Show simple item record

dc.contributor.authorVennemann, Antje
dc.contributor.authorBreitenstein, Daniel
dc.contributor.authorTallarek, Elke
dc.contributor.authorMørch, Ýrr Asbjørg
dc.contributor.authorSchmid, Ruth Baumberger
dc.contributor.authorWiemann, Martin
dc.date.accessioned2023-01-24T08:35:03Z
dc.date.available2023-01-24T08:35:03Z
dc.date.created2022-04-30T11:10:01Z
dc.date.issued2022
dc.identifier.citationVennemann, A., Breitenstein, D., Tallarek, E. et al. Subcellular detection of PEBCA particles in macrophages: combining darkfield microscopy, confocal Raman microscopy, and ToF–SIMS analysis. Drug Deliv. and Transl. Res. 12, 2075–2088 (2022). https://doi.org/10.1007/s13346-022-01128-3en_US
dc.identifier.issn2190-393X
dc.identifier.urihttps://hdl.handle.net/11250/3045674
dc.description.abstractThe detection of biomedical organic nanocarriers in cells and tissues is still an experimental challenge. Here we developed an imaging strategy for the label-free detection of poly (ethylbutyl cyanoacrylate) (PEBCA) particles. Experiments were carried out with phagocytic NR8383 macrophages exposed to non-toxic and non-activating concentrations of fluorescent (PEBCA NR668 and PEBCA NR668/IR), non-fluorescent (PEBCA), and cabazitaxel-loaded PEBCA particles (PEBCA CBZ). Exposure to PEBCA NR668 revealed an inhomogeneous particle uptake similar to what was obtained with the free modified Nile Red dye (NR668). In order to successfully identify the PEBCA-loaded cells under label-free conditions, we developed an imaging strategy based on enhanced darkfield microscopy (DFM), followed by confocal Raman microscopy (CRM) and time-of-flight secondary ion mass spectrometry (ToF–SIMS). Nitrile groups of the PEBCA matrix and PEBCA ions were used as suitable analytes for CRM and ToF–SIMS, respectively. Masses found with ToF–SIMS were further confirmed by Orbitrap-SIMS. The combined approach allowed to image small (< 1 µm) PEBCA-containing phagolysosomes, which were identified as PEBCA-containing compartments in NR8383 cells by electron microscopy. The combination of DFM, CRM, and ToF–SIMS is a promising strategy for the label-free detection of PEBCA particles.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectPEBCAen_US
dc.subjectAlveolar macrophageen_US
dc.subjectNR8383 cellen_US
dc.subjectLabel-free detectionen_US
dc.subjectBioimagingen_US
dc.titleSubcellular detection of PEBCA particles in macrophages: combining darkfield microscopy, confocal Raman microscopy, and ToF-SIMS analysisen_US
dc.title.alternativeSubcellular detection of PEBCA particles in macrophages: combining darkfield microscopy, confocal Raman microscopy, and ToF-SIMS analysisen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s) 2022en_US
dc.source.pagenumber2075–2088en_US
dc.source.volume12en_US
dc.source.journalDrug Delivery and Translational Researchen_US
dc.identifier.doi10.1007/s13346-022-01128-3
dc.identifier.cristin2020289
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal