Bioavailability of intranasal metoclopramide. 1989

M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
Department of Clinical Pharmacology, University of Wales College of Medicine, Liandough Hospital, South Glamorgan.

After intranasal administration of metoclopramide, (5 mg in 0.5 ml sterile water) the maximum plasma concentration of 13.5 +/- 7.3 (mean +/- s.d.) ng ml-1 was achieved. Absolute bioavailability was 50.5 +/- 29.5%, 110 +/- 41 min later. We conclude that the intranasal route does not allow rapid absorption of the drug and is not associated with greater bioavailability than the oral route.

UI MeSH Term Description Entries
D007275 Injections, Intravenous Injections made into a vein for therapeutic or experimental purposes. Intravenous Injections,Injection, Intravenous,Intravenous Injection
D008297 Male Males
D008787 Metoclopramide A dopamine D2 antagonist that is used as an antiemetic. 4-Amino-5-chloro-N-(2-(diethylamino)ethyl)-2-methoxybenzamide,Cerucal,Maxolon,Metaclopramide,Metoclopramide Dihydrochloride,Metoclopramide Hydrochloride,Metoclopramide Monohydrochloride,Metoclopramide Monohydrochloride, Monohydrate,Primperan,Reglan,Rimetin,Dihydrochloride, Metoclopramide,Hydrochloride, Metoclopramide,Monohydrochloride, Metoclopramide
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000042 Absorption The physical or physiological processes by which substances, tissue, cells, etc. take up or take in other substances or energy.
D000281 Administration, Intranasal Delivery of medications through the nasal mucosa. Drug Administration, Intranasal,Administration, Intranasal Drug,Administration, Nasal,Intranasal Administration,Intranasal Drug Administration,Administrations, Intranasal,Administrations, Intranasal Drug,Administrations, Nasal,Drug Administrations, Intranasal,Intranasal Administrations,Intranasal Drug Administrations,Nasal Administration,Nasal Administrations
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D001682 Biological Availability The extent to which the active ingredient of a drug dosage form becomes available at the site of drug action or in a biological medium believed to reflect accessibility to a site of action. Availability Equivalency,Bioavailability,Physiologic Availability,Availability, Biologic,Availability, Biological,Availability, Physiologic,Biologic Availability,Availabilities, Biologic,Availabilities, Biological,Availabilities, Physiologic,Availability Equivalencies,Bioavailabilities,Biologic Availabilities,Biological Availabilities,Equivalencies, Availability,Equivalency, Availability,Physiologic Availabilities

Related Publications

M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
August 1999, Drugs,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
January 1986, European journal of clinical pharmacology,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
December 1989, British journal of clinical pharmacology,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
June 1990, Arzneimittel-Forschung,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
April 1994, Journal of veterinary pharmacology and therapeutics,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
November 1999, European journal of clinical pharmacology,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
February 2013, Epilepsy research,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
August 2011, European journal of clinical pharmacology,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
January 1984, Arzneimittel-Forschung,
M J Ward, and D C Buss, and J Ellershaw, and A Nash, and P A Routledge
January 1986, European journal of drug metabolism and pharmacokinetics,
Copied contents to your clipboard!