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Spectrophotometric Determination of Some Fluoroquinolone Antibacterials through Charge-transfer and Ion-pair Complexation Reactions

机译:通过电荷转移和离子对络合反应光度法测定某些氟喹诺酮类抗生素

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Two simple, rapid and sensitive spectrophotometric methods for the determination of three fluoroquinolones, namely levofloxacin, norfloxacin and ciprofloxacin have been performed either in pure form or in their tablets. In the first method, levofloxacin and norfloxacin are directly treated with bromocresol green (BCG) in dichloromethane while ciprofloxacin is allowed to react with the same dye in aqueous acidic buffer. Highly yellow colored complex species were formed instantaneously in case of levofloxacin and norfloxacin or after extraction into dichloromethane for ciprofloxacin. The formed complexes are quantified spectrophotometrically at their absorption maxima at 411 nm for levofloxacin and 412 nm for norfloxacin and ciprofloxacin. The second method involves the reaction of levofloxacin with ヱ-chloranilic acid ( ヱ-CA) and norfloxacin with tetracyanoethylene (TCNE) in acetonitrile to give complexes with maximum absorbance at 521 and 333 nm for the two drugs, respectively. Adopting the first procedure, calibration graphs were linear over the range 1- 20 レg mL-1 with mean percentage recoveries of 100.41 【 0.72, 99.99 【 0.54 and 100.23 【 0.91 for the theree drugs, respectively. For the second procedure, the concentration ranges were 15-250 レg mL-1 for levofloxacin using ヱ-CA and 0.8-16 レg mL-1 for norfloxacin using TCNE with mean percentage recoveries of 99.88 【 0.45 and 100.26 【 0.68 for the two drugs, respectively. The proposed methods were successfully applied to determine these drugs in their tablet formulations and the results compared favorably to that of reference methods. The proposed methods are recommended for quality control and routine analysis.
机译:两种简单,快速和灵敏的分光光度法测定三种氟喹诺酮类药物,即左氧氟沙星,诺氟沙星和环丙沙星,均以纯形式或以其片剂形式进行。在第一种方法中,将左氧氟沙星和诺氟沙星直接用溴甲酚绿(BCG)在二氯甲烷中处理,同时使环丙沙星与相同的染料在酸性缓冲液中反应。在左氧氟沙星和诺氟沙星的情况下,或者在提取二氯甲烷中的环丙沙星后,会立即形成高度黄色的复合物。左旋氧氟沙星在411 nm处最大吸收峰,分光光度法定量形成的配合物,诺氟沙星和环丙沙星在412 nm处最大吸收峰。第二种方法涉及左氧氟沙星与β-氯苯甲酸(β-CA)和诺氟沙星与四氰基乙烯(TCNE)在乙腈中的反应,以得到两种药物分别在521和333 nm处具有最大吸收的复合物。采用第一种方法时,三种药物的校正曲线在1- 20μgmL -1 范围内均呈线性,平均回收率分别为100.41【0.72、99.99【0.54和100.23【0.91。对于第二种方法,使用ヱ-CA的左氧氟沙星的浓度范围为15-250レg mL -1 ,使用TCNE的诺氟沙星的浓度范围为0.8-16レg mL -1 两种药物的平均回收率分别为99.88【0.45和100.26【0.68。所提出的方法已成功地应用于确定这些药物在其片剂中的含量,其结果与参考方法相比具有优势。建议将提出的方法用于质量控制和常规分析。

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