Pharmacokinetics of mycophenolic acid in Chinese kidney transplant patients

Pharmacokinetics of mycophenolic acid in Chinese kidney transplant patients first-author †E-mail:lxy00711@yahoo.com.cn †E-mail:lxy00711@yahoo.com.cn lxy00711@yahoo.com.cn Department of Clinical Pharmacology, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China Department of Clinical Pharmacology, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China To assess the influence of cyclosporin A (CsA) and tacrolimus (FK506) on mycophenolic acid (MPA) and correlation analysis of the pharmacokinetic parameters and patient characteristics, clinical outcome in Chinese kidney transplant recipients, the pharmacokinetics of 1000 mg mycophenolate mofetil (MMF) twice daily was measured by high-performance liquid chromatography (HPLC). PKS (Pharmaceutical Kinetics Software) 1.0.2 software package was used for the calculation of pharmacokinetic parameters. The mean C max , t max , and AUC (0–12) were (21.88±10.52) µg/ml, (1.20±0.95) h, and (52.546±13.215) µg·h/ml, respectively. The level of AUC (0–12) in the FK506 group was significantly higher than that in the CsA group. MPA appeared not to be affected by renal function. MPA AUC (0–12) showed statistically significant difference according to the patient’s gender. Mycophenolate mofetil Mycophenolic acid Pharmacokinetics Kidney transplant INTRODUCTION 1 Mycophenolic acid (MPA) is the active metabolite of the registered prodrug mycophenolate mofetil (MMF) often used in combination with cyclosporin A (CsA) or tacrolimus (FK506) as an immunosuppressive agent after organ transplantation for the prophylaxis of acute rejection (Takahashi et al., 1995 1995 ; Shaw et al., 1998 1998 ). Following oral administration, MMF is completely absorbed and rapidly hydrolyzed to MPA by esterase present in the gut wall, liver, and possibly lung and peripheral tissues (Bulingham et al., 1996a 1996a ). MPA serves as a potent, selective, noncompetitive, reversible inhibitor of inosine monophosphate dehydrogenase (IMPDH), which is a key enzyme in de novo purine biosynthesis of guanine nucleotides required as a building block for DNA and RNA synthesis (Young and Sollinger, 1994 1994 ; Lee et al., 1985 1985 ). MPA has stronger cytostatic effect on lymphocytes than on other cells, since the de novo synthesis of purines is essential for the proliferation of T and B lymphocytes, unlike other types of cells that can use the salvage pathway for the generation of these compounds. A depletion of the guanine nucleotide pool in lymphocytes leads to a reduction in DNA synthesis, proliferation of lymphocytes, and subsequent immunosuppression. In addition to antilymphocyte activity, MPA prevents arterial smooth muscle cell proliferation, in contrast to conventional immunosuppressants, such as CsA. This property has potential benefits in opposing obliterative arteriopathy associated with chronic organ rejection (Rasom, 1995 1995 ). After oral administration, MPA is highly bound to serum albumin (97%) (Bullingham et al., 1998 1998 ) and only the free fraction of the drug is pharmacologically active. It has been shown that the free concentration of MPA is variable in renal transplant patients with different renal function. The bioavailability of MPA is around 94% and the maximum plasma concentration of MPA following an oral dose is reached in around 0.8 h. The average plasma half-life for healthy adults is approximately 16 h (Shaw et al., 1995 1995 ; Matsuzawa and Nakase, 1984 1984 ). MPA is extensively metabolized by uridine diphosphate glucuronosyltransferase (UDP-GT), mainly into the pharmacologically inactive metabolite MPA-glucuronide (MPAG). Due to enterohepatic recirculation MPAG plays an important role in the maintenance of steady-state plasma MPA level (Bullingham et al., 1996b 1996b ; Shaw et al., 2002 2002 ) and the appearance of a second plasma peak of MPA at 6 to 12 h following MMF administration. In addition, MPA is further metabolized to acyl glucuronide (AcMPAG) and 7-O-glucoside (Bullingham et al., 1998 1998 ). The pharmacokinetics of MPA varies widely between and within patients and with time post-transplant (Johnson et al., 1999 1999 ). Further, it was shown that the pharmacokinetics of MPA is influenced by co-administration of calcineurin inhibitors such as CsA and FK506 (Bullingham et al., 1996a 1996a ; Gregoor et al., 1999 1999 ). Some changes in free MPA concentrations, due to patient characteristics such as severe renal impairment and gender, will lead to an altered efficacy or toxicity profile. The first dose of MMF should be administered within 72 h from transplantation. The recommended fix-dose strategy of 2 g/day reduces the acute rejection rate and hence improves long-term allograft survival (European Mycophenolate Mofetil Cooperative Study Group, 1995 1995 ; Tricontinental Mycophenolate Mofetil Renal Transplantation Study Group, 1996 1996 ). Consequently, in our experiments this dosage is accepted. In addition, the pharmacokinetics of MPA in Chinese kidney transplant patients has not been characterized previously. The aims of this study were to assess the influence of CsA and FK506 on the pharmacokinetics of MPA, to conduct correlation analysis of pharmacokinetic parameters and characteristics of renal transplant patients receiving FK506 in combination with MMF, as opposed to a matched group of patients receiving the same dose of MMF in combination with CsA. A secondary objective was to conduct correlation analysis of pharmacokinetic parameters and renal impairment, gender, clinical outcome. EXPERIMENTAL DETAILS 1 Subjects 2 This study was a open-label and randomized evaluation of the pharmacokinetics of MPA in Chinese kidney transplant patients. Inclusion criteria were aged 24 to 74 male or female patients who underwent kidney transplantation for the first time at the renal disease center of the first affiliated hospital, Zhejiang University, and were treated with MMF in addition to cyclosporine or tacrolimus plus prednisone as immunosuppressants. Exclusion criteria were patients with systemic bacterial, fungal, or viral infection; patients who were pregnant or lactant; patients who had a history of malignant tumor; patients who had received combined organ transplantation; patients who are positive with hepatitis B surface antigen; patients who were peptic ulcer or severe gastrointestinal abnormalities; patients who had symptoms of anemia and decreased blood cells or platelet; patients who were allergic or intolerant to hormones, MMF, MPA, cyclosporine, and tacrolimus. Written informed consent to undergo pharmacokinetic studies was obtained from each patient. Study design 2 The study was approved by the Ethical Committee of the First Affiliated Hospital, Zhejiang University and was carried out in accordance with the Declaration of Helsinki. To evaluate the pharmacokinetics of MMF, two clinical studies were conducted. After operation, 22 patients involved in the first study took 1000 mg MMF twice daily, prednisone 10~20 mg/d, and CsA 100~480 mg/d; the other 7 patients taking 1000 mg MMF twice daily, prednisone 10~20 mg/d, and FK506 6~8 mg/d were in the second study. The MPA pharmacokinetic parameters of all patients were studied for more than 7 d posttransplant when steady serum concentration was reached. Blood samples were collected before dosing and 0.33, 0.66, 1.0, 1.5, 2.0, 4.0, 6.0, 8.0, and 12 h after dosing. Serum sample was obtained by centrifuging blood at 3500 r/min for 15 min in our laboratory. The obtained serum was pooled and stored frozen at −20 °C until analysis for MPA by HPLC. Biochemical parameters such as serum creatinine (sCr), creatinine clearance (CCr), glutamate-pyruvate transaminase (GPT), glutamine oxaloacetic transaminase (GOT), total bilirubin (TB), and direct bilirubin (DB) were monitored on the study date. Measurement of MPA in serum 2 A stock solution of MPA in acetonitrile was prepared at 500 µg/ml and further diluted with free serum to obtain 0.1 to 10.0 µg/ml standard solutions as calibrators. Then 1 ml of these standard calibration samples was vortex-mixed vigorously with 10% phosphoric acid solution for 30 s and centrifuged at 13 500 r/min for 5 min. The mixtures’ supernatants were introduced into solid-phase extraction cartridges (Oasis, Waters) pre-conditioned with methanol (1 ml) followed by water (1 ml). The loaded cartridges were washed with 5% methanol (1 ml). The analytes were eluted with methanol and solvents of all samples were removed by using a stream of nitrogen (40 °C). The residue was redissolved in acetonitrile (100 µl). An aliquot (10 µl) of the mixture was injected into the column. Serum concentration of MPA was carried out using a Waters 2690 high-performance liquid chromatography (HPLC) system with a Waters 996 diode array UV detector. Waters Symmetry C 18 cartridges (4.6 mm×250 mm, 5 µm) fitted with a Security guard cartridge were used and maintained at a temperature of 25 °C. The mobile phase consisted of acetonitrile and potassium dihydrogen phosphate buffer (2.5 mmol/L, pH 4.5) at ratio of 50:50 with a flow rate of 1.0 ml/min. Compounds were quantified by UV absorbance at a wavelength of 210 nm. The chromatography data were collected and processed on Millennium 32 software. Pharmacokinetic data analysis 2 PKS (Pharmaceutical Kinetics Software) 1.0.2 software package (Shanghai Hongneng Software Co. Ltd., China) was used for calculation of pharmacokinetic parameters. Noncompartmental analysis was used to determine several pharmacokinetic parameters. The maximum concentration ( C max ) and maximum time ( t max ) were the observed values. The area under the curve (AUC (0–12) ) was estimated by trapezoidal rule with extrapolation, and apparent clearance ( CL / F ) was determined as dose/AUC. Mean residence time (MRT) was calculated by the formula AUMC (0–12) (area under the first moment curve)/AUC (0–12) . Statistics 2 The effect of CsA and FK506 on the pharmacokinetics of MPA and analysis of correlation between MPA pharmacokinetic parameters and patient characteristics was performed using a two tailed t -test. MPA AUC (0–12) was chosen for the correlation analysis. Results are expressed as the mean± SD . A P -value of less than 0.05 was considered to be statistically significant. RESULTS 1 Patient characteristics 2 A total of 29 kidney transplant recipients (17 men and 12 women) completed the study. Characteristics of these patients are listed in Table 1 1 . There was no case of retransplantation. The mean age was (40.0±12.0) years and the mean body weight was (58.0±10.0) kg. The mean sCr of the 29 subjects was (141.79±68.54) μg/L, and the mean CCr was (58.09±19.60) ml/min. The mean GPT and GOT were (35.50±29.20) μg/L and (23.60±11.10) μg/L, respectively. The mean TB and DB were (8.0±3.95) U/L, and (2.60±1.80) U/L, respectively. The mean CsA, FK506, and prednisone dose administered were (318.0±82.30) mg/d, (7.14±1.21) mg/d, and (19.10±2.43) mg/d, respectively. All the patients took the same dose (1000 mg twice daily) of MMF on the study day. Among the 29 patients, 3 patients experienced rejection within 1 month after transplantation. Item Values Demographics Number of study patients 29 Sex (male, female) 17, 12 Age (years, mean± SD ) 40.0±12.0 Weight (kg, mean± SD ) 58.0±10.0 Number of rejection patients 3 Retransplant – Biochemical parameters (mean± SD ) Serum creatinine (μg/L) 141.79±68.54 Creatinine clearance (ml/min) 58.09±19.60 Glutamate-pyruvate transaminase (μg/L) 35.50±29.20 Glutamine oxaloacetic transaminase (μg/L) 23.60±11.10 Total bilirubin (U/L) 98.0±3.95 Direct bilirubin (U/L) 2.60±1.80 Dose of immunosuppressants (mean± SD ) Dose of mycophenolate mofetil (mg/d) 2000 Dose of cyclosporine A (mg/d) 318.0±82.30 Dose of tacrolimus (mg/d) 7.14±1.21 Dose of prednisone (mg/d) 19.10±2.43 Determination of MPA in serum 2 The calibration curve of MPA in serum was linear in the range of 0.1 to 10.0 µg/ml. The concentrations ( C ) were calculated by peak area ( A ) values. The regression equation of the calibration curve was C =2.12×10 −6 A +2.84×10 −2 , r =0.9999. The minimum detectable concentration of MPA (signal-to-noise ratio of 3) in serum was determined to be approximately 0.05 µg/ml. The overall precision, expressed as % RSD (Relative Standard Deviation) ( n =5), was not less than 3.64% and 2.62% for intra-day and inter-day assay, respectively. The absolute and relative recovery ( n =5) was 78.92% to 88.96% and 95.85% to 104.12%, respectively. MPA pharmacokinetics of Chinese kidney transplant patients 2 A large interindividual variation of pharmacokinetics data was observed. The mean serum concentration-time profile of MPA in 29 kidney transplantation patients after 10 d of MMF treatment is depicted in Fig. 1 1 . The pharmacokinetic parameters of MPA in 29 individual kidney transplant recipients are depicted in Table 2 2 . There was substantial interindividual variation of MPA AUC (0–12) , C max , t max , and CL / F values among the patients. The mean MPA AUC (0–12) after kidney transplantation in Chinese kidney transplantation recipients was (52.546±13.215) μg·h/ml. The mean values of CL / F , and AUMC (0–12) , and MRT (0–12) were (20.30±5.70) L/h, (172.73±52.87) μg·h/ml, and (3.3100±0.6295) h, respectively. t max was reached at (1.20±0.95) h after dosing, and C max was (21.88±10.52) μg/ml. Patient t max (h) C max (μg/ml) CL / F (L/h) AUC (0–12) (μg·h/ml) AUMC (0–12) (μg·h/ml) MRT (h) 1 2.00 14.672 24.37122 41.032 132.25 3.2231 2 0.67 7.295 28.11279 35.571 140.76 3.9572 3 0.33 13.708 19.95490 50.113 192.04 3.8321 4 1.00 17.441 21.20621 47.156 158.99 3.3715 5 1.00 14.530 21.96692 45.523 155.27 3.4107 6 1.50 18.443 20.25727 49.365 150.87 3.0562 7 0.67 22.752 20.41191 48.991 137.03 2.7970 8 0.67 28.483 26.27430 38.060 95.63 2.5125 9 0.67 22.768 19.03457 52.536 150.14 2.8578 10 1.00 25.623 27.02191 37.007 122.87 3.3201 11 1.00 15.238 21.90245 45.657 137.28 3.0067 12 0.33 53.766 15.16990 65.920 100.94 1.5313 13 0.33 42.521 18.23719 54.833 155.35 2.8331 14 0.33 15.793 20.92619 47.787 190.21 3.9804 15 1.00 27.037 13.23872 75.536 233.50 3.0912 16 4.00 11.626 22.52252 44.400 200.16 4.5081 17 4.00 16.136 19.97363 50.066 237.69 4.7474 18 1.50 11.644 17.22594 58.052 228.62 3.9382 19 0.67 22.752 20.74818 48.197 135.44 2.8102 20 0.67 18.134 19.38698 51.581 179.04 3.4710 21 2.00 5.627 40.84967 24.480 93.28 3.8109 22 0.33 37.470 16.21587 61.668 208.80 3.3858 23 1.00 21.780 13.23276 75.570 268.23 3.5495 24 1.50 16.118 24.05581 41.570 125.07 3.0086 25 0.67 30.750 16.87194 59.270 163.05 2.7508 26 2.00 30.771 17.01259 58.780 170.99 2.9090 27 2.00 17.074 16.57275 60.340 198.27 3.2859 28 0.33 22.967 14.25517 70.150 231.03 3.2935 29 1.50 31.492 11.81614 84.630 316.44 3.7392 Mean 1.20 21.880 20.30436 52.546 172.73 3.3100 SD 0.95 10.520 5.703189 13.215 52.87 0.6295 Effect of CsA and FK506 on the pharmacokinetics of MPA 2 There were differences in the baseline characteristics of the two groups. Mean C 0 MPA in patients receiving FK506 was significantly higher than that in the CsA group: 2.45 µg/ml versus 1.45 µg/ml ( P =0.004). MPA AUC (0–12) in the FK506 group was statistically higher: (60.9467±11.6779) µg·h/ml than that in the CsA group: (48.184±10.6598) µg·h/ml ( P =0.0045). Correlation analysis of pharmacokinetic parameters and patient characteristics 2 Correlation analysis between MPA AUC and patients’ renal function and gender was performed to determine the factors affecting the AUC value among the patients who were administered CsA. The patients’ renal function seemed not to have any effect on AUC since creatinine clearance did not correlate with AUC ( P =0.9473). However, MPA AUC showed a statistically significant difference according to the patient’s gender ( P =0.0006). MPA AUC of females was higher than that of males by 34.32%, even though they were given the same doses of MMF. Correlation analysis of pharmacokinetic parameters and clinical outcome 2 Among the 29 patients, 3 patients (10.3%) experienced acute rejection (AR) within 1 month after transplantation. MPA AUC (0–12) in the AR group was statistically lower ((40.93±14.28) µg·h/ml) than that in the non AR group ((53.88±12.70) µg·h/ml) ( P =0.038). There was no statistical difference of the accident rate of infection between the patients of MPA AUC (0–12) > 60 µg·h/ml and MPA AUC (0–12) < 60 µg·h/ml. DISCUSSION 1 The pharmacokinetics of MPA in kidney transplant patients has been reviewed many times, although few studies on the MPA pharmacokinetics in Chinese patients have been reported. Moreover, co-administration of calcineurin inhibitors such as CsA and FK506 and patients characteristics will have effect on the pharmacokinetic parameters of MPA. In this respect, the pharmacokinetic study of MPA in Chinese kidney transplant patients will be very essential. The pharmacokinetic profiles of MPA are characterized by an early and sharp increase of MPA concentration, with the first peak concentration being reached at 0.5 to 1 h after dosing. These profiles were consistent with the rapid absorption and rapid conversion of MMF to MPA, followed by rapid distribution and metabolism of the generated MPA. Analysis of MPA concentration in the 29 Chinese patients in this study revealed that the pattern of the concentration-time profile was similar to the results of other studies (Pescovitz et al., 2003 2003 ; Cho et al., 2004 2004 ), although there was some variability of AUC (0–12) , C max and t max . The mean MPA AUC ((52.546±13.215) μg·h/ml) of Chinese kidney transplant patients treated with 1000 mg MMF twice daily was higher than that of Caucasian patients ((33.3±13.7) μg·h/ml), African American patients ((26.8±14.3) μg·h/ml) who took the same dose as that in our study (Shaw et al., 2000 2000 ), and Korean patients ((18.45±4.25) μg·h/ml) taking MMF 750 mg twice a day. Only 3 of our 29 patients experienced acute rejection within 1 month after operation, maybe it was partly due to the high MPA AUC in the target range of 30 to 60 μg·h/ml reported to decrease the risk of acute rejection (Shaw et al., 2000 2000 ). But we must be careful when the patient simultaneously has CsA and MPA AUC concentrations such as above 3 acute rejection patients. In our study, calcineurin antagonists such as comedications seem to affect the MPA pharmacokinetics. For equivalent doses of MMF, combination therapy with FK506 had been reported to result in higher MPA AUC than does a CsA-based regimen (Zucker et al., 1997 1997 ). Furthermore, our study confirmed previous observations (Kuriata-kordek et al., 2003 2003 ) of significantly higher MPA C 0 in the FK506-treated group than that in patients receiving CsA. It was reported (Filler et al., 2000 2000 ) that equal MPA exposure to that achieved without calcineurin inhibitors was obtained with a 40% reduced dose in combination with FK506, or a 20% increased dose with CsA. (Zucker et al., 1999 1999 ) during an in vitro study to investigate the effect of FK506 and CsA on uridine diphosphate glucuronosyltransferase (UDPGT), an enzyme that converts MPA to MPAG. The author suggests that FK506 inhibits UDPGT significantly more efficiently than CsA through not yet determined mechanisms. MPA AUC (0–12) was significantly different between men and women and serum creatinine did not correlate with MPA AUC (0–12) , which is consistent with the report by Cho et al.( 2004 2004 ). As so many factors affect the pharmacokinetics of MPA, MPA monitoring may be beneficial for renal transplant recipients receiving MMF. Although this study has some limitations such as incomplete correlation analysis, small number of patients, and short follow-up, this is a relatively complete study to evaluate the pharmacokinetics of MPA in Chinese kidney transplant recipients. Comparison of rejection rate and side effects according to the AUC of MPA in Chinese kidney transplant patients has not been conducted, so future study in our laboratory will address this issue. References RE Bullingham , A Nicholls , M Hale . Pharmacokinetics of mycophenolate mofetil (RS61443): A short review . Transplant Proc , 1996 . 28 ( 2 ): 925 - 929 . . 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