Li Peili, Liu Shuai, Zhang Gaoke, Yang Xu, Cao Weiwei, Gong Xuedong, Xing Xiaodong
School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
ACS Appl Bio Mater. 2020 Feb 17;3(2):1105-1115. doi: 10.1021/acsabm.9b01053. Epub 2020 Feb 5.
Bacterial biofilm poses a serious threat to human health, leading to increased and prolonged bacterial infections. How to solve the problem of eliminating biofilms effectively and rapidly while being nontoxic to normal cells is still a challenge. Here, we design a pH-sensitive anti-biofilm nanosystem formed by self-assembly between negatively charged carboxyl groups of poly(ethylene glycol_-COOH-polyethylenimine-2,3-dimethylmaleic anhydride (PPD) and positively charged amines on the surface of carbon dots derived from the ashes of calcined l-lysine powder (CD) (PPD@CD for short). The outmost copolymer could make PPD@CD facilely diffuse into the dense biofilm and reverse to be positively charged via hydrolysis, which lead to the acid-triggered disassembly of the nanosystem. After hydrolyzation, PPD would turn into a biocidal cationic polymer, which is prone to attaching on bacteria inside the biofilm and efficiently killing them. In addition, the released CD could induce intracellular reactive oxygen species (ROS) across the whole biofilm to degrade the matrix of extracellular polymer substances and kill resident bacteria deep into the biofilm. Finally, the prepared nanosystem effectively inhibits the formation of biofilm and rapidly destroys the mature biofilm by the synergy antibacterial effects of the cation and ROS. We also evaluate the biocompatibility of the nanocomposites. The results show that PPD@CQD has no toxicity to L929 and 3T3 cells and exhibits a zero hemolytic rate even when the concentration is up to 2000 μg/mL. The outstanding biocompatibility coupled with rapid anti-biofilm ability of the nanosystem presents an opportunity for it to be utilized as an effective pH-responsive and targetable anti-biofilm agent for controlling bacterial infections.
细菌生物膜对人类健康构成严重威胁,导致细菌感染增加且持续时间延长。如何有效且快速地解决消除生物膜的问题,同时对正常细胞无毒,仍是一项挑战。在此,我们设计了一种pH敏感的抗生物膜纳米系统,它由聚(乙二醇)-COOH-聚乙烯亚胺-2,3-二甲基马来酸酐(PPD)带负电荷的羧基与源自煅烧l-赖氨酸粉末灰烬的碳点(CD)表面带正电荷的胺之间自组装形成(简称为PPD@CD)。最外层的共聚物可使PPD@CD轻松扩散到致密的生物膜中,并通过水解转变为带正电荷,这导致纳米系统的酸触发解离。水解后,PPD会变成一种杀菌阳离子聚合物,易于附着在生物膜内的细菌上并有效杀死它们。此外,释放出的CD可诱导整个生物膜内的细胞内活性氧(ROS),以降解细胞外聚合物物质的基质并杀死生物膜深处的驻留细菌。最后,所制备的纳米系统通过阳离子和ROS的协同抗菌作用,有效抑制生物膜的形成并快速破坏成熟生物膜。我们还评估了纳米复合材料的生物相容性。结果表明,PPD@CQD对L929和3T3细胞无毒,即使浓度高达2000μg/mL时溶血率也为零。纳米系统出色的生物相容性与快速的抗生物膜能力为其作为一种有效的pH响应和靶向抗生物膜剂用于控制细菌感染提供了机会。