Heat stable and intrinsically sterile liquid protein formulations

Over 80% of biologic drugs, and 90% of vaccines, require temperature-controlled conditions throughout the supply chain to minimize thermal inactivation and contamination. This cold chain is costly, requires stringent oversight, and is impractical in remote environments. Here, we report chemical dispersants that non-covalently solvate proteins within fluorous liquids to alter their thermodynamic equilibrium and reduce conformational flexibility. This generates non-aqueous, fluorine-based liquid protein formulations that biochemically rigidify protein structure to yield thermally stable biologics at extreme temperatures (up to 90 °C). These non-aqueous formulations are impervious to contamination by microorganismal pathogens, degradative enzymes, and environmental impurities, and display comparable pre-clinical pharmacokinetics and safety profiles to standard saline protein samples. As a result, we deliver a fluorochemical formulation paradigm that may limit the need for cold chain logistics of protein reagents and biopharmaceuticals.

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Publication Details

Journal
Nature Communications
Published
2024-12-30
DOI
https://doi.org/10.1038/s41467-024-55304-9
Citations
2
Primary Topic
Protein purification and stability
Type
article
Field-Weighted Citation Impact
0.47

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article

Heat stable and intrinsically sterile liquid protein formulations

Atip Lawanprasert, Mariangely González Vargas, Sopida Pimcharoen, Scott H. Medina et al.
2 citations
Nature Communications
Protein purification and stability
0.47
article

Heat stable and intrinsically sterile liquid protein formulations

Atip Lawanprasert, Mariangely González Vargas, Sopida Pimcharoen, Scott H. Medina, Girish S. Kirimanjeswara, Harminder Singh, Arshiya Dewan
article en
2 citations

Abstract

Over 80% of biologic drugs, and 90% of vaccines, require temperature-controlled conditions throughout the supply chain to minimize thermal inactivation and contamination. This cold chain is costly, requires stringent oversight, and is impractical in remote environments. Here, we report chemical dispersants that non-covalently solvate proteins within fluorous liquids to alter their thermodynamic equilibrium and reduce conformational flexibility. This generates non-aqueous, fluorine-based liquid protein formulations that biochemically rigidify protein structure to yield thermally stable biologics at extreme temperatures (up to 90 °C). These non-aqueous formulations are impervious to contamination by microorganismal pathogens, degradative enzymes, and environmental impurities, and display comparable pre-clinical pharmacokinetics and safety profiles to standard saline protein samples. As a result, we deliver a fluorochemical formulation paradigm that may limit the need for cold chain logistics of protein reagents and biopharmaceuticals.

Nature CommunicationsVol. 15(1)
Pennsylvania State University (US), Center for Disease Dynamics, Economics & Policy (US)
National Science Foundation, University of Pennsylvania, Pennsylvania State University, National Institutes of Health, Defense Advanced Research Projects Agency, University of California, San Francisco, Materials Research Institute, Pennsylvania State University, Division of Materials Research
Openalex Percentile: Top 33%
Protein purification and stability
0.47
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Heat stable and intrinsically sterile liquid protein formulations — Atip Lawanprasert, Mariangely González Vargas, et al. · Nature Communications (2024) | TGRS Research Map | TGRS