Using pharmacokinetics in drug therapy. VI: Comparing methods for dealing with nonlinear drugs like phenytoin.

GE Schumacher - American Journal of Hospital Pharmacy, 1980 - europepmc.org
Four methods for estimating dosage regimens for drugs exhibiting non-linear
pharmacokinetic behavior (eg, phenytoin) are described and compared. Estimations of …

Understanding the dose-effect relationship: clinical application of pharmacokinetic-pharmacodynamic models

NHG Holford, LB Sheiner - Clinical pharmacokinetics, 1981 - Springer
It is a major goal of clinical pharmacology to understand the dose-effect relationship in
therapeutics. Much progress towards this goal has been made in the last 2 decades through …

Clinical Pharmacokinetics: (First of Two Parts)

DJ Greenblatt, J Koch-Weser - New England Journal of Medicine, 1975 - Mass Medical Soc
THE intensity of the therapeutic and toxic effects of most pharmacologic agents depends on
their concentration at the sites of action. The time course of this concentration is determined …

[引用][C] Use of unbound drug concentration in blood to discriminate between two models of hepatic drug elimination

DJ Morgan, K Raymond - Journal of Pharmaceutical Sciences, 1982 - Elsevier
The preceding paper (1) discusses my earlier criticism, based on pragmatic reasons, of the
paper (2) published by Amirjahed (3). It was suggested by Amirjahed (3) that if only 10 …

[引用][C] Pharmacokinetics, science or fiction?

A RESCIGNO - Pharmacological research, 1996 - Elsevier
Pharmacokinetics, Science or Fiction? Page 1 Pharmacological Research, Vol. 33, No. 4/5,
1996 PHARMACOKINETICS, SCIENCE OR FICTION? ALDO RESCIGNO Institute of …

Pharmacokinetics of intravenous clomiphene isomers.

M Szutu, DJ Morgan, M McLeish… - British journal of …, 1989 - ncbi.nlm.nih.gov
Although clomiphene has been used extensively in the treatment of anovulation in normal
cycling women for more than 20 years, little is known about the pharmacokinetics of the …

Haemodynamic and pharmacological effects of the converting enzyme inhibitor CGS 14824A in normal volunteers

MD Schaller, J Nussberger, B Waeber… - European journal of …, 1985 - Springer
The converting enzyme inhibitor CGS 14824A was evaluated in 15 healthy male volunteers.
First, the efficacy of a single 5 or 10 mg oral dose in antagonizing the pressor response to …

Consideration of the unbound drug concentration in enzyme kinetics

NJ Waters, RS Obach, L Di - Enzyme Kinetics in Drug Metabolism …, 2014 - Springer
The study of enzyme kinetics in drug metabolism involves assessment of rates of
metabolism and inhibitory potencies over a suitable concentration range. In all but the very …

Simple transformation method for predicting plasma drug profiles from dissolution rates

DP Vaughan, RH Leach - Journal of Pharmaceutical Sciences, 1976 - Wiley Online Library
A transformation factor is described which related in vitro drug dissolution from a preparation
to the corresponding in vivo plasma drug concentrations. This factor, derived from the …

Clinical pharmacokinetics: the first 30 years

TM Speight, V Sjöqvist - Clinical pharmacokinetics, 2006 - Springer
This year, 2006, marks the 30th anniversary of dren [3] and pregnant women;[4] patients with
various the arrival of Clinical Pharmacokinetics onto the disease states including renal and …