HPLC DETERMINATION OF DACARBAZINE, DOXORUBICIN, AND ONDANSETRON MIXTURE IN 5-PERCENT DEXTROSE INJECTION ON UNDERIVATIZED SILICA WITH AN AQUEOUS-ORGANIC MOBILE-PHASE
Dt. King et Jt. Stewart, HPLC DETERMINATION OF DACARBAZINE, DOXORUBICIN, AND ONDANSETRON MIXTURE IN 5-PERCENT DEXTROSE INJECTION ON UNDERIVATIZED SILICA WITH AN AQUEOUS-ORGANIC MOBILE-PHASE, Journal of liquid chromatography, 16(11), 1993, pp. 2309-2323
A high performance liquid chromatography procedure has been developed
for the assay of a dacarbazine, doxorubicin, and ondansetron mixture i
n 5% dextrose injection. The separation and quantitation are achieved
on an 22-cm underivatized silica column at ambient temperature using a
mobile phase of 60:40 v/v 6.25 mM phosphate buffer, pH 3.0-acetonitri
le at a flow rate of 1.0 ml/min with detection of all three analytes a
t 216 nm. The separation is achieved within 10 min with sensitivity in
the ng/ml range for each analyte. It was shown that the predominant m
echanism of retention for the analytes on silica was cation exchange.
The method showed linearity for dacarbazine, doxorubicin, and ondanset
ron in the 0.79-7.90, 0.08-1.60, and 0.06-6.00 mug/ml ranges, respecti
vely. Accuracy and precision were in the 0-7% and 0.4-6% ranges, respe
ctively, for all three compounds. The limits of detection for dacarbaz
ine, doxorubicin, and ondansetron were 12.5. 10.0 and 8.0 ng/ml, respe
ctively, based on a signal to noise ratio of 3 and a 50 mul injection.