Ra. Quercia et al., STABILITY OF GRANISETRON HYDROCHLORIDE IN AN EXTEMPORANEOUSLY PREPARED ORAL LIQUID, American journal of health-system pharmacy, 54(12), 1997, pp. 1404-1406
The stability of granisetron 0.2 mg/mL (as the hydrochloride salt) in
an extemporaneously prepared oral liquid was studied. Twelve 1-mg gran
isetron tablets were pulverized and suspended in 30 mL of distilled wa
ter. This mixture was then diluted with cherry syrup to produce a 60-m
L oral liquid with a granisetron concentration of 0.2 mg/mL. Half of t
he preparation was stored at 5 degrees C, and half was stored at 24 de
grees C. Samples were taken on days 0, 1, 2, 3, 4, 6, 8, 10, 12, and 1
4 and assayed by high-performance liquid chromatography. There was no
change in the liquid's color, consistency, or pH, and the concentratio
ns of granisetron ranged from 97% to 104% of initial concentration dur
ing the 14 days at 5 and 24 degrees C. Granisetron 0.2 mg/mL (as the h
ydrochloride salt) in an extemporaneously prepared oral liquid was sta
ble for up to 14 days.