首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >LC method for the analysis of acetylsalicylic acid, caffeine and codeine phosphate in pharmaceutical preparations.
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LC method for the analysis of acetylsalicylic acid, caffeine and codeine phosphate in pharmaceutical preparations.

机译:LC方法用于分析药物制剂中的乙酰水杨酸,咖啡因和磷酸可待因。

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摘要

An accurate, simple, reproducible and sensitive method for the determination of acetylsalicylic acid, caffeine and codeine phosphate has been developed and validated. Acetylsalicylic acid, caffeine and codeine phosphate were separated using a microBondapack C(8) column by isocratic elution with flow rate 1.0 ml/min. The mobile phase composition was 125/125/250/0.5 (v/v) isopropyl alcohol, acetonitrile, water and o-phosphoric acid. The samples were detected at 215 nm using photo-diode array detector. The linear range of detection for acetylsalicylic acid, caffeine and codeine phosphate were between 0.40 and 1000, 0.25 and 250, and 0.48 and 96 microg/ml, respectively. The linearity, range, selectivity, system performance parameters, precision, accuracy, and ruggedness for acetylsalicylic acid, caffeine and codeine phosphate were also shown to have acceptable values.
机译:建立并验证了测定乙酰水杨酸,咖啡因和磷酸可待因的准确,简单,可重现和灵敏的方法。使用microBondapack C(8)色谱柱,通过等度洗脱,以1.0 ml / min的流速分离乙酰水杨酸,咖啡因和磷酸可待因。流动相组成为125/125/250 / 0.5(v / v)异丙醇,乙腈,水和邻磷酸。使用光电二极管阵列检测器在215 nm处检测样品。乙酰水杨酸,咖啡因和磷酸可待因的线性检测范围分别在0.40和1000、0.25和250之间以及0.48和96 microg / ml之间。乙酰水杨酸,咖啡因和磷酸可待因的线性,范围,选择性,系统性能参数,精度,准确度和耐用性也显示出可接受的值。

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