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Activation of Human Osteoblasts Via Different Bovine Bone Substitute Materials With and Without Injectable Platelet Rich Fibrin

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Date 2021 Mar 8
PMID 33681155
Citations 10
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Abstract

Introduction: The aim of the study was to compare the effect of four bovine bone substitute materials (XBSM) with and without injectable platelet-reach fibrin for viability and metabolic activity of human osteoblasts (HOB) as well as expression of alkaline phosphatase (ALP), bone morphogenetic protein 2 (BMP-2), and osteonectin (OCN).

Materials And Methods: Cerabone (CB), Bio-Oss (BO), Creos Xenogain (CX) and MinerOss X (MO) ± i-PRF were incubated with HOB. At day 3, 7, and 10, cell viability and metabolic activity as well as expression of ALP, OCN, and BMP-2, was examined.

Results: For non-i-PRF groups, the highest values concerning viability were seen for CB at all time points. Pre-treatment with i-PRF increased viability in all groups with the highest values for CB-i-PRF after 3 and 7 and for CX-i-PRF after 10 days. For metabolic activity, the highest rate among non-i-PRF groups was seen for MO at day 3 and for CB at day 7 and 10. Here, i-PRF groups showed higher values than non-i-PRF groups (highest values: CB + i-PRF) at all time points. There was no difference in ALP-expression between groups. For OCN expression in non-i-PRF groups, CB showed the highest values after day 3, CX after day 7 and 10. Among i-PRF-groups, the highest values were seen for CX + i-PRF. At day 3, the highest BMP-2 expression was observed for CX. Here, for i-PRF groups, the highest increase was seen for CX + i-PRF at day 3. At day 7 and 10, there was no significant difference among groups.

Conclusion: XBSM sintered under high temperature showed increased HOB viability and metabolic activity through the whole period when compared to XBSM manufactured at lower temperatures. Overall, the combination of XBSM with i-PRF improved all cellular parameters, ALP and BMP-2 expression at earlier stages as well as OCN expression at later stages.

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References
1.
Zhang Y, Tangl S, Huber C, Lin Y, Qiu L, Rausch-Fan X . Effects of Choukroun's platelet-rich fibrin on bone regeneration in combination with deproteinized bovine bone mineral in maxillary sinus augmentation: a histological and histomorphometric study. J Craniomaxillofac Surg. 2011; 40(4):321-8. DOI: 10.1016/j.jcms.2011.04.020. View

2.
El-Ghannam A, Ducheyne P, Risbud M, Adams C, Shapiro I, Castner D . Model surfaces engineered with nanoscale roughness and RGD tripeptides promote osteoblast activity. J Biomed Mater Res A. 2004; 68(4):615-27. DOI: 10.1002/jbm.a.20051. View

3.
Kubler A, Neugebauer J, Oh J, Scheer M, Zoller J . Growth and proliferation of human osteoblasts on different bone graft substitutes: an in vitro study. Implant Dent. 2004; 13(2):171-9. DOI: 10.1097/01.id.0000127522.14067.11. View

4.
El Bagdadi K, Kubesch A, Yu X, Al-Maawi S, Orlowska A, Dias A . Reduction of relative centrifugal forces increases growth factor release within solid platelet-rich-fibrin (PRF)-based matrices: a proof of concept of LSCC (low speed centrifugation concept). Eur J Trauma Emerg Surg. 2017; 45(3):467-479. PMC: 6579868. DOI: 10.1007/s00068-017-0785-7. View

5.
Anselme K . Osteoblast adhesion on biomaterials. Biomaterials. 2000; 21(7):667-81. DOI: 10.1016/s0142-9612(99)00242-2. View