Light scattering into two fixed angles vs. angle-resolved measurements for characterization of single submicron particles

A. Konokhova, M. Yurkin, V. Maltsev
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Abstract

Single particle identification and characterization based on scatter measurements is widely used in numerous biomedical applications. This scatter-based characterization approach implies a solution of the parametric inverse light-scattering (ILS) problem. The need for high-speed analysis limits the amount of collected scatter information and motivates maximum simplification of optical model of analyzed particles. We analyzed the capabilities and limitations of two existing approaches, based on measurement of either two scattering signals or angle-resolved patterns, applied to characterize single submicron particles. The standard flow cytometric approach is based on light scattering measurements into two fixed angles, forward and side scattering, which are further fitted by the Mie theory. We showed that corresponding ILS problem may have multiple solutions, and the procedure results in uncontrollable errors if the particle is not spherical. By contrast, angle-resolved scattering measurements have much larger information content at a cost of reduced analysis speed. This approach coupled with rigorous solution of ILS problem is shown to provide accurate identification and characterization of biological particles, including nonspherical ones.
两个固定角度的光散射与单个亚微米粒子表征的角度分辨测量
基于散射测量的单粒子识别和表征广泛应用于许多生物医学应用。这种基于散射的表征方法意味着参数逆光散射(ILS)问题的解决方案。高速分析的需要限制了所收集散射信息的数量,并促使所分析粒子的光学模型最大程度地简化。我们分析了两种现有方法的能力和局限性,基于测量两个散射信号或角度分辨模式,用于表征单个亚微米粒子。标准的流式细胞术方法是基于两个固定角度的光散射测量,即前散射和侧散射,并进一步通过Mie理论进行拟合。我们发现相应的ILS问题可能有多个解,并且当粒子不是球形时,该过程会导致不可控的误差。相比之下,角度分辨散射测量具有更大的信息量,但代价是降低了分析速度。该方法与ILS问题的严格解相结合,可以准确地识别和表征生物颗粒,包括非球形颗粒。
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