Development and Validation of RP-HPLC Method for the Determination of Dexrabeprazole Sodium

Yıl 2021, , 1427 - 1431, 31.12.2021

Semra Yılmazer Keskin , Ebru Nurdan Şentürk Cihansel Unlu

https://doi.org/10.16984/saufenbilder.999458

Öz

A rapid and simple liquid chromatographic method was developed for the quantitative determination of dexrabeprazole sodium in the tablet dosage form. The reverse-phase chromatographic analysis was carried out by using a C-18 column. The acetonitrile-phosphate buffer mixture was used as the mobile phase. The obtained retention time was 4.33∓0.02 min. by using 50:50 (v:v) acetonitrile:phosphate buffer(pH 7) and 1.0 mL/min. flow rate. Quantification of the analyte was based on measuring the peaks areas at 272 nm. The analytical performance of the developed RP-HPLC method was validated with respect to accuracy, precision, linearity, stability, and robustness. The obtained linearity range was 77-143 mg/L and the correlation coefficient was 0.9989. The obtained LOD and LOQ values were 0.010 mg/L and 0.034 mg/L, respectively.

Anahtar Kelimeler

Dexrabeprazole, RP-HPLC, validation

Kaynakça

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