Effects of food type on the extent of drug-drug interactions between activated charcoal and phenobarbital in rats.
Absorption
Activated charcoal
Adsorption
Drug-drug interaction
Enteral nutrient
Food type
High-fat meal
Phenobarbital
Standard breakfast
Journal
Drug metabolism and pharmacokinetics
ISSN: 1880-0920
Titre abrégé: Drug Metab Pharmacokinet
Pays: England
ID NLM: 101164773
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
26
12
2018
revised:
25
04
2019
accepted:
15
05
2019
pubmed:
1
7
2019
medline:
6
2
2020
entrez:
1
7
2019
Statut:
ppublish
Résumé
Activated charcoal is known to decrease the intestinal absorption of co-administered drug by adsorption. The extent of this drug-drug interaction (DDI) is attenuated by food intake. The aim of this study was to quantitatively evaluate the effects of food type on the extent of DDI between phenobarbital and activated charcoal using a rat model. Phenobarbital was orally administered at a dose of 1.5 mg/kg with or without 33 mg/kg of activated charcoal under fasted or fed conditions, and the plasma concentration profile of phenobarbital was monitored. Several fed conditions, such as a standard breakfast, high-fat meal or enteral nutrient used in human studies, were examined. Under the fasted conditions, activated charcoal significantly decreased the area under the plasma concentration - time curve (AUC) of phenobarbital by 45.2%. When the standard breakfast or high-fat meal was fed, this DDI was reduced to 28.3 and 18.0%, respectively, as assessed by the reduction in the AUC. On the contrary, enteral nutrient did not significantly attenuate the DDI. In conclusion, the influence of food intake on the extent of DDI between phenobarbital and activated charcoal was found to differ among the types of food concomitantly ingested.
Identifiants
pubmed: 31255507
pii: S1347-4367(18)30496-8
doi: 10.1016/j.dmpk.2019.05.002
pii:
doi:
Substances chimiques
Charcoal
16291-96-6
Phenobarbital
YQE403BP4D
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
287-291Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.