Vk. Sharma et al., Oral pharmacokinetics of omeprazole and lansoprazole after single and repeated doses as intact capsules or as suspensions in sodium bicarbonate, ALIM PHARM, 14(7), 2000, pp. 887-892
Background: Omeprazole and lansoprazole can be given in sodium bicarbonate
as, respectively, simplified omeprazole suspension and simplified lansopraz
ole suspension. We previously found the antisecretory effect of omeprazole
20 mg given as simplified omeprazole suspension to be lower than with intac
t capsules. However, lansoprazole 30 mg as simplified lansoprazole suspensi
on produced an effect similar to that seen with intact capsules.
Aim: To evaluate the absorption of both drugs when given orally as capsules
or as suspensions in sodium bicarbonate.
Methods: In random order, we gave 5-day courses of omeprazole 20 mg and lan
soprazole 30 mg as capsules and as suspensions in sodium bicarbonate to 12
healthy women. Serial blood samples were taken on days 1 and 5 of each cour
se for pharmacokinetic measurements.
Results: There was impairment of omeprazole absorption when given as simpli
fied omeprazole suspension. Maximum plasma concentration and area under the
concentration/time curve were lower with simplified omeprazole suspension
than with omeprazole capsules (P=0.034 and 0.013, respectively, on day 5).
No differences were found in lansoprazole absorption when simplified lansop
razole suspension was compared with its standard capsule formulation. Relat
ive bioavailability of omeprazole from simplified omeprazole suspension com
pared to the capsule was 58.4% on day 5. The corresponding value for lansop
razole was 84.7%.
Conclusions: Simplified omeprazole suspension 20 mg does not supply adequat
e omeprazole for systemic absorption. Lansoprazole absorption from simplifi
ed lansoprazole suspension is maintained.