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- W2002378902 abstract "Processing protein solutions into the solid state is a common approach for generating stable amorphous protein mixtures that are suitable for long-term storage. Great care is typically given to protecting the protein native structure during the various drying steps that render it into the amorphous solid state. However, many studies illustrate that chemical and physical degradations still occur in spite of this amorphous material having good glassy properties and it being stored at temperatures below its glass transition temperature (Tg). Because of these persistent issues and recent biophysical studies that have refined the debate ascribing meaning to the molecular dynamical transition temperature and Tg of protein molecules, we provide an updated discussion on the impact of assessing and managing localized, individual protein molecule nondiffusive motions in the context of proteins being prepared into bulk amorphous mixtures. Our aim is to bridge the pharmaceutical studies addressing bulk amorphous preparations and their glassy behavior, with the biophysical studies historically focused on the nondiffusive internal protein dynamics and a protein's activity, along with their combined efforts in assessing the impact of solvent hydrogen-bonding networks on local stability. We also provide recommendations for future research efforts in solid-state formulation approaches." @default.
- W2002378902 created "2016-06-24" @default.
- W2002378902 creator A5039878143 @default.
- W2002378902 creator A5052375005 @default.
- W2002378902 creator A5088530431 @default.
- W2002378902 date "2014-09-01" @default.
- W2002378902 modified "2023-10-14" @default.
- W2002378902 title "The Importance of Individual Protein Molecule Dynamics in Developing and Assessing Solid State Protein Preparations" @default.
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