Abstract

Liposomes are biodegradable nanoparticle vesicles consisting of a lipid bilayer encapsulating an aqueous core. Entrapped cargo material is shielded from the extra-vesicular medium and sustained release of encapsulated material can be achieved. However, application of liposomes as nano-carriers demands their characterization concerning size and size distribution, particle-number concentration, occurrence of vesicle building blocks in solution and determination of the resulting vesicle encapsulation capacity. These questions can be targeted via gas-phase electrophoretic mobility molecular analysis (GEMMA) based on a nano electrospray (nES) charge-reduction source. This instrument separates single-charged nanoparticles in the gas-phase according to size in a high-laminar sheath-flow by means of an orthogonal, tunable electric field. nES GEMMA analysis enables to confirm liposome integrity after passage through the instrument (in combination with atomic force microscopy) as well as to exclude vesicle aggregation. Additionally, nanoparticle diameters at peak apexes and size distribution data are obtained. Differences of hydrodynamic and dry particle diameter values, as well as the effect of number- and mass-based concentration data analysis on obtained liposome diameters are shown. Furthermore, the repeatability of liposome preparation is studied, especially upon incorporation of PEGylated lipids in the bilayer. Finally, the instruments applicability to monitor mechanical stress applied to vesicles is demonstrated.

Highlights

  • Liposomes are nanoparticles formed from a lipid bilayer encapsulating an aqueous interior

  • Application of dried compressed air leads to improved removal of solvent molecules attached to vesicle surface and more homogeneous nano electrospray (nES) gas-phase electrophoretic mobility molecular analysis (GEMMA) peaks

  • Peaks at lower EM diameter values gain in their intensity as these peaks probably originate from lipid molecular aggregates, disrupted liposome bilayers or smaller vesicles. For future measurements these results indicate that nES GEMMA is an appropriate analytical technique to investigate the impact of mechanical stress on liposomes

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Summary

Introduction

Liposomes are nanoparticles formed from a lipid bilayer encapsulating an aqueous interior. Particle distributions are shifted to lower diameter values in doing so, still smaller sized sample components cannot be detected in the given case due to the method inherent preferential detection of larger analytes.

Results
Conclusion

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