Method Development And Validation Of Odevixibat By HPLC And Characterization Of Its Novel Stress Degradation Products By Using HPLC-MS/MS
Background: For evaluating Odevixibat and its degradation products that were identified by LC-MS/MS, a sensitive and simple method was developed.Results: This method uses a 250 x 4.6 mm, 5 m long Inertsil ODS C18 column for chromatographic separation.With a flow rate of 1 mL/min and ambient temperature, a mobile phase containing 0.1% formic acid (FA) and acetonitrile in a ratio of 60:40 was utilized.At 220 nm, UV observations were made.The linearity, recoveries, and quantification limitations were found to be within the allowable range.Conclusions: Newly produced Odevixibat breakdown products and stress studies were confirmed as chemical structures using LC-MS in accordance with ICH Q2 (R) standards.
Authors
- Challa Sudheer
Institutions
- Andhra University (IN)
Publication Details
- Journal
- African Journal of Biomedical Research
- Published
- 2024-09-27
- DOI
- https://doi.org/10.53555/ajbr.v27i3s.6958
- Primary Topic
- Analytical Methods in Pharmaceuticals
- Type
- article
- Field-Weighted Citation Impact
- 0.00