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LC-MS/MS assay for the simultaneous quantitation of the ATM inhibitor AZ31 and the ATR inhibitor AZD6738 in mouse plasma.
Kiesel, Brian F; Shogan, Jeffrey C; Rachid, Madani; Parise, Robert A; Vendetti, Frank P; Bakkenist, Christopher J; Beumer, Jan H.
Afiliação
  • Kiesel BF; Cancer Therapeutics Program, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA; Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, USA.
  • Shogan JC; Department of Radiation Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Rachid M; Cancer Therapeutics Program, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
  • Parise RA; Cancer Therapeutics Program, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
  • Vendetti FP; Department of Radiation Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Bakkenist CJ; Department of Radiation Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Beumer JH; Cancer Therapeutics Program, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA; Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, USA; Division of Hematology-Oncology, Department of Medicine, University of Pittsburgh School of Medicine,
J Pharm Biomed Anal ; 138: 158-165, 2017 May 10.
Article em En | MEDLINE | ID: mdl-28213176
ABSTRACT
The ATM kinase inhibitor AZ31 and ATR kinase inhibitor AZD6738 are in various phases of preclinical and clinical evaluation for their ability to potentiate chemoradiation. To support the preclinical evaluation of their pharmacokinetics, we developed and validated an LC-MS/MS assay for the simultaneous quantification of AZ31 and AZD6738 in mouse plasma. A "dilute and shoot" method was used to precipitate proteins from a sample volume of 50µL. Chromatographic separation was achieved using a Phenomenex Polar-RP column and a gradient mobile phase consisting of methanol-water with 0.1% formic acid. Detection was accomplished using a Waters Quattro Micro mass spectrometer in positive ionization mode. The assay utilizing 50µL sample was linear from 10 to 5000ng/mL and determined to be both accurate (-8.2 to 8.6%) and precise (<5.4% CV) and achieved the criteria for U.S. FDA guidance for bioanalytical method validation. Quantification was achieved in mouse tissue homogenate using a separate 200µL sample preparation. This LC-MS/MS assay will be essential for determining the tissue distribution and pharmacokinetics in future mouse studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasma / Pirimidinas / Sulfóxidos / Cromatografia Líquida / Ligas / Espectrometria de Massas em Tandem / Proteínas Mutadas de Ataxia Telangiectasia Tipo de estudo: Guideline Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasma / Pirimidinas / Sulfóxidos / Cromatografia Líquida / Ligas / Espectrometria de Massas em Tandem / Proteínas Mutadas de Ataxia Telangiectasia Tipo de estudo: Guideline Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article