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Flow cytometer system for single-shot biosensing based on whispering gallery modes of fluorescent microspheres

机译:基于荧光微球回音壁模式的单次生物传感流式细胞仪系统

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We report an innovative label-free biosensor based on statistical analysis of several whispering gallery modes spectral shifts in polystyrene fluorescent microspheres using a custom microflow cytometer. Whispering gallery modes analysis enables detection of nanometer-sized analytes showing promising possibilities for virus, bacteria and molecular detection. To demonstrate this, fluorophore-doped microspheres of the appropriate size parameter are mixed in an aqueous solution. Then, a syringe pump pushes the solution through a fiber optic flow cell where a laser beam illuminates the analysis area to excite the microspheres and their fluorescence is collected. This device provides a low-cost and user friendly solution that could enhance spectrum acquisition rates up to 5 spectra per second thanks to the considerable amount of microspheres flowing through the excitation area per unit time. Finally, the fluorescence spectra are statistically investigated using an instantaneous measurement of apparent refractive index algorithm to determine a reliable value for the refractive index of the environment since the exact radius of the microsphere scanned is unknown. This refractive index becomes an effective value for the local perturbation caused by inhomogeneities on the microsphere surface and hence, determines whether or not inhomogeneities, such as bacteria, are adsorbed by comparing to a control sample. Combining a flow cell with our detection algorithm, we reduce the period of a 50 microspheres experiment from 161 minutes to 14 minutes when the flow rate is 2000 μl/h and the microsphere concentration is 5 μsphere/μl.
机译:我们报告了一种创新的无标签生物传感器,它基于使用定制的微流式细胞仪对聚苯乙烯荧光微球中的几种耳语画廊模式光谱变化进行统计分析。细语画廊模式分析可检测纳米级分析物,显示出病毒,细菌和分子检测的广阔前景。为了证明这一点,将适当尺寸参数的荧光团掺杂的微球在水溶液中混合。然后,注射泵将溶液推过光纤流通池,在其中激光束照射分析区域以激发微球并收集其荧光。该设备提供了一种低成本且用户友好的解决方案,由于单位时间内有大量微球流过激发区,因此可以将光谱采集速率提高到每秒5个光谱。最后,使用表观折射率算法的瞬时测量对荧光光谱进行统计研究,以确定环境折射率的可靠值,因为所扫描微球的确切半径是未知的。该折射率成为由微球表面上的不均匀性引起的局部扰动的有效值,因此,通过与对照样品比较,确定是否吸附了诸如细菌的不均匀性。将流动池与我们的检测算法相结合,当流速为2000μl/ h并且微球浓度为5μsphere/μl时,我们将50个微球实验的时间从161分钟减少到14分钟。

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