A novel uHPLC-MS/MS method for the quantitation of AZD7451 (AZ12607092) in human plasma. Academic Article uri icon

Overview

abstract

  • Tropomyosin-related kinases (Trk) are tyrosine kinase receptors implicated in tumor proliferation, invasion, and survival signaling across a number of tumors, making them potentially attractive targets for the treatment of cancer. AZD7451 is a potent and selective inhibitor of Trk kinases currently undergoing a Phase I dose escalation in glioblastoma multiforme at the National Cancer Institute. A key part of early clinical testing for AZD7451 involves demonstrating that pharmacokinetic half-life and clinical exposures of AZD7451 are sufficient to inhibit Trk receptors in preclinical models. To address this need, an ultra sensitive analytical method was developed to measure the AZD7451 profile in human plasma. A liquid-liquid extraction recovered >80% of AZD7451 before quantitative analysis by ultra HPLC-MS/MS. A Varian Polaris(®) C18-A column and a mass transition of m/z 383.5→340.5 (m/z 389.6→342.0 for the internal standard [(2)H6]-AZD7451) was used, and a dynamic calibration range of 0.5-1000ng/mL was established, which provided a sensitive (<8.5% deviation), and precise (<6%) quantitative assay for AZD7451. AZD7451 demonstrated stability in human plasma at room temperature for 24h (<7% change) and after extraction at 4°C for 24h (<8% change), and was stable through 4 freeze/thaw cycles (<8% change). This method was used to measure AZD7451 plasma levels in clinical samples to confirm the sensitivity at several time points following AZD7451 treatment in subjects with glioblastoma.

publication date

  • October 22, 2013

Research

keywords

  • 2-Aminopurine
  • Antineoplastic Agents
  • Chromatography, High Pressure Liquid
  • Protein Kinase Inhibitors
  • Pyrazoles
  • Receptor Protein-Tyrosine Kinases
  • Tandem Mass Spectrometry

Identity

PubMed Central ID

  • PMC3864870

Scopus Document Identifier

  • 84887591431

Digital Object Identifier (DOI)

  • 10.1016/j.jchromb.2013.10.023

PubMed ID

  • 24239935

Additional Document Info

volume

  • 942-943