Development and Validation of a Stability-Indicating RP-HPLC Method for Determination of Darifenacin Hydrobromide in Bulk Drugs ()
1. Introduction
Darifenacin hydrobromide (DRF), a novel antimuscarinic agent, chemically known as (S)-2-[1-[2-(2,3-dihy- drobenzofuran-5-yl)ethyl] pyrrolidin-3-yl]-2,2-diphenyl-acetamide hydrobromide, is a medication used to treat overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency. It works by blocking the M3 muscarinic acetylcholine receptor selectively, which is primarily responsible for bladder contractions, thereby decreases the urgency to urinate [1] [2] .
An extensive survey of literature revealed that few chromatographic methods have been published for the quantification of DRF and related substances. S. Thomas et al. reported a selective stability-indicating HPLC method for DRF in the presence of process related impurities and stress degradation products and characterization of degradation products by LC-MS studies [3] . Despite of the separation of several related substances and DRF, the method has limitations of using ion-pairing mobile phase additive, very high run time, and poor peak shape of DRF. M. V. Murthy et al. reported a stability-indicating UPLC method [4] . A stability-indicating LC method with chemometric evaluation of DRF was also reported [5] . A chiral stability-indicating assay method for the determination of DRF and its enantiomer and a chiral LC Method for enantiomeric purity determination of DRF in bulk drugs and extended release tablets were also reported [6] [7] . K. Srinivas et al. reported an impurity profile method for batch analysis of DRF [8] . In addition, B. Kaye et al. reported a solid phase extraction of DRF in human plasma [9] . To the best of our knowledge, no rapid stability-indicating HPLC method for the quantitative determination of DRF in drug substance in presence of more susceptible process related impurities in bulk drugs was reported.
The main target of the present research work was to develop a selective, rapid and stability-indicating HPLC method for the determination of DRF and its related substances. The developed method was validated with respect to specificity, limits of detection (LOD), limits of quantitation (LOQ), linearity, precision, accuracy, solution and mobile phase stabilities, and robustness as per International Conference on Harmonization (ICH Q2R1) guidelines [10] . Forced degradation studies were performed on the DRF drug substance to establish the stability- indicating nature of the method in accordance with established ICH guidelines [11] .
2. Experimental
2.1. Reagents and Chemicals
HPLC grade acetonitrile and methanol and AR grade ammonium acetate and ammonia solutions were purchased from S.D. Fine chemicals Pvt. Ltd., Mumbai, India. High purity water was obtained by using Millipore Milli-Q water purification system (Millipore synergy, France). Samples of DRF and its three process related impurities (Imp-1: 2,2-Diphenyl-2-[(3S)-pyrrolidin-3-yl]acetamide tartarate, Imp-2: 5-(2-bromoethyl)-2,3-dihydrobenzo- furan, Imp-3: N-(2-(2,3-dihydrobenzofuran-5-yl)ethyl)-2-(1-(2-(2,3-dihydrobenzofuran-5-yl)ethyl)pyrrolidin-3- yl)-2,2-diphenyl acetamide) were received from a local industry, Hyderabad, India. Structures of DRF and impurities are shown in Figure 1. Among three impurities Imp-1 and Imp-2 are substrates and Imp-3 is a dimeric by-product. All required sample solutions, and solvents were filtered through 0.45 µm PTFE filter papers.
2.2. Equipment
The HPLC system used for method development, forced degradation studies and method validation consisted of a quaternary UFLC LC-20AD liquid chromatograph pump module, a DGU-20A5 degasser, a SIL-20AC auto sampler, a CTO-20AC column oven compartment, a SPD-M20A photo diode array detector, and CBM-20A communications bus module (All from Shimadzu, Kyoto, Japan). The chromatographic and the integrated data were recorded using HP (Hewlett Packard, India) computer system using Lab Solutions data acquisition software (Shimadzu, Kyoto, Japan).
2.3. Chromatographic Conditions
The chromatographic column used was Prodigy C8 column (250 × 4.6 mm, 5 μm particle size, 150A˚) of Phenomenex make. The batch and serial numbers of the column are 5182-22 and 585196-1, respectively. All the chromatograms given in this paper are of this column. Another Prodigy C8 column of same dimensions but with
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Figure 1. Chemical structures of DRF, impurities (Imp-1, Imp-2, and Imp-3), and degradation of products (A1, A2, O1, and O2).
different batch (5234-033) and serial number (652229-1) is used for intermediate precision study. The mobile phase used consists of (solvent A) 0.05 M ammonium acetate pH adjusted to 7.2 by using ammonia solution, and (solvent B) methanol and acetonitrile in 64:36 v/v ratio. The separation was achieved in an isocratic elution mode at 50:50 v/v ratio of solvent A and solvent B at a flow rate of 1.0 mL/min at a column temperature of 25˚C. The chromatograms were monitored at a wavelength of 215 nm. The injection volume was 10 μL. A mixture of methanol and water (1:1 v/v) was used as diluent.
2.4. Preparation of Standard Solutions and Sample Solutions
Stock solutions of DRF (2.0 mg/mL) and all impurities (0.5 mg/mL each) were prepared by dissolving in minimum amount of methanol and made up to volume with diluent. Working solutions of DRF spiked and unspiked with impurities were prepared from the stock solution for the determinations of related substances and assay, respectively.
2.5. Forced Degradation Studies and Specificity
Specificity is the ability of the method to measure the analyte (DRF) response unequivocally in the presence of its possible impurities. The specificity of the developed HPLC method for DRF was determined in the presence of its process related impurities (Imp-1 to Imp-3 at 0.15%) and degradation products formed under stress. Forced degradation studies of drug can help to identify the likely degradation products, also they in turn can help to establish the degradation pathways and the intrinsic stability of the molecule. In order to develop a specific stability-indicating method, forced degradation studies were carried out on DRF active pharmaceutical ingredient powder. DRF was subjected to various stress conditions and generated samples were injected into HPLC at regular intervals and the final stress conditions were established in such a way to get significant degradation. Applied stress conditions are acidic hydrolysis (0.5 N HCl, reflux at 70˚C for 18 h), basic hydrolysis (1 N NaOH, reflux at 70˚C for 24 h), neutral hydrolysis (reflux at 70˚C for 24 h), oxidation (3% hydrogen peroxide, in the dark at room temperature for 10 days), thermal (DRF powder in a petri dish was placed in a temperature controlled dry air oven (Cintex Industrial Corporation, Mumbai, India) maintained at 60˚C for 10 days) , and Photo (DRF powder and solution were kept under fluorescent and UV light in a photostability chamber (Sanyo, UK) for a period of 1.2 million Lux hours and 200 Wh/m2, respectively). Samples of acid and base hydrolyses were neutralized, and all the degradation samples were diluted five times for assay determination. Assays were performed by comparison with standard and the mass balances (% assay + % impurities + % degradation products) were calculated for stressed samples. The three degradation samples of each stress were injected into an LC-PDA system to check the purity and homogeneity of the drug peak.
2.6. Method Validation
The validation of the developed HPLC method was carried out for the determination of related substances (Imp- 1 to Imp-3) and assay of DRF as per ICH guidelines to demonstrate that the method is appropriate for its intended use.
2.6.1. System Suitability
The system suitability tests were conducted and evaluated by injecting six replicates of 800 µg/mL (spiked with 0.15% of all impurities), and 100 µg/mL of DRF solutions for related substance and assay methods, respectively.
2.6.2. Precision
The system precision was evaluated by analyzing six replicates of standard solution for both assay (DRF 100 µg/mL) and related substances (DRF (800 µg/mL) spiked with 0.15% each impurity) individually. The method precisions for assay and related substances were evaluated by injecting six individual test preparations of DRF (100 µg/mL), and DRF (800 µg/mL) spiked with 0.15% each impurity, respectively. The intermediate precisions were evaluated on three different days by a different analyst using different batch column of same manufacturer and instrument located within the same laboratory. Precision at LOQ levels was also determined by injecting six individual preparations of mixture of all impurities spiked to DRF (800 µg/mL) at their LOQ level. The %RSDs of the areas of each impurity and assay of DRF were calculated for precision studies.
2.6.3. Limit of Detection (LOD) and Limit of Quantification (LOQ)
To establish the minimum concentration at which the analyte was reliably detected (LOD) and quantified (LOQ), the signal-to-noise ratios were determined. The LOD and LOQ for Imp-1, Imp-2, Imp-3 and DRF were estimated at a signal-to-noise ratio of 3:1 and 10:1, respectively, by injecting a series of dilute solutions with known concentrations.
2.6.4. Linearity
Linearity of the related substance method was established by analyzing series of dilute solutions at six different concentration levels ranging from LOQ to 250% to the specification level of impurities (i.e., LOQ, 0.6, 1.2, 1.8, 2.4, and 3.0 µg/mL) spiked into DRF drug substance (800 µg/mL). The calibration curves were drawn by plotting the peak areas of impurities against their corresponding concentrations. Similarly, assay method linearity was established by injecting DRF at five different concentration levels ranging from 50% to 150% (i.e., 50, 75, 100, 125, and 150 µg/mL) to DRF concentration 100 µg/mL. The correlation coefficients (r2), slopes and Y-in- tercepts of impurities and DRF were determined from their respective calibration plots.
2.6.5. Accuracy
Accuracy of the related substance method was evaluated by spiking known amounts of the impurities into the test sample, analyzing the same and calculating the percent recovered. For related substances, the recovery studies were performed in triplicate at three concentration levels (50%, 100% and 150%) to specification level (0.15%) of impurities (i.e., 0.6, 1.2, and 1.8 µg/mL) with respect to DRF drug substance concentration 800 µg/mL. The accuracy of the DRF assay was evaluated in triplicate at the three concentration levels 50%, 100% and 150% (i.e., 50, 100 and 150 µg/mL) to DRF concentration 100 µg/mL, and the recovery was calculated for each concentration.
2.6.6. Robustness
Robustness study was carried out to check the influence of small variations in the optimized chromatographic conditions. The typical parameters investigated include flow rate (±10% to 1.0 mL/min), mobile phase pH (±0.2 to 7.2), and column temperature (±3˚C to 25˚C). System suitability parameters and changes in assay of DRF and recoveries of impurities were checked. In all the above deliberately altered experimental conditions, the mobile phase compositions were held constant.
2.6.7. Solution Stability and Mobile Phase Stability
The solution stability of DRF and its impurities was carried out by leaving unspiked and spiked sample solutions in a tightly capped volumetric flask at 2˚C - 8˚C for 48 h. Content of impurities and assay of DRF were determined at 8 h intervals. Mobile phase stability was assessed by comparative analysis of freshly prepared sample solutions and freshly prepared reference standard solution up to 48 h.
3. Results and Discussion
3.1. Optimization of Chromatographic Conditions
The main objective of the development of a chromatographic method was to get the good separation of impurities and stress degradation products from DRF and each other. For method development DRF, DRF spiked with impurities, acid and oxidative stress generated samples were injected simultaneously. In the initial stages of method development with C18 stationary phase columns (Agilents’ XDB and Extend) showed very quick elution of Imp-1 and DRF along with peak asymmetry with several mobile phase compositions consisting of acetate/ phosphate buffers and acetonitrile/methanol due to their high polarity. To increase the retention of DRF, moderately polar C8 stationary phase column was employed instead of nonpolar C18 column. Replacement of C18 with C8 resulted in good peak parameters with increased retentions of Imp-1 and DRF compared to C18. As the pKa value of DRF (≈9.2) is higher, buffers with higher pH were chosen initially with C8 stationary phase column. Disodium hydrogen orthophosphate (0.02 M, pH adjusted to 7.0 with orthophosphoric acid) buffer with acetonitrile showed peak asymmetry (tailing > 2), but with methanol good peak parameters for DRF were resulted. At lower concentrations of methanol, peak fronting and higher retention times of analytes were observed. As the methanol concentration increases to decrease the LC run time, improvement in peak symmetry (tailing factor 1.05) with good column efficiency (Plate count > 9000) for DRF (assay peak) was observed, but showed co-elution of Imp-3 with DRF (spiked sample). Buffers with lower pH (≈4.0) showed peak asymmetry. Trails with mono phosphate buffer (KH2PO4) also resulted in same type of results.
Later, improved separation between analytes and difference in elution order was observed when phosphate buffer was replaced by ammonium acetate buffer. During method development with ammonium acetate buffer, several isocratic methods were employed and the effects of ionic strength of buffer, pH and organic modifier compositions on peak parameters were studied.
3.1.1. Effect of Buffer Concentration
The effect of concentration of ammonium acetate buffer on separation was studied by varying its concentration from 0.01 to 0.05 M on Prodigy C8 column maintained at 25˚C. The change in the concentration of ammonium acetate had shown no much effect on the retention of the analytes, and on resolution. But peak tailing of DRF was improved form >2 to <1.5 with an improvement in theoretical plates number from <2000 to >3000 with an increase in concentration of ammonium acetate from 0.01 to 0.05 M. Sharp symmetrical peaks with good resolution were obtained with 0.05 M ammonium acetate buffer. The desired symmetry and resolution were obtained with 0.05 M of ammonium acetate; it was used for further optimization of other variables.
3.1.2. Effect of Buffer pH
The effect of ammonium acetate buffer pH on peak parameters was studied from 4.0 to 7.5 (adjusted with acetic acid and ammonia solution). Buffer with pH 4.0 was found to be not suitable as the poor retention of Imp-1, Imp-3, degradation products, and DRF resulted coelution. At pH 5.0, better resolutions were also not achieved and tailing was found more for DRF. As pH increases to 6.0, DRF, impurities and degradation products were separated from each other with better resolutions, but failed to get desirable tailing factors and theoretical plates. With an increase of pH to 7.5, better resolutions were obtained with an improvement in peak parameters. Finally, after several trials with buffers at different pH, it could be seen that at pH 7.2, all the peaks with good resolutions and desirable peak tailings and theoretical plates were obtained.
3.1.3. Effect of Organic Modifier
Employment of different compositions of organic modifier using methanol and acetonitrile played key role in achieving optimized method. With methanol alone it was observed that, merging of DRF, degradation products, and Imp-3 at higher concentrations. Decrease of methanol percentage resulted in the enhanced retention of non- polar analyte Imp-2 and increase in resolutions with increase in peak fronting of DRF. Similarly, at higher percentage of acetonitrile coelution of DRF with degradation products and Imp-3 was observed. Unlike methanol, lower concentrations of acetonitrile resulted good resolutions with peak tailing. From these results we had come to a conclusion that combination of methanol and acetonitrile may result in a method that can be capable of eluting all the analytes with good resolutions with improved peak parameters. The effect of acetonitrile concentration in methanol (total organic modifier concentration was set as 60) was studied on peak parameters of DRF, and found that increase in tailing factor and increase in theoretical plates with increase in the percentage of acetonitrile. But it was observed that increase of acetonitrile percentage causes the lowering of resolution between degradation products and Imp-3. In order to increase the resolution, total organic modifier concentration was decreased to 55 without changing the acetonitrile percentage in methanol, and found increased resolution between Imp-3 and degradation products with no change in tailing factor and an additional improvement in theoretical plates number of DRF. Finally, 36% of acetonitrile was chosen as the optimized combination with methanol.
Finally, after several attempts, an optimized separation was accomplished on a Prodigy C8 (250 × 4.6 mm, 5 μm) column in an isocratic elution mode with a mobile phase composed of 0.05 M ammonium acetate (pH was adjusted to 7.2 with ammonia solution) and methanol with 36% acetonitrile in 45:55 (v/v) ratio at a flow rate of 1.0 mL/min and at a column temperature of 25˚C. The injection volume was set as 10 μL. Chromatogram showing the separation of impurities from DRF under optimized conditions is shown in Figure 2, samples of three different batches.
3.2. Specificity and Degradation Behavior of DRF
The assay of DRF for three determinations was found to be 99.5% with %RSD of 0.8; while in the presence of impurities (0.15% w/w) it was 99.2% with %RSD of 0.5. It suggests that the assay did not change in the presence of impurities. No considerable degradation of DRF was observed under neutral and basic hydrolytic, photolytic, and thermolytic stress conditions. Significant degradation of DRF drug substance was observed in acidic hydrolytic and oxidative stress conditions as shown in Figure 3. Peak purity test results obtained from PDA detector confirmed that the DRF peak was homogeneous and pure in all the analyzed stress samples. The mass balance of stressed samples was found in the range of 98.1% to 99.7%. The forced degradation results are summarized in Table 1. From references 3 and 4, the predicted structures of degradation products formed under acidic (A1 and A2) and oxidative (O1 and O2) stress are shown in Figure 1. Respective retention and relative retention times of degradation products are A1 = 8.35, 0.854; A2 = 13.02, 1.331; O1 = 6.80, 0.695; and O2 = 16.53, 1.690. Chromatogram of mixture of acidic and oxidative stress sample solution spiked with impurities showing good separation confirms the method specificity and selectivity (Figure 4).
3.3. Method Validation
3.3.1. System Suitability
System suitability data (Table 2) indicating that the system was suitable for use as the tailing factor for all the analytes was less than 1.2 and the resolution between any of the two adjacent eluting analytes was greater than 2.6. It also confirms the good selectivity of the method.
3.3.2. Sensitivity
The LOD and LOQ results of DRF and its three process related impurities estimated at a signal-to-noise ratio of 3:1 and 10:1 respectively were summarized in Table 2.
3.3.3. Precision
The %RSD results of precision studies (system, method, intermediate and at LOQ) for both DRF assay and related substances methods were found in the range of 0.23 - 0.79 and 0.32 - 4.82, respectively confirming the high precision of the method. The results of precision studies were given in Table 2.
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Figure 2. Chromatogram of DRF spiked with process related impurities.
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(b)
Figure 3. Typical chromatograms of DRF under stress (a) acidic hydrolysis, and (b) oxidation.
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Figure 4. Chromatogram of mixture of acidic and oxidative stress sample spiked with impurities.
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Table 1. Summary of forced degradation studies.
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Table 2. System suitability, linearity, sensitivity, precision, and accuracy data.
RT, retention time; Rs, resolution; kʹ, retention factor; As, tailing factor; N, number of theoretical plates; r2, correlation coefficient. aAverage of six determinations. bAverage of three determinations.
3.3.4. Accuracy
At each level, the obtained percentage recovery of DRF assay in the drug substance was ranged from 98.7 - 100.6, and the percentage recoveries of Imp-1, Imp-2, and Imp-3 were obtained in the range from 95.6 - 100.1. These good recovery results confirm the quantitative ability of the method. The recovery results were given in Table 2.
3.3.5. Linearity
The linear calibration plot for the DRF assay method was obtained over the tested calibration range (50 - 150 µg/mL) and the correlation coefficient obtained was greater than 0.999. The linear calibration plots for the related substances were drawn over the calibration ranges LOQ to 3.0 µg/mL, and correlation coefficients obtained were greater than 0.996. The obtained results for both assay and related substances methods showed an excellent correlation between the peak area and analyte concentration revealed the good linearity of the method. Linearity data of DRF and impurities is given in Table 2.
3.3.6. Robustness
Careful evaluation of deliberately varied conditions such as flow rate (0.9 and 1.1 mL/min), pH (7.0, and 7.4), and column temperature (22˚C and 28˚C) showed that the resolution between any two adjacent analytes was greater than 2.0 and tailing factors obtained below 1.5; and variability in the estimation of DRF assay and related substances recovery was within ±1% and ±9%, respectively indicating the robustness of the method.
3.3.7. Solution Stability and Mobile Phase Stability
The %RSDs of DRF assay and three impurities during the solution and mobile phase stability experiments were within 1% and 7% respectively. No significant change observed in the assay of DRF and content of impurities during solution stability and mobile phase stability experiments confirming that sample solutions and mobile phase used during the study were stable up to 48 h.
4. Conclusion
A simple and rapid isocratic stability-indicating reversed phase high-performance liquid chromatography method for the determination of DRF and its process-related impurities was developed and validated. Various forced degradations were performed on DRF according to ICH guidelines to study the specificity of the developed method. All of the degradation products and process impurities were well-separated from the drug substance confirming the stability-indicating power of the method. The developed method has been found to be selective, accurate, sensitive and precise, and is applicable for detecting process related substances and possible degradation product which may be present at trace level in bulk drugs.
NOTES
*Corresponding author.