Abstract:
A method, device and kit for the quantitative determination of lipoprotein components, especially cholesterol and triglycerides, in body fluids, especially human serum, plasma or whole blood utilizing the selective adsorption of lipoproteins on particulate silica. This selective adsorption is also useful for the quantitative separation of lipoproteins from samples of whole blood for diagnostic purposes.
Abstract:
The normality of a cell labelled with a lipid soluble fluorescent dye and excited with a beam of polarized light can be evaluated by measuring the time dependence of the state of polarization of fluorescence emitted by the cell which is determined by simultaneously measuring the intensities of fluorescence polarized in directions parallel and perpendicular to the direction of polarization of the excitation beam.The state of polarization of a cell changes markedly as a function of excitation time when the cell is abnormal (i.e., malignant), while the state of polarization of a cell remains substantially constant when the cell is normal. Classification of cells in a population by way of the stability of the state of polarization provides guidance in determining the presence of malignancy in the population.