Injectable platelet rich fibrin (i-PRF): opportunities in regenerative dentistry?

富血小板纤维蛋白 纤维蛋白 富血小板血浆 成纤维细胞 生长因子 男科 血小板源性生长因子受体 伤口愈合 化学 转化生长因子 血小板衍生生长因子 生物相容性 血小板 牙科 免疫学 医学 内分泌学 生物化学 体外 受体 有机化学
作者
Richard J. Miron,Masako Fujioka‐Kobayashi,Maria Hernandez,Umadevi Kandalam,Yufeng Zhang,Shahram Ghanaati,Joseph Choukroun
出处
期刊:Clinical Oral Investigations [Springer Nature]
卷期号:21 (8): 2619-2627 被引量:543
标识
DOI:10.1007/s00784-017-2063-9
摘要

Platelet rich plasma (PRP) has been utilized in regenerative dentistry as a supra-physiological concentrate of autologous growth factors capable of stimulating tissue regeneration. Despite this, concerns have been expressed regarding the use of anti-coagulants, agents known to inhibit wound healing. In this study, a liquid formulation of platelet rich fibrin (PRF) termed injectable-PRF (i-PRF) without the use of anti-coagulants was investigated.Standard PRP and i-PRF (centrifuged at 700 rpm (60G) for 3 min) were compared for growth factor release up to 10 days (8 donor samples). Furthermore, fibroblast biocompatibility at 24 h (live/dead assay); migration at 24 h; proliferation at 1, 3, and 5 days, and expression of PDGF, TGF-β, and collagen1 at 3 and 7 days were investigated.Growth factor release demonstrated that in general PRP had higher early release of growth factors whereas i-PRF showed significantly higher levels of total long-term release of PDGF-AA, PDGF-AB, EGF, and IGF-1 after 10 days. PRP showed higher levels of TGF-β1 and VEGF at 10 days. While both formulations exhibited high biocompatibility and higher fibroblast migration and proliferation when compared to control tissue-culture plastic, i-PRF induced significantly highest migration whereas PRP demonstrated significantly highest cellular proliferation. Furthermore, i-PRF showed significantly highest mRNA levels of TGF-β at 7 days, PDGF at 3 days, and collagen1 expression at both 3 and 7 days when compared to PRP.i-PRF demonstrated the ability to release higher concentrations of various growth factors and induced higher fibroblast migration and expression of PDGF, TGF-β, and collagen1. Future animal research is now necessary to further validate the use of i-PRF as a bioactive agent capable of stimulating tissue regeneration.The findings from the present study demonstrate that a potent formulation of liquid platelet concentrates could be obtained without use of anti-coagulants.
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