Bioceramic modular tissue-engineered bone with rapid vascularization for large bone defects
Siwei Luo
1, 2, 3
,
Zhen Wang
1, 2
,
Geng Tang
4
,
Daizhu Yuan
2
,
Zhan Yu Wu
2
,
Zihao Zou
1, 2
,
Long Yang
2
,
Tao Lu
2, 3
,
Chuan Ye
1, 2
3
Department of Orthopedics, The First People's Hospital of Guiyang, Guiyang, 550002, China
|
Publication type: Journal Article
Publication date: 2024-06-01
scimago Q1
wos Q1
SJR: 1.034
CiteScore: 9.1
Impact factor: 5.6
ISSN: 02728842, 18733956
Materials Chemistry
Surfaces, Coatings and Films
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Process Chemistry and Technology
Abstract
Tackling large bone defects remains a significant clinical challenge due to the limitations in current treatment strategies. This study presents a modular tissue-engineered bone, achieving rapid vascularization within 14 days and showing significant initial stability after implantation. This innovation is driven by the synergy of high-resolution mono-LCD mask photopolymerization 3D printing, electrospinning technology, and photosensitive gel cell carriers, resulting in a bioceramic-electrospun fiber composite scaffold (BECS) that enhances nutrient permeation and mechanical support. Emphasizing biomimicry, the scaffold incorporates an electrospun ultrafine fiber membrane that simulates the periosteum's microvascular structure, crucial for rapid endothelialization of graft lumens. This membrane acts as an advanced carrier for vascular endothelial growth factor (VEGF), facilitating targeted release that significantly promotes vascular regeneration. Our in vitro and in vivo analyses indicate that immediate vascularization and subsequent osteogenesis significantly enhance blood supply and bone regeneration in defect sites. Notably, the application of Human umbilical cord mesenchymal stem cells (UC-MSCs) within the gelatin methacrylate (GelMA) cell carrier ensures uniform distribution and proliferation, essential for balanced bone regeneration. Demonstrating a 75% increase in vascular network formation and a 60% enhancement in osteocalcin (OCN) expression within the initial four weeks, the scaffold supports both rapid vascularization and osteogenesis. This dual-functional tissue-engineered bone represents a significant advancement for treating large bone defects, with the potential to improve current therapeutic strategies substantially.
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9
Total citations:
9
Citations from 2025:
7
(77.78%)
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GOST
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Luo S. et al. Bioceramic modular tissue-engineered bone with rapid vascularization for large bone defects // Ceramics International. 2024. Vol. 50. No. 11. pp. 18275-18283.
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Luo S., Wang Z., Tang G., Yuan D., Wu Z. Yu., Zou Z., Yang L., Lu T., Ye C. Bioceramic modular tissue-engineered bone with rapid vascularization for large bone defects // Ceramics International. 2024. Vol. 50. No. 11. pp. 18275-18283.
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RIS
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TY - JOUR
DO - 10.1016/j.ceramint.2024.02.311
UR - https://linkinghub.elsevier.com/retrieve/pii/S0272884224008320
TI - Bioceramic modular tissue-engineered bone with rapid vascularization for large bone defects
T2 - Ceramics International
AU - Luo, Siwei
AU - Wang, Zhen
AU - Tang, Geng
AU - Yuan, Daizhu
AU - Wu, Zhan Yu
AU - Zou, Zihao
AU - Yang, Long
AU - Lu, Tao
AU - Ye, Chuan
PY - 2024
DA - 2024/06/01
PB - Elsevier
SP - 18275-18283
IS - 11
VL - 50
SN - 0272-8842
SN - 1873-3956
ER -
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BibTex (up to 50 authors)
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@article{2024_Luo,
author = {Siwei Luo and Zhen Wang and Geng Tang and Daizhu Yuan and Zhan Yu Wu and Zihao Zou and Long Yang and Tao Lu and Chuan Ye},
title = {Bioceramic modular tissue-engineered bone with rapid vascularization for large bone defects},
journal = {Ceramics International},
year = {2024},
volume = {50},
publisher = {Elsevier},
month = {jun},
url = {https://linkinghub.elsevier.com/retrieve/pii/S0272884224008320},
number = {11},
pages = {18275--18283},
doi = {10.1016/j.ceramint.2024.02.311}
}
Cite this
MLA
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Luo, Siwei, et al. “Bioceramic modular tissue-engineered bone with rapid vascularization for large bone defects.” Ceramics International, vol. 50, no. 11, Jun. 2024, pp. 18275-18283. https://linkinghub.elsevier.com/retrieve/pii/S0272884224008320.