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首页> 外文期刊>RSC Advances >Cationic nanomicelles derived from Pluronic F127 as delivery vehicles of Chinese herbal medicine active components of ursolic acid for colorectal cancer treatment
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Cationic nanomicelles derived from Pluronic F127 as delivery vehicles of Chinese herbal medicine active components of ursolic acid for colorectal cancer treatment

机译:源自Pluronic F127的阳离子纳米胶束作为熊果酸中草药活性成分的传递载体,用于治疗大肠癌

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摘要

Ursolic acid (UA) has shown great potential in cancer therapy but their efficacy is seriously compromised by poor water-solubility and limited cellular uptake. In this paper, cationic nanomicelles self-assembled from Pluronic F127 with the cationic polymer of C _(18) -polyethylenimine (C _(18) -PEI) as a functional component are fabricated as delivery vehicles of Chinese herbal medicine active components of ursolic acid (UA) for colorectal cancer treatment. The inhibition effects of this drug loaded cationic nanomicelles (named as FUP) on cell viability and cell colony formation were more significant than the free UA, due to their cationic surface which can increase UA uptake by colorectal cancer cells. Cell cycle analysis showed that this inhibition effect was mediated by a cell cycle arrest at the G1 checkpoint, and the cell death induced by these nanomicelles occurred via apoptosis, which was detected by annexin?V antibody and propidium iodide staining. Further western blot analysis demonstrated the apoptosis mechanism was associated with the regulation of Fas/FasL and activation of caspase-8 and caspase-3. Therefore, our cationic nanomicelles can potentially be used to enhance the therapeutic effect of UA for colorectal cancer treatment.
机译:熊果酸(UAs)在癌症治疗中已显示出巨大潜力,但水溶性差且细胞吸收受限,严重削弱了它们的功效。本文以C_(18)-聚乙烯亚胺(C_(18)-PEI)的阳离子聚合物为功能成分,由Pluronic F127自组装制备了阳离子纳米胶束,作为熊果草中草药活性成分的传递载体。酸(UA)用于大肠癌的治疗。载有这种药物的阳离子纳米胶束(称为FUP)对细胞活力和细胞集落形成的抑制作用比游离UA更为显着,因为它们的阳离子表面可增加结直肠癌细胞对UA的吸收。细胞周期分析表明,这种抑制作用是由G1检查点的细胞周期停滞介导的,这些纳米胶束诱导的细胞死亡是通过凋亡发生的,而膜联蛋白?V抗体和碘化丙啶染色可以检测到这种死亡。进一步的蛋白质印迹分析表明,其凋亡机制与Fas / FasL的调节以及caspase-8和caspase-3的激活有关。因此,我们的阳离子纳米胶束可以潜在地用于增强UA对大肠癌的治疗作用。

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