{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["53(9)"],"submitter":["Abbas Y"],"pubmed_abstract":["Oral bioavailability is a crucial pharmacokinetic (PK) parameter optimized by drug developers working on new therapeutic compounds. The goal is to obtain adequate systemic exposure and to establish safe and effective therapeutic dosages. Critical to optimizing oral bioavailability is understanding a compound's susceptibility to first-pass metabolism, determined by the intricate relationship between gut absorption, metabolism, and hepatic metabolism. Efforts to model this relationship in vitro have led to the emergence of microphysiological systems (MPSs) that consist of multiple, fluidically linked organs. Here, we describe an MPS that links the gut and liver, capable of simulating both oral and intravenous dosing routes and is made up of entirely primary human cells: a gut barrier tissue "],"journal":["Drug metabolism and disposition: the biological fate of chemicals"],"pagination":["100130"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12597587"],"repository":["biostudies-literature"],"pubmed_title":["A primary human Gut/Liver microphysiological system to estimate human oral bioavailability."],"pmcid":["PMC12597587"],"pubmed_authors":["van Wyk M","Christophi J","Spreen AA","Boazak EM","Kostrzewski T","Bliton RJ","Sze H","Abbas Y"],"additional_accession":[]},"is_claimable":false,"name":"A primary human Gut/Liver microphysiological system to estimate human oral bioavailability.","description":"Oral bioavailability is a crucial pharmacokinetic (PK) parameter optimized by drug developers working on new therapeutic compounds. The goal is to obtain adequate systemic exposure and to establish safe and effective therapeutic dosages. Critical to optimizing oral bioavailability is understanding a compound's susceptibility to first-pass metabolism, determined by the intricate relationship between gut absorption, metabolism, and hepatic metabolism. Efforts to model this relationship in vitro have led to the emergence of microphysiological systems (MPSs) that consist of multiple, fluidically linked organs. Here, we describe an MPS that links the gut and liver, capable of simulating both oral and intravenous dosing routes and is made up of entirely primary human cells: a gut barrier tissue ","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Sep","modification":"2026-06-05T12:29:14.99Z","creation":"2026-05-16T03:13:00.129Z"},"accession":"S-EPMC12597587","cross_references":{"pubmed":["40829518"],"doi":["10.1016/j.dmd.2025.100130"]}}