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基于聚(烯丙胺)包覆的 Au@Ag 纳米探针的细胞和组织中癌症相关标记物的多重微 SERS 成像。

Multiplex micro-SERS imaging of cancer-related markers in cells and tissues using poly(allylamine)-coated Au@Ag nanoprobes.

机构信息

Mass Spectrometry Laboratory, MolSys Research Unit, University of Liège, 4000, Liège, Belgium.

出版信息

Anal Bioanal Chem. 2020 Nov;412(28):7739-7755. doi: 10.1007/s00216-020-02927-8. Epub 2020 Sep 10.

DOI:10.1007/s00216-020-02927-8
PMID:32910264
Abstract

Surface-enhanced Raman scattering (SERS) nanoprobes based on Au@Ag core@shell nanoparticles coated with poly(allylamine) were functionalized with small targeting molecules to evaluate simultaneously the level of expression of two cancer-related markers, both in cells and in tissues. The Au@Ag nanoparticles provide a high SERS signal enhancement in the visible range when combined with resonant Raman-active molecules. The poly(allylamine) coating plays a dual key role in (i) protecting the metal surface against the complex biological medium, leading to a stable signal of the Raman-active molecules, and (ii) enabling specific biofunctionalization through its amine functions. Using small targeting molecules linked to the polymer coating, two different nanoprobes (duplex approach) were designed. Each was able to specifically target a particular cancer-related marker: folate receptors (FRs) and sialic acid (SA). We demonstrate that the level of expression of these targeted markers can be evaluated following the SERS signal of the probes incubated on cells or tissues. The potential overexpression of folate receptors and of sialic acid was evaluated and measured in breast and ovarian cancerous tissue sections. In addition, FR and/or SA overexpression in the tumor region can be visualized with high contrast with respect to the healthy region and with high spatial accuracy consistent with histology by SERS imaging of the nanoprobe signal. Owing to the unique spectral signature of the designed nanoprobes, this approach offers an efficient tool for the spatially resolved, in situ measurement of the expression level of several cancer-related markers in tumors at the same time.Graphical abstract.

摘要

基于 Au@Ag 核壳纳米粒子的表面增强拉曼散射 (SERS) 纳米探针,用聚丙稀胺修饰,并用小分子靶向分子进行功能化,用于同时评估两种癌症相关标志物在细胞和组织中的表达水平。当 Au@Ag 纳米粒子与共振拉曼活性分子结合时,在可见范围内提供了高的 SERS 信号增强。聚丙稀胺涂层具有双重关键作用:(i)保护金属表面免受复杂的生物介质的影响,从而使拉曼活性分子的信号稳定;(ii)通过其胺功能实现特异性的生物功能化。使用与聚合物涂层相连的小分子靶向分子,设计了两种不同的纳米探针(双探针方法)。每种探针都能特异性地靶向特定的癌症相关标志物:叶酸受体 (FR) 和唾液酸 (SA)。我们证明,通过孵育在细胞或组织上的探针的 SERS 信号,可以评估这些靶向标志物的表达水平。在乳腺癌和卵巢癌组织切片中,评估和测量了这些靶向标志物的潜在过表达。此外,通过 SERS 成像探针信号,肿瘤区域的 FR 和/或 SA 过表达可以与健康区域形成高对比度,并具有与组织学一致的高空间分辨率。由于设计的纳米探针具有独特的光谱特征,这种方法为在肿瘤中同时进行几种癌症相关标志物的空间分辨、原位表达水平测量提供了一种有效的工具。

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