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Simultaneous Derivative Spectrophotometric Analysis of Doxylamine Succinate, Pyridoxine Hydrochloride and Folic Acid in Combined Dosage Forms

机译:混合剂型同时测定琥珀酸多西拉敏胺,盐酸吡rid醇和叶酸的导数分光光度法

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摘要

Two UV spectrophotometric methods have been developed, based on first derivative spectrophotometry for simultaneous estimation of doxylamine succinate, pyridoxine hydrochloride, and folic acid in tablet formulations. In method I, the concentrations of these drugs were determined by using linear regression equation. Method II is also based on first derivative spectrophotometry however simultaneous equations (Vierdot's method) were derived on derivative spectra. The first derivative amplitudes at 270.0, 332.8 and 309.2 nm were utilized for simultaneous estimation of these drugs respectively by both methods. In both the methods, linearity was obtained in the concentration range 2.5-50 μg/ml, 1-40 μg/ml and 1-30 μg/ml for doxylamine succinate, pyridoxine hydrochloride, and folic acid respectively. The developed methods show best results in terms of linearity, accuracy, precision, LOD, LOQ and ruggedness for standard laboratory mixtures of pure drugs and marketed formulations. The common excipients and additives did not interfere in their determinations.
机译:基于一阶导数分光光度法,已开发出两种紫外分光光度法,用于同时估算片剂中丁二胺琥珀酸盐,吡ido醇盐酸盐和叶酸的含量。在方法I中,这些药物的浓度通过使用线性回归方程确定。方法II也是基于一阶导数分光光度法,但是在导数光谱上导出了联立方程(维耶多方法)。通过两种方法分别利用270.0、332.8和309.2 nm的一阶导数幅度同时估算这些药物。在这两种方法中,琥珀酸多西拉敏胺,盐酸吡ido醇和叶酸的浓度范围分别为2.5-50μg/ ml,1-40μg/ ml和1-30μg/ ml,都具有线性。对于纯药物和市售制剂的标准实验室混合物,所开发的方法在线性,准确性,精密度,LOD,LOQ和坚固性方面均显示出最佳结果。常见的赋形剂和添加剂不会影响其测定。

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  • 作者

    Pathak, A.; Rajput, S. J.;

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  • 年度 2008
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  • 原文格式 PDF
  • 正文语种 en
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