首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Assessment of radiation-induced DNA damage caused by the incorporation of 99mTc-radiopharmaceuticals in murine lymphocytes using single cell gel electrophoresis.
【24h】

Assessment of radiation-induced DNA damage caused by the incorporation of 99mTc-radiopharmaceuticals in murine lymphocytes using single cell gel electrophoresis.

机译:使用单细胞凝胶电泳评估鼠淋巴细胞中掺入99mTc-放射性药物引起的辐射诱导的DNA损伤。

获取原文
获取原文并翻译 | 示例
           

摘要

The DNA damage induced by the 99mTc-radiopharmaceuticals incorporation to the cell was determined by the single-cell gel electrophoresis in murine lymphocytes in vitro. The 99mTc-hexamethyl-propylene amine oxime (99mTc-HMPAO) and 99mTc-2, 5-dihydroxybenzoic acid (99mTc-gentisic acid) induced nearly 100% of cells with breaks and/or alkali labile sites, which is explained by the action of the Auger electrons produced by the decay of the 99mTc. These results agree with the doses of 1.6 and 1.0 Gy estimated by subcellular dosimetry for 99mTc-HMPAO that is incorporated in the cytoplasm, and the 99mTc-gentisic acid, which remains bonded to the cell membrane, respectively. The results imply that Auger electrons are able to cause important DNA damage, when the radionuclide is incorporated in the range of a few microns from the nuclei.
机译:通过体外将鼠淋巴细胞中的单细胞凝胶电泳确定99mTc-放射性药物掺入细胞所引起的DNA损伤。 99mTc-六甲基-丙烯胺肟(99mTc-HMPAO)和99mTc-2,5-二羟基苯甲酸(99mTc-龙胆酸)诱导了近100%的细胞破裂和/或碱不稳定位点,这可以通过解释99mTc衰减产生的俄歇电子。这些结果与通过亚细胞剂量法估计的掺入细胞质的99mTc-HMPAO的剂量为1.6和1.0 Gy的剂量一致,而99mTc-龙胆酸仍与细胞膜结合。结果表明,当放射性核素掺入距离核几微米的范围内时,俄歇电子能够引起重要的DNA损伤。

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