Xu Sicheng, Sun Pengfei, Yu Zikun, Chen Kai, Chu Yongzhen, Wang Shaofan, Shen Qingming, Chen Pengfei, Yao Yuyu, Fan Quli
State Key Laboratory of Organic Electronics and Information Displays & Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, Nanjing, 210023, China.
Department of Cardiology, Zhongda Hospital, Medical School of Southeast University, No 87, Dingjiaqiao, Nanjing, 210009, China.
Small. 2024 Dec;20(51):e2406159. doi: 10.1002/smll.202406159. Epub 2024 Oct 10.
Fluorescence imaging in the second near-infrared region (NIR-II, 1000-1700 nm) has garnered considerable attention for displaying the biological information of deep tissues. However, the lack of biocompatible contrast agents with bright NIR-II emission has hampered the precise clinical application of deep tissue imaging. Here, a lipophilic enhancement strategy employing donor-acceptor-donor (D-A-D) molecules, introducing long alkoxy chains and quaternary ammonium salts for the development of highly bright water-soluble NIR-II fluorophores (BBTD-2C-N), is described. Notably, liposome-encapsulated BBTD-2C-N nanoparticles (B-2C-N/DMPC) in aqueous solution exhibit a 1.8-fold increase in NIR-II fluorescence brightness compared to free BBTD-2C-N in methanol. Avoidance of the aggregation-caused quenching effect and enhanced NIR-II fluorescence are attributed to significantly attenuated π-π stacking interactions and maintained monodisperses in the hydrophobic liposome shell. Moreover, BBTD-2C-N demonstrates superior performance in visualizing lipid droplet-rich HeLa cells in vitro, as well as precise monitoring of adipose tissue and fatty liver in vivo. This study reveals a new avenue for the development of bright NIR-II fluorophores and precise in vivo imaging.
第二近红外区域(NIR-II,1000 - 1700纳米)的荧光成像因能显示深层组织的生物学信息而备受关注。然而,缺乏具有明亮NIR-II发射的生物相容性造影剂阻碍了深层组织成像在临床上的精确应用。在此,描述了一种采用供体-受体-供体(D-A-D)分子的亲脂性增强策略,引入长链烷氧基和季铵盐以开发高亮度水溶性NIR-II荧光团(BBTD-2C-N)。值得注意的是,水溶液中的脂质体包裹BBTD-2C-N纳米颗粒(B-2C-N/DMPC)与甲醇中的游离BBTD-2C-N相比,NIR-II荧光亮度提高了1.8倍。避免聚集导致的猝灭效应和增强的NIR-II荧光归因于显著减弱的π-π堆积相互作用以及在疏水脂质体壳中保持的单分散性。此外,BBTD-2C-N在体外可视化富含脂滴的HeLa细胞以及体内精确监测脂肪组织和脂肪肝方面表现出优异性能。这项研究揭示了开发明亮NIR-II荧光团和精确体内成像的新途径。