Liu Bo, Li Jianghua, Zhang Zhongtian, Roland James D, Lee Bruce P
Department of Biomedical Engineering, Michigan Technological University, Houghton, Michigan 49931, United States.
Hunan Key Laboratory of Micro & Nano Materials Interface Science, College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
Chem Eng J. 2022 Aug 1;441. doi: 10.1016/j.cej.2022.135808. Epub 2022 Mar 16.
Bacteria such as Methicillin-resistant (MRSA) causes acidic microenvironment during infection. A biomaterial that exhibits tunable antimicrobial property in a pH dependent manner is potentially attractive. Herein, we presented a novel antibacterial hydrogel consisting of pH responsive and reversible catechol-boronate linkage formed between intrinsically bactericidal chlorinated catechol (catechol-Cl) and phenylboronic acid. Fourier transformed infrared spectroscopy (FTIR), oscillatory rheometry, and Johnson Kendall Roberts (JKR) contact mechanics testing confirmed the formation and dissociation of the complex in a pH dependent manner. When the hydrogel was treated with an acidic buffer (pH 3), the hydrogel exhibited excellent antimicrobial property against multiple strains of Gram-positive and negative bacteria including MRSA (up to 4 log reduction from 10 colony forming units/mL). At an acidic pH, catechol-Cl was unbound from the phenylboronic acid and available for killing bacteria. Conversely, when the hydrogel was treated with a basic buffer (pH 8.5), the hydrogel lost its antimicrobial property but also became non-cytotoxic. At a basic pH, the formation of catechol-boronate complex effectively reduce the exposure of the cytotoxic catechol-Cl to the surrounding. When further incubating the hydrogel in an acidic pH, the reversible complex dissociated to re-expose catechol-Cl and the hydrogel recovered its antibacterial property. Overall, the combination of catechol-Cl and phenylboronic acid provide a new strategy for designing hydrogels with pH responsive antibacterial activity and reduced cytotoxicity.
耐甲氧西林金黄色葡萄球菌(MRSA)等细菌在感染过程中会导致酸性微环境。一种能以pH依赖方式展现出可调节抗菌性能的生物材料具有潜在吸引力。在此,我们展示了一种新型抗菌水凝胶,它由具有杀菌作用的氯化儿茶酚(儿茶酚-Cl)与苯硼酸之间形成的pH响应且可逆的儿茶酚-硼酸酯键组成。傅里叶变换红外光谱(FTIR)、振荡流变学和约翰逊-肯德尔-罗伯茨(JKR)接触力学测试证实了该复合物以pH依赖方式形成和解离。当水凝胶用酸性缓冲液(pH 3)处理时,它对包括MRSA在内的多种革兰氏阳性和阴性细菌菌株表现出优异的抗菌性能(从10个菌落形成单位/毫升最多可减少4个对数级)。在酸性pH条件下,儿茶酚-Cl与苯硼酸解离并可用于杀灭细菌。相反,当水凝胶用碱性缓冲液(pH 8.5)处理时,水凝胶失去其抗菌性能,但也变得无细胞毒性。在碱性pH条件下,儿茶酚-硼酸酯复合物的形成有效减少了细胞毒性的儿茶酚-Cl对周围环境的暴露。当将水凝胶在酸性pH条件下进一步孵育时,可逆复合物解离,儿茶酚-Cl重新暴露,水凝胶恢复其抗菌性能。总体而言,儿茶酚-Cl和苯硼酸的组合为设计具有pH响应抗菌活性和降低细胞毒性的水凝胶提供了一种新策略。