Scanned at very high ultrasound frame rates, injectable microbubbles can be activated sequentially as isolated punctual sources of acoustic echoes. These signals can thus be localized far beyond the diffraction limit. The resolution improvement granted by Sono-Activated Ultrasound Localization Microscopy (SAULM) was demonstrated within microfluidic channels 20 times smaller than the imaging wavelength (λ = 870 μm). The width of the channels mapped with SAULM was 13 times smaller than as they appeared under conventional ultrasound imaging. Two channels separated by λ/4.5 could be distinguished. Implementing SAULM in-vivo could lead to a complete reconstruction of the vascular tree down to the smallest capillaries at several centimeter depth.
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21 October 2013
Research Article|
October 25 2013
Sono-activated ultrasound localization microscopy
Yann Desailly;
Yann Desailly
Institut Langevin (ESPCI, CNRS, INSERM)
, 1 rue Jussieu, 75005 Paris, France
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Olivier Couture;
Olivier Couture
a)
Institut Langevin (ESPCI, CNRS, INSERM)
, 1 rue Jussieu, 75005 Paris, France
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Mathias Fink;
Mathias Fink
Institut Langevin (ESPCI, CNRS, INSERM)
, 1 rue Jussieu, 75005 Paris, France
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Mickael Tanter
Mickael Tanter
Institut Langevin (ESPCI, CNRS, INSERM)
, 1 rue Jussieu, 75005 Paris, France
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a)
e-mail: olivier.couture@espci.fr
Appl. Phys. Lett. 103, 174107 (2013)
Article history
Received:
August 19 2013
Accepted:
October 08 2013
Citation
Yann Desailly, Olivier Couture, Mathias Fink, Mickael Tanter; Sono-activated ultrasound localization microscopy. Appl. Phys. Lett. 21 October 2013; 103 (17): 174107. https://doi.org/10.1063/1.4826597
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