LC–MS/MS quantification of asymmetric dimethyl arginine and symmetric dimethyl arginine in plasma using surrogate matrix and derivatization with fluorescamine

Author:

Junnotula Venkatraman1,Jones Barry R2,Gorman Shelby3,Shen Miaoqing2,Mulvana Daniel2

Affiliation:

1. Bioanalysis, Immunogenecity & Biomarkers, IVIVT, GlaxoSmithkline Pharmaceuticals, 1250 S. Collegeville Road, Collegeville, PA 19426, USA

2. Q2 Solutions, 19 Brown Road, Ithaca, NY 14850, USA

3. Clinical Biomarkers & Translational Research, Oncology Research & Development, Glaxosmithkline Pharmaceuticals, 1250 S. Collegeville Road, Collegeville, PA 19426, USA

Abstract

Aim: A novel LC–MS/MS method using a surrogate matrix and derivatization with fluorescamine was developed and validated for simultaneous quantification of asymmetric dimethyl arginine and symmetric dimethyl arginine. Methods & results: Asymmetric dimethyl arginine, symmetric dimethyl arginine and corresponding internal standards were extracted using protein precipitation and derivatization with fluorescamine followed by SPE. Derivatives were analyzed by turbo ion spray LC–MS/MS in the positive ion mode. Methodology was successfully transferred across multiple preclinical species and utilized in the support of several investigative studies. Conclusion: A new LC–MS/MS analytical methodology that utilizes a surrogate matrix and derivatization with fluorescamine was successfully developed and validated.

Publisher

Future Science Ltd

Subject

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

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