
Department of Oral and Maxillofacial Surgery, Johannes Gutenberg University, Mainz, Germany.
Int J Oral Maxillofac Implants. 2005 Jan-Feb;20(1):118-23.
The aim of this study was to compare a new method for the production of platelet-rich plasma (PRP), the plasma-rich-in-growth-factors kit (PRGF kit; G.A.C. Medicale San Antonio, Vitoria, Spain), with an established method, the Platelet Concentrate Collection System (PCCS; 3i/Implant Innovations, Palm Beach Gardens, FL) with respect to resulting cellular and growth factor contents.
Whole blood was drawn from 51 healthy donors (20 men, 31 women) aged 19 to 59 years (mean +/- SD 35.12 +/- 9.65 years), and PRP was prepared by both methods.
Platelet counts differed significantly (signed rank test, P < .001 for all) between the donor blood (274,200 +/- 54,050/microL), the PCCS PRP preparation (1,641,800 +/- 426,820/microL), and the PRGF kit PRP preparation (513,630 +/- 139,470/microL). The PCCS concentrated leukocytes (whole blood, 6,992 +/- 2,011/microL; PCCS PRP, 14,153 +/- 7,577/microL), while the PRGF kit produced a leukocyte-poor PRP (65 +/- 108/microL). Higher concentrations of transforming growth factor beta1 (TGF-beta1) and platelet-derived growth factor AB (PDGF-AB) were found in the PCCS PRP (TGF-/beta1, 290 +/- 95 ng/mL; PDGF-AB, 157 +/- 62 ng/mL) than in the Anitua PRGF kit PRP (TGF-beta1, 73 +/- 26 ng/mL; PDGF-AB, 47 +/- 21 ng/mL). Statistical analysis showed significant differences (P < .001 for TGF-beta1 and P < .01 for PDGF-AB).
The results of this study and some data in the literature indicate that the content of growth factors in PRP can vary tremendously, depending on the system used for the preparation of PRP.
PCCS collects more platelets and leukocytes than the PRGF kit. This results in significantly higher growth factor levels. Further in vivo studies are needed to determine whether this results in a clinically different biologic effect.
本研究旨在比较一种制备富血小板血浆(PRP)的新方法——富含生长因子血浆试剂盒(PRGF试剂盒;西班牙维多利亚市G.A.C. Medicale San Antonio公司)与一种已确立的方法——血小板浓缩采集系统(PCCS;美国佛罗里达州棕榈滩花园市3i/Implant Innovations公司)所产生的细胞和生长因子含量。
从51名年龄在19至59岁(平均±标准差35.12±9.65岁)的健康献血者(20名男性,31名女性)中采集全血,并通过两种方法制备PRP。
献血者血液(274,200±54,050/微升)、PCCS法制备的PRP(1,641,800±426,820/微升)和PRGF试剂盒法制备的PRP(513,630±139,470/微升)之间的血小板计数差异显著(符号秩检验,所有P均<0.001)。PCCS法浓缩了白细胞(全血,6,992±2,011/微升;PCCS法制备的PRP,14,153±7,577/微升),而PRGF试剂盒制备出白细胞含量低的PRP(65±108/微升)。在PCCS法制备的PRP中发现的转化生长因子β1(TGF-β1)和血小板衍生生长因子AB(PDGF-AB)浓度高于Anitua PRGF试剂盒法制备的PRP(TGF-β1,290±95纳克/毫升;PDGF-AB,157±62纳克/毫升)(TGF-β1为73±26纳克/毫升;PDGF-AB为47±21纳克/毫升)。统计分析显示差异有统计学意义(TGF-β1的P<0.001,PDGF-AB的P<0.01)。
本研究结果及文献中的一些数据表明,PRP中生长因子的含量可能因制备PRP所用的系统不同而有极大差异。
PCCS比PRGF试剂盒收集到更多的血小板和白细胞。这导致生长因子水平显著更高。需要进一步的体内研究来确定这是否会产生临床上不同的生物学效应。