Dhiman Chatterjee

Micron-size bubbles encapsulated by a stabilizing layer of surface-active materials are used in medical ultrasound imaging and drug delivery. Their destruction stimulated by ultrasound plays a critical role in both applications. We investigate the destruction process of microbubbles in a commercially available contrast agent by measuring the attenuation of ultrasound through it. The measurement is performed with single-cycle bursts from an unfocused transducer (with a center frequency of 5 MHz) for varying pressure amplitudes at 50-, 100-, and 200-Hz pulse repetition frequencies (PRF) with duty cycles 0.001%, 0.002%, and 0.004%, respectively. At low excitation, the attenuation is found to increase with time. With increased excitation level, the attenuation level decreases with time, indicating destruction of microbubbles. There is a critical pressure amplitude (∼1.2 MPa) for all three PRFs, below which there is no significant bubble destruction. Above the critical pressure amplitudes the rate of destruction depends on excitation levels. But at high-pressure amplitudes the destruction becomes independent of excitation pressure amplitude. The results are interpreted to identify two different mechanisms of bubble destruction by its signature in attenuation, namely, slow dissolution by diffusion and catastrophic shell rupture. The different modes are discussed in detail with their implications in medical applications. © 2005 American Institute of Physics.

Intravenously injected encapsulated microbubbles improve the contrast of an ultrasound image. Their destruction is used in measuring blood flow, stimulating arteriogenesis, and drug delivery. We measure attenuation and scattering of ultrasound through solution of commercial contrast agents such as Sonazoid and Definity. We have developed a number of different interfacial rheology models for the encapsulation of such microbubbles. By matching with experimentally measured attenuation, we obtain the characteristic rheological parameters. We compare model predictions with measured subharmonic responses. We also investigate microbubble destruction under acoustic excitation by measuring time-varying attenuation data. © 2006 American Institute of Physics.

Broadband attenuation measurement has been widely used for characterizing ultrasound contrast agents. Chen et al. (2002) recently suggested that broadband attenuation data depend on the center frequency of the broadband excitation pulse and, therefore, that they are not a reliable measure of the bubble behavior. We investigated the suitability of measurement of broadband attenuation as a characterizing tool using the contrast agent Definity® as a test case. Analyzing the attenuation data obtained with three broadband unfocused transducers with different center frequencies (2.25, 3.5 and 5 MHz), we found that attenuation is independent of the transducer used and matches in the overlap regions of any two transducers. Attenuation does not depend on excitation pressure amplitude as long as the excitation amplitude remains below a critical value (≈ 0.26 MPa), indicating that the measurement of broadband attenuation below critical excitation can, indeed, be used for characterization. Furthermore, the linear relationship of attenuation with concentrations of Definity® is also investigated. © 2005 World Federation for Ultrasound in Medicine & Biology.

Intravenously injected encapsulated microbubbles improve the contrast of an ultrasound image. Their destruction is used in measuring blood flow, stimulating arteriogenesis, and drug delivery. We measure attenuation and scattering of ultrasound through solution of commercial contrast agents such as Optison (GE Health Care, Princeton, NJ) and Definity (Bristol Meyer-Squibb Imaging, North Ballerina, MA). We have developed an interfacial rheology model for the encapsulation of such microbubbles. By matching with experimental data, we obtain the characteristic rheological parameters. We compare model predictions with other experiments. We also investigate microbubble destruction under acoustic excitation by measuring time-varying attenuation data. Three regions of acoustic pressure amplitudes are found: at low pressure, there is no destruction; at slightly higher pressure bubbles are destroyed, and the rate of destruction depends on a combination of PRF and amplitude. At a still higher pressure amplitude, the attenuation decreases catastrophically. The last two regimes correspond respectively to 1) slow destruction of bubbles due to increased gas diffusion and 2) complete bubble destruction leading to release of free bubbles. An analytical model for the bubble growth and dissolution will be presented. The effects of membrane permeability and elasticity on the stability of microbubbles are investigated. (Supported by DOD, NSF and NIH). © 2008 American Institute of Physics.