Method development and validation of remogliflozin and tenligliptin by RP-HPLC

Authors

  • Shaik Abdul Vaseem Department of Pharmaceutical Analysis, Joginapally B. R. Pharmacy College, Moinabad, Hyderabad, Telangana-500075, India.
  • Shyamala Department of Pharmaceutical Analysis, Joginapally B. R. Pharmacy College, Moinabad, Hyderabad, Telangana-500075, India.

Keywords:

Remogliflozin, Teneligliptin, RP-HPLC, validation.

Abstract

A rapid and precise reverse phase high performance liquid chromatographic method has been developed for the validated of Remogliflozin and Teneligliptin, in its pure form as well as in tablet dosage form. Chromatography was carried out on a Zorbax C18 (4.6 x 150mm, 5µm) column using a mixture of Methanol: Phosphate Buffer pH 3.9 (55:45v/v) as the mobile phase at a flow rate of 1.0ml/min, the detection was carried out at 255nm. The retention time of the Remogliflozin   and Teneligliptin was 2.061, 2.462 ±0.02min respectively. The method produce linear responses in the concentration range of 1-5µg/ml of Remogliflozin and 100-500µg/ml of Teneligliptin. The method precision for the determination of assay was below 2.0%RSD. The method is useful in the quality control of bulk and pharmaceutical formulations.

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Published

2022-12-26