Determination of intracellular fludarabine triphosphate in human peripheral blood mononuclear cells by LC-MS/MS

J Pharm Biomed Anal. 2013 Dec:86:198-203. doi: 10.1016/j.jpba.2013.08.007. Epub 2013 Aug 23.

Abstract

Fludarabine is a nucleoside analog routinely used in conditioning regimens of pediatric allogeneic stem cell transplantation to promote stem cell engraftment. In children, it remains a challenge to accurately and precisely quantify the active intracellular triphosphate species of fludarabine in vivo, primarily due to limitations on blood volume and inadequate assay sensitivity. Here we report a liquid chromatography tandem mass spectrometry (LC-MS/MS) method for determination of fludarabine triphosphate in human peripheral blood mononuclear cells (PBMC). PBMC (∼5 million cells) were collected and lysed in 1mL 70% methanol containing 1.2mM tris buffer (pH 7.4). The lysate (80μL) was mixed with internal standard (2-chloro-adenosine triphosphate, 150ng/mL, 20μL) and injected onto an API5000 LC-MS/MS system. Separation was achieved on a hypercarb column (100mm×2.1mm, 3μm) eluted with 100mM ammonium acetate (pH 9.8) and acetonitrile in a gradient mode at a flow rate of 0.4mL/min. Multiple reactions monitoring (MRM) and electrospray ionization in negative mode (ESI(-)) were used for detection. The ion pairs 524.0/158.6 for the drug and 540.0/158.8 for the IS were selected for quantification and 524.0/425.7 used for confirmation. Retention time was 3.0 and 3.4min for fludarabine triphosphate and the IS, respectively. The concentration range for the calibration curve was 1.52-76nM. Our method is simple, fast, and has been successfully applied in a clinical dose-concentration study in children to quantify intracellular fludarabine in low volume clinical samples. The median concentration was 1.03 and 3.19pmole/million PBMC at trough and peak time points, respectively. Fludarabine triphosphate is degraded in water within hours but relatively stable in 70% methanol-tris (1.2mM, pH 7.4). One limitation is that the hypercarb column takes a longer time to equilibrate than conventional reverse phase columns, and peaks become broad and distorted if the column is not washed and stored properly.

Keywords: 2-chloroadenosine triphosphate; Cl-ara-ATP; F-ara-ATP; Fludarabine triphosphate; Hypercarb column; LC–MS/MS; PBMC; PK; Stability; alloHCT; allogeneic hematopoietic cell transplantation; fludarabine triphosphate; peripheral blood mononuclear cells; pharmacokinetic.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, Liquid / methods
  • Humans
  • Intracellular Fluid / chemistry*
  • Intracellular Fluid / metabolism*
  • Leukocytes, Mononuclear / chemistry*
  • Leukocytes, Mononuclear / metabolism*
  • Mass Spectrometry / methods
  • Tandem Mass Spectrometry / methods*
  • Vidarabine / analogs & derivatives*
  • Vidarabine / analysis
  • Vidarabine / blood

Substances

  • Vidarabine
  • fludarabine