Evidence map›Paper›PMID 27549027›Full record

ArticleThe Analyst2016

Nano electrospray gas-phase electrophoretic mobility molecular analysis (nES GEMMA) of liposomes: applicability of the technique for nano vesicle batch control.

Victor U Weiss, Carlos Urey, Andreas Gondikas, Monika Golesne, Gernot Friedbacher, Frank von der Kammer, Thilo Hofmann, Roland Andersson, György Marko-Varga, Martina Marchetti-Deschmann and 1 more

Abstract read
In one paragraph

Article in The Analyst, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Victor U WeissInstitute of Chemical Technologies and Analytics, TU Wien, Vienna, Austria. guenter.allmaier@tuwien.ac.at.
Carlos UreyDepartment of Surgery, University of Lund, Lund, Sweden.
Andreas GondikasDepartment of Environmental Geosciences and Environmental Science Research Network, University of Vienna, Vienna, Austria.
Monika GolesneInstitute of Chemical Technologies and Analytics, TU Wien, Vienna, Austria. guenter.allmaier@tuwien.ac.at.
Gernot FriedbacherInstitute of Chemical Technologies and Analytics, TU Wien, Vienna, Austria. guenter.allmaier@tuwien.ac.at.
Frank von der KammerDepartment of Environmental Geosciences and Environmental Science Research Network, University of Vienna, Vienna, Austria.
Thilo HofmannDepartment of Environmental Geosciences and Environmental Science Research Network, University of Vienna, Vienna, Austria.
Roland AnderssonDepartment of Surgery, University of Lund, Lund, Sweden.
György Marko-VargaBiomedical Center, University of Lund, Lund, Sweden.
Martina Marchetti-DeschmannInstitute of Chemical Technologies and Analytics, TU Wien, Vienna, Austria. guenter.allmaier@tuwien.ac.at.
Günter AllmaierInstitute of Chemical Technologies and Analytics, TU Wien, Vienna, Austria. guenter.allmaier@tuwien.ac.at.

Funding

Austrian Science Fund FWF P 25749
6 · The paper itself

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.

Indexed as

ElectrophoresisGasesLipidsLiposomesMicroscopy, Atomic ForceParticle SizeGasesLipidsLiposomes

Identifiers

PMID27549027
PMCPMC5066478

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.