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Article: SEAWATER-CONTAMINATED ULNAR RABBIT BONE DEFECTS REPAIR USING 3D-PRINTED β-TCP/VANCOMYCIN COMPOSITE SCAFFOLDS

TitleSEAWATER-CONTAMINATED ULNAR RABBIT BONE DEFECTS REPAIR USING 3D-PRINTED β-TCP/VANCOMYCIN COMPOSITE SCAFFOLDS
Authors
Keywordsbiomedical materials
Materials science
nanomaterials
orthopedics
Issue Date2025
Citation
European Cells and Materials, 2025, v. 52, p. 98-113 How to Cite?
AbstractBackground: 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 Identifierhttp://hdl.handle.net/10722/363066
ISSN
2023 Impact Factor: 3.2
2023 SCImago Journal Rankings: 0.700

 

DC FieldValueLanguage
dc.contributor.authorLao, H. D.-
dc.contributor.authorLiu, D.-
dc.contributor.authorYi, R.-
dc.contributor.authorYuan, Y. N.-
dc.contributor.authorZhao, M.-
dc.contributor.authorLi, G. S.-
dc.contributor.authorNie, X. Y.-
dc.contributor.authorGu, J. L.-
dc.contributor.authorCai, X. M.-
dc.contributor.authorLi, H.-
dc.contributor.authorLin, S. E.-
dc.contributor.authorZhou, J. J.-
dc.date.accessioned2025-10-10T07:44:22Z-
dc.date.available2025-10-10T07:44:22Z-
dc.date.issued2025-
dc.identifier.citationEuropean Cells and Materials, 2025, v. 52, p. 98-113-
dc.identifier.issn1473-2262-
dc.identifier.urihttp://hdl.handle.net/10722/363066-
dc.description.abstractBackground: 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.languageeng-
dc.relation.ispartofEuropean Cells and Materials-
dc.subjectbiomedical materials-
dc.subjectMaterials science-
dc.subjectnanomaterials-
dc.subjectorthopedics-
dc.titleSEAWATER-CONTAMINATED ULNAR RABBIT BONE DEFECTS REPAIR USING 3D-PRINTED β-TCP/VANCOMYCIN COMPOSITE SCAFFOLDS-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.22203/eCM.v052a07-
dc.identifier.scopuseid_2-s2.0-105014970951-
dc.identifier.volume52-
dc.identifier.spage98-
dc.identifier.epage113-

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