J Clin Pharmacol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     

Sign In to gain access to subscriptions and/or personal tools.
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Google Scholar
Right arrow Articles by Jain, A.
Right arrow Articles by Bozorgzadeh, A.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jain, A.
Right arrow Articles by Bozorgzadeh, A.

PHARMACOKINETICS

Pharmacokinetics of Mycophenolic Acid in Live Donor Liver Transplant Patients vs Deceased Donor Liver Transplant Patients

Ashok Jain, MD, Raman Venkataramanan, PhD, Rajeev Sharma, MD, Tai Kwong, PhD, Peter Abt, MD, Mark Orloff, MD, Randeep Kashyap, MD, Georgious Tsoulfas, MD and Adel Bozorgzadeh, MD

From the Department of Surgery, Division of Solid Organ Transplantation, University of Rochester Medical Center, Rochester, New York (Dr Jain, Dr Sharma, Dr Orloff, Dr Kashyap, Dr Tsoulfas, Dr Bozorgzadeh); School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania (Dr Venkataramanan); Department of Laboratory Medicine, University of Rochester Medical Center, Rochester, New York (Dr Kwong); and Department of Surgery, University of Pennsylvania, Philadelphia (Dr Abt).

The exposure of mycophenolic acid in live donor liver transplant patients (those receiving a partial hepatic volume) in comparison to deceased donor liver transplant patients (those receiving the whole hepatic volume) after administration of mycophenolate mofetil has not been reported earlier. The aim of the present study is to compare the pharmacokinetics parameters of mycophenolic acid and mycophenolic acid glucuronide in live donor liver transplant patients versus deceased donor liver transplant patients. Twelve live donor liver transplant and 12 deceased donor liver transplant recipients were studied over a dosing interval after intravenous administration of mycophenolate mofetil. The maximum concentration (Cmax) and the area under the plasma concentration versus time curve (AUC) for mycophenolic acid in live donor liver transplant patients were significantly higher than in deceased donor liver transplant patients (Cmax/AUC: live donor liver transplant patients: 16.1 ± 6.6 µg/mL/43.9 ± 12.6 µg/mL·h vs deceased donor liver transplant patients: 10.7 ± 2.0 µg/mL/28.9 ± 7.1 µg/mL·h; P = .046/.002). The volume of distribution was higher in the deceased donor liver transplant patients compared with live donor liver transplant patients. However, the mean plasma concentration at 12 hours (Clast), drug disposition rate constant, half-life (t1/2), and mean residence time were similar in both groups. The mean plasma concentration of mycophenolic acid glucuronide was 1.4 to 2.0 times higher in deceased donor liver transplant patients compared with live donor liver transplant patients. These observations point to the need to use a lower dosage (approximately 30%) of mycophenolate mofetil in live donor liver transplant patients compared with deceased donor liver transplant patients.


Key Words: Liver transplantationlive donordeceased donorpharmacokineticsmycophenolate mofetilmycophenolic acid

Address for correspondence: Ashok Jain, MD, University of Rochester Medical Center, Department of Surgery, Division of Transplantation, 601 Elmwood Avenue, Box SURG, Rochester, NY 14642; e-mail: ashok_jain{at}urmc.rochester.edu.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by the American College of Clinical Pharmacology