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Spectrophotometric Determination of Doxazosin Mesylate in Tablets by Ion-Pair and Charge-Transfer Complexation Reactions

机译:离子对和电荷转移络合反应光度法测定片剂中甲磺酸多沙唑嗪的含量

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Two accurate, easy spectrophotometric methods for the determination of doxazosin mesylate were described. The first method was based on the formation of ion-pair complexes with the acidic sulfophthalein dyes bromocresol purple (BCP) and bromophenol blue (BPB) in pH 3.3 and 4.5 citrate-phosphate buffer, respectively. The formed complexes were extracted into dichloromethane, and their absorbance was measured at 403 and 410 nm for BCP and BPB, respectively. The second method was based on the charge transfer reaction of the drug as an n-electron donor with either 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) or 7,7,8,8-tetracyanoquinodimethane (TCNQ) as pi-acceptors, to give colored radical anions. The absorbances of products were measured at 457 nm in acetonitrile and 838 nm in methanol for DDQ and TCNQ, respectively. Under the optimum reaction conditions, Beer's law was obeyed with a good correlation coefficient (r = 0.9997-0.9999) in the concentration ranges 3.0-18.0, 3.0-20.0,15.0-95.0, and 10.0-100.0 mu g/mL for the BCP, BPB, DDQ, and TCNQ methods, respectively. Limits of detection of the BCP, BPB, DDQ, and TCNQ methods were 0.314, 0.408,1.935, and 1.610 mu g/mL, respectively. The limits of quantification were 1.045,1.360, 6.449, and 5.367 mu g/mL, respectively. The parameters molar absorptivity, precision, accuracy, recovery, robustness, and stability constant were studied. The proposed methods were successfully applied for determination of the drug in tablets with good accuracy and precision. Statistical comparison of the results with those obtained by a reported method showed good agreement and indicated no significant difference in accuracy and precision.
机译:介绍了两种准确,简便的分光光度法测定甲磺酸多沙唑嗪的方法。第一种方法是基于分别在pH 3.3和4.5柠檬酸-磷酸盐缓冲液中与酸性磺基酞菁染料溴甲酚紫(BCP)和溴酚蓝(BPB)形成离子对络合物。将形成的络合物萃取到二氯甲烷中,并分别在403和410 nm下测量BCP和BPB的吸光度。第二种方法基于作为n电子供体的药物与2,3-二氯-5,6-二氰基-1,4-苯醌(DDQ)或7,7,8,8-的电荷转移反应四氰基喹二甲烷(TCNQ)作为pi受体,可生成有色自由基阴离子。在DDQ和TCNQ中,分别在457 nm的乙腈和838 nm的甲醇中测量产物的吸光度。在最佳反应条件下,对于BCP,在3.0-18.0、3.0-20.0、15.0-95.0和10.0-100.0μg / mL的浓度范围内,遵循比尔定律具有良好的相关系数(r = 0.9997-0.9999), BPB,DDQ和TCNQ方法。 BCP,BPB,DDQ和TCNQ方法的检出限分别为0.314、0.408、1.935和1.610μg / mL。定量限分别为1.045、1.360、6.449和5.367μg / mL。研究了摩尔吸光度,精度,准确度,回收率,鲁棒性和稳定性常数的参数。所提出的方法已成功地应用于片剂中药物的准确度和精密度的测定。结果与通过报告的方法获得的结果进行统计比较,结果显示出良好的一致性,并且在准确性和精密度上没有显着差异。

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