dextromethorphan and propylparaben

dextromethorphan has been researched along with propylparaben* in 2 studies

Other Studies

2 other study(ies) available for dextromethorphan and propylparaben

ArticleYear
LC for analysis of two sustained-release mixtures containing cough cold suppressant drugs.
    Journal of chromatographic science, 2010, Volume: 48, Issue:6

    A liquid chromatographic method was applied for the analysis of two sustained-release mixtures containing dextromethorphane hydrobromide, carbinoxamine maleate with either phenylephrine hydrochloride in pharmaceutical capsules (Mix 1) or phenyl-propanolamine, methylparaben, and propylparaben, which bonds as a drug base to ion exchange resin in pharmaceutical syrup (Mix 2). The method was used for their simultaneous determination using a CN column with a mobile phase consisting of acetonitrile-12 mM ammonium acetate in the ratio of 60:40 (v/v, pH 6.0) for Mix 1 and 45:55 (v/v, pH 6.0) for Mix 2.

    Topics: Antitussive Agents; Capsules; Chromatography, Ion Exchange; Delayed-Action Preparations; Dextromethorphan; Drug Stability; Least-Squares Analysis; Nasal Decongestants; Parabens; Phenylephrine; Phenylpropanolamine; Pyridines; Reproducibility of Results; Sensitivity and Specificity

2010
Simultaneous determination of bromhexine hydrochloride and methyl and propyl p-hydroxybenzoate and determination of dextromethorphan hydrobromide in cough-cold syrup by high-performance liquid chromatography.
    Journal of pharmaceutical and biomedical analysis, 1996, Volume: 15, Issue:2

    Liquid chromatographic methods were developed for the determination of bromhexine hydrochloride, methyl p-hydroxybenzoate and propyl p-hydroxybenzoate (method A) and dextromethorphan hydrobromide (method B) in cough-cold syrup formulations. Reversed-phase analytical columns (150 mm x 3.9 mm i.d.) were used with (A) C18 and (B) phenyl as stationary phases and mixtures of (A) acetonitrile and aqueous 15 mM triethylamine solution (43:57) and (B) methanol and aqueous 3% ammonium formate buffer solution (53:47) as mobile phases at a flow rate of 1.0 ml min-1. Both aqueous components were adjusted to pH 3.9. UV detection of analytes was at (A) 245 nm and (B) 278 nm. In both methods, the time required for an HPLC run giving good separations and recoveries was less than 8 min.

    Topics: Antitussive Agents; Bromhexine; Chromatography, High Pressure Liquid; Dextromethorphan; Expectorants; Parabens

1996