Identification of related substances in tofacitinib citrate by LC-MS techniques for synthetic process optimization.

Abstract

A specific LC-MS method was developed for separation, identification and characterization of the process-related substances and degradation products in tofacitinib citrate. The separation was achieved on a LiChrospher C18 column (250mm×4.6mm, 5μm) by linear gradient elution of 0.1% ammonium acetate solution (pH adjusted to 4.0 by formic acid) and acetonitrile at a flow rate of 1.0mL/min. Forced degradation studies were conducted under hydrolytic (acidic, basic), oxidative, photolytic and thermal stress conditions as described in ICH. It was found that tofacitinib was stable under photolytic condition, but degraded obviously in acidic, basic, thermal and oxidative conditions. The high resolution TOF-MS and MS/MS were used for determination and structural identification of the related substances. Eleven major related substances were detected and identified as five process-related substances and six degradation products, and three of them were further synthesized and characterized by NMR spectroscopy. The most plausible mechanisms involved in the formation of the related substances were also proposed. Since related substances have a significant impact on drug safety, quality and efficacy, the data obtained are valuable for process monitoring and quality assurance of tofacitinib citrate.

DOI: 10.1016/j.jpba.2017.05.012

Cite this paper

@article{Wu2017IdentificationOR, title={Identification of related substances in tofacitinib citrate by LC-MS techniques for synthetic process optimization.}, author={Xiao Wu and Xuefang Zeng and Lei Wang and Tai-jun Hang and Min Song}, journal={Journal of pharmaceutical and biomedical analysis}, year={2017}, volume={143}, pages={17-25} }