Poly(ethyleneglycol) column for the determination of acetaminophen, phenylephrine and chlorpheniramine in pharmaceutical formulations

被引:39
作者
García, A
Rupérez, FJ
Marín, A
de la Maza, A
Barbas, C
机构
[1] Univ S Pablo, Fac CC Expt & Salud, CEU Urbaniz Monteprincipe, Madrid 28668 3, Spain
[2] Labs CINFA SA, Poligono Areta Huarte, Pamplona, Spain
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2003年 / 785卷 / 02期
关键词
acetaminophen; phenylephrine; chlorpheniramine;
D O I
10.1016/S1570-0232(02)00904-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
New polar reversed-phase stationary phases in HPLC provide specific selectivities which can help to solve traditional chromatographic problems related to the development of chromatographic methods with widely different retention times for the sample components. One such case is the analysis of pharmaceutical formulations against the common cold. Acetaminophen, phenylephrine and chlorpheniramine, compounds with different polarities, are frequently associated in these drugs. An isocratic and rapid HPLC method for the simultaneous determination of the three compounds, acetaminophen, phenylephrine and chlorpheniramine, in capsules as pharmaceutical formulations, including the separation of impurities (4-aminophenol and 4-chloracetanilide) and excipients, has been developed and validated. The final chromatographic conditions employed a Supelco Discovery HS PEG column poly(ethyleneglycol) 15x0.46 cm, 5 mum. The mobile phase was 20 mM phosphate buffer, pH 7.0-acetonitrile (90:10, v/v) at a flow-rate of 1 ml/min. UV detection was performed at 215 nm for all the compounds except acetaminophen, which was measured at 310 nm. Validation parameters permit us to consider this method suitable. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:237 / 243
页数:7
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