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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Cytotoxic Activity of Kenaf Seed Oils from Supercritical Carbon Dioxide Fluid Extraction towards Human Colorectal Cancer (HT29) Cell Lines
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Cytotoxic Activity of Kenaf Seed Oils from Supercritical Carbon Dioxide Fluid Extraction towards Human Colorectal Cancer (HT29) Cell Lines

机译:超临界二氧化碳流体提取的洋麻籽油对人结肠直肠癌(HT29)细胞系的细胞毒活性

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Kenaf (Hibiscus cannabinus) from the family Malvaceae, is a valuable fiber plant native to India and Africa and is currently planted as the fourth commercial crop in Malaysia. Kenaf seed oil contains alpha-linolenic acid, phytosterol such as beta-sitosterol, vitamin E, and other antioxidants with chemopreventive properties. Kenaf seeds oil (KSO) was from supercritical carbon dioxide extraction fluid (SFE) at 9 different permutations of parameters based on range of pressures from 200 to 600 bars and temperature from 40 to 80° C. They were 200/40, 200/60, 200/80, 400/40,400/60, 400/80, 600/40, 600/60, and 600/80. Extraction from 9 parameters of KSO-SFE was screened for cytotoxicity towards human colorectal cancer cell lines (HT29) and mouse embryonic fibroblast (NIH/3T3) cell lines using MTS assay. KSO-SFE at 600/40 showed the strongest cytotoxicity towards HT29 with IC_(50) of 200 mug/mL. The IC_(50) for NIH/3T3 was not detected even at highest concentration employed. Cell cycle analysis showed a significant increase in the accumulation of KSO-SFE-treated cells at sub-Gl phase, indicating the induction of apoptosis by KSO-SFE. Further apoptosis induction was confirmed by Annexin V/PI and AO/PI staining.
机译:锦葵科的红麻(Kenaf cannabinus)是一种有价值的纤维植物,原产于印度和非洲,目前已作为马来西亚的第四种商业作物种植。洋麻籽油包含α-亚麻酸,植物甾醇(例如β-谷甾醇),维生素E和其他具有化学预防特性的抗氧化剂。红麻种子油(KSO)来自超临界二氧化碳萃取液(SFE),基于200至600 bar的压力范围和40至80°C的温度,在9种不同的参数排列下,分别为200 / 40、200 / 60 ,200 / 80、400 / 40、400 / 60、400 / 80、600 / 40、600 / 60和600/80。使用MTS分析,从9种KSO-SFE参数中提取提取物,以筛选对人结肠直肠癌细胞系(HT29)和小鼠胚胎成纤维细胞(NIH / 3T3)的细胞毒性。 KSO-SFE在600/40时对HT29具有最强的细胞毒性,IC_(50)为200杯/毫升。即使在最高浓度下也未检测到NIH / 3T3的IC_(50)。细胞周期分析显示在亚G1期KSO-SFE处理的细胞的积累显着增加,表明KSO-SFE诱导细胞凋亡。膜联蛋白V / PI和AO / PI染色证实了进一步的凋亡诱导。

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