Passive mapping for real-time monitoring of ultrasound therapy.

Passive mapping for real-time monitoring of ultrasound therapy.

Arrays of detectors placed co-axially with a therapeutic transducer make it possible to receive the high-frequency emissions produced by tissue during therapeutic ultrasound excitation with high sensitivity and in real time, whether in the presence or absence of cavitation activity. The signals rece...

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Bibliografiske detaljer
Main Authors:	Coussios, C, Gyongy, M, Ritchie, R, Webb, I, Nandlall, S, Jackson, E, Arvanitis, C, Bazan-Peregrino, M, Arora, M
Format:	Conference item
Udgivet:	2010

Lignende værker

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A real-time controller for sustaining thermally relevant acoustic cavitation during ultrasound therapy.
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Thin-film sparse boundary array design for passive acoustic mapping during ultrasound therapy.
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Sum-of-harmonics method for improved narrowband and broadband signal quantification during passive monitoring of ultrasound therapies
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Monitoring cell and tissue damage during ablation by high-intensity focussed ultrasound
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On the Applicability of the Thermal Dose Cumulative Equivalent Minutes Metric to the Denaturation of Bovine Serum Albumin in a Polyacrylamide Tissue Phantom
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Passive acoustic mapping of extravasation following ultrasound-enhanced drug delivery
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Real-time temperature estimation and monitoring of HIFU ablation through a combined modeling and passive acoustic mapping approach.
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Use of Passive Arrays for Characterization and Mapping of Cavitation Activity during HIFU Exposure
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Broadband ultrasonic attenuation estimation and compensation with passive acoustic mapping
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Real-time three-dimensional passive cavitation detection for clinical high intensity focused ultrasound systems.
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Spatiotemporal assessment of the cellular safety of cavitation-based therapies by passive acoustic mapping
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Ultrasound-enhanced delivery of polymer-coated oncolytic adenovirus for tumour growth inhibition
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Controlled ultrasound-induced blood-brain barrier disruption using passive acoustic emissions monitoring.
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Use of micro- and nano-sized inertial cavitation nuclei to trigger and map drug release from cavitation-sensitive liposomes.
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