Abstract

BackgroundTetrahydrocurcumin (THC), the active metabolite of curcumin, is gaining popularity amongst scientist due to its wide spectrum of pharmacological activities, better stability and colourless nature. The objective of this study was to develop a sensitive, cost-effective RP-HPLC method for the estimation of THC in bulk drug substance and formulation.ResultsEfficient chromatographic separation was achieved on Hypersil BDS, C18 column, 250 mm × 4.6 mm, 5 μm column by isocratic elution with mobile phase comprising of acetonitrile: methanol: water (40:23:37% V/V); adjusted to a pH of 3.0 ± 0.05. The flow rate of the mobile phase was 1.0 ml/min with a column temperature of 25 °C. UV detector was used for the analysis and detection was carried out at 280 nm. The developed method was validated according to ICH guidelines with respect to system suitability, linearity, accuracy, precision and robustness. The theoretical plates were found to be more than 5800. The method showed linearity over the range of 4 to 60 μg/ml with R2 = 0.9998. The accuracy of the method in terms of recovery study was 98.23-99.99%. The %RSD for intra-day and inter-day precision were 0.272 and 0.275, respectively. The method was found to be robust with respect to change in wavelength, flow rate and column temperature.ConclusionThe analytical method was found satisfactory on validation as per ICH guidelines. Hence, it can be routinely used for quantification of THC in bulk drug and formulation.

Highlights

  • Tetrahydrocurcumin (THC), the active metabolite of curcumin, is gaining popularity amongst scientist due to its wide spectrum of pharmacological activities, better stability and colourless nature

  • Tetrahydocurcumin (THC) is an active metabolite of it [2] where both the double bonds are reduced to single bonds (Fig. 1)

  • Robustness Change in wavelength, flow rate and column temperature caused not more than 2% difference in the assay value (Table 7)

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Summary

Introduction

Tetrahydrocurcumin (THC), the active metabolite of curcumin, is gaining popularity amongst scientist due to its wide spectrum of pharmacological activities, better stability and colourless nature. The objective of this study was to develop a sensitive, cost-effective RP-HPLC method for the estimation of THC in bulk drug substance and formulation. Curcumin is a principal bioactive component of plant Curcuma longa (Linn). It is a potent antioxidant exhibiting various pharmacological activities [1]. Tetrahydocurcumin (THC) is an active metabolite of it [2] where both the double bonds are reduced to single bonds (Fig. 1). It is 1,7-bis(4-hydroxy-3-methoxyphenyl)heptane-3,5-dione with empirical formula C21H24O6 and molecular weight 372.4. THC retains a range of therapeutic properties. It has been shown to ameliorate oxidative stress-induced renal injury [3] and was able to mitigate mitochondrial dysfunction in brain vasculature

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