Development and validation of a HILIC–MS/MS method for quantification of decitabine in human plasma by using lithium adduct detection
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Clinical Biochemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference17 articles.
1. Evolution of decitabine development
2. Pharmacokinetic evaluation of decitabine for the treatment of leukemia
3. Pharmacokinetics of decitabine administered as a 3-h infusion to patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS)
4. Characterization of decomposition products and preclinical and low dose clinical pharmacokinetics of decitabine (5-aza-2′-deoxycytidine) by a new liquid chromatography/tandem mass spectrometry quantification method
5. Chemical Decomposition of 5-Aza-2′-deoxycytidine (Decitabine): Kinetic Analyses and Identification of Products by NMR, HPLC, and Mass Spectrometry
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3. Pharmacokinetic Assessment of Low Dose Decitabine in Combination Therapies: Development and Validation of a Sensitive Uhplc-Ms/Ms Method for Murine Plasma Analysis;2024
4. Development and Validation of a Uplc-Ms/Ms Method for Quantification of Decitabine in Children's Plasma by Using Sodium Adduct Detection;2024
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