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引用本文:陈洋洋,李梦媛,李雪莹,王琪,郝若祎,阎雪莹.染料木素MePEG-PLGA共聚物胶束体内外抗肿瘤作用[J].中国现代应用药学,2020,37(12):1442-1447.
CHEN Yangyang,LI Mengyuan,LI Xueying,Wang Qi,HAO Ruoyi,YAN Xueying.Anti-tumor Effect of Genistein MePEG-PLGA Copolymer Micelles in vitro and in vivo[J].Chin J Mod Appl Pharm(中国现代应用药学),2020,37(12):1442-1447.
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染料木素MePEG-PLGA共聚物胶束体内外抗肿瘤作用
陈洋洋, 李梦媛, 李雪莹, 王琪, 郝若祎, 阎雪莹
黑龙江中医药大学药学院, 哈尔滨 150040
摘要:
目的 探讨染料木素MePEG-PLGA共聚物胶束对人肝癌SMMC-7721细胞的体内外抗肿瘤作用。方法 采用MTT法、Annexin V-FITC/PI染法分别考察染料木素MePEG-PLGA共聚物胶束对人肝癌SMMC-7721细胞的细胞毒性、细胞凋亡、细胞周期的影响;通过荷肝SMMC-7721瘤裸鼠体内抗肿瘤试验,考察染料木素胶束的体内抗肿瘤效应。结果 染料木素胶束对肝癌SMMC-7721细胞的抑制率均高于染料木素,最高抑制率分别可达83.26%,78.25%。流式细胞仪检测结果显示,染料木素胶束组能够提高染料木素对SMMC-7721细胞凋亡的诱导能力,并且呈浓度依赖性。5,10,20 μg·mL-1的染料木素组和染料木素胶束组药物作用于SMMC-7721细胞48 h时,染料木素胶束能够明显提高染料木素对细胞G2/M期细胞的阻滞作用,并且呈现浓度依赖性。体内抗肿瘤试验结果表明,相同浓度的染料木素胶束组的抑瘤效果显著强于染料木素乳剂组,呈浓度依赖性,最高抑瘤率可达55.41%。结论 染料木素MePEG-PLGA共聚物胶束在体内和体外均有显著的抗肝癌作用。
关键词:  染料木素  MePEG-PLGA共聚物胶束  细胞凋亡  抗肿瘤
DOI:10.13748/j.cnki.issn1007-7693.2020.12.007
分类号:R965.1
基金项目:黑龙江省自然科学基金项目(ZD2016019)
Anti-tumor Effect of Genistein MePEG-PLGA Copolymer Micelles in vitro and in vivo
CHEN Yangyang, LI Mengyuan, LI Xueying, Wang Qi, HAO Ruoyi, YAN Xueying
College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin 150040, China
Abstract:
OBJECTIVE To study the anti-tumor effect of genistein(GEN) MePEG-PLGA copolymer micelles on human hepatoma SMMC-7721 cells in vitro and in vivo. METHODS MTT assay, Annexin V-FITC/PI staining were used to investigate the effects of GEN MePEG-PLGA copolymer micelles on cytotoxicity, apoptosis and cell cycle of human hepatoma SMMC-7721 cells. The in vivo anti-tumor effect of GEN micelles was investigated in nude mice bearing hepatocellular carcinoma SMMC-7721 tumor in vivo. RESULTS The inhibitory rate of GEN micelles in SMMC-7721 cells were higher than GEN and the highest inhibition rates were 83.26% and 78.25%, respectively. The results of flow cytometry showed that the GEN micelles group could increase the ability of GEN to induce apoptosis of SMMC-7721 cells and presented a concentrationdependent manner. When the concentration of 5, 10, 20 μg·mL-1 GEN and GEN micelles groups acted on SMMC-7721 cells for 48 h, the GEN micelles could significantly enhance the ability of arrest cell in G2/M phase for GEN, and showing a concentration-dependent manner. In vivo anti-solid tumor experimental results showed that the same concentration of GEN micelles group had significantly better anti-tumor effect than GEN emulsion, and in a concentration-dependent manner, the highest tumor inhibition rate was 55.41%. CONCLUSION The GEN MePEG-PLGA copolymer micelles has significant anti-hepatocarcinoma effects both in vivo and in vitro.
Key words:  genistein  MePEG-PLGA copolymer micelles  apoptosis  antitumor
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