# Ultrasound-activated UiO-66 enables ROS-mediated antibacterial therapy and accelerates diabetic wound healing

**Authors:** Chuanwei Sun, Gaoquan Zheng, Yingying Zhao, Zuan Liu, Zhihui Jiang, Jiongliang Li, Chongquan Huang, Yuan Yan, Wen Lai, Zhifeng Huang, Lidan Liu, Feng Peng, Yu Zhang

PMC · DOI: 10.1093/rb/rbag012 · Regenerative Biomaterials · 2026-02-02

## TL;DR

This study shows that unmodified UiO-66, a metal-organic framework, can be used with ultrasound to kill bacteria and speed up wound healing in diabetic mice.

## Contribution

Pristine UiO-66 is introduced as a first-of-its-kind sonodynamic therapy platform for dual antibacterial and pro-regenerative wound healing.

## Key findings

- UiO-66 generates reactive oxygen species under ultrasound, effectively killing bacteria in vitro and in vivo.
- UiO-66 promotes cell proliferation and migration of HUVECs and L929 fibroblasts, aiding tissue repair.
- In diabetic mice, UiO-66 reduces bacterial load and accelerates wound closure in infected wounds.

## Abstract

The development of noninvasive and dual-functional therapeutic strategies is of critical importance for the treatment of infected diabetic wounds, which require both effective bacterial eradication and enhanced tissue regeneration. Conventional approaches are frequently constrained by single-function modalities or adverse side effects, emphasizing the demand for safer and more versatile alternatives. In this study, we demonstrate for the first time that pristine UiO-66, a metal–organic framework without surface modification, can serve as a novel nanoplatform for sonodynamic therapy (SDT), simultaneously achieving antibacterial and pro-regenerative effects. Comprehensive structural and photochemical analyses reveal that UiO-66 efficiently generates reactive oxygen species (ROS) under ultrasound irradiation, which endow it with broad-spectrum antibacterial capacity. These effects are validated by in vitro plate-count assays and RNA sequencing analysis. In parallel, UiO-66 exhibits excellent biocompatibility and significantly promotes the proliferation and migration of HUVECs and L929 fibroblasts, underscoring its potential to facilitate tissue repair. Importantly, in a diabetic mouse model of Staphylococcus aureus-infected wounds, UiO-66-mediated SDT markedly reduces bacterial burden and accelerates wound closure. Collectively, this work establishes pristine UiO-66 as a sonodynamically activated dual-functional therapeutic platform, offering a promising paradigm for integrated infection control and tissue regeneration in chronic wound management, and highlighting its translational potential in clinical wound care.

## Linked entities

- **Chemicals:** UiO-66 (PubChem CID 145926330)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** diabetic (MESH:D003920), infected (MESH:D007239)
- **Chemicals:** UiO-66 (MESH:C000711576), metal (MESH:D008670), ROS (MESH:D017382)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Staphylococcus aureus (species) [taxon 1280]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13012228/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC13012228/full.md

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Source: https://tomesphere.com/paper/PMC13012228