Stability-indicating HPLC-DAD method for the determination of empagliflozin

Abstract

Background

A stability-indicating RP-HPLC method was developed and validated for the estimation of empagliflozin drug and its tablet dosage form using a DAD detector. The mobile phase consisted of methanol/acetonitrile/0.1%OPA (75:20:5). The peak was observed at 2.54 min using 222.0 nm absorption maxima.

Results

Calibration curve plot was found within the range of 10–50 µg/mL. The coefficient of determination (R²) was found to be 0.9990. Forced degradation studies were performed for the empagliflozin in various conditions, and the results were calculated as %RSD values and were found to be within the limits.

Conclusion

The method was validated as per ICH guidelines with respect to all validation parameters.

Background

Empagliflozin a new oral antidiabetic drug is a selective sodium–glucose transport protein 2 (SGLT2) inhibitor. The drug is given as a film-coated pill containing either 10 or 25 mg of empagliflozin as an active pharmaceutical ingredient. The drug was permitted by The United States Food and Drug Administration (USFDA) in 2014 [1].

The chemical name of empagliflozin is (1S)-1,5-anhydro-1-(4-chloro-3-{4-[(3S)-tetrahydrofuran-3-yloxy]benzyl}phenyl)-D-glucitol, also known as D-Glucitol,1,5-anhydro-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl]methyl]phenyl]-(1S), and structure is shown in Fig. 1.

Fig. 1

Structure of empagliflozin

It is a white to yellowish non-hygroscopic crystalline solid, very slightly soluble in water, slightly soluble in acetonitrile and ethanol, sparingly soluble in methanol, and practically insoluble in toluene [2]. Being sodium–glucose co-transporter 2(SGLT2) inhibitor in nature, it is probably the latest class of medicine in the treatment of T2DM. SGLT2 being glucose-lowering agents shows an insulin-independent mechanism which also proves their use in other treatments along with combination of other anti-diabetic agents for the treatment of T2DM. Additionally, it contributes to reduced hyperglycemia, assists weight loss, and reduces blood pressure [3, 4]. The physico-chemical parameters [5] are shown in Table 1.

Table 1 Critical physico-chemical parameters

Very few studies were done on the empagliflozin as a single drug assay (HPLC) [6,7,8]. Jaiswal et al. identified and quantified empagliflozin in the presence of four related impurities using HPLC [9]. Ayoub et al. gave pharmaceutical evaluation using LC–MS technique [10]. Various studies performed the HPLC method on different combinations of drugs with empagliflozin [11,12,13,14,15,16]. One HPTLC method was reported in combination of drugs [17]. However, the reported methods are not suitable for quick analysis as the retention time is quite high and the methods are incompatible for coupling with a mass detector. Moreover, no stability-indicating assay is reported to date. Thus, in the proposed work, stress studies and tablet analysis were performed using HPLC equipped with a DAD detector. Moreover, the proposed method is economic as less solvent will be consumed due to short running time.

Methods

Chemicals

Empagliflozin (99.91%) was received as a gift sample from Manus Aktteva Biopharma LLP, Ahmedabad, India. To assess the purity of the drug, melting point was determined which was found as per the literature. Thus, the drug was used without further purification. Methanol, acetonitrile and water of HPLC grade were obtained from Spectrochem Pvt. Ltd., Mumbai. Ortho-phosphoric acid was obtained from E. Merck India Ltd. Mumbai. Film-coated tablet formulations were purchased by a local pharmacy. All analytical grade chemicals were used throughout the analysis.

Equipment

Agilent HPLC 1260 Infinity II Quaternary Pump VL system with a DAD Detector was utilized. Separation was carried out on a particle size Poroshell 120 EC-C18, 4.6 × 100 mm, 4 µm column (at ambient temperature), and isocratic runs under RP-HPLC condition. The instrument was controlled by a PC with properly connected chromatographic software.

Chromatographic conditions

Using a gradient mode, fifty trials of HPLC methods using acetonitrile, water, methanol, and various buffers in different ratios were explored to optimize the separation of empagliflozin. The optimized mobile phase was prepared by mixing methanol/acetonitrile/0.1% OPA (75:20:5) that was filtered and degassed properly before use. The UV detection was carried at 222.0 nm (Fig. 2).

Fig. 2

UV spectrum of empagliflozin

The trials were introduced via a rheodyne injector. The entire determination was performed for 10 min. All the sample and mobile phase preparation were done regularly. The separation conditions are shown in Table 2.

Table 2 Optimized chromatographic conditions of empagliflozin

Method validation

Validation parameters consist of linearity, accuracy, precision, robustness, ruggedness, detection limit, quantification limit and stability studies. Relative standard deviation less than 2% was considered and acceptable [18].

Linearity

Accurately weighed 100 mg of drug is dissolved in 100-mL volumetric flask and then suitably diluted to give 1000 µg/mL stock solution. Aliquots of 0.1, 0.2, 0.3, 0.4 and 0.5 mL from stock solution were pipetted out in 10-mL volumetric flask and volume was made up to the mark with methanol to get the concentrations of 10, 20, 30, 40, 50 µg/mL, and their chromatogram was recorded at the optimized condition. The concluding concentration of the drug was in the series of 10–50 µg/mL. Peak area was recorded for the calibration curve construction. The value of coefficient of determination (R²) evaluated the calibration curve.

Accuracy

Standard addition method was used for the evaluation of accuracy, i.e., quantification of the recovery of analyte. To known drug solution, a certain amount of standard drug was added. The different 80%, 100% and 120% levels of drug were compared with standard values of drug obtained. Replicate analysis was done on this parameter.

Precision

The precision of the method was determined by obtained peak area of different replication of a fixed amount of the drug (10 µg/mL). It is resolute in terms of inter- and intra-day precision. Variations of inter-day and intra-day in the peak areas of drug concentration on three different days are calculated in terms of %RSD.

Robustness

Robustness of method was determined by making changes in flow rate, temperature, and wavelength. The percentage relative standard deviation noted for empagliflozin should be less than 2 according to ICH guidelines.

Repeatability

It was determined by multiple homogenous analyzing sample solution 10 µg/mL of empagliflozin into system and measured the peak area. It was repeated six times.

Detection limit and quantitation limit

The limit of detection (LOD) and the limit of quantitation (LOQ) were calculated by following formulas

• LOD = 3.3 SD/Slope

• LOQ = 10 SD/Slope

SD is the standard deviation of the y-intercept of the regression line.

Analysis of marketed formulations

Two tablets from peeled off ones were powdered. The powder representing 10 mg of empagliflozin was taken in a clean beaker. Approximately, 50 mL methanol was added to solubilize the analyte. Then, the solution was filtered using a Whatman filter paper in to a 100-mL volumetric flask to remove the excipients. The whole material from the beaker was transferred quantitatively to volumetric flask then made up the volume. The final solution of 100 μg/mL was made. From this stock solution, 1 mL solution was pipetted out and added to a 10-mL volumetric flask and volume made up with methanol. Solution so obtained was filtered through with 0.2-µm nylon membrane filter paper to get the final solution ready for HPLC instrument. Using a provided rheodyne injector, 20 μL of the sample was fed to the column. The instrument was allowed to run with already established solvent system and method followed. The value of the drug sample under the peak was calculated using the graph shown in Fig. 3.

Fig. 3

HPLC chromatogram of empagliflozin at 222.0 nm

Forced degradation studies

In these studies, we can interpret the acid, base, oxidation, thermal, photolytic degradation in the sample. Separation of degradation product from the pure active ingredient is studied by the obtained peak under stressed condition [9]. In acid degradation when the drug interacts with acid it produces primary degradation in the desirable range. For acid analysis HCl or H₂SO₄ (0.1–1 M) is widely used. In basic degradation when the drug interacts with base it produces primary degradation in the desirable range. For base analysis, NaOH or KOH (0.1–1 M) is widely used. In oxidative degradation hydrogen peroxide is widely used for oxidation degradation. Drug structure will allow selecting concentration and condition of oxidizing agent. In light stress, the empagliflozin was open to direct daylight for calculating degradation. The drug was used at different intervals and injected into a system for determining degradation of the drug. In thermal degradation according to ICH Q1A accelerated testing condition, thermal degradation should be carried out in dry heat or wet heat. Study may be conducted at high temperatures for a short period [19].

Results

Various chromatographic methods were tried to optimize the separation of empagliflozin. Mobile phase, retention time, flow rate and other optimized condition are shown in Table 2.The linear relationship was determined by plotting the calibration curve. The equation of regression line showed that R², m and C for empagliflozin were 0.9990, 8997.2, and 118,538, respectively. The RT for empagliflozin was 2.54 min. Separation of empagliflozin at 222.0 nm and calibration curve are shown in Figs. 3 and 4, respectively.

Fig. 4

Calibration curve of empagliflozin

In the optimized method, the range of linearity was observed in 10–50 µg/mL. The linearity was determined by the least square regression method, and the value of R² was 0.9990 as shown in Fig. 2. The recovery result determines the accuracy of the method and is shown in Table 3.

Table 3 Accuracy of empagliflozin

Precision results of the RP-HPLC method for empagliflozin are shown in Table 4.

Table 4 Precision data of the RP-HPLC method for empagliflozin

Robustness is determined by performing the analysis at slightly different flow rate, mobile phase, temperature and wavelength from optimized chromatographic condition. The results are given in Table 5.

Table 5 Robustness results at different temperature, flow rate and wavelength for empagliflozin

The limit of detection and limit of quantitation of empagliflozin were determined to be 0.05 and 0.1 µg/mL, respectively.

Analysis of marketed formulations

The developed method was validated and effectively applied to determine empagliflozin in different formulations. Three replicates determination was made for each observation as shown in Table 6.

Table 6 Analysis of marketed formulation

Forced degradation studies of empagliflozin were done in different conditions as per the ICH guidelines. Acid degradation of empagliflozin was performed in 0.1N HCl and weighed 10 mg of drug accurately and transferred to a 100-mL clean volumetric flask and dissolved in 5 to 10 mL methanol. The volume was made up with 0.1N HCl solution and kept at room temperature. One milliliter of samples was taken out at 0-, 4-, 8-, 24-hour time intervals. It was neutralized with same volume of 0.1N NaOH solution and diluted with methanol to get the final concentration of 10 μg/mL of empagliflozin. Sample solutions were then analyzed using the HPLC method. The result obtained from the peak area of the HPLC chromatogram was extrapolated to calculate the actual drug content. In acidic degradation study there was no degradation up to 8 h. It was only after 24 h that 30% degradation was seen. Base degradation of empagliflozin was performed in 0.1N NaOH and weighed 10mg drug accurately and transferred to a 100-mL clean volumetric flask and dissolved in − 10 mL of methanol as above. The volume was made up with 0.1N NaOH solution and kept at room temperature for observation. One milliliter of samples was taken out at 0-, 4-, 8-, 24-h time intervals, and neutralized with equal value of 0.1N HCl solution. The volume was made up with methanol to get the final concentration of 10 μg/mL of empagliflozin. Samples were then analyzed using the HPLC method. In base stress condition empagliflozin indicated degradation after 8 h and the percentage of degradation is 30%. For oxidation 10% hydrogen peroxide was used. Drug sample (10 mg) was accurately weighed and taken in 5–10 mL methanol in 100-mL clean volumetric flask and H₂O₂ 10 % v/v was used to make up the volume. The sample was kept at room temperature for observation. One milliliter of samples was taken out at 0-, 4-, 8-, 24-h time intervals and diluted with methanol to get the final concentration of 10 μg/mL of empagliflozin. Sample solutions were then analyzed using a developed method. In the oxidative degradation study empagliflozin showed 33% degradation after 8 h.

Empagliflozin was exposed to the direct sunlight and observed for photolytic degradation if any. The drug was kept in a petri dish and kept for 20 days in open light. The samples were collected after 5 and 10 days and these were then analyzed using the HPLC Instrument and followed the procedure discussed in earlier sections. Even after 20 days there was no degradation found. As per the ICH Q1A accelerated testing condition, thermal degradation should be carried out in dry heat or wet heat. Studies may be conducted at high temperatures for a short period. The drug was kept in a petri dish in an oven at 80 °C for 2 days. Then, the drug content was determined using the procedure as discussed in earlier section after 24 and 48 h. Before handling the drug, the sample was allowed to cool down in a desiccator. In the thermal degradation study no degradation was observed even after 48h. The degradation results are shown in Table 7 and Fig. 5.

Table 7 Results of forced degradation study for empagliflozin

Fig. 5

Degradation study in condition of a control, b acid, c base, d oxidation, e light, f heat

Discussion

Various research articles of the same drug in combination of same category drugs are reported [20,21,22]. The developed procedure using reverse phase HPLC analysis method for empagliflozin has been developed consisting of separation of the drug on a C₁₈ column equipped with DAD indicator. The best selected solvent system was found to be methanol/acetonitrile/1%OPA (75:20:05). The flow rate of the solvent system was kept at 1.0 mL/min. The period required for the separation was obtained at 2.54 min. Linearity was obtained in over the concentration range of 10–50 μg/mL (R² = 0.9990) with a LOD and LOQ of 0.05 μg/mL and 0.1 μg/mL, respectively.

The developed procedure was applied to two marketed formulations of these two compositions of empagliflozin 25 mg and excipients to q.s. The analysis obtained was in uniformity in the claimed amount in the marketed sample. Validation performed according to the ICH guidelines where the results are fast, accurate, robust, specific and linear [18, 19].

The separation done on the method was linear over the concentration range of inter-day and intra-day precision and accuracy was between 99.14 and 99.29%. The stability-indicating assay was done in the same manner as many reported methods [23, 24]. In the degradation studies, the drug was stable up to 8 h in acidic medium, 24 h in basic medium, and 24 h under oxidative stress and there was no degradation in heat and light exposure.

Conclusion

Simple, sensitive and selective stability-indicating HPLC method for estimation of empagliflozin has been developed in pharmaceutical dosage form. On the basis of result and analysis, it is concluded that the method is applicable for the estimation of drug in the formulary of marketed tablet without obstruction from the excipients in the formulation.

The proposed method is true, simple, cost-effective and applicable for routine analysis of drug quality control in laboratories and the pharmaceutical industries. Stability studies have been carried out to assess the stability of the compound and to demonstrate the stability of the RP-HPLC method developed.