In vitro characterization of a novel, tissue-targeted ultrasonic contrast system with acoustic microscopy

被引:85
作者
Lanza, GM
Trousil, RL
Wallace, KD
Rose, JH [1 ]
Hall, CS
Scott, MJ
Miller, JG
Eisenberg, PR
Gaffney, PJ
Wickline, SA
机构
[1] Washington Univ, Barnes Jewish Hosp, Dept Med, Div Cardiol, St Louis, MO 63110 USA
[2] Washington Univ, Dept Phys, St Louis, MO 63130 USA
[3] Iowa State Univ Sci & Technol, Dept Phys & Astron, Ames, IA 50011 USA
[4] Iowa State Univ Sci & Technol, Ames Lab, Ames, IA 50011 USA
[5] Natl Inst Biol Stand & Controls, Div Hematol, Potters Bar EN6 3QG, Herts, England
关键词
D O I
10.1121/1.423948
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Targeted ultrasonic contrast systems are designed to enhance the reflectivity of selected tissues in vivo [Lanza et nl., Circulation 94, 3334 (1996)]. In particular, these agents hold promise for the minimally invasive diagnosis and treatment of a wide array of pathologies, most notably tumors, thromboses, and inflamed tissues. In the present study, acoustic microscopy was used to assess the efficacy of a novel, perfluorocarbon based contrast agent to enhance the inherent acoustic reflectivity of biological and synthetic substrates. Data from these experiments were used to postulate a simple model describing the observed enhancements. Frequency averaged reflectivity (30-55 MHz) was shown to increase 7.0+/-1.1 dB for nitrocellulose membranes with targeted contrast. Enhancements of 36.0+/-2.3 dB and 8.5+/-0.9 dB for plasma and whole blood clots, respectively, were measured between 20 and 35 MHz. A proposed acoustic transmission Line model predicted the targeted contrast system would increase the acoustic reflectivity of the nitrocellulose membrane, whole blood clot, and fibrin plasma clot by 2.6, 8.0, and 31.8 dB, respectively. These predictions were in reasonable agreement with the experimental results of this paper. In conclusion, acoustic microscopy provides a rapid and sensitive approach for in vitro characterization, development, and testing of mathematical models of targeted contrast systems. Given the current demand for targeted contrast systems for medical diagnostic and therapeutic use, the use of acoustic microscopy may provide a useful tool in the development of these agents. (C) 1998 Acoustical Society of America. [S0001-4966(98)01412-X].
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页码:3665 / 3672
页数:8
相关论文
共 39 条
[1]  
[Anonymous], ECHOCARDIOGRAPHY
[2]   ULTRASONIC CHARACTERIZATION OF ALBUNEX, A NEW CONTRAST AGENT [J].
BLEEKER, HJ ;
SHUNG, KK ;
BARNHART, JL .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1990, 87 (04) :1792-1797
[3]  
CHRISTY DH, 1995, P IEEE ULTR S, P1125
[4]   CELLULAR MECHANISMS OF CAPTOPRIL-INDUCED MATRIX REMODELING IN SYRIAN-HAMSTER CARDIOMYOPATHY [J].
DAVISON, G ;
HALL, CS ;
MILLER, JG ;
SCOTT, M ;
WICKLINE, SA .
CIRCULATION, 1994, 90 (03) :1334-1342
[5]   ULTRASONIC TISSUE CHARACTERIZATION OF END-STAGE DILATED CARDIOMYOPATHY [J].
DAVISON, G ;
HALL, CS ;
MILLER, JG ;
SCOTT, M ;
WICKLINE, SA .
ULTRASOUND IN MEDICINE AND BIOLOGY, 1995, 21 (07) :853-860
[6]   PRINCIPLES AND RECENT DEVELOPMENTS IN ULTRASOUND CONTRAST AGENTS [J].
DEJONG, N ;
TENCATE, FJ ;
LANCEE, CT ;
ROELANDT, JRTC ;
BOM, N .
ULTRASONICS, 1991, 29 (04) :324-330
[7]  
Demos S, 1996, CIRCULATION, V94, P1214
[8]  
Edgell T, 1996, THROMB HAEMOSTASIS, V75, P595
[9]  
Gramiak R, 1968, Invest Radiol, V3, P356
[10]  
HALL C, 1997, APPL TARGETED CONTRA, V97, P1605