Jf. Chaulet et al., SIMULTANEOUS DETERMINATION OF CHLOROQUINE, PROGUANIL AND THEIR METABOLITES IN HUMAN BIOLOGICAL-FLUIDS BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Journal of pharmaceutical and biomedical analysis, 12(1), 1994, pp. 111-117
A reversed-phase ion-pair high-performance liquid chromatographic meth
od with ultraviolet detection is described for the simultaneous measur
ement of chloroquine, proguanil and their major metabolites in human p
lasma, erythrocytes and urine. After a liquid-solid extraction on a Bo
nd Elut(R) C8 cartridge, the compounds are separated on a C8 Lichrosph
er 60 RP select B column by isocratic elution; the mobile phase is wat
er-acetonitrile-methanol (78:28:4, v/v/v) with 0.5 M ammonium formate
and 0.075 M perchloric acid. The eluent is monitored with an ultraviol
et detector at 254 nm. The lower limits of quantification in plasma ar
e near 6.0 ng ml-1 for chloroquine and near 9.0 ng ml-1 for proguanil.
No chromatographic interference can be detected from endogenous compo
unds or from other antimalarial drugs. The method is accurate and prec
ision is good with inter- and intra-assay relative standard deviations
lower than 6.8% for plasma samples. N-(2-6 dichlorobenzylidene amino)
guanidine is used as an internal standard. The chromatographic procedu
re takes 35 min and can be used for therapeutic drug monitoring and cl
inical studies.