Identifying the inertial cavitation threshold and skull effects in a vessel phantom using focused ultrasound and microbubbles.
Identifying the inertial cavitation threshold and skull effects in a vessel phantom using focused ultrasound and microbubbles.
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DOI:
10.1016/j.ultrasmedbio.2010.02.009
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发表时间:
2010-05
影响因子:
2.9
通讯作者:
Konofagou, Elisa E.
中科院分区:
文献类型:
--
作者:
Tung, Yao-Sheng;Choi, James J.;Baseri, Babak;Konofagou, Elisa E.
Focused ultrasound (FUS) in combination with microbubbles has been shown capable of delivering large molecules to the brain parenchyma through opening of the blood-brain barrier (BBB). However, the mechanism behind the opening remains unknown. To investigate the pressure threshold for inertial cavitation of preformed microbubbles during sonication, passive cavitation detection in conjunction with B-mode imaging was used. A cerebral vessel was simulated by generating a cylindrical hole of 610 µm in diameter inside a polyacrylamide gel and saturating its volume with microbubbles. Definity microbubbles (Mean diameter range: 1.1–3.3 µm, Lantheus Medical Imaging, N. Billerica, MA, USA) were injected prior to sonication (frequency: 1.525 MHz; pulse length: 100 cycles; PRF: 10 Hz; sonication duration: 2 s) through an excised mouse skull. The acoustic emissions due to the cavitation response were passively detected using a cylindrically focused hydrophone, confocal with the FUS transducer and a linear-array transducer with the field of view perpendicular to the FUS beam. The broadband spectral response acquired at the passive cavitation detector (PCD) and the B-mode images identified the occurrence and location of the inertial cavitation, respectively. Findings indicated that the peak-rarefactional pressure threshold was approximately equal to 0.45 MPa, with or without the skull present. Mouse skulls did not affect the threshold of inertial cavitation but resulted in a lower inertial cavitation dose. The broadband response could be captured through the murine skull, so the same PCD set-up can be used in future in vivo applications.
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影响因子:
3.5
作者:
Chomas, JE;Dayton, P;Ferrara, K
通讯作者:
Ferrara, K
影响因子:
19.7
作者:
Hynynen, K;McDannold, N;Jolesz, FA
通讯作者:
Jolesz, FA
影响因子:
2.9
作者:
Choi, James J.;Wang, Shougang;Tung, Yao-Sheng;Morrison, Barclay, III;Konofagou, Elisa E.
通讯作者:
Konofagou, Elisa E.
DOI:
10.1109/tbme.2009.2034533
发表时间:
2010-01
期刊:
IEEE transactions on bio-medical engineering
影响因子:
--
作者:
Choi JJ;Feshitan JA;Baseri B;Wang S;Tung YS;Borden MA;Konofagou EE
通讯作者:
Konofagou EE
影响因子:
2.9
作者:
Takegami, K;Kaneko, Y;Nagawa, H
通讯作者:
Nagawa, H