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Sensitive and accurate estimation of losartan potassium formulation by high-performance thin-layer chromatography
Muralidharan Selvadurai1, Subramaniya Nainar Meyyanathan
1Department of Pharmaceutical Analysis, JSS College of Pharmacy, Rocklands-Ooty, Tamilnadu, India.
Aim And Objectives:
To develop a simple, sensitive, cost-effective and reproducible UV-spectrophotometric method and validate for the estimation of disodium edetate in topical gel formulations.
Materials And Methods:
Solution of disodium edetate reacts with ferric chloride to form complex in 0.1 N HCl giving λmax at 270 nm. Beer's law was obeyed in the concentration range of 5-50 μg/mL (r (2) = 0.9997).
Results:
The limit of detection and limit of quantitation were found to be 1.190 and 3.608 μg/mL, respectively. The results show that the procedure is accurate, precise, and reproducible (relative standard deviation < 1%), while being simple and less time consuming.
Conclusions:
The study concluded that the UV-spectrophotometric method could be used for the quantification of disodium edetate in pure form as well as in pharmaceutical formulations.
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