Rasey J S, Krohn K A, Grunbaum Z, Conroy P J, Bauer K, Sutherland R M
Radiat Res. 1985 Apr;102(1):76-85.
[14C]Bromomisonidazole was prepared by direct bromination of [ring-2] [14C]misonidazole in dioxane. The uptake and binding of the two labeled sensitizers were compared in vitro in 1-mm EMT-6 spheroids which contain a necrotic core. Using liquid scintillation counting it was shown that spheroids incubated with 50 microM [14C]bromomisonidazole concentrated drug above levels in the medium by 1 1/2 hr and achieved maximum concentration by 10 hr with no further increase at 23 hr. Spheroids incubated with 50 microM [14C]misonidazole may concentrate the sensitizer more slowly but ultimately reached the same fivefold increase over levels in the medium by 23 hr as was observed for bromomisonidazole. Autoradiographs prepared from spheroids after incubation with [14C]misonidazole or [14C]bromomisonidazole showed silver grains preferentially located over viable hypoxic cells in the inner half of the spheroid rim adjacent to the necrotic center, with lower grain density over nonviable necrotic areas and many fewer grains over oxic cells at the periphery of the spheroid. The results indicate that both severely and moderately hypoxic cells may preferentially bind [14C]bromomisondiazole. The data support the potential of radiolabeled bromomisonidazole for in vivo imaging pending additional studies of the metabolism of this agent.
[14C]溴米索硝唑是通过在二氧六环中对[环-2][14C]米索硝唑进行直接溴化反应制备而成。在含有坏死核心的1毫米EMT-6球体中,对这两种标记敏化剂的摄取和结合进行了体外比较。通过液体闪烁计数法表明,用50微摩尔[14C]溴米索硝唑孵育的球体在1.5小时时药物浓度高于培养基中的水平,并在10小时时达到最大浓度,23小时时不再增加。用50微摩尔[14C]米索硝唑孵育的球体可能更缓慢地浓缩敏化剂,但最终在23小时时比培养基中的水平增加了五倍,与溴米索硝唑的情况相同。用[14C]米索硝唑或[14C]溴米索硝唑孵育后的球体制作的放射自显影片显示,银颗粒优先位于球体边缘靠近坏死中心的内半部分的存活缺氧细胞上,在无活力的坏死区域颗粒密度较低,在球体周边的有氧细胞上颗粒则少得多。结果表明,严重缺氧和中度缺氧细胞可能优先结合[14C]溴米索硝唑。这些数据支持了放射性标记的溴米索硝唑在体内成像方面的潜力,有待对该药物的代谢进行更多研究。