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β-环糊精对吩噻嗪类抗精神病药物体外诱导溶血的保护机制。

Protective mechanism of beta-cyclodextrin for the hemolysis induced with phenothiazine neuroleptics in vitro.

作者信息

Irie T, Sunada M, Otagiri M, Uekama K

出版信息

J Pharmacobiodyn. 1983 Jun;6(6):408-14. doi: 10.1248/bpb1978.6.408.

Abstract

beta-Cyclodextrin (beta-CyD) was found to protect the human erythrocytes from the hemolysis induced with ten phenothiazine neuroleptics in isotonic solution. The hemolytic activities of the phenothiazine-beta-CyD systems appeared to depend upon the free phenothiazine concentration, suggesting that the complexed form of phenothiazines is essentially inactive to cause hemolysis. The binding abilities and surface activities of the complexed form of phenothiazines were much smaller than those of free phenothiazines. These results indicate that the protective effect of beta-CyD may be due to the decrease in the effective hemolytic concentration of phenothiazines by inclusion complexation rather than the stabilizing effect of beta-CyD on the erythrocyte membrane.

摘要

发现β-环糊精(β-CyD)可保护人类红细胞免受等渗溶液中十种吩噻嗪类抗精神病药物诱导的溶血作用。吩噻嗪-β-CyD系统的溶血活性似乎取决于游离吩噻嗪的浓度,这表明吩噻嗪的络合形式基本上无溶血活性。吩噻嗪络合形式的结合能力和表面活性远小于游离吩噻嗪。这些结果表明,β-CyD的保护作用可能是由于包合络合作用降低了吩噻嗪的有效溶血浓度,而不是β-CyD对红细胞膜的稳定作用。

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