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Transplantation Proceedings
Volume 36, Issue 2
, Pages 364-366
, March 2004
The colon displays an absorptive capacity of tacrolimus
References
- Clinical pharmacokinetics of Tacrolimus. Clin Pharmacokinet. 1995;29:404
- Metabolism of the immunosuppressant Tacrolimus in the small intestine (cytochrome P450, drug interactions, and interindividual variability). Drug Metab Dispos. 1995;23:1315
- High trough levels of oral FK506 induced by loss of small intestine. Pediatr Transplant. 2001;5:434
- Enteric absorption of FK506: estimation by a block liver perfusion technique in rats. Transplant Proc. 1998;30:3777
- Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism. J Pharmacol Exp Ther. 1997;283:1552
- Metabolism of the macrolide immunosuppressant, Tacrolimus, by the pig gut mucosa in the Ussing chamber. Br J Pharmacol. 1996;117:1730
- Pharmacokinetics and pharmacodynamics of FK506 in pediatric patients receiving living related donor liver transplantations. Transplant Proc. 1995;27:1108
- Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat. Drug Metab Dispos. 1992;20:753
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The barrier function of CYP3A4 and P-glycoprotein in the small bowel.
Adv Drug Delivery Rev. 1997;27:161
- Effects of intestinal and hepatic metabolism on the bioavailability of Tacrolimus in rats. Pharm Res. 1998;15:1609
- Effect of intestinal P-glycoprotein on daily Tacrolimus trough level in a living donor small bowel recipient. Clin Pharmacol Ther. 2000;68:98
PII: S0041-1345(03)01324-1
doi: 10.1016/j.transproceed.2003.12.013
© 2004 Elsevier Inc. All rights reserved.
« Previous
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Transplantation Proceedings
Volume 36, Issue 2
, Pages 364-366
, March 2004
