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1.
Nanomedicine ; 58: 102745, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38499167

ABSTRACT

Understanding the stability of mRNA loaded lipid nanoparticles (mRNA-LNPs) is imperative for their clinical development. Herein, we propose the use of size-exclusion chromatography coupled with dual-angle light scattering (SEC-MALS) as a new approach to assessing mRNA-LNP stability in pure human serum and plasma. By applying a dual-column configuration to attenuate interference from plasma components, SEC-MALS was able to elucidate the degradation kinetics and physical property changes of mRNA-LNPs, which have not been observed accurately by conventional dynamic light scattering techniques. Interestingly, both serum and plasma had significantly different impacts on the molecular weight and radius of gyration of mRNA-LNPs, suggesting the involvement of clotting factors in desorption of lipids from mRNA-LNPs. We also discovered that a trace impurity (~1 %) in ALC-0315, identified as its O-tert-butyloxycarbonyl-protected form, greatly diminished mRNA-LNP stability in serum. These results demonstrated the potential utility of SEC-MALS for optimization and quality control of LNP formulations.


Subject(s)
Chromatography, Gel , Lipids , Nanoparticles , RNA, Messenger , Humans , RNA, Messenger/genetics , RNA, Messenger/blood , Nanoparticles/chemistry , Lipids/chemistry , Dynamic Light Scattering , Plasma/chemistry , Light , Scattering, Radiation , Serum/chemistry , RNA Stability , Liposomes
2.
Mol Cells ; 25(3): 397-406, 2008 May 31.
Article in English | MEDLINE | ID: mdl-18443420

ABSTRACT

Computational modeling of signal transduction is currently attracting much attention as it can promote the understanding of complex signal transduction mechanisms. Although several mathematical models have been used to examine signaling pathways, little attention has been given to crosstalk mechanisms. In this study, an attempt was made to develop a computational model for the pathways involving growth-factor-mediated mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3'-kinase/protein kinase B (PI3K/Akt). In addition, the dynamics of the protein activities were analyzed based on a set of kinetic data. The simulation approach integrates the information on several levels and predicts systems behavior. The in-silico analysis conducted revealed that the Raf and Akt pathways act independently.


Subject(s)
Extracellular Signal-Regulated MAP Kinases/metabolism , MAP Kinase Signaling System , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism , Computer Simulation , Enzyme Inhibitors/pharmacology , ErbB Receptors/metabolism , Kinetics , Models, Biological , Receptor, Nerve Growth Factor/metabolism , raf Kinases/metabolism
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