首页> 外文OA文献 >SIMPLE, SENSITIVE AND SELECTIVE SPECTROPHOTOMETRIC METHODS FOR THE DETERMINATION OF ATENOLOL IN PHARMACEUTICALS THROUGH CHARGE TRANSFER COMPLEX FORMATION REACTION
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SIMPLE, SENSITIVE AND SELECTIVE SPECTROPHOTOMETRIC METHODS FOR THE DETERMINATION OF ATENOLOL IN PHARMACEUTICALS THROUGH CHARGE TRANSFER COMPLEX FORMATION REACTION

机译:通过电荷转移络合物形成反应测定药物中阿替洛尔的简单,灵敏和选择性光度法

摘要

Three rapid, selective and sensitive spectrophotometric methods have been proposed for the quantitative determination of atenolol (ATN) in pure form as well as in its pharmaceutical formulation. The methods are based on charge transfer complexation reaction of ATN as n-electron donor with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), 2,4-dinitrophenol (DNP) and 2,4,6-trinitrophenol (picric acid; PA) as it-acceptors to give highly colored radical anion species. The colored products were quantified spectrophotometrically at 590 nm with DDQ (method A) and at 420 nm with both DNP (method B) and PA (method C). Under the optimized experimental conditions. Beer's law is obeyed over the concentration ranges of 3-48, 2-24 and 1.5-18 mu g/mL ATN for method A, method B and method C, respectively. The molar absorptivity. Sandell sensitivity, limits of detection and quantification are also reported. The effects of reaction medium, reaction time and reagent concentration on the sensitivity and stability of the complexes formed have been examined. The proposed methods were successfully applied to the determination of ATN in pure form and commercial tablets with good accuracy and precision. Statistical comparison of the results was performed using Student's t-test and F-ratio at 95% confidence level and the results showed no significant difference between the reference and proposed methods with regard to accuracy and precision. Further, the accuracy and reliability of the methods were confirmed by recovery studies via standard addition technique.
机译:已经提出了三种快速,选择性和灵敏的分光光度法来定量测定纯形式及其药物制剂中的阿替洛尔(ATN)。该方法基于作为正电子供体的ATN与2,3-二氯-5,6-二氰基-1,4-苯醌(DDQ),2,4-二硝基苯酚(DNP)和2,4的电荷转移络合反应,将6-6-三硝基苯酚(苦味酸; PA)作为受体,得到高度着色的自由基阴离子。用DDQ(方法A)在590 nm处用分光光度法定量着色的产物,用DNP(方法B)和PA(方法C)在420 nm处分光光度法定量。在优化的实验条件下。方法A,方法B和方法C分别在3-48、2-24和1.5-18μg/ mL ATN的浓度范围内遵守比尔定律。摩尔吸收率。还报告了Sandell的灵敏度,检测限和定量限。研究了反应介质,反应时间和试剂浓度对形成的配合物的敏感性和稳定性的影响。所提出的方法已成功地应用于纯净形式和市售片剂中ATN的测定,具有较高的准确度和精密度。使用Student的t检验和F比率以95%的置信度对结果进行统计比较,结果显示参考方法和建议方法在准确性和精密度上没有显着差异。此外,通过标准添加技术的回收率研究证实了该方法的准确性和可靠性。

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