| Abstract: | The influence of tri‐ and di‐alkyltins (TATs and DATs) as well as di‐ and triphenyltin compounds (DPhTs and TPhTs) on haemolysis of red blood cells (RBCs) and stability of planar lipid membranes (PLMs) has been studied. The results obtained show that the efficiency of TATs (trimethyl‐, triethyl‐, tri‐n‐propyl‐ and tributyl‐tin chlorides) in destroying PLMs did not differ greatly when the compounds were studied in solutions of physiological pH (phosphate buffer, pH 7.4). A decrease in pH to 5.0 caused small changes in the efficiency of the three largest TAT molecules and a significant decrease in the efficiency of trimethyltin chloride. Both haemolytic and PLM experiments showed that the most active TAT was tri‐n‐propyltin chloride. The destructive action of DAT (dimethyl‐ and dibutyltin) and DPhT dichlorides was somewhat more differentiated. Dimethyltin dichloride (DMT) interaction with model membranes was a little weaker than that of DPhT and dibutyltin dichlorides and all these compounds influenced the model membranes to a lesser extent than TATs or TPhT. To bring about comparable haemolysis effects the dichlorides had to be used at much greater concentrations than the chlorides. The haemolytic properties of the dichlorides, especially of that of DMT, significantly increased in solution at pH 5.0. TPhT chloride interacted with model membranes similarly to TAT chlorides. Also, no great difference in efficiency of this compound was found for the two buffer solutions used. Copyright © 2000 John Wiley & Sons, Ltd. |
