Although intestinal metabolism plays an important role in drug disposition, early predictions of human outcomes are challenging, in-part due to limitations of available in vitro models. To address this, we have evaluated three in vitro models of human intestine (microsomes, permeabilized enterocytes, and cryopreserved intestinal mucosal epithelium) as tools to assess intestinal metabolism and estimate the fraction escaping gut metabolism (f g) in drug discovery. The models were tested with a chemically diverse set of 32 compounds, including substrates for oxidoreductive, hydrolytic, and conjugative enzymes. Liquid chromatography-high resolution mass spectrometry (LC-HRMS) was used to quantify substrate disappearance (CL int) and qualify metabolite formation (QuanQual). Fraction unbound in the incubation (f u,inc) was determined by rapid-equilibrium dialysis (RED). Measured in vitro results [intrinsic clearance (CL int) and f u,inc ] were supplemented with literature data [passive Caco-2 A→B permeability, enterocyte blood flow (Q ent), and intestinal surface area (A)] and combined using a midazolam-calibrated Q gut model to predict human f g values. All three models showed reliable cytochrome P450 (CYP) and UDP-glucuronosyltransferase (UGT) activities, but enterocytes and mucosa may offer advantages for low clearance compounds and alternative pathways (e.g. sulfation, hydrolases, and flavin-containing monooxigenases). Early predictions of human f g values were acceptable for the high f g compounds (arbitrarily f g >0.7). However, predictions of low and moderate f g values (arbitrarily f g <0.7) remain challenging, indicating that further evaluation is needed (e.g. saturation effects and impact of transporters), but not immediate compound avoidance. Results suggest that tested models offer an additional value in drug discovery, especially for drug design and chemotype evaluation.
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