Author(s): Nagaraju Pappula, S. Ravichandra, S. Lakshmi Sindhura, P. Asha Rani, V. Seshu Madhuri, V. Ajay, P. Narsi Reddy

Email(s): pappulanagaraju@gmail.com

DOI: 10.5958/2231-5675.2019.00038.3   

Address: Nagaraju Pappula*, S. Ravichandra, S. Lakshmi Sindhura, P. Asha Rani, V. Seshu Madhuri, V. Ajay, P. Narsi Reddy
Department of Pharmaceutical Analysis, Hindu College of Pharmacy, Amravathi Road, Guntur – 522002, A.P., India
*Corresponding Author

Published In:   Volume - 9,      Issue - 4,     Year - 2019


ABSTRACT:
The study describes method development and subsequent validation of RP-HPLC method for simultaneous estimation of candesartan and hydrochlorothiazide in combined tablet dosage forms. Chromatographic separation was achieved on a Hypersil BDS C8 column (250 mm x 4.6 mm, 5 µm) using a mobile phase consisting of (40:60 v/v) acetonitrile: triethylamine (0.02%) at a flow rate of 1 mL/min. The detection wavelength is 262 nm. The retention times of candesartan and hydrochlorothiazidewere found to be 2.449 min and 4.895 min respectively. The developed method was validated as per ICH guidelines. The developed and validated method was successfully used for the quantitative analysis of candesartan and hydrochlorothiazidein tablet dosage forms.


Cite this article:
Nagaraju Pappula, S. Ravichandra, S. Lakshmi Sindhura, P. Asha Rani, V. Seshu Madhuri, V. Ajay, P. Narsi Reddy. Simultaneous Estimation of Candesartan and Hydrochlorothiazide in Combined Tablet Dosage Form by RP-HPLC. Asian J. Pharm. Ana. 2019; 9(4):224-228. doi: 10.5958/2231-5675.2019.00038.3


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DOI: 10.5958/2231–5675 

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