Comparative evaluation of the efficiency of osteoplastic materials in the reparative regeneration of an experimental punch defect of the femoral bone

Authors

DOI:

https://doi.org/10.11603/2414-4533.2026.3.16665

Keywords:

reparative osteogenesis, bone defect, osteoplastic materials, demineralized bone matrix, collagen, RANKL, OPG, sclerostin, bone remodeling markers

Abstract

The aim of the work: to establish and compare the effectiveness of a non-collagen xenogeneic bone material, a collagen-coated xenogeneic bone material, and demineralized bone matrix in stimulating reparative osteogenesis in a rat femoral perforated bone defect model, based on a comprehensive histomorphological, radiological, and biochemical assessment.
Materials and Methods. A standard 3-mm perforated femoral defect was created in rats under thiopental-sodium anesthesia. Animals were divided into 4 groups (n=10 per group per time point): 1 – uncorrected defect (control); 2 – xenogeneic material without collagen; 3 – xenogeneic material with collagen; 4 – demineralized bone matrix (DBM). Animals were euthanized on days 5, 14, 30, and 60. Light microscopy, radiography, and ELISA determination of 8 serum bone remodeling markers (CTX-I, TRAP-5b, P1NP, BALP, osteocalcin, RANKL, OPG, sclerostin) were performed. Statistical analysis (Student's t-test, Pearson correlation, multiple regression, hierarchical clustering, principal component analysis) was carried out in STATISTICA 10.0.
Results. All investigated materials were shown to pass through a single sequence of remodeling phases (acute resorptive → transitional anabolic → stabilization), differing only in the rate and amplitude of progression. DBM provided the earliest and most stable morphological maturation of the regenerate at all time points (day-5 CTX-I reduced to (0.442±0.03) ng/mL vs (0.724±0.05) ng/mL in controls, t=4.84; p<0.001); the collagen-containing material demonstrated the most dynamic osteogenic effect in the medium term (days 14–30); the collagen-free material showed consistent but slower remodeling completed by day 60. PCA demonstrated that 89.1% of total variance in the 8 markers was explained by two principal components reflecting a single resorption–formation axis; multiple regression confirmed the leading predictive role of the RANKL/OPG axis for resorption (R²=0.795) and formation markers (R²=0.698).
Conclusions. The effectiveness of stimulating reparative osteogenesis in the studied model increases in the sequence: uncorrected defect < material without collagen < material with collagen < demineralized bone matrix. These findings support a differentiated approach to selecting an osteoplastic material depending on the expected timeframe of defect consolidation.

Author Biographies

  • Pavlo Bidzilya, I. Horbachevsky Ternopil National Medical University

    PhD Student, Department of Functional and Laboratory Diagnostics

  • Yuliia Kovalova, Dnipro University of Technology

    PhD (Technical Sciences), Associate Professor

  • Mykhailo Protsaylo, I. Horbachevsky Ternopil National Medical University

    PhD (Medicine), Associate Professor, Department of Pediatric Diseases and Pediatric Surgery

  • Ivan Klishch, I. Horbachevsky Ternopil National Medical University

    DSc (Biological Sciences), Professor, Head of the Department of Pharmacology and Clinical Pharmacology

References

1. Bone grafts and synthetic substitutes in dental applications: a comprehensive review of molecular mechanisms, materials evolution, and clinical perspective. Front Bioeng Biotechnol. 2025; 13:1759864. DOI: 10.3389/fbioe.2025.1759864. DOI: https://doi.org/10.3389/fbioe.2025.1759864

2. Yang H, Li B, Qin D, et al. Global, regional, and national burden of fracture of pelvis, 1990-2021: Analysis of data from the Global Burden of Disease Study 2021. Frontiers in Public Health. 2025 Jun.; 18:13:1610604. DOI: 10.3389/fpubh. 2025.1610604.

3. Li C, Lin Q. Global epidemiology, burden, and causes of lower extremity and pelvic fractures in the past 32 years. Front Public Health. 2025; 13:1627867. DOI: 10.3389/fpubh.2025.1627867. DOI: https://doi.org/10.3389/fpubh.2025.1627867

4. Cho J, Song H. Current concepts and applications of bone graft substitutes in orthopedic surgery. Journal of Musculoskeletal Trauma. 2025; 38(4):169-77. DOI: 10.12671/jmt.2025.00248. DOI: https://doi.org/10.12671/jmt.2025.00248

5. Sergey Veselkov, Olga Samoilova, Nataliya Shaburova, Evgeny Trofimov. High-Temperature Oxidation of High-Entropic Alloys: A Review. Materials (Basel). 2021 May 16; 14(10):2595. DOI: 10.3390/ma14102595. DOI: https://doi.org/10.3390/ma14102595

6. Moghaddam A, Müller U, Roth HJ, Wentzensen A, Grützner PA, Zimmermann G. TRACP 5b and CTX as osteological markers of delayed fracture healing. Injury. 2011; 42(8):758-64. DOI: 10.1016/j.injury.2011.03.014. DOI: https://doi.org/10.1016/j.injury.2010.11.017

7. Cox G, Einhorn TA, Tzioupis C, Giannoudis PV. Bone-turnover markers in fracture healing. J Bone Joint Surg Br. 2010; 92(3):329-34. DOI: 10.1302/0301-620x.92b3.22787. DOI: https://doi.org/10.1302/0301-620X.92B3.22787

8. Ohrbach R, Sharma S. Behavioral therapy for temporomandibular disorders. Front Oral Maxillofac Med. 2021 December 10; 3:37. DOI: 10.21037/fomm-20-65. DOI: https://doi.org/10.21037/fomm-20-65

9. Brigi C, Aghila Rani KG, Selvakumar B, Hamad M, Abou Neel EA, Samsudin AR.. Decoding biomaterial-associated molecular patterns (BAMPs): influential players in bone graft-related foreign body reactions. PeerJ. 2025 Apr.; 22:13:e19299. DOI: 10.7717/peerj.19299. DOI: https://doi.org/10.7717/peerj.19299

10. Bretschneider H, Quade M, Lode A, Gelinsky M, Rammelt S, Vater C. Chemotactic and Angiogenic Potential of Mineralized Collagen Scaffolds Functionalized with Naturally Occurring Bioactive Factor Mixtures to Stimulate Bone Regeneration. Int J Mol Sci. 2021; 22(11):5836. DOI: 10.3390/ijms22115836. DOI: https://doi.org/10.3390/ijms22115836

11. Ripamonti U, Duarte R, Ferretti C, Reddi A. Osteogenic Competence and Potency of the Bone Induction Principle: Inductive Substrates That Initiate “Bone: Formation by Autoinduction”. J. of Craniofacial Surgery. 2022; 33(3): 971-84. DOI: 10.1097/SCS.0000000000008299. DOI: https://doi.org/10.1097/SCS.0000000000008299

12. Al Qabbani A, Rani KGA, AlKawas S, et al. Evaluation of the osteogenic potential of demineralized and decellularized bovine bone granules following implantation in rat calvaria critical-size defect model. PLoS One. 2023; 18(12):e0294291. DOI: 10.1371/journal.pone.0294291. DOI: https://doi.org/10.1371/journal.pone.0294291

13. Fassbender M, Minkwitz S, Thiele M, Wildemann B. Efficacy of two different demineralised bone matrix grafts to promote bone healing in a critical-size-defect: a radiological, histological and histomorphometric study in rat femurs. Int Orthop. 2014 Sep.; 38(9):1963-9. DOI: 10.1007/s00264-014-2321-2. DOI: https://doi.org/10.1007/s00264-014-2321-2

14. Tobeiha M, Moghadasian MH, Amin N, Jafarnejad S. RANKL/RANK/OPG Pathway: A Mechanism Involved in Exercise-Induced Bone Remodeling. Biomed Res Int. 2020 Feb.; 19:2020:6910312. DOI: 10.1155/2020/6910312. DOI: https://doi.org/10.1155/2020/6910312

Published

2026-09-30

Issue

Section

Experimental investigations

How to Cite

Comparative evaluation of the efficiency of osteoplastic materials in the reparative regeneration of an experimental punch defect of the femoral bone. (2026). Hospital Surgery. Journal Named by L.Ya. Kovalchuk, 3, 138-146. https://doi.org/10.11603/2414-4533.2026.3.16665