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首页> 外文期刊>Journal of analytical chemistry >Spectrophotometric determination of glimepiride in pharmaceutical preparations based on the formation of charge-transfer and ion-pair complexes
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Spectrophotometric determination of glimepiride in pharmaceutical preparations based on the formation of charge-transfer and ion-pair complexes

机译:基于电荷转移和离子对复合物形成的分光光度法测定药物制剂中格列美脲的含量

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摘要

Two rapid, simple, accurate and sensitive spectrophotometric methods were developed for the determination of glimepiride in pharmaceutical preparations. The first method was based on the formation of a charge-transfer complex of the drug, as n-electron donor, with 7,7,8,8-tetracyanoquinodimethane (TCNQ), as π-acceptor. The second method was based on the formation of ion-pair complexes between the examined drug and bromothymol blue (BTB). The proposed methods were validated for linearity, limit of detection, limit of quantification, precision, accuracy, robustness and specificity. The calibration was linear over the concentration range of 10-80 and 20-120 μg/mL for methods I and II, respectively. The limits of detection were 2.6 and 2.8 μg/mL. The proposed methods were applied to the determination of the drug in pharmaceutical preparations. The results obtained were in good agreement with those obtained using the reference method (HPLC). There was no significant difference in the accuracy and precision as revealed by the accepted values of t- and F-tests, respectively.
机译:开发了两种快速,简单,准确和灵敏的分光光度法测定药物制剂中格列美脲的含量。第一种方法是基于药物的电荷转移复合物,作为n电子供体,以7,7,8,8-四氰基喹二甲烷(TCNQ)作为π受体。第二种方法基于所检查药物与溴百里酚蓝(BTB)之间离子对络合物的形成。验证了所提出方法的线性,检测限,定量限,精密度,准确性,鲁棒性和特异性。方法I和II的校准分别在10-80和20-120μg/ mL的浓度范围内是线性的。检测限为2.6和2.8μg/ mL。所提出的方法用于药物制剂中药物的测定。获得的结果与使用参考方法(HPLC)获得的结果高度吻合。分别由公认的t检验和F检验值表明,准确性和精密度没有显着差异。

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