DocumentCode
2101237
Title
Ultrasound contrast agents phagocytosed by neutrophils demonstrate acoustic activity
Author
Dayton, Paul A. ; Lindner, Jonathan R. ; Chomas, James E. ; Morgan, Karen E. ; Simon, Scott ; Lum, Aaron ; May, Donovan ; Coggins, Matthew P. ; Ferrara, Kathy W.
Author_Institution
Div. of Biomed. Eng., California Univ., Davis, CA, USA
Volume
2
fYear
1999
fDate
1999
Firstpage
1705
Abstract
Ultrasound contrast agents are microbubbles composed of a thin lipid or albumin shell filled with air or a high molecular weight gas. These microbubbles are used for contrast-enhanced ultrasound (CEU) assessment of organ perfusion. In regions of inflammation, microbubbles are phagocytosed intact by activated neutrophils adherent to the venular wall. The authors hypothesized that microbubbles remain acoustically active following phagocytosis. Accordingly, they assessed the physical responses of both phagocytosed and free microbubbles by direct microscopic observation during delivery of repetitive single pulses of ultrasound at various acoustic pressures. Insonation results in oscillation in the bubbles volume. Microbubbles were optically recorded during insonation with a high-speed imaging system and diameter-time curves were analyzed to determine the effect of phagocytosis. Phagocytosed microbubbles retained their acoustic activity, although the intracellular environment increased viscoelastic damping experienced by microbubbles. With a pulse of high acoustic intensity (>1 MPa), phagocytosed microbubbles expanded up to 500% of their initial radii, which occasionally resulted in neutrophil rupture. Primary radiation force displaced phagocytosed microbubbles a distance of 100 microns with an acoustic pressure of -240 kPa and a pulse repetition frequency of 10 kHz, thus providing further evidence of acoustic activity. The authors conclude that phagocytosed microbubbles exhibit viscoelastic damping and yet are susceptible to acoustic destruction. They can generate non-linear echoes on the same order of magnitude as free microbubbles. These results indicate that CEU may be used to identify and assess regions of inflammation by detecting acoustic signals from microbubbles that are phagocytosed by activated neutrophils. In addition, the rapid expansion of a microbubble at high acoustic pressure may present a means to rupture a neutrophil or drug capsule at a specific site, resulting in delivery of a drug
Keywords
biomedical ultrasonics; blood; cellular biophysics; -240 kPa; 1 MPa; 10 kHz; 100 mum; acoustic activity; acoustic destruction; acoustic pressure; activated neutrophils; contrast-enhanced ultrasound assessment; drug capsule; high molecular weight gas; high-speed imaging system; inflammation regions assessment; insonation; intracellular environment; medical diagnostic imaging; neutrophil rupture; nonlinear echoes characterization; nonlinear echoes generation; optically recorded microbubbles; organ perfusion; phagocytosed ultrasound contrast agents; venular wall; viscoelastic damping; white blood cells; Acoustic pulses; Damping; Drugs; Elasticity; High speed optical techniques; Lipidomics; Microscopy; Optical pulses; Ultrasonic imaging; Viscosity;
fLanguage
English
Publisher
ieee
Conference_Titel
Ultrasonics Symposium, 1999. Proceedings. 1999 IEEE
Conference_Location
Caesars Tahoe, NV
ISSN
1051-0117
Print_ISBN
0-7803-5722-1
Type
conf
DOI
10.1109/ULTSYM.1999.849326
Filename
849326
Link To Document