首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Simultaneous Determination of Sodium, Potassium and Magnesium Counter Ions in Three Drugs: Pantoprazole Sodium, Losartan Potassium and Omeprazole Magnesium by Ion Chromatography
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Simultaneous Determination of Sodium, Potassium and Magnesium Counter Ions in Three Drugs: Pantoprazole Sodium, Losartan Potassium and Omeprazole Magnesium by Ion Chromatography

机译:三种药物中钠,钾和镁抗衡离子的同时测定:泮托拉唑钠,氯沙坦钾和奥美拉唑镁通过离子色谱法

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The present analytical method was developed for single determination of three counter ions in pantoprazole sodium, losartan potassium and omeprazole magnesium drug substances by ion chromatography. The ion chromatography method was unique and suitable for three drugs such as pantoprazole sodium, losartan potassium and omeprazole magnesium with specification limits 5.7, 8.5 and 3.3 % of percentages of sodium, potassium and magnesium counter ions, respectively. The method was developed with Metrosep C4 (150 x 4.0 mm, 5 p.) column and combination of 4.0 mM nitric acid, 0.1 % dipicolinic acid and 10 % acetonitrtle with flow of 1 mL. The injection volume used for mis analysis was 20 uL with conductivity detector. The validation was performed to single ion chromatography method for three counter ions such as sodium in pantoprazole sodium, potassium in losartan potassium and magnesium in omeprazole magnesium. The % RSD for the method precision and intermediate of sodium in the pantoprazole sodium was 1.6 % and 1.6 %, respectively. The correlation coefficient for the linearity parameter of the sodium in the pantoprazole sodium was 1.000. The accuracy of sodium in pantoprazole sodium was observed as 97, 101 and 103 % recovery at 50, 100 and 150 %, respectively. The % RSD for the method precision and intermediate of potassium in the losartan potassium was 2.0 % and 1.5 %, respectively. The correlation coefficient for the linearity of the potassium in the losartan potassium was 0.999. The accuracy of potassium in losartan potassium was observed as 97.2, 100.0 and 101.8 % recovery at 50, 100 and 150 %, respectively. The % RSD for the method precision and intermediate precision of magnesium in the omeprazole magnesium was 1.7 and 2.0 %, respectively. The correlation coefficient for the linearity of the magnesium in the omeprazole magnesium was 1.000. The accuracy of magnesium in omeprazole magnesium was observed as 113.1,98.5 and 98.5 % recovery at 50, 100 and 150 %, respectively. The robustness study was performed for flow of mobile phase from the actual flow and acetonitrile concentration. All the robustness values were less than the 10 % of initial counter ion content. The developed and validated method can be used for the simultaneous determination of sodium, potassium and magnesium counter ions in pantoprazole sodium, losartan potassium and omeprazole magnesium, respectively.
机译:通过离子色谱法,开发了本发明的分析方法,用于单次抗帕拉唑钠,氯沙坦钾和奥美拉唑镁药物物质中的三个抗衡离子。离子色谱法是独特的,适用于三种药物,如泮托拉唑钠,氯沙坦钾和奥美拉唑镁,分别具有规格限制5.7,8.5和3.3%的钠,钾和镁抗衡离子的百分比。该方法是用MetRosep C4(150×4.0mm,5 p。)柱和4.0mm硝酸,0.1%二辛酸和10%乙腈的组合而开发的,具有1mL的10%乙腈。用于MIS分析的注射体积为电导率检测器20μl。对三种抗磷唑钠钠,氯沙坦钾盐中的三个抗钙离子的单离子色谱法进行验证,在奥氨拉唑镁中的镁。泮托拉唑钠中的方法精度和中间体的%RSD分别为1.6%和1.6%。泮托拉唑钠钠线性参数的相关系数为1.000。在50,100和150%的分别观察到泮托拉唑钠的钠钠的准确性分别在50,100和150%中恢复为97,101和103%。氯沙坦钾中钾的方法精度和中间体的%RSD分别为2.0%和1.5%。氯沙坦钾钾线性的相关系数为0.999。在50,100和150%的情况下观察到氯沙坦钾的钾的准确性分别为97.2,100.0和101.8%。奥美拉唑镁中镁的方法精度和中间精度的%RSD分别为1.7和2.0%。奥美拉唑镁在奥美唑镁中的线性度的相关系数为1.000。观察到奥美拉唑镁的镁的准确性分别观察为50,100和150%的113.1,98.5%和98.5%。对从实际流动和乙腈浓度的流动相流动进行鲁棒性研究。所有稳健性值小于初始反离子含量的10%。开发和验证的方法可用于同时测定泮托拉唑钠,氯沙坦钾和奥美拉唑镁中的钠,钾和镁抗衡离子。

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