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Article: SEAWATER-CONTAMINATED ULNAR RABBIT BONE DEFECTS REPAIR USING 3D-PRINTED β-TCP/VANCOMYCIN COMPOSITE SCAFFOLDS
| Title | SEAWATER-CONTAMINATED ULNAR RABBIT BONE DEFECTS REPAIR USING 3D-PRINTED β-TCP/VANCOMYCIN COMPOSITE SCAFFOLDS |
|---|---|
| Authors | |
| Keywords | biomedical materials Materials science nanomaterials orthopedics |
| Issue Date | 2025 |
| Citation | European Cells and Materials, 2025, v. 52, p. 98-113 How to Cite? |
| Abstract | Background: Repairing extensive bone defects following seawater immersion poses a significant challenge for orthopedic surgeons. Recent advancements in three-dimensional (3D) printing technology have demonstrated considerable potential in fabricating scaffolds with optimized morphological structures and superior biological properties. However, the specific characteristics and therapeutic efficacy of 3D-printed nano beta-tricalcium phosphate (β-TCP) scaffolds in the repair of seawater-immersed rabbit ulna bone defects remain inadequately explored. Methods: Nano-β-TCP scaffolds were fabricated via stereo lithography apparatus (SLA) and characterized using scanning electron microscope (SEM), X-ray diffraction, and mechanical testing. Vancomycin-loaded scaffolds were implanted in 18 rats, with drug release profiles monitored over a 56-day period. Thirty-six rabbits were assigned to three groups to assess scaffold performance in 1.5 cm seawater-immersed ulnar defects. Serum tumor necrosis factor-alpha (TNF-α) levels were measured pre-and post-implantation to evaluate inflammatory responses. Bone repair was assessed through X-ray, histological analysis, and micro-computed tomography (micro-CT) scanning. In vitro antibacterial efficacy was also evaluated. Results: The scaffold exhibited a cylindrical porous structure with dimensions of 0.5 cm in both diameter and height. The average pore size was approximately 400 µm, with a porosity of 53 %, and a compressive strength of 170 N. The scaffold demonstrated sustained vancomycin release over 56 days. In vivo, implantation of the scaffolds resulted in a significant reduction in serum TNF-α levels (p < 0.05) and promoted new bone formation compared to controls (p < 0.05). Histological and micro-CT analyses confirmed superior bone repair, with increased expression of osteocalcin (OCN), osteopontin (OPN), and vascular endothelial growth factor (VEGF). The scaffolds exhibited robust antibacterial activity after 72 hours. Conclusions: 3D-printed nano-β-TCP scaffolds offer an effective solution for repairing seawater-immersed bone defects and significantly enhance bone regeneration. |
| Persistent Identifier | http://hdl.handle.net/10722/363066 |
| ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 0.700 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lao, H. D. | - |
| dc.contributor.author | Liu, D. | - |
| dc.contributor.author | Yi, R. | - |
| dc.contributor.author | Yuan, Y. N. | - |
| dc.contributor.author | Zhao, M. | - |
| dc.contributor.author | Li, G. S. | - |
| dc.contributor.author | Nie, X. Y. | - |
| dc.contributor.author | Gu, J. L. | - |
| dc.contributor.author | Cai, X. M. | - |
| dc.contributor.author | Li, H. | - |
| dc.contributor.author | Lin, S. E. | - |
| dc.contributor.author | Zhou, J. J. | - |
| dc.date.accessioned | 2025-10-10T07:44:22Z | - |
| dc.date.available | 2025-10-10T07:44:22Z | - |
| dc.date.issued | 2025 | - |
| dc.identifier.citation | European Cells and Materials, 2025, v. 52, p. 98-113 | - |
| dc.identifier.issn | 1473-2262 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/363066 | - |
| dc.description.abstract | Background: Repairing extensive bone defects following seawater immersion poses a significant challenge for orthopedic surgeons. Recent advancements in three-dimensional (3D) printing technology have demonstrated considerable potential in fabricating scaffolds with optimized morphological structures and superior biological properties. However, the specific characteristics and therapeutic efficacy of 3D-printed nano beta-tricalcium phosphate (β-TCP) scaffolds in the repair of seawater-immersed rabbit ulna bone defects remain inadequately explored. Methods: Nano-β-TCP scaffolds were fabricated via stereo lithography apparatus (SLA) and characterized using scanning electron microscope (SEM), X-ray diffraction, and mechanical testing. Vancomycin-loaded scaffolds were implanted in 18 rats, with drug release profiles monitored over a 56-day period. Thirty-six rabbits were assigned to three groups to assess scaffold performance in 1.5 cm seawater-immersed ulnar defects. Serum tumor necrosis factor-alpha (TNF-α) levels were measured pre-and post-implantation to evaluate inflammatory responses. Bone repair was assessed through X-ray, histological analysis, and micro-computed tomography (micro-CT) scanning. In vitro antibacterial efficacy was also evaluated. Results: The scaffold exhibited a cylindrical porous structure with dimensions of 0.5 cm in both diameter and height. The average pore size was approximately 400 µm, with a porosity of 53 %, and a compressive strength of 170 N. The scaffold demonstrated sustained vancomycin release over 56 days. In vivo, implantation of the scaffolds resulted in a significant reduction in serum TNF-α levels (p < 0.05) and promoted new bone formation compared to controls (p < 0.05). Histological and micro-CT analyses confirmed superior bone repair, with increased expression of osteocalcin (OCN), osteopontin (OPN), and vascular endothelial growth factor (VEGF). The scaffolds exhibited robust antibacterial activity after 72 hours. Conclusions: 3D-printed nano-β-TCP scaffolds offer an effective solution for repairing seawater-immersed bone defects and significantly enhance bone regeneration. | - |
| dc.language | eng | - |
| dc.relation.ispartof | European Cells and Materials | - |
| dc.subject | biomedical materials | - |
| dc.subject | Materials science | - |
| dc.subject | nanomaterials | - |
| dc.subject | orthopedics | - |
| dc.title | SEAWATER-CONTAMINATED ULNAR RABBIT BONE DEFECTS REPAIR USING 3D-PRINTED β-TCP/VANCOMYCIN COMPOSITE SCAFFOLDS | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.22203/eCM.v052a07 | - |
| dc.identifier.scopus | eid_2-s2.0-105014970951 | - |
| dc.identifier.volume | 52 | - |
| dc.identifier.spage | 98 | - |
| dc.identifier.epage | 113 | - |
