A. Macgowan et al., In vitro models, in vivo models, and pharmacokinetics: What can we learn from in vitro models?, CLIN INF D, 33, 2001, pp. S214-S220
In vitro pharmacokinetic models of infection can make an important contribu
tion to the study of the pharmacodynamic properties of an antibacterial age
nt. In conjunction with animal and human pharmacodynamic evaluations, they
provide data to allow for the optimization of drug dosing regimens. In vitr
o models can be used simply to describe the effect of a drug on a bacterial
population as well as to provide data for more-analytical studies, includi
ng hypothesis testing. Analytical study designs provide information on the
pharmacodynamic parameter best related to the chosen outcome, as well as it
s magnitude. Factors such as the characteristics of the model (method of dr
ug removal, inoculum density, and growth phase), doses simulated, species a
nd susceptibility range of bacteria, and methods and analytical tools used
to measure antibacterial effect will have an effect on the conclusions draw
n. In vitro models have an important future role in ensuring antibiotic eff
icacy and in reducing the risks of resistance.