The evolution of medical ultrasonics requires continual evaluation of safety issues. Concern presently centers on the nonthermal bioeffects mechanisms of gas body activation (GBA) and inertial cavitation, particularly in relation to the use of gas-body contrast agents in diagnostic ultrasound procedures. If suitable gas bodies are present initially, GBA occurs with a possibility of cell membrane damage. At higher amplitudes, inertial cavitation may be initiated with a risk of cellular DNA damage. In mammals, these phenomena can be subtle or dramatically destructive: the potential exists for both harmful side effects and therapeutic benefit. This research has four specific aims: (1) Sensitive non- rotating exposure systems are planned, which can bring out micro-scale interactions between cells and bubbles and reveal the fundamental dosimetric relationships. (2) Gas-body contrast agents inject the potential for cavitational bioeffects into otherwise risk-free exposure conditions. Experiments will be aimed at characterizing the behavior of these agents at low levels and at determining if they can lead to inertial cavitation under medically-relevant conditions. In addition, the bioeffects capability of the agents will be examined with emphasis on specific targeting of cancer cells for therapeutic purposes. (3) DNA strand breaks induced by direct exposure of cells to inertial cavitation have recently been revealed by the novel """"""""comet"""""""" assay. The mechanisms and genetic consequences of such DNA damage will be examined, and its relation, if any to medical ultrasonics will be determined. (4) Intestinal hemorrhage can be induced by either ultrasonic heating or by cavitation acting alone. The possible synergistic enhancement of this effect will be studied when both mechanisms operate. Finally, tissue damage related to cavitation or activation of gas-body contrast agents in other organs, such as the kidney, will be investigated and defined. The quantitative dosimetric information resulting from this research is urgently needed for risk assessment and guidance of sonographers, and for developing the full therapeutic potential of medical ultrasound.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA042947-17
Application #
6172523
Study Section
Diagnostic Radiology Study Section (RNM)
Program Officer
Baker, Houston
Project Start
1987-01-01
Project End
2001-03-31
Budget Start
2000-04-19
Budget End
2001-03-31
Support Year
17
Fiscal Year
2000
Total Cost
$344,116
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Miller, Douglas L; Quddus, Jawaid (2002) Diagnostic ultrasound-induced membrane damage in phagocytic cells loaded with contrast agent and its relation to Doppler-mode images. IEEE Trans Ultrason Ferroelectr Freq Control 49:1094-102
Miller, D L; Quddus, J (2001) Lysis and sonoporation of epidermoid and phagocytic monolayer cells by diagnostic ultrasound activation of contrast agent gas bodies. Ultrasound Med Biol 27:1107-13
Miller, D L; Spooner, G J; Williams, A R (2001) Photodisruptive laser nucleation of ultrasonic cavitation for biomedical applications. J Biomed Opt 6:351-8
Miller, D L; Quddus, J (2000) Sonoporation of monolayer cells by diagnostic ultrasound activation of contrast-agent gas bodies. Ultrasound Med Biol 26:661-7
Miller, D L; Quddus, J (2000) Diagnostic ultrasound activation of contrast agent gas bodies induces capillary rupture in mice. Proc Natl Acad Sci U S A 97:10179-84
Miller, D L; Gies, R A (2000) The influence of ultrasound frequency and gas-body composition on the contrast agent-mediated enhancement of vascular bioeffects in mouse intestine. Ultrasound Med Biol 26:307-13
Miller, D L; Bao, S; Gies, R A et al. (1999) Ultrasonic enhancement of gene transfection in murine melanoma tumors. Ultrasound Med Biol 25:1425-30
Miller, D L; Bao, S; Morris, J E (1999) Sonoporation of cultured cells in the rotating tube exposure system. Ultrasound Med Biol 25:143-9
Miller, D L; Gies, R A (1999) Consequences of lithotripter shockwave interaction with gas body contrast agent in mouse intestine. J Urol 162:606-9
Williams, A R; Bao, S; Miller, D L (1999) Filtroporation: A simple, reliable technique for transfection and macromolecular loading of cells in suspension. Biotechnol Bioeng 65:341-6

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