HPTLC Method for the Simultaneous Estimation of Valsartan and Hydrochlorothiazide in Tablet Dosage Form

A simple, precise, accurate and rapid high performance thin layer chromatographic method has been developed and validated for the simultaneous estimation of valsartan and hydrochlorothiazide in combined dosage forms. The stationary phase used was precoated silica gel 60F 254 . The mobile phase used was a mixture of chloroform: methanol: toluene: glacial acetic acid (6:2:1:0.1 v/v/v/v). The detection of spots were carried out at 260 nm. The method was validated in terms of linearity, accuracy, precision and specificity. The calibration curve was found to be linear between 300 to 800 ng/spot for valsartan and 100 to 600 ng/spot for hydrochlorothiazide. The limit of detection and the limit of quantification for the valsartan were found to be 100 and 300 ng/spot respectively and for hydrochlorothiazide 30 and 100 ng/spot respectively. The proposed method can be successfully used to determine the drug content of marketed formulation.

Valsartan and hydrochlorothiazide (25 mg) each were weighed accurately, dissolved and diluted with methanol to obtain the final concentration of 100 µg/ml of each drug.Twenty tablets were weighed accurately and ground to a fine powder.Weight equivalent to 25 mg of valsartan and hydrochlorothiazide were transferred to conical flask and mixed with methanol.The solution was sonicated for 15 min.The extracts were filtered through Whatman filter paper No. 41 and residue was washed thoroughly with methanol.The extracts and washing were pooled and transferred to a 250 ml volumetric flask and volume was made up to 250 ml with methanol.Required dilutions were made to get 100 µg/ml of valsartan and hydrochlorothiazide.
TLC plates were prewashed with methanol.Activation of plates was done in an oven at 50 0 for 5 min.The chromatographic conditions maintained were precoated silica gel 60F 254 aluminum sheets (10×10 cm) as stationary phase, chloroform:meth anol:toluene:glacial acetic acid (6:2:1:0.1 v/v/v/v) as mobile phase, chamber and plate saturation time of 30 min, migration distance allowed was 72 mm, wavelength scanning was done at 260 nm keeping the slit dimensions at 5×0.45 mm.A deuterium lamp provided the source of radiation.Standard solutions of valsartan and hydrochlorothiazide were spotted and developed.Photometric measurements were performed at 260 nm in reflectance mode with Camag TLC scanner 3 using WinCATS software.
The standard calibration curve was generated using regression analysis with Microsoft excel.Sample solutions of the marketed formulation were spotted on to the same plate followed by development scanning.The analysis was repeated in triplicate.The content of the drug was calculated from the peak areas recorded.The developed method was validated in terms of linearity, accuracy, limit of detection, limit of quantification, intra-day and inter-day precision and repeatability of measurement as well as repeatability of sample application [8] .
A solvent system that would give dense and compact spots with significant R f values were desired for quantification of valsartan and hydrochlorothiazide in pharmaceutical formulations.The mobile phase consisting of chloroform:methano l:toluene:glacial acetic acid (6:2:1:0.1 v/v/v/v) gave R f values of 0.36±0.04 and 0.63±0.03for valsartan and hydrochlorothiazide, respectively (fig.1).The linear regression data (n=5, Table 1) showed a good linear relationship over a concentration range of 300-800 ng/spot and 100-600 ng/spot for valsartan and hydrochlorothiazide, respectively.The limit of detection and limit of quantification for valsartan was found to be 100 and 300 ng/spot and for hydrochlorothiazide, 30 and 100 ng/spot, respectively.
The intra-day precision was determined by analyzing standard solutions in the concentration range of 400 ng/spot to 700 ng/spot for valsartan and 200 ng/ spot to 500 ng/spot for hydrochlorothiazide for 3 times on the same day while inter-day precision was determined by analyzing corresponding standards daily for 3 day over a period of one week.The intra-day and inter-day coefficients of variation for both drugs were found to be in the range of 0.27-1.19%and 0.12-1.05%,respectively.These values indicate that the method is precise.Repeatability of sample application was assessed by spotting 4 µl of drug solution 5 times on a TLC plate followed by development of plate and recording the peak area for 5 spots.The % RSD for peak area values of valsartan and hydrochlorothiazide were found to be 0.98 and 0.83, respectively.Repeatability of measurement of peak area was determined by spotting 4 µl of valsartan and hydrochlorothiazide solution on a TLC plate and developing the plate.The separated spot was scanned five times without changing the position of the plate and % RSD for measurement of peak area of valsartan and hydrochlorothiazide were found to be 0.43 and 0.49, respectively.To  confirm the specificity of the proposed method, the solution of the formulation was spotted on the TLC plate, developed and scanned.It was observed that the excipients present in the formulation did not interfere with the peaks of valsartan and hydrochlorothiazide.
Recovery studies of the drugs were carried out for the accuracy parameter.These studies were carried out at three levels i.e. multiple level recovery studies.Sample stock solutions from tablet formulation of 100 µg/ml were prepared.Dilutions were made and recovery studies were performed.Percentage recovery was found to be within the limits as listed in Table 2.The assay value for the marketed formulation was found to be within the limits as listed in Table 2.The low RSD value indicated the suitability of the method for routine analysis of valsartan and hydrochlorothiazide in pharmaceutical dosage forms.
The developed HPTLC technique is simple, precise, specific and accurate and the statistical analysis proved that method is reproducible and selective for the analysis of valsartan and hydrochlorothiazide in bulk drug and tablet formulations.