Preterm Physiologically Based Pharmacokinetic Model. Part II: Applications of the Model to Predict Drug Pharmacokinetics in the Preterm Population

• Published in: Clinical pharmacokinetics Vol. 59; no. 4; pp. 501 - 518
• Main Authors: Abduljalil, Khaled, Pan, Xian, Pansari, Amita, Jamei, Masoud, Johnson, Trevor N.
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.04.2020; Springer Nature B.V
• Subjects: Cytochrome; Drug development; Drug dosages; Enzymes; Internal Medicine; Liver; Medicine; Medicine & Public Health; Metabolism; Newborn babies; Nonsteroidal anti-inflammatory drugs; Original Research Article; Pharmaceutical industry; Pharmacokinetics; Pharmacology/Toxicology; Pharmacotherapy; Physiology; Premature birth
• ISSN: 0312-5963; 1179-1926
• DOI: 10.1007/s40262-019-00827-4

Background Preterm neonates are usually not part of a traditional drug development programme, however they are frequently administered medicines. Developing modelling and simulation tools, such as physiologically based pharmacokinetic (PBPK) models that incorporate developmental physiology and maturation of drug metabolism, can be used to predict drug exposure in this group of patients, and may help to optimize drug dose adjustment. Objective The aim of this study was to assess and verify the predictability of a preterm PBPK model using compounds that undergo diverse renal and/or hepatic clearance based on the knowledge of their disposition in adults. Methods A PBPK model was developed in the Simcyp Simulator V17 to predict the pharmacokinetics (PK) of drugs in preterm neonates. Drug parameters for alfentanil, midazolam, caffeine, ibuprofen, gentamicin and vancomycin were collated from the literature. Predicted PK parameters and profiles were compared against the observed data. Results The preterm PBPK model predicted the PK changes of the six compounds using ontogeny functions for cytochrome P450 (CYP) 1A2, CYP2C9 and CYP3A4 after oral and intravenous administrations. For gentamicin and vancomycin, the maturation of renal function was able to predict the exposure of these two compounds after intravenous administration. All PK parameter predictions were within a twofold error criteria. Conclusion While the developed preterm model for the prediction of PK behaviour in preterm patients is not intended to replace clinical studies, it can potentially help with deciding on first-time dosing in this population and study design in the absence of clinical data.