Pharmacokinetics of diltiazem hydrochloride delay-onset sustained-release pellet capsules in healthy volunteers

ARTICLE

Pharmacokinetics of diltiazem hydrochloride delay-onset sustained-release pellet capsules in healthy volunteers

Xi-Qing Yan^I; Zhi-Gang Chen^II; Rong-Liang Wang^II; Jun Yang^I,*; Fang Ai^III; Yan-Juan Pan^I; Pei-Yong Qiu^I; Da-Xin Wang^IV

^ICollege of Pharmacy, Xinxiang Medical University, Xinxiang, China

^IIFirst affiliated Hospital of Xinxiang Medical University

^IIIDepartment of Pediatric Surgery, First affiliated Hospital of Xinxiang Medical University, China

^IVClinical Medical College of Yangzhou University, China

ABSTRACT

The pharmacokinetics (PK) of ordinary tablets and sustained release capsules of diltiazem hydrochloride in human clinical trials had been studied. The PK of diltiazem hydrochloride delay-onset sustained-release pellet capsules, a new dosage form, has not been reported, although it is very important to clinical use. In this paper, we investigated the PK of diltiazem hydrochloride delay-onset sustained-release pellet capsules and the food influence in Chinese healthy volunteers. The PK parameters indicated that the diltiazem hydrochloride delay-onset sustained-release pellet capsules appeared marked characteristics of delayed and controlled release. An opened-label, randomized and parallel clinical trial was conducted in 36 Chinese healthy volunteers with single oral dose (90 mg, 180 mg or 270 mg) and a multiple oral dose (90 mg d^-1×6 d) administration. The effect of food on the PK of one single oral dose (360 mg) was investigated in 24 healthy Chinese volunteers. Plasma diltiazem concentration was determined by reversed-phase high-performance liquid chromatography (RP-HPLC) and the main pharmacokinetic parameters were analyzed by PKSolver (Ver 2.0). All clinical studies were conducted in the Clinical Pharmacological Center (No. JDX1999064) of Xiangya Hospital Affiliated Central South University, China. The PK parameters suggested that the new formulation had marked characteristics of delayed and controlled release of diltiazem, and food intake did not alter significantly diltiazem pharmacokinetic parameters.

Uniterms: Diltiazem hydrochloride/delay-onset sustained-release pellet capsules/pharmacokinetics. Food/ingestion/effect in pharmacokinetic profile. High-performance liquid chromatography/quantitative analysis.

RESUMO

Embora a farmacocinética (PK) do cloridrato de diltiazem nas formas de comprimidos de liberação imediata e cápsulas de liberação modificada em ensaios clínicos já tenha sido relatada, a pesquisa da PK do cloridrato de diltiazem na forma de cápsulas com peletes de liberação retardada e sustentada ainda é muito importante. Neste trabalho, propusemos avaliar a farmacocinética do cloridrato de diltiazem administrado através desta nova forma farmacêutica em voluntários chineses sadios, assim como a influência da ingestão de alimentos neste perfil farmacocinético. Foi realizado um ensaio clínico aberto, randomizado e paralelo em 36 voluntários, que receberam dose oral única de 90 mg, 180 mg ou 270 mg e dose múltiplas (90 mg/d × 6 d) pela mesma via de administração. Para avaliar o efeito da ingestão de alimentos sobre a PK do diltiazem foi realizada a administração de dose única (360 mg) em 24 voluntários chineses sadios. A concentração plasmática do diltiazem foi determinada por Cromatografia Liquida de Alta Eficiência em fase reversa (CLAE-FR) e os principais parâmetros farmacocinéticos foram analisados através do emprego do software PKSolver (Ver 2.0). O ensaio de farmacocinética clínica foi conduzido na clínica Pharmacological Center (No.JDX1999064) do Hospital de Xiangya, Central South University, China. Os parâmetros PK obtidos indicaram que a nova formulação de cápsulas de liberação retardada e sustentada de cloridrato de diltiazem possue marcantes características de liberação retardada e controlada do fármaco.

Unitermos: Cloridrato de diltiazem/peletes de liberação retardada e sustentada/farmacocinética. Alimentos/ingestão/efeito no perfil famacocinético. Cromatografia Líquida de Alta Eficiência/análise quantitativa.

INTRODUCTION

Diltiazem, a calcium channel blocker of the benzodiazepine family, has been widely used for the treatment of angina pectoris (Chaffman, Brogden, 1985; Théroux et al., 1985; Hossack et al., 1981) and hypertension (Zhang et al., 2010; Bertere et al., 2009; Färbom et al., 2008), especially treatment of the hypertension with angina pectoris (Ezeugo, Glasser, 2009; Claas, Glasser, 2005). Pharmacodynamic studies showed that diltiazem might affect heart muscle by blocking influx of extracellular fluid calcium (Britt, 1985) and improving affinity of 1, 4-dihydropyridines for the Ca²⁺ channel (Glossmann et al., 1980).

Diltiazem has been introduced into clinical practice as the ordinary tablets and delay-onset capsules. The patient has to take the drug three times a day because the effective plasma concentration of diltiazem sustains so short time after the administration (Hekmatara et al., 2006; Mazzo et al., 1994). Although the sustained-release capsules of diltiazem hydrochloride keeps the diltiazem release and absorption slowly, the blood concentration is relatively low and flat, which is not suitable to the circadian rhythm of blood pressure (Weir, 1995; Scholz, 1997). So the extended and controlled release diltiazem form is better for the clinical requirement.

As a new form, diltiazem hydrochloride delay-onset sustained-release pellet is prepared by spraying diltiazem solution onto the surface of celpheres and then coating with hydroxy propyl methyl cellulose as swelling layer and Surelease as coating layer (Dey et al., 2008). There are two pellet kinds depending on adjusting the proportion of the surface macromolecular layer: one is a rapid release pellet after a long certain delayed time, and the other is an extended release pellet after a long certain delayed time. The two pellet kinds that are loaded in one single capsule ensure to delay the release of the active ingredient effecting in sufficient amount and extend for enough time. The delayed drug release is compatible with the chrono-pharmacologic drug delivery systems (Smolensky et al., 2007). These capsules delay the release of diltiazem for 4-6 h and be effectively compatible with the circadian variation of the disease.

The pharmacokinetics (PK) of ordinary tablets and sustained capsules of diltiazem hydrochloride in human trials were already studied (Yeung et al., 1999; Sista et al., 2003; Caillé et al., 1991; Weiner et al., 1986). The PK of diltiazem hydrochloride delay-onset sustained-release pellet capsules with the delayed and controlled drug release is very important for this new medicine, although it has not been reported. The aim of the present work was to evaluate the PK of diltiazem hydrochloride delay-onset sustained-release pellet capsules and the influence of food on drug absorption in Chinese healthy volunteers, via establishing an analytical method to quantify human plasma diltiazem concentration by reversed-phase high-performance liquid chromatography (RP-HPLC).

MATERIAL AND METHODS

Drug and reagents

Four dosages (90 mg, 180 mg, 270 mg and 360 mg) of diltiazem hydrochloride delay-onset sustained-release pellet capsules (Batch: 111202, Specifications: 90 mg/capsule) for single, multiple and food-effect oral administrations were made. Each capsule was contained of two kinds of pellets consisted of HPMC and Surelease, in which one was the short delayed release and the other was the long delayed release, respectively. Diltiazem hydrochloride reference substance (Batch: 070223-201101) was purchased from Chinese National Institutes for Food and Drug Control with the purity of diltiazem more than 98.4%. Alprazolam reference substance (Batch: 0912) was obtained from State Narcotics Laboratory, China, with the purity of alprazolam more than 99.8%. Acetonitrile (HPLC grade) was purchased from Caledon Company, Canada. Double Distilled water and other reagents were analytical grade.

Instruments

The HPLC system was an Agilent Chemistation Rev.A.08.03 System (HPLC1100, Agilent, American) equipped with a G1313A quaternary pump, a vacuum degasser, a G-1316 column oven, and a G1315B photodiode array detector. Low speed centrifuge (80-20) was from Shanghai Medical Instrument Co., Ltd. (Shanghai, China).

Test subjects

Thirty six Chinese volunteer, half male and half female, with mean age of 23.4 ± 3.7 (18-27 years), mean weight of 64.5 ± 5.8 kg with body mass index (BMI) 23.4-24.6 kg m^-2, and mean height of 167.0 ± 5.8 cm were enrolled in the study. All the subjects were confirmed to be healthy by physical examination, passing through the clinical laboratory tests, and screening the medical histories. None of the subjects had any surgery or took any alterative medications other than diltiazem hydrochloride. No medications were taken for at least two weeks before the study. Tobacco, alcohol, beverage containing alcohol and caffeine were forbidden 48 h before the study and during the study. During process of the single and multiple dose clinical studies, all subjects were fed with the unified light foods diet and confined in special wards. In the food-effect study, the high fat food diet used was based on the Guideline Recommendation of US FDA but adopted to Chinese dietary habit include: one fried egg, pork (fat: lean=2:1) 75 g, rape 100 g, colza oil 20 ml for cooking, the steamed bread 100 g and rice gruel 150 mL as staple food. The above Chinese food could provide approximately 1118 calories. Following the Guidance of Helsinki Declaration, all subjects signed the informed consent. The study protocol was approved by Ethic Committee of Xiangya Hospital Affiliated Central South University, China (Protocol JDX1999064).

Study design

Single dose study

An opened-label, randomized, parallel and single dose clinical study was carried out in 36 Chinese healthy volunteers. The subjects were equally (12 subjects one group, male and female equalization) divided to three groups as A, B, and C, and were administrated with specified doses of 90, 180 and 270 mg diltiazem respectively. All subjects were supplied with unified light diet, and then fasted but water supplied overnight before the drug administration and given corresponding diltiazem hydrochloride delay-onset sustained-release pellet capsules (Group A, 1 capsule; Group B, 2 capsules, Group C, 3 capsules) with 240 mL warm water for oral administration. And food was withheld for an additional 4 hours. Venous blood (5 ml) for pharmacokinetics study was collected into the heparinized tubes before drug administration (0 hour) and at 0.25, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 24, and 36 h after drug oral administration. The blood was immediately centrifuged for 10 min at 3000 rpm·min^-1 to separate the plasma, which then was frozen and stored at -40 ºC for assay. Adverse events of each subject were carefully observed and recorded during the study.

Multiple dose study

Multiple dose studies were carried out in Group A (12 volunteers) 14 days after the single dose study when the wash-out period passed. All subjects were fasted but water supplied overnight before each drug administration, and then given corresponding diltiazem hydrochloride delay-onset sustained-release pellet capsules (one capsule, 90 mg) with 240 mL warm water at 8:00 in the next morning. It was continued the drug administration (one capsule) for 6 days. Venous blood (5 mL) for pharmacokinetics study was collected into the heparinized tubers before drug administration (0 hour) in the 4^th, 5^th, 6^th day and after oral administration at 0.25, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 24 and 36 h in the 6^th day. The blood was immediately centrifuged for 10 min at 3000 r·min^-1 to separate the plasma, which was frozen and stored at -40 ºC for assay. Adverse events of each subject were carefully observed and recorded during the study.

Food-effect study

The effect of food on corresponding diltiazem hydrochloride delay-onset sustained-release pellet capsules was carried out in group B and C (24 volunteers) after the single dose study. A randomized, open-label, two-period crossover method was designed to take a single dose of diltiazem (360 mg, 4 capsules) with a 14 days wash-out period between the two occasions. Subjects were admitted to ward on the day before the drug administration. From 7:00 pm after dinner to the dosing on the day, subjects were not allowed to eat any food expect water. Subjects were randomized to treat (the delay-onset sustained-release pellet capsules 360 mg without food (fasting condition), or with high-fat food (fed). After a 14-days washout period, subjects were crossed over to the alternate treatment. All subjects received the same lunch and supper following drug administration. After administration, the subjects in the fasted group remained fasting for 4 hours. Water was allowed ad libitum throughout the study period except for 4 hours pre- and post-study drug administration. Strenuous exercise was not permitted during the 36-hour post-dose monitoring period. Blood (5 mL) was collected into heparinized tubes before and at 0.25, 0.5, 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 24 and 36 hours after drug administration. The blood was immediately centrifuged for 10 min at 3000 r·min^-1 to separate the plasma, which was frozen and stored at -40 ºC for assay.

Analysis of blood samples

• Blood preparation

To 1 mL of spiked plasma sample, 30 µL of a solution containing alprazolam (2.44 µg.mL^-1, internal standard) and 1 mL of sodium hydroxide solution (0.1 mol.L^-1) were added, and then the obtained mixture was vortex-mixed for 1 min. An aliquot of the hexane: trichloromethane: isopropanol (60:40:5) (5 mL) was then added to the mixture, vortex-mixed for another 2 min and then centrifuged at 3000 rpm for 10 min. The supernatant was collected and evaporated to dryness under a nitrogen stream at -40 ºC. The residues were reconstituted with 100 µL of the mobile phase, respectively, and an aliquot of 50 µL of each sample was injected to HPLC for LC-UV analysis.

• RP-HPLC conditions

The blood was separated on Gemini ODS C₁₈ (4.6 mm×550 mm, 5 µm) column and detected at the UV wavelength of 215 nm. The HPLC separation temperature was set at 35 ^oC. The mobile phase was made up of acetonitrile: 0.08% triethylamine solution 37: 63 (v/v) (adjusted to pH 3.01-3.06 using phosphoric acid) at a flow rate at 1.2 mL·min^-1.

Method validation

• Calibration curve and limit of quantification

The RP-HPLC analytical method was validated by evaluated linearity of standard curve, intra-day and inter-day precision and accuracy, and recovery of diltiazem extracted in plasma. The calibration curve was constructed using seven different concentration levels of diltiazem without 0.

The limit of the quantification was defined as the lowest amount of the analyte in plasma that was quantitatively determined with suitable precision (<20%) of the true concentration.

• Recovery, accuracy and precision

To determine the absolute recovery of diltiazem in plasma, three different concentration levels at 10.1, 80.8, and 646.4 ng.mL^-1 of diltiazem were obtained by spiked diltiazem into the blank plasma, in which the diltiazem level was so low that was difficult to be measured, with six replicates for each concentration, and then the samples were extracted and analyzed by the RP-HPLC as described above. The absolute recoveries of diltiazem were obtained by dividing peak areas of extracted samples by those of corresponding spiked standard solution in the extracted blank plasma.

Accuracy and precision of the method were assessed by intra-day and inter-day analysis of six replicates for each concentration at 3 different concentration levels (10.1, 80.8, and 646.4 ng.mL^-1, respectively). The coefficient of variation (CVs) at each concentration level was expressed as precision. The intra-day and inter-day precision was analyzed by one-way analysis of variance (ANOVA) method.

• Sample stability tests

The stability tests were to measure the concentrations of the spiked diltiazem in the blank plasma which were placed on the laboratory desk at room temperature for 24 h, which were frozen and defrosted for 1 to 3 times, or which were stored at frozen condition for 0 to 28 days.

• Quality control samples

Diltiazem was spiked into the blank plasma to reach the final concentration levels at 10.1, 80.8, and 646.4 ng.mL^-1, respectively as quality control samples. The quality control concentrations should cover the concentrations of the target analyses.

The data processing and statistical analysis

Plasma diltiazem concentration profiles of 36 subjects were presented as mean ± standard deviation (SD). Main pharmacokinetics parameters were calculated for each subject. T_max and C_max were obtained directly from the observed data. Plasma concentrations that lower than the lower limit of quantification (LLOQ) were assigned as a value of zero for the calculation of plasma concentrations and pharmacokinetic parameters. All the PK parameters were calculated by the PK-Solver 2.0 (China Medicine University, China).

RESULTS

Method validation

Chromatographic behaviors

The typical chromatograms of diltiazem were shown in Figure 1. The analyte and Internal standard (IS) were separated very well, where the retention time of diltiazem and IS was at 6.8 min and 9.3 min, respectively. It was not found any endogenous interference peaks on their chromatograms.

Linearity of the calibration curve and the limit of quantification

The diltiazem was added into blank plasma to obtain the concentrations of standard solutions at 10.1, 20.2, 40.4, 80.8, 161.6, 323.2 and 646.6 ng.mL^-1. The samples were prepared and analyzed by RP-HPLC as above. A good linear correlations regression equation of diltiazem was fitted as: Y = (0.00586) X + 0.02481, r = 0.9990, (where X was the plasma concentration of diltiazem hydrochloride, and Y was the peak area ratio of IS diltiazem hydrochloride). The calibration curve linearity of diltiazem hydrochloride was from the range of 10.1 to 646.4 ng.mL^-1.

Recovery, accuracy and precision

The absolute recoveries of diltiazem extracted in plasma were 82.9 ± 18.4, 94.6 ± 14.9 and 70.5 ± 7.1%, respectively, corresponding for the three concentration levels of 10.1, 80.8, and 646.4 ng.mL^-1 listed in Table I. The recovery of IS was 97.2 ± 5.4 %. The absolute recovery rates of this method were suitable for the PK studies of diltiazem in human plasma (Werghese et al., 1983).

Table II was the precision and accuracy of intra-day and inter-day. The results showed the precision of intra-day analysis of diltiazem spiked in the blank plasma at three different concentration levels were 6.2%, 5.6%, 2.7%, respectively, and that of the inter-day were 7.3%, 3.0% and 4.4%, respectively. These data demonstrated high precision and accuracy of the method.

Sample stability

• Stability of plasma diltiazem at room temperature

The blank plasma with diltiazem levels at 10.1, 80.8, or 646.4 ng.mL^-1 was kept at room temperature for 24 hours. The RSD at 0, 2, 6, 12, or 24 h was not more than 11.1% (LLOQ sample), 1.8%, and 2.1%, respectively.

• Stability of plasma diltiazem after freeze-thaw circles

The blank plasma with diltiazem levels at 10.1, 80.8, or 646.4 ng.mL^-1 was frozen at -40 ºC and followed three freeze-thaw cycles. The RSD was not more than 7.6% (LLOQ sample), 3.2%, and 1.7%, respectively.

• Stability of plasma diltiazem after frozen storage

The blank plasma with diltiazem levels at 10.1, 80.8, or 646.4 ng.mL^-1 was analyzed after the samples were frozen at -20 ºC for 0 to 28 days. The RSD was not more than 19.5 % (LLOQ sample), 6.1%, and 4.7%, respectively.

These results showed that the plasma diltiazem was quite stable during the whole PK studies.

Pharmacokinetics

Diltiazem was quite well tolerated, in which neither serious unexpected events occurred nor drop-out in the volunteers during the study. All volunteers were in good condition in the clinical trials.

Single dose trial

The mean plasma concentration-time profiles of 36 healthy volunteers in single oral administration with the dose of 90 mg, 180 mg, or 270 mg of diltiazem hydrochloride delayed-onset sustained-release pellet capsules were shown in Figure 2. The main PK parameters were summarized in Table III. Mean C_max values were 128.26 ± 22.61, 162.69 ± 32.24, and 191.00 ± 40.26 ng.mL^-1. The corresponding T_max values were 11.15 ± 1.10, 11.76 ± 1.25, and 11.48 ± 1.03 hours, respectively and t_1/2β values were 14.47 ± 0.42, 14.41 ± 2.32, and 14.89 ± 1.16 hours; The T_lag values were 4.85 ± 0.51, 4.81 ± 0.73, 4.58 ± 0.42 hours. The AUC₃₆ were 2597.97 ± 313.22, 3511.52 ± 324.90, and 4245.90 ± 468.82 ng.h.mL^-1, while the AUC_∞ were 3131.61 ± 765.71, 4307.71 ± 628.42, and 5341.92 ± 861.74 ng.h.mL^-1 respectively.

Multiple-dose trials

The mean plasma concentration-time profiles of multiple oral doses (90 mg) of diltiazem hydrochloride delayed-onset sustained-release pellet capsules in 6^th day were shown in Figure 3. Considering the factual dosing interval was 24 h, the PK parameters that were calculated by PKSolver 2.0 as Table IV. The mean C_mas,ss value was 181.33 ± 23.09 ng.mL^-1, the corresponding T_max value was 10.39 ± 1.32 hour and t_1/2β was 14.38 ± 0.72 hour. The C_min,ss was 44.08 ± 3.06 ng.mL^-1 and the AUC_0~24,ss was 3127.61 ± 233.37 ng.h.mL^-1. The oral clearance (CL/F) of multiple-dose group was 28775 ± 216 mL.h^-1.

Food-effects trials

The mean plasma concentration-time profiles of high calories food-effects on diltiazem hydrochloride delayed-onset sustained-release pellet capsules (360 mg) and parameters of fasted condition in plasma were shown in Figure 4. The corresponding PK parameters in steady-state were reported in Table V. The Mean C_max values were 216.09 ± 34.68 and 206.51 ± 41.23 ng.mL^-1; the corresponding T_max values were 11.8 ± 1.8 and 11.6 ± 2.1 hours; the t_1/2β were 16.1 ± 4.2 and 14.3 ± 5.7 hours; and the AUC₃₆ were 4663.8 ± 1521.3 and 4530.6 ± 1671.2 ng.h.mL^-1, while the AUC_∞ were 5851.3 ± 1625.7 and 5622.9 ± 1756.2 ng.h.mL^-1. The oral clearance (CL/F) of multiple-dose group from fed and fasted group were 61.5 ± 8.72 and 64.2 ± 1.31 mL.h ^-1, respectively.

DISCUSSION

Several RP-HPLC methods for measuring human plasma diltiazem concentration have been reported (Sultana et al., 2010; Zargh et al., 2005). The method that sodium hydroxide was used as alkaline extraction solution remarkably increased the extraction rates of diltiazem from plasma sample (Höglund, Nilsson, 1987). This method was simple and sensitive in short analysis time for diltiazem determination in plasma. The lower limit of quantification (LLOQ) (10.1 ng.mL^-1) for the plasma diltiazem concentration was suitable for the detection in this experiment following the FDA advice (RSD < 20 %).

Compared with the PK parameters obtained from the same oral dose of tablets, the main PK parameters of t_max, C_max, AUC_t and t_1/2 of diltiazem hydrochloride delayed-onset sustained-release pellet capsules in three single oral dose groups were much higher in the present study than the corresponding PK parameters reported in the previous literatures (Murata et al., 1989; Turner, 2002).

The parameters of AUC₃₆ and AUC_∞ in group B with the oral administration of 180 mg single dose were higher than those in group A with 190 mg, and lower than those in group C with 270 mg. The T_lag (about 5 hours) indicted that the diltiazem release from the pellets was a delayed release character. Moreover, the point deviation in the concentration-time curves should be attributed to big individual differences among the volunteers.

Theoretically, the main PK parameters obtained from single dose and multiple doses are in accordance with each other, of which the multiple parameters could be calculated out by single. In this process, the multiple parameters of t_max, C_max,ss, C_min,ss, C_ss,average and AUC_0~24h,ss calculated from single were 5.95 h, 182.24 ng.mL^-1, 43.34 ng.mL^-1, 130.48 ng.mL^-1, 3131.61 ng.mL^-1 respectively, which were well coincided with the corresponding actual values listed as Table IV. The only exceptional parameter was that the real multiple t_max was 10.39 h, which was thought as the total of t_lag (4.41 h) and the calculated t_max by single (5.95 h). Response to the reported pharmacokinetic parameters of the same multiple oral dose, the present results showed that the time to maximum plasma concentration [t_max = (10.39 ± 1.32) h] was prolonged significantly. However, the elimination half-life (t_1/2β = 14.38 ± 0.72 h) remained extending (Lefebvre et al., 1994; Roberts et al., 1991; Ochs et al., 1984).

A dose of 360 mg diltiazem could be found using in clinical practice, thus a dumping dose in high fat food condition effect should be investigated. The comparisons of parameters AUC and C_max after taking delay-onset pellets of diltiazem in food and fasted state appeared only slight increase (C_max from 206.51 to 216.09 ng.mL^-1; t_1/2β from 14.3 to 16.1 h; AUC_∞ from 5622.9 to 5851.3 ng.mL.h^-1), but the T_max of fed (11.8±1.8 hour) almost appeared equal to that of fasted condition (11.6±2.1 hour). That means the delay-onset dosage form was well tolerated under food and fast condition. No marked difference was observed in the PK parameters and curves. The data showed that the delayed-onset dosage form could be administrated without regards of food effect.

The diltiazem hydrochloride delayed-onset release capsules were mainly used to treat the blood pressure and cardiac disease. Indeed, the prominent 24-hour variation in the occurrence of a variety of acute cardiovascular events, such as myocardial infarction, angina pectoris, cardiac arrest and sudden cardiac death have been shown to be closely related to the circadian blood pressure pattern of hypertensive subjects (Portaluppi et al., 1999). The objective of the pellets capsules was to adject the diltiazem release to vary with the variation of blood pressure in 24-hour time. Such model could match the circadian pattern of blood pressure characterized by a low span associated with sleep, rest, or inactivity, followed by a steep rise over a 4-hour period that occurs with awakening and/or arousal and a high span for the remainder of the 24-hour period during wakefulness, increased activity, or work (White, 1996; Weber et al., 1988). Therefore, considering the delayed lag time of about 5 hours, it suggests that patients take the capsules in the bedtime of about 22:00 pm so that the diltiazem will release at about 2~3 am and peak blood concentration appears in morning (T_max=11.6 h, 360 mg/dose), or patients take the capsules at 8:00 am to allow the peak drug level between 6:00 and 8:00 pm according to patient conditions (Hermida et al., 2007). So the diltiazem hydrochloride delayed-onset sustained-release pellet capsules should be better for the patients to prevent the attack of heart disease in sleeping time.

There had a limitation in this study. This study was conducted mainly in a small number of young healthy subjects (between 19 and 30 years of age) who did not receive additional medications or tobacco. The study population cannot be representative population of patients totally who might be treated with this medication or with tobacco or alcohol. Meanwhile, the drug interactions potentially were not assessed, and the influence of co-morbid conditions (e.g. motility disorders, malabsorption disorders and achlorhydria) on other aspects of pharmacokinetics could not be accounted for either.

CONCLUSIONS

The present study suggested that diltiazem hydrochloride delayed-onset sustained-release pellet capsules possessed marked characteristics of delayed and controlled release. From the PK analysis, the pellets administrated showed delayed release time in about 5 hours which will comply with the chronopharmacology. The sustained release pellets capsules could be orally administrated without regard to the food factor.

ACKNOWLEDGEMENT

This work was supported by National Natural Science Foundation of China (No. 81240105), China Postdoctoral Science Fund (No. 20080430856) and High educated talents fund of Xinxiang Medical University (No. 100778), Hunan province combining achievement transformation project (No. 2009XK6020) and a grant from Clinical Medical College of Yangzhou University and Hunan KAMP Institute for Medical Reaserch.

The authors have no conflicts of interest that are directly relevant to the content of this study.

Received for publication on 07^th February 2012

Accepted for publication on 06^th November 2012

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Publication Dates

• Publication in this collection
  19 Apr 2013
• Date of issue
  Mar 2013

History

• Received
  07 Feb 2012
• Accepted
  06 Nov 2012