Gao Duyang, Luo Zichao, He Yang, Yang Lixiang, Hu Dehong, Liang Yongye, Zheng Hairong, Liu Xiaogang, Sheng Zonghai
Paul C. Lauterbur Research Center for Biomedical Imaging, CAS Key Laboratory of Health Informatics, Shenzhen Key Laboratory of Ultrasound Imaging and Therapy, Institute of Biomedical and Health Engineering, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, P. R. China.
Department of Chemistry and Center for NanoMedicine, National University of Singapore, Singapore, 117543, Singapore.
Small. 2023 Apr;19(17):e2206544. doi: 10.1002/smll.202206544. Epub 2023 Jan 29.
Fluorescence imaging in the second near-infrared window (NIR-II, 1000-1700 nm) provides a powerful tool for in vivo structural and functional imaging in deep tissue. However, the lack of biocompatible contrast agents with bright NIR-II emission has hindered its application in fundamental research and clinical trials. Herein, a liposome encapsulation strategy for generating ultrabright liposome-cyanine dyes by restricting dyes in the hydrophobic pockets of lipids and inhibiting the aggregation, as corroborated by computational modeling, is reported. Compared with free indocyanine green (ICG, an US Food and Drug Administration-approved cyanine dye), liposome-encapsulated ICG (S-Lipo-ICG) shows a 38.7-fold increase in NIR-II brightness and enables cerebrovascular imaging at only one-tenth dose over a long period (30 min). By adjusting the excitation wavelength, two liposome-encapsulated cyanine dyes (S-Lipo-ICG and S-Lipo-FD1080) enable NIR-II dual-color imaging. Moreover, small tumor nodules (2-5 mm) can be successfully distinguished and removed with S-Lipo-ICG image-guided tumor surgery in rabbit models. This liposome encapsulation maintains the metabolic pathway of ICG, promising for clinical implementation.
第二近红外窗口(NIR-II,1000 - 1700纳米)中的荧光成像为深部组织的体内结构和功能成像提供了一个强大的工具。然而,缺乏具有明亮NIR-II发射的生物相容性造影剂阻碍了其在基础研究和临床试验中的应用。在此,报道了一种脂质体包封策略,通过将染料限制在脂质的疏水口袋中并抑制聚集来产生超亮脂质体 - 花菁染料,计算模型证实了这一点。与游离吲哚菁绿(ICG,一种美国食品药品监督管理局批准的花菁染料)相比,脂质体包封的ICG(S-Lipo-ICG)在NIR-II亮度上提高了38.7倍,并且仅用十分之一的剂量就能在长时间(30分钟)内实现脑血管成像。通过调整激发波长,两种脂质体包封的花菁染料(S-Lipo-ICG和S-Lipo-FD1080)能够实现NIR-II双色成像。此外,在兔模型中,通过S-Lipo-ICG图像引导的肿瘤手术可以成功区分并切除小的肿瘤结节(2 - 5毫米)。这种脂质体包封保持了ICG的代谢途径,有望用于临床应用。