Ajpm. Smout et al., EFFECT OF AN EVENING DOSE OF REGULAR AND EFFERVESCENT FORMULATIONS OFRANITIDINE OR CIMETIDINE ON INTRAGASTRIC PH IN HEALTHY-VOLUNTEERS, Alimentary pharmacology & therapeutics, 9(1), 1995, pp. 51-56
Aims: To compare the effects on intragastric acidity of a single eveni
ng dose of either standard or effervescent formulations of ranitidine
(300 mg) or cimetidine (800 mg). Methods: Twelve healthy subjects were
studied, using a four-period randomized cross-over design and an ambu
latory intragastric pH monitoring technique. The subjects received a s
tandard evening meal at 17.00 hours and one of the H-2-receptor antago
nist formulations was given at 23.00 hours. Results: Both effervescent
formulations caused a transient rapid increase in intragastric pH, re
aching a maximum at about 3 min after ingestion. After both effervesce
nt formulations a significantly higher pH was measured during the firs
t 45 min after ingestion (P < 0.05), compared to the regular formulati
ons. The onset of action of the H-2-receptor antagonists was similar f
or both formulations of ranitidine and the effervescent cimetidine, bu
t tended to be slower for the regular cimetidine (P = 0.06). Nocturnal
intragastric pH was significantly increased by all four formulations,
but more effectively so by the two ranitidine formulations. The durat
ion of action (taken as time with pH > 4) of both ranitidine formulati
ons was longer than that of both cimetidine formulations (P < 0.002).
Conclusions: A single evening dose of 300 mg ranitidine produces a str
onger decrease of nocturnal gastric acid secretion than 800 mg cimetid
ine. The effervescent formulations of both drugs offer the advantage o
f a rapid decrease (within minutes) of intragastric acidity, with pres
ervation of the sustained systemic effect.