Literature DB >> 27890509

Small-scale screening method for low-viscosity antibody solutions using small-angle X-ray scattering.

Masakazu Fukuda1, Atsushi Watanabe2, Akira Hayasaka3, Masaru Muraoka4, Yuji Hori3, Tadao Yamazaki2, Yoshimi Imaeda5, Akiko Koga2.   

Abstract

In this study, we investigated the concentration range in which self-association starts to form in humanized IgG monoclonal antibody (mAb) solutions. Furthermore, on the basis of the results, we developed a practical method of screening for low-viscosity antibody solutions by using small-angle X-ray scattering (SAXS) measurements utilizing small quantities of samples. With lower-viscosity mAb3, self-association was not detected in the range of 1-80mg/mL. With higher-viscosity mAb1, on the other hand, self-association was detected in the range of 10-20mg/mL and was clearly enhanced by a decrease in temperature. The viscosities of mAb solutions at 160, 180, and 200mg/mL at 25°C quantitatively correlated very well with the particle size parameters obtained by SAXS measurements of mAb solutions at 15mg/mL at 5°C. The quantity of mAb sample required for the SAXS measurements was only 0.15mg, which is about one-hundredth of that required for actual viscosity measurements at a high concentration, and such quantities could be available even at an early stage of development. In conclusion, the SAXS analysis method proposed in this study is a valuable tool for the development of concentrated mAb therapeutics with high manufacturability and high usability for subcutaneous injection.
Copyright © 2016 Elsevier B.V. All rights reserved.

Keywords:  Cluster; High concentration; Monoclonal antibody; Self-association; Small-angle X-ray scattering; Viscosity

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Year:  2016        PMID: 27890509     DOI: 10.1016/j.ejpb.2016.11.027

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  3 in total

Review 1.  The role of small-angle scattering in structure-based screening applications.

Authors:  Po-Chia Chen; Janosch Hennig
Journal:  Biophys Rev       Date:  2018-10-10

2.  The solution structure of the human IgG2 subclass is distinct from those for human IgG1 and IgG4 providing an explanation for their discrete functions.

Authors:  Gar Kay Hui; Antoni D Gardener; Halima Begum; Charles Eldrid; Konstantinos Thalassinos; Jayesh Gor; Stephen J Perkins
Journal:  J Biol Chem       Date:  2019-05-14       Impact factor: 5.157

3.  Dissecting the molecular basis of high viscosity of monospecific and bispecific IgG antibodies.

Authors:  Cholpon Tilegenova; Saeed Izadi; Jianping Yin; Christine S Huang; Jiansheng Wu; Diego Ellerman; Sarah G Hymowitz; Benjamin Walters; Cleo Salisbury; Paul J Carter
Journal:  MAbs       Date:  2020 Jan-Dec       Impact factor: 5.857

  3 in total

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