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Talanta. 2001 May 30;54(4):621-30. doi: 10.1016/s0039-9140(01)00315-0.

Determination of active ingredients in cough-cold preparations by micellar liquid chromatography.

Talanta

M Gil-Agustí, L Monferrer-Pons, M C García-Alvarez-Coque, J Esteve-Romero

Affiliations

  1. Dpto de Ciencias Experimentales, Area de Quimica Analitica, Universitat Jaume I, Campus Riu Sec, 12080, Castelló, Spain.

PMID: 18968285 DOI: 10.1016/s0039-9140(01)00315-0

Abstract

The chromatographic behaviour of some active ingredients in cough-cold pharmaceutical preparations, the antihistamine chlorpheniramine (or the dextro enantiomer dexchlorpheniramine), and the phenethylamines phenylephrine, phenylpropanolamine and pseudoephedrine, has been studied using a C(18) column, micellar mobile phases of sodium dodecyl sulphate (SDS) and pentanol, and with UV detection. All possible combinations of chlorpheniramine/phenethylamine were resolved and determined using a mobile phase of 0.15 M SDS-6% (v/v) pentanol at pH 7, with analysis time below 7 min. Repeatabilities and within laboratory precisions were evaluated at four different drug concentrations in the range 0.5-25 mug ml(-1) (n=5), resulting RSDs below 1.6%. The drug amounts found in the analysis of 14 commercialised preparations agreed with those declared by the manufacturers within the tolerance limits, and with those obtained using an aqueous 60% (v/v) methanol reference mobile phase. No interference was observed from other accompanying drugs such as acetylsalicylic acid, ascorbic acid, betamethasone, caffeine, codeine phosphate, diphenhydramine, lactose, paracetamol, and prednisolone. The studied combinations required a rather high amount of methanol in conventional RPLC to be eluted from the column. In contrast, the proposed procedure used a much lower amount of organic solvent (pentanol), which is highly retained in the SDS solution, being also less toxic than methanol.

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