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基于等离子体氧化物纳米探针的高精确、无标记单细胞癌症检测。

Highly accurate and label-free discrimination of single cancer cell using a plasmonic oxide-based nanoprobe.

机构信息

School of Engineering, RMIT University, Melbourne, Victoria, 3000, Australia.

School of Mathematics and Physics, Hebei University of Engineering, Handan, 056038, China; School of Life Science and Technology, Xidian University, Xi'an, 710126, China.

出版信息

Biosens Bioelectron. 2022 Feb 15;198:113814. doi: 10.1016/j.bios.2021.113814. Epub 2021 Nov 19.

Abstract

The detection of cancer cells at the single-cell level enables many novel functionalities such as next-generation cancer prognosis and accurate cellular analysis. While surface-enhanced Raman spectroscopy (SERS) has been widely considered as an effective tool in a low-cost and label-free manner, however, it is challenging to discriminate single cancer cells with an accuracy above 90% mainly due to the poor biocompatibility of the noble-metal-based SERS agents. Here, we report a dual-functional nanoprobe based on dopant-driven plasmonic oxides, demonstrating a maximum accuracy above 90% in distinguishing single THP-1 cell from peripheral blood mononuclear cell (PBMC) and human embryonic kidney (HEK) 293 from human macrophage cell line U937 based on their SERS patterns. Furthermore, this nanoprobe can be triggered by the bio-redox response from individual cells towards stimuli, empowering another complementary colorimetric cell detection, approximately achieving the unity discrimination accuracy at a single-cell level. Our strategy could potentially enable the future accurate and low-cost detection of cancer cells from mixed cell samples.

摘要

单细胞水平的癌细胞检测能够实现许多新的功能,如下一代癌症预后和精确的细胞分析。虽然表面增强拉曼光谱(SERS)已被广泛认为是一种低成本、无标记的有效工具,但由于贵金属基 SERS 试剂的生物相容性差,很难将准确率提高到 90%以上。在这里,我们报告了一种基于掺杂驱动等离子体氧化物的双功能纳米探针,该探针在基于其 SERS 模式区分 THP-1 细胞与外周血单个核细胞(PBMC)和人胚肾(HEK)293 与人类巨噬细胞系 U937 方面的准确率超过 90%。此外,该纳米探针可以被单个细胞对刺激的生物氧化还原反应触发,实现另一种互补的比色细胞检测,在单细胞水平上大约达到了 100%的区分准确率。我们的策略有可能实现未来从混合细胞样本中准确、低成本地检测癌细胞。

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