Absolute quantification of a therapeutic domain antibody using ultra-performance liquid chromatography-mass spectrometry and immunoassay

被引:22
|
作者
Szapacs, Matthew E. [1 ]
Urbanski, James J. [1 ]
Kehler, Jonathan R. [1 ]
Wilson, Robert [2 ]
Boram, Sharon L. [1 ]
Hottenstein, Charles S. [1 ]
Citerone, David R. [1 ]
机构
[1] GlaxoSmithKline Inc, Worldwide Bioanal, Drug Metab & Pharmacokinet, King Of Prussia, PA 19406 USA
[2] GlaxoSmithKline Inc, Biopharmaceut R&D Unit, Stevenage, Herts, England
关键词
PROTEIN; PLASMA; LC/MS/MS; DISSOCIATION; EXTRACTION; INHIBITOR; BIOMARKER; PEPTIDES; ELASTASE; STANDARD;
D O I
10.4155/BIO.10.70
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Domain antibodies (dAbs; similar to 10-15 kDa) are made up of the variable heavy chain or the variable light chain of the antibody structure, and retain binding capability, dAbs have proved difficult to detect in plasma using immunoassay without specific antibodies raised against the dAb. Results: A sensitive and selective UPLC-MS/MS method for the absolute quantification of a dAb in monkey plasma was developed (range: 1 to 500 ng/ml) without the need for a specific capture antibody. This method was used to analyze pharmacokinetic studies early on in drug development. Furthermore, an immunoassay was developed and the pharmacokinetic samples were reanalyzed. Conclusion: The two assays show good correlation (r(2) = 0.92), giving confidence in using either method for quantification of the dAb.
引用
收藏
页码:1597 / 1608
页数:12
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