Abstract
A simple, sensitive, precise, specific and stability indicating high-performance thin-layer chromatographic (HPTLC) method for the determination of emtricitabine both in bulk drug and pharmaceutical dosage form was developed and validated. The method employed aluminium plates precoated with silica gel G60 F254 as the stationary phase. The solvent system consisted of tolueneโ:โethyl acetateโ:โmethanol (2โ:โ8โ:โ1, v/v/v). This solvent system was found to give compact spots for emtricitabine with value . Densitometric analysis of emtricitabine was carried out in the absorbance mode at 284โnm. Linear regression analysis showed good linearity with respect to peak area in the concentration range of 30โ110โngโspotโ1. The method was validated for precision, limit of detection (LOD), limit of quantitation (LOQ), robustness, accuracy and specificity. Emtricitabine was subjected to acid and alkali hydrolysis, oxidation, neutral hydrolysis, photodegradation and dry heat treatment. Also the degraded products peaks were well resolved from the pure drug with significantly different values. Statistical analysis proved that the method is repeatable and specific for the estimation of the said drug. As the method could effectively separate the drugs from their degradation products, it can be employed as a stability indicating method.
1. Introduction
Emtricitabine is chemically known as 4-amino-5-fluoro-1-[(2R, 5S)-2-(hydroxymethyl)-1, 3-oxathiolan-5-yl] pyrimidin-2-one [1]. The chemical structure of emtricitabine is shown in Figure 1. Emtricitabine, a nucleoside reverse transcriptase inhibitor, is phosphorylated by cellular enzymes to emtricitabine 5โฒ-triphosphate, which, in turn, inhibits the activity of HIV-1 (HIV) reverse transcriptase by competing with the endogenous substrate. Incorporation of the triphosphate into the viral DNA causes chain termination, thereby inhibiting viral replication [2]. Quantification of emtricitabine has been performed in the past using UV spectrophotometry [3โ5], HPLC coupled with UV or fluorometric detection [6โ11], HPTLC [12], and LC/MS/MS [13, 14] either alone or in combination with other drugs.
To our knowledge, no article related to the stability indicating high-performance thin-layer chromatographic (HPTLC) determination of emtricitabine in pharmaceutical dosage forms has been reported in the literature. The international conference on harmonization (ICH) guideline entitled Stability Testing of New Drug Substances and Products requires the testing to be carried out to elucidate the inherent stability characteristics of the active substance [15].
Nowadays HPTLC is becoming a routine analysis technique due to advantages of low operating cost, high sample throughput, and need for minimum sample cleanup. The major advantage of HPTLC is that several samples can be run simultaneously using a small quantity of mobile phase unlike HPLC, thus lowering analysis time and cost per analysis [16, 17].
The aim of the present work was to develop an economic, precise, accurate, specific, and stability-indicating HPTLC method using densitometric detection for the determination of emtricitabine in the presence of its degradation products, either in bulk form or in pharmaceutical dosage form as per ICH guidelines [15, 18].
2. Experimental
2.1. Materials
Pharmaceutical grade of emtricitabine (batch no. EM0030606) was kindly supplied as a gift sample by Matrix Laboratories, Hyderabad, India, used without further purification, and certified to contain 99.57% (w/w) on dried basis. Pharmaceutical dosage form (Emtriva Capsules 200โmg; Batch no. 29832AF21) was procured as a gift sample from Gilead Sciences Inc, USA. All chemicals and reagents used were of analytical grade and were purchased from Merck Chemicals, Mumbai, India.
2.2. HPTLC Instrumentation and Chromatographic Conditions
The HPTLC plates were prewashed with methanol and activated at 110ยฐC for 5โmin prior to chromatography. The samples were spotted in the form of bands 6โmm width with a Camag 100 microlitre sample syringe (Hamilton, Bonaduz, Switzerland) on silica gel precoated HPTLC aluminum plate G60 F254, [(โcm) with 250โฮผm thickness; E. Merck, Darmstadt, Germany, supplied by Anchrom Technologists, Mumbai] using a Camag Linomat IV applicator (Switzerland). A constant application rate of 0.1โฮผLโsโ1 was used and the space between two bands was 6โmm. Linear ascending development was carried out in 20โcmโรโ10โcm twin trough glass chamber (Camag, Muttenz, Switzerland) saturated with the mobile phase. The mobile phase was consisted of tolueneโ:โethyl acetateโ:โmethanol (2โ:โ8โ:โ1, v/v/v) and 20โmL were used per chromatography run. The optimized chamber saturation time for mobile phase was 30โmin using saturation pads at room temperature (). The length of chromatogram run was 8โcm. Densitometric scanning was performed using a Camag TLC scanner III in the reflectance-absorbance mode and operated by CATS software (V 3.15, Camag). The slit dimension was kept at 5โmmโรโ0.45โmm and the scanning speed was 10โmmโsโ1. The source of radiation used was a deuterium lamp emitting a continuous UV spectrum between 190 and 400โnm. All determinations were performed at ambient temperature with a detection wavelength of 284โnm. Concentrations of the compound chromatographed were determined from the intensity of the diffused light. Evaluation was by peak areas with linear regression.
2.3. Preparation of Standard Solution
Accurately weighed 100โmg of emtricitabine was transferred to a 100โmL volumetric flask and dissolved in and diluted up to the mark with methanol to obtain a standard solution of emtricitabine (1000โฮผgโmLโ1). This solution was further diluted with methanol to obtain working standard solutions of emtricitabine in concentration range of 30โ110โฮผgโmLโ1.
2.4. Method Validation
The HPTLC method was validated as per the ICH guidelines [18].
2.4.1. Linearity and Range
One microlitre from each working standard solution was spotted on the HPTLC plate to obtain final concentration range of 30โ110โngโspotโ1. Each concentration was spotted six times on the HPTLC plate. The plate was developed using the previously described mobile phase and scanned. The peak areas were plotted against the corresponding concentrations to obtain the calibration graph. Linear calibration curve was generated using least-squares linear-regression analysis. Residual analysis was performed to ascertain linearity.
2.4.2. Precision
Precision of the method was verified by repeatability and intermediate precision studies. Repeatability studies were performed by analyses of three different concentrations (70, 90, 110โngโspotโ1) of the drug in hexaplicate on the same day. Intermediate precision of the method was checked by repeating studies on different days.
2.4.3. Limit of Detection and Limit of Quantitation
In order to estimate the limit of detection (LOD) and limit of quantitation (LOQ), blank methanol was spotted following the same method. The signal-to-noise ratio was determined. An LOD was considered as 3โ:โ1 and LOQ as 10โ:โ1. The LOD and LOQ were experimentally verified by diluting known concentrations of standard solution of emtricitabine until the average responses were approximately 3 or 10 times the standard deviation of the responses for six replicate determinations.
2.4.4. Robustness of the Method
By introducing small changes in the mobile-phase composition (ยฑ0.1โmL for each component), the effects on the results were examined. Mobile phases having different composition like tolueneโ:โethyl acetateโ:โmethanol (2.1โ:โ8.0โ:โ1.0 v/v/v), (2.0โ:โ8.1โ:โ1.0 v/v/v), and (2.0โ:โ8.0โ:โ1.1 v/v/v) were tried, and chromatograms were run. Amount of mobile phase was varied by ยฑ5%. Time from spotting to chromatography and from chromatography to scanning was varied by +10โmin. Robustness of the method was done at three different concentration levels 70, 90, 110โngโspotโ1 for emtricitabine.
2.4.5. Accuracy
Accuracy of the method was determined by standard addition method in which the known amount of standard emtricitabine solutions were added to preanalyzed capsule solution. These amounts corresponded to 50, 100, and 150% of the amounts claimed on the label. The amounts of emtricitabine were estimated by applying these values to the regression equation of the calibration curve. Accuracy study was performed for six times, and % recovery of emtricitabine was calculated.
2.4.6. Specificity
Specificity of the method was by means of complete separation of pure drug from the degradation products. Peak purity of emtricitabine and degradation products was assessed by comparing their respective spectra at peak start (S), peak apex (M), and peak end (E) position of the spots.
2.4.7. Solution Stability
The stability of standard solutions was tested after 0, 6, 12, 24, 48, and 72โh of storage. The stability of the solutions was determined by comparing peak area percentage and peak purity at 1000โngโspotโ1.
2.5. Analysis of Marketed Pharmaceutical Dosage Form
To determine the content of emtricitabine in marketed pharmaceutical dosage form (Emtriva Capsules 200โmg; Batch no. 29832AF21), powder of twenty capsules was weighed. An accurate weight of the powder equivalent to 200โmg emtricitabine was weighed and transferred into a 100โmL volumetric flask containing 50โmL methanol, sonicated for 30โmin, and diluted to 100โmL with methanol. The resulting solution was centrifuged at 4000โrpm for 5โmin, and supernatant was analyzed for drug content. 1โmL of the above supernatant solution was transferred into 20โmL volumetric flask and diluted to volume with methanol. The concentration achieved after the above dilution was 100โฮผgโmLโ1. 1โฮผL volume was spotted for six times to achieve a final concentration of 100โngโspotโ1. The plate was developed in the previously described chromatographic conditions. The possibility of excipient interference in the analysis was studied.
2.6. Forced Degradation Studies
Decomposition studies were performed in solutions containing emtricitabine at a concentration of 1000โฮผgโmLโ1. Samples were withdrawn at suitable time intervals and subjected to HPTLC analysis. The drug was subjected under different stress conditions as follows.
2.6.1. Acid-Induced Degradation
To 10โmL of methanolic stock solution 10โmL of 0.1โN HCl was added. This mixture was refluxed at 80ยฐC.
2.6.2. Base-Induced Degradation
To 10โmL of methanolic stock solution 10โmL of 0.01โN NaOH was added, and the solution was refluxed at 80ยฐC.
2.6.3. Oxidative Degradation
To 10โmL of methanolic stock solution 10โmL each of hydrogen peroxide 6% (v/v) and 3% (v/v) was added separately. The solution was kept at room temperature and then heated in boiling water bath for 10โmin to completely remove the excess of hydrogen peroxide.
2.6.4. Wet Heat Degradation
Studies under neutral conditions were performed by dissolving the drug substance in distilled water, and solution was refluxed at 80ยฐC for 5 days.
2.6.5. Dry Heat Degradation
For dry heat degradation, the standard drug was placed in an oven at 80ยฐC for 12 days.
2.6.6. Photochemical Degradation
The photochemical stability of the drug was studied by exposing the solution to direct sunlight for 5 days (~40โh) kept on a terrace.
3. Results and Discussion
3.1. Selection of Analytical Wavelength
Stock solution of emtricitabine was prepared in methanol. UV spectrum of 10โฮผgโmLโ1 concentration of emtricitabine showed absorbance of less than 1, and two maxima were obtained at 242 and 282โnm (Figure 2). Further, in situ HPTLC spectrum of emtricitabine was taken. ฮปmax was found to be 284โnm and was selected as scanning wavelength (Figure 3).
3.2. Optimization of the Chromatographic Conditions
The HPTLC procedure was optimized with a view to develop stability-indicating assay method. Both the pure drug and degraded drug solutions were spotted on HPTLC plates and run in different solvent systems. Initially, ethyl acetate and methanol were tried in different ratio. Ethyl acetate and methanol in the ratio of 9โ:โ1.5 v/v was selected, and was found to be 0.51, but in the subsequent run while performing the forced degradation studies, it was found that the degradation peak was eluted out. So, the toluene was added to bring down the of degradation peak. Finally, toluene, ethyl acetate, and methanol were tried in different ratio. The optimum mobile phase was found to be consisted of tolueneโ:โethyl acetateโ:โmethanol (2โ:โ8โ:โ1 v/v/v). The drug in presence of their degradation products was satisfactorily resolved with value at (Figure 4). In order to reduce the neckless effect, the TLC chamber was saturated for 30โmin using saturation pads. The mobile phase was run upto distance of 8โcm, which takes approximately 30โmin for development of HPTLC plate.
3.3. Validation of the Method
3.3.1. Linearity and Range
Linear relationship was observed by plotting drug concentration against peak areas. Emtricitabine showed linear response in the concentration range of 30โ110โngโspotโ1. The corresponding linear regression equation was with square of correlation coefficient (r2) of 0.9997 for emtricitabine. Residual analysis was performed to ascertain linearity (Figure 5). Slope was significantly different from zero (Table 1).
3.3.2. Precision
The results of the repeatability and intermediate precision experiments are shown in Table 2. The developed method was found to be precise as the RSD% values for repeatability and intermediate precision studies were <2%, respectively.
3.3.3. Limit of Detection and Limit of Quantitation
The signalโ:โnoise ratios of 3โ:โ1 and 10โ:โ1 were considered as LOD and LOQ respectively. The LOD and LOQ were found to be 10โngโspotโ1 and 30โngโspotโ1 respectively.
3.3.4. Robustness of the Method
The standard deviation of peak areas was calculated for each parameter, and RSD% was found to be less than 2%. The low values of RSD% as shown in Table 3. indicated robustness of the method.
3.3.5. Accuracy
As shown from the data in Table 4. good recovery % of the drug in the range from 99.84 to 101.46% was obtained at various added concentrations.
3.3.6. Specificity
The peak purity for standard emtricitabine was assessed by comparing spectra acquired at the start (S), apex (M), and end (E) of the peak obtained from the scanning of spot, that is, and . Spots obtained of degradation products were well resolved from the active ingredient. Peak purity of spots of emtricitabine resolved during stability study was assessed by comparing the respective spectra at peak start, peak middle, and peak end, that is, and . The peak purity data indicated that peaks of emtricitabine resolved after application of stress conditions were pure (Table 6).
The data of summary of validation parameters are listed in Table 5.
3.4. Solution Stability
There was no indication of degradation in sample solutions of emtricitabine as revealed by peak purity data and from the value of RSD% (<2%) for peak areas of bands of solution stored at different times. The solution was found to be stable at ambient temperature for 72โh, and no unknown peaks were observed.
3.5. Analysis of Marketed Pharmaceutical Dosage Form
A single spot at value of 0.26 was observed in the chromatogram of the drug samples extracted from capsules. There was no interference from the excipients that are commonly present in the formulations. The drug content was found to be 99.87% ยฑ 0.56 with a RSD% of 0.56 for six replicate determinations. It may, therefore, be inferred that degradation of emtricitabine had not occurred in the marketed formulations that were analyzed by this method. The good performance of the method indicated the suitability of this method for routine analysis of emtricitabine in pharmaceutical dosage form.
3.6. Forced Degradation Studies
Stress testing of emtricitabine under different conditions using tolueneโ:โethyl acetateโ:โmethanol (2โ:โ8โ:โ1 v/v/v) as the mobile solvent system suggested the following degradation behaviour.
3.6.1. Acid-Induced Degradation
The rate of degradation in acid was slower as compared to that of alkali. Initially 0.1โN HCl was used at 80ยฐC for 8โh, but more than 80% degradation was observed hence the duration of reaction with acid decreased to 3โh to obtain a reasonable degradation between 20โ30%. The degradation peaks were observed at 0.03, 0.09 and 0.75 (Figure 6).
3.6.2. Base-Induced Degradation
The drug was found to be highly labile to alkaline degradation. The reaction in 0.1โN NaOH at 80ยฐC was so fast that around 80% of the drug was degraded in 1โh. Subsequently, studies were performed by reducing the alkali strength to 0.01โN NaOH. Drug showed degradation around 30% within 3.5โh at 80ยฐC associated with rise in a two major and one minor degradation peaks at 0.03, 0.71, and 0.07, respectively (Figure 7).
3.6.3. Oxidative Degradation
The drug was found to be highly labile under oxidative conditions. Reaction in 6% peroxide at room temperature shown complete degradation in 1โh. Hence drug was exposed to 3% hydrogen peroxide for 8โh at room temperature. The degradation peaks were observed at 0.07 and 0.43 (Figure 8).
3.6.4. Wet Heat Degradation
The drug was found to be stable when refluxed with water at 80ยฐC for 12โh. No significant degradation was observed, reflux time was then increased for 5 days. No degradation peaks were observed.
3.6.5. Dry Heat Degradation
Drug was found to be stable when subjected to thermal degradation at 80ยฐC for 12 days. No degradation peaks were observed.
3.6.6. Photochemical Degradation
Emtricitabine was found to be stable to photochemical degradation as no degradation peaks were observed after exposing drug to sunlight for 5 days.
Degradation products obtained under different stress conditions are summarized in Table 6.
4. Conclusion
The developed HPTLC technique is precise, specific, accurate, and stability indicating. Statistical analysis proves that the method is repeatable and selective for the analysis of emtricitabine as bulk drug and in pharmaceutical dosage form. As the method separates the drug from its degradation products, it can be employed as a stability-indicating one. The proposed HPTLC method reduces the duration of analysis and is suitable for routine determination of emtricitabine in pharmaceutical formulation in quality-control laboratories, where economy and time are essential. This study is a typical example of development of a stability-indicating assay, established following the recommendations of ICH guidelines.
Acknowledgments
The authors thank Matrix Laboratories, Hyderabad, India, for providing gift sample of standard emtricitabine and AICTE, New Delhi, for financial support of the project. The authors declare no conflict of interests for competing financial gain.