数字农科院2.0

Aggregation-Induced Emission Ionic Liquids for Bacterial Imaging, Biofilm Inhibition, and Mixed Bacterial Infection Wound Healing

文献类型: 外文期刊

作者: Gao, Chenxi;Fu, Lei;Wang, Juanjuan;Chu, Yuefeng;Gao, Luyao;Qiu, Hongdeng;Chen, Jia

作者机构:

关键词: Ionic liquids;Aggregation-induced emission;Bacterial imaging;Biofilm inhibition;Woundhealing

期刊名称: CHEMICAL & BIOMEDICAL IMAGING

ISSN: 2832-3637

年卷期: 2025 年

页码:

收录情况: CSCD(2025-2026年度) ; ; ESCI(2025版)

摘要: The excessive utilization of antibiotics escalates the susceptibility to bacterial infections in the general populace. The misuse of antibiotics and the emergence of bacterial resistance can be effectively regulated through the implementation of bacterial detection technology. Therefore, the construction of a multifunctional platform for bacterial detection and removal holds immense significance. In this research, we have effectively developed an imidazolium ionic liquid (TPE-IL) based on the tetraphenylethylene (TPE) structure with aggregation-induced emission (AIE), enabling effective bacterial imaging, biofilm inhibition, and mixed bacterial infection wound healing. TPE-IL effectively targets and penetrates bacterial surfaces via the electrostatic interactions of its imidazole groups and the hydrophobic interactions of its alkyl chains. This dual-action mechanism not only enhances fluorescence emission from the bacterial surface, enabling precise bacterial imaging, but also exhibits significant bactericidal activity. TPE-IL revealed superior antibacterial activity against both Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). The in vitro anti-biofilm experiments demonstrated that TPE-IL exhibited remarkable inhibitory effects on biofilms formed by S. aureus and E. coli. The in vivo antibacterial experiments confirmed the potent in vivo bactericidal activity of TPE-IL, which significantly reduced inflammatory responses, enhanced collagen deposition, and promoted wound healing without inducing organ damage in mice. Moreover, TPE-IL displayed low cytotoxicity and hemolysis rate. This work has successfully developed a safe and effective platform for bacterial identification and antimicrobial treatment, thereby offering significant implications in addressing the challenges associated with antibiotic resistance and misuse.

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