Department of Periodontology, College of Dental Medicine, Nova Southeastern University, Fort Lauderdale, FL.
Department of Cranio-Maxillofacial Surgery, University of Bern, Bern, Switzerland.
J Periodontol. 2017 Jan;88(1):112-121. doi: 10.1902/jop.2016.160443. Epub 2016 Sep 2.
Over the past decade, use of leukocyte platelet-rich fibrin (L-PRF) has gained tremendous momentum in regenerative dentistry as a low-cost fibrin matrix used for tissue regeneration. This study characterizes how centrifugation speed (G-force) along with centrifugation time influence growth factor release from fibrin clots, as well as the cellular activity of gingival fibroblasts exposed to each PRF matrix.
Standard L-PRF served as a control (2,700 revolutions per minute [rpm]-12 minutes). Two test groups using low-speed (1,300 rpm-14 minutes, termed advanced PRF [A-PRF]) and low-speed + time (1,300 rpm-8 minutes; A-PRF+) were investigated. Each PRF matrix was tested for growth factor release up to 10 days (eight donor samples) as well as biocompatibility and cellular activity.
The low-speed concept (A-PRF, A-PRF+) demonstrated a significant increase in growth factor release of platelet-derived growth factor (PDGF), transforming growth factor (TGF)-β1, epidermal growth factor, and insulin-like growth factor, with A-PRF+ being highest of all groups. Although all PRF formulations were extremely biocompatible due to their autogenous sources, both A-PRF and A-PRF+ demonstrated significantly higher levels of human fibroblast migration and proliferation compared with L-PRF. Furthermore, gingival fibroblasts cultured with A-PRF+ demonstrated significantly higher messenger RNA (mRNA) levels of PDGF, TGF-β, and collagen1 at either 3 or 7 days.
The findings from the present study demonstrate modifications to centrifugation speed and time with the low-speed concept favor an increase in growth factor release from PRF clots. This, in turn, may directly influence tissue regeneration by increasing fibroblast migration, proliferation, and collagen mRNA levels. Future animal and clinical studies are now necessary.
在过去的十年中,作为一种用于组织再生的低成本纤维基质,白细胞富血小板纤维蛋白(L-PRF)在再生牙科领域的应用得到了迅猛发展。本研究旨在探讨离心速度(G 力)和离心时间对纤维蛋白凝块中生长因子释放的影响,以及牙龈成纤维细胞暴露于各 PRF 基质后的细胞活性。
标准 L-PRF 作为对照(2700 转/分-12 分钟)。研究了两种使用低速(1300 转/分-14 分钟,称为先进 PRF [A-PRF])和低速+时间(1300 转/分-8 分钟;A-PRF+)的实验组。每个 PRF 基质均进行生长因子释放测试,时间长达 10 天(8 个供体样本),同时还进行了生物相容性和细胞活性测试。
低速方案(A-PRF、A-PRF+)显示血小板衍生生长因子(PDGF)、转化生长因子(TGF)-β1、表皮生长因子和胰岛素样生长因子的释放显著增加,其中 A-PRF+组最高。尽管所有 PRF 制剂因其自体来源而具有极高的生物相容性,但 A-PRF 和 A-PRF+的人成纤维细胞迁移和增殖水平均显著高于 L-PRF。此外,与 L-PRF 相比,培养于 A-PRF+的牙龈成纤维细胞在第 3 天或第 7 天的 PDGF、TGF-β 和胶原 1 的信使 RNA(mRNA)水平显著升高。
本研究结果表明,通过改变离心速度和时间的低速方案可增加 PRF 凝块中生长因子的释放,这可能通过增加成纤维细胞迁移、增殖和胶原 mRNA 水平直接影响组织再生。未来有必要进行动物和临床研究。