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用于测量病毒及其他亚微观颗粒光散射的流式细胞仪。

Flow cytometer for measurement of the light scattering of viral and other submicroscopic particles.

作者信息

Steen Harald B

机构信息

Department of Biophysics, Institute for Cancer Research, Oslo, Norway.

出版信息

Cytometry A. 2004 Feb;57(2):94-9. doi: 10.1002/cyto.a.10115.

Abstract

BACKGROUND

Light scattering is an essential parameter in flow cytometry, facilitating functions such as size measurement, discrimination of cell types on the basis of shape and morphology, detection of fluorescence-negative cells, and gating of fluorescence measurements. Light scattering measurement of viruses is generally not feasible with current flow cytometers due to their small size. The problem is aggravated by the fact that the light scattering of particles in this size range (< 200 nm) falls off with roughly the sixth power of their linear dimensions.

METHODS

A new optical layout using darkfield illumination and detection has been developed. A 532-nm laser was used for excitation, and scattered light was collected with large aperture optics.

RESULTS

Light scattering histograms of polymer particles with diameters of 70-300 nm were recorded without gating by other parameters. By extrapolation, a detection limit of about 50 nm was obtained. Different species of virus with sizes of approximately 100 nm also were recorded.

CONCLUSIONS

Flow cytometric light scattering measurement of submicroscopic particles, in a size range that includes many viral species, is now feasible. The results indicate that it may be practically impossible to measure by flow cytometry the light scattering of particles smaller than 40 nm.

摘要

背景

光散射是流式细胞术的一个重要参数,有助于诸如大小测量、基于形状和形态区分细胞类型、检测荧光阴性细胞以及荧光测量的设门等功能。由于病毒尺寸小,使用当前的流式细胞仪对病毒进行光散射测量通常不可行。在这个尺寸范围(<200 nm)内,颗粒的光散射随其线性尺寸的大约六次方下降,这一事实加剧了该问题。

方法

已开发出一种使用暗场照明和检测的新光学布局。使用532 nm激光进行激发,并用大孔径光学器件收集散射光。

结果

记录了直径为70 - 300 nm的聚合物颗粒的光散射直方图,无需通过其他参数设门。通过外推,获得了约50 nm的检测限。还记录了大小约为100 nm的不同病毒种类。

结论

对包括许多病毒种类的亚微观颗粒进行流式细胞术光散射测量现在是可行的。结果表明,通过流式细胞术测量小于40 nm颗粒的光散射实际上可能是不可能的。

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