ArticleThe AAPS journal2025
Optimization of In Vitro CYP3A4 TDI Assay Conditions and Use of Derived Parameters for Clinical DDI Risk Assessment Using Static and Dynamic Models.
Article in The AAPS journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Cytochrome P450 3A4 (CYP3A4) is a key target for time-dependent inhibition (TDI) assessment during drug development. However, translating in vitro TDI data to in vivo drug-drug interaction (DDI) risk remains challenging due to the acknowledged overestimation when incorporating in vitro kinetics in predictive models. We investigated different in vitro TDI assay conditions in human liver microsomes (HLM) and evaluated their impact on the predictive accuracy for CYP3A4-related DDI for 32 marketed drugs. Considering assay sensitivity and in vivo DDI prediction accuracy with mechanistic static modeling (MSM), optimal incubation parameters were identified as: a pre-incubation time of 40 min for precipitants and 10 min incubation time for CYP3A4 substrate midazolam (10 μM) at 0.1 mg/mL HLM. A tendency to overestimate the DDI magnitude (AFE = 4.83, AAFE = 4.87) was still observed in MSM when using the unbound drug inhibition constant (KI,
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