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Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits

Osteochondral defects caused by degenerative diseases of joints, traumas and inflammation are important issues in clinical practice. Different types of autologous platelet concentrate (PCs) are used in bone and cartilage regeneration. The present study aimed to investigate the effect of lyophilized...

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Autores principales: Sun, Jianwei, Han, Leng, Liu, Chundong, Ma, Junli, Li, Xiao, Sun, Shuohui, Wang, Zhifa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632968/
https://www.ncbi.nlm.nih.gov/pubmed/37954116
http://dx.doi.org/10.3892/etm.2023.12268
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author Sun, Jianwei
Han, Leng
Liu, Chundong
Ma, Junli
Li, Xiao
Sun, Shuohui
Wang, Zhifa
author_facet Sun, Jianwei
Han, Leng
Liu, Chundong
Ma, Junli
Li, Xiao
Sun, Shuohui
Wang, Zhifa
author_sort Sun, Jianwei
collection PubMed
description Osteochondral defects caused by degenerative diseases of joints, traumas and inflammation are important issues in clinical practice. Different types of autologous platelet concentrate (PCs) are used in bone and cartilage regeneration. The present study aimed to investigate the effect of lyophilized platelet-rich fibrin (L-PRF) on the repair of osteochondral defects in rabbits. L-PRF was first prepared from fresh PRF (F-PRF) through freeze-drying, and histological and microstructural observations were performed to compare the characteristics of L-PRF and F-PRF. Thereafter, these bioactive scaffolds were implanted into osteochondral defects surgically created in rabbits to assess their effects on tissue repair using micro-CT scanning, histological observations and the evaluation scoring method for cartilage repair established by the International Cartilage Repair Society (ICRS). L-PRF had a histological structure similar to F-PRF. At 16 weeks after implantation surgery, full-thickness osteochondral defects with a diameter of 5 mm and a depth of 4 mm were well-filled with newly regenerated tissues, exhibiting the simultaneous regeneration of avascular articular cartilage and well-vascularized subchondral bone, as proven through macroscopic and microscopic observations in PRF-treated groups compared with that in the untreated group. The application of L-PRF and F-PRF for osteochondral defects in rabbits contributed to massive host remodeling and reconstruction of osteochondral tissues, thus offering a prospective bioactive scaffold for the simultaneous reconstruction of articular cartilage and subchondral bone tissue.
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spelling pubmed-106329682023-11-10 Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits Sun, Jianwei Han, Leng Liu, Chundong Ma, Junli Li, Xiao Sun, Shuohui Wang, Zhifa Exp Ther Med Articles Osteochondral defects caused by degenerative diseases of joints, traumas and inflammation are important issues in clinical practice. Different types of autologous platelet concentrate (PCs) are used in bone and cartilage regeneration. The present study aimed to investigate the effect of lyophilized platelet-rich fibrin (L-PRF) on the repair of osteochondral defects in rabbits. L-PRF was first prepared from fresh PRF (F-PRF) through freeze-drying, and histological and microstructural observations were performed to compare the characteristics of L-PRF and F-PRF. Thereafter, these bioactive scaffolds were implanted into osteochondral defects surgically created in rabbits to assess their effects on tissue repair using micro-CT scanning, histological observations and the evaluation scoring method for cartilage repair established by the International Cartilage Repair Society (ICRS). L-PRF had a histological structure similar to F-PRF. At 16 weeks after implantation surgery, full-thickness osteochondral defects with a diameter of 5 mm and a depth of 4 mm were well-filled with newly regenerated tissues, exhibiting the simultaneous regeneration of avascular articular cartilage and well-vascularized subchondral bone, as proven through macroscopic and microscopic observations in PRF-treated groups compared with that in the untreated group. The application of L-PRF and F-PRF for osteochondral defects in rabbits contributed to massive host remodeling and reconstruction of osteochondral tissues, thus offering a prospective bioactive scaffold for the simultaneous reconstruction of articular cartilage and subchondral bone tissue. D.A. Spandidos 2023-10-24 /pmc/articles/PMC10632968/ /pubmed/37954116 http://dx.doi.org/10.3892/etm.2023.12268 Text en Copyright: © Sun et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Sun, Jianwei
Han, Leng
Liu, Chundong
Ma, Junli
Li, Xiao
Sun, Shuohui
Wang, Zhifa
Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits
title Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits
title_full Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits
title_fullStr Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits
title_full_unstemmed Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits
title_short Effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits
title_sort effect of autologous lyophilized platelet‑rich fibrin on the reconstruction of osteochondral defects in rabbits
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632968/
https://www.ncbi.nlm.nih.gov/pubmed/37954116
http://dx.doi.org/10.3892/etm.2023.12268
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