Institute of Chemical Kinetics and Combustion SB RAS, Institutskaya 3, 630090, Novosibirsk, Russia.
J Biomed Opt. 2012 May;17(5):057006. doi: 10.1117/1.JBO.17.5.057006.
We describe a novel approach to study blood microparticles using the scanning flow cytometer, which measures light scattering patterns (LSPs) of individual particles. Starting from platelet-rich plasma, we separated spherical microparticles from non-spherical plasma constituents, such as platelets and cell debris, based on similarity of their LSP to that of sphere. This provides a label-free method for identification (detection) of microparticles, including those larger than 1 μm. Next, we rigorously characterized each measured particle, determining its size and refractive index including errors of these estimates. Finally, we employed a deconvolution algorithm to determine size and refractive index distributions of the whole population of microparticles, accounting for largely different reliability of individual measurements. Developed methods were tested on a blood sample of a healthy donor, resulting in good agreement with literature data. The only limitation of this approach is size detection limit, which is currently about 0.5 μm due to used laser wavelength of 0.66 μm.
我们描述了一种使用扫描流动细胞仪研究血液微粒的新方法,该方法测量单个颗粒的光散射模式(LSP)。从富含血小板的血浆开始,我们根据其 LSP 与球体的相似性,将球形微粒与非球形血浆成分(如血小板和细胞碎片)分离。这为微粒的识别(检测)提供了一种无标记的方法,包括大于 1μm 的微粒。接下来,我们严格表征了每个测量的颗粒,确定了其大小和折射率,包括这些估计值的误差。最后,我们采用了一种反卷积算法来确定整个微粒群体的大小和折射率分布,考虑到个体测量的可靠性有很大差异。在健康供体的血液样本上测试了所开发的方法,结果与文献数据吻合良好。这种方法的唯一限制是尺寸检测极限,目前由于使用的激光波长为 0.66μm,因此约为 0.5μm。