C. Tharassebloch et al., DETERMINATION OF SINEFUNGIN IN RAT PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Journal of chromatography B. Biomedical applications, 674(2), 1995, pp. 247-252
Citations number
7
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Journal title
Journal of chromatography B. Biomedical applications
A reversed-phase high-performance liquid chromatographic method for th
e determination of sinefungin, a new antiprotozoal drug, in rat plasma
has been developed and validated. Sample preparation was performed at
4 degrees C by deproteinization with acetonitrile. Vidarabine was use
d as an internal standard. Both sinefungin and vidarabine were separat
ed on a C-18 column with a mobile phase of ammonium dihydrogenphosphat
e-acetonitrile (95:5, v/v) and detected by ultraviolet absorbance at 2
60 nm. Recoveries of sinefungin from plasma were 75 +/- 3.2% and 81 +/
- 4.8% following dosage at concentrations of 10 mu g/ml and 30 mu g/ml
, respectively. Using 250 mu l of rat plasma, the limit of quantitatio
n was 1 mu g/ml sinefungin, and the assay was linear from 1 to 30 mu g
/ml. This method appears sensitive enough to be used in further pharma
cokinetic studies of sinefungin in animal models.