Issue 11, 2026, Issue in Progress

Injectable ε-poly-lysine/hyaluronic acid hydrogel for targeted prevention of cardiovascular implantable electronic device pocket infections

Abstract

Cardiovascular implantable electronic device (CIED) pocket infections represent a grave threat to the survival quality and life safety of patients with cardiovascular diseases, while also imposing a substantial economic burden on healthcare systems. However, the efficacy of current approaches employed for preventing CIED pocket infections remains suboptimal. In this study, an injectable antibacterial hydrogel was successfully constructed by physically crosslinking carboxyl groups on the surface of hyaluronic acid microspheres (HAG) with amino groups on poly-L-lysine (PLL). The developed HAG/PLL hydrogel exhibited not only non-toxicity toward L929 cells but also excellent cytocompatibility, accompanied by a low hemolysis rate when tested with red blood cells. Furthermore, in vivo experiments demonstrated that the HAG/PLL hydrogel showed no toxicity to vital organs (including the heart, liver, and kidney) as well as local tissues at the implantation site. Moreover, the HAG/PLL hydrogel effectively eliminated Staphylococcus aureus and Escherichia coli bacteria by promoting ROS production, thereby inducing bacterial cell membrane disruption. In conclusion, HAG/PLL hydrogels were simply and conveniently prepared and showed considerable potential in the prevention of CIED infections owing to their excellent biocompatibility and antimicrobial properties.

Graphical abstract: Injectable ε-poly-lysine/hyaluronic acid hydrogel for targeted prevention of cardiovascular implantable electronic device pocket infections

Article information

Article type
Paper
Submitted
05 Nov 2025
Accepted
09 Feb 2026
First published
17 Feb 2026
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2026,16, 9440-9454

Injectable ε-poly-lysine/hyaluronic acid hydrogel for targeted prevention of cardiovascular implantable electronic device pocket infections

J. Liu, Z. Cheng, P. Zhao, Y. Wu, L. Zhu, C. Yu, W. Zhou, T. Wang, X. Cheng, Q. Dong and H. Bao, RSC Adv., 2026, 16, 9440 DOI: 10.1039/D5RA08511J

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