Self-Assembly of Giant Unilamellar Vesicles by Film Hydration Methodologies

被引:49
|
作者
Rideau, Emeline [1 ]
Wurm, Frederik R. [1 ]
Landfester, Katharina [1 ]
机构
[1] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
关键词
film hydration; GUV; solvent-free self-assembly; LIPID VESICLES; MEMBRANE-PROTEINS; DISORDERED PHASE; GENTLE HYDRATION; SYNTHETIC CELLS; HYBRID VESICLES; RAPID FORMATION; ELECTROFORMATION; LIPOSOMES; POLYMER;
D O I
10.1002/adbi.201800324
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Self-assembly of lipids or polymeric amphiphiles into vesicular structures has been achieved by various methods since the first generation of liposomes in the 1960s. Vesicles can be obtained with diameters from the nanometer to the micrometer regime. From the perspective of cell mimicking, vesicles with diameters of several micrometers are most relevant. These vesicles are called giant unilamellar vesicles (GUVs). Commonly used methods to form GUVs are solvent-displacement techniques, especially since the development of microfluidics. These methodologies however, trap undesirable organic solvents in their membrane as well as other potentially undesired additives (surfactants, polyelectrolytes, polymers, etc.). In contrast to those strategies, summarized herein are solvent-free approaches as suitable clean alternatives. The vesicles are formed from a dry thin layer of the lipid or amphiphilic polymers and are hydrated in aqueous media using the entropically favored self-assembly of amphiphiles into GUVs. The rearrangement of the amphiphilic films into vesicular structures is usually aided by shear forces such as an alternative current (electroformation) or the swelling of water-soluble polymeric supports (gel-assisted hydration).
引用
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页数:13
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