阿霉素、道诺霉素和放线菌素dna复合物的抑囊作用。埃利希-腹水肿瘤的体内比较研究。

S Seeber, R B Schilcher, K P Brucksch, J Käding, C G Schmidt
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引用次数: 3

摘要

比较了阿霉素、道诺霉素和放线菌素D及其dna复合物在体内对埃利希腹水肿瘤的抑细胞作用。在接种10(6)个埃利希腹水细胞8天后,将不同剂量的单个药物及其dna复合物腹腔注射到雌性NMRI小鼠。动物生存分析表明,添加DNA可提高阿霉素、道诺霉素和放线菌素D的治疗指标,而单独添加DNA对该肿瘤无影响。由于早期的生化数据(Seeber et al., 1977)显示dna结合抗生素的体外细胞毒性降低,这种治疗效果的增加可能是由于复合物形成后药理学行为的改变,延长了有效的腹腔内药物水平,降低了全身毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cystostatic efficacy of DNA-complexes of adriamycin, daunomycin, and actinomycin D. II. Comparative in vivo studies in an Ehrlich-ascites tumor.

The cytostatic efficacy of the antibiotics adriamycin, daunomycin and actinomycin D and of DNA-complexes of these compounds was compared in an Ehrlich ascites tumor in vivo. Various doses of the individual drugs and their DNA-complexes were injected intraperitoneally into female NMRI mice following 8 days after inoculation of 10(6) Ehrlich ascites cells. Survival analyses of animals demonstrated that by addition of DNA therapeutic indices were improved for adriamycin, daunomycin and actinomycin D, DNA alone had no effect on this tumor. Since earlier biochemical data (Seeber et al., 1977) had shown decreased in vitro cytotoxicity of DNA-bound antibiotics, this increase in therapeutic efficacy is probably due to an altered pharmacological behaviour after complex formation with a prolongation of effective intraperitoneal drug levels and decreased systemic toxicity.

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