In vitro characterization of liposomes and Optison® by acoustic scattering at 3.5 MHz

被引:39
作者
Coussios, CC
Holland, CK
Jakubowska, L
Huang, SL
MacDonald, RC
Nagaraj, A
McPherson, DD
机构
[1] Univ Cincinnati, Dept Biomed Engn, Cincinnati, OH USA
[2] Northwestern Univ, Dept Biochem Mol Biol & Cell Biol, Evanston, IL USA
[3] Northwestern Univ, Dept Internal Med, Chicago, IL 60611 USA
[4] Northwestern Univ, Feinberg Cardiovasc Res Inst, Chicago, IL 60611 USA
关键词
liposome; Optison (R); contrast agent; backscattering coefficient; acoustic scattering; attenuation;
D O I
10.1016/j.ultrasmedbio.2003.10.015
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Liposomes are phospholipid vesicles that can encapsulate both gas and fluid. With antibody conjugation, new formulations, known as immunoliposomes, can be targeted to atheroma and other pathologic components and are, thus, being developed as novel diagnostic ultrasound (US) echo contrast agents to enhance atherosclerosis imaging. The majority of these echogenic liposomes range in diameter from 0.25 to 5.0 mum. To quantify the echogenicity of liposome suspensions of varying concentrations, the backscattering coefficient at 3.5 MHz was determined experimentally. The backscattering coefficient was also estimated theoretically as a function of air volume fraction by modeling the encapsulated air as a free air bubble and assuming single bubble scattering. For most of the liposome concentrations examined in this study (on the order of 10(8)/mL), the backscattering coefficient equals or exceeds that of Optison(R) at the human clinical dosage (on the order of 10(4)/mL). Experimental measurement of the decrease in backscattering coefficient shows promise as a sensitive method for determining whether liposomes are left intact or destroyed during imaging; thus, helping to explore their potential as a vehicle for targeted drug delivery. In addition, the attenuation of US through liposome suspensions is negligible at 3.5 MHz relative to the attenuation through Optison(R) (0.25 dB/cm), suggesting that liposomes have a much higher scatter-to-attenuation ratio and could be more efficient as contrast agents.
引用
收藏
页码:181 / 190
页数:10
相关论文
共 41 条
[21]   Feasibility of mitral flow assessment by echo-contrast ultrasound, part I: Determination of the properties of echo-contrast agents [J].
Herman, B ;
Einav, S ;
Vered, Z .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2000, 26 (05) :787-795
[22]   Compressibility and density of lipid bilayers composed of polyunsaturated phospholipids and cholesterol [J].
Hianik, T ;
Haburcak, M ;
Lohner, K ;
Prenner, E ;
Paltauf, F ;
Hermetter, A .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1998, 139 (02) :189-197
[23]  
Hoff L., 2001, ACOUSTIC CHARACTERIZ
[24]   Physical correlates of the ultrasonic reflectivity of lipid dispersions suitable as diagnostic contrast agents [J].
Huang, SL ;
Hamilton, AJ ;
Pozharski, E ;
Nagaraj, A ;
Klegerman, ME ;
McPherson, DD ;
MacDonald, RC .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2002, 28 (03) :339-348
[25]   Improving ultrasound reflectivity and stability of echogenic liposomal dispersions for use as targeted ultrasound contrast agents [J].
Huang, SL ;
Hamilton, AJ ;
Nagaraj, A ;
Tiukinhoy, SD ;
Klegerman, ME ;
McPherson, DD ;
MacDonald, RC .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (12) :1917-1926
[26]  
JONES JP, 1989, ULTRASONIC IMAGING, V11, P137
[27]   EVALUATION OF FREQUENCY-DEPENDENCE OF BACKSCATTER COEFFICIENT IN NORMAL AND ATHEROSCLEROTIC AORTIC WALLS [J].
LANDINI, L ;
SARNELLI, R ;
PICANO, E ;
SALVADORI, M .
ULTRASOUND IN MEDICINE AND BIOLOGY, 1986, 12 (05) :397-401
[28]   METHOD OF DATA REDUCTION FOR ACCURATE DETERMINATION OF ACOUSTIC BACKSCATTER COEFFICIENTS [J].
MADSEN, EL ;
INSANA, MF ;
ZAGZEBSKI, JA .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1984, 76 (03) :913-923
[29]   Frequency and concentration dependence of the backscatter coefficient of the ultrasound contrast agent Albunex® [J].
Marsh, JN ;
Hughes, MS ;
Hall, CS ;
Lewis, SH ;
Trousil, RL ;
Brandenburger, GH ;
Levene, H ;
Miller, JG .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1998, 104 (03) :1654-1666
[30]  
NG KH, 1993, CIRCULATION, V88, P502