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Research Article | Open Access

Enhancing diabetic muscle repair through W-GA nanodots: a nanomedicinal approach to ameliorate myopathy in type 2 diabetes

Shan Liu1,‡, Renwen Wan2,‡, QingRong Li3,‡, Yisheng Chen2, Yanwei He2, Xingting Feng2,  Yung Patrick Shu-Hang4( ), Zhiwen Luo2,‡ ( ), Xianwen Wang3 ( ), Chen Chen5( )
Department of Endocrinology, Huashan Hospital, Fudan University, No. 12. Middle Wulumuqi Road, Jingan District, Shanghai 20040, China
Department of Sports Medicine, Huashan Hospital, Fudan University, No. 12. Middle Wulumuqi Road, Jingan District, Shanghai 200040, China
School of Biomedical Engineering, No. 81 Meishan Road, Shushan District, Anhui Medical University, Hefei 230032, China
Department of Orthopaedics and Traumatology, Faculty of Medicine, The Chinese University of Hong Kong, Shatin 999077, Hong Kong
Department of Arthroscopic Surgery, Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, No. 600 Yishan Road, Xuhui District, Shanghai 200233, China

‡Shan Liu, Renwen Wan, QingRong Li and Zhiwen Luo made equal contributions to this work.

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Abstract

Objective

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder that significantly impairs muscle regeneration following injuries, contributing to numerous complications and reduced quality of life. There is an urgent need for therapeutic strategies that can enhance muscle regeneration and alleviate these pathological mechanisms. In this study, we evaluate the therapeutic efficacy of W-GA nanodots, which are composed of gallic acid (GA) and tungstate (W6+), on muscle regeneration in type 2 diabetes mellitus (T2D)-induced muscle injury, with a focus on their anti-inflammatory and antioxidative effects.

Methods

This study synthesized ultrasmall W-GA nanodots that were optimized for improved stability and bioactivity under physiological conditions. In vitro assessments included cell viability, apoptosis, reactive oxygen species (ROS) generation, and myotube differentiation in C2C12 myoblasts under hyperglycemic conditions. In vivo, T2D was induced in C57BL/6 mice, followed by muscle injury and treatment with W-GA. Muscle repair, fibrosis, and functional recovery were assessed through histological analysis and gait analysis using the CatWalk system.

Results

The W-GA nanodots significantly enhanced muscle cell proliferation, decreased ROS, and reduced apoptosis in vitro. In vivo, compared with the control group, the W-GA-treated group exhibited notably improved muscle regeneration, decreased fibrosis, and enhanced functional recovery. The treatment notably modulated the inflammatory response and oxidative stress in diabetic muscle tissues, facilitating improved regenerative dynamics and muscle function.

Conclusions

W-GA nanodots effectively counter the pathological mechanisms of diabetic myopathy by enhancing regenerative capacity and reducing oxidative stress and inflammation. This nanomedicine approach offers a promising therapeutic avenue for improving muscle health and overall quality of life in individuals suffering from T2D. However, further studies are needed to explore the clinical applications and long-term efficacy of these nanodots in preventing diabetic complications.

References

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Burns & Trauma
Article number: tkae059

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Cite this article:
Liu S, Wan R, Li Q, et al. Enhancing diabetic muscle repair through W-GA nanodots: a nanomedicinal approach to ameliorate myopathy in type 2 diabetes. Burns & Trauma, 2025, 13(3): tkae059. https://doi.org/10.1093/burnst/tkae059

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Received: 11 May 2024
Revised: 22 August 2024
Accepted: 24 August 2024
Published: 10 October 2026
© The Author(s) 2025. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.