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Metabolite Kinetics: The Segregated Flow Model for Intestinal and Whole Body Physiologically Based Pharmacokinetic Modeling to Describe Intestinal and Hepatic Glucuronidation of Morphine in Rats In Vivo.
- Source :
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Drug metabolism and disposition: the biological fate of chemicals [Drug Metab Dispos] 2016 Jul; Vol. 44 (7), pp. 1123-38. Date of Electronic Publication: 2016 Apr 20. - Publication Year :
- 2016
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Abstract
- We used the intestinal segregated flow model (SFM) versus the traditional model (TM), nested within physiologically based pharmacokinetic (PBPK) models, to describe the biliary and urinary excretion of morphine 3β-glucuronide (MG) after intravenous and intraduodenal dosing of morphine in rats in vivo. The SFM model describes a partial (5%-30%) intestinal blood flow perfusing the transporter- and enzyme-rich enterocyte region, whereas the TM describes 100% flow perfusing the intestine as a whole. For the SFM, drugs entering from the circulation are expected to be metabolized to lesser extents by the intestine due to the segregated flow, reflecting the phenomenon of shunting and route-dependent intestinal metabolism. The poor permeability of MG crossing the liver or intestinal basolateral membranes mandates that most of MG that is excreted into bile is hepatically formed, whereas MG that is excreted into urine originates from both intestine and liver metabolism, since MG is effluxed back to blood. The ratio of MG amounts in urine/bile [Formula: see text] for intraduodenal/intravenous dosing is expected to exceed unity for the SFM but approximates unity for the TM. Compartmental analysis of morphine and MG data, without consideration of the permeability of MG and where MG is formed, suggests the ratio to be 1 and failed to describe the kinetics of MG. The observed intraduodenal/intravenous ratio of [Formula: see text] (2.55 at 4 hours) was better predicted by the SFM-PBPK (2.59 at 4 hours) and not the TM-PBPK (1.0), supporting the view that the SFM is superior for the description of intestinal-liver metabolism of morphine to MG. The SFM-PBPK model predicts an appreciable contribution of the intestine to first pass M metabolism.<br /> (Copyright © 2016 by The American Society for Pharmacology and Experimental Therapeutics.)
- Subjects :
- Administration, Intravenous
Administration, Oral
Animals
Cell Membrane Permeability
Hepatobiliary Elimination
Inactivation, Metabolic
Male
Morphine administration & dosage
Morphine blood
Morphine urine
Morphine Derivatives blood
Morphine Derivatives urine
Rats, Sprague-Dawley
Regional Blood Flow
Renal Elimination
Duodenum blood supply
Duodenum metabolism
Liver blood supply
Liver metabolism
Liver Circulation
Models, Biological
Morphine pharmacokinetics
Morphine Derivatives pharmacokinetics
Splanchnic Circulation
Subjects
Details
- Language :
- English
- ISSN :
- 1521-009X
- Volume :
- 44
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Drug metabolism and disposition: the biological fate of chemicals
- Publication Type :
- Academic Journal
- Accession number :
- 27098743
- Full Text :
- https://doi.org/10.1124/dmd.116.069542