Pharmacokinetics and protein binding of mycophenolic acid in stable lung transplant recipients

被引:28
作者
Ensom, MHH
Partovi, N
Decarie, D
Dumont, RJ
Fradet, G
Levy, RD
机构
[1] Childrens & Womens Hlth Ctr British Columbia, Dept Pharm, Vancouver, BC V6H 3V4, Canada
[2] Univ British Columbia, Fac Pharmaceut Sci, Vancouver, BC V5Z 1M9, Canada
[3] Vancouver Hosp & Hlth Sci Ctr, Pharmaceut Sci CSU, Vancouver, BC V5Z 1M9, Canada
[4] Univ British Columbia, Div Cardiovasc Surg, Dept Surg, Vancouver, BC V5Z 1M9, Canada
[5] Univ British Columbia, Div Thorac Surg, Dept Surg, Vancouver, BC V5Z 1M9, Canada
[6] Univ British Columbia, Fac Med, Vancouver, BC, Canada
[7] Vancouver Hosp & Hlth Sci Ctr, Div Resp Med, Vancouver, BC V5Z 1M9, Canada
[8] British Columbia Transplant Soc, Vancouver, BC, Canada
关键词
mycophenolic acid; mycophenolate; pharmacokinetics; protein binding; lung transplant recipients;
D O I
10.1097/00007691-200204000-00013
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Mycophenolate mofetil (MMF) use is increasing in solid organ transplantation. Mycophenolic acid (MPA), the active metabolite of MMF, is highly protein bound and only free MPA is pharmacologically active. The average MPA free fraction in healthy adult individuals, stable renal transplant recipients, and heart transplant recipients is approximately 2 to 3%. However, no data are currently available on MPA protein binding in stable lung transplant recipients and little is known regarding MPA's pharmacokinetic characteristics after lung transplantation. The purpose of this study Was to characterize the pharmacokinetic profile and protein binding of MPA in this patient population. Seven patients were entered into the study. On administration of a steady-state morning MMF dose, blood samples were collected at 0, 1, 2, 3, 4, 5, 6, 8, 9, 10, and 12 hours post-dose. Total MPA concentrations were measured by a validated HPLC method with UV detection and followed by ultrafiltration of pooled samples for free MPA concentrations. Area under the curve (AUC), peak concentration (C-max), time to peak concentration (T-max), trough concentration (C-min), free fraction (f), and free MPA AUC Were calculated by traditional pharmacokinetic methods, Patient characteristics included; 3 males and 4 females, an average of 4.4 years post-lung transplant (rance, 0.3-11.5 yr), mean (+/-SD) age of 50 +/- 10 years and weight 69 +/- 20 kg. Mean albumin concentration was 37 +/- 3 g/L and serum creatinine was 142 +/- 49 mumol/L. All patients Were on cyclosporine and prednisone. MMF dosage ranged from I to 3 a day (35.5 +/- 14.1 mg/kg/d; range, 15.2-60.0 mg/kg/d), Mean (+/-SD) AUC was 45.78 +/- 18.35 mug.h/mL (range, 16.56-74.22 mug.h/mL), C-max was 17.37 +/- 7.69 mug/mL (range, 4.92-26.63 mug.h/mL), T-max was 1.2 +/- 0.4 hours (range, 1.0-2,0 h), C-min was 3.12 +/- 1.41 mug/mL (range, 1.47-4-.82 mug/mL), f was 2.90 +/- 0.56% (range, 2.00 +/- 3.40%), and free MPA AUC was 1.29 +/- 0.50 mug.h/mL (range, 0.54-1.88 mug.h/mL) This is the first study to determine these pharmacokinetic characteristics of MPA in the lung transplant population. Further studies should focus on identification of MMF dosing strategies that optimize immunosuppressive efficacy and minimize toxicity in lung allograft recipients.
引用
收藏
页码:310 / 314
页数:5
相关论文
共 17 条
[1]   Clinical pharmacokinetics of mycophenolate mofetil [J].
Bullingham, RES ;
Nicholls, AJ ;
Kanmm, BR .
CLINICAL PHARMACOKINETICS, 1998, 34 (06) :429-455
[2]   EXPERIENCE WITH MYCOPHENOLATE MOFETIL (RS61443) IN RENAL-TRANSPLANTATION AT A SINGLE-CENTER [J].
DEIERHOI, MH ;
KAUFFMAN, RS ;
HUDSON, SL ;
BARBER, WH ;
CURTIS, JJ ;
JULIAN, BA ;
GASTON, RS ;
LASKOW, DA ;
DIETHELM, AG ;
MCDONALD, JC ;
FLYE, MW ;
ROHR, MS ;
HOWARD, RJ .
ANNALS OF SURGERY, 1993, 217 (05) :476-484
[3]   Mycophenolic acid concentrations are associated with cardiac allograft rejection [J].
DeNofrio, D ;
Loh, E ;
Kao, A ;
Korecka, M ;
Pickering, FW ;
Craig, KA ;
Shaw, LM .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2000, 19 (11) :1071-1076
[4]   Measurement of mycophenolate mofetil plasma levels after heart transplantation and a potential side effect of high levels [J].
Dubrey, SW ;
Holt, DW ;
Banner, N .
THERAPEUTIC DRUG MONITORING, 1999, 21 (03) :325-326
[5]   Pharmacokinetics of mycophenolic acid after mycophenolate mofetil administration in liver transplant patients treated with tacrolimus [J].
Jain, A ;
Venkataramanan, R ;
Hamad, IS ;
Zuckerman, S ;
Zhang, SM ;
Lever, J ;
Warty, VS ;
Fung, JJ .
JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 41 (03) :268-276
[6]   Decreased protein binding of mycophenolic acid associated with leukopenia in a pancreas transplant recipient with renal failure [J].
Kaplan, B ;
Gruber, SA ;
Nallamathou, R ;
Katz, SM ;
Shaw, LM .
TRANSPLANTATION, 1998, 65 (08) :1127-1129
[7]   The effect of renal insufficiency on mycophenolic acid protein binding [J].
Kaplan, B ;
Meier-Kriesche, HU ;
Friedman, G ;
Mulgaonkar, S ;
Gruber, S ;
Korecka, M ;
Brayman, KL ;
Shaw, LM .
JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 39 (07) :715-720
[8]   Combination therapy with tacrolimus and mycophenolate mofetil following cardiac transplantation: Importance of mycophenolic acid therapeutic drug monitoring [J].
Meiser, BM ;
Pfeiffer, M ;
Schmidt, D ;
Reichenspurner, H ;
Ueberfuhr, P ;
Paulus, D ;
von Scheidt, W ;
Kreuzer, E ;
Seidel, D ;
Reichart, B .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 1999, 18 (02) :143-149
[9]  
Muller MM, 1997, THERAPIE, V52, P341
[10]  
NOWAK I, 1995, CLIN CHEM, V41, P1011