Potential effect of cationic liposomes on interactions with oral bacterial cells and biofilms

脂质体 阳离子脂质体 生物膜 阳离子聚合 Zeta电位 生物物理学 表面电荷 变形链球菌 化学 药物输送 细菌 材料科学 生物化学 纳米技术 生物 纳米颗粒 有机化学 转染 基因 物理化学 遗传学
作者
Marika Sugano,Hirobumi Morisaki,Yoichi Negishi,Yoko Endo‐Takahashi,Hirotaka Kuwata,Takashi Miyazaki,Masahide Yamamoto
出处
期刊:Journal of Liposome Research [Taylor & Francis]
卷期号:: 1-7 被引量:24
标识
DOI:10.3109/08982104.2015.1063648
摘要

Although oral infectious diseases have been attributed to bacteria, drug treatments remain ineffective because bacteria and their products exist as biofilms. Cationic liposomes have been suggested to electrostatically interact with the negative charge on the bacterial surface, thereby improving the effects of conventional drug therapies. However, the electrostatic interaction between oral bacteria and cationic liposomes has not yet been examined in detail.The aim of the present study was to examine the behavior of cationic liposomes and Streptococcus mutans in planktonic cells and biofilms.Liposomes with or without cationic lipid were prepared using a reverse-phase evaporation method. The zeta potentials of conventional liposomes (without cationic lipid) and cationic liposomes were -13 and 8 mV, respectively, and both had a mean particle size of approximately 180 nm. We first assessed the interaction between liposomes and planktonic bacterial cells with a flow cytometer. We then used a surface plasmon resonance method to examine the binding of liposomes to biofilms. We confirmed the binding behavior of liposomes with biofilms using confocal laser scanning microscopy.The interactions between cationic liposomes and S. mutans cells and biofilms were stronger than those of conventional liposomes. Microscopic observations revealed that many cationic liposomes interacted with the bacterial mass and penetrated the deep layers of biofilms.In this study, we demonstrated that cationic liposomes had higher affinity not only to oral bacterial cells, but also biofilms than conventional liposomes. This electrostatic interaction may be useful as a potential drug delivery system to biofilms.
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