Liquid chromatography-tandem mass spectrometric method for trace quantification of ethyl methanesulfonate: a genotoxic impurity in dapoxetine hydrochloride

Abstract

Background

Dapoxetine hydrochloride is a selective serotonin reuptake inhibitor drug for treating premature ejaculation. This study was designed to develop and validate a sensitive and selective LC–MS/MS method for trace analysis of genotoxic impurity ethyl methanesulfonate in Dapoxetine hydrochloride.

Results

Chromatographic separation was achieved on the Shodex RSpak DS-413 column, 150 × 4.6 mm, 3.0 µm using eluent containing a equal volumes of acetonitrile and 0.1% v/v formic acid in water was used in the isocratic elution mode at a pump flow of 1.0 mL/min. No interference was observed at the retention time of ethyl methanesulfonate, indicating that the developed method is specific and selective for trace level quantification.The developed method was found to be linear in the concentration range of 1–50 ppm with coefficient of regression of 0.9997. Detection limit and quantification limit were determined to be 0.6 ppm and 1.0 ppm respectively. Acceptable RSD values (< 10.0%) and recovery results (> 90%) obtained from the accuracy and precison experiments indicate that the developed method is precise and accurate in the concentration range of 1–50 ppm. Ethyl methanesulfonate solutions were stable for two days when stored at room and refrigerated temperatures.

Conclusion

The developed method has the ability to quantify ethyl methanesulfonate in dapoxetine hydrochloride. Thus, the anticipated method has high probability to adopt in the quality testing laboratories of pharmaceutical industry.

Background

Over the last decade, regulatory agencies acorss the world are increasingly vigilant on the assessment and control of mutagenic impurities in active pharmaceutical ingridents (API) and drug products. A drug substance can contain different types of trace-level impurities resulting from residues of starting materials, reagents, intermediates, by-prodcuts generated during the course of synthesis and degradation products [1]. These trace-level impurities present in the drug substance yield no therapeutic benefit to the pateint but in fact have the potential to cause risk to safety of the patient. Some of trace-level impurities present in the drug substance may cause deleterious changes in the genetic material of cells. Therefore, the levels of such potential gentoxic impurities (GTIs) present in the drug substances should be assessed and controlled for ensuring the safety of the patient. The International Council on Harmonization (ICH) covers both the safety and quality frameworks for establishing acceptable limits that will assure negligible risk to patients [2]. The ICH M7 recommended limits for daily intake of GTIs are 120, 20, 10 and < 1.5 µg/day, for < 1 month, > 1–12 months, > 1- 10 years and > 10 years to lifetime, respectively. Based on the maximum daily dose (MDD) of the drug substance, limit for the quantitation of mutagenic impurities will be established.

Dapoxetine hydrochloride (DAPO) is a novel short acting selective serotonin reputake inhibitor drug for treating premature ejaculation (PE) and depression [3]. Unlike other selective serotonin reputake inhibitors, DAPO is absorbed and eliminated rapidly from the body. Due to its absorption, distribution, metabolism, and excretion (ADME) properties, DAPO is recommended and prescribed for the treatment of PE rather than depression. The maximum recommended oral dose of DAPO is 60 mg per day for adults in the age group of 18–65 years. DAPO is available as tablets with 30 mg as well as 60 mg dose strengths. It is reported to have several side effects including diarrhea, anxiety, dry mouth etc. Presence of any GTIs in the DAPO can further aggravate the side effects of the drug in patients receiving drug prodcuts containing DAPO. Therefore, it is very important to identify and quantify any GTIs that could be present in DAPO.

In the synthesis of DAPO, methane sulfonylchloride is used to protect alcohol group in the stage three intermediate of the synthesis. During the down stream processing of DAPO ethanol is used as the solvent. It is highly likely that ethanol (used in the down stream processing) can react with residual amount of methane sulfonylchloride (remaining from stage III reaction) or metahne sulfonic acid (formed due the hydrolysis of methane sulfonylchloride due its to high reactivity with water) to generate EMS. Therefore, in the bulk synthesis of DAPO, it is quite possible that there will be trace levels of EMS in DAPO. Based on the structural alerts [4, 5] and more importantly as per the guidelines issued by European Directorate for the Quality of Medicines and Healthcare (EDQMH), EMS is considerd to be gentoxic in nature and should be measured at trace levels [2, 6, 7]. The complete synthetic scheme of DAPO is shown in Fig. 1. Based on the MDD, EMS should be controlled at 25 ppm in the DAPO drug substance.

Fig. 1

Synthetic scheme of dapoxetine hydrochloride

There are few methods reported in the literature for determination of EMS using gas chromatography (GC) with flame-ionization detector (FID) and mass analyzer. Some of the reported GC methods involve direct determination of EMS [8,9,10,11], while the reminaing involve derivatization of EMS using different reagents [12, 13]. The reported GC methods couple with FID or mass analyzer for direct determination of EMS were found to have less sensitivity and higher injection volumes which are not ideal for regular GC analysis. While the GC methods involving derivatization of EMS can suffer from false-positive results due to the possibility of residual alcohols present in the drug substances also undergoing derivitization. The mass spectrometric methods reported [14,15,16,17] for the determination of EMS in different drug substances were found to have either higher injection volume or higher LOQ or narrow linearity ranges.

Till date, no method is reported for quantification of EMS in DAPO by LC–MS/MS. In this current work, simple and sensitive LC–MS/MS method was developed and validated for the determination of EMS in DAPO. The developed method was used for trace-level quantification of EMA in three batches of DAPO and its advanced intermediate.

Methods

Safety concerns

All samples of EMS were handled under a fume hood due to its genotoxic properites. Appropritae institutional safety procedures were followed in the collection and disposal of eluent obtained from the liquid chromatpographic anlaysis of samples.

Chemicals and materials

DAPO was obtained as gift sample from Herrlich Pharma, Hyderabad, India. EMS (Purity > 99%), formic acid and acetonitrile (ACN) was procured from Merck, Mumbai, Inida. Reagents and solvents used in this study were of mass spectrometric grade. Chromatographic grade water obtained from water purification system (Merck/Milli-Q® Integral 3 system, MA, USA) was used in the preparation of mobile phase and the diluents.

Instrumentation

Shimadzu Nexera-X2 chromatographic separation unit (Shimadzu Corp, Kyoto, Japan) attached with 8040 triple quadrupole mass analyzer (Shimadzu Corp, Kyoto, Japan) was used for this study. Data acquisition and integration was performed using automated software (Shimadzu Corp, Kyoto, Japan). During the preparation of sample and standard solutions calibrated auto-pipettes were used. Filteration of premixed eluent was performed using 0.45 µm membrane filter (Millipore® MA, USA). Before injection, all the standard and sample solutions were filtered using 0.45 µm polyvinylidene difluoride (PVDF) syringe filter (Millipore® MA, USA).

Liquid chromatographic and mass spectrometric conditions

LC conditions

Separation was performed on Shodex RSpak DS-413 (150 × 4.6 mm, 3.0 µm) column in reverse phase mode. The eluent solution containing a mixture of an organic phase and aqueous phase. Aqueous phase consisted of 0.1% v/v of formic acid in water, while the organic phase contains ACN. Separation between EMS and DAPO was achieved in isocratic elution mode with eluent flow of 1.0 mL min⁻¹. The sample injection volume was 20 µL. Autosampler and column oven temperatures were set at 25 °C (± 2 °C) and 30 °C (± 2 °C), respectively. Method conditions are detailed in Table 1.

Table 1 Summary of method conditions

MS conditions

Electron-spray inonization (ESI) source in positive mode using multiple reaction monitoring (MRM) was employed for the ionization of EMS. Source and desolvation line (DL) temperatures were set at 150 °C and 320 °C, respectively. Ultra-high pure nitrogen gas (99.95% purity) was used as nebulizing and drying gas at a flow rate of 1.5 mL min⁻¹ and 15 mL min⁻¹, respectively. Ultra-high pure argon gas was used as collision-induced dissociation (CID) gas to enhance the response. MRM transition of m/z 125.1 > 97.0 was employed for the quantification of EMS.

Preparation of stock solutions and sample solutions

Primary stock solution of EMS was prepared at a concentration of 0.125 mg mL⁻¹ using a mixture of water:ACN (10:90 v/v) as diluent and stored under refrigerated conditions. First intermediate stock solution (1.25 µg mL⁻¹) of EMS was prepared from the primary stock solution (0.125 mg mL⁻¹). First intermediate stock solution of EMS was further diluted to yield a second intermediate stock solution of EMS with a concentration of 250 ng mL⁻¹. Calibration curve standard solutions were prepared by drawing appropriate aliquots of either first intermediate stock solution or second intermediate stock solution and diluting with a mixture of water:ACN (10:90 v/v). Six different calibration curve standard solutions (10, 125, 250, 375, 500 ng mL⁻¹) were prepared for EMS in the range of 10–500 ng mL⁻¹ (≈ 1–50 ppm with respect to DAPO amount).

System suitability was established by injecting six replicate injections of second intermediate stock solutions (250 ng mL⁻¹) of EMS and determining the relative standard deviation [RSD (%)] of response obtained for the replicate injections.

For determining the LOD and LOQ concentration of EMS in the optimized method, different concentratios of EMS standard solutions ranging from 2 to 25 ng mL⁻¹ (≈ 0.2–5 ppm w.r.t 10 mg mL⁻¹ concentration of DAPO) were prepared from the second intermediate stock solution of EMS (250 ng mL⁻¹).

The precision of the optimized method was established by performing method precision (intra-day precision, repeatability) and intermediate precision (reproducibility) studies using the spiked sample solution. In the method precision study, six different spiked samples were prepared by spiking the EMS at 100% level in the DAPO sample. Reproducibility was performed by repeating method precision experiment by different analyst on different day using different column.

Accuracy of the method was evaluated using un-spiked and spiked samples of DAPO. Unspiked DAPO sample (0% level) and spiked samples at five different levels (LOQ, 50%, 100%, 150% and 200%), with respect to the DAPO concentration (10 mg mL⁻¹) were prepared in triplicate using the the same diluent used for the preparation of primary and secondary stock solutions.

For robustness studies, second intermediate stock solution (250 ng mL⁻¹) of EMS and spiked samples of DAPO (10 mg mL⁻¹) with EMS at 100% concentration level were used. The study was done in triplicates. Test samples of DAPO and its process intermediate were prepared in duplicate at 10 mg mL⁻¹.

Method validation

The developed method for the low-level quantification of EMS in DAPO was systematically validated as per the regulatory guidelines [18, 19]. As part of method validation, sensitivity, selectivity, accuracy, linearity, precision, solution stability and robustness.

Results

Optimization of liquid chromatographic and mass spectrometric method conditions

In the development of a LC–MS/MS method for quantification of EMS (a non-volatile GTI) in DAPO, first the LC conditions were optimized followed by the mass spectrometric conditions. Optimizaion of LC conditions was done based on elution time of EMS and DAPO, peak area of EMS and resolution between EMS and DAPO. Based on the trials, Shodex RSpak DS-413 column (150 mm × 4.6 mm × 3.5 µm) using premixed eluent containing equal ratio of 0.1% v/v formic acid in water and ACN in isocratic elution mode were selected as final LC conditions.

Various experimental runs were performed by changing the mass spectrometric parameters. Finally, better sensitivity was achevied using the conditions mentioned in Table 1.

Method validation

Specificity

The total ion chromatogram clearly indicate that baseline is clean and free from interference at the elution time of EMS and there is good separation of EMS from DAPO. The MRM transition chromatograms at m/z of 125.1(Q1)/79.1(Q3) for blank, un-spiked DAPO sample (10 mg mL⁻¹), standard EMS solution (25 ppm), and a spiked sample of DAPO with EMS is presented in Fig. 2.

Fig. 2

Overlay MRM signal of a Blank, b standard solution of EMS and c spiked sample of DAPO with EMS

Sensitivity

Limit of detection (LOD) and limit of quantification (LOQ) concentrations for EMS were determined to be 0.6 ppm and 1.0 ppm, respectively, w.r.t. 10 mg mL⁻¹ sample concentration of DAPO. The MRM transition chromatograms at m/z of 125.1(Q1)/79.1(Q3) for blank, LOD solution and LOQ solution is presented in Fig. 3. RSD values of six replicate injections of EMS at LOQ level was found to be 2.58%.

Fig. 3

Overlay MRM signal of a Blank, b LOD solution and c LOQ solution

Linearity

The calibration curve for EMS in DAPO (Range: 1–50 ppm with respect to DAPO amount) was constructed with concentration of EMS on the x-axis and peak area response on the y-axis. From the regression analysis; r², intercept, slope, and residual plots pattern were calculated and results are briefed in Table 2.

Table 2 Summary of data obtained from method validation

Precision

RSD values for EMS content from six individual preparations of spiked solution in the repeatability and reproducibility experiments were found to be within the predefined acceptance criteria of ≤ 10.0%. Cumulative RSD (%) values for the results obtained from precision (analyst 1) and intermediate precision (analyst 2) were found to be within the satisfactory limit of ≤ 10%. Results from the precision studies are detailed in Table 2.

Accuracy

Percentage recovery values of EMS, at all the five levels in the range of LOQ-200%, were found to be > 90% with RSD value of < 7.2%. These results indicate the trueness of the method as the percentage recovery and %RSD values were found to be within the satisfactory limits of 80–120% and ≤ 10%, respectively. The results from accuracy studies are summarized in Table 2.

Robustness

Developed method robustness was assessed for the eluent flow rate (0.8 and 1.2 mL min⁻¹) and nebulization gas flow rate (1.3 and 1.8 mL min⁻¹) and the results are summarized in Table 2. RSD value from six replicate injections of system suitability solution of EMS for the change in eluent flow rate and nebulization gas flow rate was found to be < 5.3%. Percentage recovery values of EMS from triplicate spiked sample preparations for the change in eluent flow rate and nebulization gas flow rate were found to be in the range of 91–103%. Results from different robustness parameters were found to be within the acceptance criteria of ≤ 10% (RSD) and within limit of 80–120% for recovery.

Solution Stability

Solution stability of secondary intermediate stock solution (250 ng mL⁻¹) of EMS and spiked samples of DAPO (10 mg mL⁻¹) containing EMS at 100% concentration level were evaluated up to two days at ambient laboratory temperature (25 ± 5 °C) and refrigerated condition (2–8 °C). The percent recoveries of EMS in secondary intermediate stock solution and spiked sample were calculated by matching against the freshly prepared secondary intermediate stock solution of EMS. The data obtained from the stability studies for EMS are presented in Fig. 4.

Fig. 4

Overlay of stability data of EMS in standard and spiked sample at ambient laboratory and refrigerated (2–8 °C) conditions

Method application

The level of EMS present in the three batches of bulk samples of DAPO and its advanced intermediate was found to be less than LOD of the method.

Discussion

The objective was to develop a capable method for fast and accurate quantification of EMS in the shortest run time with realistic accuracy [20, 21]. Optimizaion of LC conditions was done based on elution time of EMS and DAPO, peak area of EMS and resolution between EMS and DAPO. During the optimization of LC conditions, first different stationary phases (such as Luna C18, Zorbax C8, Shodex RSpak DS-413, and Atlantis T3) with varied polarity were evaluated with different aqueous and non-aqueous mobile phase compostions. As a part of selecting the LC–MS compatible aqeuous mobile phase (mobile phase A), two different solvents, namely, 10 mM ammonium acetate in water and 0.1% v/v formic acid were tried. Methanol and ACN were tried to identify the suitable non-aqueous mobile phase (mobile phase B).

In the optimization of MS conditions, the sample was ionized using electrospray ionization technique and analyzed in scan mode with m/z range of 50–500. The resultant MS signal was found to have good intensity for the parent ion (Q1). Subsequently the parent ion (Q1) was fragmented by providing collision energy in the presence of collision indiced dissociation (CID) gas in the seond quadrupole (MS2) to yiled daughter ion (Q3) with good intensity. The CID gas and collision energy parameters were fine tuned to get stable daughter ion (Q3). Futher, instrument dependent parameters like desolvation line (DL) and source temperature, CID and drying gas flows were optimized for quantification of EMS. Two different transitions at m/z values of 125.1(Q1)/79.1(Q3) and 125.1(Q1)/97.0(Q3) were monitored during the optimization studies. The response obtained for the transition 125.1(Q1)/79.1 (Q3) was not intense and therefore it was not considered for further experiments. In the final optimized method, 125.1(Q1)/97.0 (Q3) was selected for sample analysis.

No interference was observed in the MRM transition chromatograms of blank and DAPO at m/z of 125.1(Q1)/79.1(Q3) at the retention time of EMS, indicating that the developed method is specific and selective for EMS. LOQ value found to be lower or equal to the reported LC–MS/MS methods [14, 16, 17]. F_cal values from the linear regression analysis were found to be significantly greater than their corresponding F_crit at 5% level of significance, suggesting that the regression model is significant. Lower %Y-intercept and higher r² values from the calibration curve standards in the entire range demonstrates that the method is linear. Residual plots obtained from the linear regression analysis have shown a random distribution of the residuals across zero, indicating the absence of a trend/bias in the results.

RSD values and recovery results obtained from the method validation (Table 2) indicate that the developed method is precise and accurate for the low level quantification of EMS in DAPO. The data from the robustness experiments had appreciably indicated that the optimized method is robust to the small deliberate changes in the method parameters.

The data from solution stability experiments indicated that no significant difference in the stability of the samples when stored at room (25 ± 5 °C) and refrigerated (2–8 °C) temperature for a period of two days.

Conclusions

The developed method is rapid, sensitive and selective, accurate and precise for trace-level determination of EMS in DAPO and its advanced intermediate. Standard solutions of EMS as well as the spiked sample solutions of EMS were found to be stable for two days at room temperature and refrigerated conditions. The method was successfully employed in the quantification of EMS in three batches of DAPO and its advanced intermediate. This method can be applied in pharmaceutical testing labs for trace level quantification of the EMS in DAPO and can be easily adopted to other sample API’s.