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RP-HPLC Determination of Paracetamol-Containing Components in Quaternary and Binary Mixtures

机译:RP-HPLC测定四元和二元混合物中扑热息痛的成分

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A simple reversed-phase high-performance liquid chromatographic (RP - HPLC) method for the simultaneous determination of ascorbic acid, methionine, paracetamol and caffeine is developed and validated. The cited components are separated completely using Brownlee Bio C18 column (250 x 4.6 mm, 5 μm) by isocratic elution of water - acetonitrile (85:15) (v/v) mobile phase flowing at 1.0 ml/min at ambient temperature. The spectrophotometric detection is carried out sequentially at 260 nm for ASC (2 min), 200 nm for MET (1 min), 240 nm for PAR (1.5 min) and 270 nm for CAF (1.5 min). Total chromatographic analysis time per sample was approximately 6 min. The linear range of determination for ASC, MET,PAR and CAF are 40-160 μg/ml, 40-200 μg/ml, 20-400 μg/ml and 40-160 μg/ml, respectively. Thus, proposed method can be successfully applicable to analysis the pharmaceutical preparation containing the above mentioned drugs without any interference of excipients. Recovery ranges and relative standard deviation are in turn 96.46 to 102.70%, 2.65% for ASC, 96.33 to 103.43%, 2.93% for MET, 98.31 to 102.73%,2.09% for PAR and 95.82 to 102.13%, 2.68% for CAF.
机译:建立并验证了同时测定抗坏血酸,蛋氨酸,扑热息痛和咖啡因的简单反相高效液相色谱(RP-HPLC)方法。使用Brownlee Bio C18色谱柱(250 x 4.6 mm,5μm)通过水-乙腈(85:15)(v / v)流动相的等度洗脱,在环境温度下完全分离所列举的组分。分光光度检测依次在ASC的260 nm(2分钟),MET的200 nm(1分钟),PAR的240 nm(1.5分钟)和CAF的270 nm(1.5分钟)上进行。每个样品的总色谱分析时间约为6分钟。 ASC,MET,PAR和CAF的线性测定范围分别为40-160μg/ ml,40-200μg/ ml,20-400μg/ ml和40-160μg/ ml。因此,所提出的方法可以成功地用于分析含有上述药物的药物制剂,而没有任何赋形剂的干扰。回收率和相对标准偏差依次为96.46至102.70%,ASC为2.65%,MET为96.33至103.43%,2.93%,PAR为98.31至102.73%,2.09%,CAF为95.82至102.13%,2.68%。

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