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Probing Intrinsic and Extrinsic Components in Single Osteosarcoma Cells by Near-Infrared Surface-Enhanced Raman Scattering

机译:通过近红外表面增强拉曼散射探测单个骨肉瘤细胞内在和外在成分

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摘要

We report on the capabilities of near-infrared surface-enhancedRaman scattering (SERS) using gold nanoparticles to obtain detailed chemical information with high spatial resolution from within single cancer cells, living or fixed. Colloidal gold particles, 60 nm in size, were introduced into live human osteosarcoma cells by endocytosis by adding them to the growth medium. Rapid SERS mapping of cells indicated that not only could rich vibrational spectra be obtained from intrinsic cellular constituents both in the cytoplasm and nucleus and but also the distribution of extrinsic molecules introduced into the cells, in this case, rhodamine 6G could be characterized, suggesting that the intracellular distribution of chemotherapeutic agents could potentially be measured by this technique. We show that the SERS signal intensity from the cellular components increases and more spectral detail is acquired from dried cells when compared with hydrated cells in buffer. The data also show spectral fluctuations, mainly in intensity but also in peak position, which are dependent upon the intensity of the excitation light and are probably due to diffusion of molecules on the surface of the gold nanoparticles. A detailed understanding of the origins of these effects is still not complete, but the ability to acquire very sensitive SERS inside living cancer cells indicates the potential of this technique as a useful tool in biomedicine.
机译:我们报告了近红外表面增强拉曼散射(SERS)的功能,使用金纳米颗粒可从单个或活的或固定的癌细胞内获得具有高空间分辨率的详细化学信息。通过内吞作用将大小为60 nm的胶体金颗粒通过添加到生长培养基中而通过内吞作用引入到人骨肉瘤活细胞中。细胞的快速SERS定位表明,不仅可以从细胞质和细胞核中固有的细胞成分中获得丰富的振动光谱,而且还可以检测引入细胞中的外在分子的分布,在这种情况下,罗丹明6G可以被表征,这表明化疗药物在细胞内的分布有可能通过这种技术进行测量。我们显示,与缓冲液中的水合细胞相比,来自细胞成分的SERS信号强度增加,并且从干燥细胞中获得了更多的光谱细节。数据还显示光谱波动,主要在强度上而且在峰位置上,这取决于激发光的强度,并且可能是由于分子在金纳米颗粒表面上的扩散所致。对这些作用的起因的详细了解仍不完全,但是在活癌细胞中获取非常敏感的SERS的能力表明该技术作为生物医学中有用工具的潜力。

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