Literature DB >> 15018786

Measurement of the anticancer agent gemcitabine and its deaminated metabolite at low concentrations in human plasma by liquid chromatography-mass spectrometry.

Yan Xu1, Bruce Keith, Jean L Grem.   

Abstract

A liquid chromatography/mass spectrometry (LC-MS) method has been developed and validated for the determination of the anticancer agent gemcitabine (dFdC) and its metabolite 2',2'-difluoro-2'-deoxyuridine (dFdU) in human plasma. An Oasis((R)) HLB solid phase extraction cartridge was used for plasma sample preparation. Separation of the analytes was achieved with a YMC ODS-AQ (5 microm, 120 A, 2.0 mm x 150 mm) column. The initial composition of the mobile phase was 2% methanol/98% 5mM ammonium acetate at pH 6.8 (v/v), and the flow rate was 0.2 ml/min. An isocratic gradient was used for 3min, followed by a linear gradient over 4 min to 30% methanol/70% 5mM ammonium acetate at pH 6.8. The gradient returned to the initial conditions over 2 min and remained there for 6 min. The retention times of dFdC, dFdU, and the internal standard 5'-deoxy-5-fluorouridine (5'-DFUR) were 11.46, 12.63, and 13.58 min. The mass spectrometer was operated under negative electrospray ionization conditions. Single-ion-monitoring (SIM) mode was used for analyte quantitation at m/z 262 for [dFdC-H](-), m/z 263 for [dFdU-H](-), and m/z 245 for [5'-DFUR-H](-). The average recoveries for dFdC, dFdU, and 5'-DFUR were 88.4, 84.6, and 99.3%, respectively. The linear calibration ranges were 5-1000 ng/ml for dFdC, and 5-5000 ng/ml for dFdU. The intra- and inter-assay precisions (%CV) were </=3 and </=7% at three concentration levels (50.0, 500, and 5000 ng/ml). The limits of quantitation (defined as 10 times of signal-to-noise ratio) were 3.16 ng/ml for dFdC, and 1.35 ng/ml for dFdU with 50-microl sample injections. This method has been used for measuring plasma concentrations of dFdC and dFdU in samples from adult cancer patients in a Phase I trial of weekly dFdC given as 150 (or lower) mg/(m(2) 24-h) infusion. The average plasma dFdC concentrations at 22- and 23-h into the infusion were 18.3 and 16.8 ng/ml at 150 and 100mg/m(2), respectively; the values for dFdU averaged 2950 and 1372 ng/ml.

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Year:  2004        PMID: 15018786     DOI: 10.1016/j.jchromb.2003.11.038

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  4 in total

1.  Rapid Homogeneous Immunoassay to Quantify Gemcitabine in Plasma for Therapeutic Drug Monitoring.

Authors:  Daniel Kozo; Matt W Ross; Justin Jarrah; Michael Barrett; Rebecca L Harney; Jodi B Courtney; Irina Baburina; Julianne L Holleran; Jan H Beumer; Godefridus J Peters; Richard J Honeywell; Salvatore J Salamone
Journal:  Ther Drug Monit       Date:  2017-06       Impact factor: 3.681

2.  A novel method for quantification of gemcitabine and its metabolites 2',2'-difluorodeoxyuridine and gemcitabine triphosphate in tumour tissue by LC-MS/MS: comparison with (19)F NMR spectroscopy.

Authors:  Tashinga E Bapiro; Frances M Richards; Mae A Goldgraben; Kenneth P Olive; Basetti Madhu; Kristopher K Frese; Natalie Cook; Michael A Jacobetz; Donna-Michelle Smith; David A Tuveson; John R Griffiths; Duncan I Jodrell
Journal:  Cancer Chemother Pharmacol       Date:  2011-03-23       Impact factor: 3.333

3.  Stability-indicating HPLC determination of gemcitabine in pharmaceutical formulations.

Authors:  Rahul Singh; Ashok K Shakya; Rajashri Naik; Naeem Shalan
Journal:  Int J Anal Chem       Date:  2015-03-08       Impact factor: 1.885

4.  Pharmacokinetic Study of Adjuvant Gemcitabine Therapy for Biliary Tract Cancer following Major Hepatectomy (KHBO1101).

Authors:  Yutaka Fujiwara; Shogo Kobayashi; Hiroaki Nagano; Masashi Kanai; Etsuo Hatano; Masanori Toyoda; Tetsuo Ajiki; Yuki Takashima; Kenichi Yoshimura; Akinobu Hamada; Hironobu Minami; Tatsuya Ioka
Journal:  PLoS One       Date:  2015-12-03       Impact factor: 3.240

  4 in total

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