Starosolski Zbigniew, Bhavane Rohan, Ghaghada Ketan B, Vasudevan Sanjeev A, Kaay Alexander, Annapragada Ananth
Edward B. Singleton Department of Pediatric Radiology, Texas Children's Hospital, Houston, Texas, United States of America.
Department of Surgery, Baylor College of Medicine, Houston, Texas, United States of America.
PLoS One. 2017 Nov 9;12(11):e0187563. doi: 10.1371/journal.pone.0187563. eCollection 2017.
Indocyanine green (ICG), a FDA approved near infrared (NIR) fluorescent agent, is used in the clinic for a variety of applications including lymphangiography, intra-operative lymph node identification, tumor imaging, superficial vascular imaging, and marking ischemic tissues. These applications operate in the so-called "NIR-I" window (700-900 nm). Recently, imaging in the "NIR-II" window (1000-1700 nm) has attracted attention since, at longer wavelengths, photon absorption, and scattering effects by tissue components are reduced, making it possible to image deeper into the underlying tissue. Agents for NIR-II imaging are, however, still in pre-clinical development. In this study, we investigated ICG as a NIR-II dye. The absorbance and NIR-II fluorescence emission of ICG were measured in different media (PBS, plasma and ethanol) for a range of ICG concentrations. In vitro and in vivo testing were performed using a custom-built spectral NIR assembly to facilitate simultaneous imaging in NIR-I and NIR-II window. In vitro studies using ICG were performed using capillary tubes (as a simulation of blood vessels) embedded in Intralipid solution and tissue phantoms to evaluate depth of tissue penetration in NIR-I and NIR-II window. In vivo imaging using ICG was performed in nude mice to evaluate vascular visualization in the hind limb in the NIR-I and II windows. Contrast-to-noise ratios (CNR) were calculated for comparison of image quality in NIR-I and NIR-II window. ICG exhibited significant fluorescence emission in the NIR-II window and this emission (similar to the absorption profile) is substantially affected by the environment of the ICG molecules. In vivo imaging further confirmed the utility of ICG as a fluorescent dye in the NIR-II domain, with the CNR values being ~2 times those in the NIR-I window. The availability of an FDA approved imaging agent could accelerate the clinical translation of NIR-II imaging technology.
吲哚菁绿(ICG)是一种经美国食品药品监督管理局(FDA)批准的近红外(NIR)荧光剂,在临床上用于多种应用,包括淋巴管造影、术中淋巴结识别、肿瘤成像、浅表血管成像以及标记缺血组织。这些应用在所谓的“NIR-I”窗口(700 - 900纳米)内进行。最近,“NIR-II”窗口(1000 - 1700纳米)的成像引起了关注,因为在更长的波长下,组织成分对光子的吸收和散射效应会降低,从而能够对更深层的底层组织进行成像。然而,用于NIR-II成像的试剂仍处于临床前开发阶段。在本研究中,我们研究了ICG作为一种NIR-II染料的情况。在不同介质(磷酸盐缓冲盐水、血浆和乙醇)中,针对一系列ICG浓度测量了ICG的吸光度和NIR-II荧光发射。使用定制的光谱近红外组件进行体外和体内测试,以促进在NIR-I和NIR-II窗口同时成像。使用嵌入脂质乳剂溶液和组织模型中的毛细管(作为血管模拟)进行ICG的体外研究,以评估在NIR-I和NIR-II窗口中的组织穿透深度。在裸鼠中进行ICG的体内成像,以评估NIR-I和II窗口中后肢的血管可视化情况。计算对比度噪声比(CNR)以比较NIR-I和NIR-II窗口中的图像质量。ICG在NIR-II窗口中表现出显著的荧光发射,并且这种发射(类似于吸收谱)受到ICG分子环境的显著影响。体内成像进一步证实了ICG作为NIR-II领域荧光染料的效用,其CNR值约为NIR-I窗口中的2倍。一种经FDA批准的成像剂的可用性可以加速NIR-II成像技术的临床转化。