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In vitro demonstration of focused ultrasound thrombolysis using bifrequency excitation.

作者信息

Saletes Izella, Gilles Bruno, Auboiroux Vincent, Bendridi Nadia, Salomir Rares, Béra Jean-Christophe

机构信息

Inserm, U1032, LabTau and Université de Lyon, 69003 Lyon, France ; Université Lyon 1, 69003 Lyon, France.

Faculty of Medicine, University of Geneva, 1211 Geneva, Switzerland ; Clinatec/LETI/CEA, 38054 Grenoble, France.

出版信息

Biomed Res Int. 2014;2014:518787. doi: 10.1155/2014/518787. Epub 2014 Aug 27.

DOI:10.1155/2014/518787
PMID:25243147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4163449/
Abstract

Focused ultrasound involving inertial cavitation has been shown to be an efficient method to induce thrombolysis without any pharmacological agent. However, further investigation of the mechanisms involved and further optimization of the process are still required. The present work aims at studying the relevance of a bifrequency excitation compared to a classical monofrequency excitation to achieve thrombolysis without any pharmacological agent. In vitro human blood clots were placed at the focus of a piezoelectric transducer. Efficiency of the thrombolysis was assessed by weighing each clot before and after sonication. The efficiencies of mono- (550 kHz) and bifrequency (535 and 565 kHz) excitations were compared for peak power ranging from 70 W to 220 W. The thrombolysis efficiency appears to be correlated to the inertial cavitation activity quantified by passive acoustic listening. In the conditions of the experiment, the power needed to achieve 80% of thrombolysis with a monofrequency excitation is reduced by the half with a bifrequency excitation. The thermal effects of bifrequency and monofrequency excitations, studied using MR thermometry measurements in turkey muscle samples where no cavitation occurred, did not show any difference between both types of excitations when using the same power level.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/3f04f31c1034/BMRI2014-518787.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/89944688c623/BMRI2014-518787.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/ecb79ec0c7d5/BMRI2014-518787.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/034099d90f8d/BMRI2014-518787.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/fe999cea7149/BMRI2014-518787.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/6107e6632519/BMRI2014-518787.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/78d29650017b/BMRI2014-518787.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/5eeaef3cdc27/BMRI2014-518787.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/3f04f31c1034/BMRI2014-518787.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/89944688c623/BMRI2014-518787.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/ecb79ec0c7d5/BMRI2014-518787.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/034099d90f8d/BMRI2014-518787.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/fe999cea7149/BMRI2014-518787.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/6107e6632519/BMRI2014-518787.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/78d29650017b/BMRI2014-518787.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/5eeaef3cdc27/BMRI2014-518787.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/4163449/3f04f31c1034/BMRI2014-518787.008.jpg

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