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Ultraviolet refractometry using field-based light scattering spectroscopy

机译:使用基于场的光散射光谱法进行紫外折光法

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摘要

Accurate refractive index measurement in the deep ultraviolet (UV) range is important for the separate quantification of biomolecules such as proteins and DNA in biology. This task is demanding and has not been fully exploited so far. Here we report a new method of measuring refractive index using field-based light scattering spectroscopy, which is applicable to any wavelength range and suitable for both solutions and homogenous objects with well-defined shape such as microspheres. The angular scattering distribution of single microspheres immersed in homogeneous media is measured over the wavelength range 260 to 315 nm using quantitative phase microscopy. By least square fitting the observed scattering distribution with Mie scattering theory, the refractive index of either the sphere or the immersion medium can be determined provided that one is known a priori. Using this method, we have measured the refractive index dispersion of SiO2 spheres and bovine serum albumin (BSA) solutions in the deep UV region. Specific refractive index increments of BSA are also extracted. Typical accuracy of the present refractive index technique is ≤0.003. The precision of refractive index measurements is ≤0.002 and that of specific refractive index increment determination is ≤0.01 mL/g.
机译:深紫外(UV)范围内的准确折射率测量对于生物学中蛋白质和DNA等生物分子的单独定量非常重要。这项任务要求很高,到目前为止尚未得到充分利用。在这里,我们报告了一种使用基于场的光散射光谱法测量折射率的新方法,该方法适用于任何波长范围,并且适用于溶液和形状明确的均质物体(例如微球)。使用定量相显微镜在260至315 nm的波长范围内测量浸没在均匀介质中的单个微球的角散射分布。通过用米氏散射理论对观测到的散射分布进行最小二乘拟合,可以确定球体或浸没介质的折射率,前提是先验已知。使用这种方法,我们测量了SiO2球和牛血清白蛋白(BSA)溶液在深紫外区域的折射率分散。还提取了BSA的特定折射率增量。本折射率技术的典型精度为≤0.003。折射率测量的精度≤0.002,比折射率增量测定的精度≤0.01mL / g。

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