Zwitterion‐Lubricated Hydrogel Microspheres Encapsulated with Metformin Ameliorate Age‐Associated Osteoarthritis

Author:

Hou Jiahui12ORCID,Lin Yanpeng3,Zhu Chencheng12,Chen Yupeng45,Lin Rongmin12,Lin Hancheng12,Liu Dahai6,Guan Daogang45,Yu Bin12,Wang Jun6,Wu Hangtian12,Cui Zhuang12ORCID

Affiliation:

1. Devision of Orthopaedics and Traumatology Department of Orthopaedics Nanfang Hospital Southern Medical University Guangzhou Guangdong 510515 China

2. Guangdong Provincial Key Laboratory of Bone and Cartilage Regeneration Medicine Nanfang Hospital Southern Medical University Guangzhou Guangdong 510515 China

3. Department of Radiology Nanfang Hospital Southern Medical University Guangzhou Guangdong 510515 China

4. Department of Biochemistry and Molecular Biology School of Basic Medical Sciences Southern Medical University Guangzhou Guangdong 510515 China

5. Guangdong Provincial Key Laboratory of Single Cell Technology and Application Southern Medical University Guangzhou Guangdong 510515 China

6. School of Medicine Foshan University Foshan Guangdong 528000 China

Abstract

AbstractChondrocyte senescence and reduced lubrication play pivotal roles in the pathogenesis of age‐related osteoarthritis (OA). In the present study, highly lubricated and drug‐loaded hydrogel microspheres are designed and fabricated through the radical polymerization of sulfobetaine (SB)‐modified hyaluronic acid methacrylate using microfluidic technology. The copolymer contains a large number of SB and carboxyl groups that can provide a high degree of lubrication through hydration and form electrostatic loading interactions with metformin (Met@SBHA), producing a high drug load for anti‐chondrocyte senescence. Mechanical, tribological, and drug release analyses demonstrated enhanced lubricative properties and prolonged drug dissemination of the Met@SBHA microspheres. RNA sequencing (RNA‐seq) analysis, network pharmacology, and in vitro assays revealed the extraordinary capacity of Met@SBHA to combat chondrocyte senescence. Additionally, inducible nitric oxide synthase (iNOS) has been identified as a promising protein modulated by Met in senescent chondrocytes, thereby exerting a significant influence on the iNOS/ONOO‐/P53 pathway. Notably, the intra‐articular administration of Met@SBHA in aged mice ameliorated cartilage senescence and OA pathogenesis. Based on the findings of this study, Met@SBHA emerges as an innovative and promising strategy in tackling age‐related OA serving the dual function of enhancing joint lubrication and mitigating cartilage senescence.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Wiley

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