Characterization of Five Oxidative Degradation Impurities and One Process Impurity of Suvorexant Drug Substance by LC-MS/MS, HR-MS and 1D, 2D NMR: Validation of Suvorexant Drug Substance and Process Impurities by HPLC and UPLC

• Published in: Journal of chromatographic science Vol. 58; no. 5; pp. 433 - 444
• Main Authors: Rajana, Nagaraju, Devi, Dharamasoth Rama, Kumar Reddy, Dinne Naresh, Babu, J Moses, Basavaiah, K, Balakumaran, K
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 25.04.2020
• Subjects: Azepines - analysis; Azepines - chemistry; Calorimetry, Differential Scanning; Chromatography, High Pressure Liquid - methods; Chromatography, Liquid - methods; Drug Contamination; Magnetic Resonance Spectroscopy - methods; Molecular Structure; Oxidation-Reduction; Spectroscopy, Fourier Transform Infrared; Tandem Mass Spectrometry - methods; Triazoles - analysis; Triazoles - chemistry
• ISSN: 0021-9665; 1945-239X
• DOI: 10.1093/chromsci/bmaa003

Abstract During the oxidative (10% H2O2) degradation of suvorexant drug substance, around 1.0% of one impurity and less than 1.0% four impurities were found by a new high-performance liquid chromatography (HPLC) assay and related substance method. The mass numbers of 1.0% impurity was 469 [M + H]+, remaining four impurities were 172 [M + H]+, 467 [M + H]+, 483 [M + H]+ and 485 [M + H]+. The 469 [M + H]+, 485[M + H] and 172 [M + H]+ impurities were characterized by using the LC-MS/MS, HR-MS and 1D, 2D NMR spectroscopic data. The 172 [M + H]+ impurity was prepared synthetically and co-injected in HPLC. The retention time of synthesized 172 [M + H]+ impurity was matching with the unknown degradation impurity in HPLC. The developed mass compatible HPLC and ultra performance liquid chromatography methods were validated for drug substance and process impurities by following ICH Q2 (R1) guidelines.