Micellar High Performance Liquid Chromatographic Method for Simultaneous Determination of Clonazepam and Paroxetine HCl in Pharmaceutical Preparations Using Monolithic Column

A new and accurate micellar high performance liquid chromatographic method coupled with ultraviolet detection was developed for simultaneous determination of Clonazepam (CLZ) and Paroxetine (PRX) using a monolithic C-18 column, and mobile phase consisting of 0.175M Sodium dodecyl sulphate, 12% n-propanol prepared in 0.02M phosphoric acid at pH 6.0. The analysis was performed at a flow rate of 1 mL/min with ultravioletdetection at 300 nm. The method was linear over the concentration range (1.0-20 μg) and (4.0-250 μg) with limits of detection of 0.277, 2.675 μg/mL and limits of quantification of 0.838, 8.106 μg/mL for CLZ and PRX respectively. The average % recovery was found to be 100.08 ± 1.31 and 100.22 ± 1.15 for CLZ and PRX respectively. Method validation according to ICH Guidelines recommendation was evaluated. Statistical analysis of the results obtained by the proposed method was compared successfully with those obtained using the reference one. There was no significance difference between the two methods regarding accuracy and precision respectively.

Paroxetine was the first antidepressant formally approved in the United States for the treatment of panic attacks [21].
Paroxetine co administered with clonazepam demonstrated significant improvement by endpoint. Combined treatment with paroxetine and clonazepam resulted in more rapid response than with the SSRI alone [37].
Up till now there was not any micellar HPLC method for simultaneous determination of Paroxetine and Clonazepam in the tablet dosage forms. There is one method for the simultaneous determination of clonazepam and paroxetine by RP-HPLC [38]. Our method is more sensitive and we use a smaller amount of organic solvent comparing to the other method (using 60% acetonitrile). For these reasons we are encouraged to perform the present work which determines CLZ and PAX simultaneously using monolithic column.

Experimental
Apparatus HPLC using a Chromatograph separation was carried out using a (Merck Hitachi model L-7100) equipped with a Rheodyne injector valve with a 20 µL loop, and an ultraviolet detector (Merck Hitachi L-7400), operated at 300 nm. The chromatograms were recorded on a Shimadzu C-R6A integrator. Mobile phase was filtered using membrane filters (Millipore, Ireland) and degassed using Merck solvent L-7612 degasser. pH-meter used is Consort P-901. Ultrasonic bath, model SS 101 H 230, USA. Volumes of 20.0 µL were injected (triplicate) and eluted with the mobile phase under the optimum chromatographic conditions. The peak areas against the final concentration of the drugs in µg/mL were drawn. And the corresponding regression equations were obtained.
Analysis of CLZ/PRX laboratory prepared mixtures by the proposed method: Aliquots of CLZ and PRX standard solutions at a pharmaceutical ratio of 1: 50 [39]. Were transferred into a series of 10.0 mL volumetric flasks. The solutions were diluted to the volume with the mobile phase and mixed well. Procedure described under "Construction of the Calibration Graphs" was then applied. The mean percentage recoveries were calculated by referring to the calibration graphs, or using the corresponding regression equations.

Analysis of the two drugs in their single tablets by the proposed method:
The content of ten tablets (Amotril ® , Seroxat ® CR) were accurately weighed, finely powdered, and thoroughly mixed. Accurately weighed amounts of the powdered tablets equivalent to 0.5 mg of CLZ or 12.5 mg of PRX were transferred into a 100 ml volumetric flask and extracted with 80 mL of methanol. The contents of the flask were sonicated for 30 min, completed to the volume with the same solvent and filtered. Filtration utilizing syringe filter was performed to get clear solutions. Aliquots containing suitable concentrations of the studied drugs were analyzed as described under "construction of the calibration graphs". The nominal content of each drug was calculated either from a previously plotted calibration graph or using the corresponding regression equation.
Analysis of the two drugs in their laboratory prepared co-formulated tablets by the proposed method: Co-formulated tablets were prepared, according to their pharmaceutical ratio (1:50). Weighed quantity of mixed laboratory prepared tablets equivalent to 0.25 mg CLZ and 12.5 mg PRX were transferred into 100 mL volumetric flasks and about 80 mL of methanol were added. The contents of the flask were sonicated for 30 min, completed to the volume with the same solvent and filtered twice using syringe filters to get highly clear filtrate. Volumes containing different concentrations of CLZ and PRX were taken and analyzed as described under construction of the calibration graphs. The content of each drug was calculated either from the already plotted calibration graphs or by using the corresponding regression equations.

Results and Discussion
A micellar HPLC method coupled with ultraviolet detection was developed and fully validated for the simultaneous determination of CLZ and PRX.
The proposed method can separate CLZ and PRX with good resolution, as the retention time between CLZ and PRX less than 5 min. The experimental parameters influencing the chromatograms of the studied drugs were accurately considered and optimized. The optimal parameter gives the highest number of theoretical plates and the best resolution within a reasonable time. Figure 2 shows a typical chromatogram for laboratory prepared mixture of CLZ and PRX under the described chromatographic conditions and the detection was performed at 300 nm. The separation was achieved within short retention time (t r =1.36 and 4.9 min) for CLZ and PRX, respectively.

Materials and reagents
• Clonazepam CLZ: was kindly provided from Egyptian International Pharmaceutical Industry Company (EIPICO), with a purity of 99.3% as determined by the comparison method.
• Paroxetine HCl: was kindly provided by Pharaonia pharmaceuticals company (Alexandria, Egypt), with a purity of 99.8% as determined by the comparison method.
• All the pharmaceuticals used were obtained from Egyptian market.

Chromatographic conditions:
Chromolith® speed ROD C-18 (50 mm × 4.6 mm i.d., 2 µm particle sizes), Merck, Germany. Mobile phase: a solution consists of a mixture of 12% n-propanol and 0.175 MSDS and the pH was adjusted to 6.0 using orthophosphoric acid. The mobile phase was filtered through Millipore membrane filter. Flow rate: 1 mL/ min. Ultraviolet detection: 300 nm.
Standard solutions: Stock solutions were prepared by dissolving either 10.0 mg of CLZ or 10.0 mg PRX in 100.0 mL of methanol to give solution containing 100 µg/ml using ultrasonic bath for good solubility. Working standard solutions were prepared by appropriate dilution of the stock solutions with methanol. All solutions were stored in the refrigerator at 2°C and found to be stable for at least 7 days. Choice of column: Two different columns were tried for performance investigations, including: Promosil ODS C18 column (250 × 4.6 mm i.d., 5 µm particle size), Agela Technologies, USA and Chromolith® speed ROD C-18 (50 mm × 4.6 mm i.d., 2 µm particle sizes), Merck, Germany. Experimental studies revealed that, the second column was the appropriate one, giving symmetrical, well defined peaks with good resolution within reasonable time. The first column was not suitable as it showed disturbed overlapped peaks.

Concentration of SDS:
The effect of the concentration of SDS on the selectivity and retention time of the drugs was studied using mobile phase containing concentration of 0.1 to 0.2M SDS. It was found that 0.175M of SDS was the optimum conc.
pH of the mobile phase: The influence of pH changing on the retention time of CLZ and PRX was studied over the range of (4.0-6.5), pH 6.0 was the most appropriate pH as it gives symmetrical peaks within reasonable time and high number of theoretical plates as shown in Table 1.
Type of organic modifier: Different organic modifiers were tried including methanol, n-propanol and n-butanol. It was found that n-propanol was the organic modifier of choice as it gives the most symmetrical separated peaks. Methanol was found to give a precipitate in the mobile phase and n-butanol gives non symmetrical peaks.

Concentration of organic modifier:
The effect of increasing the % concentration of n-propanol on the chromatographic behavior was studied over the range of (8% -14%). It was found that 12% (v/v) was the most appropriate concentration as it gives the highest number of theoretical plate and good resolution. As shown in Table 1.

Choice of detection wavelengths:
The effect of changing wavelength on the chromatographic behavior of both drugs was investigated over the range (290-320 nm). We use the wavelength that gives the maximum peak for paroxetine to enable us to determine both drugs simultaneously. It was found that 300 nm was the most suitable wavelength found for the determination and separation since it gives the symmetrical peaks for both drugs with high number of theoretical plates and good resolution.

Development and validation of the analytical method
The validity of the proposed method was tested regarding linearity, specificity, accuracy, repeatability and precision according to ICH Q2R1 recommendations [40]. Where the P is the peak area, C is the concentration of the drug in µg/ mL and r is the correlation coefficient.
Statistical analysis [41] of the data gave a reasonable value of the correlation coefficient (r) of the regression equation, accepted values of the standard deviation of residuals (S y/x ), standard deviation of intercept (S a ), and standard deviation of slope (S b ), and accepted value of the percentage relative standard deviation and the percentage relative error ( Table 2). These data proved the linearity of the calibration curve and low scattering of the points around the calibration curve.

Limit of Quantitation (LOQ) and limit of detection (LOD):
The limit of quantitation (LOQ) is the minimal concentration which can be determined based on ICH Q2R1 recommendations (40) under which the calibration plot is non linear.
The limit of detection (LOD) is the minimum analyte concentration which can be detected (41).
Where S a =standard deviation of the intercept of the calibration curve and b=slope of the calibration curve.
LOQ and LOD values for CLZ and PRX by the suggested method were showed in Table 2 using the comparison chromatographic methods [42,43] for CLZ and PAX respectively. The comparison method for CLZ involved the use of methanol and ammonium phosphate (50:50 v/v) adjusted to pH 8.0 and detected ultravioletly at 254 nm, and for PAX involved the use of dipotassium hydrogen phosphate and Acetonitrile (90: 10 v/v), adjusted to pH 6.5 and detected spectrophotometrly at 295 nm. Statistical analysis of the results obtained by the proposed method and comparison methods using Student's t-test and variance ratio F-test [41] revealed no significant difference between the performance of the two methods regarding the accuracy and precision, respectively (Table 3).

Precision
I. Intra-day precision: Intra-day precision was assessed through replicate analysis of three concentrations of the studied drugs on three successive times within the same day. The results are shown in Table 4.
II. Inter-day precision: Inter-day precision was carried out through replicate analysis of three concentrations of the studied drugs on three successive days. The results are summarized in Table 4.

Robustness of the method:
The robustness of the method was assessed by evaluating the influence of small variation of experimental variables: concentrations of organic modifier (12% ± 1), pH (6.0 ± 0.1), and conc. of SDS (0.175M ± 0.01) on the analytical performance of the method. In these experiments, one experimental parameter was changed while the other parameters were kept unchanged, and the recovery percentage was calculated each time. The minor changes in these experiment parameters did not significantly affect the peak areas; recovery percentage in case of CLZ is 100.08 ± 1.31 and in case of PRX is 100.22 ± 1.15 respectively.

Selectivity:
The proposed MLC method was considered selective by detecting any change resulted from common tablet additives such as lactose, starch, magnesium stearate, and talc. The high mean % recovery and high accuracy with low SD indicated that excipients did not affect the results of the proposed method.

Applications
Application of the proposed method to the analysis of CLZ/ PRX laboratory prepared mixtures: CLZ and PRX can be determined in laboratory prepared mixtures simultaneously by the suggested method in ratios of 1:50 (Figure 3). Both drugs can be quantitated in the laboratory prepared mixtures concerning the linear regression equations of the calibration plots.
The results shown in Table 5 are in good agreement with those obtained using the official methods [42,43]. Student's t-test and variance ratio F-test statistically analyzed the results [41] and showed no significant difference between the two methods concerning the accuracy and precision, respectively. Good recoveries, 99.86 ± 1.58 and 100.25 ± 1.443 were achieved for CLZ and PRX, respectively.

Pharmaceutical application
Application of the proposed method to the analysis of laboratory prepared co-formulated tablets: The proposed method was successfully applied to the estimation of CLZ and PRX in their laboratory prepared co-formulated tablets. The results listed in Table  6 show a good agreement with those by the official method [42,43]. Student's t-test and variance ratio F-test [41] analyzed the results obtained by the proposed method and showed no significant difference   between it and the official method [42,43] concerning the accuracy and precision, respectively. Good recoveries, 100.02 ± 0.59 and 100.19 ± 1.33 were achieved for CLZ and PRX respectively, from their prepared tablets in 1:50 ratio, respectively. Figure 4 shows chromatograms indicating good resolved peaks of CLZ and PRX in their laboratory prepared co-formulated tablets.

Analysis of CLZ and PRX tablets:
The proposed method was successfully applied to the assay of the studied drugs in single dosage forms. The results of the proposed method were favorably compared with those obtained using the comparison method [42,43]. Mean percent recoveries from Amotril ® 0.5 mg CLZ tablets and Seroxat ® CR 12.5 mg PRX tablets were 99.96 ± 0.59 and 99.99 ± 1.27, respectively.
The results shown in Table 7 are in good agreement with those obtained with the comparison method [42,43]. Statistical analysis of the results obtained using Student's t-test and variance ratio F-test [41] revealed no significant difference between the performance of the two methods regarding the accuracy and precision, respectively. Figure 5 shows chromatograms indicating good resolved peaks of CLZ and PRX in their dosage forms.

Conclusion
A simple, accurate and validated chromatographic method with ultraviolet detection was proposed for the simultaneous determination          of CLZ and PRX in binary mixtures. In addition, it could be applied to the analysis of both drugs in their single and laboratory prepared coformulated dosage forms without any interference from the common excipients and the results show good agreement with those obtained by the comparison method.