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Ultrasonic contrast agent shell rupture detected by inertial cavitation and rebound signals

  • Azzdine Y. Ammi
  • , Robin O. Cleveland
  • , Jonathan Mamou
  • , Giace I. Wang
  • , S. Lori Bridal
  • , William D. O'Brien

Research output: Contribution to journalArticlepeer-review

Abstract

Determining the rupture pressure threshold of ultrasound contrast agent microbubbles has significant applications for contrast imaging, development of therapeutic agents, and evaluation of potential bioeffects. Using a passive cavitation detector, this work evaluates rupture based on acoustic emissions from single, encapsulated, gas-filled microbubbles. Sinusoidal ultrasound pulses were transmitted into weak solutions of Optison™ at different center frequencies (0.9, 2.8, and 4.6 MHz), pulse durations (three, five, and seven cycles of the center frequencies), and peak rarefactional pressures (0.07 to 5.39 MPa). Pulse repetition frequency was 10 Hz. Signals detected with a 13-MHz, center-frequency transducer revealed postexcitation acoustic emissions (between 1 and 5 μs after excitation) with broadband spectral content. The observed acoustic emissions were consistent with the acoustic signature that would be anticipated from inertial collapse followed by "rebounds" when a microbubble ruptures and thus generates daughter/free bubbles that grow and collapse. The peak rarefactional pressure threshold for detection of these emissions increased with frequency (e.g., 0.53, 0.87, and 0.99 MPa for 0.9, 2.8, and 4.6 MHz, respectively; five-cycle pulse duration) and decreased with pulse duration. The emissions identified in this work were separated from the excitation in time and spectral content, and provide a novel determination of microbubble shell rupture.

Original languageEnglish (US)
Pages (from-to)126-135
Number of pages10
JournalIEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control
Volume53
Issue number1
DOIs
StatePublished - Jan 2006
Externally publishedYes

Funding

Manuscript received December 29, 2004; accepted June 16, 2005. This work was supported by NIH Grant EB02641 (formerly HL58218) awarded to the University of Illinois at Urbana-Champaign. This work was supported by the cooperative project for biomedical engineering between the University of Illi- nois at Urbana-Champaign, and the Centre National de la Recherche Scientifique, France. R. O. C. was supported by a “Bourses de Recherche” from the Scientific Advisory Board of the Mayor of Paris.

FundersFunder number
Author National Institutes of Health National Institutes of Health National Institutes of Health National Institutes of Health The Bev Hartig Huntington's Disease Foundation National Institutes of HealthHL58218
National Institute of Biomedical Imaging and BioengineeringR37EB002641
University of Illinois Urbana-Champaign
Centre National de la Recherche Scientifique

    ASJC Scopus subject areas

    • Instrumentation
    • Acoustics and Ultrasonics
    • Electrical and Electronic Engineering

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