Bazhanov V S, Gol'dberg L E, Berdnikova V V, Shepelevtseva N G, Dudnik Iu V
Antibiotiki. 1977 Apr;22(4):357-61.
Studies with the use of intact inbred albino mice showed that in intravenous administration the acute toxicity of antibiotic No. 6270 and echinomycin in complexes with DNA increased 3--4 times as compared to the toxicity of the same antibiotics used without the complex. Under the experimental conditions with 3-fold intravenous administration at 72-hour intervals in doses equivalent by their acute toxicity, the antitumor activity of the echinomycin complex with DNA against the solid form of lymphosarcoma L10-1 was approximately 4 times lower than the activity of the antibiotic used alone. Like echinomycin, antibiotic No. 6270 in complex with DNA used according to the same administration scheme in doses equivalent by their acute toxicity had a lower inhibitory effect on growth of lymphosarcoma L10-1 and sarcoma 180 as compared to its use alone.
使用完整的近交白化小鼠进行的研究表明,静脉给药时,抗生素6270和放线菌素与DNA形成复合物后的急性毒性比未形成复合物时使用的相同抗生素的毒性增加了3至4倍。在实验条件下,以72小时间隔进行3次静脉给药,剂量按急性毒性等效,放线菌素与DNA的复合物对实体型淋巴肉瘤L10-1的抗肿瘤活性比单独使用抗生素时低约4倍。与放线菌素一样,抗生素6270与DNA形成复合物后,按照相同的给药方案以急性毒性等效剂量使用时,与单独使用相比,对淋巴肉瘤L10-1和肉瘤180生长的抑制作用较低。