Research Article | Open Access
K. Susmitha, M. Thirumalachary, T. Charan Singh, G. Venkateshwarlu, "Extractive Spectrophotometric Determination of Tenofovir Disoproxil Fumarate Using Acidic Triphenylmethane Dyes", International Scholarly Research Notices, vol. 2014, Article ID 856760, 6 pages, 2014. https://doi.org/10.1155/2014/856760
Extractive Spectrophotometric Determination of Tenofovir Disoproxil Fumarate Using Acidic Triphenylmethane Dyes
Tenofovir disoproxil fumarate is a nucleotide reverse transcriptase inhibitor that has activity against the hepatitis B and HIV viruses. Three simple and sensitive extractive spectrophotometric methods have been described for the assay of tenofovir disoproxil fumarate either in pure form or in pharmaceutical formulations. The developed methods involve formation of colored chloroform extractable ion-pair complexes of the drugs with triphenylmethane dyes, namely, bromothymol blue (BTB), bromophenol blue (BPB), and bromocresol purple (BCP) in acidic medium. The extracted complexes showed absorbance maxima between 410 and 415 nm. Beer’s law is obeyed in the concentration ranges 1.5–25, 1.0–25, and 1.25–25 μg mL−1 with BTB, BPB, and BCP, respectively. The effectc of concentration of dye, pH, and interference of excipients have been studied and optimized. The limits of detection and quantification have been determined. All three methods are validated as per the guidelines of ICH. The methods have been applied to the determination of drug in commercial tablets and results of analysis were validated statistically through recovery studies.
Tenofovir disoproxil fumarate (TDF) 9-[(R)-2-[[bis[(isopropoxycarbonyl)oxy]methoxy]phosphinyl]methoxy]propyl] adenine fumarate is antiviral agent acts as nucleoside reverse transcriptase enzyme inhibitor . It is a nucleoside analogue which is phosphorylated by host cell enzyme to give 5-triphosphate derivative. This moiety competes with the equivalent host cellular triphosphate for proviral DNA synthesis by viral reverse transcriptase which is viral RNA-dependent DNA polymerase. Incorporation of the 5-triphosphate moiety into the growing viral DNA chain results in chain termination. It is indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults [2, 3].
The literature survey revealed that only few methods are available for the determination of tenofovir in dosage forms and include liquid chromatography with tandem mass spectrometry [4, 5]; HPLC with solid phase extraction ; reversed phase HPLC [7, 8]; HPLC with spectrophotometric detection ; HPTLC ; gradient ion-pair LC with fluorescent detector ; and HPLC-UV, HPLC-MS , and first-order UV derivative spectrophotometry [13, 14]. Visible spectrophotometry, because of its simplicity, cost-effectiveness, sensitivity, selectivity, fair accuracy, and precision, has remained competitive in pharmaceutical analysis. In a method described by Onah and Ajima, tenofovir  was quantified by complexation with ammonium molybdate-stannous chloride having maximum absorption at 495 nm, and, with picric acid, it forms blue coloured complex that is absorbed maximally at 465 nm.
Because of its physiological significance, the quantitative determination of tenofovir attracted the attention of analytical chemists and almost all analytical methods have been applied to accomplish the purpose. However, methods based on spectrophotometric determination of this drug involving ion-pair complexes with common and versatile acidic dyes namely, bromothymol blue (BTB), bromocresol purple (BCP), and bromophenol blue (BPB) are not reported yet. This prompted the authors to develop extractive spectrophotometric methods for the determination of tenofovir using the above mentioned dyes.
In this paper, we report three simple and sensitive extractive spectrophotometric methods for the assay of tenofovir. The methods are based on ion-pair complexation of drug with dyestuffs such as BTB, BCP, and BPB and subsequent extraction into chloroform and to measure the absorbance of colour complex. The proposed methods have the advantages of speed and simplicity besides being accurate and precise and can be adopted by the pharmaceutical laboratories for industrial quantitative analysis.
2.1. Materials and Methods
Tenofovir disoproxil fumarate (TDF) is procured from Aurobindo Pharmaceuticals, Hyderabad, as a gift sample. The dyestuffs, namely, BTB, BPB, and BCP (AR grade) supplied by SD Fine Chemicals Ltd., Mumbai, are used without any further purification. The dyestuffs were used as 0.025% solutions in doubly distilled water.
Sodium acetate-hydrochloric acid buffers of pH 2.5 for BPB and BCP and 2.8 for BTB were prepared by mixing 50 mL of 1.0 M sodium acetate solution with 50.50, 49.50, respectively, of 1.0 M HCl solution and diluted to 250 mL with doubly distilled water. The pH of each solution was adjusted to an appropriate value with the aid of a pH meter. Chloroform (HPLC grade) supplied by SD Fine Chemicals Ltd., Mumbai, is used throughout the work. Stock solutions were prepared for all the dyes and drug (25 mg/100 mL).
The spectra (Figure 1) of ion-pair complexes have been recorded on SHIMADZU 140 double beam spectrophotometer, Thermo Nicolet 1000, and also on ELICO 159 UV-Visible single beam spectrophotometer using quartz cells of 10 mm path length. An Elico model Li-120 pH meter was used for pH measurement.
3. Results and Discussion
TDF forms ion-pair complexes in acidic buffer with dyestuffs, namely, bromothymol blue (BTB), bromophenol blue (BPB), and bromocresol purple (BCP), and these complexes are quantitatively extracted into chloroform. Ion-pair complexes of drug with BTB, BPB, and BCP are absorbed maximally between 410 and 415 nm. The reagent blank under similar conditions showed no absorption.
Tenofovir disoproxil fumarate undergoes protonation of adenine ring in acidic medium, while sulphonic acid group is present in BTB, BPB, and BCP that is the only group undergoing dissociation in the pH range 1–5. The color of such dyes is due to the opening of lactoid ring and subsequent formation of quinoid group. It is supposed that the two tautomers are present in equilibrium, but, due to strong acidic nature of the sulphonic acid group, the quinoid body must predominate. Finally, the protonated TDF forms ion-pairs with the dyestuffs which are quantitatively extracted into chloroform. The drug-dye ion-pair complex behaves as a single unit held together by an electrostatic force of attraction as shown in Scheme 1.
3.1. Calibration Curves
Different aliquots of drug solution were transferred into 125 mL separating funnel. To this 5 mL of buffer (pH 2.5, 2.8, and 2.5), 5 mL of dye was added and total volume was made up to 20 mL with water. 10 mL of chloroform was added and the contents were shaken for 5 min. The two layers were allowed to separate for 5 min. The organic layer was separated and absorbance of yellow colored solution which is stable at least for 3 hrs is measured between 410 and 415 nm against blank similarly prepared.
The same procedure of analysis is followed either for assay of pure drug or for dosage form. The calibration graphs (Figure 2) that are linear over the concentration ranges are within the permissible range. The optical characteristics and statistical data for the regression equation of the proposed methods are presented in Table 1.
3.2. Procedure for the Assay of Pure Drug
Four different solutions of pure drug in the range of calibration curve were selected and the recovery experiments were performed. The recoveries and their relative standard deviations are tabulated in Table 2 for five replicates.
3.3. Procedure for the Assay of Dosage Forms
2 Tablets of VIREAD 150 mg are powdered and dissolved in doubly distilled water, stirred thoroughly, and filtered through a Whatman number 42 filter paper. This solution was transferred into 100 mL standard volumetric flask and diluted with doubly distilled water as required. Different solutions of drug in the range of calibration curve were chosen and the assay was estimated using the calibration curve. The results of the recovery experiments are tabulated in Table 3.
In order to establish molar ratio between TDF and dyestuffs used, the Job’s method of continuous variation [16, 17] has been applied. In this method, solutions of drug and dyestuff with identical molar concentrations ( M) were mixed in varying volume ratios in such a way that the total volume of each mixture was the same. The absorbance of each solution was measured and plotted against the mole fraction of the drug, (drug)/(drug) + (dyestuff) (Figure 3). This measurement showed that 1 : 1 complex was formed with each dyestuff. The formation constants [18, 19] were also estimated and found to be , , and M−1 for complexes with BTB, BPB, and BCP, respectively.
The influence of pH on the ion-pair formation of Tenofovir disoproxil fumarate with various dyestuffs has been studied using sodium acetate-hydrochloric acid buffer. The results are shown in Figure 4. It is evident that absorbance of complexes with BTB, BPB, and BCP was found to be constant within the pH ranges 2.2–3.3 (BTB), 2.0-3.0 (BPB, BCP), respectively. Thus, all the absorbance measurements were made at pH 2.8, 2.5, and 2.5 with BTB, BPB, and BCP, respectively.
The effect of dyestuff concentrations was also studied by adding different volumes of dyestuff to a constant amount of TDF (15.0 μg mL−1). It is apparent from Figure 5 that the maximum absorbance in each case was found with 2.0 mL of dyestuff, beyond which absorbance was constant. Thus, 5 mL of each dyestuff was used for ion-pair formation throughout the experiment.
A systematic study of the effect of foreign species present along with TDF at 15.0 μg mL−1 levels was undertaken. This study was carried out by following the proposed procedures for a 10 mL sample system, by adding a known amount of foreign species to TDF solution of 15.0 μg mL−1 summarizes the results obtained. However, the drug content from the powdered tablets was extracted into chloroform, which completely removes any interference by the common excipients found in formulations.
4. Validation of the Proposed Methods
All the three proposed methods have been validated in terms of guideline proposed by ICH , namely, selectivity, specificity, accuracy, precision, limits of calibration curve, LOD, LOQ, robustness, ruggedness, and regression equation. The student -test and variance -test have been performed in comparison with a reference method. (Table 1) summarizes the values for Beer’s law limits, molar absorptivity, regression equation, correlation coefficients, relative standard deviation, and recoveries. To test the reproducibility of the proposed methods, six replicate determinations of 15 μg mL−1 of studied TDF are made. The coefficient of variation was found to be less than 1.0% for all the procedures.
The proposed methods have been successfully applied to the determination of TDF in pharmaceutical preparations. The performance order of the proposed methods is BCP > BTB > BPB. The results obtained and shown in (Tables 2 and 3) were compared to those obtained by a reference method  by means of -test at 95% confidence level. In all cases, the average results obtained by proposed methods and reference method were statistically identical, as the difference between average values had no significance at 95% confidence level.
The proposed methods are simple, sensitive, and reproducible and can be used for routine analysis of tenofovir in pure form and in formulation.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors are thankful to the Principal and Head, Department of Chemistry, Nizam College, and to the authorities of Jawaharlal Nehru Technology University, Hyderabad, for providing laboratory facilities.
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