Quantitative Determination of Dextromethorphan and Three Metabolites in Urine by Reverse-Phase High-Performance Liquid Chromatography

Autor: Park, Young Han, Peter Kullberg, M., Hinsvark, Orville N.
Zdroj: Journal of Pharmaceutical Sciences; January 1984, Vol. 73 Issue: 1 p24-29, 6p
Abstrakt: □ A high-performance liquid chromatographic (HPLC) method for the quantitation of dextromethorphan (I) and its three metabolites, dextrorphan (II), 3-hydroxy-9α,13α,14α -morphinan (III), and 3-methoxy-9α,13α,14α:-morphinan (IV), in urine was developed. For the analysis of nonconjugated compounds, urine samples at pH11-11.5, containing 3-methoxy-17-methyl-10-oxo-9α,13α,14α -morphinan as an internal standard, were applied to an extraction column, and the compounds were eluted with 10% n-butyl alcohol-hexane. The organic eluant was extracted with 0.1M HC1, and an aliquot of the acidic extract was analyzed by HPLC utilizing a 5-μm phenyl column (25×0.46-cm i.d.) with a mobile phase of 10mM potassium phosphate-acetonitrile (45:55, pH4.0); the column effluent was monitored by UV detection at 280nm. Free and conjugated metabolites in the enzyme-treated urine were analyzed by selective extraction of I and IV with hexane from urine samples at pH>12 and extraction of II and III with 10% n-butyl alcohol-hexane from urine samples at pH11-11.5. The minimum quantifiable levels of I-IV ranged from 0.017 to 0.09μg of base/mL and from 0.11 to 0.21μg of base/mL in nonhydrolyzed and hydrolyzed urine, respectively.
Databáze: Supplemental Index