Zhou Jiaqi, Li Hao, Li Hui, Ding Jiayi, Du Zhong, Xiong Jiabao, Yao Hongyang, Zhang Xueliang, Alifu Nuernisha, Dong Biao
State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, School of Medical Engineering and Technology, Xinjiang Medical University, Urumqi, 830054, China.
Institute of Public Health, Xinjiang Medical University, Urumqi, 830011, China.
Mater Today Bio. 2025 Mar 27;32:101693. doi: 10.1016/j.mtbio.2025.101693. eCollection 2025 Jun.
Cyanine molecules with the second near-infrared (NIR-II) emission hold great potential for bioimaging owing to their great biocompatibility, but the scissor-like structure of these molecules poses a major bottleneck in obtaining efficient NIR-II fluorescence probes. Constructing J-aggregates represents a promising strategy for obtaining biomedical NIR-II emissive materials. However, achieving J-aggregates in cyanine dyes with large torsion angles between the heterocyclic rings poses a challenge. In this study, we introduced the guanidine of tumor molecular targeted peptide 1 (TMTP1) to increase steric hindrance of IR-783 and reduce the angle of IR-783 scissors. The near-coplanar structure of IR-783@peptide TMTP1 composite facilitates the formation of a novel J-aggregates (IR-783-LP-TMTP1) with super-stable effect for NIR-II in vivo dynamic vascular imaging and remarkable tumor targeting capability. The stable emission wavelength and high spatial resolution of J-aggregates was demonstrated for brain and ear vasculature bioimaging under 808 nm laser excitation. Additionally, J-aggregates exhibits robust tumor-targeting capability towards cervical tumors, indicating their potential in cervical cancer diagnosis. This work develops a molecular design strategy to construct bright NIR-II J-aggregates with super-stable and robust tumor-targeting properties and paving the way for improving bioimaging performance of similar molecules.
具有第二近红外(NIR-II)发射的花菁分子由于其良好的生物相容性而在生物成像方面具有巨大潜力,但这些分子的剪刀状结构在获得高效的NIR-II荧光探针方面构成了主要瓶颈。构建J-聚集体是获得生物医学NIR-II发光材料的一种有前景的策略。然而,在杂环之间具有大扭转角的花菁染料中实现J-聚集体是一项挑战。在本研究中,我们引入肿瘤分子靶向肽1(TMTP1)的胍基以增加IR-783的空间位阻并减小IR-783剪刀的角度。IR-783@肽TMTP1复合物的近共面结构有利于形成一种新型的J-聚集体(IR-783-LP-TMTP1),其对体内NIR-II动态血管成像具有超稳定作用,并具有显著的肿瘤靶向能力。在808nm激光激发下,J-聚集体的稳定发射波长和高空间分辨率在脑和耳血管系统生物成像中得到了证明。此外,J-聚集体对宫颈癌表现出强大的肿瘤靶向能力,表明其在宫颈癌诊断中的潜力。这项工作开发了一种分子设计策略,以构建具有超稳定和强大肿瘤靶向特性的明亮NIR-II J-聚集体,并为改善类似分子的生物成像性能铺平道路。