共 32 条
Elucidation of lipid nanoparticle surface structure in mRNA vaccines
被引:23
作者:
Wang, Mingzhang Maple
[1
]
Wappelhorst, Caitlin N.
[1
]
Jensen, Erika L.
[1
]
Chi, Ying-Chih Thomas
[1
]
Rouse, Jason C.
[2
]
Zou, Qin
[1
]
机构:
[1] Pfizer Inc, Analyt Res & Dev, BioTherapeut Pharmaceut Sci, 875 Chesterfield Pkwy West, Chesterfield, MO 63017 USA
[2] Pfizer Inc, Analyt Res & Dev, BioTherapeut Pharmaceut Sci, 1 Burtt Rd, Andover, MA 01810 USA
关键词:
POLYETHYLENE-GLYCOL;
TRIGGERED RELEASE;
NMR-SPECTROSCOPY;
EX-VIVO;
SIRNA;
PH;
IMPACT;
D O I:
10.1038/s41598-023-43898-x
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Lipid nanoparticles (LNPs) have been used as a carrier for messenger RNA (mRNA) vaccines. Surface properties of LNPs are important to the stability and function of mRNA vaccines. Polyethylene-glycol (PEG) is a functional lipid at the surface of LNPs that improves colloidal stability, increases circulation time, and impacts cellular uptake. In this study, we explore in-depth lipid composition at the surface of mRNA-LNPs using high-field nuclear magnetic resonance (NMR) spectroscopy. Our results provide a unique surface lipid profile of intact LNPs identifying PEG chains and partial ionizable lipids are present with quantification capability. The surface PEG density is determined to reveal the brush-like conformation on the surface of mRNA-LNPs. Furthermore, we implement a diffusion NMR strategy for routine testing of formulated drug products during drug development. Comparative NMR analysis of different vaccine preparations and stability samples provides a global view of the mRNA-LNP surface structure for enhanced product knowledge.
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页数:8
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