Platelet-rich plasma activation in combination with biphasic  osteochondral scaffolds–conditions for maximal growth factor  production

Platelet-rich plasma activation in combination with biphasic osteochondral scaffolds–conditions for maximal growth factor production

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Alan Getgood • Frances Henson • Roger Brooks • Lisa A. Fortier • Neil Rushton
  • چاپ و سال / کشور: 2011

Description

Purpose The combination of scaffolds and biological factors may enhance articular cartilage repair. Little is known regarding the activation and subsequent growth factor release of platelet-rich plasma (PRP) in contact with biosynthetic scaffolds. The purpose of this study was i) to identify whether the addition of thrombin was required to activate PRP in the presence of a collagen osteochondral scaffold and ii) to compare the activity of PRP when applied to both collagen- and polylactide-based osteochondral scaffolds. Methods Equal combined volumes of test substances were used (n = 3): 500 ll PRP alone or on scaffolds; 375 ll PRP ? 125 ll autologous thrombin on scaffolds; 455 ll PRP ? 45 ll bovine thrombin on scaffolds. Scaffolds and/or PRP were cultured in vitro in DMEM/F12 medium for 10 days. TGF-b1, PDGF-AB and bFGF were measured using ELISA. Results A similar cumulative release profile in all growth factors was found over the 10-day period i.e. a burst release and further physiological prolonged release. A significantly higher release of PDGF-AB was seen in the PRP ? collagen scaffold groups at all time points, compared to scaffold ? PRP ? thrombins (P\0.001). A significantly increased cumulative volume of PDGF-AB was released from the collagen scaffold compared to the polylactide scaffold (P\0.001). Conclusion This study shows that polylactide and particularly collagen osteochondral scaffolds activate PRP in vitro. If PRP is combined with these scaffolds clinically, no exogenous activation with thrombin is required to achieve growth factor release, which m
Knee Surg Sports Traumatol Arthrosc DOI 10.1007/s00167-011-1456-6 Received: 9 November 2010 / Accepted: 10 February 2011
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