Effect of Dimeticone and Pepsin on the Bioavailability of Metoclopramide in Healthy Volunteers
Autor: | R A de Moraes, M. O. de Moraes, Gisela Costa Camarão, F A Frota Bezerra, A L A e Silva Leite, D F do Nascimento, M.E.A. de Moraes |
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Rok vydání: | 2014 |
Předmět: |
Adult
Male Adolescent Metoclopramide Metabolic Clearance Rate Administration Oral Biological Availability Absorption (skin) Pharmacology Bioequivalence Young Adult Pepsin Pharmacokinetics Tandem Mass Spectrometry Drug Discovery medicine Humans Dimethylpolysiloxanes Dosing Chromatography High Pressure Liquid Cross-Over Studies biology business.industry General Medicine Middle Aged Crossover study Healthy Volunteers Pepsin A Bioavailability Drug Combinations Area Under Curve biology.protein Female business Brazil Tablets medicine.drug |
Zdroj: | Drug Research. 64:537-540 |
ISSN: | 2194-9387 2194-9379 |
DOI: | 10.1055/s-0033-1363250 |
Popis: | Objective To assess the effect of dimeticone and pepsin on the bioavailability of metoclopramide (CAS 7232-21-5) in healthy volunteers. Methods The study was conducted using a randomized, open, 2-period crossover design. The volunteers received single administration of 7-mg conventional metoclopramide capsule and a formulation containing metoclopramide (7 mg) plus dimeticone (40 mg) and pepsin (50 mg), with a 7-day interval between treatments. Serial blood samples were collected before dosing and during 24 h post-treatment. Plasma metoclopramide concentrations were analyzed by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). The pharmacokinetics parameters AUC(last) and C(max) were obtained from the metoclopramide plasma concentration vs. time curves. Results Metoclopramide's association was bioequivalent to conventional capsule; 90% CIs for geometric mean treatment ratios of C(max) [108.0% (90% CI, 100.4-116.3%)], AUC(last) [103.3% (90% CI, 99.5-107.4%)] were within the predefined range. The metoclopramide formulations were well tolerated at the administered doses and no significant adverse reactions were observed. Thus, these results confirm the good bioavailability of metoclopramide in the new formulation and rule out any impaired absorption when the drugs are formulated in combination. |
Databáze: | OpenAIRE |
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