Regulated LC-MS/MS bioanalysis technology for therapeutic antibodies and Fc-fusion proteins using structure-indicated approach

被引:4
作者
Iwamoto, Noriko [1 ,2 ]
Shimada, Takashi [1 ,2 ]
机构
[1] Shimadzu Co Ltd, Leading Technol Bioanal & Prot Chem, Kyoto, Japan
[2] Shimadzu Sci Instruments, Shimadzu Biosci Res Partnership, Bothell, WA USA
关键词
nSMOL; LC-MS/MS; Bioanalysis; Monoclonal antibody; Fc-fusion protein; Clinical pharmacokinetics; Therapeutic drug monitoring; LINKED-IMMUNOSORBENT-ASSAY; COMPLEMENTARITY-DETERMINING REGIONS; NANO-SURFACE; MONOCLONAL-ANTIBODY; SELECTIVE DETECTION; MASS-SPECTROMETRY; MS BIOANALYSIS; PLASMA; TRASTUZUMAB; SERUM;
D O I
10.1016/j.dmpk.2018.10.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent studies, the development of bioanalysis technologies using liquid chromatography-tandem mass spectrometry (LC-MS/MS) has attracted attention. Our developed nano-surface and molecularorientation limited (nSMOL) proteolysis enables Fab-specific proteolysis and is optimal for LC-MS/MS analysis of antibody drugs and Fc-fusion proteins in biological samples. In this nSMOL method, antibodies and Fc-fusion proteins are held in pores of the particle and the subsequent proteolysis is carried out with protease-immobilized nanoparticles. The Fab of antibodies or fused region of Fc-fusion protein can be held to orient toward the reaction solution. The access of the immobilized protease is limited to a part in the structure of protein substrate on the particle surface. Thus, nSMOL proteolysis reacts selectively at the Fab complementarity-determining region of antibodies or N-terminal specific domain of Fc-fusion proteins and can be applied to both types of drugs. We have already evaluated drug concentrations in biological samples pretreated with nSMOL proteolysis using LC-MS/MS for more than twenty drugs, of which ten drugs have been fully validated and published. In this review, we discuss the development and application of LC-MS/MS bioanalysis, which enables the bioanalysis of therapeutic antibodies and Fc-fusion proteins by focusing on a structure-based approach. (c) 2018 The Japanese Society for the Study of Xenobiotics. Published by Elsevier Ltd.
引用
收藏
页码:19 / 24
页数:6
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