Observations on the viability of C6-glioma cells after sonoporation with low-intensity ultrasound and microbubbles

Ultrasound (US) and microbubbles can be used to facilitate cellular uptake of drugs through a cavitationinduced enhancement of cell membrane permeability. The mechanism is, however, still incompletely understood. A direct contact between microbubbles and cell membrane is thought to be essential to c...

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Veröffentlicht in:IEEE transactions on ultrasonics, ferroelectrics, and frequency control. - 1986. - 60(2013), 1 vom: 14. Jan., Seite 34-45
1. Verfasser: Van Ruijssevelt, Lisbeth (VerfasserIn)
Weitere Verfasser: Smirnov, Pierre, Yudina, Anna, Bouchaud, Veronique, Voisin, Pierre, Moonen, Chrit
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:IEEE transactions on ultrasonics, ferroelectrics, and frequency control
Schlagworte:Journal Article Annexin A5 Carbocyanines Fluoresceins Fluorescent Dyes Tetrazolium Salts Thiazoles calcein AM 148504-34-1 N(10)-nonylacridine orange mehr... 4C467Q911Y 3,3'-dihexyl-2,2'-oxacarbocyanine 54501-79-0 thiazolyl blue EUY85H477I Acridine Orange F30N4O6XVV
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245 1 0 |a Observations on the viability of C6-glioma cells after sonoporation with low-intensity ultrasound and microbubbles 
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520 |a Ultrasound (US) and microbubbles can be used to facilitate cellular uptake of drugs through a cavitationinduced enhancement of cell membrane permeability. The mechanism is, however, still incompletely understood. A direct contact between microbubbles and cell membrane is thought to be essential to create membrane perturbations lasting from seconds to minutes after US exposure of the cells. A recent study showed that the effect may even last up to 8 h after cavitation (with residual permeability up to 24 h after cavitation). In view of possible membrane damage, the purpose of this study was to further investigate the evolution of cell viability in the range of the 24-h temporal window. Furthermore, a description of the functional changes in tumor cells after US exposure was initiated to obtain a better understanding of the mechanism of membrane perturbation after sonication with microbubbles. Our results suggest that US does not reduce cell viability up to 24 h post-exposure. However, a perturbation of the entire cell population exposed to US was observed in terms of enzymatic activity and characteristics of the mitochondrial membrane. Furthermore, we demonstrated that US cavitation induces a transient loss of cell membrane asymmetry, resulting in phosphatidylserine exposure in the outer leaflet of the cell membrane 
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650 7 |a Carbocyanines  |2 NLM 
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700 1 |a Smirnov, Pierre  |e verfasserin  |4 aut 
700 1 |a Yudina, Anna  |e verfasserin  |4 aut 
700 1 |a Bouchaud, Veronique  |e verfasserin  |4 aut 
700 1 |a Voisin, Pierre  |e verfasserin  |4 aut 
700 1 |a Moonen, Chrit  |e verfasserin  |4 aut 
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