Randhawa V S, Stewart F A, Denekamp J, Stratford M R
Br J Cancer. 1985 Feb;51(2):219-28. doi: 10.1038/bjc.1985.32.
The effect of melphalan alone or combined with various schedules of misonidazole (MISO) has been tested on a murine fibrosarcoma. The tumoricidal effect has been determined using the growth delay assay. Large single doses (500-1000 mgkg-1) of MISO enhanced the anti-tumour effect of melphalan, especially at high melphalan doses. This was accompanied by a drop in body and tumour temperature and an increase in the melphalan half-life. The MISO-induced hypothermia was prevented in one experiment by keeping the mice in an ambient temperature of 35 degrees C for 3 h. This reduced the exposure to melphalan but did not diminish the cytotoxic effect of the drug combination. Chronic administration of MISO for an 8 h period gave no enhancement of melphalan damage, whether melphalan was given half-way through or at the end of the period of dosing. It seems that a threshold tumour concentration of MISO, in excess of 70 micrograms g-1, is needed for enhancement of melphalan cytotoxicity; prolonged exposures to very low doses are ineffective.
已在小鼠纤维肉瘤上测试了美法仑单独使用或与不同给药方案的米索硝唑(MISO)联合使用的效果。使用生长延迟试验确定了杀肿瘤效果。大剂量单次给予米索硝唑(500 - 1000 mgkg-1)可增强美法仑的抗肿瘤作用,尤其是在美法仑高剂量时。这伴随着体温和肿瘤温度下降以及美法仑半衰期延长。在一项实验中,通过将小鼠置于35摄氏度的环境温度中3小时,防止了米索硝唑诱导的体温过低。这减少了美法仑的暴露,但并未降低药物组合的细胞毒性作用。连续8小时给予米索硝唑,无论美法仑是在给药期中途还是结束时给予,均未增强美法仑的损伤作用。似乎增强美法仑细胞毒性需要米索硝唑的肿瘤浓度阈值超过70微克/克;长时间暴露于极低剂量无效。