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Development and Validation of a UHPLC–MS/MS Method for Quantitation of Almonertinib in Rat Plasma: Application to an in vivo Interaction Study Between Paxlovid and Almonertinib
Almonertinib was approved for the first-line treatment of advanced NSCLC patients with EGFR-TKI-sensitive genetic mutations by National Medical Products Administration (NMPA) in 2021.The purpose of this study was to establish and validate a fast, accurate, stable and facile ultra-performance liquid...
Autores principales: | Tang, Peng-fei, Bao, Su-su, Gao, Nan-yong, Shao, Chuan-feng, Xie, Wei-fei, Wu, Xue-meng, Zhao, Le-ping, Xiao, Zhong-xiang |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355496/ https://www.ncbi.nlm.nih.gov/pubmed/35935882 http://dx.doi.org/10.3389/fphar.2022.960311 |
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