Pr3+and Yb3+co-doped phosphate glasses are prepared to study their optical properties.Excitation and emission spectra and decay curves are used to characterize their luminescence.We demonstrate that upon excitation of...Pr3+and Yb3+co-doped phosphate glasses are prepared to study their optical properties.Excitation and emission spectra and decay curves are used to characterize their luminescence.We demonstrate that upon excitation of Pr3+ion with one high energy photon at 470 nm,two near-infrared(NIR)photons are emitted at 950-1100 nm(Yb3+:2F 5/2 →2F 7/2)through an efficient cooperative energy transfer(CET)from Pr3+to Yb3+.The maximum energy transfer efficiency(ETE)and the corresponding quantum efficiency approach up to 90.17%and 190.17%,respectively.The glass materials might find potential application for improving the efficiency of silicon-based solar cells.展开更多
Protein microarrays based on fluorescence detection have been widely utilized for high-throughput functional proteomic analysis. However, a drawback of such assays has been low sensitivity and narrow dynamic range, li...Protein microarrays based on fluorescence detection have been widely utilized for high-throughput functional proteomic analysis. However, a drawback of such assays has been low sensitivity and narrow dynamic range, limiting their capabilities, especially for detecting low abundance biological molecules such as cytokines in human samples. Here, we present fluorescence-enhancing microarrays on plasmonic gold films for multiplexed cytokine detection with up to three orders of magnitude higher sensitivity than on conventional nitrocellulose and glass substrates. Cytokine detection on the gold plasmonic substrate is about one to two orders of magnitude more sensitive than enzyme-linked immunosorbent assay （ELISA） and can be multiplexed. A panel of six cytokines （Vascular endothelial growth factor （VEGF）, Interleukin 1β （IL-1β）, Interleukin 4 （IL-4）, Interleukin 6 （IL-6）, Interferon γ （IFN-γ）, and Tumor necrosis factor （TNF）） were detected in the culture media of cancer cells. This work establishes a new method of high throughput multiplexed cytokine detection with higher sensitivity and dynamic range than ELISA.展开更多
基金supported by the National Natural Science Foundation of China(Nos.61275180,51272109and50972061)the Natural Science Foundation of Zhejiang Province(Nos.Z4110072and R4100364)+1 种基金the Opening Foundation of Zhejiang Provincial Top Key DisciplineK.C.Wong Magna Fund in Ningbo University
文摘Pr3+and Yb3+co-doped phosphate glasses are prepared to study their optical properties.Excitation and emission spectra and decay curves are used to characterize their luminescence.We demonstrate that upon excitation of Pr3+ion with one high energy photon at 470 nm,two near-infrared(NIR)photons are emitted at 950-1100 nm(Yb3+:2F 5/2 →2F 7/2)through an efficient cooperative energy transfer(CET)from Pr3+to Yb3+.The maximum energy transfer efficiency(ETE)and the corresponding quantum efficiency approach up to 90.17%and 190.17%,respectively.The glass materials might find potential application for improving the efficiency of silicon-based solar cells.
文摘Protein microarrays based on fluorescence detection have been widely utilized for high-throughput functional proteomic analysis. However, a drawback of such assays has been low sensitivity and narrow dynamic range, limiting their capabilities, especially for detecting low abundance biological molecules such as cytokines in human samples. Here, we present fluorescence-enhancing microarrays on plasmonic gold films for multiplexed cytokine detection with up to three orders of magnitude higher sensitivity than on conventional nitrocellulose and glass substrates. Cytokine detection on the gold plasmonic substrate is about one to two orders of magnitude more sensitive than enzyme-linked immunosorbent assay （ELISA） and can be multiplexed. A panel of six cytokines （Vascular endothelial growth factor （VEGF）, Interleukin 1β （IL-1β）, Interleukin 4 （IL-4）, Interleukin 6 （IL-6）, Interferon γ （IFN-γ）, and Tumor necrosis factor （TNF）） were detected in the culture media of cancer cells. This work establishes a new method of high throughput multiplexed cytokine detection with higher sensitivity and dynamic range than ELISA.
