...
首页> 外文期刊>Drug and Chemical Toxicology >In vitro cytotoxicity study of oxaziridines generated after chlordiazepoxide,demoxepam,and desmethylchlordiazepoxide UV irradiation
【24h】

In vitro cytotoxicity study of oxaziridines generated after chlordiazepoxide,demoxepam,and desmethylchlordiazepoxide UV irradiation

机译:氯氮卓,地西x和去甲基氯氮卓紫外线照射后产生的恶唑烷的体外细胞毒性研究

获取原文
获取原文并翻译 | 示例
           

摘要

The cytotoxicity of oxaziridines photogenerated after irradiation of chlordiazepoxide (CDZ) and its metabolites was investigated in vitro by a MTT assay on P388 leukemia and B16 melanoma cell lines and compared with that of the anticancer drug,melphalan. For the longer time-exposure experiment,oxaziridines had the same cytotoxicity as melphalan and this toxicity was higher when oxaziridines were photogenerated in the presence of cells. In conclusion,oxaziridines generated after CDZ,demoxepam,and desmethylchlordiazepoxide ultraviolet irradiation exhibited cytotoxicity activity against cancer cell lines. A possibility of CDZ use within the context of photodynamic therapy as a treatment for small,superficial tumors should not be excluded,because oxaziridines can be generated locally by skin-tumor local irradiation after CDZ topical administration.
机译:用MTT法对氯二氮卓(CDZ)及其代谢产物照射后光生的恶唑烷的细胞毒性进行了体外研究,该试验对P388白血病和B16黑素瘤细胞系进行了比较,并与抗癌药物美法仑进行了比较。对于更长的时间暴露实验,恶唑烷具有与美法仑相同的细胞毒性,当在细胞存在下光产生恶唑烷时,该毒性更高。总之,CDZ,地西,和去甲基氯二氮杂dia紫外线照射后产生的恶唑烷对癌细胞系表现出细胞毒性。在光动力疗法的背景下使用CDZ作为治疗小,浅表肿瘤的可能性不应该被排除,因为在局部施用CDZ后皮肤肿瘤局部照射可产生恶唑烷定。

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