Time-varying compartmental models capture hours-scale variation in the elimination kinetics of vancomycin in rats

• Published in: British journal of pharmacology Vol. 182; no. 13; p. 2986
• Main Authors: McDonough, Matthew H, Gerson, Julian, Kippin, Tod, Meiring, Wendy, Plaxco, Kevin W
• Format: Journal Article
• Language: English
• Published: England 01.07.2025
• Subjects: Animals; Anti-Bacterial Agents - blood; Anti-Bacterial Agents - pharmacokinetics; Male; Models, Biological; Rats; Rats, Sprague-Dawley; Time Factors; Vancomycin - blood; Vancomycin - pharmacokinetics; compartment models; renal function; animal models; Bayesian information criterion; nonlinear least squares regression
• ISSN: 1476-5381
• DOI: 10.1111/bph.70020

Pharmacokinetics have traditionally been assessed using concentration measurements with relatively low temporal resolution, such as from blood draws, leading to pharmacokinetic profiles estimated from sparse data, often averaged across subjects. Recent advances in in vivo sensors, however, now enable the collection of hundreds of observations over a few hours in individual subjects. Previous analyses of such data for the antibiotic tobramycin identified significant (several-fold), hours-scale changes in the efficiency with which this renally cleared drug is eliminated in anaesthetised rats. Here, we apply similar analyses to study the pharmacokinetics of another renally cleared drug, the antibiotic vancomycin. We estimate vancomycin pharmacokinetic profiles using previously collected time-dense plasma concentration measurements within six anaesthetised rats. Specifically, we fit standard one- and two-compartment models, as well as time-varying one-compartment models (in which the proportionality relating concentration to elimination rate is time-varying), to these data to investigate if the time-varying models are statistically preferred for describing individual-level vancomycin pharmacokinetics, over standard one- and two-compartment models. One-compartment models incorporating time-varying elimination proportionalities are statistically preferred over standard one- and two-compartment models for five of our six vancomycin time courses. When the initial impact of the distribution phase is removed from these data, a reciprocally time-varying one-compartment model is preferred over the standard-one compartment model in four of five considered datasets. These results provide further animal-model evidence that the pharmacokinetics of renally cleared drugs can vary significantly over timescales as short as a few hours.