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用于基于表面增强共振拉曼的图像引导肿瘤手术的靶向糖纳米颗粒的稳健合成

Robust Synthesis of Targeting Glyco-nanoparticles for Surface Enhanced Resonance Raman Based Image-Guided Tumor Surgery.

作者信息

Liu Kunli, Ullah A K M Atique, Juhong Aniwat, Yang Chia-Wei, Yao Cheng-You, Li Xiaoyan, Bumpers Harvey L, Qiu Zhen, Huang Xuefei

机构信息

Department of Chemistry, Michigan State University, East Lansing, MI, 48824 USA.

Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI, 48824 USA.

出版信息

Small Sci. 2024 May;4(5). doi: 10.1002/smsc.202300154. Epub 2024 Feb 22.

Abstract

Surface Enhanced Resonance Raman (SERS) is a powerful optical technique, which can help enhance the sensitivity of Raman spectroscopy aided by noble metal nanoparticles (NPs). However, current SERS-NPs are often suboptimal, which can aggregate under physiological conditions with much reduced SERS enhancement. Herein, a robust one-pot method has been developed to synthesize SERS-NPs with more uniform core diameters of 50 nm, which is applicable to both non-resonant and resonant Raman dyes. The resulting SERS-NPs are colloidally stable and bright, enabling NP detection with low-femtomolar sensitivity. An algorithm has been established, which can accurately unmix multiple types of SERS-NPs enabling potential multiplex detection. Furthermore, a new liposome-based approach has been developed to install a targeting carbohydrate ligand, i.e., hyaluronan, onto the SERS-NPs bestowing significantly enhanced binding affinity to its biological receptor CD44 overexpressed on tumor cell surface. The liposomal HA-SERS-NPs enabled visualization of spontaneously developed breast cancer in mice in real time guiding complete surgical removal of the tumor, highlighting the translational potential of these new glyco-SERS-NPs.

摘要

表面增强共振拉曼光谱(SERS)是一种强大的光学技术,它可以借助贵金属纳米颗粒(NPs)提高拉曼光谱的灵敏度。然而,目前的SERS-NPs往往并非最优,它们在生理条件下会聚集,导致SERS增强效果大幅降低。在此,人们开发了一种稳健的一锅法来合成核心直径更均匀、为50纳米的SERS-NPs,该方法适用于非共振和共振拉曼染料。所得的SERS-NPs具有胶体稳定性且亮度高,能够以低飞摩尔灵敏度进行NP检测。已建立一种算法,它可以准确地对多种类型的SERS-NPs进行解混,从而实现潜在的多重检测。此外,还开发了一种基于脂质体的新方法,将靶向碳水化合物配体,即透明质酸,安装到SERS-NPs上,赋予其对在肿瘤细胞表面过度表达的生物受体CD44显著增强的结合亲和力。脂质体HA-SERS-NPs能够实时可视化小鼠体内自发形成的乳腺癌,指导肿瘤的完整手术切除,突出了这些新型糖基化SERS-NPs的转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83f9/11935228/bffe6ca37a83/SMSC-4-2300154-g004.jpg

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