Keyur B. Ahir, Emanual M. Patelia* and Falgun A. Mehta
Department of Pharmaceutical Chemistry and Analysis, Indukaka Ipcowala College of Pharmacy, New Vallabh Vidyanagar – 388121, Gujarat, India
Received date: August 02, 2012; Accepted date: September 20, 2012; Published date: September 25, 2012
Citation: Ahir KB, Patelia EM, Mehta FA (2012) Simultaneous Estimation of Nebivolol Hydrochloride and Hydrochlorothiazide in Tablets by TLC-Densitometry. J Chromat Separation Techniq 3:141. doi:10.4172/2157-7064.1000141
Copyright: © 2012 Ahir KB, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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A simple, rapid and accurate thin-layer chromatography (TLC)–densitometric method has been established and validated for the simultaneous determination of nebivolol hydrochloride and hydrochlorothiazide in tablets. The method is based on TLC separation of the two drugs followed by densitometric measurements of their spots at 281 nm. The separation was carried out on Merck TLC aluminium plate of silica gel 60F 254 using toluene:ethyl acetate:methanol:ammonia (3:2.7:1.7:0.1 v/v/v) as a mobile phase. Nebivolol hydrochloride and hydrochlorothiazide gave sharp and well defined peak at Rf 0.68 and 0.38, respectively. Calibration curves for nebivolol hydrochloride and hydrochlorothiazide were linear in range 500-3000 ng/spot and 1000-6000 ng/spot, respectively. Method was successively applied to tablet formulation. No chromatographic interferences from the tablet excipients were found. The method was validated in accordance with the requirements of ICH guidelines.
Nebivolol hydrochloride; Hydrochlorothiazide; TLCdensitometry; Validation; ICH guidelines
Nebivolol hydrochloride (NEB), α, α’ [iminobis (methylene)] bis [6-fluro-3, 4- dihydro-2H -1-benzopyran-2-methanol] hydrochloride is an antihypertensive [1,2].Nebivolol hydrochloride occurs in two isomeric forms . (+) Nebivolol acts as strong adrenergic β1 blocker whereas (-) nebivolol as vasodilator [4,5].
Hydrochlorothiazide (HCTZ), 6- chloro-3, 4-dihydo-2H-1, 2, 4-benzothizdiazine-7-sulfonamide1, 1 dioxide is a popular thiazide diuretics acts on the kidneys to reduce sodium (Na) reabsorption in the distal convoluted tubule .
Both these drugs are used in the treatment of arterial hypertension. The chemical structures of drugs are shown in Figure 1. A combination of both drugs is recently launched in the market.
In literature, various methods have been reported for the estimation of Nebivolol hydrochloride from pharmaceutical dosage form and biological fluids. The first order UV-spectrophotometry , reverse-phase HPLC/UV detection , enantiomeric resolution using HPLC , enantioseparation using chiral stationary phase , liquid chromatography/tandem mass spectrometry , liquid chromatography coupled with electro spray ionization tandem mass spectroscopy , are some of those. HPTLC densitometric quantitative analysis from tablet formulation [13,14] has been reported. Also several analytical methods are studied for determination of hydrochlorothiazide alone and in combinations with other drugs [15-21]. RP-HPLC method has been found for simultaneous determination of NEB and HCTZ in combined dosage form . NEB is not official in I.P., B.P or U.S.P. while HCTZ is official in I.P. B.P and U.S.P.
However, to our knowledge, no information related to the TLCdensitometry determination of NEB and HCTZ in pharmaceutical dosage forms has ever been mentioned in literature.
The present paper describes a reliable, rapid and accurate method for determination of NEB and HCTZ using TLC-densitometry.
Materials and reagents
Nebivolol hydrochloride and hydrochlorothiazide were kindly supplied as a gift sample by Cadila Pharmaceuticals Ltd., Dholka, and Ahmadabad India. All the reagents used were of analytical reagent grade (S.D. Fine Chemicals, Mumbai, India) and used without further purification.
Instrumentation and chromatographic conditions
The samples were spotted on TLC aluminium plate 60 F254 (20 cm×10 cm) with 200 μm thickness; (E MERCK, Darmstadt, Germany) using a Camag Linomat V (Switzerland).The samples were streaked in the form of narrow bands of width 6 mm with a constant application rate of 150 nl/ sec using nitrogen aspirator and the space between two bands was kept constant at 15.4 mm. The slit dimension was kept at 6 mm×0.45 mm. The mobile phase consists of toluene:ethyl acetate:methanol:ammonia (3:2.7:1.7:0.1 v/v/v). Linear ascending development was carried out in 20 cm×10 cm twin trough glass chamber (Camag, Muttenz, Switzerland). The optimized chamber saturation time for mobile phase was 20 min, at temperature (25°C ± 2°C); the relative humidity (60% ± 5%); the length of chromatogram run was 8 cm and TLC plates were air dried. Densitometric scanning was performed on Camag TLC Scanner 3 equipped with winCATS software version 1.3.0 at 281 nm. The source of radiation utilized was deuterium lamp.
Preparation of standard solutions and calibration graphs
The working standard solution 500 μg/mL of NEB and 1000 μg/mL of HCTZ were separately prepared in methanol. Different volumes in the range 1–6 μL of NEB and HCTZ solutions were over spotted on TLC plates with the help of microlitre syringe, using Linomat V sample applicator. The plate was developed and scanned in above established chromatographic conditions. Peak area was recorded for each concentration of drugs and curves (concentration vs. peak area) were constructed.
Precision: System precision of the method was assessed as repeatability and performed by spotting 1000 ng /spot of NEB and 2500 ng/spot of HCTZ.
Method precision was assessed as intra-day and inter-day variations. Intra-day and inter-day variations for the determinations of NEB and HCTZ was carried at three different concentration levels 1000, 1500, 2000 ng of NEB and 2500, 3750, 5000 ng of HCTZ, respectively.
Accuracy: Recovery experiment was checked by over spotting 80%, 100% and 120% of the mixed standard drug solution of NEB and HCTZ and the spots were reanalyzed by the proposed method. The experiment was conducted in triplicate. This was performed to check the recovery of the drug at different levels in formulation
Specificity: Specificity of the method was ascertained by analysing standard drug and sample solution. The mobile phase resolved both the drugs very efficiently, as shown in Figure 2. The spot for NEB and HCTZ was confirmed by comparing the Rf and spectra of the spot with that of standard. A typical absorption overlain spectrum of NEB and HCTZ shown in Figure 3; wavelength 281 nm was selected for densitometric scanning. Peak purity of NEB and HCTZ was assessed by comparing the spectra of sample with that of standard at three different levels, i.e., peak start (S), peak apex (M) and peak end (E) positions of the spot, as shown in Figure 4.
Robustness: Robustness was studied in six replicate at the concentration 1000 ng/spot of NEB and 2500 ng/spot of HCTZ. In this study, seven parameters (mobile phase composition, mobile phase volume, development distance, relative humidity, duration of saturation, time from spotting to chromatography and chromatography to spotting) were studied and the effects on the results were examined.
Ruggedness: The ruggedness of the proposed method was evaluated by two different analysts.
Limit of detection (LOD) and limit of quantification (LOQ): In order to determine detection and quantification limit, concentrations in the lower part of the linear range of the calibration curve were used. Stock solution of NEB and HCTZ was prepared and different volume of stock solution in the range 500 to 1000 ng for NEB and 1000 to 2000 ng for HCTZ were over spotted in triplicate. The amount of both the drugs by spot versus average response (peak area) was graphed and the equation for this was determined. The standard deviations (S.D.) of responses were calculated. The average of standard deviations was calculated (A.S.D.). LOD was calculated by (3.3×A.S.D.)/b and LOQ calculated by (10×A.S.D.)/b, where “b” corresponds to the slope obtained in the linearity study of method.
Analysis of nebivolol and hydrochlorothiazide marketed formulation
To determine the content of NEB and HCTZ simultaneously in conventional tablets (label claim 5 mg nebivolol and 12.5 mg hydrochlorothiazide); twenty tablets were accurately weighed, average weight determined and ground to fine powder. A quantity of powder equivalent to 5 mg nebivolol and 12.5 mg of hydrochlorothiazide was transferred into 25 ml volumetric flask containing 15 ml methanol, sonicated for 10 min and diluted to mark with same solvent and filtered using 0.45 μm filter (Millifilter, MA). Appropriate volume 5 μL was applied on TLC plate followed by development and scanning as described in section 2.2. The analysis was repeated for six times. Nebivolol and hydrochlorothiazide gave sharp and well defined peaks at Rf 0.68 and 0.38, respectively, when scanned at 281 nm. The results are shown in Table 1 indicate that there was no interferences from the excipients commonly present in the tablets.
|Component||Label Claim (mg)||% Label Claim*||% R.S.D.|
*mean of six estimations
Table 1: Assay of tablet formulation.
Optimization of HPTLC method
TLC procedures were optimized with a view to separate and quantify NEB and HCTZ from tablet formulation. Initially, mobile phase consisting of toluene, ethyl acetate and methanol was tried in the ratio of 3:2.5:1 (v/v/v), but the typical peak nature of chromatogram was missing. Therefore, the ratio of toluene, ethyl acetate and methanol was changed to 3:2.7:1.7 v/v/v. HCTZ showed symmetrical but tailing was observed with NEB. The peak tailing was overcome by adding 0.1 ml of ammonia to the mobile phase. Finally, the mobile phase consisting of toluene:ethyl acetate:methanol:ammonia (3:2.7:1.7:0.1 v/v/v) gave symmetric peak with good resolution. The Rf of NEB and HCTZ was found to be 0.68 ± 0.02 and 0.38 ± 0.02, respectively.
Linearity responses for NEB and HCTZ were assessed in the concentration ranges 500-3000 ng/spot and 1000- 6000 ng/spot, respectively. The linear equations for the calibration plots were Y=3.7582X+157.12 and Y=1.0178 X+8947.5, with correlation coefficient (r) being 0.9995 and 0.9991 for NEB and HCTZ, respectively. Calibration range was established with six replicate readings of each concentration.
Validation of the method
Precision: Precision of the method was determined in the terms of intra-day and inter-day variation (%R.S.D.). Intra-day precision (%R.S.D.) was assessed by analyzing standard drug solutions within the calibration range, three times on the same day.
Inter-day precision (%R.S.D.) was assessed by analyzing standard drug solutions within the calibration range on three different days over a period of week. The results are shown in Table 2.
|Drug||Amount applied ng/spot||Intra-day precision [%R.S.D., n = 3]||Inter-day precision [% R.S.D., n = 3]|
Table 2: Result of precision study.
Repeatability: Repeatability of sample application was assessed by spotting 1000 ng/spot of NEB and 2500 ng/spot of HCTZ solutions six times on a TLC, followed by development and scanning as described in section 2.2. The %R.S.D. for peak area of NEB and HCTZ was found to be 0.73 and 1.21, respectively.
Accuracy: To the preanalysed sample a known amount of standard solution of pure drug (NEB and HCTZ) was over spotted at three different levels. These solutions were subjected to re-analysis by the proposed method and results of the same are shown in Table 3.
|Component||Initial Amount (ng/spot)||% Amount of standard drug added||% Drug recovered *||% R.S.D.|
*mean of three estimations at each level
Table 3: Results of recovery studies.
c: The standard deviation of peak areas was calculated for each parameter and %R.S.D. was found to be less than 2%. The low values of %R.S.D. shown in Table 4 proved robustness of the method.
|S.D. of Peak Area||% R.S.D.||S.D. of Peak Area||% R.S.D|
|Mobile Phase Composition|
|Toluene: ethyl acetate: methanol: ammonia (3.2:2.9:1.9:0.1)||67.14||1.78||145.80||1.25|
|Toluene: ethyl acetate: methanol: ammonia (2.8:2.5:1.5:0.1)||50.08||1.34||133.44||1.16|
|Mobile Phase Volume|
|Duration of saturation|
|Activation of prewashed plates|
|Time from spotting to chromatography|
|Time from chromatography to scanning|
Table 4: Results from robustness studies.
Ruggedness: The ruggedness of the proposed method was evaluated by two different analysts. The results for NEB and HCTZ were found to be 98.66%, 99.79% and 100.03%, 100.42%, respectively.
LOD and LOQ: Detection limit and quantification limit was calculated by the method as described in section 2.4.6 The LOD and LOQ for NEB were 73.58 ng and 223.09 ng. For HCTZ, LOD and LOQ were found to be 101.12 ng and 309.46 ng, respectively. This indicates that adequate sensitivity of the method.
The summery of validation parameters were listed in Table 5.
|Linearity range (ng /spot )||500 - 3000||1000 - 6000|
|Limit of detection (ng /spot )||73.58||101.12|
|Limit of quantitation (ng/ spot)||223.09||309.46|
|% Recovery (n = 9)||1.45||1.62|
|Analyst I (n = 6)||1.88||1.82|
|Analyst II ( n = 6)||1.85||1.65|
|Repeatability (n = 6)||0.73||1.21|
|Inter-day (n = 3)||1.25 - 1.77||0.39 - 0.65|
|Intra-day (n = 3)||0.76 - 1.53||0.34 - 0.63|
Table 5: Summary of validation parameter.
The proposed HPTLC method provides simple, accurate and reproducible quantitative analysis for simultaneous determination of NEB and HCTZ in tablets. The method was validated as per ICH guidelines.
authors are thankful to R.C. Patel College of Pharmacy, Shirpur Dist: Dhule (M.S.) India 425 405 for providing necessary facilities.
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