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人转铁蛋白-阿霉素结合物的制备及其体外细胞毒作用
引用本文:林溪,黄秀旺.人转铁蛋白-阿霉素结合物的制备及其体外细胞毒作用[J].肿瘤,2000,20(4):263-265.
作者姓名:林溪  黄秀旺
作者单位:福建医科大学临床药理研究所!福州350004
摘    要:目的 介绍人转铁蛋白-阿霉素结合物的制备及细胞毒性。方法 采用氧化葡聚糖(DEX)T-40作为中介体,联结人转铁蛋白(HTF)与阿霉素(ADR)制备人转铁蛋白-阿霉素交联物9HTF-DEX-ADR)。HTF与ADR的克分子比为1:40 ̄45。以MTT法测其细胞毒性。结果 交联物对肿瘤细胞K5621h处理的IC50中游离ADR的4.2倍,对正常人单核细胞48h处理的杀伤只有游离ADR的1/9。结论

关 键 词:转铁蛋白  阿霉素  肿瘤细胞  体外细胞毒作用

PREPARATION OF HUMAN TRANSFERRIN-ADRIAMYCIN CONJUGATE AND CYTOTOXIC EFFECT OF THE CONJUGATES IN VITRO
LIN Xi,HUANG Xiu wang Institute of Clinical Pharmacology,Fujian Medical University,Fu zhou China.PREPARATION OF HUMAN TRANSFERRIN-ADRIAMYCIN CONJUGATE AND CYTOTOXIC EFFECT OF THE CONJUGATES IN VITRO[J].Tumor,2000,20(4):263-265.
Authors:LIN Xi  HUANG Xiu wang Institute of Clinical Pharmacology  Fujian Medical University  Fu zhou China
Institution:LIN Xi,HUANG Xiu wang Institute of Clinical Pharmacology,Fujian Medical University,Fu zhou 350004 China
Abstract:Objective Preparation of human transferrin adriamycin conjugate and its cytotoxicity was described. Methods Human transferrin (HTF) was conjugatd with adriamycin (ADR), via oxidative dextran T 40 as linker, to construct HTF DEX ADR. The molarratio of HTF to drug was to 40 45. The cytotoxicity of HTF DEX ADR to K562 cells was determined by MTT method.Results The cytotoxicity of HTF DEX ADR to K562 cells was 4 2 times than that of free ADR, while to normal peripheral blood mononuclear cells was only 1/9 that of free ADR. Conclusion It suggests that the conjugate shows a selective cytotoxicity to K562 cells.$$$$
Keywords:Transferrin  Adriamycin  Tumor cells  cultured
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