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载瑞香素泊洛沙姆/聚乙烯吡咯烷酮热敏水凝胶的制备及抗菌活性评价

Preparation and Antibacterial Activity Evaluation of Daphnetin-Loaded Poloxamers/Polyvinylpyrrolidone Thermosensitive Hydrogels.

作者信息

Fan Junhong, An Fengli, Li Shaohua, Guo Yuqin, Zhang Haolan, Zhang Yaxin, Cao Yujie, Yu Lan

机构信息

School of Pharmacy, Lanzhou University, Lanzhou 730000, China.

出版信息

ACS Appl Bio Mater. 2025 Jan 20;8(1):374-385. doi: 10.1021/acsabm.4c01348. Epub 2024 Dec 12.

Abstract

Antibiotic misuse and bacterial resistance are pressing issues threatening public health. Natural plant extracts with bactericidal properties offer potential alternatives to reduce or replace antibiotic use. This study aims to develop a thermosensitive hydrogel containing daphnetin (DAP-TG) using poloxamers 407 (P407), polyvinylpyrrolidone (PVP), and poloxamers 188 (P188). We systematically evaluated the gel's antibacterial activity against () and (), as well as its antibacterial mechanisms. By examining the gelation temperature and time, degradation time, and in vitro release performance of DAP-TG, we produced a sustained-release DAP-TG with a rapid phase transition at (31.6 ± 0.1) °C. Its structure was characterized through Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). The results indicated that the DAP thermosensitive hydrogel was formed and presented a 3D network spatial structure. The biocompatibility of DAP-TG was explored through the hemolysis test and cytotoxicity test. The results indicated that DAP-TG possessed excellent biocompatibility. The antibacterial efficacy of DAP-TG against and was assessed using minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), growth curve, and inhibition zone tests. Results showed that DAP-TG exhibited excellent antibacterial activity against both and , with MIC values of 1.28 and 0.32 mg/mL. The antibacterial mechanism of DAP-TG was preliminarily explored through the investigation of bacterial cell content leakage, AKP leakage, membrane permeability, SEM, ROS production, and biofilm inhibition activity. DAP-TG induced irreversible damage to the cell membranes of and , resulting in enhanced permeability, elevated ROS levels, and inhibited biofilm formation. Our study indicates that DAP-TG exhibits effective sustained-release and antibacterial properties against and in vitro, making it a promising candidate for antibacterial applications in food and pharmaceutical products.

摘要

抗生素的滥用和细菌耐药性是威胁公众健康的紧迫问题。具有杀菌特性的天然植物提取物为减少或替代抗生素的使用提供了潜在的替代方案。本研究旨在使用泊洛沙姆407(P407)、聚乙烯吡咯烷酮(PVP)和泊洛沙姆188(P188)开发一种含有瑞香素的热敏水凝胶(DAP-TG)。我们系统地评估了该凝胶对()和()的抗菌活性及其抗菌机制。通过考察DAP-TG的凝胶化温度和时间、降解时间以及体外释放性能,我们制备了一种在(31.6±0.1)℃具有快速相转变的缓释DAP-TG。通过傅里叶变换红外(FTIR)光谱和扫描电子显微镜(SEM)对其结构进行了表征。结果表明,形成了DAP热敏水凝胶并呈现出三维网络空间结构。通过溶血试验和细胞毒性试验探索了DAP-TG的生物相容性。结果表明,DAP-TG具有优异的生物相容性。使用最低抑菌浓度(MIC)、最低杀菌浓度(MBC)、生长曲线和抑菌圈试验评估了DAP-TG对()和()的抗菌效果。结果表明,DAP-TG对()和()均表现出优异的抗菌活性,MIC值分别为1.28和0.32mg/mL。通过研究细菌细胞内容物泄漏、碱性磷酸酶(AKP)泄漏、膜通透性、SEM、活性氧(ROS)产生和生物膜抑制活性,初步探索了DAP-TG的抗菌机制。DAP-TG对()和()的细胞膜造成了不可逆的损伤,导致通透性增强、ROS水平升高并抑制生物膜形成。我们的研究表明,DAP-TG在体外对()和()表现出有效的缓释和抗菌性能,使其成为食品和药品抗菌应用的有前途的候选者。

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