Author(s): Sushil D. Patil, Tejashri Dugaje, Sanjay J. Kshirsagar

Email(s): sushilpharma@rediffmail.com

DOI: 10.5958/2231-5713.2019.00030.8   

Address: Sushil D. Patil*, Tejashri Dugaje*, Dr. Sanjay J. Kshirsagar
MET’s Institute of Pharmacy, MET League of Colleges, Bhujbal Knowledge City, Adgaon, Nashik,
Savitribai Phule Pune University, Maharashtra, India
*Corresponding Author

Published In:   Volume - 9,      Issue - 3,     Year - 2019


ABSTRACT:
A simple and precise high performance liquid chromatography method for determination of candesartan cilexetil in their pharmaceutical formulation was developed and validated. The separation was carried out on Cosmosil C18 (250mm X 4.6, 5µ) RP-HPLC column using an 0.8ml/min as flow rate with methanol: water (80:20 v/v) mobile phase. Quantification was performed with a UV detector at 214nm, solubility and stability was determined individually in simulated biological fluids at various pH was investigated. The calibration curves of candesartan cilexetil were linear in the range of 10-50 µg/ml (R²=0.999). The developed method was applied to pharmaceutical formulation successfully with no interfering peaks. The percentage recovery was 99.71-100.29%. It was observed that solubility of candesartan cilexetil was increased in all invitro medium, in 1.2 and slightly 7.4 pH and the stability of candesartan cilexetil was stable in pH 1.2 or degraded in pH 7.4 for 24 hours.


Cite this article:
Sushil D. Patil, Tejashri Dugaje, Sanjay J. Kshirsagar. Development and Validation of HPLC Method for Estimation of Pharmaceutical Drug and its Stability Studies in Simulated Biological Fluid: Comparative Study. Asian J. Pharm. Tech. 2019; 9(3):179-184. doi: 10.5958/2231-5713.2019.00030.8


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DOI: 10.5958/2231–5713 


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