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American Journal of PharmTech Research

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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)

Development and Validation of RP HPLC Method for Simultaneous Estimation of Ebastine and Montelukast Sodium In Combined Dosage Form - Issue cover

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.

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Article Information

AJPTR33064

AJPTR-01-000887

2013-06-01

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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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