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Simultaneous Estimation of Quinapril Hydrochloride and Hydrochlorothiazide from Pharmaceutical Formulation by Using UV, IR and RP-HPLC
Corresponding Author(s) : Avinash Mahajan
Asian Journal of Chemistry,
Vol. 26 No. 13 (2014): Vol 26 Issue 13
Abstract
The objective of present investigation was to develop and validate assay methods for simultaneous estimation of quinapril hydrochloride and hydrochlorothiazide in combined dosage form by using three different analytical approaches viz. UV, FT-IR and RP-HPLC. Drugs were estimated by dual wavelength method and calibration curve methods by using UV and FT-IR spectrophotometer, respectively. The stability indicating assay method was developed by using HPLC. The stress degradation study was carried out according to International Conference on Harmonization (ICH) guideline Q1A (R2). Chromatographic separation was carried out on HIQ-Sil (150 × 4.6 mm, 5 μm) column using 0.01 M KH2PO4 buffer (pH 3.5, adjusted with orthophosphoric acid): methanol as mobile phase in gradient elution mode.
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- U.S. Pharmacopoeia 30/ NF25, U.S. Pharmacopoeial Convention, Rockville, MD, pp. 954-955 (2005).
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References
M.E. Roberts and B.J. Epstein, J. Cardiovasc. Nurs., 24, 380 (2009); doi:10.1097/JCN.0b013e3181aed18e.
U.S. Pharmacopoeia, 30/ NF25, U. S. Pharmacopoeial Convention, Rockville, MD, pp. 1689-1690 (2005).
Indian Pharmacopoeia Volume II, Govt. of India, New Delhi: Ministry of Health and Family Welfare, pp. 1194-1195 (2007).
European Pharmacopoeia, Convention on the Elaboration of European Pharmacopoeia, Vol. 2, pp. 1756-1757 (2004).
U.S. Pharmacopoeia 30/ NF25, U.S. Pharmacopoeial Convention, Rockville, MD, pp. 954-955 (2005).
R. Gangola, S. Kaushik and P. Sharma, J. Appl. Pharm. Sci., 1, 46 (2011).
A.T. Hemke, M.V. Bhure, K.S. Chouhan, K.R. Gupta and S.G. Wadodkar, E.-J. Chem., 7, 1156 (2010); doi:10.1155/2010/826585.
N. Jain, R. Jain, N. Thakur and B. Gupta, Int. J. Appl. Pharm., 2, 212 (2010).
K.R. Patel, S.A. Patel, D. Vinayc and R.N. Sonpal, Indian Res. J. Pharm., 2, 202 (2011).
S.T. Kumbhar, G.K. Chougule, V.S. Tegeli, G.B. Gajeli, Y.S. Thorat and U.S. Shivsharan, Int. J. Pharm. Sci. Drug Res., 3, 62 (2011).
K.S. Chouhan, M.V. Bhure, A.T. Hemke, K.R. Gupta and S.G. Wadodkar, Res. J. Pharm. Biol. Chem. Sci., 1, 81 (2010).
N. Devanaboyina, T. Satyanarayana and G.B. Rao, Res. J. Pharm. Biol. Chem. Sci., 3, 270 (2012).
A. Gumieniczek and H. Hopkala, Pharm. Acta Helv., 73, 183 (1998); doi:10.1016/S0031-6865(98)00019-3.
R.D. Sreenivas, M.K. Srinivasu, C.L. Narayana and G.O. Reddy, Indian Drugs, 37, 80 (2000).
V.A. Chatpalliwar, D.D. Patil, S.J. Surana and G.B. Bhavar, Indian J. Pharm. Sci., 70, 529 (2008); doi:10.4103/0250-474X.44612.
M. Gandhimathi and T.K. Ravi, Indian J. Pharm. Sci., 71, 311 (2009); doi:10.4103/0250-474X.56035.
E. Dinç and D. Baleanu, J. Braz. Chem. Soc., 18, 962 (2007); doi:10.1590/S0103-50532007000500013.
R. Savithri, N.S. Bindu, P.S. Bhargavi, D.H. Theja and P. Ramalingam, Der Pharm. Sinica, 2, 251 (2011).
International Conference on Harmonization Triplicate, Guideline: Validation of Analytical Procedures Text and Methodology, Q2[R1], p. 1-13 (2005).
M. Bakshi and S. Singh, J. Pharm. Biomed. Anal., 28, 1011 (2002); doi:10.1016/S0731-7085(02)00047-X.
International Conference on Harmonization, Guidance for Industry: Stability Testing of New Drug Substances and Products, Q1A [R2] (1996).
International Conference on Harmonization, Impurities in New Drug Products, Q3B (R2) (2006).
International Conference on Harmonization, Test Procedures and Acceptance Criteria for New Drug Substances and New Drug Products: Chemical Substances, Q6A (2000).
Food and Drug Administration, Code of Federal Regulations Title 21, Section 211 (available on http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm).
S. Singh and M. Bakshi, Pharm. Tech. On-line, 24, 1 (2000).