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pH/有机溶剂双梯度高效液相色谱法同时测定氨酚曲麻片中五种感冒药成分

[Simultaneous determination of five cold medicine ingredients in paracetamol triprolidine hydrochloride and pseudoephedrine hydrochloride tablets by pH/organic solvent double-gradient high performance liquid chromatography].

作者信息

Xuan Xueyi, Huang Lina, Pan Xiaoling, Li Ning

机构信息

Guangdong College of Pharmacy, Guangzhou 510006, China.

出版信息

Se Pu. 2013 Feb;31(2):133-8. doi: 10.3724/sp.j.1123.2012.09023.

Abstract

A pH/organic solvent double-gradient mode in reversed-phase high performance liquid chromatography (HPLC) has been established as a new approach to the simultaneous determination of acetaminophen, caffeine, salicylamide, pseudoephedrine hydrochloride and triprolidine hydrochloride in paracetamol triprolidine hydrochloride and pseudoephedrine hydrochloride tablets. Through the optimization of the organic solvent gradient mode and pH/organic solvent double-gradient mode, the optimum double-gradient HPLC system of the five cold medicine ingredients has been built. The determination was carried out on a Diamonsiol C18 column (250 mm x 4.6 mm, 5 microm). The mobile phase consisted of methanol, 0.05 mol/L ammonium acetate solution and 0.08 mol/L acetic acid solution. The column temperature was set at 30 degrees C. The flow rate was 1.0 mL/min. The sample was measured at multiple wavelengths: 0-6 min, 280 nm; 6-7 min, 257 nm; 7-14 min, 280 nm; 14 min, 233 nm. The separation of the five cold medicine ingredients in the tablets was achieved in 25.5 min. The linear ranges of acetaminophen, pseudoephedrine hydrochloride, caffeine, salicylamide and triprolidine hydrochloride were 0.055 -0.998 g/L, 0.053-0.946 g/L, 0.007-0.129 g/L, 0.035-0.622 g/L and 0.002-0.039 g/L, respectively, with their correlation coefficients greater than 0.999 0. The detection limits (S/N = 3) were 0.09, 6, 0.02, 0.128 and 0.02 mg/L, respectively. Their mean recoveries were 97.9%-102.8%. The advantage of the method is the simultaneous determination of acidic, neutral and basic compounds. It also can improve the column efficiency of the analyte, compress the half-peak width and reduce the trailing. The optimized and validated method can be used for the simultaneous determination of the five cold medicine ingredients in the tablets.

摘要

已建立反相高效液相色谱(HPLC)中的pH/有机溶剂双梯度模式,作为同时测定氨酚曲麻片中对乙酰氨基酚、咖啡因、水杨酰胺、盐酸伪麻黄碱和盐酸曲普利啶的新方法。通过优化有机溶剂梯度模式和pH/有机溶剂双梯度模式,构建了这五种感冒药成分的最佳双梯度HPLC系统。测定在Diamonsiol C18柱(250 mm×4.6 mm,5μm)上进行。流动相由甲醇、0.05 mol/L醋酸铵溶液和0.08 mol/L醋酸溶液组成。柱温设定为30℃。流速为1.0 mL/min。样品在多个波长下测定:0 - 6分钟,280 nm;6 - 7分钟,257 nm;7 - 14分钟,280 nm;14分钟,233 nm。片剂中五种感冒药成分在25.5分钟内实现分离。对乙酰氨基酚、盐酸伪麻黄碱、咖啡因、水杨酰胺和盐酸曲普利啶的线性范围分别为0.055 - 0.998 g/L、0.053 - 0.946 g/L、0.007 - 0.129 g/L、0.035 - 0.622 g/L和0.002 - 0.039 g/L,其相关系数均大于0.999 0。检测限(S/N = 3)分别为0.09、6、0.02、0.128和0.02 mg/L。它们的平均回收率为97.9% - 102.8%。该方法的优点是可同时测定酸性、中性和碱性化合物。它还能提高分析物的柱效,压缩半峰宽并减少拖尾。该优化且经过验证的方法可用于同时测定片剂中这五种感冒药成分。

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