Chromatography Research International

Chromatography Research International / 2012 / Article

Research Article | Open Access

Volume 2012 |Article ID 273604 | 6 pages | https://doi.org/10.1155/2012/273604

Development and Validation of a Stability-Indicating HPTLC Method for Analysis of Rasagiline Mesylate in the Bulk Drug and Tablet Dosage Form

Academic Editor: Wenkui Li
Received02 May 2011
Revised18 Jul 2011
Accepted02 Oct 2011
Published06 Feb 2012

Abstract

A simple and sensitive thin-layer chromatographic method has been established for analysis of rasagiline mesylate in pharmaceutical dosage form. Chromatography on silica gel 60 F254 plates with 6 : 1 : 2(v/v/v) butanol-methanol water as mobile phase furnished compact spots at   . Densitometric analysis was performed at 254 nm. To show the specificity of the method, rasagiline mesylate was subjected to acid, base, neutral hydrolysis, oxidation, photolysis, and thermal decomposition, and the peaks of degradation products were well resolved from that of the pure drug. Linear regression analysis revealed a good linear relationship between peak area and amount of rasagiline mesylate in the range of 100–350 ng/band. The minimum amount of rasagiline mesylate that could be authentically detected and quantified was 11.12 and 37.21 ng/band, respectively. The method was validated, in accordance with ICH guidelines for precision, accuracy, and robustness. Since the method could effectively separate the drug from its degradation products, it can be regarded as stability indicating.

1. Introduction

Rasagiline mesylate (Figure 1) is a chemical inhibitor of the enzyme monoamine oxidase type-B which has a major role in the inactivation of biogenic and diet-derived amines in the central nervous system. Rasagiline is a propargylamine-based drug indicated for the treatment of idiopathic Parkinson’s disease. It is designated chemically as (R)-N-(prop-2-ynyl)-2,3-dihydro-1H-inden-1-amine. Rasagiline is freely soluble in water and ethanol and sparingly soluble in isopropyl alcohol. It is a chiral compound with one asymmetric carbon atom in a five-member ring with an absolute R-configuration which is produced as single enantiomer [1].

There are many methods reported in the literature for analysis of rasagiline mesylate, for example, GC-MS [2], HPLC methods [35], LC-MS/MS in human plasma [6], and spectrophotometric methods [7, 8]. However, no available densitometric method for the simultaneous separation of rasagiline mesylate from degradation products has been reported. Hence, the objective of the present study is to develop and validate a new HPTLC method for the estimation of rasagiline mesylate in bulk drug and its dosage form.

Today, HPTLC is rapidly becoming a routine analytical technique due to its advantages of low operating costs high sample throughput, and need for minimum sample preparation. The major advantage of HPTLC is that several samples can be run simultaneously using a small quantity of mobile phase unlike HPLC, thus reducing the analysis time and cost per analysis [9]. Accordingly, the aim of the present study was to establish the inherent stability of rasagiline mesylate through stress studies under a variety of ICH recommended test conditions [10, 11] and to develop a stability-indicating HPTLC assay [12]. The proposed method was validated according to the ICH guidelines [13].

2. Experimental

2.1. Materials and Reagents

Rasagiline mesylate was obtained from Orchid Pharmaceuticals Ltd (Chennai, India). It was used without further purification and certified to contain 99.67% (w/w) on dry weight basis. Rasagiline Mesylate Pharmaceutical preparation, Rasipron was purchased from a local drug store; it contained 1 mg active material. The other chemicals and reagents used were of AR grade and procured from S.D. Fine-Chem (New Delhi, India).

2.2. HPTLC Instrumentation

Chromatography was performed on 10 cm × 10 cm aluminium foil plates precoated with 0.2 mm layers of silica gel 60 F254 (E. Merck, Germany). Before use, the plates were prewashed by development with methanol then dried in the current of dry air and activated at 60°C for 5 min. Samples were applied as bands 6 mm wide, 15 mm apart, by use of a Camag (Switzerland) Linomat 5 equipped with a microlitre syringe. A constant application rate of 150 nL s−1 was used. Butanol methanol water 6 : 1 : 2 (v/v/v) was used as the mobile phase. Linear ascending development was performed in a twin-trough glass chamber previously saturated with mobile phase vapour for 30 min at room temperature (RT, 25 ± 2°C) and relative humidity 60 ± 5%. The development distance was approximately 80 mm. After development, the plates were dried in current of air by use of an air dryer. Densitometric scanning, at 254 nm, was performed with a Camag TLC scanner 3 in absorbance mode. The source of radiation was a deuterium lamp emitting a continuous UV spectrum in the range 190–400 nm.

2.3. Calibration Plots of Rasagiline Mesylate

A stock solution containing 100 μg/mL of rasagiline mesylate was prepared by dissolving an accurately weighed 10 mg portion of the drug in methanol in 100 mL volumetric flask. Different volumes of stock solution (1, 1.5, 2, 2.5, 3, 3.5 μL) were spotted on an HPTLC plate in triplicate to obtain concentrations of 100, 150, 200, 250, 300, and 350 ng/band of rasagiline mesylate, respectively. The data of peak area versus drug concentration were treated by linear least-squares regression.

2.4. Method Validation
2.4.1. Precision

The precision of the method was verified by repeatability and intermediate precision studies. Repeatability studies were performed by analyzing three different concentrations (100, 200, and 300 ng/spot) of the drug by six times on the same day. The intermediate precision of the method was checked by repeating on three different days.

2.4.2. Robustness

The analytical conditions were deliberately changed, by introducing small changes in mobile phase composition (±2%), mobile phase volume (±2%), chamber saturation period (±10%), and development distance (±10%), and time from application to development (0, 10, 15, 20 min) and time from development to scanning (0, 30, 60, 90 min) were carried out.

2.4.3. LOD and LOQ

The method was used to determine the LOD and LOQ. Blank methanol was spotted six times, and the SD of the peak area of the blanks was calculated. The limits were determined from the slope of the calibration plot and the SD of the response for the blank sample by use of the formula:

2.4.4. Accuracy

To check the degree of accuracy of the method, recovery studies were performed in triplicate by standard addition method at 50, 100, and 150%. Known amount of standard rasagiline mesylate was added to preanalysed samples and was subjected to the proposed HPTLC method.

2.4.5. Specificity

The specificity of the method was determined by comparing the results for the standard drug and the sample. The peak purity of the sample was assessed by comparing the spectra at peak start, peak apex, and peak end positions of the band.

2.4.6. Forced Degradation Studies of Rasagiline Mesylate

A stock solution containing 10 mg rasagiline mesylate in 100 mL methanol (100 μg/mL) was used for forced degradation to provide an indication of the stability-indicating ability and specificity of the proposed method. Studies of acid-induced decomposition were performed by exposing the solution of the drug to 5 M hydrochloric acid by heating the solution under reflux at 80°C for 5 h. Studies of base-induced decomposition were performed in 5 M sodium hydroxide, and the solution was heated under reflux for 3 h at 80°C. The resulting solutions were applied on TLC plate in triplicate (2.5 μL each, i.e. 250 ng/band). The plate was chromatographed as described above. Oxidative degradation was studied by refluxing the drug solution to 30% hydrogen peroxide for 4 h at 80°C. The resulting solution was applied to TLC plates such that 250 ng per band was applied to the plates. Neutral hydrolysis was carried out by accurately weighing 25 mg of the drug in 25 mL HPLC grade water, and the solution was refluxed for 12 hrs at 50°C. Appropriate aliquot was taken from the above solution and diluted with methanol to obtain a final concentration of 100 ng/μL. The resultant solution (2.5 μL) was applied to TLC plate (250 ng/spot), and the chromatogram was run to evaluate the degradation effect. Similarly, dry heat degradation also carried out by placing the standard drug in solid form in an oven at 100°C for 10 hrs. Rasagiline mesylate 1 mg was accurately weighed and separately dissolved in methanol in 10 m L volumetric flask. The resultant solution was applied to TLC plate in such a way that final concentration achieved was 250 ng/spot. The photochemical stability of the drug was also studied by exposing the stock solution to direct sunlight (60,000–70,000 lux) for 24 h on a wooden plank and kept on terrace. The solution (2.5 μL, equivalent to 250 ng/band) was then applied to TLC plates, and densitograms were obtained as described above. The densitogram was run in triplicate in all the conditions to evaluate the degradative effect.

2.5. Analysis of Rasagiline Mesylate in Tablet Dosage Form

To determine the rasagiline mesylate content of conventional tablets, twenty tablets were weighed and powdered in a glass mortar. An amount of powder equivalent to 10 mg rasagiline mesylate was transferred to a 100 mL volumetric flask, extracted with methanol, sonicated for 20 min, and diluted to volume with same solvent. The resulting solution was filtered through a 0.45 μm filter (Millifilter; Milford, MA; USA). The solution (2.5 μL, 250 ng rasagiline mesylate) was applied in triplicate on an HPTLC plate for quantification using the proposed method.

3. Results and Discussion

3.1. Optimization of the Mobile Phase

Several solvent mixtures in different ratios were tested to obtain a compact band of rasagiline mesylate. Butanol : methanol : water 6 : 1 : 2 v/v/v) was found to give a compact band for rasagiline mesylate with an value of (Figure 2). This mobile phase gave good resolution for the separation of rasagiline mesylate, all degradation products, and was selected for the proposed stability-indicating method. Thirty minutes was found to be sufficient for saturation of the development chamber with the mobile phase vapor in order to obtain separation of the compounds. A 20 mL aliquot of mobile phase was used for a 20 min development over a distance of 80 mm.

3.2. Calibration Plots of Rasagiline Mesylate

The linear regression analysis data for the calibration plots showed a good linear relationship () with respect to peak area in the concentration range of 100–350 ng/band (Figure 3). The mean values of the slope and intercept were and , respectively, for densitometric analysis at 254 nm (Table 1).


ParameterRasagiline mesylate

Linearity100–350 ng/band
Correlation coefficient, ±SD
Slope ±SD
Intercept ±SD
LOD, ng/band11.12
LOQ, ng/band37.21

3.3. Method Validation
3.3.1. Precision

The results of the repeatability and intermediate precision experiments are shown in Table 2. Inter precision studies were checked by both interday and intraday analysis. Interday analysis was carried out by repeating the experiments on three different days, whereas intraday analysis was done for 3 times on the same day. The developed method was found to be precise as the RSD values for repeatability and intermediate precision studies were <2%, respectively, as recommended by ICH guideline.


Concentration (ng/spot)RepeatabilityIntermediate precision
Mean ± SD (ng/spot)RSD (%)Mean ± SD (ng/spot)RSD (%)

100 1.98 1.76
200 0.84 0.76
300 0.36 0.60

3.3.2. Robustness

The low values of RSD obtained after introducing small, deliberate changes in the mobile phase composition, mobile phase volume, chamber saturation time, time from application to development, and time from development to scanning in the developed HPTLC method indicated the robustness of the method. The % RSD values of all the above-mentioned parameters are shown in Table 3.


Parameters% RSD

% change in mobile phase
Chamber saturation time
Development distance
Time from application to development
Time from development to scanning

3.3.3. LOD and LOQ

LOD and LOQ were determined by the SD method and were found to be 11.12 and 37.21 ng/band, respectively (Table 1).

3.3.4. Accuracy

Accuracy of the method was obtained by recovery after spiking with 50, 100, and 150% of additional drug. The study was carried out in triplicate by standard addition method and found to be in the range of 99.10–101.0% (Table 4).


Excess drug added to the analyte (%)Amount of drug found (ng)% Recovery% RSD

0100.099.100.72
50151.6101.060.49
100198.499.210.31
150252.2100.880.44

Matrix containing 100 ng of drug. .
3.3.5. Specificity

The value () of the sample and standard was almost identical, and spectra of the sample and the standard were superimposable. These results indicated the specificity of the method.

3.3.6. Stability in Sample Solution

Solutions of two different concentrations (150 and 200 ng/spot) were prepared from sample solution and stored at room temperature for 6.0, 12.0, 24.0, 48.0, and 72.0 h, respectively. They were then applied on the same TLC plate after development, the chromatogram was evaluated as listed in (Table 5) for additional spots if any. The % RSD for the samples analyzed at different elapsed assay times was found to be <2%. Thus, the drug was stable in solution state. There was no indication of compound instability in the sample solution.


Actual (ng)Area meanArea range% RSD

813.1943809.0121–819.58170.58
200 1120.82681116.3661–1129.7529 1.58

.
3.3.7. Forced Degradation Studies of Rasagiline Mesylate

The bands of degradation products were well resolved from the drug bands. The peak of rasagiline mesylate was not significantly shifted in the presence of degradation peaks, which indicated the stability-indicating property of the proposed method. The number of degradation products with their values under different stress conditions is shown in Table 6.


ConditionTime (h)Recovery (%)(%) value of degraded products

5 M HCl refluxed at 80°C547.507.53, 44.96
5 M NaOH refluxed at 80°C346.9222.92, 11.96, 18.75
H2O2 30% v/v refluxed at 80°C463.305.45, 9.89, 21.37
Daylight24100None detected
Dry heat degradation10100None detected
Neutral hydrolysis (Reflux at 50º C)12100None detected

The chromatograms, of the samples treated with acid, base, hydrogen peroxide, and sunlight showed well-separated bands of pure rasagiline mesylate as well as some additional bands of the degradation products at different values (Table 6).

Drug recovery from the acid-stressed sample was found to be 47.50%. Base-stressed samples showed recovery at the level of 46.92% (Table 6). The chromatogram of the acid-degraded sample showed two additional bands at values of 0.20 and 0.42 (Figure 4). The chromatogram of the base-degraded sample showed three additional bands at values of 0.26, 0.52, and 0.67 (Figure 5).

The chromatogram of the sample of rasagiline mesylate treated with 30% (v/v) H2O2 had three additional bands at 0.43, 0.53, and 0.68 showing that rasagiline mesylate was susceptible to oxidation-induced degradation (Figure 6). Rasagiline mesylate remained stable in neutral, thermal, and photolytic conditions. All the above conditioned parameters showed recovery at the level of 100% suggesting that the drug does not undergo degradation in neutral, thermal, and photolytic conditions.

3.3.8. Analysis of Rasagiline Mesylate in Tablet Dosage Form

A single spot at was observed in the chromatogram of the drug samples extracted from tablets. There was no interference from the excipients commonly present in the tablets. The drug content was found to be 99.98% with a % RSD of 0.57 (). The low % RSD value indicated the suitability of this method for routine analysis of rasagiline mesylate in pharmaceutical dosage form.

4. Conclusion

The introduction of HPTLC to pharmaceutical analysis is a major step in quality assurance. This HPTLC technique is precise, specific, accurate, and stability indicating. Statistical analysis proved the method is suitable for analysis of rasagiline mesylate as the bulk drug and in a pharmaceutical formulation without interference from excipients. This is a typical stability-indicating assay, established in accordance with the recommendations of the ICH guidelines. The method can be used to determine the purity of a drug, and it is also proposed for analysis of drug and degradation products in stability samples obtained during industrial production.

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Copyright © 2012 Singaram Kathirvel et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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