首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Potential Antiproliferative Activity and Evaluation of Essential Oil Composition of the Aerial Parts of Tamarix aphylla (L.) H.Karst.: A Wild Grown Medicinal Plant in Jordan
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Potential Antiproliferative Activity and Evaluation of Essential Oil Composition of the Aerial Parts of Tamarix aphylla (L.) H.Karst.: A Wild Grown Medicinal Plant in Jordan

机译:Tamarix aphylla(L.)H.Karst。的空中部分的潜在抗增殖活性和精油成分评估:约旦的一种野生植物

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Essential (volatile) oil from aerial parts of Tamarix aphylla (L.) H.Karst. (Tamaricaceae) grown wild in Jordan was hydrodistilled by Clevenger apparatus and analyzed by means of GC and GC-MS techniques. In vitro screening of potential cytotoxicity of the aqueous (AE) and ethanol (EE) extracts was also evaluated against human breast adenocarcinoma (MCF-7), colorectal adenocarcinoma (Caco-2), and pancreatic carcinoma (Panc-1) cancer cell lines as well as normal human fibroblasts. GC-MS analysis of T. aphylla EO revealed its richness in nonterpenoid nonaromatic hydrocarbons (52.39%), with predominance of 6,10,14-trimethyl-2-pentadecanone as the principal component. Biologically, the plant extracts exhibited cytotoxicity effects in dose-dependent manner against most of the tested cell lines, but potent effects were only predicted against MCF-7 cells with IC50 values of 2.17 ± 0.10 and 26.65 ± 3.09 μg/mL for T. aphylla AE and EE, respectively. T. aphylla AE demonstrated a comparable cytotoxic effect with that offered by the control drug cisplatin (IC50 value of 1.17 ± 0.13 μg/mL), even with higher safety profile against normal fibroblast cells (IC50 values of T. aphylla AE versus cisplatin 79.99 ± 4.90 versus 9.08 ± 0.29 μg/mL). T. aphylla extracts could be a valuable source for cytotoxic agents with high safety and selective cytotoxicity profiles. Unfortunately, no antiproliferative potential against Caco-2 or Panc-1 cancer cell lines was detected at a concentration less than 30 μg/mL.
机译:Ta柳(L.)H.Karst地上部分的挥发油。用Clevenger仪器对在约旦野生的金枪鱼科(Tamaricaceae)进行水蒸馏,并通过GC和GC-MS技术进行分析。还评估了水性提取物(AE)和乙醇(EE)的潜在细胞毒性对人乳腺腺癌(MCF-7),结直肠腺癌(Caco-2)和胰腺癌(Panc-1)癌细胞系的影响以及正常的人类成纤维细胞。 GC-MS分析显示,无叶丁香EO具有丰富的非萜类非芳香烃含量(52.39%),其中主要成分为6,10,14-三甲基-2-十五烷酮。从生物学上讲,植物提取物对大多数受试细胞系均表现出剂量依赖性的细胞毒性作用,但仅预测其对MCF-7细胞的强效作用,其无花T. IC50值为2.17±0.10和26.65±3.09μg/ mL。 AE和EE。 T. aphylla AE表现出与对照药物顺铂相同的细胞毒性作用(IC50值为1.17±0.13μg/ mL),即使对正常成纤维细胞的安全性更高(T. aphylla AE相对于顺铂的IC50值为79.99± 4.90对9.08±0.29μg/ mL)。紫苏提取物可能是具有高安全性和选择性细胞毒性特征的细胞毒性剂的有价值来源。不幸的是,当浓度低于30μg/ mL时,未检测到针对Caco-2或Panc-1癌细胞的抗增殖潜能。

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