Efficacy of Contrast-enhanced US and Magnetic Microbubbles Targeted to Vascular Cell Adhesion Molecule-1 for Molecular Imaging of Atherosclerosis

被引:55
|
作者
Wu, Juefei [1 ]
Leong-Poi, Howard [3 ]
Bin, Jianping [1 ]
Yang, Li [2 ]
Liao, Yulin [4 ,5 ]
Liu, Ying [1 ]
Cai, Jingjing [1 ]
Xie, Jiajia [1 ]
Liu, Yili [1 ]
机构
[1] So Med Univ, Nanfang Hosp, Dept Cardiol, Guangzhou 510515, Guangdong, Peoples R China
[2] So Med Univ, Nanfang Hosp, Dept Pharmacol, Guangzhou 510515, Guangdong, Peoples R China
[3] Univ Toronto, Div Cardiol, Li Ka Shing Knowledge Inst, St Michaels Hosp,Keenan Res Ctr, Toronto, ON, Canada
[4] So Med Univ, Dept Pathophysiol, China Japan Collaborat Lab Cardiovasc Physiol, Guangzhou 510515, Guangdong, Peoples R China
[5] So Med Univ, Key Lab Shock & Microcirculat Res, Guangzhou 510515, Guangdong, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
RECENT MYOCARDIAL-ISCHEMIA; P-SELECTIN; INFLAMMATION; RHEOLOGY; DELIVERY;
D O I
10.1148/radiol.11102251
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To evaluate whether microbubbles targeted to vascular cell adhesion molecule-1 (VCAM-1) (CD106) coupled with a magnetic guidance system could improve the efficacy of contrast-enhanced molecular ultrasonography (US) of atherosclerosis in the aorta. Materials and Methods: The animal research committee at Southern Medical University approved all experiments. Adherence of magnetic VCAM-1-targeted microbubbles, control inactive magnetic microbubbles, and nonmagnetic VCAM-1-targeted microbubbles to VCAM-1-Fc was determined in vitro by using a flow chamber at variable shear stress (1-24 dyne/cm(2)) under magnetic field guidance. Attachment of microbubbles under magnetic field guidance was determined in vivo with fluorescent microscopy and contrast-enhanced US of the abdominal aorta in wild-type (C57BL/6) or apolipoprotein E (APOE)-deficient mice on a regular or hypercholesterolemic diet. General factorial analysis of variance was used to compare the targeted effect of the microbubbles among different animal groups to identify significant differences. Results: Attachment was noted for magnetic and nonmagnetic microbubbles but not for inactive magnetic microbubbles; firm attachment at high shear stress (16-20 dyne/cm(2)) was achieved only with magnetic microbubbles. Fluorescence intensity and video intensity were significantly higher in magnetic microbubbles with magnetic field guidance than in inactive magnetic microbubbles and nonmagnetic microbubbles (P < .05). Video intensity from retained magnetic microbubbles in APOE-deficient mice was significantly greater than that in wild-type mice (mean video intensity for APOE-deficient mice: 28.25 [interquartile range, or IQR, 26.55-29.20] with a hypercholesterolemic diet and 16.10 [IQR, 14.15-18.75] with a regular diet; mean video intensity for wild-type mice: 9.55 [IQR, 8.85-10.5] with a hypercholesterolemic diet and 2.90 [IQR, 1.25-3.85] with a regular diet; P < .001). Conclusion: Use of a magnetic targeted microbubble system results in greater attachment to endothelial VCAM-1 in atherosclerotic aortas in conditions of high shear stress and improved detection of early inflammatory changes of atherosclerosis. (C) RSNA, 2011
引用
收藏
页码:463 / 471
页数:9
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