Growth factor and pro-inflammatory cytokine contents in platelet-rich plasma (PRP), plasma rich in growth factors (PRGF), advanced platelet-rich fibrin (A-PRF), and concentrated growth factors (CGF)

被引:32
作者
Masuki, Hideo [1 ]
Okudera, Toshimitsu [1 ]
Watanebe, Taisuke [1 ]
Suzuki, Masashi [1 ]
Nishiyama, Kazuhiko [1 ]
Okudera, Hajime [1 ]
Nakata, Koh [2 ]
Uematsu, Kohya [4 ]
Su, Chen-Yao [3 ]
Kawase, Tomoyuki [4 ]
机构
[1] Tokyo Plast Dent Soc, Kita Ku, Tokyo, Japan
[2] Niigata Univ, Med & Dent Hosp, Biosci Med Res Ctr, Niigata, Japan
[3] Natl Yang Ming Univ, Dept Dent, Taipei, Taiwan
[4] Niigata Univ, Inst Med & Dent, Div Oral Bioengn, Niigata, Japan
关键词
Growth factor; Platelet-rich plasma; Platelet-rich fibrin; Plasma rich in growth factors; Concentrated growth factors;
D O I
10.1186/s40729-016-0052-4
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: The development of platelet-rich fibrin (PRF) drastically simplified the preparation procedure of platelet-concentrated biomaterials, such as platelet-rich plasma (PRP), and facilitated their clinical application. PRF's clinical effectiveness has often been demonstrated in pre-clinical and clinical studies; however, it is still controversial whether growth factors are significantly concentrated in PRF preparations to facilitate wound healing and tissue regeneration. To address this matter, we performed a comparative study of growth factor contents in PRP and its derivatives, such as advanced PRF (A-PRF) and concentrated growth factors (CGF). Methods: PRP and its derivatives were prepared from the same peripheral blood samples collected from healthy donors. A-PRF and CGF preparations were homogenized and centrifuged to produce extracts. Platelet and white blood cell counts in A-PRF and CGF preparations were determined by subtracting those counts in red blood cell fractions, supernatant acellular serum fractions, and A-PRF/CGF exudate fractions from those counts of whole blood samples. Concentrations of growth factors (TGF-beta 1, PDGF-BB, VEGF) and pro-inflammatory cytokines (IL-1 beta, IL-6) were determined using ELISA kits. Results: Compared to PRP preparations, both A-PRF and CGF extracts contained compatible or higher levels of platelets and platelet-derived growth factors. In a cell proliferation assay, both A-PRF and CGF extracts significantly stimulated the proliferation of human periosteal cells without significant reduction at higher doses. Conclusions: These data clearly demonstrate that both A-PRF and CGF preparations contain significant amounts of growth factors capable of stimulating periosteal cell proliferation, suggesting that A-PRF and CGF preparations function not only as a scaffolding material but also as a reservoir to deliver certain growth factors at the site of application.
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页数:6
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