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Preparation of nanoliposomes by microfluidic mixing in herring-bone channel and the role of membrane fluidity in liposomes formation

J. Kotouček, F. Hubatka, J. Mašek, P. Kulich, K. Velínská, J. Bezděková, M. Fojtíková, E. Bartheldyová, A. Tomečková, J. Stráská, D. Hrebík, S. Macaulay, I. Kratochvílová, M. Raška, J. Turánek,

. 2020 ; 10 (1) : 5595. [pub] 20200327

Jazyk angličtina Země Velká Británie

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc20028356

Grantová podpora
NV16-30299A MZ0 CEP - Centrální evidence projektů

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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$a Preparation of nanoliposomes by microfluidic mixing in herring-bone channel and the role of membrane fluidity in liposomes formation / $c J. Kotouček, F. Hubatka, J. Mašek, P. Kulich, K. Velínská, J. Bezděková, M. Fojtíková, E. Bartheldyová, A. Tomečková, J. Stráská, D. Hrebík, S. Macaulay, I. Kratochvílová, M. Raška, J. Turánek,
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$a 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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$a Mašek, Josef $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic.
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$a Kulich, Pavel $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic.
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$a Velínská, Kamila $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic.
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$a Bezděková, Jaroslava $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic. Mendel University in Brno, Department of Chemistry and Biochemistry, Zemedelska 1, 61300, Brno, Czech Republic.
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$a Fojtíková, Martina $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic.
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$a Bartheldyová, Eliška $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic.
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$a Tomečková, Andrea $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic.
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$a Stráská, Jana $u Regional Centre of Advanced Technologies and Materials, Palacký University, Šlechtitelů 11, 78371, Olomouc, Czech Republic.
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$a Hrebík, Dominik $u Central European Institute of Technology CEITEC, Structural Virology, Masaryk University, Kamenice 753/5, 62500, Brno, Czech Republic.
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$a Macaulay, Stuart $u Malvern Panalytical, Malvern, Worcestershire, United Kingdom.
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$a Kratochvílová, Irena $u Institute of Physics, Czech Academy of Sciences, Na Slovance 2, Prague 8, Czechia. krat@fzu.cz.
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$a Raška, Milan $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic. milan.raska@upol.cz. Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Hněvotínská 3, 775 15, Olomouc, Czech Republic. milan.raska@upol.cz.
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$a Turánek, Jaroslav $u Department of Pharmacology and Immunotherapy, Veterinary Research Institute, v.v.i., Hudcova 70, 621 00, Brno, Czech Republic. turanek@vri.cz.
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