...
首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Catechol amide derivatized polyhydroxylated fullerene as potential chelating agents of radionuclides: Synthesis, reactive oxygen species scavenging, and cytotoxic studies
【24h】

Catechol amide derivatized polyhydroxylated fullerene as potential chelating agents of radionuclides: Synthesis, reactive oxygen species scavenging, and cytotoxic studies

机译:儿茶酚酰胺衍生的多羟基化富勒烯作为放射性核素的潜在螯合剂:合成,活性氧物种清除和细胞毒性研究

获取原文
获取原文并翻译 | 示例

摘要

Radionuclide internal contamination can induce chemical and radioactive intoxication and produce harmful free radicals in vivo. At present, administration of chelating agents is the most effective treatment against nuclide contamination. However, traditional studies on chelating agents have ignored the damage caused by free radicals to the body. The present study aimed to develop a type of a bifunctional sequestering agent that can chelates nuclides and scavenges free radicals simultaneously. Therefore, a novel catechol amide-derivatized polyhydroxylated fullerene was designed and prepared. The poor water solubility of fullerene was ameliorated by chemically modifying hydrophilic catechol amide and multiple hydroxyl groups, and obtaining high water-soluble fullerene derivatives. The affinities of chelators were investigated via sulfochlorophenol competitive complexing method and antioxidant capacities were examined by electron paramagnetic resonance. The results revealed the good complexation of the designed and synthesized chelating agent with uranyl ions; and its efficiency in scavenging hydroxyl radicals. This chelating agent showed extremely low toxicity and notable protective effect against oxidative stress on A549 cells. Besides, in U(VI)-exposed A549 cells, immediate treatment with catechol amide-derivatized polyhydroxylated fullerene significantly decreased the lactate dehydrogenase (LDH) release by inhibiting the cellular U(VI) intake, promoting the intracellular U(VI) release and inhibiting the production of intracellular reactive oxygen species (ROS). These results suggest that this fullerene derivative may be a valuable in vivo antioxidant and radionuclide decorporation agent.
机译:放射性核素内部污染可以诱导化学和放射性中毒,并在体内产生有害的自由基。目前,螯合剂的施用是针对核素污染的最有效的处理。然而,对螯合剂的传统研究忽略了由自由基对身体引起的损伤。本研究旨在开发一种双官能螯合剂,可以螯合核素并同时清除自由基。因此,设计并制备了一种新型的儿茶酚酰胺衍生的多羟基化富勒烯。通过化学改性亲水性儿茶酚酰胺和多个羟基和多种羟基来改善富勒烯的不良水溶性,得到高水溶性富勒烯衍生物。通过磺氯苯酚竞争络合方法研究螯合剂的亲和力,通过电子顺磁共振检查抗氧化能力。结果表明,设计和合成螯合剂与铀酰离子的良好络合;及其在清除羟基自由基中的效率。该螯合剂对A549细胞的氧化应激表现出极低的毒性和显着的保护作用。此外,在U(VI)中,通过抑制细胞U(VI)摄入,通过抑制细胞U(VI)释放并抑制促进细胞U(VI)释放并抑制,在U(VI)中,与儿茶酚酰胺 - 衍生化的多羟基化富勒烯的立即处理显着降低了乳酸脱氢酶(LDH)释放,促进细胞内U(VI)释放和抑制生产细胞内反应性氧(ROS)。这些结果表明,该富勒烯衍生物可以是体内抗氧化剂和放射性核素装饰剂的价值。

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