Abstract
A simple, sensitive, rapid, precise and accurate method has been developed for simultaneous estimation of tazarotene and hydroquinone in their pharmaceutical dosage form (gel preparation). The chromatographic separation was carried out on a reversed-phase Inertsil C18 (4.6 mm I.D. × 250 mm, 5 μm) column using a mobile phase consisting of 0.02 M KH2PO4‒acetonitrile (80 : 20, v/v) at a flow rate of 1.0 mL/min and UV detection at λmax = 254 nm. The method showed linearity with the correlation coefficient of 0.999 for both tazarotene and hydroquinone over the concentration range of 5‒25 and 1‒5 µg/mL, respectively. The mean recoveries were found to be in the range of 98‒101% for both components. The method was validated as per International Conference on Harmonization guidelines for linearity, limit of detection, limit of quantification, specificity, accuracy, precision and robustness. As a result, this method can be successfully applied for routine quantification of tazarotene and hydroquinone in pharmaceutical dosage form (gel preparation).
Similar content being viewed by others
REFERENCES
Brenna, E., Frigoli, S., Fronza, G., and Serra, S., J. Pharm. Biomed. Anal., 2008, vol. 46, no. 3, p. 574.
Tazarotene on Drugs.com. www.drugs.com/search. php?searchterm=tazarotene. Accessed December 18, 2016.
Sheliya, K., Shah, K., and Kapupara, P., J. Chem. Pharm. Res., 2014, vol. 6, no. 4, p. 934.
Odumosu, P. and Ekwe, T., Afr. J. Pharm. Pharmacol., 2010, vol. 4, no. 5, p. 231.
Desiderio, C., Ossicini, L., and Fanali, S., J. Chromatogr. A, 2000, vol. 887, p. 489.
Lowe, N., Horwitz, S., Tanghetti, E., Draelos, Z., and Menter, A., J. Cosmet. Laser Ther., 2006, vol. 8, no. 3, p. 121.
Elzanfaly, E., Saad, A., and Elaleem, A., Saudi Pharm. J., 2012, vol. 20, p. 249.
Jogarami, R., Jain, P., and Sharma, S., J. Pharm. Res., 2012, vol. 5, p. 2273.
Patel, M., Patel, R., Parikh, J., and Patel, B., Anal. Methods, 2010, vol. 2, p. 275.
Pathare, D., Jadhav, S., and Shingare, M., Chromatographia, 2007, vol. 66, p. 247.
Badawy, A.M., El-Alim, A.A., and Saad, A.S., Drug Test. Anal., 2010, vol. 2, p. 130.
Roy, C. and Chakrabarty, J., J. Sci. Pharm., 2013, vol. 81, no. 4, p. 951.
Roy, C., Patel, H., and Chakrabarty, J., Indo Am. J. Pharm. Sci., 2012, vol. 3, p. 1400.
International Conference on Harmonization (ICH) Guidelines Topic Q2(R1): Validation of Analytical Procedures: Text and Methodology, Geneva, 2005. http://www. ich.org/fileadmin/Public_Web_Site/ICH_Products/ Guidelines/Quality/Q2_R1/Step4/Q2_R1__Guideline.pdf. Accessed October 10, 2016.
ACKNOWLEDGMENTS
Authors gratefully acknowledge Vice-chancellor, Banasthali Vidyapith for providing necessary research facilities. The financial assistance provided by the DST, New Delhi under the CURIE program is duly acknowledged.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Yadav Rajkumar, Divya, Y. & Rakesh, Y. Development and Validation of Analytical Method for Simultaneous Estimation of Tazarotene and Hydroquinone in their Gel Formulation by Reversed-phase High Performance Liquid Chromatography. J Anal Chem 74, 467–471 (2019). https://doi.org/10.1134/S1061934819050095
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1061934819050095