Single dose pharmacokinetics of the novel transdermal donepezil patch in healthy volunteers
Authors Kim YH, Choi HY, Lim H, Lee SH, Jeon HS, Hong D, Kim SS, Choi YK, Bae K
Received 2 December 2014
Accepted for publication 5 February 2015
Published 10 March 2015 Volume 2015:9 Pages 1419—1426
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Professor Shu-Feng Zhou
Yo Han Kim,1 Hee Youn Choi,1 Hyeong-Seok Lim,1 Shi Hyang Lee,1 Hae Sun Jeon,1 Donghyun Hong,2 Seong Su Kim,2 Young Kweon Choi,2 Kyun-Seop Bae1
1Department of Clinical Pharmacology and Therapeutics, College of Medicine, University of Ulsan, Asan Medical Center, Seoul, Republic of Korea; 2iCure Pharmaceutical lncorporated, Anseong, Gyeonggi-do, Republic of Korea
Background: Donepezil is an acetylcholinesterase inhibitor indicated for Alzheimer’s disease. The aim of this randomized, single-blind, placebo-controlled, single-dose, dose-escalation study was to investigate the safety, tolerability, and pharmacokinetics of the donepezil patch in healthy male subjects.
Methods: Each healthy male subject received a single transdermal donepezil patch (72 hours patch-on periods) of 43.75 mg/12.5 cm2, 87.5 mg/25 cm2, or 175 mg/50 cm2. Serial blood samples were collected up to 312 hours after patch application. The plasma concentrations of donepezil were determined by using a validated liquid chromatography–tandem mass spectrometry method. Pharmacokinetic parameters were obtained by noncompartmental analysis. Tolerability of the patches and performance of the patches (adhesion, skin irritation, residual donepezil content in the patch) were assessed throughout the study.
Results: The study was completed by 36 healthy subjects. After patch application, the maximal plasma donepezil concentration (Cmax) and the area under the curve (AUC) increased in a dose-proportional manner. Median time to Cmax was ~74–76 hours (~2–4 hours after patch removal), and mean t1/2ß was ~63.77–93.07 hours. The average donepezil residue in the patch after 72 hours was ~73.9%–86.7% of the loading dose. There were neither serious adverse events nor adverse events that lead to discontinuation. Skin adhesion of the patch was good in 97.2% of the subjects. All skin irritations after patch removal were mild and were resolved during the study period.
Conclusion: The donepezil patch appeared to be generally well tolerated and adhesive. Pharmacokinetic analysis of the donepezil patch demonstrated linear kinetics.
Keywords: donepezil, transdermal patch, pharmacokinetics, healthy subjects
Alzheimer’s disease (AD) is the most common cause of senile dementia.1 It was first described by Alois Alzheimer in 1906.2 In 2012, there were 36 million people worldwide with AD. It is predicted to affect more than 115 million people globally by 2050.3 It is a progressive, neurodegenerative disorder that is usually diagnosed in people over 65 years of age.4
Donepezil is a reversible acetylcholinesterase inhibitor that has been approved for use for AD. It is believed to inhibit the breakdown of the neurotransmitter acetylcholine and compensate for the deficiency of acetylcholine in brain.5,6 In previous clinical trials, it has been shown to improve cognitive function in patients for a wide range of AD severity, from very mild to moderate-to-severe.7–11
The most common adverse events (AEs) with donepezil, as well as with other cholinesterase inhibitors, are nausea, vomiting, diarrhea, and dizziness, all of which are symptoms linked to cholinergic hyperstimulation.12,13 These effects are dose-related and largely depend on the plasma fluctuations.14 When donepezil is orally administered, it is well absorbed and reaches peak plasma concentrations (Cmax) in 3–4 hours.15 The plasma concentration of donepezil then decreases until the next dose is administered.16 By reducing Cmax and slowing the time that it takes to reach Cmax (tmax), the potential for these AEs may be attenuated.
The advantages of transdermal drug delivery for AD have already been reported: reduced dosing frequency, improved bioavailability, reduced side effects, and improved patient compliance due to simple application.17–19 For this reason, rivastigmine, one of the acetylcholinesterase inhibitors, has already been developed as a transdermal patch.16,20,21
The transdermal donepezil patch was also developed for the advantage of providing smooth and steady delivery of donepezil through the skin; a transdermal patch would decrease Cmax and lengthen tmax while maintaining drug exposure.17 According to in vivo studies, when transdermal donepezil (40 mg/kg, 2.14 cm2) was applied to the abdominal skin of male Sprague-Dawley rats, the Cmax at steady state (52.2 ng/mL) was maintained for 48 hours with the donepezil formulation using oleic acid.22 The company iCure Pharmaceutical lncorporated (Anseong, Gyeonggi-do, Republic of Korea), which manufactures the donepezil patch that was used in this study, also conducted in vivo studies to evaluate pharmacokinetics. When a single dose of 5 mg/kg oral solution was administered to Hairless Wistar Yagi rats, the Cmax was 41.4 ng/mL with a tmax of 1 hour. When 8.75 mg/2.5 cm2, 17.5 mg/5 cm2, and 35 mg/10 cm2 donepezil patches were applied to Hairless Wistar Yagi rats, the Cmax values were dose-proportional (36.5 ng/mL, 64.4 ng/mL, and 129.1 ng/mL, respectively) with tmax values of 24–36 hours.23
The aim of this randomized, single-blind, placebo-controlled, single-dose, dose-escalation study was to investigate the tolerability and the pharmacokinetics of the novel donepezil patch in healthy male subjects.
Materials and methods
Each healthy male volunteer who was 20–45 years of age and had a body mass index (BMI) of 20–26 kg/m2 was eligible for this study. Volunteers were considered to be in good health on the basis of these criteria, which were assessed within the 4 weeks prior to the first administration of the study drug: medical history; physical examinations; vital sign measurements (blood pressure, heart rate, and body temperature); 12-lead electrocardiograms (ECGs); clinical laboratory tests (hematology, blood chemistry, and urinalysis); serology (hepatitis B surface antigen, hepatitis C virus antibody, and HIV antigen/antibody); and urine drug screening (amphetamine, methamphetamine, barbiturate, cocaine, opiate, benzodiazepine, cannabinoid, and methadone). Each subject with a known allergy or hypersensitivity to donepezil or with a history of drug abuse was excluded from the study.
The study protocol was approved by the Ministry of Food and Drug Safety (MFDS) and the institutional review board of the Asan Medical Center (AMC), Seoul, Republic of Korea. The study was conducted at the Clinical Trial Center of the AMC from May 2013 to September 2013. All subjects provided written informed consent before screening tests, and this study was conducted in accordance with the Declaration of Helsinki and International Conference of Harmonization (ICH) guidelines for good clinical practice. This trial was registered with the identifier number NCT01860625 at ClinicalTrials.gov.
This study was designed as a randomized, single-blind, placebo controlled, dose-escalation study. In this study, a 3.5 mg/cm2 donepezil patch was applied as a single dose of 43.75 mg/12.5 cm2, 87.5 mg/25 cm2, or 175 mg/50 cm2. There were 12 subjects per group, nine of whom were given active patches and three of whom were given placebos. The subjects were admitted to the hospital on the day before drug administration. On the morning of day 1, each subject received a single application to the upper back with a patch-on period of 72 hours. All subjects were discharged on day 5 (24 hours after patch removal), and they revisited the hospital on days 6, 7, 8, 10, 12, and 14 to assess the tolerability and the pharmacokinetics of donepezil. Follow-up visits were performed 18–22 days after the patch application.
For pharmacokinetic analysis, sequential blood samples were collected prior to and at 4, 8, 12, 24, 48, 70, 72, 74, 76, 80, 96, 120, 144, 168, 216, 264, and 312 hours after patch administration. All blood samples for the determination of donepezil concentrations were drawn into heparinized tubes and separated by centrifugation at 1,800× g for 8 minutes at 4°C and stored at −70°C until analysis.
The adhesive properties of each patch were evaluated every 12 hours (within approximately 30 minutes) from time 0 (the time of adhesion) through 72 hours (before patch removal) after the application of donepezil patch. The adhesiveness of patch was graded according to the criteria in Table 1.24
Table 1 Adhesion score and skin irritation score systems in this study
Tolerability was assessed throughout the study by using vital sign measurements; ECGs; clinical laboratory tests (hematology, blood chemistry, and urinalysis); physical examinations; and monitoring of AEs. AEs were recorded in terms of symptoms and signs, duration, intensity, relationship to the study drug, action taken, outcome, and seriousness.
Assessment of skin irritation was performed immediately after the removal of the patch (72 hours) as well as 1, 12, and 24 hours after patch removal (at 73, 84, and 96 hours after patch application, respectively) by using a skin irritation scoring system (Table 1).24 After the subject was discharged, the skin irritation score was assessed at every outpatient visit until that subject experienced an irritation score of 0.
Determination of donepezil concentrations
Plasma concentrations of donepezil were determined by using validated high performance liquid chromatography (HPLC) coupled with tandem mass spectrometry. The internal standard was diphenhydramine hydrochloride. The sample extracts were analyzed by using HPLC (Nonospace SI-2 3133; Shiseido, Tokyo, Japan) and an Unison UK-C18 column (3.0 μm, 50 mm * 2.0 mm; Imtakt, Kyoto, Japan) with a mobile phase consisting of ammonium formate with 0.1% formic acid and acetonitrile with 0.1% formic acid (40:60, v/v).
The MS system (API-4000™; AB Sciex, Framingham, MA, USA) was operated in positive ion electrospray mode with multiple reaction monitoring. For donepezil and the internal standard, the precursor-to-production reactions that were monitored were mass-to-charge ratios (m/z), 380.3→91.1 and 256.2→167.1, respectively. All separations were achieved at a flow rate of 0.2 mL/min.
Calibration curves covered the concentration range of 0.1–80 ng/mL (R2>0.99). By using this assay, interday accuracy ranged from 96.27% to 105.98%, and interday precision, expressed as percent coefficient of variation (%CV), ranged from 0.7% to 4.3%. In addition, intraday accuracy and precision (%CV) ranged from 97.23% to 104.92% and from 1.4% to 5.3%, respectively.
Pharmacokinetic assessment and statistical analysis
The plasma concentration–time profiles of donepezil in the subjects were analyzed by using a noncompartmental method and WinNonlin 6.1 (Pharsight Corporation, Princeton, NJ, USA). All analyses were made by using actual times of sampling. The Cmax and tmax were determined from the observed values. The terminal elimination rate constant (λz) was estimated by linear regression of the terminal log-linear portion of the plasma concentration–time curves. The area under the time–concentration curve (AUC) from time 0 to the last measurable time (AUClast) was calculated by the trapezoidal rule, and the AUC extrapolated to infinity (AUCinf) was obtained as follows:
AUCinf = AUClast + Clast/λz
for which Clast is the last quantifiable concentration.
The t1/2β was calculated for each participant as follows:
t1/2β = ln(2)/λz
All statistical analyses were performed by using SAS 9.3 (SAS Korea, Seoul, Republic of Korea) and Phoenix WinNonlin 6.1 (Pharsight Corporation). Demographic data and pharmacokinetic parameters were summarized by using descriptive statistics. Dose linearity was investigated by using the Kruskal–Wallis test to evaluate the dose-normalized Cmax and AUCinf values.
A total of 36 healthy Korean volunteers were enrolled, and 36 subjects were administered the study drugs and completed the study. Expressed as mean ± standard deviation, the mean characteristics of the study participants were as follows: the mean age was 27.65±4.54 years; the mean weight was 67.06±7.76 kg; and the mean height was 173.79±4.87 cm.
The mean plasma concentration–time profiles of donepezil are shown in Figure 1. After the application of the donepezil patch, serum donepezil concentration increased slowly and peaked between ~74–76 hours (~2–4 hours after patch removal) and declined with a t1/2β of ~63.77–94.07 hours (Table 2). In this study, the dose-normalized Cmax and AUCinf values were not statistically significant (P=0.5986 and P=0.3392, respectively). After patch application, the Cmax and AUCinf increased in a dose-proportional manner (Figure 2). Patch adhesiveness was good in 97.2% of subjects. Only one subject reported that the “patch detached”; this happened more than 61 hours after patch application (Table 3). Used patches from all subjects in each group were analyzed for residual donepezil. The values for average donepezil residue (residual dose/loading dose * 100 [%]) in the patch 72 hours after application were as follows: 81.1%±3.2% for the 43.75 mg/12.5 cm2 group, 80.4%±4.4% for the 87.5 mg/25 cm2 group, and 78.4%±2.5% for the 175 mg/50 cm2 group.
Figure 1 Plasma concentration-time curves of donepezil 72 hour after patch application.
Included in the tolerability analysis were 36 subjects, all of whom applied donepezil patch. Eleven subjects experienced a total of 14 AEs, among which ten events in seven subjects were considered “possibly related” to the study drug (Table 4). All AEs were mild except for one case of hypertriglyceridemia in the 43.75 mg/12.5 cm2 group. An increase in triglycerides (1,318 mg/dL) without any symptoms was observed at the follow-up visit, and the decreased level was checked on subsequent visit. Two application-site AEs included skin discoloration and papules; both were resolved without sequelae. No death or serious AEs occurred during the entire course of the study. Likewise, there were no clinically significant abnormalities in vital signs, physical examinations, or electrocardiograms.
Table 4 Summary of AEs and causal relationship after donepezil patch administration
The distributions of individual skin irritation scores after patch removal are shown in Figure 3. Immediately after patch removal (72 hours after application), most of the subjects experienced irritation scores of 1 (minimal erythema). All subjects experienced irritation scores of 0 (no evidence of irritation) by the day 12 outpatient visit (approximately 264 hours after patch application). Irritation scores of 4, 5, 6, or 7 were not observed during the entire study.
To our knowledge, this is the first published study to investigate the tolerability and pharmacokinetics of the donepezil patch in healthy subjects. After application, the donepezil patch provided a smooth and sustained plasma concentration–time profile over the entire patch-on period of 72 hours. For the highest dose of donepezil (175 mg/50 cm2) administered in this study, about 20% of the dose (approximately 35 mg) was released from the patch over the 72-hour application. As per the clinical pharmacology and biopharmaceutics review, the pharmacokinetic profile of 10 mg single-dose oral donepezil was reported to produce an AUCinf of 885.30±249.10 ng/mL and a Cmax of 20.90±5.00 ng/mL.25 Systemic exposure (AUCinf) after a 72-hour application of 175 mg/50 cm2 was about three times higher than after the single dose of a 10 mg oral tablet, while the Cmax with the patch was similar to the Cmax with a 10 mg dose of oral donepezil. Thus, this transdermal dose (about 35 mg/72 hours) is expected to produce exposure (AUC) similar to 3 days of 10 mg oral donepezil but with a lower Cmax.
In the 43.75 mg/12.5 cm2 group, the %CV of AUCinf was larger than in the other treatment groups (58.6% in the 43.75 mg/12.5 cm2 group, 24.5% in the 87.5 mg/25 cm2 group, and 32.2% in the 175 mg/50 cm2 group). Of the nine subjects in the group, two showed lower clearances (28.1 and 28.7 L/hour) than average (72.3 L/hour), so the AUCinf of each of these subjects was higher (1556.5 ng·h/mL and 1526.8 ng·h/mL, respectively) than average AUCinf (808.5 ng·h/mL). Although we did not evaluate the different genotypes, the difference between CYP2D6 could have been one of the reasons for the large interindividual variability. In a recent population pharmacokinetic study in which donepezil clearance was evaluated in CYP2D6 genotypes, CYP2D6-poor metabolizers demonstrated a 32% lower clearance than did CYP2D6-extensive metabolizers.26
The disadvantages of transdermal delivery include skin irritation and imperfect adhesion to the skin.19 In this study, the results for skin irritation indicate that the skin reactions to the study drug were mild. The highest score was 3 (erythema and papules); this was seen in two subjects, and the condition was resolved to 0 (no evidence of irritation) within 8 days. The adhesiveness of the donepezil patch was also good. Except for one subject, the individual adhesion scores ranged between 0 (≥90% adherence) and 2 (adherence of ≥50% to <75%) for 72 hours.
Our study had limitations that should be considered. First, these results were obtained from healthy male subjects; the tolerability and pharmacokinetics of donepezil patch may differ in female or elderly AD patients. Second, donepezil accumulated in plasma by four to seven-fold until the steady state; further evaluation and comparison of the steady-state pharmacokinetics of the donepezil patch is needed.27 On the basis of the findings of this study, the investigation of multiple doses in healthy volunteers or elderly AD patients may be helpful to evaluate steady-state pharmacokinetics and to prove the optimal way to treat AD with donepezil.
This study represents the first assessment of a single-dose donepezil patch in human subjects. Overall, the donepezil patch appeared to be generally well tolerated and adhesive. The pharmacokinetic characteristics of the donepezil patch demonstrated linear kinetics.
This study was conducted by the AMC and was supported by a grant from the Korean Health Technology R&D Project, Ministry of Health and Welfare, Republic of Korea (HI14C1061). This study was also supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute, funded by the Ministry of Health and Welfare, Republic of Korea (HI12C1449).
All of the authors report that they have no conflicts of interest in this work. The study was funded by iCure Pharmaceutical Inc., the manufacturer of the donepezil patch that was used in this study. The sponsor’s financial support did not include bonuses for the success of the present study or for the recruitment of subjects.
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