Victorelli Francesca Damiani, Calixto Giovana Maria Fioramonti, Ramos Matheus Aparecido Dos Santos, Bauab Taís Maria, Chorilli Marlus
J Biomed Nanotechnol. 2018 Jan 1;14(1):227-237. doi: 10.1166/jbn.2018.2484.
Staphylococcus aureus is a common gram-positive bacterium of the human skin microbiota. It is also a dangerous pathogen that can cause serious and even lethal skin infections. The topical administration of metronidazole via nanotechnology-based drug delivery systems, such as liquid crystalline systems, can modulate both the drug permeation and activity, decreasing its side effects and increasing the drug potent activity against the gram-positive bacteria. This study aimed at: (1) structurally developing and characterizing a liquid crystalline systems composed of chitosan and polyethyleneimine dispersion as the aqueous phase, oleic acid as the oily phase, and ethoxylated and propoxylated cetyl alcohol as the surfactant (FPC) for metronidazole incorporation (0.5% w/w); (2) evaluating the in vitro release and skin permeation and retention properties of the metronidazole-loaded liquid crystalline systems (FPC-M); (3) investigating the in vitro antibacterial activity of FPC-M against Staphylococcus aureus. Polarised light microscopy indicated that both FPC and FPC-M are hexagonal systems. Rheological, texture, and bioadhesion assays showed that both are elastic and bioadhesive systems. According to the results of the in vitro release, permeation, and retention assays, FPC can modulate metronidazole release and allow metronidazole to stay for a longer time on the skin. The determination of FPC-M activity against Staphylococcus aureus showed that it could target the bacterial cell. In conclusion, the liquid crystalline systems developed in this study can improve the clinical performance of metronidazole in the treatment of staphylococcal skin infections.
金黄色葡萄球菌是人类皮肤微生物群中一种常见的革兰氏阳性细菌。它也是一种危险的病原体,可引起严重甚至致命的皮肤感染。通过基于纳米技术的药物递送系统(如液晶系统)局部施用甲硝唑,可以调节药物的渗透和活性,减少其副作用,并增强药物对革兰氏阳性菌的有效活性。本研究旨在:(1)在结构上开发并表征一种液晶系统,该系统以壳聚糖和聚乙烯亚胺分散体为水相,油酸为油相,乙氧基化和丙氧基化十六醇为表面活性剂(FPC)用于掺入甲硝唑(0.5% w/w);(2)评估负载甲硝唑的液晶系统(FPC-M)的体外释放、皮肤渗透和滞留特性;(3)研究FPC-M对金黄色葡萄球菌的体外抗菌活性。偏光显微镜显示FPC和FPC-M均为六方系统。流变学、质地和生物粘附测定表明两者均为弹性和生物粘附系统。根据体外释放、渗透和滞留测定的结果,FPC可以调节甲硝唑的释放,并使甲硝唑在皮肤上停留更长时间。对FPC-M对金黄色葡萄球菌活性的测定表明它可以靶向细菌细胞。总之,本研究中开发的液晶系统可以改善甲硝唑在治疗葡萄球菌皮肤感染中的临床性能。