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Preparative resolution of gatifloxacin enantiomers with pre-column esterification strategy and comparing their enantioselectivity to bacteria and antibody / 生物医学与环境科学(英文)
Article in English | WPRIM (Western Pacific) | ID: wpr-264605
Responsible library: WPRO
ABSTRACT
Gatifloxacin (GFX) is a kind of chiral fluoroquinolones compound due to the methyl group at the C-3 position of the piperazine ring[1]. Although the enantiomers of GFX show similar levels of antimicrobial activity and pharmacokinetics[2], the other biological activities (i.e., toxicity or enantioselective recognition to various receptors in vivo) of GFX enantiomers have not yet been studied. With this in mind, we developed a rapid and cost-effective high performance liquid chromatographic (HPLC) separation procedure for GFX enantiomers with a pre-column esterification strategy. With significant enhancement of drug solubility and optimization for chromatographic conditions, the proposed method was scaled up to preparative HPLC to obtain optical active S-(-)- and R-(+)-GFX. The antibacterial activities of GFX enantiomers after preparative separation were further verified by measuring the Minimum Inhibitory Concentration (MIC) values against Escherichia coli ATCC 25922. In addition, the binding selectivity of GFX enantiomers to protein receptor were evaluated by antibody using enzyme-linked immunosorbent assay (ELISA) for the first time.
Subject(s)
Full text: Available Health context: Neglected Diseases Health problem: Neglected Diseases / Zoonoses Database: WPRIM (Western Pacific) Main subject: Pharmacology / Structure-Activity Relationship / Molecular Structure / Microbial Sensitivity Tests / Chemistry / Fluoroquinolones / Escherichia coli / Esterification / Anti-Bacterial Agents Language: English Journal: Biomedical and Environmental Sciences Year: 2015 Document type: Article
Full text: Available Health context: Neglected Diseases Health problem: Neglected Diseases / Zoonoses Database: WPRIM (Western Pacific) Main subject: Pharmacology / Structure-Activity Relationship / Molecular Structure / Microbial Sensitivity Tests / Chemistry / Fluoroquinolones / Escherichia coli / Esterification / Anti-Bacterial Agents Language: English Journal: Biomedical and Environmental Sciences Year: 2015 Document type: Article
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