# Platelet-Rich Fibrin Low-Speed Centrifugation Protocols and Particulate Bovine Bone on Bone Defects Repair

**Authors:** Lélio Fernando Ferreira Soares, Thaisa Macedo Iunes Carrera, Roberta de Oliveira Alves, Camila Chiérici Marcantonio, Juliana dos Santos Neves, Joni Augusto Cirelli, Guilherme José Pimentel Lopes de Oliveira, Suzane Cristina Pigossi

PMC · DOI: 10.1590/0103-644020256428 · Brazilian Dental Journal · 2025-11-21

## TL;DR

This study compares how PRF membranes and bovine bone affect bone repair in rats, finding that bovine bone alone or with PRF improves healing.

## Contribution

The study introduces low-speed centrifugation protocols for PRF and evaluates their combination with bovine bone in bone defect repair.

## Key findings

- PRF membranes increased early bone formation and Bglap expression compared to control.
- DBBM alone or with i-PRF enhanced cortical and medullary bone formation over time.
- Adding i-PRF did not further improve DBBM's regenerative effects.

## Abstract

Platelet-rich fibrin (PRF) membranes and injectable PRF (i-PRF) are biological agents used to enhance healing, often combined with deproteinized bovine bone mineral (DBBM) for bone regeneration. This study evaluated low-speed centrifugation protocols for the preparation of PRF membranes and i-PRF combined with DBBM (sticky bone, SB) in repairing rat tibial bone defects. Sixty-four rats received tibial defects filled with blood clot (CO), PRF membrane alone (PRF), DBBM alone (BO), or i-PRF associated with DBBM (SB). Micro-computed tomography (μCT), histological analysis, and gene expression of molecular markers were assessed at 15 and 45 days. PRF membranes led to greater early bone formation and elevated Bglap expression compared to control (p < 0.05). μCT analysis showed that the BO group had significantly greater cortical bone formation at 15 days than the control group (p < 0.05). Additionally, both BO and SB groups promoted increased cortical bone formation at 45 days (p < 0.05), with SB also enhancing cortical thickness at the defect margins. In the medullary region, both BO and SB exhibited higher bone formation and trabecular number (p < 0.05) after 15 and 45 days. Gene expression analysis revealed higher levels of Alpl, Bglap, and Runx2 in the BO group than in SB and control groups (p < 0.05). In conclusion, PRF membranes improved early bone formation compared to a blood clot. DBBM, whether used alone or in combination with i-PRF, also enhanced bone regeneration compared to control. However, the addition of i-PRF did not improve the regenerative potential of DBBM.

## Linked entities

- **Genes:** BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632], ALPL (alkaline phosphatase, biomineralization associated) [NCBI Gene 249], RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** RUNX2 (RUNX family transcription factor 2) [NCBI Gene 536911], ALPL (alkaline phosphatase, biomineralization associated) [NCBI Gene 280994] {aka TNAP, TNS-AP}, BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 281646] {aka BGP}
- **Diseases:** BO (MESH:C537104), Bone Defects (MESH:D001847)
- **Chemicals:** SB (MESH:D000965), i (MESH:D007455)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12641583/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12641583/full.md

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Source: https://tomesphere.com/paper/PMC12641583