Wilkott L J, Dulmadge E A, Lloyd H H
J Natl Cancer Inst. 1978 May;60(5):1117-20. doi: 10.1093/jnci/60.5.1117.
Proliferating cultured P388 cells exhibited a greater degree of sensitivity to adriamycin than did proliferating cultured L1210 cells, although both leukemia cell populations had approximately the same doubling time. The rate of reduction in viability when cultured L1210 cell populations were exposed to adriamycin (0.0625-2.0 microgram/ml, concentrations that are comparable to tissue drug levels during therapy) was concentration-dependent. Therefore, the results indicated a possible therapeutic advantage to be gained by an increase in drug concentrations (within the limits of acceptable host toxicity) at the target cell site.
尽管两种白血病细胞群体的倍增时间大致相同,但增殖培养的P388细胞比增殖培养的L1210细胞对阿霉素表现出更高的敏感性。当培养的L1210细胞群体暴露于阿霉素(0.0625 - 2.0微克/毫升,与治疗期间组织药物水平相当的浓度)时,活力降低的速率呈浓度依赖性。因此,结果表明在靶细胞部位增加药物浓度(在可接受的宿主毒性范围内)可能获得治疗优势。