Colombia Médica, Vol. 42, No. 1, January-March, 2011, pp. 81-87
Bioavalaibility and pharmacokinetic comparison of two formulations of metformin 850 mg tablets in healthy Colombian volunteers
Comparación de la biodisponibilidad y la farmacocinética entre dos formulaciones de tabletas de metformina de 850 mg en voluntarios colombianos sanos
Gloria Holguín, Esp1, Fanny Cuesta, IQ2, Rosendo Archbold, MSc3, Margarita Restrepo, MSc4, Sergio Parra, MSc5, Lina Peña, Esp6, Blanca Montoya, Bact7, Juan Carlos Ríos, MSc8, Victoria Eugenia Toro, QF9, Adriana Ruiz, PhD10
1Full Professor, Department
of Pharmacy, Faculty of Pharmaceutical Chemistry, Universidad de
Antioquia, Medellín, Colombia. e-mail: email@example.com
Received for publication December 17, 2009
Code Number: rc11011
Purpose: The aim of this study was to compare the bioavailability of two
formulations of metformin 850 mg tablets: Glucophage® from Merck
Santè laboratories (reference product) and Metformin from
Winthrop Pharmaceuticals de Colombia SA (test product) in healthy
Keywords: Metformin; Bioequivalence; Bioavailability; Pharmacokinetics; Interchange of drugs; Area under curve.
Objetivo: El objetivo de este estudio es comparar la bioequivalencia de dos
formulaciones de tabletas de metformina de 850 mg: Glucophage® del
Laboratorio Merck Santè (producto de referencia) y metformina de
Laboratorios Winthrop Pharmaceuticals de Colombia SA (producto de
prueba), en voluntarios colombianos sanos.
Palabras clave: Metformina; Bioequivalencia; Biodisponibilidad; Farmacocinética; Intercambiabilidad de medicamentos; Área bajo la curva.
Metformin is a biguanide drug that became commercially available in 1957. It is for oral administration and has a specific anti-hyperglycemic effect on patients with type 2 diabetes mellitus (DM). Therapeutic doses of metformin do not produce hypoglycemia, and it is a therapeutic advantage when compared with sulfonylureas1.
Doses of 0.5-1.5 g have a bioavailability of 50%-60%2. Absorption is slow and incomplete in the upper gastrointestinal tract, because of the high polarity and low liposolubility of the molecule. At intestinal pH between 7 and 8, metformin is mainly ionized (pka=2.8 and 11.5), which slows its absorption rate3.
Metformin is rapidly distributed after absorption, and it is accumulated in the esophagus, stomach, duodenum, salivary glands, and kidneys4. It has neither binding to plasma proteins nor metabolism, and it undergoes renal excretion.
Nowadays, metformin is a first-choice drug for type 2 DM treatment because of its broad therapeutic advantages. Therefore, Colombian pharmaceutical industries have been motivated to produce a generic form of this drug.
Because of the low bioavailability and high inter-individual variability in the absorption of the different pharmaceutical forms of metformin, it is necessary to perform comparative bioavailability studies. Thus, regulatory authorities and medical prescribers would have the scientific support to expect a therapeutic equivalence if bioequivalence among the compared pharmaceutical forms is demonstrated.
The aim of this study was to evaluate, in healthy Colombian volunteers, the bioequivalence of the generic metformin, from Laboratorios Lakor Farmacéutica SA now Winthrop Pharmaceuticals de Colombia SA manufactured by Sanofi~Synthelabo, Cali, Colombia, with the reference product Glucophage® from Merck Santè laboratories.
MATERIALS AND METHODS
Drug products. Test product (T): metformin, 850-mg tablets, owned by Winthrop Pharmaceuticals de Colombia SA manufactured by Sanofi~Synthelabo, Cali, Colombia, lot: P1320804, and containing 850 mg of the active ingredient per tablet, corresponding to 100% of the labeled quantity of metformin.
Reference product (R): Glucophage®, 850 mg tablets, owned by Merck, manufactured by Merck Santè, Lyon, France, lot: 104031, and containing 872.95 mg of the active ingredient per tablet, corresponding to the 102.7% of the labeled quantity of metformin.
The pharmaceutical products used in this study were previously evaluated to determine the drug content of each product, according to the British Pharmacopoeia Quality Specifications. They were declared pharmaceutical equivalents because the test product did not differ from the reference product by more than 5%.
Study subjects. The study was conducted according to the Helsinki Declaration and Resolution 8430 of 1993 by the Ministry of Social Protection. It was also approved by the Ethics Committee of the School of Medicine, at Universidad de Antioquia. 24 subjects were recruited for this study, (10 male, 14 female; ages 21.2±2.1 years; weight 60.5±7.7 kg; height 1.67±0.08 m). Subjects were assessed healthy volunteers, after having been medically examined and clinically tested: complete blood count, urinalysis, blood biochemistry were normal, and HIV, hepatitis B, and pregnancy screenings (for women) were negative. All subjects were briefed on the bioequivalence study details and they all agreed and signed a written informed consent. All volunteers were free to leave the study at any time. The number of subjects was determined by the coefficient of variation from published data5 and by applying the method proposed by Zapater6 and Julious7 to obtain 80% power.
Clinical trial design. In order to evaluate the bioequivalence of the two metformin formulations, we performed a random, double blind, two-period crossover study. On the first dosing day, each subject took a metformin tablet of either test or reference formulations (850 mg of metformin) with 240 ml of water. After a 2-week wash out period, each subject took a tablet of the other product.
The volunteers for this study were admitted to the Corporación de Estudios en Salud clinic (CES) in Medellín (Colombia), and they were under direct medical supervision during 24 hours. The first day at 6:00 am, their urine samples were tested for alcohol and drug abuse. Subjects received formulations after 12 hours of fasting.
Standard breakfast, lunch, refection, and dinner were given at 2, 5, 8, and 11 hours after dosing. All meals were the same for both periods. Food with xanthines (such as chocolate), and carbonated drinks were not allowed.
Ten milliliter blood samples were taken through an indwelling cannula in heparinized tubes (Becton Dickinson, NY) before (0.0 h) and at 0.50, 1, 1.50, 2, 2.50, 3, 3.50, 4, 5, 6, 8, 10, 12, 14, and 24 hours after drug administration. Samples were centrifuged at 2000 rpm for 15 minutes and plasma was separated and stored at -20°C for analysis.
Analytical procedure and method validation. Metformin extraction from plasma was accomplished by the liquid-liquid extraction method proposed by Yuen et al.8 One half ml of plasma was vortex during 30 seconds in a screw-capped glass tube after adding 2 ml of acetonitrile to precipitate plasma proteins. After centrifugation (2500 rpm) for 5 minutes at 5ºC, 2 ml of supernatant was transferred to another clean glass tube. The drug was extracted with 2 ml of the extraction solvent (n-hexan) and vortex for thirty seconds followed by centrifugation (2800 rpm) for 5 minutes. The organic phase was then transferred by aspiration to a clean glass tube. The extraction procedure was repeated with the remaining samples. A gentle air flow and a water bath were used to dry the organic phase. The residue was reconstituted in 400 µl of a mixture of KH2PO4 buffer 10 mM (pH 7.5) and acetonitrile (72:28, v/v), and filtered by using a vacuum pump. One hundred microlitres of the sample were injected directly into a chromatographic system.
The HPLC system is comprised of an Agilent, model HP1100 (California, USA), pump, an Agilent diode array detector, and an auto-injector. The software package ChemStation (2000 Version) was used to control the chromatographic system. The Analytical column was a LiChrospher C18 RP-Select B (Agilent, 250 mm, 4 mm ID, 5 µm particle size). The mobile phase consisted of dihydrogen phosphate buffer 0.01M (pH 7.5) and acetonitrile (40:60 v/v). The flow rate was 1.5 ml/min.
The method was validated following criteria established by FDA Guidelines9. Calibration was linear in the concentration range of 62.5-2000.0 ng/ml, with an intra-day correlation coefficient of 0.9995 and inter-day of 0.9976. The intra-day and inter-day calibration curve showed consistent linearity, as seen by a slope coefficient of variation (CV) of 7.6% and 9.6%, respectively.
Other validation parameters were also fulfilled by this method. Intra-day precision was determined by replicate analysis (six times) of standard samples in plasma containing 125, 500, and 2000 ng/ml. Intra-day precision in this study, expressed as means of percent of CV, was 7.3%.
Inter-day precision was determined at six concentrations (62.5, 125, 250, 500, 1000, and 2000 ng/ml) in plasma, in six replicate runs (6 days). Inter-day precision in this study expressed, as the mean of CV was 12.3%. The limit of quantification based on CV smaller than 20% was 62.5 ng/ml; estimated on values obtained in intra-day and inter-day assays.
Two concentrations of metformin (250 and 1000 ng/ml-quality control (QC) samples in three replicates were used for stability studies, including freeze and thaw, short-term temperature and long-term stability; they fulfilled validation parameters. Standard curves were performed daily, over a 12-week period, with each volunteer’s plasma samples and showed consistent linearity (intercept, slope, and correlation coefficient).
Pharmacokinetic analysis. Pharmacokinetic data were calculated by non-compartmental method. The maximum plasma concentration (Cmax) and the time to reach it (Tmax) were determined by inspecting each individual plasma level-time curves. The elimination rate constant (ke) was obtained by ln-linear regression of the terminal decay phase. The area under the plasma level-time curve (AUC0-96h) was obtained by the trapezoidal rule, and the AUC96h-∞ time was determined by dividing the last plasma concentration by ke, and adding this result to the AUC0-96h. The partial AUC (as an early exposure measure) was obtained by truncating the partial area at the population median of Tmax values for the reference formulation.
Statistical analysis. In order to assess the effects of treatment, period, sequence of administration, and subjects, ln-transformed data for AUC0-∞ and Cmax, and non-transformed Tmax were evaluated by means of analysis of variance (ANOVA) for the cross design (Statistica 6.0, Statsoft Inc, 2001).
The method suggested by Schuirmann and accepted by the FDA10 (known as the two one-sided tests) was used to evaluate whether these two formulations of metformin were bioequivalent. Bioequivalence was accepted if 90% confidence intervals for test/reference ratios of AUCs and Cmax fell in the range of 0.80-1.25. A p value of less than 0.05 was considered statistically significant11.
At the first period, all 24 subjects concluded the study without any adverse effects. However, in the second period, one subject presented diarrhea with the test product, another reported epigastric pain with the reference product. At the beginning of this period, a subject was excluded because she was taking antibiotics to treat a urinary infection. Pharmacokinetic parameters were calculated for all 23 volunteers who ended the second period.
Concentrations over the quantification limit (62.5 ng/ml) were observed within 5 to 14 hours. Although blood samples were taken until 24 hours after drug administration, plasma levels were not detected at this time. The mean concentration profiles for the 2 formulations were quite similar, as observed in Figure 1.
To obtain paired data
for 22 subjects, one of 23 was excluded randomly. All parameters had
normality for intra-subject and inter-subject residues. However, two
volunteers presented extreme outcomes: one had lower AUC0-∞ and early exposure area (AUC0-Tmax) values for the test as compared with the reference formulation; Tmax was also very different in this volunteer (test 5 hours, and reference 1.5 hours). The other one had higher AUC0-Tmax values for the test as compared with the reference formulation. The
pharmacokinetic parameters for both formulations are shown in Table 1.
The mean values and 90% CI for the pharmacokinetic parameters compared are summarized in Table 2. ANOVA for AUC0-∞ and Cmax, after logarithmic transformation of the data, revealed that none of the effects examined (formulation, period, within and between-subject variances and carry over) was statistically significant. The 90% CI was within the bioequivalence acceptable range from 80% to 125%, suggesting that both formulations are similar.
Although we planned a study with 24 volunteers, we had to exclude two of them; nevertheless, the power test calculated by using the variability data obtained in the ANOVA analysis and the equations proposed by Julious7 revealed that a sample size of 22 volunteers was sufficient to reject bio-inequivalence (power 88.3%).
The available pharmacokinetic data on metformin have shown that oral bioavailability, ranges from approximately 32% to 61%. The drug disposition exhibits multi-compartmental characteristics. Metformin is rapidly eliminated by the kidney by combined glomerular filtration and tubular secretion. Its metabolism and protein-binding in plasma are negligible. Studies with small numbers of patients suggest that bioavailability decreases with increasing dose12. There are only scarce data on the relationship between plasma metformin concentrations and metabolic effects13.
Pharmacokinetic parameters such as ke, t1/2, and Cmax, present large differences when several papers are compared5,14,15 including the results obtained in this study and in another research we conducted16. This variability could be explained by the metformin accumulation in the intestinal wall17, the subject variation attributed to the drug transporter polymorphisms18, and physiological factors, such as gastric emptying and small-intestine transit. Changes in the gastric emptying and intestinal transit of a metformin dosage form may alter absorption processes and, therefore, bioavailability19.
The reference product reached slightly higher plasmatic levels than the test product and the amount absorbed seemed to be slightly greater (Figure 1). Although there was no significant difference for Cmax and AUC0-∞, the Tmax parameter showed a higher inter-subject variability, with one subject being the most extreme case, who showed a Tmax for the test product of 5 hours, while for the reference product it was 1.5 hours. For this reason, the partial AUC0-Tmax was measured.
The variability in Tmax had implications on the AUC0-Tmax, the 90% CI calculated for this parameter was 78.9-93.5 %, out the range of 80-125%. We might explain this result by the drug class, because in the biopharmaceutical classification it belongs to a substance with high solubility and low permeability (Class III)20. In a solution, the permeability may be the limiting factor for the absorption rate. Thus, the absorption kinetics should be ruled more by physio-logical conditions and the drug distribution than by factors related with the formulation21.
The differences found in this study for the Tmax can be demonstrated because it was performed with one dose only; however, with the chronic administration and the achievement of a stable concentration, no clinical repercussions are expected for such difference.
Although several parameters are important at the time of a product interchange, according to the FDA, the extension of the absorption (AUC0-∞), and the Cmax are the key parameters to declare the bioequivalence.
The generic product metformin, tablets of 850 mg, is bioequivalent regarding AUC0-∞ and Cmax when compared with the reference product (Glucophage®).
Conflict of interest. None of the authors has conflicts of interest related to this study.
This study was sponsored by Winthrop Pharmaceuticals de Colombia SA, contract 8716-002 2003. We thank Professor Abel Díaz for his suggestions and advice with the statistical analysis, and the Pharmaceutical Chemistry students Andrés Restrepo and Iván Darío Gómez for their collaboration when the clinical trial was performed. We disclose no conflict of interest with the companies Winthrop Pharmaceuticals de Colombia S.A., Sanofi-Aventis or Merck-La Santé.
Copyright 2011 - Colombia Médica
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