Papadopoulou M V, Epperly M W, Shields D S, Bloomer W D
Pittsburgh Cancer Institute, PA 15213.
Jpn J Cancer Res. 1992 Apr;83(4):410-4. doi: 10.1111/j.1349-7006.1992.tb00123.x.
Two new bioreductive compounds, 9-[3-(2-nitro-1-imidazolyl)propylamino]acridine hydrochloride (NLA-1) and 9-[2-(2-nitro-1-imidazolyl)ethylamino]acridine hydrochloride (NLA-2), have been prepared. They feature an acridine ring to intercalate with DNA, a 2-nitroimidazole ring as the radiosensitizing moiety and an amino functionality for increased DNA-binding and hydrophilicity. Time and concentration dependent cytotoxicity as well as radiosensitization efficacy of the two compounds under hypoxic or aerobic conditions were determined in vitro using V-79 cells and an MTT colorimetric or clonogenic assay. The isosensitization point (ISP), defined as that drug concentration which results in the same survival decrement upon exposure of hypoxic or oxygenated cells to a given radiation dose, has been determined for both compounds at 7.5 Gy and the values are significantly lower than the ISPs of 5-[3-(2-nitro-1-imidazolyl)propyl]phenanthridinium bromide, 2-(2-nitro-1-imidazolyl)ethylamine or misonidazole (MISO). NLA-1 and NLA-2 are potent hypoxic cytotoxins and on a concentration basis, more potent than MISO as radiosensitizers in vitro. The sensitization enhancement ratios were significantly increased when 1 h drug preincubation under hypoxia at 37 degrees C was applied, before irradiation at room temperature.
已制备出两种新型生物还原化合物,即9-[3-(2-硝基-1-咪唑基)丙基氨基]吖啶盐酸盐(NLA-1)和9-[2-(2-硝基-1-咪唑基)乙基氨基]吖啶盐酸盐(NLA-2)。它们具有一个可与DNA嵌入的吖啶环、一个作为放射增敏部分的2-硝基咪唑环以及一个用于增强DNA结合和亲水性的氨基官能团。使用V-79细胞以及MTT比色法或克隆形成试验在体外测定了这两种化合物在缺氧或有氧条件下的时间和浓度依赖性细胞毒性以及放射增敏效果。已针对这两种化合物在7.5 Gy剂量下测定了等敏点(ISP),其定义为使缺氧或充氧细胞暴露于给定辐射剂量时导致相同存活降低的药物浓度,该值显著低于5-[3-(2-硝基-1-咪唑基)丙基]菲啶溴化物、2-(2-硝基-1-咪唑基)乙胺或米索硝唑(MISO)的等敏点。NLA-1和NLA-2是强效的缺氧细胞毒素,并且在体外作为放射增敏剂,按浓度计算比MISO更有效。当在37℃缺氧条件下进行1小时药物预孵育,然后在室温下进行照射时,增敏增强率显著增加。