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dc.contributor.authorNawijn, Charlotte
dc.contributor.authorSegers, Tim
dc.contributor.authorLajoinie, Guillaume
dc.contributor.authorMørch, Ýrr Asbjørg
dc.contributor.authorBerg, Sigrid
dc.contributor.authorSnipstad, Sofie
dc.contributor.authorDavies, Catharina de Lange
dc.contributor.authorVersluis, Michel
dc.date.accessioned2023-08-16T06:10:49Z
dc.date.available2023-08-16T06:10:49Z
dc.date.created2021-08-20T08:45:19Z
dc.date.issued2021
dc.identifier.citationJournal of Visualized Experiments. 2021, 2021 (172), .en_US
dc.identifier.issn1940-087X
dc.identifier.urihttps://hdl.handle.net/11250/3084254
dc.description.abstractMicrobubble contrast agents hold great promise for drug delivery applications with ultrasound. Encapsulating drugs in nanoparticles reduces systemic toxicity and increases circulation time of the drugs. In a novel approach to microbubble-assisted drug delivery, nanoparticles are incorporated in or on microbubble shells, enabling local and triggered release of the nanoparticle payload with ultrasound. A thorough understanding of the release mechanisms within the vast ultrasound parameter space is crucial for efficient and controlled release. This set of presented protocols is applicable to microbubbles with a shell containing a fluorescent label. Here, the focus is on microbubbles loaded with poly(2-ethyl-butyl cyanoacrylate) polymeric nanoparticles, doped with a modified Nile Red dye. The particles are fixed within a denatured casein shell. The microbubbles are produced by vigorous stirring, forming a dispersion of perfluoropropane gas in the liquid phase containing casein and nanoparticles, after which the microbubble shell self-assembles. A variety of microscopy techniques are needed to characterize the nanoparticle-stabilized microbubbles at all relevant timescales of the nanoparticle release process. Fluorescence of the nanoparticles enables confocal imaging of single microbubbles, revealing the particle distribution within the shell. In vitro ultra-high-speed imaging using bright-field microscopy at 10 million frames per second provides insight into the bubble dynamics in response to ultrasound insonation. Finally, nanoparticle release from the bubble shell is best visualized by means of fluorescence microscopy, performed at 500,000 frames per second. To characterize drug delivery in vivo, the triggered release of nanoparticles within the vasculature and their extravasation beyond the endothelial layer is studied using intravital microscopy in tumors implanted in dorsal skinfold window chambers, over a timescale of several minutes. The combination of these complementary characterization techniques provides unique insight into the behavior of microbubbles and their payload release at a range of time and length scales, both in vitro and in vivo.en_US
dc.language.isoengen_US
dc.publisherJournal of Visualized Experimentsen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleMulti-timescale microscopy methods for the characterization of fluorescently-labeled microbubbles for ultrasound-triggered drug releaseen_US
dc.title.alternativeMulti-timescale microscopy methods for the characterization of fluorescently-labeled microbubbles for ultrasound-triggered drug releaseen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber24en_US
dc.source.volume2021en_US
dc.source.journalJournal of Visualized Experimentsen_US
dc.source.issue172en_US
dc.identifier.doi10.3791/62251
dc.identifier.cristin1927505
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal