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Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc

Intervertebral disc degeneration (IVDD) is one of the main causes of low back pain. Although local delivery strategies using biomaterial carriers have shown potential for IVDD treatment, it remains challenging for intervention against multiple adverse contributors by a single delivery platform. In t...

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Autores principales: Zhu, Zhuang, Yu, Qifan, Li, Hanwen, Han, Feng, Guo, Qianping, Sun, Heng, Zhao, He, Tu, Zhengdong, Liu, Zhuang, Zhu, Caihong, Li, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225820/
https://www.ncbi.nlm.nih.gov/pubmed/37256210
http://dx.doi.org/10.1016/j.bioactmat.2023.05.005
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author Zhu, Zhuang
Yu, Qifan
Li, Hanwen
Han, Feng
Guo, Qianping
Sun, Heng
Zhao, He
Tu, Zhengdong
Liu, Zhuang
Zhu, Caihong
Li, Bin
author_facet Zhu, Zhuang
Yu, Qifan
Li, Hanwen
Han, Feng
Guo, Qianping
Sun, Heng
Zhao, He
Tu, Zhengdong
Liu, Zhuang
Zhu, Caihong
Li, Bin
author_sort Zhu, Zhuang
collection PubMed
description Intervertebral disc degeneration (IVDD) is one of the main causes of low back pain. Although local delivery strategies using biomaterial carriers have shown potential for IVDD treatment, it remains challenging for intervention against multiple adverse contributors by a single delivery platform. In the present work, we propose a new functionalization strategy using vanillin, a natural molecule with anti-inflammatory and antioxidant properties, to develop multifunctional gelatin methacrylate (GelMA) microspheres for local delivery of transforming growth factor β3 (TGFβ3) toward IVDD treatment. In vitro, functionalized microspheres not only improved the release kinetics of TGFβ3 but also effectively inhibited inflammatory responses and promoted the secretion of extracellular matrix (ECM) in lipopolysaccharide-induced nucleus pulposus (NP) cells. In vivo, functionalized platform plays roles in alleviating inflammation and oxidative stress, preserving the water content of NP and disc height, and maintaining intact structure and biomechanical functions, thereby promoting the regeneration of IVD. High-throughput sequencing suggests that inhibition of the phosphatidylinositol 3-kinase (PI3K)-Akt signaling might be associated with their therapeutic effects. In summary, the vanillin-based functionalization strategy provides a novel and simple way for packaging multiple functions into a single delivery platform and holds promise for tissue regeneration beyond the IVD.
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spelling pubmed-102258202023-05-30 Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc Zhu, Zhuang Yu, Qifan Li, Hanwen Han, Feng Guo, Qianping Sun, Heng Zhao, He Tu, Zhengdong Liu, Zhuang Zhu, Caihong Li, Bin Bioact Mater Article Intervertebral disc degeneration (IVDD) is one of the main causes of low back pain. Although local delivery strategies using biomaterial carriers have shown potential for IVDD treatment, it remains challenging for intervention against multiple adverse contributors by a single delivery platform. In the present work, we propose a new functionalization strategy using vanillin, a natural molecule with anti-inflammatory and antioxidant properties, to develop multifunctional gelatin methacrylate (GelMA) microspheres for local delivery of transforming growth factor β3 (TGFβ3) toward IVDD treatment. In vitro, functionalized microspheres not only improved the release kinetics of TGFβ3 but also effectively inhibited inflammatory responses and promoted the secretion of extracellular matrix (ECM) in lipopolysaccharide-induced nucleus pulposus (NP) cells. In vivo, functionalized platform plays roles in alleviating inflammation and oxidative stress, preserving the water content of NP and disc height, and maintaining intact structure and biomechanical functions, thereby promoting the regeneration of IVD. High-throughput sequencing suggests that inhibition of the phosphatidylinositol 3-kinase (PI3K)-Akt signaling might be associated with their therapeutic effects. In summary, the vanillin-based functionalization strategy provides a novel and simple way for packaging multiple functions into a single delivery platform and holds promise for tissue regeneration beyond the IVD. KeAi Publishing 2023-05-23 /pmc/articles/PMC10225820/ /pubmed/37256210 http://dx.doi.org/10.1016/j.bioactmat.2023.05.005 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 Article
Zhu, Zhuang
Yu, Qifan
Li, Hanwen
Han, Feng
Guo, Qianping
Sun, Heng
Zhao, He
Tu, Zhengdong
Liu, Zhuang
Zhu, Caihong
Li, Bin
Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc
title Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc
title_full Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc
title_fullStr Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc
title_full_unstemmed Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc
title_short Vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc
title_sort vanillin-based functionalization strategy to construct multifunctional microspheres for treating inflammation and regenerating intervertebral disc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225820/
https://www.ncbi.nlm.nih.gov/pubmed/37256210
http://dx.doi.org/10.1016/j.bioactmat.2023.05.005
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