Helmholtz Zentrum München, Institute for Biological and Medical Imaging, Ingolstädter Landstr. 1, 85764, Neuherberg, Germany; Chair for Biological Imaging (CBI), Technische Universität München (TUM), Trogerstr. 9, 81675, Munich, Germany.
Cardiovascular Research Center and Cardiology Division, Massachusetts General Hospital, Harvard Medical School, 185 Cambridge Street, Boston, MA 025114, USA.
Eur Heart J Cardiovasc Imaging. 2017 Nov 1;18(11):1253-1261. doi: 10.1093/ehjci/jew222.
(i) to evaluate a novel hybrid near-infrared fluorescence-intravascular ultrasound (NIRF-IVUS) system in coronary and peripheral swine arteries in vivo; (ii) to assess simultaneous quantitative biological and morphological aspects of arterial disease.
Two 9F/15MHz peripheral and 4.5F/40MHz coronary near-infrared fluorescence (NIRF)-IVUS catheters were engineered to enable accurate co-registrtation of biological and morphological readings simultaneously in vivo. A correction algorithm utilizing IVUS information was developed to account for the distance-related fluorescence attenuation due to through-blood imaging. Corrected NIRF (cNIRF)-IVUS was applied for in vivo imaging of angioplasty-induced vascular injury in swine peripheral arteries and experimental fibrin deposition on coronary artery stents, and of atheroma in a rabbit aorta, revealing feasibility to intravascularly assay plaque structure and inflammation. The addition of ICG-enhanced NIRF assessment improved the detection of angioplasty-induced endothelial damage compared to standalone IVUS. In addition, NIRF detection of coronary stent fibrin by in vivo cNIRF-IVUS imaging illuminated stent pathobiology that was concealed on standalone IVUS. Fluorescence reflectance imaging and microscopy of resected tissues corroborated the in vivo findings.
Integrated cNIRF-IVUS enables simultaneous co-registered through-blood imaging of disease related morphological and biological alterations in coronary and peripheral arteries in vivo. Clinical translation of cNIRF-IVUS may significantly enhance knowledge of arterial pathobiology, leading to improvements in clinical diagnosis and prognosis, and helps to guide the development of new therapeutic approaches for arterial diseases.
(i)评估新型近红外荧光-血管内超声(NIRF-IVUS)系统在体内冠状动脉和外周猪动脉中的应用;(ii)评估动脉疾病的同时定量生物学和形态学方面。
设计了两种 9F/15MHz 外周和 4.5F/40MHz 冠状动脉近红外荧光(NIRF)-IVUS 导管,以实现体内生物和形态学读数的精确同步配准。开发了一种利用 IVUS 信息的校正算法,以校正由于透血成像导致的距离相关荧光衰减。校正后的 NIRF(cNIRF)-IVUS 用于活体成像,以研究猪外周动脉球囊血管成形术后血管损伤、冠状动脉支架上实验性纤维蛋白沉积以及兔主动脉粥样硬化,揭示了血管内评估斑块结构和炎症的可行性。与单独的 IVUS 相比,ICG 增强的 NIRF 评估的加入提高了对血管成形术后内皮损伤的检测。此外,通过体内 cNIRF-IVUS 成像对冠状动脉支架纤维蛋白的 NIRF 检测揭示了单独 IVUS 掩盖的支架病理生物学。切除组织的荧光反射成像和显微镜检查证实了体内发现。
集成的 cNIRF-IVUS 能够同时对活体冠状动脉和外周动脉的与疾病相关的形态和生物学改变进行同步配准的血管内透血成像。cNIRF-IVUS 的临床转化可能显著增强对动脉病理生物学的认识,从而改善临床诊断和预后,并有助于指导动脉疾病新治疗方法的发展。