Novel LC–MS/MS method for the determination of selumetinib (AZD6244) in whole blood collected with volumetric absorptive microsampling

Author:

Voggu Ramakrishna R1,Brus Theodore S1,Barksdale Chineta T1,Severin Paul2,Hansen Patricia1,Chudnovskiy Ross1,Thomas Eric1,Bailey Christopher3

Affiliation:

1. Covance Laboratories, Inc., 8211 Scicor Dr, IN 46214, USA

2. Covance Laboratories, Inc., 3301 Kinsman Blvd., Madison, WI 53704, USA

3. Clinical Pharmacology & Safety Sciences, AstraZeneca, Da Vinci Building, Melbourn Science Park, Melbourn, Hertfordshire, SG8 6HB, UK

Abstract

Aim: A method has been developed and validated for quantitation of selumetinib in human whole blood collected using a Mitra™ volumetric absorptive microsampling device. This device is patient-friendly, affording less-invasive sampling with broad applicability to clinical and diagnostic applications – specifically in pediatric populations. Materials & methods: In this method, drug is extracted from the Mitra device via sonication in methanol: Ammonium hydroxide, then analyzed by LC–MS/MS. The linear range for selumetinib analysis is 2.00–2000 ng/ml. Results: All validation parameters met acceptance criteria established in agreement with current regulatory guidance for bioanalytical method validation. The stability of selumetinib in Mitra tips was established at both ambient and frozen conditions. Conclusion: A simple method has been developed and validated for determination of selumetinib from human whole blood, collected using volumetric absorptive microsampling and analyzed by LC–MS/MS.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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