首页> 外文期刊>Journal of Analytical Methods in Chemistry >Spectrophotometric Determination of Gemifloxacin Mesylate, Moxifloxacin Hydrochloride, and Enrofloxacin in Pharmaceutical Formulations Using Acid Dyes
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Spectrophotometric Determination of Gemifloxacin Mesylate, Moxifloxacin Hydrochloride, and Enrofloxacin in Pharmaceutical Formulations Using Acid Dyes

机译:用酸性染料分光光度法测定药物制剂中的甲磺酸吉米沙星,盐酸莫西沙星和恩诺沙星

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摘要

Simple, rapid, and extractive spectrophotometric methods were developed for the determination of some fluoroquinolones antibiotics: gemifloxacin mesylate (GMF), moxifloxacin hydrochloride (MXF), and enrofloxacin (ENF) in pure forms and pharmaceutical formulations. These methods are based on the formation of ion-pair complexes between the basic drugs and acid dyes, namely, bromocresol green (BCG), bromocresol purple (BCP), bromophenol blue (BPB), bromothymol blue (BTB), and methyl orange (MO) in acidic buffer solutions. The formed complexes were extracted with chloroform and measured at 420, 408, 416, 415, and 422 nm for BCG, BCP, BPB, BTB, and MO, respectively, for GMF; at 410, 415, 416, and 420 nm for BCP, BTB, BPB, and MO, respectively, for MXF; and at 419 and 414 nm for BCG and BTB, respectively, in case of ENF. The analytical parameters and their effects are investigated. Beer's law was obeyed in the ranges 1.0-30, 1.0-20, and 2.0-24 mu g mL(-1) for GMF, MXF, and ENF, respectively. The proposed methods have been applied successfully for the analysis of the studied drugs in pure forms and pharmaceutical formulations. Statistical comparison of the results with the reference methods showed excellent agreement and indicated no significant difference in accuracy and precision.
机译:开发了用于测定某些氟喹诺酮类抗生素的简单,快速和萃取分光光度法:纯形式和药物制剂中的甲磺酸吉西沙星(GMF),盐酸莫西沙星(MXF)和恩诺沙星(ENF)。这些方法基于基本药物和酸性染料之间的离子对络合物的形成,即溴甲酚绿(BCG),溴甲酚紫(BCP),溴酚蓝(BPB),溴百里酚蓝(BTB)和甲基橙( MO)在酸性缓冲溶液中。形成的复合物用氯仿萃取,对于GCG,BCG,BCP,BPB,BTB和MO分别在420、408、416、415和422 nm处测量。对于MXF,BCP,BTB,BPB和MO分别在410、415、416和420 nm处;对于ENF,BCG和BTB分别在419和414 nm处。分析了分析参数及其影响。对于GMF,MXF和ENF,分别遵循的啤酒定律分别在1.0-30、1.0-20和2.0-24μg mL(-1)范围内。所提出的方法已成功地用于分析纯药物和药物制剂中的药物。结果与参考方法的统计比较显示出极好的一致性,并且在准确性和精密度上没有显着差异。

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