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Recent Advances in Reactive Oxygen Species (ROS)-Responsive Polyfunctional Nanosystems 3.0 for the Treatment of Osteoarthritis.

作者信息

Ding Dao-Fang, Xue Yan, Wu Xi-Chen, Zhu Zhi-Heng, Ding Jia-Ying, Song Yong-Jia, Xu Xiao-Ling, Xu Jian-Guang

机构信息

Center of Rehabilitation Medicine, Yueyang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.

School of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.

出版信息

J Inflamm Res. 2022 Aug 31;15:5009-5026. doi: 10.2147/JIR.S373898. eCollection 2022.


DOI:10.2147/JIR.S373898
PMID:36072777
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9443071/
Abstract

Osteoarthritis (OA) is an inflammatory and degenerative joint disease with severe effects on individuals, society, and the economy that affects millions of elderly people around the world. To date, there are no effective treatments for OA; however, there are some treatments that slow or prevent its progression. Polyfunctional nanosystems have many advantages, such as controlled release, targeted therapy and high loading rate, and have been widely used in OA treatment. Previous mechanistic studies have revealed that inflammation and ROS are interrelated, and a large number of studies have demonstrated that ROS play an important role in different types of OA development. In this review article, we summarize third-generation ROS-sensitive nanomaterials that scavenge excessive ROS from chondrocytes and osteoclasts in vivo. We only focus on polymer-based nanoparticles (NPs) and do not review the effects of drug-loaded or heavy metal NPs. Mounting evidence suggests that polyfunctional nanosystems will be a promising therapeutic strategy in OA therapy due to their unique characteristics of being sensitive to changes in the internal environment.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/9660f15029ea/JIR-15-5009-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/b3d58e6beb77/JIR-15-5009-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/3b79d18bd262/JIR-15-5009-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/668cdd1fabba/JIR-15-5009-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/9660f15029ea/JIR-15-5009-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/b3d58e6beb77/JIR-15-5009-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/3b79d18bd262/JIR-15-5009-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/668cdd1fabba/JIR-15-5009-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1816/9443071/9660f15029ea/JIR-15-5009-g0004.jpg

相似文献

[1]
Recent Advances in Reactive Oxygen Species (ROS)-Responsive Polyfunctional Nanosystems 3.0 for the Treatment of Osteoarthritis.

J Inflamm Res. 2022-8-31

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Fibroblast-Myofibroblast Transition in Osteoarthritis Progression: Current Insights.

Int J Mol Sci. 2025-8-15

[2]
Controlled Stimulus-Responsive Delivery Systems for Osteoarthritis Treatment.

Int J Mol Sci. 2024-11-2

[3]
Nanoparticles and bone microenvironment: a comprehensive review for malignant bone tumor diagnosis and treatment.

Mol Cancer. 2024-11-1

[4]
Fibrotic pathways and fibroblast-like synoviocyte phenotypes in osteoarthritis.

Front Immunol. 2024

本文引用的文献

[1]
Activation and Function of NLRP3 Inflammasome in Bone and Joint-Related Diseases.

Int J Mol Sci. 2022-5-11

[2]
Itaconate attenuates osteoarthritis by inhibiting STING/NF-κB axis in chondrocytes and promoting M2 polarization in macrophages.

Biochem Pharmacol. 2022-4

[3]
Reactive Oxygen Species (ROS)-Responsive Biomaterials for the Treatment of Bone-Related Diseases.

Front Bioeng Biotechnol. 2022-1-11

[4]
Reactive oxygen species (ROS)-responsive nanoprobe for bioimaging and targeting therapy of osteoarthritis.

J Nanobiotechnology. 2021-11-27

[5]
Betaine Attenuates Osteoarthritis by Inhibiting Osteoclastogenesis and Angiogenesis in Subchondral Bone.

Front Pharmacol. 2021-9-29

[6]
Bardoxolone-Methyl Prevents Oxidative Stress-Mediated Apoptosis and Extracellular Matrix Degradation in vitro and Alleviates Osteoarthritis in vivo.

Drug Des Devel Ther. 2021

[7]
Cartilage-targeting poly(ethylene glycol) (PEG)-formononetin (FMN) nanodrug for the treatment of osteoarthritis.

J Nanobiotechnology. 2021-7-3

[8]
ROS-Responsive Boronate-Stabilized Polyphenol-Poloxamer 188 Assembled Dexamethasone Nanodrug for Macrophage Repolarization in Osteoarthritis Treatment.

Adv Healthc Mater. 2021-10

[9]
Targeted apoptosis of macrophages and osteoclasts in arthritic joints is effective against advanced inflammatory arthritis.

Nat Commun. 2021-4-12

[10]
Structural Transformative Antioxidants for Dual-Responsive Anti-Inflammatory Delivery and Photoacoustic Inflammation Imaging.

Angew Chem Int Ed Engl. 2021-6-21

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