Pharmacokinetics of caffeine

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Through an exhaustive search of the literature, caffeine in vivo pharmacokinetics has been reviewed on the basis of available systematic studies. History and physicochemical variables related to caffeine, and the physiological factors (dosing, age, genetic factors, disease states, pregnancy, smoking, and drug interactions) which can affect caffeine disposition in humans and animals, have been considered. Interspecies variation in caffeine pharmacokinetics has been treated as a property and consequence of body size (allometry). Linear relationships have been reported between pharmacokinetic parameters, pharmacokinetic time (a variable in terms of chronological time), and body weight across seven mammalian species, taking into account species-longevity differences too. The urinary excretion pattern of caffeine metabolites was found to be more species specific, each species presenting its own metabolic profile. This peculiar pharmacokinetic profile may render caffeine useful in the future as a natural biological probe to clarify genetic, phylogenetic, and ontogenetic events in drug metabolism, and for determining intra- and interspecies physiopathological characteristics.

Original languageEnglish
Pages (from-to)33-39
Number of pages7
JournalISI Atlas of Science: Pharmacology
Volume2
Issue number1
Publication statusPublished - 1988

Fingerprint

Caffeine
Pharmacokinetics
Inborn Genetic Diseases
Metabolome
Age Factors
Body Size
Drug Interactions
Smoking
History
Body Weight
Pregnancy
Pharmaceutical Preparations

ASJC Scopus subject areas

  • Pharmacology, Toxicology and Pharmaceutics(all)

Cite this

Pharmacokinetics of caffeine. / Bonati, M.; Garattini, S.

In: ISI Atlas of Science: Pharmacology, Vol. 2, No. 1, 1988, p. 33-39.

Research output: Contribution to journalArticle

@article{de1d82201d424b33bec734104c912e15,
title = "Pharmacokinetics of caffeine",
abstract = "Through an exhaustive search of the literature, caffeine in vivo pharmacokinetics has been reviewed on the basis of available systematic studies. History and physicochemical variables related to caffeine, and the physiological factors (dosing, age, genetic factors, disease states, pregnancy, smoking, and drug interactions) which can affect caffeine disposition in humans and animals, have been considered. Interspecies variation in caffeine pharmacokinetics has been treated as a property and consequence of body size (allometry). Linear relationships have been reported between pharmacokinetic parameters, pharmacokinetic time (a variable in terms of chronological time), and body weight across seven mammalian species, taking into account species-longevity differences too. The urinary excretion pattern of caffeine metabolites was found to be more species specific, each species presenting its own metabolic profile. This peculiar pharmacokinetic profile may render caffeine useful in the future as a natural biological probe to clarify genetic, phylogenetic, and ontogenetic events in drug metabolism, and for determining intra- and interspecies physiopathological characteristics.",
author = "M. Bonati and S. Garattini",
year = "1988",
language = "English",
volume = "2",
pages = "33--39",
journal = "ISI Atlas of Science: Pharmacology",
issn = "0890-9083",
number = "1",

}

TY - JOUR

T1 - Pharmacokinetics of caffeine

AU - Bonati, M.

AU - Garattini, S.

PY - 1988

Y1 - 1988

N2 - Through an exhaustive search of the literature, caffeine in vivo pharmacokinetics has been reviewed on the basis of available systematic studies. History and physicochemical variables related to caffeine, and the physiological factors (dosing, age, genetic factors, disease states, pregnancy, smoking, and drug interactions) which can affect caffeine disposition in humans and animals, have been considered. Interspecies variation in caffeine pharmacokinetics has been treated as a property and consequence of body size (allometry). Linear relationships have been reported between pharmacokinetic parameters, pharmacokinetic time (a variable in terms of chronological time), and body weight across seven mammalian species, taking into account species-longevity differences too. The urinary excretion pattern of caffeine metabolites was found to be more species specific, each species presenting its own metabolic profile. This peculiar pharmacokinetic profile may render caffeine useful in the future as a natural biological probe to clarify genetic, phylogenetic, and ontogenetic events in drug metabolism, and for determining intra- and interspecies physiopathological characteristics.

AB - Through an exhaustive search of the literature, caffeine in vivo pharmacokinetics has been reviewed on the basis of available systematic studies. History and physicochemical variables related to caffeine, and the physiological factors (dosing, age, genetic factors, disease states, pregnancy, smoking, and drug interactions) which can affect caffeine disposition in humans and animals, have been considered. Interspecies variation in caffeine pharmacokinetics has been treated as a property and consequence of body size (allometry). Linear relationships have been reported between pharmacokinetic parameters, pharmacokinetic time (a variable in terms of chronological time), and body weight across seven mammalian species, taking into account species-longevity differences too. The urinary excretion pattern of caffeine metabolites was found to be more species specific, each species presenting its own metabolic profile. This peculiar pharmacokinetic profile may render caffeine useful in the future as a natural biological probe to clarify genetic, phylogenetic, and ontogenetic events in drug metabolism, and for determining intra- and interspecies physiopathological characteristics.

UR - http://www.scopus.com/inward/record.url?scp=0023944590&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0023944590&partnerID=8YFLogxK

M3 - Article

VL - 2

SP - 33

EP - 39

JO - ISI Atlas of Science: Pharmacology

JF - ISI Atlas of Science: Pharmacology

SN - 0890-9083

IS - 1

ER -