| 摘要 |
The proposed method for determining the activity of free radical lipid peroxidation in biological substrates consists in mixing small quantity of undiluted arterial and venous blood of a human being, blood of an experimental animal, and the homogenates of the internal organs of an experimental animal with potassium-phosphate buffer solution, treating the obtained biological substrate by centrifuge, holding the treated substrate at a specified constant temperature, and determining the activity of free radical lipid peroxidation by the intensity of the spontaneous induced chemiluminescence and the intensity of the weak luminescence of the substrate.
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