Eisert W G, Beisker W
Biophys J. 1980 Jul;31(1):97-112. doi: 10.1016/S0006-3495(80)85042-9.
An epi-illumination design for fluorescence polarization measurements is introduced in flow cytometry with the optical axis orthogonally aligned to the cell stream. Various optical components and designs are discussed with respect to their influence on polarization measurements. Using the epi-configuration, paired measurements with the direction of polarization of the exciting light changed orthogonally are proposed for the compensation of system anisotropies and electronic mismatch. Large aperture corrections are employed for the excitation as well as for the emission pathway. Additional parameters such as fluorescence at 90 degrees, multiangle light scattering, and high precision cell-sizing by internally calibrated time of the flight measurements, as described previously, remain available with the design proposed here. Fluorescent latex microspheres, stained intracellular DNA, and algae have been used to test performance.
在流式细胞术中引入了一种落射照明设计用于荧光偏振测量,其光轴与细胞流正交对齐。讨论了各种光学组件和设计对偏振测量的影响。利用落射配置,提出了在激发光偏振方向正交变化的情况下进行配对测量,以补偿系统各向异性和电子失配。对激发光路和发射光路都采用了大孔径校正。如前所述,这里提出的设计仍可获得其他参数,如90度荧光、多角度光散射以及通过内部校准飞行时间测量实现的高精度细胞大小测定。已使用荧光乳胶微球、细胞内DNA染色样本和藻类来测试性能。