Time for phenytoin concentration to peak: consequences of first-order and zero-order absorption. 1989

D L McCauley, and T N Tozer, and M E Winter
Division of Clinical Pharmacy, School of Pharmacy, University of California, San Francisco 94143-0622.

An increase in the time required to achieve the peak plasma concentration is observed following the oral administration of increasing doses of phenytoin. Zero-order absorption is the usual explanation for this observation. The presence of Michaelis-Menten elimination also increases the peak time when absorption is first order. The contribution of each of these mechanisms in vivo is unknown.

UI MeSH Term Description Entries
D007408 Intestinal Absorption Uptake of substances through the lining of the INTESTINES. Absorption, Intestinal
D008954 Models, Biological Theoretical representations that simulate the behavior or activity of biological processes or diseases. For disease models in living animals, DISEASE MODELS, ANIMAL is available. Biological models include the use of mathematical equations, computers, and other electronic equipment. Biological Model,Biological Models,Model, Biological,Models, Biologic,Biologic Model,Biologic Models,Model, Biologic
D010672 Phenytoin An anticonvulsant that is used to treat a wide variety of seizures. It is also an anti-arrhythmic and a muscle relaxant. The mechanism of therapeutic action is not clear, although several cellular actions have been described including effects on ion channels, active transport, and general membrane stabilization. The mechanism of its muscle relaxant effect appears to involve a reduction in the sensitivity of muscle spindles to stretch. Phenytoin has been proposed for several other therapeutic uses, but its use has been limited by its many adverse effects and interactions with other drugs. Diphenylhydantoin,Fenitoin,Phenhydan,5,5-Diphenylhydantoin,5,5-diphenylimidazolidine-2,4-dione,Antisacer,Difenin,Dihydan,Dilantin,Epamin,Epanutin,Hydantol,Phenytoin Sodium,Sodium Diphenylhydantoinate,Diphenylhydantoinate, Sodium
D006207 Half-Life The time it takes for a substance (drug, radioactive nuclide, or other) to lose half of its pharmacologic, physiologic, or radiologic activity. Halflife,Half Life,Half-Lifes,Halflifes
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000284 Administration, Oral The giving of drugs, chemicals, or other substances by mouth. Drug Administration, Oral,Administration, Oral Drug,Oral Administration,Oral Drug Administration,Administrations, Oral,Administrations, Oral Drug,Drug Administrations, Oral,Oral Administrations,Oral Drug Administrations
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor

Related Publications

D L McCauley, and T N Tozer, and M E Winter
May 1994, International journal of clinical pharmacology and therapeutics,
D L McCauley, and T N Tozer, and M E Winter
May 1990, Journal of pharmaceutical sciences,
D L McCauley, and T N Tozer, and M E Winter
September 1986, Journal of pharmaceutical sciences,
D L McCauley, and T N Tozer, and M E Winter
September 1988, Journal of pharmaceutical sciences,
D L McCauley, and T N Tozer, and M E Winter
January 1981, Biopharmaceutics & drug disposition,
D L McCauley, and T N Tozer, and M E Winter
February 1984, Computers and biomedical research, an international journal,
D L McCauley, and T N Tozer, and M E Winter
December 1976, Food and cosmetics toxicology,
D L McCauley, and T N Tozer, and M E Winter
December 1976, Food and cosmetics toxicology,
Copied contents to your clipboard!