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Coherent versus noncoherent optical probing of dynamic shape fluctuations in red blood cells

机译:红细胞动态形状波动的相干和非相干光学探测

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Abstract: Optical registration technique is developed and frequency spectra are measured for dynamic shape fluctuations (flicker) in erythrocytes. Flicker spectra are studied in the range 0.03 - 500 Hz, using dynamic microphotometering of single cells in two optical modes: phase contrast regime, and reflection-mode laser probing. The registered spectra are similar to those typical of 1/f noise, with an essential difference: their slope in log-log scale varies with frequency, from $MIN@(0.8 $DIV 1.2) below 10 Hz to $MIN@(1.6 $DIV 2.4) above 50 Hz. The spectra measured with backward laser light scattering go systematically higher then those measured in the phase contrast regime. The theory of erythrocyte flicker is developed, based on the eigenmodes analysis of the bending oscillations of the cell envelope, and on the optical problem solution for the contribution from these oscillations to the registered signal. The theory describes quantitatively the spectral curves, and relates their parameters to the main mechanical and shape parameters of erythrocytes: bending modulus of cell membrane, viscosity coefficient of hemoglobin solution, and thickness-diameter ratio of a cell. The difference in the spectra obtained by coherent and noncoherent probing of erythrocytes is explained by specificity of optical mechanisms of the registered signal formation. No firm evidence is obtained for the contribution from the active processes in erythrocytes to the flicker. !15
机译:摘要:开发了光学配准技术,并测量了频谱以检测红细胞的动态形状波动(闪烁)。使用动态显微光度法在两种光学模式下对单个单元进行动态显微光度法研究了在0.03-500 Hz范围内的闪烁光谱:相衬状态和反射模式激光探测。记录的频谱类似于典型的1 / f噪声,但有一个本质区别:它们的对数对数刻度的斜率随频率变化,从低于10 Hz的$ MIN @(0.8 $ DIV 1.2)到$ MIN @(1.6 $)。 50 Hz以上的DIV 2.4)。用反向激光散射测得的光谱要比在相衬条件下测得的光谱更高。基于细胞包膜弯曲振荡的本征模式分析,以及基于光学振动问题解决方案(这些信号对注册信号的贡献),开发了红细胞闪烁理论。该理论定量描述了光谱曲线,并将其参数与红细胞的主要力学和形状参数相关:细胞膜的弯曲模量,血红蛋白溶液的粘度系数和细胞的厚度直径比。通过对红细胞进行相干和非相干探测而获得的光谱差异由配准信号形成的光学机制的特异性解释。对于红细胞的活跃过程对闪烁的贡献,没有得到确凿的证据。 !15

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