| 注册
首页|期刊导航|国际医药卫生导报|菲并咪唑衍生物的体外抗肿瘤活性及其对斑马鱼胚胎发育的毒性效应研究

菲并咪唑衍生物的体外抗肿瘤活性及其对斑马鱼胚胎发育的毒性效应研究

陈坚平 余楚钦 郑康帝 杨怡 刘杰 邬凤娟

国际医药卫生导报2017,Vol.23Issue(18):2839-2844,6.
国际医药卫生导报2017,Vol.23Issue(18):2839-2844,6.DOI:10.3760/cma.j.issn.1007-1245.2017.18.008

菲并咪唑衍生物的体外抗肿瘤活性及其对斑马鱼胚胎发育的毒性效应研究

Evaluation on in vitro anticancer effect against cancer cells and toxicity in vivo of phenanthroimidazole derivatives on zebrafish embryos

陈坚平 1余楚钦 2郑康帝 2杨怡 2刘杰 3邬凤娟3

作者信息

  • 1. 510080 广州,中山大学附属第一医院
  • 2. 510006 广州,广东药科大学药学院
  • 3. 510623广州,无限极(中国)有限公司
  • 折叠

摘要

Abstract

Objective To design and synthesize phenanthroimidazole derivatives L271,and to evaluate in vitro antitumor activity and toxicity in vivo of phenanthroimidazole derivatives on zebrafish embryos.Methods Using 1,10-phenanthroline-5,6-dione and 2-methylbenzaldehyde as raw material,phenanthroimidazole derives L271 was prepared by microwave-assisted synthesis technology.The inhibition effects of phenanthroimidazole derivatives L271 on the growth of human cervical cancer cells Hela and human lung adenocarcinoma cells A549 were detected by MTT assay.With zebrafish embryos as a model,the effects of phenanthroimidazole derivatives L271 on the morphology,hatching rates,mortality rates,and malformation rates of zebrafish embryos were investigated to study acute toxicity.Results The chemical structure of target compound L271 was characterized by ESI-MS.Phenanthroimidazole derives L271 showed anti-proliferation effect on human cervical cancer Hela cells and human lung adenocarcinoma A549 cells cultured in vitro,especially for human cervical cancer Hela cells.The inhibitory activity (IC5o) of L271 against human cervical cancer Hela cells was about (8.38±0.09)μμmol/L,which was close to pirarubicin [IC50 =(6.97±0.07)μmol/L] at the same conditions.Compared with control groups,several abnormalities caused by L271 at ≥> 15p.mol/L were observed including caudal fin atrophy,spinal curvature,yolk sac edema,pericardial edema,tail bending and etc..When the concentration of L271 was equal or great than 30μmol/L,hatching rates of zebrafish embryos were reduced significantly,while mortality rates were increased significantly (P<0.05).The median lethal concentration (LC50) of L271 on zebrafish embryos at 48,72,96 hpf were 37.331 μ.mol/L(95%CI:35.535-39.301),34.911 μmol/L(95%CI:33.213-36.7290),30.283μmol/L(95%CI:29.590-30.980),respectively.When the concentration of L271 was equal or great than 15p.mol/L,the percentage of normal reduced,and the percentage of mortality increased,while the percentage of mortality increased firstly and then decreased as the concentration of L271 increased.Conclusion L271 exhibit considerable inhibitory effects on human cervical cancer cells Hela,which is comparable to that of pirarubicin.And no obvious toxic effects of L271 on zebrafish embryo when the concentration of L271 is less than 10μmol/L.

关键词

菲并咪唑衍生物/抗肿瘤活性/斑马鱼/毒性

Key words

Phenanthroimidazole derivatives/Antitumor activity/Zebrafish/Toxicity

引用本文复制引用

陈坚平,余楚钦,郑康帝,杨怡,刘杰,邬凤娟..菲并咪唑衍生物的体外抗肿瘤活性及其对斑马鱼胚胎发育的毒性效应研究[J].国际医药卫生导报,2017,23(18):2839-2844,6.

国际医药卫生导报

1007-1245

访问量0
|
下载量0
段落导航相关论文