首页> 外文期刊>Current radiopharmaceuticals >Nitroimidazole Radiopharmaceuticals in Hypoxia: Part II Cytotoxicity and Radiosensitization Applications
【24h】

Nitroimidazole Radiopharmaceuticals in Hypoxia: Part II Cytotoxicity and Radiosensitization Applications

机译:缺氧硝基咪唑放射性药物:第二部分细胞毒性和放射增敏应用

获取原文
获取原文并翻译 | 示例
           

摘要

Feasibility paper explores the cytotoxicity of nitroimidazole on tumor cells and liver cells to establish the 2'-nitroimidazole as radiosensitizer in cancer therapy and hypoxia monitoring. Hypothesis is that the presence of substituted nitro group on 2' position of imidazole ring is more enzyme sensitive and determinant of biochemical cytotoxicity as hypoxia reporter in isolated tumor cells or tumor tissues. Radiolabeling of nitroimidazole imparts tracer properties to locate the distribution (radiosensitizer) of nitroimidazole in the body. A 'theradiagnostic criteria of hypoxia' using nitroimidazole radiosensitizer is proposed based on tumor killing by enhanced tumor oxygen tension (therapeutics) and altered metabolizing enzymes (diagnostics) due to cytotoxicity of radiosensitizer. Both properties of nitroimidazole cytotoxicity and oxygen sensitivity place the nitroimidazole compounds in the class of tumor therapy and hypoxia detection. Initially nitroimidazole cytotoxicity was reported as antiparasitic drug. Now radiolabeled 2'-nitroimidazole is potential radiosensitizer in hypoxia treatment and monitoring in last two decades. Hydrophilic double radiolabel groups on imidazole ring offer multimodal imaging and active nitro- or imidazole ring in nitroimidazoles interact with intracellular metabolism in liver by biotransformation and biooxidation to cause cytotoxicity as biomarker of hypoxia. Nitroimidazole metabolizing and xenobiotic enzymes showed regulatory role to excrete out nitroimidazole from the body and reduced stay time in tissue. Nitroimidazoles showed physicochemical properties with poor tissue diffusion, less antioxidant redox potential and long retention time in tissue making them poor choice of hypoxia markers. Key of success is achieving 2'-Nitroimidazole based multimodal radiopharmaceuticals as less cytotoxic, more tumor oxygen specific multifunctional reporters of apop-tosis, proliferation, and hypoxia in theradiagnostics and radiation oncology.
机译:可行性文件探讨了硝基咪唑对肿瘤细胞和肝细胞的细胞毒性,以建立2'-硝基咪唑作为放射增敏剂用于癌症治疗和缺氧监测。假设是咪唑环2'位上存在取代的硝基基团,在分离的肿瘤细胞或肿瘤组织中作为缺氧报告基因对酶更敏感,并决定了生化细胞毒性。硝基咪唑的放射性标记赋予示踪剂特性以定位硝基咪唑在体内的分布(放射增敏剂)。提出了一种使用硝基咪唑放射增敏剂的“缺氧放射诊断标准”,其基于通过放射增敏剂的细胞毒性而增强的肿瘤氧张力(治疗)和改变的代谢酶(诊断)来杀死肿瘤。硝基咪唑的细胞毒性和氧敏感性的特性均使硝基咪唑化合物成为肿瘤治疗和缺氧检测的类别。最初报道硝基咪唑具有细胞毒性作为抗寄生虫药。现在,放射性标记的2'-硝基咪唑是近二十年来在缺氧治疗和监测中潜在的放射增敏剂。咪唑环上的亲水性双放射性标记基团可提供多模态成像,硝基咪唑中的活性硝基或咪唑环可通过生物转化和生物氧化作用与肝脏中的细胞内代谢相互作用,从而引起细胞毒性,作为缺氧的生物标志物。硝基咪唑代谢和异种酶显示出从体内排泄硝基咪唑并减少在组织中停留时间的调节作用。硝基咪唑显示出理化性质,具有较差的组织扩散,较少的抗氧化还原电位和较长的在组织中的保留时间,因此它们是缺氧标记物的较差选择。成功的关键在于实现2'-硝基咪唑基多峰放射性药物,因为它在放射诊断学和放射肿瘤学中具有细胞毒性较小,细胞凋亡,增殖和缺氧的肿瘤氧特异性多功能报道分子。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号