Tg. Venkateshwaran et al., HPLC DETERMINATION OF MORPHINE-ONDANSETRON AND MEPERIDINE-ONDANSETRONMIXTURES IN 0.9-PERCENT SODIUM-CHLORIDE INJECTION, Journal of liquid chromatography & related technologies, 19(8), 1996, pp. 1329-1338
Citations number
16
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
High performance liquid chromatography procedures have been developed
for the assay of morphine-ondansetron and meperidine-ondansetron mixtu
res in 0.9% sodium chloride injection. The separation and quantitation
of morphine-ondansetron were performed on an underviatized silica col
umn at ambient temperature using a mobile phase of 60:40 v/v 0.01 M mo
nobasic potassium phosphate pH 4.0 - methanol at a now rate of 1.0 mL/
min with the detection set at 233 nm. The separation was achieved with
in 20 min. Morphine and ondansetron were linear in the 134 - 536 and 6
8 - 271 mu g/mL, ranges, respectivly. Accuracy and precision were in t
he range 0.04 - 4 and 0.2 - 1%, respectively, for the two analytes and
the limits of detection for morphine and ondansetron were 210 and 110
ng/mL, respectively, based on a signal to noise ratio of 3 and a 20 m
u L injection. The separation and quantitation of the meperidine-ondan
setron mixture were also achieved on an underivatized silica column at
ambient temperature using a mobile phase of 60:40 v/v 0.01 M monobasi
c potassium phosphate pH 4.0 - methanol at a flow rate of 1.0 mL/min w
ith detection of the two analytes at 254 nm. The separation was achiev
ed within 20 min. Meperidine and ondansetron were linear in the 556 -
3331 and 89 - 536 mu g/mL ranges, respectively. Accuracy and precision
were in the range 0.7 - 5.1 and 0.1 - 0.6%, respectively, for the two
analytes and the limits of detection for meperidine and ondansetron w
ere 1.73 mu g/mL and 47 ng/mL, respectively, based on a signal to nois
e ratio of 3 and a 20 mu L injection.