METHOD DEVELOPMENT AND VALIDATION OF FINERENONE BY RP-HPLC METHOD

  • Unique Paper ID: 166111
  • Volume: 11
  • Issue: 2
  • PageNo: 751-761
  • Abstract:
  • A simple, sensitive, accurate, rapid and specific RP-Hplc method was developed for estimation and validation of Finerenone in pure drug and tablet dosage form. chromatographic separation was achieved on an symmetry ODS C analytical column using mobile phase composition of methanol and phosphate buffer in ratio of 35:65% that was set at the flow rate of 1.0 ul/min with detection of 235 nm. The presentation of method was validated according to present ICH guideline for accuracy precision and robustness, linearity, limit of quantification, limit of detection linearity.

Cite This Article

  • ISSN: 2349-6002
  • Volume: 11
  • Issue: 2
  • PageNo: 751-761

METHOD DEVELOPMENT AND VALIDATION OF FINERENONE BY RP-HPLC METHOD

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