RT Journal Article
SR Electronic
T1 Optimized Experimental Design for the Estimation of Enzyme Kinetic Parameters: An Experimental Evaluation
JF Drug Metabolism and Disposition
JO Drug Metab Dispos
FD American Society for Pharmacology and Experimental Therapeutics
SP 2273
OP 2279
DO 10.1124/dmd.112.047373
VO 40
IS 12
A1 Erik Sjögren
A1 Petter Svanberg
A1 Kajsa P. Kanebratt
YR 2012
UL http://dmd.aspetjournals.org/content/40/12/2273.abstract
AB A set of compounds (n = 30), including traditional cytochrome P450 substrates and compounds from AstraZeneca's compound library, was used in an experimental evaluation of an optimal design approach (ODA) for the estimation of enzyme kinetic parameters (CLint, Vmax, and Km). A depletion method previously shown to provide reliable results, the multiple depletion curves method (MDCM), was used as reference. Experiments were conducted with human liver microsomes, and samples were analyzed using liquid chromatography-tandem mass spectrometry. CLint estimated with the ODA were in >90% of the cases within a 2-fold difference compared with MDCM estimates. In addition, good agreement was generally seen for Vmax and Km estimates between the two methods as >80% of the estimates were within or almost within a 2-fold difference. The variability in Vmax and Km estimates were generally higher than for CLint estimates. In addition, decreased substrate turnover considerably increased the variability in Vmax and Km estimates, whereas only a modest increase was observed for CLint estimates. The experimental design of using multiple starting concentrations for the estimation of enzyme kinetics was shown to be appropriate even when there was a limitation to the number of samples. The method allowed for good estimates of CLint and also for Vmax and Km in many cases. Hence, this approach is a good alternative for the estimation of enzyme kinetic parameters, especially if enzyme saturation and an assessment of a potential risk for nonlinear metabolism are of interest.