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Today's Medical & Research News



Biotechnology Business


Studies from Amgen, Inc. reveal new findings on biotechnology business



November 6th, 2009




Related Topics
United States
Thousand Oaks
Amgen Inc
Biotechnology Business
Biotechnology Company
Pharmaceutical Business
Pharmaceutical Company
Pharmaceutical Sciences
Pharmaceuticals
Amgen Inc
According to a study from the United States, "Antibody formulation development relies on accelerated stability data at elevated temperatures to optimize formulation parameters. However, the pH- and temperature-dependence of aggregation is complicated for antibody formulations."

"In this study, a human monoclonal IgG2 antibody exhibited typical pH-dependent dimer formation under normal storage conditions (4 and/or 29 degrees C). However, an inversed pH-dependence was discovered for high molecular weight aggregate formation at elevated temperatures (37 degrees C). The different stability profiles exhibited at the various storage conditions resulted in nonlinearity of the Arrhenius kinetics. Thermal unfolding at or below 37 degrees C was not evident by differential scanning calorimetry. Enriched populations of the structural isoforms of the IgG2 subclass were tested for their unique temperature and pH-dependence of aggregation. The Arrhenius kinetics of aggregation for each of the individual IgG2 isoforms was also nonlinear. However, the temperature-dependence of clipping suggested that clip-mediated aggregation was responsible for the increased higher order aggregates at low pH and elevated temperatures. Unique clip species resulting from the conformational differences between the IgG2 isoforms lead to increased aggregation," wrote N. Perico and colleagues, Amgen, Inc.

The researchers concluded: "These results have implications on the mechanisms of antibody aggregation and on the validity of accelerated data to predict shelf-life accurately."

Perico and colleagues published the results of their research in the Journal of Pharmaceutical Sciences (Conformational Implications of an Inversed pH-Dependent Antibody Aggregation. Journal of Pharmaceutical Sciences, 2009;98(9):3031-3042).

For additional information, contact M.S. Ricci, Amgen Inc., Formulat & Analyt Resources, Processing & Prod Development, 1 Amgen Center Dr., Thousand Oaks, CA 91320, USA.

The publisher of the Journal of Pharmaceutical Sciences can be contacted at: John Wiley & Sons Inc., 111 River St., Hoboken, NJ 07030, USA.

Keywords: United States, Thousand Oaks, Amgen Inc., Biotechnology Business, Biotechnology Company, Pharmaceutical Business, Pharmaceutical Company, Pharmaceutical Sciences, Pharmaceuticals, Amgen, Inc.

This article was prepared by NewsRx editors from staff and other reports. Copyright 2009, NewsRx.com.

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