Evidence map›Paper›PMID 39738105›Full record

ArticleNature communications2024

Heat stable and intrinsically sterile liquid protein formulations.

Atip Lawanprasert, Harminder Singh, Sopida Pimcharoen, Mariangely González Vargas, Arshiya Dewan, Girish S Kirimanjeswara, Scott H Medina

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Atip LawanprasertDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, USA.ORCID 0009-0001-3163-8803
Harminder SinghDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, USA.ORCID 0000-0001-9261-6651
Sopida PimcharoenDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, USA.
Mariangely González VargasDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, USA.
Arshiya DewanDepartment of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, PA, USA.
Girish S KirimanjeswaraDepartment of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, PA, USA.ORCID 0000-0002-9216-1105
Scott H MedinaDepartment of Biomedical Engineering, Pennsylvania State University, University Park, PA, USA. shm126@psu.edu.ORCID 0000-0001-5441-2164

Funding

Resource for Biocomputing Visualization and InformaticsP41GM103311 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2012 to 2017
$8.2M
Understanding and controlling the cellular fate of fluorine-modified biologicsR35GM142902 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Scott Hammond Medina · 2021 to 2026
$2.2M
TA Instruments Low Volume AutoAffinity ITCS10OD025145 · OD · PENNSYLVANIA STATE UNIVERSITY, THE · PI YENNAWAR, NEELA H. · 2018 to 2018
$247k
National Science Foundation (NSF) 1845053NIGMS NIH HHS P41 GM103311NIGMS NIH HHS R35 GM142902NIH HHS S10 OD025145United States Department of Defense | Defense Advanced Research Projects Agency (DARPA) D21AP10182U.S. Department of Health & Human Services | National Institutes of Health (NIH) 1R35-GM142902
6 · The paper itself

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.

Indexed as

Hot TemperatureAnimalsChemistry, PharmaceuticalHumansMiceProteinsProtein StabilityThermodynamicsProteins

Identifiers

PMID39738105
PMCPMC11685576

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.