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两性霉素B介导柔红霉素的红细胞内摄取且不发生溶血。

Erythrocyte entrapment of daunomycin by amphotericin B without hemolysis.

作者信息

Kitao T, Hattori K

出版信息

Cancer Res. 1980 Apr;40(4):1351-3.

PMID:7357561
Abstract

Amphotericin B is a polyene that binds to sterols and perforates cell membranes. An antileukemic drug such as daunomycin added exogenously is impermeable to the red cell membrane. However, when the cells are incubated with a low concentration of amphotericin B, daunomycin is entrapped in the red cells without hemolysis or alteration in the chemical parameter of the erythrocytes. The erythrocyte has been used as a carrier vehicle to enhance the cytotoxic activity of daunomycin against L1210 leukemic cells. In comparison to control preparations, the greatest increase in survival was obtained in vivo when the erythrocytes with entrapped daunomycin were given to C57BL X DBA/2 F1 mice bearing L1210 cells.

摘要

两性霉素B是一种与固醇结合并使细胞膜穿孔的多烯类药物。外源性添加的抗白血病药物如柔红霉素不能透过红细胞膜。然而,当细胞与低浓度的两性霉素B一起孵育时,柔红霉素会被包封在红细胞内,而不会发生溶血或红细胞化学参数的改变。红细胞已被用作载体,以增强柔红霉素对L1210白血病细胞的细胞毒活性。与对照制剂相比,当将包封有柔红霉素的红细胞给予携带L1210细胞的C57BL X DBA/2 F1小鼠时,在体内获得了最大的生存期延长。

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