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蟾酥抗肿瘤有效成分的活性追踪分离及急性毒性研究
引用本文:于垂亮,侯惠民. 蟾酥抗肿瘤有效成分的活性追踪分离及急性毒性研究[J]. 中草药, 2011, 42(2): 307-311
作者姓名:于垂亮  侯惠民
作者单位:上海医药工业研究院,药物制剂国家工程研究中心,上海,201203
摘    要:目的从传统中药蟾酥中寻找抗肿瘤活性强而毒性低的化合物。方法采用追踪分离的方式,以体外肿瘤细胞生长抑制强度为活性指标,同时结合小鼠急性毒性实验,对蟾酥的主要化学成分进行初步研究。结果采用活性追踪分离方式,从蟾酥中分离得到具有抑制肿瘤细胞生长活性同时对小鼠急性毒性较低的化合物蟾毒它灵,其对人非小细胞肺癌A549细胞具有较好的生长抑制作用,小鼠iv给药的LD50约为蟾毒灵的4倍,而且稳定性较好。结论综合化合物的活性、毒性及稳定性等因素,初步判断蟾毒它灵较其他同类化合物具有更好的抗肿瘤药物开发前景。

关 键 词:蟾酥  蟾毒它灵  抗肿瘤  急性毒性  蟾毒灵
收稿时间:2010-06-21

Bioassay-guided separation and acute toxicity evaluation of antitumor ingredient in Bufonis Venenum
YU Chui-liang and HOU Hui-min. Bioassay-guided separation and acute toxicity evaluation of antitumor ingredient in Bufonis Venenum[J]. Chinese Traditional and Herbal Drugs, 2011, 42(2): 307-311
Authors:YU Chui-liang and HOU Hui-min
Affiliation:National Pharmaceutical Engineering and Research Center,Shanghai Institute of Pharmaceutical Industry,Shanghai 201203,China
Abstract:Objective To obtain antitumor active compounds with lower toxicity from main ingredients of Chinese materia medicaBufonis Venenum. Methods Taking inhibition of in vitro tumor cells as active indexes, a bioassay-guided separation and toxicityevaluation in mice of ingredients in Bufonis Venenum were applied. Results Bufotalin was seperated from Bufonis Venenum withsignificant inhibition and lower acute toxicity by active tracking method. The inhibitory effect on the proliferation of A549 was better,LD50 of bufotalin by iv administration to mice is about four times of bufalin, and bufotalin is stable. Conclusion Integrated theactivity, toxicity, and stability factors of the compounds, bufotalin from Bufonis Venenum will deserve further research than any othersimilar compounds in potential antitumor activity.
Keywords:Bufonis Venenum   bufotalin   antitumor   acute toxicity   bufalin
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