Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, Guangdong 510640, China.
Nano Lett. 2022 Oct 26;22(20):8109-8114. doi: 10.1021/acs.nanolett.2c02486. Epub 2022 Oct 10.
The construction of luminescent gold nanoparticles (AuNPs) with highly redshifted emission in the second near-infrared window (NIR-II) and good biocompatibility is still challenging. Herein, using an amphiphilic block copolymer (ABC) template with controllable hydrophobic interactions in the diverse forms of unimers and micelles, we report a facile strategy for redshifting the emission and enhancing the biological interactions of luminescent AuNPs. While the uniform clusters of NIR-II AuNPs are formed inside the hydrophobic cores of ABC micelles with strong interparticle hydrophobic interactions and enhanced emission at 1080 nm with a high quantum yield (QY) of 1.6%, the rigid NIR-II AuNPs are generated with strong intraparticle hydrophobic interactions as ABC unimers on the surface, leading to a redshifted emission of 1280 nm with a QY of 0.25% and enhancing the affinities toward injured intestinal mucosa in colitis imaging. These findings open new possibilities for the design of highly redshifted luminescent AuNPs with enhanced biological interactions.
具有高红移发射的发光金纳米粒子(AuNPs)在第二近红外窗口(NIR-II)中的构建和良好的生物相容性仍然具有挑战性。在此,我们使用具有多种形式的单体和胶束的具有可控疏水性相互作用的两亲嵌段共聚物(ABC)模板,报道了一种简便的策略,用于红移发光 AuNPs 的发射并增强其生物相互作用。虽然在 ABC 胶束的疏水性核内形成了均匀的 NIR-II AuNP 簇,其中具有强粒子间疏水性相互作用,并且在 1080nm 处的发射增强,量子产率(QY)高达 1.6%,但是由于 ABC 单体上的刚性 NIR-II AuNP 具有强的粒子内疏水性相互作用,导致发射红移至 1280nm,QY 为 0.25%,并增强了结肠炎成像中对受损肠黏膜的亲和力。这些发现为设计具有增强生物相互作用的高红移发光 AuNPs 开辟了新的可能性。