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中国精品科技期刊2020
陈建平, 庞艺萌, 刘颖, 刘海, 钟赛意, 谌素华, 秦小明. 姜黄素超分子包合物的体外抗肿瘤活性评价[J]. 食品工业科技, 2018, 39(12): 6-10. DOI: 10.13386/j.issn1002-0306.2018.12.002
引用本文: 陈建平, 庞艺萌, 刘颖, 刘海, 钟赛意, 谌素华, 秦小明. 姜黄素超分子包合物的体外抗肿瘤活性评价[J]. 食品工业科技, 2018, 39(12): 6-10. DOI: 10.13386/j.issn1002-0306.2018.12.002
CHEN Jian-ping, PANG Yi-meng, LIU Ying, LIU Hai, ZHONG Sai-yi, CHEN Su-hua, QIN Xiao-ming. Evaluation on anti-cancer activity in vitro of curcumin supramolecular inclusion complex[J]. Science and Technology of Food Industry, 2018, 39(12): 6-10. DOI: 10.13386/j.issn1002-0306.2018.12.002
Citation: CHEN Jian-ping, PANG Yi-meng, LIU Ying, LIU Hai, ZHONG Sai-yi, CHEN Su-hua, QIN Xiao-ming. Evaluation on anti-cancer activity in vitro of curcumin supramolecular inclusion complex[J]. Science and Technology of Food Industry, 2018, 39(12): 6-10. DOI: 10.13386/j.issn1002-0306.2018.12.002

姜黄素超分子包合物的体外抗肿瘤活性评价

Evaluation on anti-cancer activity in vitro of curcumin supramolecular inclusion complex

  • 摘要: 对姜黄素超分子包合物的体外抗肿瘤活性进行评价。采用Cell Counting Kit-8(CCK-8)比色法检测包合物(40、80、160、320、640 μg/mL)对不同肿瘤细胞(A375黑色素瘤细胞、A549肺癌细胞、Hela宫颈癌细胞和MCF-7乳腺癌细胞)处理不同时间(24、48、72 h)后对其细胞存活率的影响,并进一步运用Annexin-V/PI双染检测包合物抑制肿瘤细胞增殖的原因。结果表明,四种细胞的存活率均随着包合物浓度和处理时间的增加呈下降趋势,并且包合物对A375细胞的增殖具有最强的抑制作用,其IC50达到最低,为476.4 μg/mL。进一步的检测发现,当包合物处理A375细胞后,细胞凋亡的数量随着包合物浓度的升高而升高,从对照组的3.3%上升到35.0%,这表明,包合物通过诱导细胞凋亡来抑制A375细胞增殖。

     

    Abstract: The anti-cancer activity of curcumin supramolecular inclusion complex was evaluated. The cell viability of different cancer cells(A375 cells,A549 cells,Hela cells and MCF-7 cells)exposed to different concentrations of curcumin supramolecular inclusion complex(40,80,160,320,640 μg/mL)for different time(24,48,72 h)was measured by Cell Counting Kit-8(CCK-8)assay. Furthermore,the reason of inclusion complex inhibiting cancer cells growth was measured by Annexin-V/PI staining assay. The results showed that the cell viability of four cancer cells gradually decreased with the increasing of concentration and treatment time of inclusion complex. And inclusion complex exhibited the strongest inhibitory effect on A375 cells,and IC50 of inclusion complex reached to minimum as 476.4 μg/mL. Further studies by Annexin-V/PI staining assay showed that after treatment of the A375 cells with inclusion complex,the ratios of apoptotic cells increased from 3.3%(control group)to 35.0% with the increasing of concentration of inclusion complex,indicating that inclusion complex inhibited A375 cells growth through induction of apoptosis.

     

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