Novel Facile Nanoformulation of levofloxacin quinolone antibiotic

U. Haroon, Asra Mustafa, S. Gul
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Abstract

In this study, new levofloxacin loaded mesoporous silica nanoparticles were prepared by sol–gel technique using tetraethyl orthosilicate (TEOS) as silica precursor and cetyltrimethylammonium bromide (CTAB) as pore generating agent. The synthesis conditions were tailored by varying the molar ratio of water, NaOH and amount of CTAB used. The synthesized silica carriers were characterized by Scanning Electron Microscope (SEM) which showed that spherical particles with an average size between 80-87 nm were prepared. UV and Infra Red Spectroscopy (FTIR) confirmed the formation of levofloxacin-nano particulate system and showed the participation of carboxylic group in the synthetic process. It is envisaged that nano based drug delivery of levofloxacin would serve as a promising and innovative tool against resistant bacterial infection. Keywords: Levofloxacin, Nanoparticles, cetyltrimethylammonium bromide, sol–gel
新型纳米左氧氟沙星喹诺酮类抗生素的制备
以正硅酸四乙酯(TEOS)为硅前驱体,十六烷基三甲基溴化铵(CTAB)为生孔剂,采用溶胶-凝胶法制备了新型负载左氧氟沙星的介孔二氧化硅纳米颗粒。通过改变水、NaOH的摩尔比和CTAB的用量来调整合成条件。通过扫描电子显微镜(SEM)对所合成的二氧化硅载体进行了表征,结果表明所制备的二氧化硅载体平均粒径在80 ~ 87 nm之间。紫外和红外光谱(FTIR)证实了左氧氟沙星纳米颗粒体系的形成,并表明羧基参与了合成过程。预计左氧氟沙星纳米药物递送将成为一种有前途的创新工具,用于抵抗耐药细菌感染。关键词:左氧氟沙星,纳米颗粒,十六烷基三甲基溴化铵,溶胶-凝胶
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