Biopharmaceutical characterization : the NISTmAb case study
著者
書誌事項
Biopharmaceutical characterization : the NISTmAb case study
（ACS symposium series, 1201 . State-of-the-art and emerging technologies for therapeutic monoclonal antibody characterization ; 2）
American Chemical Society , Distributed in print by Oxford University Press, c2014
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注記
Includes bibliographical references and index
内容説明・目次
内容説明
The focus of this volume is the characterization of monoclonal antibodies (mAbs). The book focuses both on general aspects, techniques, and regulatory concerns common to any recombinant protein, as well as specific analytical results. Volume 2 therefore serves as both a foundational body of NISTmAb product knowledge as well as an evaluation of its suitability as an industry-appropriate reference material (RM).
In Volume 1, a framework was presented, detailing what potential critical quality attributes (PCQAs) should be measured when developing mAbs; offering a risk-based approach to determining and quantifying PCQAs; specifying to what level PCQAs must be measured; and ultimately, explaining why it all matters. In Volume 2, the editors use that framework as a guide to deduce key biochemical and biophysical parameters of the NIST RM. The ultimate goal of Volume 2 is helping researchers have the
clearest picture possible of the NIST RM specifically and mAb characterization in general.
目次
1. Determination of the NISTmAb Primary Structure
2. Sequence Variants and Sequence Variant Analysis in Biotherapeutic Proteins
3. Structural Elucidation of Post-Translational Modifications in Monoclonal Antibodies
4. Orthogonal Technologies for NISTmAb N-Glycan Structure Elucidation and Quantitation
5. Separation Methods and Orthogonal Techniques
6. Biophysical Techniques for Characterizing the Higher Order Structure and Interactions of Monoclonal Antibodies
7. Developability Assessment of a Proposed NIST Monoclonal Antibody
8. Protein Particles (0.1 ?m to 100 ?m)
9. Analytical Methods for the Measurement of Host Cell Proteins and Other Process-Related Impurities
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