脂质体
脂质双层
双层
膜流动性
生物物理学
微流控
膜
小泡
荧光各向异性
化学
磷脂
色谱法
材料科学
纳米技术
生物化学
生物
作者
Jan Kotouček,František Hubatka,Josef Mašek,Pavel Kulich,Kamila Velínská,Jaroslava Bezděková,Martina Fojtíková,Eliška Bartheldyová,Andrea Tomečková,Jana Stráská,D. Hrebik,Stuart Macaulay,Irena Kratochvílová,Milan Raška,Jaroslav Tuřánek
标识
DOI:10.1038/s41598-020-62500-2
摘要
Introduction of microfluidic mixing technique opens a new door for preparation of the liposomes and lipid-based nanoparticles by on-chip technologies that are applicable in a laboratory and industrial scale. This study demonstrates the role of phospholipid bilayer fragment as the key intermediate in the mechanism of liposome formation by microfluidic mixing in the channel with "herring-bone" geometry used with the instrument NanoAssemblr. The fluidity of the lipid bilayer expressed as fluorescence anisotropy of the probe N,N,N-Trimethyl-4-(6-phenyl-1,3,5-hexatrien-1-yl) was found to be the basic parameter affecting the final size of formed liposomes prepared by microfluidic mixing of an ethanol solution of lipids and water phase. Both saturated and unsaturated lipids together with various content of cholesterol were used for liposome preparation and it was demonstrated, that an increase in fluidity results in a decrease of liposome size as analyzed by DLS. Gadolinium chelating lipids were used to visualize the fine structure of liposomes and bilayer fragments by CryoTEM. Experimental data and theoretical calculations are in good accordance with the theory of lipid disc micelle vesiculation.
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