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Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing

Modified macroporous structures and active osteogenic substances are necessary to overcome the limited bone regeneration capacity and low degradability of self-curing calcium phosphate cement (CPC). Curcumin (CUR), which possesses strong osteogenic activity and poor aqueous solubility/bioavailabilit...

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Autores principales: Zhang, Ying, Xu, Hailiang, Wang, Jing, Fan, Xiaochen, Tian, Fang, Wang, Zhiyuan, Lu, Botao, Wu, Weidong, Liu, Youjun, Ai, Yixiang, Wang, Xiaohui, Zhu, Lei, Jia, Shuaijun, Hao, Dingjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127129/
https://www.ncbi.nlm.nih.gov/pubmed/37114092
http://dx.doi.org/10.1016/j.mtbio.2023.100630
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author Zhang, Ying
Xu, Hailiang
Wang, Jing
Fan, Xiaochen
Tian, Fang
Wang, Zhiyuan
Lu, Botao
Wu, Weidong
Liu, Youjun
Ai, Yixiang
Wang, Xiaohui
Zhu, Lei
Jia, Shuaijun
Hao, Dingjun
author_facet Zhang, Ying
Xu, Hailiang
Wang, Jing
Fan, Xiaochen
Tian, Fang
Wang, Zhiyuan
Lu, Botao
Wu, Weidong
Liu, Youjun
Ai, Yixiang
Wang, Xiaohui
Zhu, Lei
Jia, Shuaijun
Hao, Dingjun
author_sort Zhang, Ying
collection PubMed
description Modified macroporous structures and active osteogenic substances are necessary to overcome the limited bone regeneration capacity and low degradability of self-curing calcium phosphate cement (CPC). Curcumin (CUR), which possesses strong osteogenic activity and poor aqueous solubility/bioavailability, esterifies the side chains in hyaluronic acid (HA) to form a water-soluble CUR-HA macromolecule. In this study, we incorporated the CUR-HA and glucose microparticles (GMPs) into the CPC powder to fabricate the CUR-HA/GMP/CPC composite, which not only retained the good injectability and mechanical strength of bone cements, but also significantly increased the cement porosity and sustained release property of CUR-HA in vitro. CUR-HA incorporation greatly improved the differentiation ability of bone marrow mesenchymal stem cells (BMSCs) to osteoblasts by activating the RUNX family transcription factor 2/fibroblast growth factor 18 (RUNX2/FGF18) signaling pathway, increasing the expression of osteocalcin and enhancing the alkaline phosphatase activity. In addition, in vivo implantation of CUR-HA/GMP/CPC into femoral condyle defects dramatically accelerated the degradation rate of cement and boosted local vascularization and osteopontin protein expression, and consequently promoted rapid bone regeneration. Therefore, macroporous CPC based composite cement with CUR-HA shows a remarkable ability to repair bone defects and is a promising translational application of modified CPC in clinical practice.
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spelling pubmed-101271292023-04-26 Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing Zhang, Ying Xu, Hailiang Wang, Jing Fan, Xiaochen Tian, Fang Wang, Zhiyuan Lu, Botao Wu, Weidong Liu, Youjun Ai, Yixiang Wang, Xiaohui Zhu, Lei Jia, Shuaijun Hao, Dingjun Mater Today Bio Full Length Article Modified macroporous structures and active osteogenic substances are necessary to overcome the limited bone regeneration capacity and low degradability of self-curing calcium phosphate cement (CPC). Curcumin (CUR), which possesses strong osteogenic activity and poor aqueous solubility/bioavailability, esterifies the side chains in hyaluronic acid (HA) to form a water-soluble CUR-HA macromolecule. In this study, we incorporated the CUR-HA and glucose microparticles (GMPs) into the CPC powder to fabricate the CUR-HA/GMP/CPC composite, which not only retained the good injectability and mechanical strength of bone cements, but also significantly increased the cement porosity and sustained release property of CUR-HA in vitro. CUR-HA incorporation greatly improved the differentiation ability of bone marrow mesenchymal stem cells (BMSCs) to osteoblasts by activating the RUNX family transcription factor 2/fibroblast growth factor 18 (RUNX2/FGF18) signaling pathway, increasing the expression of osteocalcin and enhancing the alkaline phosphatase activity. In addition, in vivo implantation of CUR-HA/GMP/CPC into femoral condyle defects dramatically accelerated the degradation rate of cement and boosted local vascularization and osteopontin protein expression, and consequently promoted rapid bone regeneration. Therefore, macroporous CPC based composite cement with CUR-HA shows a remarkable ability to repair bone defects and is a promising translational application of modified CPC in clinical practice. Elsevier 2023-04-07 /pmc/articles/PMC10127129/ /pubmed/37114092 http://dx.doi.org/10.1016/j.mtbio.2023.100630 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Zhang, Ying
Xu, Hailiang
Wang, Jing
Fan, Xiaochen
Tian, Fang
Wang, Zhiyuan
Lu, Botao
Wu, Weidong
Liu, Youjun
Ai, Yixiang
Wang, Xiaohui
Zhu, Lei
Jia, Shuaijun
Hao, Dingjun
Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing
title Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing
title_full Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing
title_fullStr Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing
title_full_unstemmed Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing
title_short Incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing
title_sort incorporation of synthetic water-soluble curcumin polymeric drug within calcium phosphate cements for bone defect repairing
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127129/
https://www.ncbi.nlm.nih.gov/pubmed/37114092
http://dx.doi.org/10.1016/j.mtbio.2023.100630
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