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[摘要]
目的 研究胀果甘草药渣总黄酮和其指标性成分甘草查尔酮A的制备及其体外抗肿瘤活性。方法 利用大孔树脂柱色谱、聚酰胺柱色谱等方法,制备甘草药渣总黄酮,并结合色谱法和波谱法分离鉴定指标性甘草查尔酮A,应用HPLC法测定了总黄酮中甘草查尔酮A。应用A549、H1792、Calu-1 3种人癌细胞系,采用MTT法和流式细胞术法系统评价甘草药渣总黄酮和甘草查尔酮A的体外抗肿瘤活性和作用机制。结果 制备得到甘草药渣总黄酮,并从中分离鉴定了特征性指标性成分甘草查尔酮A,测定其在甘草药渣总黄酮中质量分数为7.41%。甘草药渣总黄酮和甘草查尔酮A对A549、H1792、Calu-1人癌细胞系均具有显著的抑制活性,可诱导肿瘤细胞凋亡。经流式细胞术检测,推测其作用机制为诱导肿瘤细胞凋亡。结论 甘草查尔酮A为胀果甘草药渣总黄酮发挥体外抗肿瘤活性的有效成分。
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[Abstract]
Objective To prepare the total flavonoids and its characteristic constituent licochalcone A from the residues of Glycyrrhiza inflata, which were further assayed for the antitumor activities in vitro. Methods The total flavonoids and licochalcone A were purified by chromatography. The structure of licochalcone A was identified on the basis of spectral data. The concentration of licochalcone A was determined by HPLC analysis method. Using MTT and flow cytometry, the antitumor activities in vitro were tested against A549, H1972, and Calu-1 human cancer cell lines. Results The total flavonoids and licochalcone A were prepared respectively and the concentration of licochalcone A was determined as 7.41% in the total flavonoids. The total flavonoids and licochalcone A showed the significant antitumor activities against the above three cancer cell lines. Its possible mechanism was the induction of apoptosis. Conclusions Licochalcone A is the effective antitumor constituent of the total flavonoids from the residues of G. inflata.
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[基金项目]
新疆维吾尔自治区科技支撑计划项目(201333102);新疆维吾尔自治区卫生厅青年科技人才专项科研项目(2012Y06)