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A Comprehensive Evaluation of Nanoparticle Tracking Analysis (NanoSight) for Characterization of Proteinaceous Submicron Particles
被引:46
作者:

Tian, Xinsheng
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Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark
Leiden Univ, Leiden Acad Ctr Drug Res, Cluster BioTherapeut, Div Drug Delivery Technol, Leiden, Netherlands Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark

Nejadnik, M. Reza
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Leiden Univ, Leiden Acad Ctr Drug Res, Cluster BioTherapeut, Div Drug Delivery Technol, Leiden, Netherlands Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark

Baunsgaard, Dorrit
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Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark

Henriksen, Anette
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Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark

Rischel, Christian
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Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark

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机构:
[1] Novo Nordisk AS, Large Prot Biophys & Formulat, Malov, Denmark
[2] Leiden Univ, Leiden Acad Ctr Drug Res, Cluster BioTherapeut, Div Drug Delivery Technol, Leiden, Netherlands
关键词:
monoclonal IgG antibody;
subvisible particle;
nanoparticle tracking analysis;
protein aggregation;
stability;
protein formulation;
SUBVISIBLE PARTICLES;
MONOCLONAL-ANTIBODY;
IMMUNOGENICITY;
AGGREGATION;
IGG1;
FRACTIONATION;
MODEL;
MASS;
D O I:
10.1016/j.xphs.2016.08.009
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Nanoparticle tracking analysis (NTA) has attracted great interest for application in the field of submicron particle characterization for biopharmaceuticals. It has the virtue of direct sample visualization and particle-by-particle tracking, but the complexity of method development has limited its routine applicability. We systematically evaluated data collection and processing parameters as well as sample handling methods using shake-stressed protein samples. The camera shutter and gain were identified as the key factors influencing NTA results. We also demonstrated that sample filtration was necessary for NTA analysis if there were high numbers of micron particles, whereas the choice of filter membrane was critical for data quality. Sample dilution into corresponding formulation buffer did not affect particle size distributions in our study. Finally, NTA analysis exhibited excellent repeatability in intraday comparison of multiple measurements on the same sample and interday comparison on different batches of samples. Shaking-induced protein aggregation could also be sensitively monitored by NTA. In conclusion, NTA analysis can be used as a robust stability-indicating method for the characterization of proteinaceous submicron particles and thereby complement other analytical methods, provided that consistent sample handling and parametric settings are established for the specific case study. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
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页码:3366 / 3375
页数:10
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