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Print version ISSN 0100-4670On-line version ISSN 1678-4618
Eclet. Quím. vol.28 no.1 São Paulo 2003
Potentiometric determination of captopril in pharmaceutical formulations
Determinação potenciométrica de captopril em formulações farmacêuticas
P. R. da S. RibeiroI; A. O. SantiniII; H. R. PezzaI; L. PezzaII
IDepartamento de Química Analítica Instituto de Química UNESP CEP 14801-970 Araraquara SP Brasil
IIDepartamento de Química Orgânica Instituto de Química UNESP CEP 14801-970 Araraquara SP Brasil
A simple, precise, rapid and low-cost potentiometric method for captopril determination in pure form and in pharmaceutical preparations is proposed. Captopril present in tablets containing known quantity of drug was potentiometrically titrated in aqueous solution with NaOH using a glass pH electrode, coupled to an autotitrator. No interferences were observed in the presence of common components of the tablets as lactose, microcrystalline cellulose, croscarmellose sodium, starch and magnesium stearate. The analytical results obtained by applying the proposed method compared very favorably with those obtained by the United States Pharmacopoeia Standard procedure. Recovery of captopril from various tablet dosage formulations range from 98.0 to 102.0%.
Keywords: potentiometric determination; captopril; pharmaceutical formulations.
Um método potenciométrico simples, preciso, rápido e de baixo custo foi proposto para a determinação de captopril na forma pura e em formulações farmacêuticas. O captopril presente em comprimidos em uma quantidade conhecida foi potenciometricamente titulado em meio aquoso com um titulador automático, empregando-se como titulante uma solução aquosa de NaOH e um eletrodo combinado de vidro sensível a pH. Interferências não foram observadas na presença de componentes comumente encontrados nos comprimidos, tais como, lactose, celulose microcristalina, croscarmelose sódica, amido e estearato de magnésio. Os resultados analíticos obtidos a partir da aplicação do método proposto estão em muito boa concordância com aqueles obtidos pelo método oficial descrito na Farmacopéia Americana. O recobrimento obtido para o captopril a partir de um estudo realizado com várias formulações farmacêuticas variou de 98.0 a 102.0%.
Palavras-chave: determinação potenciométrica, captopril, formulações farmacêuticas.
Captopril, chemically know as 1-[(2S)-3-mercapto-2-methylpropionyl]-L-proline, (CPT) is used therapeutically as an antihypertensive agent [11, 15], which is also prescribed for the treatment of congestive hart failure .
Several types of analytical procedures have been proposed for the analysis of captopril in pharmaceuticals formulations. These procedures include capillary electrophoresis , high-performance liquid chromatography (HPLC) [3, 4, 5, 9], polarography , voltammetry , coulometry , amperometry , conductometry , fluorimetry  , colorimetry [1, 2, 7, 14, 22, 24] and flow injection methods.[12, 21, 28]. Some of the ses procedures are not simple for routine analysis and required expensive or sophisticated instruments.
Potentiometric methods with ion-selective membranes electrodes (ISE's) can provide valuable and straightforward means of assaying captopril in pharmaceutical formulations because of the possibility to determine directly the active ions in the solution. ISEs' low-cost, easy of use and maintenance, and the simplicity and speed of assay procedure, and the reliability of the analytical information make them very attractive for the assay of pharmaceutical products.
Potentiometric methods based in the reactivity of thiol group have been used for captopril determination in pharmaceutical formulations [8, 17, 26].
To the best of our knowledge, despite the advantages of the glass membrane pH electrode, there are no previous reports for the potentiometric determination of captopril based in the reactivity of this carboxyl group using the glass pH electrode.
For this reason, the purpose of this work was to develop a potentiometric method for direct determination of captopril in tablet dosage formulations. The method is based in a potentiometric titration of captopril (carboxyl group) in aqueous solutions with sodium hydroxide solution using a combined glass electrode, coupled to an autotitrator. The proposed method is simple, rapid, precise, accurate and inexpensive.
The results agreed fairly well with those obtained by the United States Pharmacopoeia (USP) standard procedure  (iodimetric titration). The influence of interferents normally found along with captopril in tablet dosage formulations in also studied.
Potentiometric measurements were carried out using a Metrohm autotitrator, model 716 (Metrohm Ltd., Herisau, Switzerland). The indicator electrode was a Metrohm combined pH electrode model 60234.100. A thermostated titration cell (25.0±0.1)OC was employed. Volume measurements (±0.001mL) were performed with a Metrohm automatic burettes model 665.
All chemicals were analytical grade and solutions were prepared with deionized water (conductivity = 18.2MWcm). Captopril (standard substance) was purchased from sigma (St Louis, MO, USA). It was analysed as prescribed in the USP  and contains 99.7% of 1-[(2S)-3-mercapto-2-methylpropionyl]-L-proline, calculated with reference to the dried substance. It was used as a standard. The captopril tablets (25 mg) manufactured respectively by Medley (Campinas, Brazil), Azupharma Gmbh (Gerlingen, Germany) and Apotex (Toronto, Canadian) were used for the analysis. Sodium hydroxide and sodium nitrate were purchased from Merck (Darmstadt, Germany).
A freshly prepared 1.000 x 10-1 mol L-1 aqueous of solutions of captopril (standard substance) was used as the stock solution.
The sodium hydroxide 2.00 x 10-2 mol L-1 was prepared, standardized and stored according to recommendation of the literature .
The ionic strength (I) of the final solutions used for the potentiometric determination was kept constant at 0.500 mol L-1 by addition of sodium nitrate.
For pure form
A standard solution (100 mL) of captopril 1,000 x 10-2 mol L-1 (I adjusted to 0.500 mol L-1 with NaNO3) was prepared by suitable dilution of the stock solution with water.
An aliquot of 15.000 mL of this solution was transferred to a thermostated glass cell (25.0±0.1)ºC and potentiometrically titrated with a standard solution of NaOH 2.00 x 10-2 mol L-1 (I = 0.500 mol L-1 in NaNO3).
Fifteen tablets were weighed to calculate the average tablet weight. They were finely powdered and homogenized. A portion of the powder equivalent to about 217.3 mg of captopril was accurately weighed and dissolving with 40 mL of water by sonicating for 20 min in an ultrasonic bath. The resulting mixture was filtered and its ionic strength was adjusted to 0.500 mol L-1 with NaNO3. Finally, this solution was diluted with water in a 100 mL flask and analysed under the same procedure described for captopril in pure form.
Results and discussion
The development of the titration curves of polyprotic acids depends on the absolute and relative values of the respective stepwise ionization constants. Theoretically, there will be one inflection for each labile hydrogen. However, so that an inflection is associated to an adequate variation in pH, it is necessary in the first place for the relationship of the respective ionization constant to the next one to be greater than 104 (K1/K2 > 104 or pk2 pk1 > 4). In the second place, it is necessary for the corresponding ionization constant not to be that of a very weak acid.
Captopril is dibasic acid having dissociation constants pk1 = 3.7 (carboxyl group) and pk2 = 9.8 (thiol group). Observing the values of pk1 and pk2 of captopril, it can be foreseen that the titration curve presents a clear inflection for the first point of equivalence since k1 = 2 x 10-4 and the relationship of k1/k2=106 (pk2 pk1 = 6). However, captopril is a very weak acid in relation to its second hydrogen (k2 @ 10-10) that its titration curve does not present a perceivable inflection for the second point of equivalence.
Figure 1 (a) shows a typical potentiometric titration curve with only one inflection point. In the proposed method changes at the titration end point were enough pronounced to give potentiometric titration curves of satisfactory shape for an accurate and reproducible end point detection. The time required for the analyses of captopril (after the samples preparation) in tablet dosage formulations by potentiometric method was 8 min. per sample.
Figure 1(b) shows the first derivative of the potentiometric titration curve generated by the internal algorithm of the autotitrator. The evaluation of the potentiometric titration curve by the autotitrator is fully automatic yielding an accurate end point. The determination limit of the proposed method determined as described by Leite  was 180 mg mL-1.
Effect of interferents
To assess the usefulness of the proposed method, the effect of the common components (additives, adjuvants and excipients), which often accompany captopril in tablet formulations (lactose, microcrystalline cellulose, croscarmellose sodium, starch and magnesium stearate) were investigated in a concentration range of least 20 times higher than that of captopril. No interferences were observed in the presence of the substances tested.
The proposed method was successfully applied for captopril determination in tablet formulations. The results presented in Table 1, agreed fairly well with those obtained by the USP standard procedure  (iodimetric titration).
For further confirmation, the standard addition method was applied to test the reliability and recovery of the proposed method. The recovery studies were carried out after adding known quantities of the standard substance (pure drug) to the preanalyzed formulations. The results presented in Table 2 show that the percentage recoveries were found to be close to 100%; the SDs were within 0.48 0.85. These results point out the accuracy and precision of the method and the absence of significant matrix effects on potentiometric measurements at least for the samples analysed.
Compared with many of the already existing procedures for the determination of captopril, which required special instrumentation, reagents, precautions and experience, the propose potentiometric method employing the glass pH electrode exhibited the advantages of simple operation, reasonable selectivity, fast response, low-cost, and sufficient accuracy for the determination of captopril in pharmaceutical formulations.
We would like to thank FUNDUNESP, CAPES, CNPq and FAPESP Foundations (Brazil) for financial support.
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