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Chemical Probing of Single Cancer Cells with Gold Nanoaggregates by Surface-Enhanced Raman Scattering

机译:通过表面增强拉曼散射化学探测含金纳米聚集体的单个癌细胞

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By using near-infrared surface-enhanced Raman scattering (SERS) with 60 nm gold nanoparticles (Au-NPs) to probe the chemical composition inside single human osteosarcoma cells we have shown that the SERS intensity may increase by a factor of 3-6 times in different parts of the cells depending on the density of gold nanoaggregates within the probed volume after the cell is dehydrated. The cellular points of low-density gold nanoaggregates exhibit more significant increase of SERS signal levels, the cellular macrochemicals such as nucleic acids show conformational changes, and new components can be probed after the cell is completely dried. A comparative study between viable and apoptotic cells indicates that most of the Au-NPs that enter the living cell reside in the cytoplasm and around the nucleus, whereas glyoxal-induced apoptotic cells show relatively uniform distribution of Au-NPs and, interestingly, the presence of DNA fragments is detected throughout the cell, including the cell surface.
机译:通过使用具有60 nm金纳米颗粒(Au-NPs)的近红外表面增强拉曼散射(SERS)来探测单个人骨肉瘤细胞内部的化学组成,我们证明了SERS强度可能会增加3-6倍细胞脱水后,取决于探针空间内金纳米聚集体的密度,从而确定细胞中不同部位的金属离子浓度。低密度金纳米聚集体的细胞点表现出更显着的SERS信号水平增加,细胞大分子化学物质(如核酸)显示构象变化,并且在细胞完全干燥后可以探测新的成分。活细胞和凋亡细胞之间的比较研究表明,进入活细胞的大多数Au-NP位于细胞质中和细胞核周围,而乙二醛诱导的凋亡细胞显示Au-NP分布相对均匀,有趣的是,存在在整个细胞(包括细胞表面)中检测到DNA片段的数量。

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