Premium
Determination of in vivo absorption, metabolism, and transport of drugs by the human intestinal wall and liver with a novel perfusion technique
Author(s) -
Richter Oliver,
Greiner Bernd,
Fromm Martin F.,
Fraser Robert,
Omari Taher,
Barclay Murray L.,
Dent John,
Somogyi Andrew A.,
Eichelbaum Michel
Publication year - 2001
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1067/mcp.2001.117937
Subject(s) - perfusion , in vivo , metabolism , pharmacology , absorption (acoustics) , liver perfusion , chemistry , human liver , pharmacokinetics , drug metabolism , medicine , biochemistry , biology , in vitro , materials science , microbiology and biotechnology , composite material
Background and Aims The contribution of the gastrointestinal tract in comparison with the liver for the low and variable bioavailability of orally administered drugs is still poorly understood. Here we report on a new intestinal perfusion technique for the direct assessment of absorption, metabolism, and transport of drugs by the intestinal wall. Methods In 6 healthy volunteers a multilumen perfusion catheter was used to generate a 20‐cm isolated jejunal segment that was perfused with 80 mg verapamil. Simultaneously, 5 mg [ 2 H 7 ]verapamil was given intravenously. Blood, perfusate, and bile samples were analyzed for parent verapamil and its major metabolites. Results The mean fraction of the verapamil dose absorbed from the 20‐cm segment was 0.76 but substantial interindividual variability (0.51–0.96) was shown. Bioavailability was low (19.3%). The intestinal wall contributed to the same extent as the liver to extensive first‐pass metabolism (mean extraction ratio, 0.49 versus 0.48). Substantial transport of verapamil metabolites from the systemic circulation via the enterocytes into the intestinal lumen was observed. Compared with biliary excretion, intestinal secretion into a 20‐cm jejunal segment contributed to drug elimination to a similar extent. Conclusion First‐pass metabolism by the intestinal wall is extensive and contributes to the same extent as the liver to low bioavailability of some drugs such as verapamil. Moreover, intestinal secretion is as important as biliary excretion for the elimination of metabolites. Clinical Pharmacology & Therapeutics (2001) 70 , 217–227; doi: 10.1067/mcp.2001.117937