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在金膜上观察到具有高对比度的碳点标记细菌细胞的强表面增强荧光。

Strong Surface Enhanced Florescence of Carbon Dot Labeled Bacteria Cells Observed with High Contrast on Gold Film.

机构信息

Department of Chemistry, Nazarbayev University, Kabanbay Batyr ave. 53, Astana, 010000, Kazakhstan.

Department of Biology, Nazarbayev University, Kabanbay Batyr ave. 53, Astana, 010000, Kazakhstan.

出版信息

J Fluoresc. 2018 Jan;28(1):1-4. doi: 10.1007/s10895-017-2194-z. Epub 2017 Nov 10.

DOI:10.1007/s10895-017-2194-z
PMID:29127572
Abstract

Strong surface (metal) enhanced fluorescence (SEF or MEF) is observed from clusters and single E coli bacteria cells labeled with Carbon nanodots (CDs), which were synthesized from date pits. The enhancement factor (EF) for SEF of the cell clusters were close to 50 for both 533 and 633 nm laser excitation wavelength. Those EFs are ratios of emission peak areas from CD labeled cell clusters on gold film to the peak areas of the same batch cell clusters on glass substrate. SEF with 633 nm excitation performed better than SEF with 532 nm excitation, achieving higher fluorescence intensity and much higher contrast. The contrast as high as 66 for cell clusters on gold film is a ratio of fluorescent emission peak area measured at the CD labeled cell clusters to the fluorescent peak area measured at unlabeled cell clusters (autofluorescence) on the same substrate. The contrast with the background (S/N) or the ratio of fluorescent peak area measured at bacteria cells to area measured at bare substrate was as high as 200. This report may pave a way for the broader application of surface enhanced fluorescence and especially metal enhanced fluorescence imaging of CD labeled cells and other biological objects. Graphical abstract Carbon dots, synthesized from dates, are used for direct staining of E coli cells. Emission fluorescent spectroscopy of those CD labelled cells on gold film and glass, demonstrated enhancement factor about 50 for emission on gold as compared to glass, Excitation at 633 nm appears far superior to excitation at 532 nm in terms of contrast (up to 67) with unlabeled cells /control due to decrease in auto fluorescence of cells. Maximum Signal to noise ratio is 200.

摘要

用从枣核中合成的碳点直接对大肠杆菌细胞进行染色。在金膜和玻璃上对这些 CD 标记细胞的发射荧光光谱进行了研究,结果表明,与玻璃相比,金上的发射增强因子约为 50。与未经标记的细胞/对照相比,633nm 激发时的对比度(高达 67)由于细胞的自发荧光减少,明显优于 532nm 激发。最大信噪比较高,达到 200。

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