Hl. Zhang et al., HPLC DETERMINATION OF IDARUBICIN-ETOPOSIDE AND IDARUBICIN-ONDANSETRONMIXTURES IN 0.9-PERCENT SODIUM-CHLORIDE INJECTION USP, Journal of liquid chromatography & related technologies, 21(7), 1998, pp. 979-988
Citations number
17
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
High performance liquid chromatographic methods have been developed fo
r the assays of idarubicin-etoposide and idarubicin-ondansetron mixtur
es in 0.9% sodium chloride injection USP. The separation and quantitat
ion of the idarubicin-etoposide mixture was achieved on an octylsilane
column at ambient temperature using a mobile phase of 73:27 v/v 0.02
M aqueous monobasic sodium phosphate - acetonitrile at a flow rate of
1.0 mL/min with UV detection at 254 nm. The separation was achieved wi
thin 13 min. The method showed linearity for idarubicin hydrochloride
and etoposide in the 2 - 32 and 10 - 160 mu g/mL, ranges, respectively
. Accuracy and precision were in the 0.1 - 2.9% and 0.1 - 2.1% ranges,
respectively, for both analytes. The separation and quantitation of t
he idarubicin-ondansetron mixture was accomplished on an octadecylsila
ne column at ambient temperature using a mobile phase of 57:43 v/v 0.0
2 M aqueous monobasic potassium phosphate - acetonitrile at a flow lat
e of 1.8 mL/min with UV detection at 254 nm. The separation was achiev
ed within 15 min. The method showed Linearity for idarubicin hydrochlo
ride and ondansetron in the 2.4-38 and 2.3-37 mu g/mL, ranges, respect
ively, for both analytes.