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Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration

Although artificial bone repair scaffolds, such as titanium alloy, bioactive glass, and hydroxyapatite (HAp), have been widely used for treatment of large‐size bone defects or serious bone destruction, they normally exhibit unsatisfied bone repair efficiency because of their weak osteogenic and angi...

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Autores principales: Wang, Guanyun, Lv, Zehui, Wang, Tao, Hu, Tingting, Bian, Yixin, Yang, Yu, Liang, Ruizheng, Tan, Chaoliang, Weng, Xisheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811441/
https://www.ncbi.nlm.nih.gov/pubmed/36394157
http://dx.doi.org/10.1002/advs.202204234
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author Wang, Guanyun
Lv, Zehui
Wang, Tao
Hu, Tingting
Bian, Yixin
Yang, Yu
Liang, Ruizheng
Tan, Chaoliang
Weng, Xisheng
author_facet Wang, Guanyun
Lv, Zehui
Wang, Tao
Hu, Tingting
Bian, Yixin
Yang, Yu
Liang, Ruizheng
Tan, Chaoliang
Weng, Xisheng
author_sort Wang, Guanyun
collection PubMed
description Although artificial bone repair scaffolds, such as titanium alloy, bioactive glass, and hydroxyapatite (HAp), have been widely used for treatment of large‐size bone defects or serious bone destruction, they normally exhibit unsatisfied bone repair efficiency because of their weak osteogenic and angiogenesis performance as well as poor cell crawling and adhesion properties. Herein, the surface functionalization of MgAlEu‐layered double hydroxide (MAE‐LDH) nanosheets on porous HAp scaffolds is reported as a simple and effective strategy to prepare HAp/MAE‐LDH scaffolds for enhanced bone regeneration. The surface functionalization of MAE‐LDHs on the porous HAp scaffold can significantly improve its surface roughness, specific surface, and hydrophilicity, thus effectively boosting the cells adhesion and osteogenic differentiation. Importantly, the MAE‐LDHs grown on HAp scaffolds enable the sustained release of Mg(2+) and Eu(3+) ions for efficient bone repair and vascular regeneration. In vitro experiments suggest that the HAp/MAE‐LDH scaffold presents much enhanced osteogenesis and angiogenesis properties in comparison with the pristine HAp scaffold. In vivo assays further reveal that the new bone mass and mineral density of HAp/MAE‐LDH scaffold increased by 3.18‐ and 2.21‐fold, respectively, than that of pristine HAp scaffold. The transcriptome sequencing analysis reveals that the HAp/MAE‐LDH scaffold can activate the Wnt/β‐catenin signaling pathway to promote the osteogenic and angiogenic abilities.
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spelling pubmed-98114412023-01-05 Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration Wang, Guanyun Lv, Zehui Wang, Tao Hu, Tingting Bian, Yixin Yang, Yu Liang, Ruizheng Tan, Chaoliang Weng, Xisheng Adv Sci (Weinh) Research Articles Although artificial bone repair scaffolds, such as titanium alloy, bioactive glass, and hydroxyapatite (HAp), have been widely used for treatment of large‐size bone defects or serious bone destruction, they normally exhibit unsatisfied bone repair efficiency because of their weak osteogenic and angiogenesis performance as well as poor cell crawling and adhesion properties. Herein, the surface functionalization of MgAlEu‐layered double hydroxide (MAE‐LDH) nanosheets on porous HAp scaffolds is reported as a simple and effective strategy to prepare HAp/MAE‐LDH scaffolds for enhanced bone regeneration. The surface functionalization of MAE‐LDHs on the porous HAp scaffold can significantly improve its surface roughness, specific surface, and hydrophilicity, thus effectively boosting the cells adhesion and osteogenic differentiation. Importantly, the MAE‐LDHs grown on HAp scaffolds enable the sustained release of Mg(2+) and Eu(3+) ions for efficient bone repair and vascular regeneration. In vitro experiments suggest that the HAp/MAE‐LDH scaffold presents much enhanced osteogenesis and angiogenesis properties in comparison with the pristine HAp scaffold. In vivo assays further reveal that the new bone mass and mineral density of HAp/MAE‐LDH scaffold increased by 3.18‐ and 2.21‐fold, respectively, than that of pristine HAp scaffold. The transcriptome sequencing analysis reveals that the HAp/MAE‐LDH scaffold can activate the Wnt/β‐catenin signaling pathway to promote the osteogenic and angiogenic abilities. John Wiley and Sons Inc. 2022-11-17 /pmc/articles/PMC9811441/ /pubmed/36394157 http://dx.doi.org/10.1002/advs.202204234 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Wang, Guanyun
Lv, Zehui
Wang, Tao
Hu, Tingting
Bian, Yixin
Yang, Yu
Liang, Ruizheng
Tan, Chaoliang
Weng, Xisheng
Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration
title Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration
title_full Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration
title_fullStr Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration
title_full_unstemmed Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration
title_short Surface Functionalization of Hydroxyapatite Scaffolds with MgAlEu‐LDH Nanosheets for High‐Performance Bone Regeneration
title_sort surface functionalization of hydroxyapatite scaffolds with mgaleu‐ldh nanosheets for high‐performance bone regeneration
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811441/
https://www.ncbi.nlm.nih.gov/pubmed/36394157
http://dx.doi.org/10.1002/advs.202204234
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