LC–ESI-MS Characterization of Degradents of Brivaracetam; Development and Validation of a Stability-Indicating RP-HPLC Method

The planned study demonstrates the validation of the developed simple, precise, and robust stability-indicating assay method by high-pressure liquid chromatography and the identification and characterization of Brivaracetam (BRV) degradants by High-Performance Liquid Chromatography-Tandem Mass Spectrometry. The drug was exposed to a few stressors i.e. acidic, basic, oxidative, thermal, and UV light to study the stability-indicating behavior of the planned method and observed sufficient degradation in the acidic stressor. All separations were done on Hi-Q SiliC-18 (I250 x 4.6mm, 5µm particle size) by isocratic elution flow at 1ml/min. Detection was set at 210nm. All obtained results indicate that the present method is helpful in the quality control (QC) laboratory to the day-to-day investigation of (BRV) for the assay and degradation products. HPLC method development and validation have been done per the current ICH guidelines. The m/z value obtained in LC-MS analysis of the degradant was used to study further fragmentation patterns, structural elucidation of the degradant, and its pathway.

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Publication Details

Journal
Research Journal of Pharmacy and Technology
Published
2025-03-27
DOI
https://doi.org/10.52711/0974-360x.2025.00176
Citations
1
Primary Topic
Epilepsy research and treatment
Type
article
Field-Weighted Citation Impact
1.47
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article

LC–ESI-MS Characterization of Degradents of Brivaracetam; Development and Validation of a Stability-Indicating RP-HPLC Method

Sanjay D. Sawant, Shital D. Godse
1 citations
Research Journal of Pharmacy and Technology
Epilepsy research and treatment
1.47
article

LC–ESI-MS Characterization of Degradents of Brivaracetam; Development and Validation of a Stability-Indicating RP-HPLC Method

Sanjay D. Sawant, Shital D. Godse
article en
1 citations

Abstract

The planned study demonstrates the validation of the developed simple, precise, and robust stability-indicating assay method by high-pressure liquid chromatography and the identification and characterization of Brivaracetam (BRV) degradants by High-Performance Liquid Chromatography-Tandem Mass Spectrometry. The drug was exposed to a few stressors i.e. acidic, basic, oxidative, thermal, and UV light to study the stability-indicating behavior of the planned method and observed sufficient degradation in the acidic stressor. All separations were done on Hi-Q SiliC-18 (I250 x 4.6mm, 5µm particle size) by isocratic elution flow at 1ml/min. Detection was set at 210nm. All obtained results indicate that the present method is helpful in the quality control (QC) laboratory to the day-to-day investigation of (BRV) for the assay and degradation products. HPLC method development and validation have been done per the current ICH guidelines. The m/z value obtained in LC-MS analysis of the degradant was used to study further fragmentation patterns, structural elucidation of the degradant, and its pathway.

Research Journal of Pharmacy and Technology
Smt. Kashibai Navale Medical College and General hospital (IN), Utkal University (IN)
Openalex Percentile: Top 21%
Epilepsy research and treatment
1.47
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