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Brazilian Journal of Pharmaceutical Sciences

On-line version ISSN 2175-9790

Braz. J. Pharm. Sci. vol.46 no.1 São Paulo Jan./Mar. 2010

https://doi.org/10.1590/S1984-82502010000100010 

ARTICLE

 

Sensitive spectrophotometric assay of simvastatin in pharmaceuticals using permanganate

 

 

Kalsang TharpaI; Kanakapura BasavaiahI, *; Nagaraju RajedraprasadI; Kanakapura Basavaiah VinayI; Salmara Ganeshbhat HiriyannaII

IDepartment of Chemistry, University of Mysore
IIProcess Analytical Laboratory, Advinus Therapeutics

 

 


ABSTRACT

Two simple, sensitive, selective and inexpensive spectrophotometric methods are described for the determination of simvastatin (SMT) in bulk drug and in tablets using permanganate as the oxidimetric reagent. In method A, SMT is treated with a measured excess of permanganate in acetic acid medium and the unreacted oxidant is measured at 550 nm, whereas in method B the reaction is carried out in alkaline medium and the resulting manganate is measured at 610 nm. In method A, the amount of permanganate reacted corresponds to the SMT content and the absorbance is found to decrease linearly with the concentration; and in method B, the absorbance increases with concentration. The working conditions of assays were optimized, and the methods were validated according to the current ICH guidelines. Under optimum conditions, SMT could be assayed in the concentration ranges, 1.47 - 17.67x10-5 and 2.27 - 27.18 x10-6 mol/L by method A and method B, respectively. The calculated molar absorptivities are 3.2 x 103 and 2.5 x 104 L/mol/cm for method A and method B, respectively with corresponding Sandell sensitivity values of 0.0387 and 0.0178 μg/cm2. The limits of detection (LOD) and quantification (LOQ) have also been reported. Accuracy and precision for the assay were determined by calculating the intra-day and inter-day at three concentrations; the intra-day RSD was < 2% and the accuracy was better than 2.15 % (RE). The methods were applied successfully for the determination of SMT in tablet dosage form with a high percentage of recovery, good accuracy and precision, and without measurable interference by the excipients. The accuracy was further ascertained from placebo and synthetic mixture analysis and also from the spike-recovery method.

Uniterms: Simvastatin assay. Spectrophotometry. Permanganate. Pharmaceutical products.


RESUMO

Dois métodos espectrofotométricos simples, sensíveis, seletivos e baratos são descritos para a determinação de sinvastatina (SMT) a granel e em comprimidos, utilizando permanganato como reagente oxidimétrico. No método A, a SMT é tratada com excesso conhecido de permanganato em meio de ácido acético e o oxidante que não reage é medido a 550 nm, enquanto no método B, a reação é efetuada em meio alcalino e o manganato resultante é medido a 610 nm. No método A, a quantidade de permanganato que reage corresponde ao conteúdo de SMT e a absorbância diminui linearmente com o aumento da concentração; no método B, a absorbância aumenta com o aumento da concentração. As condições de trabalho do ensaio foram otimizadas e os métodos, validados de acordo com as normas do ICH. Sob condições ótimas, a SMT pode ser ensaiada nas faixas de concentração de 1,47- 17,67x10-5 e de 2,27-27,18 x10-6 mol/L pelo método A e B, respectivamente. As absortividades molares calculadas são 2 x 103 e 2,5 x 104 L/ mol/cm, respectivamente, para os métodos A e B, com os valores correspondentes de sensibilidade de Sandell de 0,0387 e 0,0178 μg/cm2. Os limites de detecção (LOQ) também foram relatados. A exatidão e a precisão do ensaio foram determinadas pelo cálculo de três concentrações intra- e inter-dia; a RSD intra-dia foi <2% e a exatidão foi melhor que 2,15% (RE). Os métodos foram aplicados com sucesso à determinação de SMT em comprimidos com alta porcentagem de recuperação, boa exatidão e precisão e sem interferência mensurável dos excipientes. A exatidão foi posteriormente determinada no placebo e na mistura sintética e, também, pelo método de spike recovery.

Unitermos: Sinvastatina/ensaio. Espectrofotometria. Permanganato. Produtos farmacêuticos.


 

 

INTRODUCTION

Simvastatin (SMT), chemically known as (1S, 2S, 8S, 8aR)-1,2,6,8,8a-hexahydro-1-(2-((2R, 4R)-tetrahyro-4-hydroxy-6-oxo-2H-pyran-2-yl)-2,6-dimethylnapthalen-8-yl 2,2-dimethylbutanoate (Figure 1), belongs to the group of cholesterol-lowering lactones known as statins which, in 2007, were identified as being among the most widely prescribed drugs in the world. Statins lower cholesterol by inhibiting the synthesis of movalinic acid, which is the key precursor in cholesterol synthesis. SMT has been shown to be effective as an antilipemic agent. It is administered as a pro drug, and in the liver it is hydrolysed to the ß-hydroxy acid form (Mc Evoy, 2002). The drug is officially listed in the 2004 United States Pharmacopoeia and the official method of its determination is high-performance liquid chromatography (The United State Pharmacopoeia, 2002). Various other methods such as UV-spectrophotometry (Erk, 2002; Xu, 2001; Zhonghong, Shurong 2000; Wang, Asgharnejad, 2000; Arayne et al., 2007; Carlcucci, Mazzeo, 1992), HPLC (Carlcucci, Mazzeo, 1992; Jianwei, Ying, 2005; Ali et al., 2006; Carolina et al., 2004, Xan et al., 2000; Wang, 2000), HPTLC (Chandhari et al., 2007), micellar electrokinetic chromatography (Srinivasu et al., 2002) and voltammetry (Coruh, Ozkan, 2006) have been reported for the assaying of SMT in pharmaceuticals. There is only one report on the use of visible spectrophotometry which describes three methods (Saradhi et al. 2007) for SMT. One procedure is based on the reduction of iron (III) by SMT to iron (II) and subsequent formation of prussian blue with ferricyanide measurable at 730 nm. In the other two procedures, the iron (II) formed is chelated with 1,10-phenanthroline or 2,2'-bipyridine followed by measurement of absorbance at 480 or 490 nm. The present paper describes two visible spectrophotometric methods using KMnO4 as an oxidizing agent in both acid and basic medium. Simplicity, sensitivity wide linear ranges, mild experimental conditions and above all cost-effectiveness characterize the proposed methods. Further, the methods were found to possess adequate accuracy and precision.

 

 

EXPERIMENTAL

Apparatus

A Systronics model 106 digital spectrophotometric with 1-cm matched quartz cells was used for all absorbance measurements.

Reagents and materials

All chemicals used were of analytical reagent grade and distilled water was used to prepare all solutions. Potassium permanganate (1x10-2 mol/L) was prepared by dissolving about 0.395 g of the chemical (Merck, Mumbai, India) in water and diluting to 250 mL; and standardized using H.A Bright's procedure (A.I. Vogel, 3rd edition, 1961, p. 280). It was further diluted to 3.164 x 10-3 mol/L KMnO4 for method A and 6.328 x 10-3 mol/L KMnO4 for method B. Acetic acid (3:2) was prepared by diluting concentrated acetic acid (Merck, Mumbai, India, Sp. gr. 1.05) appropriately with water. Sodium hydroxide solution (0.3 and 0.5 mol/L) was prepared by dissolving the chemical (Merck, Mumbai, India) in water. Pharmaceutical grade SMT, certified to be 99.88% pure, was kindly provided by Jubiliant Organosis, Nanjangud, India, as a gift and was used as received. A 2.944x10-3 mol/L SMT was prepared by dissolving 32.5 mg of SMT in 3:2 acetic acid and made up to 250 mL with the same acid used for method A. A 9.059x10-5 mol/L SMT was prepared by dissolving 10 mg of SMT in 0.3 mol/L NaOH with the aid of heat and made up to 250 mL with 0.3 mol/L NaOH and used in method B. Tablets containing SMT such as Zosta (USV Ltd, India) and Simvas (Micro labs Ltd, India) were purchased from the local market.

 

METHODS

Method A

Different aliquots of standard solution (0.5-6.0 mL, 2.944 x 10-4 mol/L ) of pure SMT were transferred into a series of 10 mL calibrated flasks by means of micro burette and the total volume was adjusted to 6.0 mL with 3:2 acetic acid. A volume of 1 mL of 3.164 x 10-3 mol/L KMnO4 was added to each flask accurately, and kept aside for 10 min with occasional swirling before diluting to the mark with water. The absorbance was recorded at 550 nm against a water blank.

Method B

Into a series of 10 mL calibrated flasks, 0.25-3.0 mL of 9.059 x 10-5 mol/L pure SMT solution were buretted and the total volume was made up to 3.0 mL with 0.3 mol/L NaOH. To each flask was added 1 mL of 0.5 mol/L NaOH followed by 1 mL of 6.328 x 10-3 mol/L KMnO4 solution. The flasks were kept aside for 20 min with occasional shaking and the volume was made up to the mark with water. The absorbance was recorded at 610 nm against the reagent blank.

Assay procedure for tablets

Twenty tablets were accurately weighed and powdered. A portion of tablet powder equivalent to 20 mg of SMT was accurately weighed into a 100 mL calibrated flasks, 40 mL of 3:2 acetic acid was added and shaken for 20 min. Then, the volume was made up to the mark with the same acid, mixed well and filtered using a Whatman No. 42 filter paper. First, a 10 mL portion of the filtrate was rejected and a convenient aliquot (around 2 or 3 mL) was subjected to analysis by the procedure described under method A. Another portion of the tablet powder containing 20 mg of SMT was accurately weighed and transferred to a separating funnel containing about 40 mL of water and mixed. The content was extracted with 5 x 5mL portions of chloroform, where the combined organic layer was dried over anhydrous sodium sulphate, and transferred into a dry beaker and evaporated to dryness in a water bath. The residue was dissolved in 0.3 mol/L NaOH with the aid of heat and transferred to a 100 mL volumetric flask and diluted to the mark with 0.3 mol/L NaOH. The solution was diluted to 9.059 x 10-5 mol/L SMT with the same alkali solution and the analysis was completed by following the procedure given under method B.

 

RESULTS AND DISCUSSION

The methods are based on the oxidation of SMT by KMnO4 in either acid or alkaline medium followed by measurement of the residual permanganate at 550 nm in method A or the reduced manganate at 610 nm in method B. The possible reaction scheme is given in Figure 2.

Optimization of experimental conditions

In method A, when a fixed concentration of permanganate was reacted with increasing concentrations of SMT in acetic acid medium, there occurred a concomitant fall in the concentration of permanganate as revealed by the decreasing absorbance at 550 nm (Figure 3 and Figure 4), which served as the basis for quantification. A preliminary experiment showed that permanganate can be determined up to 3.164 x 10-4 mol/L at 550 nm in the acid medium employed (Figure 5). Hence, different concentrations of SMT were reacted with 1 mL of 3.164 x 10-3 mol/L KMnO4 to determine the concentration range over which SMT could be determined. One ml of 3.164 x 10-3 mol/L KMnO4 must be accurately added in all the reaction flasks since KMnO4 absorbs maximally at the analytical wavelength, and small changes in the volume of KMnO4 have a critical effect on the absorbance reading. The solvent used to dissolve SMT was 3:2 acetic acid, and below this concentration of acetic acid, SMT remained insoluble. The same acid concentration was used as a reaction medium. There was no effect of increasing the concentration of acetic acid on the reaction parameters. To check the effect of acid concentration on the reaction, 1-5 mL of 1 mol/L H2SO4 was added to the fixed concentration of SMT and KMnO4, and it was observed that there was absolutely no change in the absorbance. The effect of hydrochloric acid was not studied since KMnO4 being a strong oxidizing agent would react with HCl to liberate chlorine. The reaction between SMT and KMnO4 in acetic acid medium was complete in 10 min (Figure 6), and the absorbance of the measured unreacted KMnO4 was found to be stable up to 40 min thereafter. Two blanks were prepared for the study. The reagent blank consisted of acid and permanganate showed maximum absorbance (equal to the intercept). A second blank in the absence of SMT and KMnO4 had negligible absorbance, and hence measurements were made against a water blank.

 

 

 

 

 

 

Potassium permanganate quantitatively oxidizes SMT in the presence of NaOH in method B, resulting in the formation of a bluish-green color manganate ion (Mann and Sounders, 1974) which showed an absorption peak at 610 nm (Figure 7) and served as the basis for the calibration graph (Figure 3). Increase in the concentration of KMnO4 could enhance sensitivity of the method but the blank absorbance also increased concomitantly. The effect of KMnO4 concentration on the sensitivity of the reaction (Figure 8) was ascertained, and based on this the optimum concentration was fixed at 6.3278 x 10-4 mol/L. Order of addition of NaOH is critical. When NaOH was added after the addition of KMnO4 to SMT, small brown particles with slightly greenish turbidity developed, possibly due to the formation of MnO2 in weak alkaline medium. One mL of 0.5 mol/L NaOH in the total volume of 10 mL was fixed because there was no appreciable effect on the reaction time and sensitivity when the volume of 0.5 mol/L NaOH was varied from 0.5-2.0 mL. The reaction was complete in 20 min where the contact time was not critical and any delay up to 40 min had no effect on the absorbance. The absorbance of the measured color was constant for 50 min in the presence of unreacted KMnO4 and the reaction product. In both the methods, the reaction rate was not studied at higher temperature since both the reactions reached completion within a reasonable time. The Job's method of continuous variation was applied to establish the stoichiometric ratio of SMT to KMnO4 in basic medium and was found to be 1: 4 (SMT:KMnO4) (Figure 9).

 

 

 

 

 

 

Analytical data

A linear correlation was found between absorbance at λmax and concentration of SMT in the ranges given in Table I. This correlation establishes an inverse relation between SMT and permanganate. This behavior was possible because the latter follows the Beer-Lambert's law. The inverse linear relationship in method A is described by the regression equation:

Y = a - bX

(Where Y = absorbance of 1-cm layer of solution; a = intercept; b = slope and X = concentration in mol/L). Regression analysis of the linear relation data using the method of least squares was performed to evaluate the slope (b), intercept (a) and correlation coefficient (r) for each system, and the values are presented in Table I. The optical characteristics such as range concentration limits, apparent molar absorptivity and Sandell sensitivity values of both methods are also given in Table I. The limits of detection (LOD) and quantification (LOQ) calculated according to ICH guidelines (1996) are also presented in Table I.

 

 

Method Validation

Assay precision and accuracy

The precision of the methods was calculated in terms of intermediate precision (intra-day and inter-day) (SHABIR, G.A, 2003). Three different concentrations of SMT were analyzed in seven replicates during the same day (intra-day precision) and for five consecutive days (inter-day precision). The RSD (%) values of intra-day and inter-day studies showed that the precision was good (Table III). The accuracy of an analytical method expresses the closeness between the reference value and the found value. Accuracy was evaluated as percentage relative error between the measured concentrations and concentrations taken for SMT (Bias %). The results obtained are compiled in Table II and show that the accuracy is good.

Method Selectivity

Selectivity was evaluated by recovery studies. A synthetic mixture consisting of 20 mg sodium alginate, 30 mg magnesium stearate, 20 mg lactose, 20 mg acacia, 50 mg talc and 30 mg starch besides 20 mg of SMT was prepared and analyzed after extraction into acetic acid in method A, and into chloroform in the case of method B, as described under analysis of tablets. The percent recovery of SMT was 98.64 ± 0.86 and 96.58 ± 0.63 for method A and method B, respectively. This confirms the selectivity of methods under the optimized conditions.

Placebo analysis

Placebo analysis was carried out in order to find the interference. A placebo blank consisting of 20 mg sodium alginate, 30 mg magnesium stearate, 20 mg lactose, 20 mg acacia, 50 mg talc and 30 mg starch but without SMT was prepared and analyzed as described under "procedure for tablets". There was absolutely no interference from the placebo in method A but huge interference was encountered in method B. The interference from placebo mixture in method B was successfully overcome by extraction of SMT into chloroform and by performing the analysis as described under tablets.

Application to analysis of pharmaceutical formulations

Method A does not suffer from interference from the tablet excipients and results in Table III show close agreement between the results obtained by the proposed methods and the label claim. Method B entails extraction of SMT into chloroform since there was some interference from the excipients when applied directly to the tablet extract in NaOH. The chloroform was later evaporated and residue was dissolved in NaOH where an appropriate working concentration of SMT was prepared and analyzed as given under assay procedure for tablets. The results were compared statistically by applying Student's t-test for accuracy and the variance ratio F-test for precision with results from the literature method (Arayne et al., 2007) at a 95% confidence level. The calculated t-test and F-values (Table III) did not exceed the tabulated values of 2.37 and 6.39, respectively, indicating no significant difference between the proposed methods and the reference method in terms of accuracy and precision. The validity of the methods was confirmed by applying the standard addition technique. Pre-analyzed tablet powder containing SMT was spiked with pure SMT at three concentration levels and the totals were found by the proposed methods. Each determination was done three times. The results of this study are compiled in Table IV.

 

CONCLUSIONS

Two simple, rapid, fairly accurate and precise, and sensitive spectrophotometric methods were developed for the determination of SMT in bulk drug and in tablets. The methods are free from rigid experimental conditions and are characterized by wide linear dynamic ranges and high sensitivity, and employ inexpensive and easily available chemicals. The low detection and quantification limits, simplicity and selectivity make the method suitable for quality control in the pharmaceutical industry for routine analysis. However, method B entails an extraction step when applied to tablets to overcome the interference from some inactive ingredients.

 

ACKNOWLEDGEMENT

Authors thank M/S. Jubiliant Organosis, Mysore, for providing the gift of pure simvastatin. Three of the authors (KT, NRP, KBV and SGH) thank the authorities of the University of Mysore, Mysore, for permission and facilities. Kalsang Tharpa also thanks the Department of Education, Central Tibetan Administration of His Holiness the Dalai Lama, for providing a research scholarship.

 

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Received for publication on 31st July 2008
Accepted for publication on 19th November 2009

 

 

* Correspondence: K. Basavaiah. Department of Chemistry, University of Mysore, Manasagangothri, Mysore-570006, India. Fax: 0091-821-2421263, 2516133). E-mail: basavaiahk@yahoo.co.in

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