| Literature DB >> 32341538 |
Thomas von Erlach1, Sarah Saxton1, Yunhua Shi1, Daniel Minahan1, Daniel Reker1,2, Farhad Javid1, Young-Ah Lucy Lee1, Carl Schoellhammer1, Tina Esfandiary1, Cody Cleveland1,2, Lucas Booth1, Jiaqi Lin1, Hannah Levy1, Sophie Blackburn1, Alison Hayward3, Robert Langer4,5,6, Giovanni Traverso7,8,9.
Abstract
Monolayers of cancer-derived cell lines are widely used in the modelling of the gastrointestinal (GI) absorption of drugs and in oral drug development. However, they do not generally predict drug absorption in vivo. Here, we report a robotically handled system that uses large porcine GI tissue explants that are functionally maintained for an extended period in culture for the high-throughput interrogation (several thousand samples per day) of whole segments of the GI tract. The automated culture system provided higher predictability of drug absorption in the human GI tract than a Caco-2 Transwell system (Spearman's correlation coefficients of 0.906 and 0.302, respectively). By using the culture system to analyse the intestinal absorption of 2,930 formulations of the peptide drug oxytocin, we discovered an absorption enhancer that resulted in a 11.3-fold increase in the oral bioavailability of oxytocin in pigs in the absence of cellular disruption of the intestinal tissue. The robotically handled whole-tissue culture system should help advance the development of oral drug formulations and might also be useful for drug screening applications.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32341538 PMCID: PMC8357188 DOI: 10.1038/s41551-020-0545-6
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 25.671