TY - JOUR
T1 - Identification of Degradation Products of the New Anticancer Drug Substance ONC201 by Liquid Chromatography–High-Resolution Multistage Mass Spectrometry
AU - Annereau, Maxime
AU - Vignes, Marina
AU - Bouchema, Tahar Sif Eddine
AU - Denis, Lucas
AU - Solgadi, Audrey
AU - Vieillard, Victoire
AU - Paul, Muriel
AU - Rieutord, André
AU - Grill, Jacques
AU - Secretan, Philippe Henri
AU - Do, Bernard
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/5/1
Y1 - 2023/5/1
N2 - ONC201 (dordaviprone) is a new drug substance used in a compassionate manner to treat patients with glioblastoma. Given the clinical context and the particularly promising preclinical results, we have been asked by the medical authorities to make a first treatment available throughout France as a hospital preparation to allow access to treatment and to conduct clinical trials. However, to control the quality and safety conditions inherent in this academic manufacturing process, while there is virtually no data available to date to understand the stability of ONC201, we had to determine the stability profile of ONC201, i.e., its sensitivity to different stressors and the types of impurities that could form during its degradation. We found that ONC201 was sensitive to oxidation in the presence of hydrogen peroxide or under light irradiation. Both conditions resulted in the formation of 20 degradation products detected and identified by liquid chromatography–high-resolution mass spectrometry. Their structural elucidation required an in-depth study of the fragmentation pattern of protonated ONC201, described for the first time. The product ions of the degradation products were compared to those of ONC201 protonated ion to assign the most plausible structures for all the detected degradation products. Of these degradation products, those that were rapidly produced, of high intensity and/or identified as potentially having a different toxicity profile to ONC201 by in silico studies, were selected to be monitored during batch release testing and stability studies.
AB - ONC201 (dordaviprone) is a new drug substance used in a compassionate manner to treat patients with glioblastoma. Given the clinical context and the particularly promising preclinical results, we have been asked by the medical authorities to make a first treatment available throughout France as a hospital preparation to allow access to treatment and to conduct clinical trials. However, to control the quality and safety conditions inherent in this academic manufacturing process, while there is virtually no data available to date to understand the stability of ONC201, we had to determine the stability profile of ONC201, i.e., its sensitivity to different stressors and the types of impurities that could form during its degradation. We found that ONC201 was sensitive to oxidation in the presence of hydrogen peroxide or under light irradiation. Both conditions resulted in the formation of 20 degradation products detected and identified by liquid chromatography–high-resolution mass spectrometry. Their structural elucidation required an in-depth study of the fragmentation pattern of protonated ONC201, described for the first time. The product ions of the degradation products were compared to those of ONC201 protonated ion to assign the most plausible structures for all the detected degradation products. Of these degradation products, those that were rapidly produced, of high intensity and/or identified as potentially having a different toxicity profile to ONC201 by in silico studies, were selected to be monitored during batch release testing and stability studies.
KW - LC-MS
KW - MS fragmentation patterns
KW - ONC201
KW - control specifications
KW - degradation products
KW - dordaviprone
KW - in silico
KW - oxidation
KW - structural elucidation
UR - http://www.scopus.com/inward/record.url?scp=85160343671&partnerID=8YFLogxK
U2 - 10.3390/chemosensors11050294
DO - 10.3390/chemosensors11050294
M3 - Article
AN - SCOPUS:85160343671
SN - 2227-9040
VL - 11
JO - Chemosensors
JF - Chemosensors
IS - 5
M1 - 294
ER -