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1.
Tsitologiia ; 28(9): 954-63, 1986 Sep.
Article in Russian | MEDLINE | ID: mdl-3798561

ABSTRACT

A mathematical model of erythrocyte lysis by detergents is developed which takes into consideration the kinetics of detergent binding to plasma membrane. Experimentally obtained sigmoidal kinetic and concentration curves of hemolysis are well described by the model. A comparative study is carried out in terms of the model of hemolytic action for five detergents: Triton X-100, sodium dodecylsulfate, sodium deoxycholate, cetyltrimethylammonium bromide, and cetylpyridinium chloride. The amount of detergent which should be bound to an erythrocyte membrane to induce lysis was found to be roughly the same for all detergents studied. However, detergents vary in their affinity to the membrane. Cetylpyridinium displays the highest affinity (and consequently the highest hemolytic activity), whereas deoxycholate has the least one.


Subject(s)
Detergents/pharmacology , Hemolysis/drug effects , Models, Biological , Surface-Active Agents/pharmacology , Detergents/metabolism , Dose-Response Relationship, Drug , Erythrocyte Membrane/drug effects , Erythrocyte Membrane/metabolism , Humans , Kinetics , Mathematics
2.
Tsitologiia ; 28(9): 964-9, 1986 Sep.
Article in Russian | MEDLINE | ID: mdl-3798562

ABSTRACT

Possible reasons are discussed for the abnormal erythrocyte concentration influence on the course of detergent hemolysis curves. The data obtained lead to a conclusion that erythrocyte plasma membrane properties and, as a consequence, the parameters of erythrocyte-detergent interaction are dependent on cell concentration. The dependence is more sharply expressed for concentrations 5.10(7) cell/ml. In the concentration range (5-20) X 10(7) cell/ml the state of erythrocyte membrane remains apparently unchanged.


Subject(s)
Cell Communication/drug effects , Detergents/pharmacology , Hemolysis/drug effects , Surface-Active Agents/pharmacology , Erythrocyte Aggregation/drug effects , Erythrocyte Count/drug effects , Erythrocyte Membrane/drug effects , Humans , Micelles , Suspensions
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