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Updated: May 11, 2026
In Vivo Imaging of Reactive Oxygen Species in a Murine Wound Model
Published on: November 17, 2018
Zn ion-incorporated injected hydrogels with reactive oxygen species and glucose scavenging capacity for diabetic
Sicong Chen1,2, Jiajun Qiu2, Shuhan Chen2
1College of Material Science and Engineering, Hunan University, No. 2 Lushan South Road, Yuelu District, Changsha, Hunan 410082, P. R. China.
Background:
Patients with diabetic wounds often experience challenges in the repair process, owing to increased concentration of glucose and reactive oxygen species (ROS). In addition, high glucose levels usually result in bacterial infections, which in turn worsen wound healing. This study aims to develop a multifunctional hydrogel with integrated antibacterial activity, ROS scavenging, and glucose-responsive properties to accelerate healing of infected diabetic wounds.
Methods:
A Zn ion-incorporated injected hydrogel was prepared using 4-carboxyphenylboronic acid-modified gelatine, tannic acid, and zinc ions. The spectra were detected using a Fourier transform infrared spectrometer and surface morphologies of hydrogels were obtained using a scanning electron microscopy. The release behavior of Zn ions was investigated using an inductively coupled plasma mass spectrometry instrument. To evaluate the antimicrobial properties of the GPT and GPT@Zn hydrogels, strains of Escherichia coli and Staphylococcus aureus were utilized. Cytocompatibility was evaluated using mouse fibroblasts (L929 cells) and human umbilical vein endothelial cells (HUVECs). Finally, diabetic wound models were constructed in rats to evaluate the effects of hydrogels on wound healing.
Results:
The results show that the hydrogels are injectable and have self-healing properties. Moreover, borate ester bonds are formed in the hydrogels, which are responsive to H2O2 and glucose and can eliminate them. At the same time, zinc ions were released, giving the hydrogels good antibacterial efficacy, with antibacterial rates of 99.7% and 99.9% against S. aureus and E. coli, respectively. Furthermore, the hydrogels demonstrated good cell compatibility with L929 cells and HUVECs and increased the gene expression of VEGF, COL I, and COL III because of the addition of zinc ions. Based on the ROS, glucose scavenging capacity, and biological functions of zinc ions, the hydrogels advanced the recovery of S. aureus-contaminated whole skin wounds in diabetic rats.
Conclusions:
This study provides a novel treatment strategy for diabetic wound healing by constructing Zn ion-incorporated injected hydrogels with reactive oxygen species and glucose-scavenging capacity.
