Abstract
Gradient, reverse phase liquid chromatographic methods were developed separately for the related compounds and solifenacin succinate, an active pharmaceutical ingredient used for the treatment of overactive bladder. Gradient LC method was employed for related compounds. The mobile phase-A contains a 0.01 M phosphate buffer pH: with orthophosphoric acid (88%) and mobile phase-B contains a mixture of acetonitrile and water in the ratio of 90 : 10(v/v). The flow rate was 1.0 mL/minute, column temperature was kept at 35°C, and detection was monitored at 220 nm. In the developed HPLC method the resolution between solifenacin succinate and its closely eluting impurity, that is, solifenacin N-oxide was found to be greater than 3.0. The drug was subjected to stress conditions such as hydrolysis, oxidation, photolysis, and thermal degradation. Considerable degradation was found to occur in only oxidative stress condition. Degradation product formed during oxidative stress condition was found to be impurity-C and it can be identified by LC-MS. The stress samples were assayed against a qualified reference standard and the mass balance was found close to 99.5%. The developed RP-LC method was validated as per ICH guidelines. We also developed LC-MS/MS method for determination and identification of these impurities in solifenacin succinate.
1. Introduction
Muscarinic receptors play an important role in several major cholinergically mediated functions, including contractions of urinary bladder smooth muscle and stimulation of salivary secretion. The muscle in the wall of the bladder is called the detrusor muscle. It can sometimes contract in uncontrollable spasms, and this is often referred to as having an overactive bladder. The anticholinergic agents are widely used for the treatment of overactive bladder [1]. Solifenacin succinate is a muscarinic receptor antagonist belongs to anticholinergics and has higher selectivity for the urinary bladder over salivary glands [2, 3]. It acts as a selective antagonist to the M (3) receptor and works by relaxing the bladder muscles to prevent urgent, frequent, or uncontrolled urination. Chemically, solifenacin succinate is butanedioic acid, compound with (1S)-(3R)-1-azabicyclo [2.2.2] oct-3-yl 3,4-dihydro-1-phenyl-2(1H)-iso-quinolinecarboxylate (1 : 1) having an empirical formula of C23H26N2O2 C4H6O4 and a molecular weight of 480.55.
Solifenacin succinate (Figure 1) is a white to pale-yellowish-white crystal or crystalline powder. It is freely soluble at room temperature in water, glacial acetic acid, dimethyl sulfoxide, and methanol. Solifenacin succinate is available in the market under the brand name of VESIcare in the form of tablets. It is available in two dosage strengths, that is, 5 mg or 10 mg and is formulated for oral administration. In addition to the active ingredient solifenacin succinate, each VESIcare tablet also contains the following inert ingredients: lactose monohydrate, corn starch, hypromellose 2910, magnesium stearate, talc, polyethylene glycol 8000 and titanium dioxide with yellow ferric oxide (5 mg VESIcare tablet), or red ferric oxide (10 mg VESIcare tablet). The recommended dose of VESIcare is 5 mg once daily. If the 5 mg dose is well tolerated, the dose may be increased to 10 mg once daily. VESIcare should be taken with water and swallowed whole. VESIcare can be administered with or without food.
Angioedema of the face, lips, tongue, and/or larynx has been reported with solifenacin. In some cases angioedema occurred after the first dose. Cases of angioedema have been reported to occur hours after the first dose or after multiple doses. Angioedema associated with upper airway swelling may be life threatening. If involvement of the tongue, hypopharynx, or larynx occurs, solifenacin should be promptly discontinued and appropriate therapy and/or measures necessary to ensure a patent airway should be promptly provided. Anaphylactic reactions have been reported rarely in patients treated with solifenacin succinate. Solifenacin succinate should not be used in patients with a known or suspected hypersensitivity to solifenacin succinate. In patients who develop anaphylactic reactions, solifenacin succinate should be discontinued and appropriate therapy and/or measures should be taken.
Solifenacin succinate is principally (98%) bound to α1 acid glycoprotein’s of human plasma and is highly distributed to non-CNS tissues, having a mean steady-state volume of distribution of 600 L. The elimination half-life of solifenacin following chronic dosing is approximately 45–68 hours. Solifenacin is a substrate for cytochrome P450 enzyme CYP3A4 and extensively metabolized in the liver. Inducers or inhibitors of CYP3A4 may alter solifenacin pharmacokinetics. Administration of 10 mg VESIcare in the presence of 400 mg of ketoconazole, a potent inhibitor of CYP3A4, the mean Cmax and AUC of solifenacin increased by 1.5 and 2.7-fold, respectively. Therefore, it is recommended not to exceed 5 mg daily dose of VESIcare when administered with therapeutic doses of ketoconazole or other potent CYP3A4 inhibitors.
The primary metabolic routes of solifenacin are through N-oxidation of the quinuclidin ring and 4R-hydroxylation of tetrahydroisoquinoline ring. One pharmacologically active metabolite (4R-hydroxy solifenacin), occurring at low concentrations and unlikely to contribute significantly to clinical activity, and three pharmacologically inactive metabolites (N-glucuronide and the N-oxide and 4R-hydroxy-Noxide of solifenacin) have been found in human plasma after oral dosing.
Stability testing is performed during drug development to provide evidence of how the quality of a drug substance or drug product changes over time in response to a variety of environmental factors. Factors such as temperature, humidity, and light are studied to establish shelf life for the drug products and recommended storage conditions or packing.
Solifenacin succinate is not appearing in any pharmacopeia and no literature is available for determination of all process-related compounds and degradants in bulk drugs/pharmaceutical ingredient (API). Only few high performance liquid chromatography (HPLC) and mass spectroscopy methods were reported in literature for determination of solifenacin and related substances. High sensitive and rapid LC-electrospray ionization-MS-MS (in human plasma) and semi-micro-HPLC (in rat plasma) methods were reported for the determination of solifenacin succinate and its major metabolites in biological samples [4–6]. Ultrafast liquid chromatography for determination of related substances in solifenacin succinate, HPLC method for determination of solifenacin in bulk formulations and stereo selective HPLC method to quantify all the stereoisomers of solifenacin succinate in drug products [7–10], spectrophotometric, and HPTLC methods [11–13] were reported.
However the reported methods cannot be used for determination of all process-related compounds and degradation products, particularly solifenacin N-Oxide (Impurity-C) and also observed blank interferences. As per the requirements of various regulatory authorities, the impurity profile study of drug substances and drug products has to be carried out using a suitable analytical method in the final product [14, 15].
The main aim of this work was to develop a specific, accurate, and stability indicating gradient RP-HPLC method for the determination of all process-related compounds, degradation products, and assay in presence of its degradation products without any blank interferences. The developed-related compounds and assay methods were validated as per the International Conference on Harmonization (ICH) guidelines [16]. Stability testing of new drug substances requires the stress testing to carry out and to elucidate the inherent stability characteristic of the active substance [17]. The advantages of the methods presented here are that they are simple, rapid, and stability indicative.
2. Experimental
2.1. Chemicals
Samples of solifenacin succinate and its three-related compounds, namely, impurity-A, impurity-B, and impurity-C were received from analytical research and Development Department of Hetero Research Foundation, Hyderabad, India. HPLC grade acetonitrile was purchased from Merck, Darmstadt, Germany. Analytical reagent grade potassium dihydrogen orthophosphate and orthophosphoric acid (88%) were purchased from Qualizens fine chemicals, Mumbai, India. High pure water was prepared by using Millipore Milli “Q” plus purification system.
2.2. Equipment
A Waters Alliance HPLC system equipped with 2695 separation module with quaternary gradient pumps with inbuilt auto injector, 270852 thermostatic compartment, and 2996 photo diode array detector was utilized for method development and validation which was located in Analytical Research and Development Department of Hetero Research Foundation (Lab-I), Hyderabad, India. Empower chromatography manager software (Waters) was used for data acquisition and system suitability calculations. Photo diode array detector was used for determining peak purity. The second instrument LC system consisted of quaternary gradient pump, auto sampler, column oven, and a UV-Visible dual wavelength detector. The output signal was monitored and integrated using LC Solutions chromatography Manager Software (2010 series HPLC, Shimadzu, Japan).
Shimadzu HPLC system was utilized in ruggedness study which was located in Analytical Research and Development Department of Hetero Research Foundation, Hyderabad, India (Lab-II).
2.3. Chromatographic Conditions
The chromatographic separation was achieved on waters symmetry shield RP-18 , column by performing gradient programme. The gradient HPLC method for related compounds employs variable solutions of mobile phase-A and mobile phase-B used as mobile phase. The mobile phase-A contains (1.36 g in 1000 mL of water) potassium dihydrogen orthophosphate, adjusted to pH: using orthophosphoric acid (88%) solution and mobile phase-B contains mixture of acetonitrile and water in the ratio of 90 : 10(v/v). The flow rate of the mobile phase was kept 1.0 mL/minute. The HPLC gradient programme performed for related compounds separation was shown in Table 1.
The column temperature was maintained at 35°C and the detector wavelength was monitored at a wavelength of 220 nm. The injection volume was and mixture of mobile phase-A and acetonitrile in the ratio of 90 : 10(v/v) was used as diluent. To reduce the analysis time, gradient programme was modified for assay determination, and all other remaining chromatographic parameters kept same as related compounds method. The HPLC gradient programme performed for assay determination was shown in Table 2. All calculations concerning the quantitative analysis were performed with external standardization by measurement of peak areas.
2.4. LC-MS Conditions
Equipment. A Waters Alliance 2695 HPLC and Micromass ZQ-2000 MS (Waters Assoc., Milford, MA, USA.), controlled with Mass Lynx version 4.0 software, were used for detection. The analytical column was a symmetry shield RP-18 , used for separation of desired impurities. For mass spectroscopy detection, the parameters were checked by injecting spiked sample of solifenacin succinate and oxidative stressed sample. Mass spectrometer was provided with electrospray ionization source and operating parameters were as follows.
LC-MS and Mass Spectrometric Conditions. The chromatographic separation was achieved on waters symmetry shield RP-18 , column by performing gradient programme. The gradient HPLC method employs variable solutions of mobile phase-A and mobile phase-B used as mobile phase. The mobile phase-A contains 0.01 M ammonium formate in water, adjusted to pH: with formic acid solution and mobile phase-B contains mixture of acetonitrile and water in the ratio of 90 : 10(v/v). The flow rate of the mobile phase was kept 0.9 mL/minute. The HPLC gradient program for related compounds method was set as: time/% mobile phase-B: 0.01/20, 20/40, 30/40, and 32/20 with a postrun time of 8 minutes. The HPLC column temperature was maintained at 35°C and the detector wavelength was monitored at 220 nm. The injection volume was . A mixture of mobile phase-A and acetonitrile in the ratio of 90 : 10(v/v) was used as diluent.
The mass spectrometer was operated in positive ion electrospray mode. The capillary sprayer voltage was 3.5 kV and the sample cone voltage was 25 V. The source temperature was 120°C and the desolvation temperature was 350°C. The desolvation and cone gas flow rates were set to 100 and 650 L/hr, respectively. The acquisition mass range is m/z 0–1000 at 0.5 s per scan with a 0.1 s interscan delay. All mass spectra are acquired in centroid mode.
2.5. Preparation of Standard Solutions
A stock solution of solifenacin succinate (5.0 mg/mL) was prepared by dissolving appropriate amount in the diluent. Working solutions of 0.5 mg/mL and 0.1 mg/mL were prepared from above stock solution for related compounds determination and assay determination, respectively. A stock solution of impurity mixture (impurity-A, impurity-B, and impurity-C) at 0.03 mg/mL was also prepared in diluent.
2.6. Specificity
Specificity is the ability of the method to measure the analyte response in the presence of its potential impurities [18]. Stress testing of the drug substance can help identify the likely degradation products, which can in turn help establish the degradation pathways and the intrinsic stability of the molecule and validate the stability indicating power of the analytical procedures used. The specificity of the developed HPLC method for solifenacin succinate was determined in the presence of its impurities, namely, impurity-A, impurity-B, and impurity-C and degradation products. Forced degradation studies were also performed on solifenacin succinate to provide an indication of the stability indicating property and specificity of the proposed method. The stress conditions employed for degradation study included Light 1.2 million LUX hrs (carried out as per ICH Q1B), heat (105°C), acid hydrolysis (0.1N HCl), base hydrolysis (0.1N NaOH), water hydrolysis, and oxidation (10% H2O2). For heat and light studies, study period was two days whereas for acid, base, water hydrolysis, and oxidation, it was 4 hrs.
The photo degradation was carried out by exposing the solifenacin succinate sample in solid state to light providing an overall illumination of not less than 1.2 million lux hours and an integrated near ultraviolet energy of not less than , which took about 10 days period in photo stability chamber. Stressed samples of solifenacin succinate generated were checked for peak purity of by using waters 2695 photo-diode array detector. The purity factor is within the threshold limit obtained in all stressed samples demonstrates the analyte peak homogeneity. Assay studies were carried out for stress samples against qualified reference standard and the mass balance (%assay + %impurities + %degradation products) was calculated. The assay was also calculated for bulk sample by spiking all three impurities (impurity-A, -B, and impurity-C) at the specification level (i.e., 0.15% of impurity-A, B, and C with respect to analyte concentration, which is 0.5 mg/mL).
2.7. Method Validation
2.7.1. Precision
The system precision of the assay method was evaluated by carrying out five replicate injections of solifenacin succinate standard solution. The percentage of RSD was calculated for area of solifenacin peak from five replicate injections. The method precision of the assay method was evaluated by carrying out six independent assays of test sample of solifenacin succinate against qualified reference standard. The percentage of RSD of six assay values obtained was calculated.
The system precision of the related compounds method was checked by injecting six replicate runs of solifenacin spiked with impurity blend solution (solifenacin 0.1% and each impurity 0.15% level with respect to test solution concentration, which is 0.5 mg/mL). The percentage of RSD for area of each impurity-A, impurity-B, impurity-C, and solifenacin was calculated.
The method precision of the related compounds method was checked by injecting six individual test preparations and the percentage of RSD for each impurity-A, impurity-B, and impurity-C, was calculated. The intermediate precision of the method was also evaluated using different analysts and a different instrument in the same laboratory.
2.7.2. Limit of Detection (LOD) and Limit of Quantification (LOQ)
The LOD and LOQ for solifenacin, impurity-A, impurity-B, and impurity-C were estimated at a signal-to-noise ratio of 3 : 1 and 10 : 1, respectively, by injecting a series of dilute solutions with known concentration [19]. Precision study was also carried at the LOQ level by injecting six replicates of solifenacin spiked with impurity-A, impurity-B, and impurity-C blend and calculating the percentage of RSD of the peak areas.
2.7.3. Linearity
Linearity test solutions for assay method were prepared from stock solution at six concentration levels from 80 to 120% of assay analyte concentration (80, 90, 100, 110, and 120%). The peak area versus concentration data was performed by least-squares linear regression analysis. Linearity test solutions for related compounds method were prepared by diluting the impurity stock solution (2.5) to the required concentrations. The solutions were prepared at six concentration levels from LOQ to 150% of the specification level [LOQ, 0.075(50%), 0.12(80%), 0.135(90%), 0.15(100%), 0.18(120%), and 0.225(150%)].
2.7.4. Accuracy
The accuracy of the assay method was evaluated in triplicate at three concentration levels, that is, 80, 100, and 120% in bulk drug sample. The percentage of recoveries was calculated. Accuracy/recovery experiments were performed in triplicate. The bulk sample, provided by Hetero Research Foundation, does not show the presence of impurity-A and impurity-B. Some of the bulk samples show the presence of impurity-C in between 0.03 and 0.05% levels. Standard addition and recovery experiments were conducted to determine accuracy of the related compounds method for the quantification of all three impurities in bulk drug samples.
The accuracy study was carried out in triplicate at LOQ, 0.075%, 0.15%, and 0.225% of the analyte concentration (0.5 mg/mL). The percentage of recoveries for impurity-A, impurity-B, and impurity-C were calculated.
2.7.5. Robustness
To determine the robustness of the developed assay and related compound methods, experimental conditions were purposely altered and the resolution between solifenacin succinate and impurity-C, impurity-A, and impurity-B was evaluated. The flow rate of the mobile phase was 1.0 mL/minute. To study the effect of flow rate on the resolution, it was changed by 0.2 units, from 0.8 to 1.2 mL/minute, while other mobile phase components were held constant as stated in Section 2.3. The effect of change in the composition of organic modifier was checked by changing in the mobile phase composition. The effect of pH on resolution of impurities was studied by varying units (at 3.3 and 3.7 buffer pH). The effect of column temperature on resolution was studied at 33°C and 37°C instead of 35°C. In all the above varied conditions, the components of the mobile phase were held constant as stated in Section 2.3.
2.7.6. Solution Stability and Mobile Phase Stability
The solution stability of solifenacin succinate in the assay method was carried out by leaving both the test solutions of sample and reference standard in tightly capped volumetric flasks at room temperature for 12 hrs and 24 hrs (for related compounds study period is 12 hrs, 24 hrs, 36 hrs, and 48 hrs). The same sample solutions were assayed for 6-hour interval up to the study period. The mobile phase stability was also carried out by assaying the freshly prepared sample solutions against freshly prepared reference standard solutions for 6-hour interval up to 24 hours. Mobile phase prepared was kept constant during the study period. The percentage recovery of assay of solifenacin succinate was calculated for the study period during mobile phase and solution stability experiments.
The solution stability of solifenacin succinate and its impurities in the related compounds method was carried out by leaving spiked sample solution in tightly capped volumetric flask at room temperature for 48 hours. Content of impurity-A, impurity-B, and impurity-C was determined for every 12-hour interval up to the study period. Mobile phase stability was also carried out for 48 hours by injecting the freshly prepared sample solutions for every 12-hourinterval. Content of impurity-A, impurity-B, and impurity-C was checked in the test solutions. Mobile phase prepared was kept constant during the study period. The percentage of RSD for content of each impurity-A, impurity-B and impurity-C was calculated from initial, 12, 24, 36 and 48 hrs samples of the study period.
3. Results and Discussion
3.1. Method Development and Optimization
Impurity-C is the potential impurity present in bulk samples of solifenacin succinate. The main target of the chromatographic method is to get the separation of critical closely eluting impurities, namely, impurity-A and impurity-B, solifenacin, and impurity-C. Impurities were eluted very closely to each other by using different stationary phases like CN, C18, C8, and phenyl and different mobile phases containing buffers like phosphate, sulfate, and acetate with different pH (2.5–5) and using organic modifiers like acetonitrile and methanol in the mobile phase. pH of the buffer has played a significant role in achieving the separation between impurity-A and impurity-B, solifenacin and impurity-C.
The chromatographic separation was achieved on a waters symmetry shield RP-18, , 5 μm column, by using variable mixtures of mobile phase-A and mobile phase-B as mobile phase. The mobile phase-A contains 0.01 M potassium dihydrogen orthophosphate, pH adjusted to using orthophosphoric acid solution (88%) and mobile phase-B contains a mixture of acetonitrile and water in the ratio of 90 : 10 (v/v). The flow rate of the mobile phase was 1.0 mL/minute. The HPLC gradient program for related compounds method was set as time/% mobile phase-B: 0.01/20, 20/40, 30/40 and 32/20 with a postrun time of 8 minutes. At 35°C column temperature, the peak shape of solifenacin succinate was found symmetrical. In the optimized conditions solifenacin succinate, impurity-A, impurity-B, and impurity-C were well separated with a resolution of greater than 3 and the typical retention times of impurity-A, impurity-B, impurity-C, and solifenacin succinate were about 4.1, 6.1, 8.2, and 14.0 minutes, respectively. The system suitability results for related compounds method are given in Table 3 and the developed HPLC method was found to be specific for solifenacin succinate and its three related compounds, namely, impurity-A, impurity-B, and impurity-C. For the determination of assay of solifenacin succinate the HPLC gradient programme was set as time/% mobile phase-B: 0.01/30, 7/60 and 10/30 with a postrun time of 5 minutes. In the optimized assay method the resolution between solifenacin and impurity-C is greater than 2.5 and peak shape is symmetrical. The typical retention time of solifenacin is 6 minutes. The system suitability results for assay method were given in Table 4 and the developed method is specific for assay determination.
3.2. Method Validation
3.2.1. Precision
The %RSD for assay of solifenacin succinate during assay system precision and method precision study was within 2.0 and the %RSD for area of impurity-A, impurity-B, and impurity-C in related compounds method precision study was within 5.0. The %RSD of assay results obtained in intermediate precision study was within 2.0 and the %RSD for area of impurity-A, impurity-B, and impurity-C was well within 10.0 confirmed good precision of the method.
3.2.2. Limit of Detection and Limit of Quantification
The limit of detection of solifenacin, impurity-A, impurity-B, and impurity-C was 0.0064%, 0.0034%, 0.0025%, and 0.0068% (analyte concentration, i.e., 0.5 mg/mL) for injection volume. The limit of quantification of solifenacin, impurity-A, impurity-B, and impurity-C was 0.02%, 0.01%, 0.01%, and 0.02% (analyte concentration, i.e., 0.5 mg/mL) for injection volume. The precision at LOQ concentration for impurity-A, impurity-B, and impurity-C was below 10.0%. The accuracy/recovery experiments were carried out for impurity-A, impurity-B, and impurity-C at LOQ concentration in triplicate and the recoveries were found to be well within 80–115%, which demonstrates that the developed method can accurately measure the impurities present in solifenacin succinate.
3.2.3. Linearity
Linear calibration plot for assay method was obtained over the calibration ranges tested, that is, 0.08–0.12 mg/mL and the correlation coefficient obtained was greater than 0.999. The percentage of RSD values for each level is within 2.0 and %Y-intercept of the calibration curve is −0.3 (within ). These results show that an excellent correlation existed between the peak area and concentration of the analyte.
Linearity calibration plot for related compounds method was obtained over the calibration ranges tested, that is, LOQ, 0.075%, 0.12%, 0.135%, 0.15%, 0.18%, and 0.225% for impurity-A, impurity-B, and impurity-C. The correlation coefficient obtained was greater than 0.995. The percentage of RSD values for each level are within the limit (<5.0). The %Y-intercept of the calibration curves is for impurity-A, impurity-B, and impurity-C, respectively. These results show that an excellent correlation existed between the peak area and concentration of the impurity-A, impurity-B, and impurity-C.
3.2.4. Accuracy
The percentage recovery of solifenacin succinate in assay method is within the limit (98–102). The percentage recovery of impurity-A, impurity-B, and impurity-C in related compounds method are within the limit (85% to 115%) and recovery data shown for both methods in Table 5. HPLC chromatograms of blank, pure solifenacin succinate, solifenacin succinate spiked with 0.15% of each impurity and solifenacin succinate assay chromatograms are shown in Figures 2, 3, 4, and 5.
3.2.5. Robustness
In all the deliberate varied chromatographic conditions carried out as per Section (flow rate, pH, and column temperature), the resolution between closely eluting impurities (Table 6), namely, impurity-A and impurity-B, solifenacin and impurity-C was greater than 3.0, illustrating the robustness of the method.
3.2.6. Solution Stability and Mobile Phase Stability
The %Recovery for assay of solifenacin succinate during solution stability and mobile phase stability experiments was within limit (98–102%). No significant changes were observed in the content of impurity-A, impurity-B, and impurity-C during solution stability and mobile phase experiments when performed using related compounds method. The variation content (%) of each impurity obtained from fresh sample and each time interval of the solution stability should be %. The solution stability and mobile phase stability experiments data confirm that sample solutions and mobile phase used during assay (up to 24 hours) and related compounds determination were stable up to 48 hours.
4. Results of Forced Degradation Studies
Significant degradation was not observed in solifenacin succinate stressed sample that was subjected to light, heat, acid, base, and water hydrolysis (Figures 6, 7, 9, 10 and 11). The degradation of drug substance was observed under oxidative conditions (Figure 8). Solifenacin Succinate was degraded into impurity-C during oxidative (10% after 1 hr treatment). The same was confirmed by coinjection with a qualified impurity-C standard and identified by LC-MS. Peak purity test results derived from photo diode array detector, confirmed by that solifenacin succinate peak, are homogeneous and pure in all the analyzed stress samples. The mass balance of samples (Table 7) was closed to 99.5%. The %assay of solifenacin succinate is unaffected in the presence of impurity-A, impurity-B, impurity-C, and its degradation products confirm the stability indicating power of the developed method.
5. Impurities Identification by LC-MS
For identification of impurity-A, impurity-B, and impurity-C, the ESI mass spectrum of impurities eluted at RRT 0.28 and 0.37 (Figure 12) in positive ion mode showed a molecular ion peaks at m/z 208, 210 [(mH)+], indicating the molecular weights of these compounds are 207 and 209, respectively. From this data we conclude that these two are intermediates, which were used in manufacturing process of solifenacin succinate and these two were also confirmed with photo diode array detector by comparing the spectra’s with known standards. These two impurities further were characterized by UV, FT-IR, Mass, and NMR ().
ESI mass spectrum of major impurity formed during the oxidative stress condition at RRT 1.10 in positive ion mode showed a molecular ion peak at m/z 379 [(mH)+] indicating the molecular weight of the compound as 378 (Figure 13). This molecular ion mass was 16 mass units higher than that of solifenacin and this indicates the probability of the formation of N-oxide. The same impurity was also formed in base degradation,but in smaller quantities. Further this impurity was synthesized and characterized by UV, FT-IR, Mass, and NMR ().
6. Conclusions
New, accurate, and selective gradient RP-LC methods were proposed for the determination of related compounds and assay of solifenacin succinate drug substance and validated as per ICH guidelines. The method has higher sensitivity for the determination of related compounds than previously reported methods. The method was found to be simple, selective, precise, accurate, and robust. The method was completely validated showing satisfactory data for all the method parameters tested. The developed method is stability indicating and can be used for routine analysis of production samples and also to check the stability of bulk samples of solifenacin succinate.
Acknowledgments
The authors wish to thank the management of Hetero Research Foundation for their support, encouragement, and permitting this work to communicate for publication. Authors also wish to thank the chemical research and analytical research departments for their cooperation.