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感冒止咳糖浆的离子对反相高效液相色谱法 I:盐酸伪麻黄碱、马来酸溴苯那敏和氢溴酸右美沙芬

Ion-pair reversed-phase high-pressure liquid chromatography of cough-cold syrups I: pseudoephedrine hydrochloride, brompheniramine maleate, and dextromethorphan hydrobromide.

作者信息

Chao M K, Holcomb I J, Fusari S A

出版信息

J Pharm Sci. 1979 Nov;68(11):1463-4. doi: 10.1002/jps.2600681137.

DOI:10.1002/jps.2600681137
PMID:512904
Abstract

Pseudoephedrine hydrochloride (I), brompheniramine maleate (II), and dextromethorphan hydrobromide (III) in a cough-cold sytup were separated and determined by ion-pair reversed-phase high-pressure liquid chromatography. The separation was carried out using a muBondapak C18 column (30 cm x 3.9 mm i.d.) and a mobile phase of acetonitrile-water-acetic acid (40:60:1) with 0.01 N 1-octanesulfonic acid sodium salt and 0.05 N potassium nitrate. Detection was accomplished using a UV detector at 265 nm for I and II; III was monitored at 280 nm. Concentration versus peak height plots in the ranges of 0.37-1.9 mg/ml for I, 0.025-0.126 mg/ml for II, and 0.125-0.625 mg/ml for III were linear. Ten consecutive injections of a mixture gave a percent relative standard deviation of less than 1% for all three components. Average recoveries from laboratory-prepared samples were 100.5% for I, 100.9% for II, and 100.1% for III. No precolumn cleanup was necessary, and the chromatogram was complete in 16 min.

摘要

采用离子对反相高效液相色谱法对止咳感冒药中的盐酸伪麻黄碱(I)、马来酸溴苯那敏(II)和氢溴酸右美沙芬(III)进行分离和测定。分离采用μBondapak C18柱(30 cm×3.9 mm内径),流动相为乙腈 - 水 - 乙酸(40:60:1),含0.01 N 1 - 辛烷磺酸钠盐和0.05 N硝酸钾。I和II在265 nm处用紫外检测器检测;III在280 nm处监测。I在0.37 - 1.9 mg/ml范围内、II在0.025 - 0.126 mg/ml范围内、III在0.125 - 0.625 mg/ml范围内浓度与峰高的关系呈线性。对混合物进行十次连续进样,所有三种组分的相对标准偏差百分比均小于1%。实验室制备样品的平均回收率I为100.5%、II为100.9%、III为100.1%。无需柱前净化,16分钟内可完成色谱分析。

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