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机构地区:[1]华中科技大学同济医学院药学院药物研究室,武汉430030
出 处:《中国药师》2006年第3期198-200,共3页China Pharmacist
摘 要:目的:对艾迪注射液体外抗癌活性进行研究,探讨其抗肿瘤作用及机制。方法:应用四甲基偶氮盐(MTT)法检测艾迪注射液在体外对小鼠S180,H22及人HepG2细胞的生长抑制作用;流氏细胞仪(FCM)分析其诱导HepG2细胞凋亡和对周期的阻滞作用;用荧光显微镜观察其诱导HepG2细胞凋亡作用。结果:艾迪注射液对小鼠S180、H22及人HepG2细胞的IC50分别为(9.82±0.272),(4.25±0.333),(6.78±0.268)mg·ml-1。4.1 mg·ml-1艾迪注射液作用48 h后的HepG2细胞凋亡率达到12.43%。结论:艾迪注射液对肿瘤细胞具有直接杀伤和促进肿瘤细胞凋亡的作用。Objective: The anti-cancer activity of AiDi and the related mechanism was studied. Method: The effect of AiDi on tumor cell proliferation, cell cycle distribution and apoptosis inducing were determined by cell biological methods including MTT assay, flow cytometry and fluorescent staining. Result: The IC50 of AiDi on S180 and H22 mice cell lines and HepG2 cell line were (9.82 ± 0.272), (4.25 ±0.333) and (6.78 ±0.268)mg·ml^-1 respectively, After offering AiDi of 4.1 mg·ml^-1 for 48 hours, the apoptosis rate of HepG2 cells was 12. 43%. Conclusion: AiDi showed proliferation inhibition on Si50 and H22 mice tumor cell lines and HepG2 human hepatocellular-carcinoma cell line by killing tumor cells directly and inducing apoptosis.
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