Population pharmacokinetics of olprinone in healthy male volunteers
Authors Kunisawa T, Kasai H, Suda M, Yoshimura M, Sugawara A, Izumi Y, Iida T, Kurosawa A, Iwasaki H
Received 27 June 2013
Accepted for publication 15 November 2013
Published 4 March 2014 Volume 2014:6 Pages 43—50
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Takayuki Kunisawa,1 Hidefumi Kasai,2 Makoto Suda,2 Manabu Yoshimura,3 Ami Sugawara,3 Yuki Izumi,3 Takafumi Iida,3 Atsushi Kurosawa,3 Hiroshi Iwasaki3
1Surgical Operation Department, Asahikawa Medical University Hospital, Hokkaido, Japan; 2Clinical Study Management Division, Bell Medical Solutions Inc, Tokyo, Japan; 3Department of Anesthesiology and Critical Care Medicine, Asahikawa Medical University, Hokkaido, Japan
Background: Olprinone decreases the cardiac preload and/or afterload because of its vasodilatory effect and increases myocardial contractility by inhibiting phosphodiesterase III.
Purpose: The objective of this study was to characterize the population pharmacokinetics of olprinone after a single continuous infusion in healthy male volunteers.
Methods: We used 500 plasma concentration data points collected from nine healthy male volunteers for the study. The population pharmacokinetic analysis was performed using the nonlinear mixed effect model (NONMEM®) software.
Results: The time course of plasma concentration of olprinone was best described using a two-compartment model. The final pharmacokinetic parameters were total clearance (7.37 mL/minute/kg), distribution volume of the central compartment (134 mL/kg), intercompartmental clearance (7.75 mL/minute/kg), and distribution volume of the peripheral compartment (275 mL/kg). The interindividual variability in the total clearance was 12.4%, and the residual error variability (exponential and additive) were 22.2% and 0.129 (standard deviation). The final pharmacokinetic model was assessed using a bootstrap method and visual predictive check.
Conclusion: We developed a population pharmacokinetic model of olprinone in healthy male adults. The bootstrap method and visual predictive check showed that this model was appropriate. Our results might be used to develop the population pharmacokinetic model in patients.
Keywords: phosphodiesterase III inhibitor, men, pharmacokinetic model
Phosphodiesterase (PDE) III inhibitors induce myocardial contractility and peripheral vasodilation through accumulation of intracellular cyclic adenosine monophosphate (cAMP) in myocardial and vascular smooth muscle cells.1–3 PDE III inhibitors increase cAMP levels without activating beta receptors and are thus useful for controlling acute exacerbation of chronic heart failure in patients resistant to catecholamines or those receiving beta blockers. In addition, PDE III inhibitors act without increasing myocardial oxygen consumption.4,5 They are commonly used for perioperative circulation management, especially at the time of weaning from cardiopulmonary bypass after procedures such as aortocoronary bypass surgery and mitral valve replacement, which improves peripheral circulation and hemodynamic stability.6,7 However, development of hypotension and arrhythmia after administration of such inhibitors should be carefully monitored.1,7 Therefore, PDE III inhibitors are not established as a standard treatment for perioperative circulation management in the current clinical settings. Among PDE III inhibitors, olprinone exerts stronger vasodilatory effects, especially pulmonary vasodilatory effect and reduction in arterial afterload, than milrinone.3,8,9
Target-controlled infusion (TCI) is an infusion system that allows physicians to adjust the infusion rate by using a pharmacokinetic model and to control drug concentration at the target site.10,11 Therefore, TCI of olprinone enables effective and safe administration of olprinone. We performed a population pharmacokinetic analysis to develop a pharmacokinetic model of olprinone by using plasma concentration data obtained from Phase I studies.
Material and methods
Subjects and studies
In this study, we collected 530 plasma concentration data points of olprinone from nine healthy male volunteers (subject numbers 1, 2, 3, 4, 5, 6, 7, 8, and 9; total number of subjects, 39) who participated in two clinical trials (Study I and II, Table 1). Missing data and concentrations below the lower limit of quantitation were excluded from the analysis. These two studies were performed to evaluate the safety, pharmacokinetics, and pharmacological effect after intravenous administration of olprinone. The eligible subjects were healthy adult male volunteers with no clinical abnormality in a medical interview, physical examination, electrocardiogram test, blood pressure measurement, blood test, and urine test. The study protocols were reviewed and approved by the Institutional Review Boards of each clinical study site. Written informed consent was obtained from each subject.
Table 1 Cumulative numbers of subjects and background factors
This clinical trial was conducted in two separate steps (Table 2). In the first step, seven single doses of olprinone were administered as a 5-minute infusion (Study I). After Study I, three doses were administered as a 3-hour infusion combination of a 165-minute maintenance infusion following a 15-minute loading dose (Study II). Each stage comprised four evaluation periods as follows: 1) a screening period; 2) a baseline period, a 24-hour period before the start of the study treatment period, during which baseline evaluations were made; 3) a study treatment period, 24 hours after drug administration; and 4) a follow-up period, 7 days after drug administration. The intervals between administrations were at least 7 days.
We randomized eight subjects to the two treatment groups (Group A and Group B). Subjects in Group A (subject numbers 1, 2, 3, and 4) received 5, 20, and 50 μg/kg olprinone as a single continuous infusion over 5 minutes. Subjects in Group B (subject numbers 5, 6, 7, and 8) received 2.5, 10, and 30 μg/kg olprinone as a single continuous infusion over 5 minutes. In addition, six subjects (Group C), including five who participated in Study I, were randomized in a double-blind, manner to the either the 1.25 μg/kg olprinone (subject numbers 1, 5, and 9) or placebo subgroup. The treatments were administered to each of the three subjects over 5 minutes. We collected 5 mL venous blood samples from each subject before the administration; at 5, 7.5, 10, 15, 30, and 45 minutes; and at 1, 1.5, 2, 3, 4, 6, 8, and 24 hours after the administration to measure the plasma concentration of olprinone.
Subjects in Group B (subject numbers 5, 6, 7, and 8) received a loading dose at a rate of 1.33 μg/kg/minute for 15 minutes followed by continuous infusion at a rate of 0.25 μg/kg/minute for 165 minutes; subjects in Group A (subject numbers 1, 2, 3, and 9) received a loading dose at a rate of 2.67 μg/kg/minute for 15 minutes followed by continuous infusion at a 0.5 μg/kg/minute for 165 minutes; and subjects in Group B’ (subject numbers 1, 5, 6, and 7) received a loading dose at a rate of 2.67 μg/kg/minute for 15 minutes followed by continuous infusion at a rate of 0.75 μg/kg/minute for 165 minutes. Group B’ consists of three subjects from Group B and one subject from Group A of Study I. Group A consists of three subjects from Group A of Study I and a newly enrolled subject from Group C of Study I. We collected 5 mL venous blood samples from each subject before the administration, at 15 and 30 minutes, and at 1, 2, 3, 3.04, 3.08, 3.16, 3.25, 3.5, 4, 4.5, 5, 6, 7, 9, 11, and 24 hours after the administration to measure the plasma concentration of olprinone.
Plasma concentration of olprinone
The concentrations of unchanged olprinone in the plasma were measured using a sensitive and specific high-performance liquid chromatography (HPLC) method. To each 1 mL of plasma, 100 μL of internal standard solution (milrinone 10 ng/100 μL methanol) and 1 mL of 0.2 M phosphate buffer solution (pH 5.5) were added and mixed on a vortex mixer. The mixture was applied on the top of a Bond Elut C18® column (Analytichem International, Harbor City, CA, USA). After washing the column with 2 mL H2O and 2 mL H2O containing 10% methanol, olprinone was eluted twice with 0.5 mL of methanol, and the effluent was evaporated to dryness at 50°C under a gentle stream of nitrogen gas. Then the dried residue was dissolved in 100 μL of methanol and a 50 μL portion was injected onto the HPLC column. The quantification limit was 0.1 ng/mL.
This analytical method was validated for selectivity (no peak interfering with peak of olprinone), linearity (r=0.999), precision (intraday assay, 1.25% to 9.79%, n=4; interday assay, 3.24% at 4.90 ng/mL, n=3), recovery (89.2% to 125.1% in 0.1–10 ng/mL, 92.5% to 107.3% in 10–100 ng/mL), and calibration curve (0.1–100 ng/mL).
Development of a population pharmacokinetic model for olprinone
The population pharmacokinetic analysis of olprinone was performed using the nonlinear mixed effect model (NONMEM®; ICON Development Solutions, Ellicott City, MD, USA) software package, version 7.2.0, with the PREDPP subroutines (ADVAN1, ADVAN3, or ADVAN11). The first-order conditional estimation with interaction method was used for estimation of the parameters. Bootstrap resampling was performed using the MULTTEST procedure of the SAS® 9.2 software (SAS Institute Inc, Cary, NC, USA).
We fitted one-, two-, or three-compartment models to the data when selecting the basic structural model. We examined the interindividual variability for all pharmacokinetic parameters. The interindividual variability was calculated using an exponential error model. The residual variability was determined by using an exponential error model or a mixed error model. Dose and all pharmacokinetic parameters such as total clearance (CL), distribution volume of the central compartment (V1), intercompartmental clearance (Q or Q2 and Q3) and distribution volume of the peripheral compartment (V2 and V3) were adjusted for body weight. The model was selected by statistical evaluation of the objective function value difference (ΔOBJ) using χ2-test, goodness of fit plots, and 95% confidence interval of parameter estimates. The 95% confidence interval of parameter estimate was calculated using the point estimate ±1.96 × standard error (SE), which was taken from the covariance step. Coefficient of variation (CV) or standard deviation (SD) of interindividual variability and residual error variability were calculated from square root of variance estimate. The significance level for the forward selection step and backward elimination step were 0.05 (ΔOBJ <3.84) and 0.01 (ΔOBJ <6.63), respectively.
Age as a covariate candidate was tested using the following formula:
where Pi denotes the pharmacokinetic parameter estimates of subject i, P denotes the population estimates of the pharmacokinetic parameter, BG denotes the background factor of subjects, and θBG denotes the impact of background factor. The linear relation model was used because the range of the background factor was too narrow to use other models.
The bootstrap method was used to evaluate the robustness and stability of the final model.12 One thousand bootstrap data sets were reconstructed by resampling the subjects from the original data set. The mean and SD of parameter estimates obtained from the bootstrap replications were compared to the final parameter estimates and SE obtained from the original data set. Successful run in NONMEM was defined as normal completion of both estimation and covariance steps. Moreover, a visual predictive check (VPC) was used to assess the final model.
The demographic factors of the subject are summarized in Table 1. Nine subjects participated in this study. The total number of subjects in Study I was 27, and in Study II was 12. We collected 312 plasma concentration data points in Study I and 218 in Study II. Summary statistics (mean ± SD) of age, height and body weight were 27.2±2.8 years, 171.5±4.4 cm, and 64.1±6.9 kg, respectively.
Plasma concentration-time profiles of olprinone for each dose (5, 10, and 2.5 μg/kg in Study I) are shown in Figure 1. Plasma concentration of olprinone rapidly decreased after termination of the continuous infusion. In subject numbers 2 and 5, plasma concentrations of olprinone were 0 at 1,440 minutes in the prior stage, and the dose intervals to the next stage were more than 7 days. Olprinone (0.053 ng/mL and 2.002 ng/mL) was detected in the plasma of subject numbers 2 and 5 before the administration. Therefore, these data (number 2 in Stage IV and number 5 in Stage X) were excluded from this analysis.
Selection of the base model of population pharmacokinetic model
The OBJ of one-, two-, and three-compartment models were 2,762.341, 1,835.064, and 1,268.120, respectively. The three-compartment model showed minimum OBJ. Generally, the OBJ decreases with an increase in the number of compartments. In the three-compartment model, the estimates of Q3 (0.174 mL/minute/kg) and V3 (79.5 mL/kg) were smaller than the other estimates (CL, 7.34 mL/minute/kg and V1, 125 mL/kg; Q2, 8.74 mL/minute/kg and V2, 260 mL/kg), which indicated a minimum and clinically negligible effect of the third compartment on the time-concentration curve. Thus, we selected the two-compartment model, and the concentrations predicted using this model were mostly fitted to the observed data (Figure 2). Then, the residual error variability was used for a mixed error model (exponential and additive model) (OBJ, 1,323.213). Therefore, the two-compartment model with the interindividual variability on CL was selected as a base model.
Selection of the final population pharmacokinetic model
Correlation coefficient between the post hoc estimate of pharmacokinetic parameter (CL), which was obtained from the base model, and the background factor of subjects (age) was 0.240. In the forward selection step, age was not included as covariate on CL in the pharmacokinetic model (P=0.363). The final model was therefore identical with the base model.
Pharmacokinetic parameters from the final model are shown in Table 3. Estimates of CL, V1, Q, and V2 were 7.37 mL/minute/kg, 134 mL/kg, 7.75 mL/minute/kg, and 275 mL/kg, respectively. The CV of the interindividual variability on the CL was 12.4%, and the residual error variability (exponential and additive) was 22.2% and 0.129 (SD). The relationships between the observed values and predicted values (PRED) or individual predicted values of the final model are shown in Figure 2. The relationships between conditional weighted residuals13 and time or PRED of the final model are shown in Figure 3. The PRED obtained from the final model well described the observed data.
The results of the bootstrap validation are shown in Table 4. The success rate was 99.3%, and the parameter estimates and SD of the final model were consistent with those of the bootstrap, which suggested good robustness and stability of the final model. Furthermore, the result of VPC is shown in Figure 4. The distribution of predictions simulated from the final model fitted well with those of the observations.
We constructed a population pharmacokinetics model with full sampling data (average 13.6 points per subject) using nine healthy male volunteers. Tsubokawa et al14 reported a population pharmacokinetics model for olprinone using 26 patients undergoing cardiac surgery with cardiopulmonary bypass. In this study, the plasma concentration of olprinone was best described using a two-compartment model. The half-life of olprinone in the alpha and beta phases was 5.4 and 57.7 minutes, respectively. Tsubokawa et al14 reported that CL, V1, and half-life were 7.13 mL/minute/kg, 802 mL/kg, and 97.1 minutes, respectively. The half-life of olprinone in the beta phase in our study was shorter than that reported previously. Kimata et al3 reported a positive correlation between the serum creatinine clearance and elimination half-life of olprinone. Tsubokawa et al14 reported a mean creatinine clearance of 57 mL/minute, which was lower than the creatinine clearance in healthy male volunteers. Therefore, the difference in half-life was attributed to renal function.
Clinical application of TCI infusion for drugs commonly used for anesthesia such as propofol,15,16 remifentanil,17 and rocuronium18 has been reported previously. However, to date, no study has described the clinical application of TCI infusion for PDE III inhibitors such as olprinone and milrinone.
Olprinone is metabolized as a glucuronate conjugate in the liver. The plasma concentrations of olprinone that exert vasodilatory or cardiotonic effects in the extracted radial artery sections are 0.107 μmol/L (32.6 ng/mL) or 0.35 μmol/L (106.7 ng/mL), respectively.9,19 However, in the study by Arai et al20 on off-pump coronary artery bypass, the blood concentration of olprinone 2 hours after administration at 0.2 μg/kg/minute was 27 ng/mL. Subsequently, olprinone was administered at an infusion rate of 0.1 μg/kg/minute, and the blood concentration was maintained over 15 ng/mL for 3 hours after returning to the ICU. Compared to the cardiac index after induction of anesthesia, that for 3 hours after returning to the ICU significantly increased.20 Currently, PDE III inhibitors are not used as standard agents in perioperative circulation management because of the possibility of development of adverse reactions such as hypotension and arrhythmia. After establishing the TCI infusion system, PDE III inhibitors may be used as standard agents in perioperative circulation management. The TCI infusion system may be used in the same manner as the drugs such as propofol and remifentanil in the future; however, this system has not been validated for other drugs thus far. Further studies are required to develop a TCI system for olprinone.
Our results showed that no background factors affected the pharmacokinetics of olprinone. However, our study included a limited number of subjects, limited study population, and limited range of covariates (age). Therefore, our results are not sufficient to conclude that no covariate affected the pharmacokinetics of olprinone. Further studies in patients are required to discuss the pharmacokinetics of olprinone.
We developed a population pharmacokinetic model of olprinone in healthy male volunteers. The final model was found to be appropriate using a bootstrap method and VPC. However, our study had limitations such as a small number of subjects, limited study population, and limited range of covariates. Thus, further studies in patients are required to determine the pharmacokinetics of olprinone. Our results might be useful to develop a population pharmacokinetic model in patients.
This study was sponsored by Eisai Co, Ltd (Tokyo, Japan).
The authors declare no conflict of interest in this work.
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