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Optimization of a UV light-emitting diode based fluorescence-phase sensor

机译:基于紫外线发光二极管的荧光相位传感器的优化

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摘要

A set of UV light-emitting diodes (LEDs) with the peak wavelengths ranging from 255 nm to 375 nm was applied for the investigation of spectral and decay-time fluorescence signatures in dry B. globigii spores and common airborne interferants (albuminous, epithelium, and cellulosous materials as well as aromatic hydrocarbons). The fluorescence decay signature was represented by a phase shift of the sinusoidal fluorescence waveform in respect of excitation provided by high-frequency modulated LEDs. The obtained data matrix was used for the optimization a bioparticle fluorescence sensor with a minimized number of excitation sources and detection channels and maximized discrimination ability of bioparticles against common interferants. Based on the optimization, a new concept for a UV LED based "detect-to-warn" bioparticle fluorescence sensor is proposed. The sensor contains a single deep-UV LED emitting at 280 nm that is harmonically modulated at a high frequency (of about 70 MHz) and a dual-channel fluorescence detector with the spectral windows peaked at 320 nm and 450 nm. The output parameters of the sensor are the ratio of the fluorescence intensity in the two windows and the phase shift of the fluorescence waveform in the 320-nm detection channel in respect of the excitation one. Such a sensing scheme has a smaller number of optical components and a potentially higher discrimination ability of bioparticles against common interferants in comparison with the conventional approach based on just fluorescence intensity measurement under dual-wavelength excitation (280 nm and 340 nm).
机译:一组峰值波长范围为255 nm至375 nm的UV发光二极管(LED)用于研究干燥的球形双歧杆菌孢子和常见的空气传播干扰物(白蛋白,上皮细胞,以及纤维素材料以及芳烃)。相对于高频调制LED提供的激发,荧光衰减特征由正弦荧光波形的相移表示。将获得的数据矩阵用于优化具有最小数量的激发源和检测通道以及最大程度地区分生物粒子对常见干扰物的生物粒子荧光传感器。基于优化,提出了一种基于紫外线LED的“检测到警告”生物粒子荧光传感器的新概念。该传感器包含一个在280 nm处发射的深紫外LED,该LED在高频(约70 MHz)下被谐波调制,以及一个双通道荧光检测器,其光谱窗口在320 nm和450 nm处达到峰值。传感器的输出参数是两个窗口中的荧光强度与320 nm检测通道中的荧光波形相对于激发光的相移之比。与仅基于双波长激发(280nm和340nm)下的荧光强度测量的常规方法相比,这种感测方案具有较少的光学组件数量,并且生物粒子对常见干扰物的潜在区分能力更高。

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