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一种具有超大斯托克斯位移的不对称近红外-II 有机荧光团,用于成像引导和靶向光疗。

An Asymmetric NIR-II Organic Fluorophore with an Ultra-Large Stokes Shift for Imaging-Guided and Targeted Phototherapy.

机构信息

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P. R. China.

School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei 230026, P. R. China.

出版信息

ACS Biomater Sci Eng. 2024 Jul 8;10(7):4541-4551. doi: 10.1021/acsbiomaterials.4c00496. Epub 2024 Jun 9.

Abstract

NIR-II imaging-guided phototherapy is an attractive, yet challenging, tumor treatment strategy. By monitoring the accumulation of phototherapy reagents at the tumor site through imaging and determining the appropriate therapy window, the therapeutic effect could be significantly improved. Probes with NIR-II (1000-1700 nm) fluorescence emission and a large Stokes shift hold great promise for fluorescence imaging with deep penetration, minimized self-quenching, and high spatiotemporal resolution. However, due to the lack of a suitable molecular framework, the design of a simple small-molecule dye with a large Stokes shift and NIR-II fluorescence emission has rarely been reported. Herein, we prepare an asymmetric D-π-A type NIR-II fluorescence probe (TBy). The probe is incapsulated in an amphiphilic polymer and modified with a fibronectin targeting peptide CREKA, which could recognize the fibrin-fibronectin complex overexpressed in multiple malignant tumors. The nanoparticles thus constructed (TByC-NPs) have maximum fluorescence emission at 1037 nm with a large Stokes shift of 426 nm, which is the largest Stokes shift among organic NIR-II fluorescent dyes reported in the literature. The TByC-NPs exhibit a good NIR-II imaging performance, active tumor targeting, and good photothermal and photodynamic capabilities. and studies verify that the TByC nanoplatform shows outstanding biocompatibility for NIR-II imaging-guided phototherapy and provides an excellent antitumor effect.

摘要

近红外二区(NIR-II)成像引导的光疗是一种很有吸引力但极具挑战性的肿瘤治疗策略。通过成像监测治疗试剂在肿瘤部位的积累,并确定适当的治疗窗口,可以显著提高治疗效果。具有近红外二区(1000-1700nm)荧光发射和大斯托克斯位移的探针在具有深穿透性、最小自猝灭和高时空分辨率的荧光成像方面具有很大的应用前景。然而,由于缺乏合适的分子框架,具有大斯托克斯位移和近红外二区荧光发射的简单小分子染料的设计很少有报道。在此,我们制备了一种不对称的 D-π-A 型近红外二区荧光探针(TBy)。该探针被包裹在两亲性聚合物中,并修饰有纤维连接蛋白靶向肽 CREKA,该肽可以识别多种恶性肿瘤中过度表达的纤维蛋白-纤维连接蛋白复合物。构建的纳米颗粒(TByC-NPs)在 1037nm 处具有最大荧光发射,斯托克斯位移为 426nm,这是文献报道的有机近红外二区荧光染料中最大的斯托克斯位移。TByC-NPs 表现出良好的近红外二区成像性能、主动肿瘤靶向性以及良好的光热和光动力性能。体内和体外研究验证了 TByC 纳米平台在近红外二区成像引导的光疗中具有优异的生物相容性,并提供了优异的抗肿瘤效果。

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