TY - JOUR T1 - Evaluation of in vitro models for assessment of human intestinal metabolism in drug discovery JF - Drug Metabolism and Disposition JO - Drug Metab Dispos DO - 10.1124/dmd.120.000111 SP - DMD-AR-2020-000111 AU - Mari Davies AU - Prabha Peramuhendige AU - Lloyd King AU - Melanie Golding AU - Apoorva Kotian AU - Mark Penney AU - Syeda Shah AU - Nenad Manevski Y1 - 2020/01/01 UR - http://dmd.aspetjournals.org/content/early/2020/08/29/dmd.120.000111.abstract N2 - 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 (fg)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 (CLint) and qualify metabolite formation (QuanQual). Fraction unbound in the incubation (fu,inc) was determined by rapid-equilibrium dialysis (RED). Measured in vitro results [intrinsic clearance (CLint) and fu,inc] were supplemented with literature data [passive Caco-2 A→B permeability, enterocyte blood flow (Qent), and intestinal surface area (A)] and combined using a midazolam-calibrated Qgut model to predict human fg 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 fg values were acceptable for the high fg compounds (arbitrarily fg>0.7). However, predictions of low and moderate fg values (arbitrarily fg<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. Significance Statement We found that cellular models of the human gut (permeabilized enterocytes and cryopreserved intestinal mucosa) offer an alternative to and potential advantage over intestinal microsomes in studies of drug metabolism, particularly for low clearance compounds and alternative pathways (e.g. sulfation, hydrolases, and flavin-containing monooxigenases). The predictivity of human fg for common CYP- and UGT-substrates based on the Qgut model is still limited, however, and appropriate further evaluation is recommended. ER -