Lance C Visser 1 , Steven P Arnoczky , Oscar Caballero , Monika Egerbacher . Show Affiliations »
Abstract
OBJECTIVE: To compare the concentration of a representative growth factor (transforming growth factor-beta [TGF-β]1) eluted from a platelet-rich fibrin matrix (PRFMatrix), a platelet-rich fibrin membrane (PRFMembrane), and a whole blood clot (BC) over time, and to compare the mitogenic effect of the eluents from each construct. STUDY DESIGN: In vitro study. SAMPLE POPULATION: PRFMatrix, PRFMembrane, and BC (n=4/construct/time point). METHODS: Each construct was placed in tissue culture wells containing media for 7 days. The media was collected and replenished on days 1, 3, 5, and 7 and the concentration of eluted TGF-β1 was measured by enzyme-linked immunosorbent assay. Canine tendon cells were subjected to additional aliquots of the conditioned media and the amount of cell proliferation compared. RESULTS: The media from both PRFM (PRFMatrix and PRFMembrane) constructs contained significantly more (P≤.026) TGF-β1 at days 1 and 3 and produced a significant increase (P≤.044) in cell proliferation at all time points compared with the BC. The PRFMembrane media contained significantly more (P≤.05) TGF-β1 at days 1 and 3 and produced a significant increase (P≤.002) in cell proliferation at all time points compared with the PRFMatrix. CONCLUSIONS: Both PRFM constructs are comprised of a dense fibrin scaffold that contains increased concentrations of TGF-β1 and are capable of increasing tendon cell proliferation over time when compared with a BC. CLINICAL RELEVANCE: The sustained increase in growth factor availability in PRFM constructs may be beneficial in the healing of biologically compromised tissues. © Copyright 2010 by The American College of Veterinary Surgeons.
OBJECTIVE: To compare the concentration of a representative growth factor (transforming growth factor-beta [TGF-β]1) eluted from a platelet-rich fibrin matrix (PRFMatrix), a platelet-rich fibrin membrane (PRFMembrane ), and a whole blood clot (BC) over time, and to compare the mitogenic effect of the eluents from each construct. STUDY DESIGN: In vitro study. SAMPLE POPULATION: PRFMatrix, PRFMembrane , and BC (n=4/construct/time point). METHODS: Each construct was placed in tissue culture wells containing media for 7 days. The media was collected and replenished on days 1, 3, 5, and 7 and the concentration of eluted TGF-β1 was measured by enzyme-linked immunosorbent assay. Canine tendon cells were subjected to additional aliquots of the conditioned media and the amount of cell proliferation compared. RESULTS: The media from both PRFM (PRFMatrix and PRFMembrane ) constructs contained significantly more (P≤.026) TGF-β1 at days 1 and 3 and produced a significant increase (P≤.044) in cell proliferation at all time points compared with the BC. The PRFMembrane media contained significantly more (P≤.05) TGF-β1 at days 1 and 3 and produced a significant increase (P≤.002) in cell proliferation at all time points compared with the PRFMatrix. CONCLUSIONS: Both PRFM constructs are comprised of a dense fibrin scaffold that contains increased concentrations of TGF-β1 and are capable of increasing tendon cell proliferation over time when compared with a BC. CLINICAL RELEVANCE: The sustained increase in growth factor availability in PRFM constructs may be beneficial in the healing of biologically compromised tissues. © Copyright 2010 by The American College of Veterinary Surgeons.
Entities: Chemical
Gene
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Year: 2010
PMID: 20825593 DOI: 10.1111/j.1532-950X.2010.00739.x
Source DB: PubMed Journal: Vet Surg ISSN: 0161-3499 Impact factor: 1.495