Abstract
Studying lipid peroxidation (LPO) processes is an actual problem of modern biology and medicine because of important role of LPO products at diseases and normal functioning of biomembranes and cells. A number of analytical methods based on LPO products fluorescent characteristics measurement are successfully used [1–3]. A phosphorescent method of LPO products analysis wasn’t practically applied up to date. This study is devoted to phosphorescent analysis of lipid peroxidation products in vitro (in solution, in composition of liposomes) and in situ — in composition of isolated membranes and cells (at norm and pathology).
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