A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration

We demonstrate a simple, effective and feasible method to address the shrinkage of Poly (lactic-co-glycolic acid) (PLGA) through a core-shell structure fiber strategy. The results revealed that introducing size-stable poly-caprolactone (PCL) as the core fiber significantly improved the PLGA-based fi...

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Autores principales: Shue Jin, Jing Gao, Renli Yang, Chen Yuan, Ruili Wang, Qin Zou, Yi Zuo, Meifang Zhu, Yubao Li, Yi Man, Jidong Li
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Publicado: KeAi Communications Co., Ltd. 2022
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Acceso en línea:https://doaj.org/article/cb987c41d73949f58ee6f624546c5d2d
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spelling oai:doaj.org-article:cb987c41d73949f58ee6f624546c5d2d2021-11-04T04:35:59ZA baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration2452-199X10.1016/j.bioactmat.2021.06.028https://doaj.org/article/cb987c41d73949f58ee6f624546c5d2d2022-02-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2452199X21003145https://doaj.org/toc/2452-199XWe demonstrate a simple, effective and feasible method to address the shrinkage of Poly (lactic-co-glycolic acid) (PLGA) through a core-shell structure fiber strategy. The results revealed that introducing size-stable poly-caprolactone (PCL) as the core fiber significantly improved the PLGA-based fibrous scaffold's dimensional maintenance. We further utilized fish collagen to modify the PLGA shell layer (PFC) of coaxial fibers and loaded baicalin (BA) into the PCL core layer (PCL-BA) to endow fibrous scaffold with more functional biological cues. The PFC/PCL-BA fibrous scaffold promoted the osteogenic differentiation of bone mesenchymal stem cells and stimulated the RAW264.7 cells to polarize into a pro-reparative phenotype. Importantly, the in vivo study demonstrated that the PFC/PCL-BA scaffold could regulate inflammation and osteoclast differentiation, favor neovascularization and bone formation. This work tactfully combined PLGA and PCL to establish a drug release platform based on the core-shell fibrous scaffold for vascularized bone regeneration.Shue JinJing GaoRenli YangChen YuanRuili WangQin ZouYi ZuoMeifang ZhuYubao LiYi ManJidong LiKeAi Communications Co., Ltd.articleCoaxial nanofiberBaicalinInflammationOsteoclast differentiationVascularized bone regenerationMaterials of engineering and construction. Mechanics of materialsTA401-492Biology (General)QH301-705.5ENBioactive Materials, Vol 8, Iss , Pp 559-572 (2022)
institution DOAJ
collection DOAJ
language EN
topic Coaxial nanofiber
Baicalin
Inflammation
Osteoclast differentiation
Vascularized bone regeneration
Materials of engineering and construction. Mechanics of materials
TA401-492
Biology (General)
QH301-705.5
spellingShingle Coaxial nanofiber
Baicalin
Inflammation
Osteoclast differentiation
Vascularized bone regeneration
Materials of engineering and construction. Mechanics of materials
TA401-492
Biology (General)
QH301-705.5
Shue Jin
Jing Gao
Renli Yang
Chen Yuan
Ruili Wang
Qin Zou
Yi Zuo
Meifang Zhu
Yubao Li
Yi Man
Jidong Li
A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration
description We demonstrate a simple, effective and feasible method to address the shrinkage of Poly (lactic-co-glycolic acid) (PLGA) through a core-shell structure fiber strategy. The results revealed that introducing size-stable poly-caprolactone (PCL) as the core fiber significantly improved the PLGA-based fibrous scaffold's dimensional maintenance. We further utilized fish collagen to modify the PLGA shell layer (PFC) of coaxial fibers and loaded baicalin (BA) into the PCL core layer (PCL-BA) to endow fibrous scaffold with more functional biological cues. The PFC/PCL-BA fibrous scaffold promoted the osteogenic differentiation of bone mesenchymal stem cells and stimulated the RAW264.7 cells to polarize into a pro-reparative phenotype. Importantly, the in vivo study demonstrated that the PFC/PCL-BA scaffold could regulate inflammation and osteoclast differentiation, favor neovascularization and bone formation. This work tactfully combined PLGA and PCL to establish a drug release platform based on the core-shell fibrous scaffold for vascularized bone regeneration.
format article
author Shue Jin
Jing Gao
Renli Yang
Chen Yuan
Ruili Wang
Qin Zou
Yi Zuo
Meifang Zhu
Yubao Li
Yi Man
Jidong Li
author_facet Shue Jin
Jing Gao
Renli Yang
Chen Yuan
Ruili Wang
Qin Zou
Yi Zuo
Meifang Zhu
Yubao Li
Yi Man
Jidong Li
author_sort Shue Jin
title A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration
title_short A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration
title_full A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration
title_fullStr A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration
title_full_unstemmed A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration
title_sort baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration
publisher KeAi Communications Co., Ltd.
publishDate 2022
url https://doaj.org/article/cb987c41d73949f58ee6f624546c5d2d
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