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利用新型靶向分子探针局部递送进行动脉粥样硬化的体内近红外荧光成像。

In Vivo Near-Infrared Fluorescence Imaging of Atherosclerosis Using Local Delivery of Novel Targeted Molecular Probes.

机构信息

Montreal Heart Institute, 5000 Belanger street, Montreal, Quebec, H1T 1C8, Canada.

Department of medicine, Université de Montréal, 2900 Édouard-Montpetit, Montreal, Quebec, H3T 1J4, Canada.

出版信息

Sci Rep. 2019 Feb 25;9(1):2670. doi: 10.1038/s41598-019-38970-4.

DOI:10.1038/s41598-019-38970-4
PMID:30804367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6389905/
Abstract

This study aimed to evaluate the feasibility and accuracy of a technique for atherosclerosis imaging using local delivery of relatively small quantities (0.04-0.4 mg/kg) of labeled-specific imaging tracers targeting ICAM-1 and unpolymerized type I collagen or negative controls in 13 rabbits with atheroma induced by balloon injury in the abdominal aorta and a 12-week high-cholesterol diet. Immediately after local infusion, in vivo intravascular ultrasonography (IVUS)-NIRF imaging was performed at different time-points over a 40-minute period. The in vivo peak NIRF signal was significantly higher in the molecular tracer-injected rabbits than in the control-injected animals (P < 0.05). Ex vivo peak NIRF signal was significantly higher in the ICAM-1 probe-injected rabbits than in controls (P = 0.04), but not in the collagen probe-injected group (P = 0.29). NIRF signal discrimination following dual-probe delivery was also shown to be feasible in a single animal and thus offers the possibility of combining several distinct biological imaging agents in future studies. This innovative imaging strategy using in vivo local delivery of low concentrations of labeled molecular tracers followed by IVUS-NIRF catheter-based imaging holds potential for detection of vulnerable human coronary artery plaques.

摘要

本研究旨在评估使用局部递送相对少量(0.04-0.4mg/kg)标记的特异性成像示踪剂靶向 ICAM-1 和未聚合的 I 型胶原或阴性对照物的技术在 13 只通过腹主动脉球囊损伤和 12 周高胆固醇饮食诱导动脉粥样硬化的兔子中的可行性和准确性。在局部输注后立即,在 40 分钟的时间内进行不同时间点的体内血管内超声(IVUS)-NIRF 成像。与对照物注射的动物相比,分子示踪剂注射的兔子的体内 NIRF 信号峰值明显更高(P<0.05)。与对照组相比,ICAM-1 探针注射的兔子的体外 NIRF 信号峰值明显更高(P=0.04),但胶原探针注射组则不然(P=0.29)。还表明,在单个动物中进行双探针递送后的 NIRF 信号区分也是可行的,因此为在未来的研究中组合几种不同的生物成像剂提供了可能性。这种使用体内局部递送低浓度标记分子示踪剂然后进行基于 IVUS-NIRF 导管的成像的创新成像策略有可能检测到易损的人类冠状动脉斑块。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/467948d27a1c/41598_2019_38970_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/3ddee6e495c4/41598_2019_38970_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/b1c1a8900595/41598_2019_38970_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/6796dc00e2d5/41598_2019_38970_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/0331fb7e0e67/41598_2019_38970_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/f0f01457df78/41598_2019_38970_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/467948d27a1c/41598_2019_38970_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/3ddee6e495c4/41598_2019_38970_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/b1c1a8900595/41598_2019_38970_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/6796dc00e2d5/41598_2019_38970_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/0331fb7e0e67/41598_2019_38970_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/f0f01457df78/41598_2019_38970_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c68/6389905/467948d27a1c/41598_2019_38970_Fig6_HTML.jpg

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