Zhao Zhiwei, Yan Rong, Wang Jianhao, Wu Hao, Wang Yanhao, Chen Aihong, Shao Shilong, Li Yong-Qiang
School of Radiation Medicine and Protection, Medical College of Soochow University, Collaborative Innovation Center of Radiological Medicine of Jiangsu Higher Education Institutions, Suzhou 215123, China.
J Mater Chem B. 2017 May 21;5(19):3572-3579. doi: 10.1039/c7tb00199a. Epub 2017 Apr 26.
In this study, we present a novel and robust strategy to develop a bacteria-activated photodynamic nanosystem based on polyelectrolyte-coated silica nanoparticles modified with chlorin e6 photosensitizer. Due to the aggregation of chlorin e6 on silica nanoparticles to induce excited-state quenching, the fluorescence and singlet oxygen generation of the obtained nanosystem are quenched. We demonstrate that polyelectrolyte-chlorin e6 complexes can be effectively extracted, by bacteria, from silica nanoparticles and form stable binding on the bacterial surface, changing the aggregation state of chlorin e6 and leading to the recovery of fluorescence and singlet oxygen generation. Based on this activatable photodynamic nanosystem, complete elimination of methicillin-resistant Staphylococcus aureus (MRSA) is achieved via a mechanism involving cell wall and membrane disruption, showing great potential to combat drug-resistant bacterial infections in clinical settings. Different from the bacterial enzyme-activated photodynamic systems responsive to specific bacterial strains, our activatable nanosystem exerts a broad-spectrum bacteria-triggered photodynamic effect by exploiting the unique charge characteristics of the cell envelope structure of bacteria. More importantly, we believe that the mechanism of bacteria-triggered polyelectrolyte dissociation from nanoparticles proposed in this work could be further used as a general strategy for the fabrication of bacteria-responsive multifunctional nanomaterials.
在本研究中,我们提出了一种新颖且稳健的策略,以开发一种基于用二氢卟吩e6光敏剂修饰的聚电解质包覆二氧化硅纳米颗粒的细菌激活光动力纳米系统。由于二氢卟吩e6在二氧化硅纳米颗粒上聚集导致激发态猝灭,所得纳米系统的荧光和单线态氧生成被猝灭。我们证明,聚电解质 - 二氢卟吩e6复合物可被细菌有效地从二氧化硅纳米颗粒中提取出来,并在细菌表面形成稳定结合,改变二氢卟吩e6的聚集状态,从而导致荧光和单线态氧生成的恢复。基于这种可激活的光动力纳米系统,通过涉及细胞壁和细胞膜破坏的机制实现了对耐甲氧西林金黄色葡萄球菌(MRSA)的完全消除,在临床环境中对抗耐药细菌感染显示出巨大潜力。与响应特定细菌菌株的细菌酶激活光动力系统不同,我们的可激活纳米系统通过利用细菌细胞膜结构独特的电荷特性发挥广谱细菌触发的光动力效应。更重要的是,我们认为这项工作中提出的细菌触发聚电解质从纳米颗粒解离的机制可进一步用作制造细菌响应多功能纳米材料的通用策略。