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A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level

机译:具有显着SERS活性的新型三元异质结构可在单细胞水平评估PD-L1表达

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摘要

Surface-enhanced Raman scattering (SERS) probes based on a charge transfer (CT) process with high stability and reproducibility are powerful tools under open-air conditions. However, the key problem ahead of practical usage of CT-based SERS technology is how to effectively improve sensitivity. Here, a novel ternary heterostructure SERS substrate, Fe3O4@GO@TiO2, with a significant enhancement factor of 8.08 × 106 was first synthesized. We found the remarkable enhanced effect of SERS signal to be attributed to the resonance effect of CuPc, CT between GO and TiO2, and enrichment from a porous TiO2 shell. In addition, we developed a robust SERS probe with good recyclability under visible light illumination on Fe3O4@GO@TiO2 nanocomposites toward ultrasensitive detection of cancer cells down to three cells. We have now successfully applied this probe for in situ quantification and imaging of programmed cell death receptor ligand 1 (PD-L1) on triple-negative breast cancer cell surface at the single-cell level and for monitoring the expression variation of PD-L1 during drug treatment.
机译:基于电荷转移(CT)工艺且具有高稳定性和可重复性的表面增强拉曼散射(SERS)探针在露天条件下是功能强大的工具。但是,基于CT的SERS技术实际应用之前的关键问题是如何有效提高灵敏度。在此,首次合成了具有显着增强因子8.08×10 6 的新型三元异质结构SERS衬底Fe3O4 @ GO @ TiO2。我们发现SERS信号的显着增强作用归因于CuPc的共振效应,GO和TiO2之间的CT以及从多孔TiO2壳中富集。此外,我们开发了一种坚固的SERS探针,在Fe3O4 @ GO @ TiO2纳米复合材料上的可见光照射下具有良好的可回收性,可对多达3个细胞的癌细胞进行超灵敏检测。现在,我们已经成功地将该探针用于单细胞水平的三阴性乳腺癌细胞表面上的程序性细胞死亡受体配体1(PD-L1)的原位定量和成像,并监测PD-L1在表达过程中的变化药物治疗。

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