mRNA-LNP formulations package mRNA for vaccine and gene therapy use. The paper studies how their physicochemical stability changes with composition and storage conditions.
First-pass extracted concept
mRNA-lipid nanoparticles
Candidate: concept label1 source documents6 linked claims
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LNPs, mRNA-LNPs
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increasing Tris buffer concentration accelerated 5'-cap hydrolysis in mRNA-LNP formulations.
Quoted textsource-backed
Increasing Tris buffer concentration accelerated 5'-cap hydrolysis, emphasizing the importance of a low-ionic-strength buffer for LNP formulations.
deep-cold storage at or below -20 °C is necessary to preserve mRNA-LNP integrity.
Quoted textsource-backed
Findings re-emphasize the necessity of deep-cold storage (≤-20 °C) and optimized formulation components to preserve mRNA-LNP integrity
mRNA-LNP formulation stability depends on formulation composition and storage temperature.
Quoted textsource-backed
The long-term stability of mRNA-lipid nanoparticles (LNPs)... relies on managing physicochemical properties to preserve their integrity and effectiveness through optimized formulation components... systematically evaluated LNP formulations with varied compositions... stored at -80 °C, -20 °C, 5 °C, and 25 °C
storage of mRNA-LNP formulations at 25 °C led to complete loss of transfection within six months.
Quoted textsource-backed
Storage at 25 °C led to complete loss of transfection within six months.
storage of mRNA-LNP formulations at 5 °C caused aggregation, reduced in vivo expression, and mRNA degradation.
Quoted textsource-backed
storage at 5 °C caused aggregation, reduced in vivo expression, and mRNA degradation
mRNA-LNP formulations stored at -80 °C and -20 °C retained acceptable stability over the tested period.
Quoted textsource-backed
Formulations stored at -80 °C and -20 °C retained acceptable stability