Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration

IntroductionOsteoarthritis (OA) is a degenerative disease of the joints characterized by cartilage degradation and synovial inflammation. Due to the complex pathogenesis of OA, multifaceted therapies that modulate inflammatory and immune microenvironmental disturbances while promoting cartilage rege...

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Main Authors: Zhuoming Xu, Jun Ma, Hanyin Hu, Jintao Liu, Haiyang Yang, Jiayi Chen, Hongwei Xu, Xinyu Wang, Huanhuan Luo, Gang Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Bioengineering and Biotechnology
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Online Access:https://www.frontiersin.org/articles/10.3389/fbioe.2025.1540592/full
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author Zhuoming Xu
Zhuoming Xu
Jun Ma
Hanyin Hu
Hanyin Hu
Jintao Liu
Jintao Liu
Haiyang Yang
Haiyang Yang
Jiayi Chen
Hongwei Xu
Xinyu Wang
Huanhuan Luo
Gang Chen
author_facet Zhuoming Xu
Zhuoming Xu
Jun Ma
Hanyin Hu
Hanyin Hu
Jintao Liu
Jintao Liu
Haiyang Yang
Haiyang Yang
Jiayi Chen
Hongwei Xu
Xinyu Wang
Huanhuan Luo
Gang Chen
author_sort Zhuoming Xu
collection DOAJ
description IntroductionOsteoarthritis (OA) is a degenerative disease of the joints characterized by cartilage degradation and synovial inflammation. Due to the complex pathogenesis of OA, multifaceted therapies that modulate inflammatory and immune microenvironmental disturbances while promoting cartilage regeneration are key to control the progression of OA.MethodsHerein, a multifunctional nanoparticle (DIC/Mg-PDA NPs) was constructed successfully by the metal chelation effect between Mg2+ and catecholamine bond from dopamine, followed by the amidation with diclofenac (DIC), which was then prepared into an injectable hydrogel microsphere (DIC/Mg-PDA@HM) with immune-regulating and cartilage-repairing abilities through microfluidic technology for the treatment of osteoarthritis.Results and discussionThe sustained release of Mg2+ from the composite hydrogel microspheres achieved inflammatory immune regulation by converting macrophages from M1 to M2 and promoted cartilage regeneration through the differentiation of BMSCs. Moreover, the enhanced release of DIC and polydopamine (PDA) effectively downregulated inflammatory factors, and finally achieved OA therapy. In addition, in vivo MRI and tissue section staining of OA model proved the significant efficacy of the hydrogel microspheres on OA. In conclusion, these novel hydrogel microspheres demonstrated a promising prospect for multidisciplinary repairing of OA.
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spelling doaj-art-66abb6985405410f849fe565e003f3992025-01-28T06:41:17ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852025-01-011310.3389/fbioe.2025.15405921540592Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regenerationZhuoming Xu0Zhuoming Xu1Jun Ma2Hanyin Hu3Hanyin Hu4Jintao Liu5Jintao Liu6Haiyang Yang7Haiyang Yang8Jiayi Chen9Hongwei Xu10Xinyu Wang11Huanhuan Luo12Gang Chen13Jiaxing University Master Degree Cultivation Base, Zhejiang Chinese Medical University, Hangzhou, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaJiaxing University Master Degree Cultivation Base, Zhejiang Chinese Medical University, Hangzhou, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaJiaxing University Master Degree Cultivation Base, Zhejiang Chinese Medical University, Hangzhou, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaJiaxing University Master Degree Cultivation Base, Zhejiang Chinese Medical University, Hangzhou, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaDepartment of Radiology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaDepartment of Orthopaedics, Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, The Second Affiliated Hospital of Jiaxing University, Jiaxing, ChinaIntroductionOsteoarthritis (OA) is a degenerative disease of the joints characterized by cartilage degradation and synovial inflammation. Due to the complex pathogenesis of OA, multifaceted therapies that modulate inflammatory and immune microenvironmental disturbances while promoting cartilage regeneration are key to control the progression of OA.MethodsHerein, a multifunctional nanoparticle (DIC/Mg-PDA NPs) was constructed successfully by the metal chelation effect between Mg2+ and catecholamine bond from dopamine, followed by the amidation with diclofenac (DIC), which was then prepared into an injectable hydrogel microsphere (DIC/Mg-PDA@HM) with immune-regulating and cartilage-repairing abilities through microfluidic technology for the treatment of osteoarthritis.Results and discussionThe sustained release of Mg2+ from the composite hydrogel microspheres achieved inflammatory immune regulation by converting macrophages from M1 to M2 and promoted cartilage regeneration through the differentiation of BMSCs. Moreover, the enhanced release of DIC and polydopamine (PDA) effectively downregulated inflammatory factors, and finally achieved OA therapy. In addition, in vivo MRI and tissue section staining of OA model proved the significant efficacy of the hydrogel microspheres on OA. In conclusion, these novel hydrogel microspheres demonstrated a promising prospect for multidisciplinary repairing of OA.https://www.frontiersin.org/articles/10.3389/fbioe.2025.1540592/fullhydrogel microspheremagnesium ioncartilage regenerationosteoarthritisanti-inflammatoryimmunomodulation
spellingShingle Zhuoming Xu
Zhuoming Xu
Jun Ma
Hanyin Hu
Hanyin Hu
Jintao Liu
Jintao Liu
Haiyang Yang
Haiyang Yang
Jiayi Chen
Hongwei Xu
Xinyu Wang
Huanhuan Luo
Gang Chen
Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration
Frontiers in Bioengineering and Biotechnology
hydrogel microsphere
magnesium ion
cartilage regeneration
osteoarthritis
anti-inflammatory
immunomodulation
title Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration
title_full Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration
title_fullStr Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration
title_full_unstemmed Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration
title_short Metal ion-crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration
title_sort metal ion crosslinking multifunctional hydrogel microspheres with inflammatory immune regulation for cartilage regeneration
topic hydrogel microsphere
magnesium ion
cartilage regeneration
osteoarthritis
anti-inflammatory
immunomodulation
url https://www.frontiersin.org/articles/10.3389/fbioe.2025.1540592/full
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