Ruddock G W, Greenstock C L
Biochim Biophys Acta. 1977 Jan 24;496(1):197-202. doi: 10.1016/0304-4165(77)90128-3.
The half-wave reduction potentials of a range of nitroheterocyclic compounds were measured polarographically and compared with their radiosensitizing abilities in a simple radiation biochemical assay for damage to 5'-GMP. The chemical enhancement ratio for sensitization of inorganic phosphate release from irradiated 5'-GMP, increased with sensitizer electron affinity, but in a non-linear manner. An onset of sensitization was observed for nitroheterocyclics with half-wave potentials less negative then -0.05V vs. standard calomel electrode and maximum sensitization, approaching the oxygen effect, was obtained at a sensitizer half-wave potential of -0.25 V vs. standard calomel electrode. Nitroheterocyclic sensitizers with half-wave potentials in this range may be potential clinical radiotherapeutic agents.
通过极谱法测量了一系列硝基杂环化合物的半波还原电位,并在一项针对5'-GMP损伤的简单辐射生化测定中,将其与它们的放射增敏能力进行了比较。对于辐照的5'-GMP释放无机磷酸盐的增敏作用,化学增强比随敏化剂电子亲和力的增加而增加,但呈非线性关系。对于相对于标准甘汞电极半波电位负性小于-0.05V的硝基杂环化合物,观察到了增敏作用的起始;当敏化剂相对于标准甘汞电极的半波电位为-0.25V时,获得了接近氧效应的最大增敏效果。半波电位在此范围内的硝基杂环敏化剂可能是潜在的临床放射治疗剂。