Evaluation of Biocomposite Cements for Bone Defect Repair in Rat Models

Repairing or reconstructing significant bone defects is typically challenging. In the present study, two composite cements were used as scaffolds in a sub-critical femoral defect in rats. A control group and two experimental batches were used to compare the outcomes. This research aimed to investigate the osteogenic potential and toxicological tolerance of the bioproducts through histopathology and computed tomography imaging analysis at 14, 28, 56, and 90 days post-implantation. The biomaterials used in the investigation consisted of a 65% bioactive salinized inorganic filler and a 25% weight organic matrix. The organic part of the biomaterial was composed of Bis-GMA (bisphenol A-glycidyl methacrylate), UDMA (urethane dimethacrylate), HEMA (2-Hydroxyethyl methacrylate), and TEGDMA (triethylene glycol dimethacrylate), while the inorganic filler was composed of silica, barium glass, hydroxyapatite, and fluor aluminosilicate glass. The first findings of this research are encouraging, revealing that there is a slight difference between the groups treated with biomaterials, but it might be an effective approach for managing bone abnormalities. Material C1 exhibited a faster bone defect healing time compared to material C2, where bone fractures occurred in some individuals. It is unclear if the fractures were caused by the presence of the biomaterial C2 or whether additional variables were to blame. By the end of the research, the mice appeared to tolerate the biomaterials without exhibiting any inflammatory or rejection responses.

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Publication Details

Journal
Life
Published
2024-08-30
DOI
https://doi.org/10.3390/life14091097
Citations
7
Primary Topic
Orthopaedic implants and arthroplasty
Type
article
Field-Weighted Citation Impact
4.01
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article

Evaluation of Biocomposite Cements for Bone Defect Repair in Rat Models

Sorin Marian Mârza, R. Marica, Mădălina Florina Dragomir, Mărioara Moldovan et al.
7 citations
Life
Orthopaedic implants and arthroplasty
4.01
article

Evaluation of Biocomposite Cements for Bone Defect Repair in Rat Models

Sorin Marian Mârza, R. Marica, Mădălina Florina Dragomir, Mărioara Moldovan, Alina Ioana Ardelean, Alina Oana Rusu-Moldovan, Paula Maria Pașca, Liviu Oană
article en
7 citations

Abstract

Repairing or reconstructing significant bone defects is typically challenging. In the present study, two composite cements were used as scaffolds in a sub-critical femoral defect in rats. A control group and two experimental batches were used to compare the outcomes. This research aimed to investigate the osteogenic potential and toxicological tolerance of the bioproducts through histopathology and computed tomography imaging analysis at 14, 28, 56, and 90 days post-implantation. The biomaterials used in the investigation consisted of a 65% bioactive salinized inorganic filler and a 25% weight organic matrix. The organic part of the biomaterial was composed of Bis-GMA (bisphenol A-glycidyl methacrylate), UDMA (urethane dimethacrylate), HEMA (2-Hydroxyethyl methacrylate), and TEGDMA (triethylene glycol dimethacrylate), while the inorganic filler was composed of silica, barium glass, hydroxyapatite, and fluor aluminosilicate glass. The first findings of this research are encouraging, revealing that there is a slight difference between the groups treated with biomaterials, but it might be an effective approach for managing bone abnormalities. Material C1 exhibited a faster bone defect healing time compared to material C2, where bone fractures occurred in some individuals. It is unclear if the fractures were caused by the presence of the biomaterial C2 or whether additional variables were to blame. By the end of the research, the mice appeared to tolerate the biomaterials without exhibiting any inflammatory or rejection responses.

LifeVol. 14(9)
University of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca (RO), Babeș-Bolyai University (RO), Institutul Oncologic Bucuresti (RO)
Openalex Percentile: Top 6%
Orthopaedic implants and arthroplasty
4.01
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