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A method for quantitative analysis of multicomponent DRUGS antipyretic, analgesic, cough ACTION

机译:一种多组分药物解热,镇痛,止咳作用的定量分析方法

摘要

FIELD: medicine, pharmacy, analytical pharmaceutical chemistry.;SUBSTANCE: invention proposes a method for simultaneous determination of composition of multicomponent medicinal preparations by reversed HPLC method with ultraviolet detector. Method is used in carrying out analysis of preparations comprising the following drugs: (1) paracetamol, propifenazone, caffeine, phenobarbital, codeine phosphate; or (2) paracetamol, ascorbic acid, codeine phosphate, phenylephrine hydrochloride, chlorphenylamine maleate; or (3) paracetamol, theophylline, caffeine, phenobarbital, ephedrine hydrochloride; or (4) codeine phosphate, nipagin, nipazol for a single stage in linear gradient regimen wherein the composition of mobile phase changes from phosphate buffer solution with pH 3.0 to its mixture with acetonitrile taken in the volume ratio = 1:1. Invention provides the complete separation of peaks of all analyzed and interfering substances and to obtain precise quantitative results.;EFFECT: improved assay method.;2 cl, 17 dwg, 16 tbl, 6 ex
机译:领域:本发明提出了一种通过反相HPLC法与紫外检测器同时测定多组分药物制剂组成的方法。该方法用于对包含以下药物的制剂进行分析:(1)扑热息痛,丙ifenanazone,咖啡因,苯巴比妥,磷酸可待因; (2)对乙酰氨基酚,抗坏血酸,磷酸可待因,盐酸去氧肾上腺素,马来酸氯苯胺;或(3)扑热息痛,茶碱,咖啡因,苯巴比妥,盐酸麻黄碱;或(4)线性梯度方案中的单级磷酸可待因,尼泊金,尼巴唑,其中流动相的组成从pH值为3.0的磷酸盐缓冲溶液变为其与乙腈的混合物(体积比= 1:1)。本发明提供了所有被分析和干扰物质的峰的完全分离并获得精确的定量结果。效果:改进的测定方法; 2 cl,17 dwg,16 tbl,6 ex

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