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首页> 外文期刊>Journal of Cancer Research and Therapeutics >Cytotoxic activity of extracts and fractions from Paramignya trimera root and Phyllanthus amarus against pancreatic cancer cell lines
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Cytotoxic activity of extracts and fractions from Paramignya trimera root and Phyllanthus amarus against pancreatic cancer cell lines

机译:虎尾草根和余生的提取物和级分的提取物对胰腺癌细胞的细胞毒活性

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Objective: The aim of this study was to assess cytotoxic activity of extracts and fractions from the Paramignya trimera root (PTR) and Phyllanthus amarus (PA) against two pancreatic cancer cell lines (primary: BxPc3 and secondary: CFPAC1). Materials and Methods: The root of PT and whole plant of PA were used in this study. The extracts and fractions from the PTR and PA were prepared using microwave-assisted extraction and high-performance liquid chromatography, respectively. The cytotoxic activity was assessed using the Dojindo Cell Counting Kit-8 assay. Results: The findings showed impressive cytotoxic capacity of the PTR extract against both pancreatic cancer cells of BxPc3 and CFPAC1 in a range of concentrations from 50 to 200 μg/mL, which was higher than those of ostruthin (67 μM), gemcitabine (50 nM), and four its fractions (50 μg/mL), and to be comparable to a saponin-enriched extract from Quillaja bark at 200 μg/mL. In contrast, the cytotoxic capacity of the PA extract and nine its fractions against these pancreatic cancer cell lines was significantly lower (P 0.05) than those of gemcitabine (50 nM) and Quillaja bark extract (200 μg/mL) and being comparable to phyllanthin (4.8 μM). The ICsub50/sub values of the PTR extract against BxPc3 and CFPAC1 cancer cells were 32.12 and 36.65 μg/mL, respectively, which was much lower than that of the PA extract against CFPAC1 cancer cells (128.81 μg/mL). Conclusion: The outcomes obtained from this study reveal that the PTR extract is a lead source for the potential development of novel antipancreatic cancer drugs and/or functional foods.
机译:目的:本研究的目的是评估三生草根(PTR)和Ph兰(PA)的提取物和级分对两种胰腺癌细胞系(原代:BxPc3和次代:CFPAC1)的细胞毒活性。材料与方法:本研究采用PT的根和PA的全株。 PTR和PA的提取物和级分分别使用微波辅助提取和高效液相色谱法制备。使用Dojindo Cell Counting Kit-8分析法评估细胞毒性。结果:研究结果表明,PTR提取物在50至200μg/ mL的浓度范围内对BxPc3和CFPAC1的两种胰腺癌细胞具有惊人的细胞毒性能力,高于ostruthin(67μM),gemcitabine(50 nM) )及其四个馏分(50μg/ mL),可与Quillaja树皮中富含皂苷的提取物(200μg/ mL)相媲美。相比之下,PA提取物及其9个组分对这些胰腺癌细胞系的细胞毒性能力显着低于吉西他滨(50 nM)和Quillaja树皮提取物(200μg/ mL)(P <0.05),与phyllanthin(4.8μM)。 PTR提取物对BxPc3和CFPAC1癌细胞的IC 50 值分别为32.12和36.65μg/ mL,远低于PA提取物对CFPAC1癌细胞的IC 50 (128.81μg/ mL)。 )。结论:从这项研究中获得的结果表明,PTR提取物是潜在开发新型抗胰腺癌药物和/或功能性食品的主要来源。

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