Quantitative evaluation and pharmacokinetic characteristics of the irreversible BTK inhibitor zanubrutinib in mouse plasma using LC-MS/MS
Author:
Affiliation:
1. Department of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China
2. Health Science Center, Xi'an Jiaotong University, Xi'an, China
Abstract
Funder
National Natural Science Foundation of China
Publisher
SAGE Publications
Subject
Spectroscopy,Atomic and Molecular Physics, and Optics,General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/14690667221128934
Reference20 articles.
1. B-cell receptor signaling as a driver of lymphoma development and evolution
2. New insights into pre-BCR and BCR signalling with relevance to B cell malignancies
3. The clinically active BTK inhibitor PCI-32765 targets B-cell receptor– and chemokine-controlled adhesion and migration in chronic lymphocytic leukemia
4. Targeting BTK with Ibrutinib in Relapsed Chronic Lymphocytic Leukemia
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1. A novel UHPLC‒MS/MS method for quantitative analysis of zanubrutinib in rat plasma: application to an in vivo interaction study between zanubrutinib and triazole antifungal;BMC Chemistry;2023-08-30
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