Dr. GampaVijayKumar1*, Dr. T. Rajesh2, Jaya Chandhra3
1Professor and Head, Dept. of Pharmacy, KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India.2KGR Institute of Technology and Management, Rampally, Kesara, Rangareddy, Telangana, India.
A B S T R A C
A new method was established for simultaneous estimation of Faxofenadine and Montelukast by RP-HPLC method. The chromatographic conditions were successfully developed for the separation of Faxofenadine and Montelukast by using XterraC185µm (4.6*250mm) column, flow rate was1ml/min, mobile phase ratio was Phosphate buffer (0.05M) pH4.6: ACN (55:45%v/v) (pH was adjusted with orthophosphoric acid), detection wavelength was 255nm.Theinstrumentused was Shimadzu, model No. SPD-20MA LC+20AD, Software- LC-20 Solution. The retention times were found to be 2.399 mins and 3.907mins. The % purity of Faxofenadine and Montelukast was foundtobe100.7% and 101.4% respectively. The system suitability parameters for Faxofenadine and Montelukast such as the or etical plates and tailing factor were found to be 1.3, 5117.5 and 1.4,3877.3the resolution was found to be 8.0.The analytical method was validated according to ICH guidelines (ICH,Q2(R1)). The linearity study for Faxofenadine and Montelukast was found in concentration range of 1μg-5μg and 100μg-500μg and correlation coefficient(r2)was found to be 0.999and 0.999, % mean recovery was found to be 100%and 100.5%,% RSD for repeatability was 0.2 and 0.4,% RSD for intermediate precision was 0.5and 0.1 respectively. The precision study was precise, robust and repeatable. LOD value was 2.95 and 3.04, and LOQ value was 9.87and10 respectively.
Keyword: Faxofenadine and Montelukast, RP-HPLC method