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非共振间隙增强拉曼标签的拉曼光稳定性

Raman photostability of off-resonant gap-enhanced Raman tags.

作者信息

Gu Yuqing, Zhang Yuqing, Li Yi, Jin Xiulong, Huang Chengjun, Maier Stefan A, Ye Jian

机构信息

State Key Laboratory of Oncogenes and Related Genes, School of Biomedical Engineering, Shanghai Jiao Tong University Shanghai P. R. China

The Blackett Laboratory, Department of Physics, Imperial College London London SW7 2AZ UK

出版信息

RSC Adv. 2018 Apr 17;8(26):14434-14444. doi: 10.1039/c8ra02260g.

Abstract

Surface-enhanced Raman scattering (SERS) nanoprobes show promising potential for biosensing and bioimaging applications due to advantageous features of ultrahigh sensitivity and specificity. However, very limited research has been reported on the SERS photostability of nanoprobes upon continuous laser irradiation, which is critical for high-speed and time-lapse microscopy. The core-shell off-resonant gap-enhanced Raman tags (GERTs) with built-in Raman reporters, excited at near-infrared (NIR) region but with a plasmon resonance at visible region, allow decoupling the plasmon resonance behaviors with the SERS performance and therefore show ultrahigh Raman photostability during continuous laser irradiation. In this work, we have synthesized five types of off-resonant GERTs with different embedded Raman reporters, numbers of shell layer, or nanoparticle shapes. thorough examination of time-resolved SERS trajectories and quantitative analysis of photobleaching behaviors, we have demonstrated that double metallic-shell GERTs embedded with 1,4-benzenedithiol molecules show the best photostability performance, to the best of our knowledge, among all SERS nanoprobes reported before, with a photobleaching time constant up to 4.8 × 10 under a laser power density of 4.7 × 10 W cm. Numerical calculations additionally support that the local plasmonic heating effect in fact can be greatly minimized using the off-resonance strategy. Moreover, double-shell BDT-GERTs are highly potential for high-speed and high-resolution Raman-based cell bioimaging.

摘要

表面增强拉曼散射(SERS)纳米探针由于具有超高灵敏度和特异性等优势特性,在生物传感和生物成像应用中展现出了广阔的前景。然而,关于纳米探针在连续激光照射下的SERS光稳定性的研究报道非常有限,而这对于高速和延时显微镜至关重要。具有内置拉曼报告分子的核壳非共振间隙增强拉曼标签(GERTs),在近红外(NIR)区域被激发,但在可见光区域具有等离子体共振,能够将等离子体共振行为与SERS性能解耦,因此在连续激光照射期间表现出超高的拉曼光稳定性。在这项工作中,我们合成了五种类型的非共振GERTs,它们具有不同的嵌入拉曼报告分子、壳层数或纳米颗粒形状。通过对时间分辨SERS轨迹的全面检查和光漂白行为的定量分析,我们证明,据我们所知,在之前报道的所有SERS纳米探针中,嵌入1,4 - 苯二硫醇分子的双金属壳GERTs表现出最佳的光稳定性性能,在4.7×10 W cm的激光功率密度下,光漂白时间常数高达4.8×10 。数值计算还支持,使用非共振策略实际上可以大大最小化局部等离子体加热效应。此外,双壳BDT - GERTs在基于拉曼光谱的高速和高分辨率细胞生物成像方面具有很大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/635b/9079950/7c400352be54/c8ra02260g-f1.jpg

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