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Journal of the Chilean Chemical Society

versión On-line ISSN 0717-9707

J. Chil. Chem. Soc. vol.57 no.2 Concepción  2012

http://dx.doi.org/10.4067/S0717-97072012000200010 

J. Chil. Chem. Soc., 57, N° 2 (2012), págs: 1104-1108.

 

EXTRACTIVE SPECTROPHOTOMETRIC DETERMINATION OF KETOCONAZOLE, CLOTRIMAZOLE AND FLUCONAZOLE BY ION-PAIR COMPLEX FORMATION WITH BROMOTHYMOL BLUE AND PICRIC ACID

 

*NINA ALIZADEH, ZAHRA REZAKHANI

*Department of Chemistry, University of Guilan, Namjoo Street, Rasht, P.B. 41335-1914, Iran. e-mail address: nializadeh@yahoo.com


ABSTRACT

The reactions of picric acid and bromothymol blue with three important antifungal drugs containing an imidazole ring ketoconazole (KC) and clotrimazole (CT) and fluconazole (FC) have been studied for the development of simple, rapid, sensitive an extractive-spectrophotometric method for determining the concentration of these drugs. This method is based on the formation of yellow ion-pair complexes between the basic nitrogen of the drug and sulphonphthalein acid dyes, namely; bromothymol blue (BTB) in phosphate buffer of pH =3 and picric acid (PA) in citrate buffer of pH=2.5. The formed complexes were extracted with chloroform and measured at 410 and 415nm for KC, at 410 and 413nm for CT and at 373 and 415nm for FC using PA and BTB, respectively. The analytical parameters and their effects on the reported systems are investigated. Beer's law was obeyed in the range 1-60 , 1-58 and 3-60 μg/ mL with PA and 3-55, 2-50 and 5-55 μg/ mL with BTB for CT, KC and FC, respectively. The composition of the ion pairs was found 1:1 by mole ratio and job0 s method in all cases. The proposed methods have been applied successfully for the analysis of the studied drugs in pure forms and pharmaceutical formulations.The results are in good agreement with those obtained by official methods.

Keywords: Ketoconazole; Clotrimazole; Fluconazole ; Bromothymol blue; Picric acid; Spectrophotometry.


 

INTRODUCTION

Ketoconazole (KC), cis-1-acetyl-4-[4-2-(2,4-dichlorophenyl)-2-(1H-imidazole-1-yl methyl)-1,3-dioxolan-4-yl] methoxy piperazine(I), is widely used as a typical antifungal drug in the treatment of tinea infections [1]. KC is a potent inhibitor of cytochrome P-450-dependent steroid hydroxylation in the adrenals [2]. In addition, KC enhances microsomal epoxid hydrolase activity with some epoxide substrates [3].

Clotrimazole (CT), 1-[(2-chlorophenyl) diphenyl methyl]-1H-imidazole(II), is an imidazole antifungal agent with similar action and activity to KC [4]. Most clinical studies indicate that systemic CT has little efficacy and considerable toxicity compared to other systemic imidazoles (miconazole and KC) [4]. Fluconazole(FC), [2-(2,4-difluorophenyl)-1,3-bis(1H-1,2, 4-triazol-1-yl) propan-2-ol](III), is an orally active antifungal agent, which is used in the treatment of superficial and systemic candidiasis and cryptococcal infections in patients with the acquired immunodeficiency syndromes (AIDS). It acts by blocking the synthesis of ergosterol, an essential component of the fungal cell membrane. Thus, due to the vital importance of determination of these drugs in pharmaceutical preparations and biological fluids, several spectroscopic[5-12]. high per- formance liquid chromatographic[13-/17] and electrochemical [18/23] methods for assay of KC and also, various methods such as derivative spectrophotometry [24-25],colorimetry [5-6-26-27], HPLC[28-/30], electrochemistry[18] and differential scanning calorimetry (DSC) [31] have been reported for the determination of CT in the literature. The official method normally involves titration in non-aqueous solvent[32-33]. To the best of our knowledge, despite the important ionassociation complex formation and extractive spectrophotometric methods, there are no previous reports based on the reaction of KC and CT and fluconazole with picric acid (PA) and reaction this drugs with bromothymol blue (BTB) as ion pairing reagents.

In the present investigation, we report that the development of accurate, reproducible, less time consuming and adequately sensitive three extractive-spectrophotometric methods based on the formation of ion-pair complexes between KC,CT and FC with anionic dye namely bromothymol blue (BTB) and picric acid (PA) in acidic buffer compared with other reported methods. The compositions of the complexes formed in proposed method have been established and after optimizing various analytical parameters, the obtained results were compared with those of official methods.

EXPERIMENTAL

Materials and Reagents

All chemicals used in this study were of highest purity available (Merck) and used without further purification. Doubly distilled deionized water was used throughout. The picric acid and bromothymol blue solution were freshly prepared and standardized Reagent grade KC and its 200 mg tablet as well as 2% cream samples and reagent grade CT, 100 mg vaginal tablet, 1% cream. were obtained from Behvazan Pharmaceutical Company (Rasht Iran) and standardized. capsules containing fluconazole containing100 mg and 200 mg of the drug were obtained from Loghman Darou (Tehran Iran).

A working standard solution of 100 μg/ mL ketoconazole or clotrimazole or fluconazole was prepared by dissolving 50 mg of pure drug in 50 ml of water containing few drops of hydrocholoric acid (about 0.04 M for KC and 2M for CT and FC) followed by further diluting of 5 ml of this solution to 50 ml.

Apparatus

A Shimadzu 2100 UV-Vis spectrophotometer with matched quartz cells of 1 cm path length, was used for all spectral measurements. The pH values were determined with a model 825 metrohm using a combined electrod.

General procedure

Aliquots (1mL, 100 μg/ mL) of standard KC, CT and FC solution were transferred into a series of 25 mL separating funnels containing 3 mL of 0.1% w/v picric acid (or BTB) and 1 mL of citrate buffer of pH 2.5 (or phosphate buffer of pH 3) were added. Then, 5 ml chloroform were added and the solution was shaken for 10 min.The solution was allowed to stand for clear separation of the two phases. The formed complexes were extracted with chloroform and measured at 410 and 415 nm for KC, at 410 and 413 nm for CT and at 373 and 415nm for FC using PA and BTB, respectively.

Blood serum sample

0.25 mL of a 0.5 mol/L FC solution was added into 0.5 mL of a blood serum samole. The volume of the mixture was made to 5 mL in a calibrating volumetric flask and the general procedure of the proposed method was followed.

Tablet sample solution

Five capsules of fluconazole were weighed accurately and their contents were mixed and powdered thoroughly and Ten tablets of each drug (CT and KC) after determining the average weight were powdered. Powder of each drug equivalent to 25 mg was accurately weighed and shaken with water containing a few drops of HCl (2M for CT, FC and 0.04 M for KC) and the volume was filled up to 50 ml in a volumetric flask, then, the recommended procedures for the determination of KC and CT were followed.The method of standard addition was used for the accurate determination of the ketoconazole and clotrimazole and fluconazole contents.

Cream sample solution

An accurately weighed portion of the cream or typical solution samples equivalent to 25 mg of the drug was shaken and gently heated in ethanol until they were completely dissolved and then filtered. The resulting clear solution was diluted to 50 ml with ethanol and recommended procedure was followed. The standard addition method was also employed for the accurate determination of the drug contents.

RESULTS AND DISCUSSION

Ion-pair complex extractive-spectrophotometry has been frequently used for the quantitative analysis of many pharmaceutical compounds [34]. In this study, we used PA and BTB as a suitable anionic dye, to form an intense yellow color ion-pair complex with KC and CT and FC, in acidic pH, which is soluble in chloroform and can be measured at at 410 and 415nm for KC, at 410 and 413 nm for CT and at 373 and 415 nm for FC using PA and BTB, respectively.

Absorption spectra of 2.5x 10-5 mol.L-1 of drugs (CT, KC and FC ) and PA ion-pair complexes in chloroform are shown in Fig. 1 with a maximum absorbance at 410 nm for CT, KC and 373 nm for FC with PA.The colorless blanks have practically negligible absorbance. Absorption spectra of 2.5x 10-5 mol.L-1 of drugs (CT, KC and FC) and BTB ion pair complexes in chloroform are shown in Fig.2








Such pronounced spectral changes are presumably due to the occurrence of both charge-transfer and proton-transfer during the formation of the resulting molecular complex, as pointed out previously[36,38].

The absorbance vs. bromothymol blue or picric acid /drug mole ratio plot obtained at 410 nm for CT, KC and 373 nm for FC with PA (Fig.3) at 413 nm for CT, 415 nm for KC and FC with bromothymol blue is shown in Fig. 4. The resulting mole ratio plots show a distinct inflection point at a dye-to-drug mole ratio of about 1, emphasizing the formation of a relatively strong 1:1 molecular complex in solution. The 1:1 stoichiometry was further supported by the method of continuous variations.



Optimization of conditions

The optimum conditions for quantitative estimation of the associated ion-pair formed were established via a number of preliminary experiments. The effect of pH for the quantitative extraction of KC, CT and FC with PA in chloroform was studied over the range 1-5, as it was established by using a proper citrate buffer. The resulting data at higher pH values show that the extent of ion-pair extraction decreases drastically, most probably due to the decreased amount of protonated form of drugs. At pH below 1-5, ion-pair extraction decrease . Thus, pH 2.5 was chosen for further studies. The optimum pH value for the quantitative extraction of of KC, CT and FC with bromothymol blue in chloroform was studied over the pH range of 2.5-7.0. According to the results a pH below 4.5 is recommended. At higher pH values, the fluconazole existed mainly in its neutral form (pKa=2.03) [37]. and the extent of ion pairing between anionic bromothymol blue and cationic fluconazole decreased, thus decreasing the color developed in chloroform phase. A pH value of 3.0 was used for further studies.

In preliminary experiments, a number of immiscible organic solvents were examined in order to provide an applicable extraction procedure. Chloroform was found to be the most suitable extractant as it was observed that a single extraction was adequate to achieve a quantitative recovery of the complex. Despite the higher molar absorptivity of the complexes in methylene chloride, chloroform was preferred for its selective extraction of the drug-dye complex from the aqueous phase, mainly due to the lower volatility in comparison with methylene chloride. It is important to mentioned that the colored ion-pair complex in the chloroform phase is quite stable for several days. There was no appreciable change in the absorbance or colour of the product if the order of addition of the reactants is varied.

Moreover, the optimum volume of citrate buffer at pH =2.5 and volume of phosphate buffer at pH =3 was investigated and 1 mL of citrate and phosphate buffer was used for further studies.

The influence of the volume of picric acid (0.1% w/v) solution and bromothymol blue solution on the extraction of CT, KC and FC was studied, as well. The absorbance of drug-picric acid complex and drug-bromothymol blue complexes in the organic phase increases with increasing amount of picric acid and bromothymol blue in the aqueous phase. Maximum extraction occurs when the volume of reagent added is 3 ml. A further excess of the reagent has no considerable effect on the fraction of the complex extracted.

The optimum volume of the organic phase and the number of extractions required were also studied. Maximum absorbance values were obtained by using 5 ml of chloroform during a single stage extraction. In addition, the extraction of drug with dye under the conditions recommended was found to be rapid. A shaking time of 8-10 min is sufficient for the complete extraction of the resulting 1:1 ion pair complexes. Absorbances of the separated extracts were stable for more than 1 h. The blanks did not absorb at λmax..

Linearity of calibration graphs

After the optimization of all the variables, the calibration graphs were constructed for the three drugs by plotting absorbance versus concentration in μg/mL. Beer's law was obeyed over the concentration range 1-58, 1-60 and 3-60 μg/mL for KC, CT and FC by using picric acid indicator and 3-55, 2-50 and 5-55 μg/ mL for KC, CT and FC by using bromothymol blue. Conformity with Beer0s law was evident in the concentration ranges shown in Table 1. Regression analysis of the Beer0s law plots at λmax. reveal a good correlation, (R2 = 0.981-0.995). Regression equations, intercepts, slopes and correlation coefficients for the calibration data are presented in Table 1. The following equations correspond to the linear ranges for KC and CT and FC with picric acid:

A= absorbance; C= drug concentration. The detection limit, calculated following the expression a+3S [35], where a=/intercept and S =/error standard deviation, was 1.32 , 0.¾ and 4.1 μg/mL for KC, CT and FC with picric acid and 1.02, 0.41 and 3.6 μg/mL for KC, CT and FC with bromothymol blue respectively.

Quantification, accuracy and precision

The validity of the proposed procedure for the determination of the studied drugs in their pure state and in their pharmaceutical formulations, was tested by analyzing these products using the proposed procedure and the official method [33]. The results obtained for pure drugs (Table 1) were reproducible with low relative standard deviations and the mean recoveries were comparable to these obtained using the official method (Table 2) for each of the studied drugs. The results of analysis obtained for pharmaceutical forms obtained by the proposed and the official methods are in good agreement.


Effects of interference

The effects of common excipients that often accompany the studied drugs in pharmaceutical dosage were tested for possible interference in the assay. An attractive feature of the procedure is its relative freedom from interference by the usual tablet diluents and excipients such as talc, sucrose, starch, gelatin, and magnesium stearate. Amounts far in excess of their normal occurrences in dosage forms were added, and no effects due to these excipients were noted in the experimental procedure. Moreover, no interference due to yhe degradation products of the studied drugs was observed.

Application to dosage forms

In order to establish the validity of the proposed analytical methods, the assay of KC, CT and FC in their formulations were carried out on proprietary drugs. The same samples were analyzed by the official non-aqueous potentiometric method (Table 2) [32,33]. The recovery experiments shown in Table 2 indicated a good agreement between the KC and CT and FC contents determined by the proposed and official methods as well as the declared amount of drug in the preparations used. This is indicative of non-interference of the other ingredients and the excipients, which are present in the formulations.

Recovery offluconazole from blood serum

In order to investigate the applicability of the proposed method to the determination of the fluconazole in biological fluids, it was applied to the recovery of the fluconazole from a blood serum sample. The recovery of the fluconazole using the proposed method and the standard addition technique[12] was found to be 84 % ± 4.

ACKNOWLEDGMENTS

Financial support from the Research Affairs of Guilan University is acknowledged. The authors are grateful to the Behvazan Pharmaceutical Company, ( Rasht industrial city, Iran) for the donation of pure drugs and its preparations.

 

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(Received: July 15, 2011 - Accepted: March 15, 2012).