Citation: | Yuxiong Gao, Zhendong Chen, Changyong Yang, Dafang Zhong. Liquid chromatography-mass spectrometry method for the quantification of an anti-sclerostin monoclonal antibody in cynomolgus monkey serum[J]. Journal of Pharmaceutical Analysis, 2021, 11(4): 472-479. doi: 10.1016/j.jpha.2020.08.005 |
H. Kaplon, M. Muralidharan, Z. Schneider, et al., Antibodies to watch in 2020, Mabs. 12 (2020) 1703531. https://doi.org/10.1080/19420862.2019.1703531
|
C.W. Lindsley, New 2016 Data and statistics for global pharmaceutical products and projections through 2017. ACS Chem. Neurosci. 8 (2017) 1635-1636. https://doi.org/10.1021/acschemneuro.7b00253
|
Y. Rosenberg-Hasson, L. Hansmann, M. Liedtke, et al., Effects of serum and plasma matrices on multiplex immunoassays. Immunol. Res. 58 (2014) 224-233. https://doi.org/10.1007/s12026-014-8491-6
|
W. Wang, E.Q. Wang, J.P. Balthasar, Monoclonal antibody pharmacokinetics and pharmacodynamics, Clin. Pharmacol. Ther. 84 (2008) 548-558. https://doi.org/10.1038/clpt.2008.170
|
O.H. Brekke, I. Sandlie, Therapeutic antibodies for human diseases at the dawn of the twenty-first century, Nat. Rev. Drug Discov. 2 (2003) 52-62. https://doi.org/10.1038/nrd1060
|
M. Kelley, B. DeSilva, Key elements of bioanalytical method validation for macromolecules, AAPS J. 9 (2007) E156-E163. https://doi.org/10.1208/aapsj0902017
|
A.S. Rosenberg, A. Worobec, A risk-based approach to immunogenicity concerns of therapeutic protein products Part 1 Considering consequences of the immune response to a protein, Biopharm. Int. 17 (2004) 22
|
G. Shankar, C. Pendley, K.E. Stein, A risk-based bioanalytical strategy for the assessment of antibody immune responses against biological drugs, Nat. Biotechnol. 25 (2007) 555-561. https://doi.org/10.1038/nbt1303
|
G. Shankar, D. Finko-Kent, B. Rup, et al., Recommendations on risk-based strategies for detection and characterization of antibodies against biotechnology products, J. Immunol. Methods. 333 (2008) 1-9. https://doi.org/10.1016/j.jim.2008.01.001
|
C.W.N. Damen, J.H.M. Schellens, J.H. Beijnen, Bioanalytical methods for the quantification of therapeutic monoclonal antibodies and their application in clinical pharmacokinetic studies, Hum. Antibodies. 18 (2009) 47-73. https://doi.org/10.3233/HAB-2009-0206
|
J.W. Lee, M. Kelley, L. E. King, et al., Bioanalytical approaches to quantify "total" and "free" therapeutic antibodies and their targets: technical challenges and PK/PD applications over the course of drug development, AAPS J. 13 (2011) 99-110. https://doi.org/10.1208/s12248-011-9251-3
|
B.A.P. Buscher, H. Gerritsen, I.V. Scholl, et al., Quantitative analysis of Tenecteplase in rat plasma samples using LC-MS/MS as an alternative for ELISA, J. Chromatogr. B. 852 (2007) 631-634. https://doi.org/10.1016/j.jchromb.2006.12.053
|
S.T. Wu, Z. Ouyang, T.V. Olah, et al., A strategy for liquid chromatography/tandem mass spectrometry based quantitation of pegylated protein drugs in plasma using plasma protein precipitation with water-miscible organic solvents and subsequent trypsin digestion to generate surrogate peptides for detection Rapid Commun. Mass SP. 25 (2011) 281-290. https://doi.org/10.1002/rcm.4856
|
H.C. Liu, A.V. Manuilov, C. Chumsae, et al., Quantitation of a recombinant monoclonal antibody in monkey serum by liquid chromatography-mass spectrometry, Anal. Chem. 414 (2011) 147-153. https://doi.org/10.1016/j.ab.2011.03.004
|
H. Jiang, J Zeng, C. Titsch C, et al., Fully validated LC-MS/MS assay for the simultaneous quantitation of co-administered therapeutic antibodies in cynomolgus monkey serum, Anal. Chem. 85(2013), 9859-9867. https://doi.org/10.1021/ac402420v
|
Y.X. Gao, D. Zhang, C.Y. Yang, et al., Two validated liquid chromatography-mass spectrometry methods with different pretreatments for the quantification of an anti-CD47 monoclonal antibody in rat and cynomolgus monkey serum compared with an electrochemiluminescence method, J. Pharm. Biome. Anal. 175 (2019) 112792. https://doi.org/10.1016/j.jpba.2019.112792
|
A.S. Rosenberg, A. Worobec, A risk-based approach to immunogenicity concerns of therapeutic protein products. Part II: Considering host-specific and product-specific factors impacting immunogenicity, Biopharm Int. 17 (2004) 34-42
|
G. Shankar, C. Pendley, K.E. Stein. A risk-based bioanalytical strategy for the assessment of antibody immune responses against biological drugs, Nat. Biotechnol. 25 (2007) 555-561. https://doi.org/10.1038/nbt1303
|
A. Johansson, A. Erlandsson, D. Eriksson, et al., Idiotypic-anti-idiotypic complexes and their in vivo metabolism, Cancer 94 (2002) 1306-1313
|
J.M. Sailstad, L. Amaravadi, Clements-Egan A, et al., A white paper-consensus and recommendations of a global harmonization team on assessing the impact of immunogenicity on pharmacokinetic measurements, AAPS J. 16 (2014) 488-498. https://doi.org/10.1208/s12248-014-9582-y
|
T.M. Thway, L. Magana, A. Bautista, et al., Impact of anti-drug antibodies in preclinical pharmacokinetic assessment, AAPS J. 15 (2013) 856-863. https://doi.org/10.1208/s12248-013-9484-4
|
J.S. Wang, S.T. Wu, J. Gokemeijer, et al., Attribution of the discrepancy between ELISA and LC-MS/MS assay results of a PEGylated scaffold protein in post-dose monkey plasma samples due to the presence of anti-drug antibodies, Anal. Bioanal. Chem. 402 (2012) 1229-1239. https://doi.org/10.1007/s00216-011-5527-9
|
J.R. Rojas, R.P. Taylor, M.R. Cunningham, et al., Formation, distribution, and elimination of infliximab and anti-infliximab immune complexes in cynomolgus monkeys, J. Pharm. Exp. Ther. 313 (2005) 578-585. https://doi.org/10.1124/jpet.104.079277
|
R. Jenkins, J.X. Duggan, A.F. Aubry, et al., Recommendations for validation of LC-MS/MS bioanalytical methods for protein biotherapeutics, AAPS J. 17 (2015) 1-16
|
C. Paszty, C.H. Turner, M.K. Robinson, Sclerostin: A gem from the genome leads to bone-building antibodies, J. Bone Miner. Res. 25 (2010) 1897-1904. https://doi.org/10.1002/jbmr.161
|
Z.D. Zhong, S. Dinnogen, M. Hokom, et al., Identification and inhibition of drug target interference in immunogenicity assays, J. Immunol. Methods. 355 (2010) 21-28. https://doi.org/10.1016/j.jim.2010.02.008
|
E.M. Lewiecki. Monoclonal antibodies for the treatment of osteoporosis, Expert. Opin. Biol. Ther. 13 (2013) 183-196. https://doi.org/10.1517/14712598.2012.740006
|
F. Cosman, D.B. Crittenden, J.D. Adachi, et al., Romosozumab treatment in postmenopausal women with osteoporosis, New Engl. J. Med. (2016) NEJMoa1607948. https://doi.org/10.1056/NEJMoa1607948
|
D. Zhang, C.Y. Yang, X.Y. Chen, et al., A bridging immunogenicity assay for monoclonal antibody: case study with SHR-1222, Bioanalysis. (2018) bio-2017-0289-. https://doi.org/10.4155/bio-2017-0289
|
Chinese Pharmacopoeia Commission, General Chapter 0912, Chinese Pharmacopoeia. Beijing, China, 2015
|
European Medicines Agency (EMA), Guideline on Bioanalytical Method Validation, EMA, London, U.K., 2012
|