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Development and Validation of RP HPLC Method for Simultaneous Estimation of Ebastine and Montelukast Sodium In Combined Dosage Form
Published in June 2013 Issue 3 (Vol. 3, Issue 3, 2013)

Abstract
A specific and accurate reverse phase high performance liquid chromatographic method was developed for the simultaneous determination Ebastine (EBA) and Montelukast Sodium (MONTE) in Combined dosage forms. The analysis was carried out using Phenomenex C18, column (250 mm × 4.6 mm id, 5 µm particle size) with Mobile phase consisting of Methanol : Phosphate buffer (65:35 v/v) pH 5.0+0.05 was pumped at a flow rate was 1.0 ml/ min and Quantification was achieved with photodiode array (PDA) detection at 261 nm over the concentration range of 10 - 50 µg/mL for ebastine & Montelukast Sodium with mean recovery of 100.32 ± 0.85 % and 100.15 ± 0.94 % for Ebastine and Montelukast Sodium, respectively. These methods were found to be simple, sensitive, accurate, precise and economical and applicable for the simultaneous determination of Ebastine & Montelukast Sodium in combined dosage form.
Authors (2)
Anand Jigna
View all publications →Mohan Sellappan
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June 2013 Issue 3 (Vol. 3, Issue 3, 2013)Article Impact
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How to Cite
Jigna & Sellappan (2013). Development and Validation of RP HPLC Method for Simultaneous Estimation of Ebastine and Montelukast Sodium In Combined Dosage Form. American Journal of PharmTech Research, 3(3), xx-xx. https://ajptr.com/articles/AJPTR33064
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