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

被引:288
|
作者
Miron, Richard J. [1 ,2 ,3 ]
Fujioka-Kobayashi, Masako [1 ,4 ,5 ]
Hernandez, Maria [1 ]
Kandalam, Umadevi [6 ]
Zhang, Yufeng [7 ]
Ghanaati, Shahram [8 ]
Choukroun, Joseph [9 ]
机构
[1] Nova Southeastern Univ, Coll Dent Med, Dept Periodontol, Ft Lauderdale, FL 33314 USA
[2] Nova Southeastern Univ, Ctr Collaborat Res, Cell Therapy Inst, Ft Lauderdale, FL 33314 USA
[3] Univ Michigan, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
[4] Univ Bern, Dept Craniomaxillofacial Surg, Bern, Switzerland
[5] Tokushima Univ, Inst Biomed Sci, Dept Oral Surg, Grad Sch, Tokushima, Japan
[6] Nova Southeastern Univ, Coll Dent Med, Dept Pediat Dent, Ft Lauderdale, FL 33314 USA
[7] Univ Wuhan, Dept Oral Implantol, Wuhan, Hubei, Peoples R China
[8] FORM, Frankfurt, Germany
[9] Pain Clin, Nice, France
关键词
Fibrin; Blood platelets; Regeneration; Wound healing; Fibroblasts; Platelet rich fibrin; GROWTH-FACTORS; PLASMA RICH; EXTRACTION; LEUKOCYTE; EFFICACY;
D O I
10.1007/s00784-017-2063-9
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
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-beta, 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-beta 1 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-beta 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-beta, 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.
引用
收藏
页码:2619 / 2627
页数:9
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