Isolation, identification and structural characterization of forced degradation products of mobocertinib using LC-MS/MS and NMR
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Elsevier
Abstract
The main objective of this study is to develop and validate an LC-MS/MS stability-indicating method for the
isolation, identification, and characterization of forced degradation products of mobocertinib under various
stress conditions, utilizing LC-MS/MS and NMR techniques. Four degradation products (DP1, DP2, DP3 and DP4)
were isolated. Degradation under acidic and oxidative conditions provides DP1 and DP4, respectively. Both DP2
and DP3 were obtained under basic conditions. Chromatographic development and separation were achieved
using an ODS C18 column (Chemsil) with a constant flow rate of 1.0 ml/min. The mobile phase consisted of 40 %
water containing 0.1 % formic acid in methanol, and detection was performed at a wavelength of 225 nm. The
application of LC-MS/MS technology was utilized to separate the above degradation products. The LC-MS/MS
method has validated which includes specificity, linearity, LOD and LOQ, precision, accuracy and robustness.
The chemical structure of the degradation products were characterized by 1
H NMR and mass spectroscopy. The
above listed degradation impurities are novel and not listed in the literature. In conclusion, this study provides
vital information about mobocertinib’s chemical stability and helpful in further drug development process.
Description
The main objective of this study is to develop and validate an LC-MS/MS stability-indicating method for the
isolation, identification, and characterization of forced degradation products of mobocertinib under various
stress conditions, utilizing LC-MS/MS and NMR techniques. Four degradation products (DP1, DP2, DP3 and DP4)
were isolated. Degradation under acidic and oxidative conditions provides DP1 and DP4, respectively. Both DP2
and DP3 were obtained under basic conditions. Chromatographic development and separation were achieved
using an ODS C18 column (Chemsil) with a constant flow rate of 1.0 ml/min. The mobile phase consisted of 40 %
water containing 0.1 % formic acid in methanol, and detection was performed at a wavelength of 225 nm. The
application of LC-MS/MS technology was utilized to separate the above degradation products. The LC-MS/MS
method has validated which includes specificity, linearity, LOD and LOQ, precision, accuracy and robustness.
The chemical structure of the degradation products were characterized by 1
H NMR and mass spectroscopy. The
above listed degradation impurities are novel and not listed in the literature. In conclusion, this study provides
vital information about mobocertinib’s chemical stability and helpful in further drug development process.
Citation
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