Generic MS-based method for the bioanalysis of therapeutic monoclonal antibodies in nonclinical studies

Author:

Hashii Noritaka1,Tousaka Yoshiko1,Arai Koji2,Goda Ryoya3,Inoue Noriko45,Murata Kazuyuki6,Okuzono Takeshi7,Sasahara Satomi4,Shigeyama Takuma6,Tachiki Hidehisa4,Yamane Shinichi7,Saito Yoshiro8,Ishii-Watabe Akiko1

Affiliation:

1. Division of Biological Chemistry and Biologicals, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-9501, Japan

2. Bioanalysis Department, Advanced Technology Center, Medical Solution Segment, LSI Medience Corp., 30-1, Shimura 3-chome, Itabashi-ku, Tokyo 174-8555, Japan

3. Drug Metabolism & Pharmacokinetics Research Laboratories, R&D Division, Daiichi Sankyo Co., Ltd, 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan

4. Scientific Research and Business Development Department, Towa Pharmaceutical Co., Ltd, Kyoto Research Park KISTIC #202, 134 Chudoji Minami-machi, Shimogyo-ku, Kyoto 600-8818, Japan

5. Current address: Scientific Research and Business Development Department, Towa Pharmaceutical Co., Ltd, National Cerebral & Cardiovascular Center #30602, 6-1, Kishibe Shinmachi, Suita, Osaka 564-8565, Japan

6. Osaka Laboratory, Technical Solution Headquarters Sumika Chemical Analysis Service, Ltd, 1-135, Kasugade-naka 3-chome, Konohana-ku, Osaka 554-0022, Japan

7. Drug Development Solutions Center, Sekisui Medical Co., Ltd, 2117 Muramatsu, Tokai-mura, Naka-gun, Ibaraki 319-1182, Japan

8. Division of Medical Safety Science, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-9501, Japan

Abstract

Aim: A generic bioanalytical method was developed to quantify therapeutic IgG1 monoclonal antibodies (mAbs) in mouse sera by combining an easy sample preparation method with LC/MS using selected reaction monitoring. Materials & methods: Rituximab and trastuzumab were used as model mAbs. A synthetic stable isotope-labeled peptide or a stable isotope-labeled mAb was used as an internal standard. The method feasibility was evaluated by a collaborative study involving six laboratories. Results: The calibration curve ranged from 1.0 to 1000.0 μg/ml (correlation coefficient >0.99). The validation parameters including selectivity, linearity of calibration curve, accuracy and precision met the predefined acceptance criteria. Conclusion: Our method is a useful bioanalytical method for the quantification of therapeutic IgG mAbs in nonclinical animal studies.

Publisher

Future Science Ltd

Subject

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

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