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Simple HPLC method for simultaneous determination of acetaminophen, caffeine and chlorpheniramine maleate in tablet formulations

机译:同时测定片剂中对乙酰氨基酚,咖啡因和马来酸氯苯那敏的简单HPLC方法

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A simple, rapid and accurate, routine-HPLC method is described for simultaneous determination of acetaminophen, caffeine and chlorpheniramine maleate in a new tablet formulation. Chromatographic separation of the three pharmaceuticals was achieved on a Hypersil CN column (150 x 5.0 mm, 5 mum) using a mobile phase comprising a mixture of acetonitrile, an ion-pair solution and tetrahydrofuran (13:14:87 v/v, pH 4.5). The flow-rate was changed from 1.0 mL min(-1) (in 0 similar to 7.5 min) to 1.8 mL min(-1) (after 3.5 min). Detection was 223 nm. Separation was complete in < 10 min. The method was validated for system suitability, linearity, accuracy, precision, limits of detection and quantitation, and robustness. Linearity, accuracy and precision were found to be acceptable over the ranges 31.6 similar to 315.8 mug mL(-1) for acetaminophen, 9.5 similar to 94.6 mug mL(-1) for caffeine and 1.4 similar to 13.8 mug mL(-1) for chlorpheniramine maleate. [References: 4]
机译:描述了一种简单,快速,准确的常规HPLC方法,用于同时测定新片剂中对乙酰氨基酚,咖啡因和马来酸氯苯那敏。在Hypersil CN色谱柱(150 x 5.0 mm,5 mum)上使用包含乙腈,离子对溶液和四氢呋喃(13:14:87 v / v,pH的混合物)的流动相实现三种药物的色谱分离4.5)。流速从1.0 mL min(-1)(在0中类似于7.5分钟)更改为1.8 mL min(-1)(在3.5分钟后)。检测为223nm。在不到10分钟的时间内完成分离。验证了该方法的系统适用性,线性,准确性,精密度,检测和定量限以及稳健性。线性,准确度和精密度在对乙酰氨基酚的31.6类似于315.8毫升(-1),对咖啡因的9.5类似于94.6毫升(-1)和1.4与13.8毫升的3.8毫升之间可接受。马来酸氯苯那敏。 [参考:4]

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