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首页> 外文期刊>Nanobiotechnology, IET >Evaluation of potential anti-cancer activity of cationic liposomal nanoformulatedLycopodium clavatumin colon cancer cells
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Evaluation of potential anti-cancer activity of cationic liposomal nanoformulatedLycopodium clavatumin colon cancer cells

机译:阳离子脂质体纳米配制的 italic> Clavatum Clavatum 在结肠癌细胞中的潜在抗癌活性评估

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摘要

Research dealing with early diagnosis and efficient treatment in colon cancer to improve patient's survival is still under investigation. Chemotherapeutic agent result in high systemic toxicity due to their non-specific actions on DNA repair and/or cell replication. Traditional medicine such asnLycopodium clavatumn(LC) has been claimed to have therapeutic potentials against cancer. The present study focuses on targeted drug delivery of cationic liposomal nanoformulated LC (CL-LC) in colon cancer cells (HCT15) and comparing the efficacy with an anti-colon cancer drug, 7-ethyl-10-hydroxy-camptothecin (SN38) along with its nanoformulated form (CL-SN38). The colloidal suspension of LC was made using thin film hydration method. The drugs were characterised using ultraviolet, dynamic light scattering, scanning electron microscopy, energy, dispersive X-ray spectroscopy.nInvitrondrug release showed kinetics of 49 and 89% of SN38 and LC, whereas CL-SN38 and CL-LC showed 73 and 74% of sustained drug release, respectively. Studies on morphological changes, cell viability, cytotoxicity, apoptosis, cancer-associated gene expression analysis of Bcl-2, Bax, p53 by real-time polymerase chain reaction and western blot analysis of Bad and p53 protein were performed. Nanoformulated LC significantly inhibited growth and increased the apoptosis of colon cancer cells indicating its potential anti-cancer activity against colon cancer cells.
机译:结肠癌的早期诊断和有效治疗以提高患者生存率的研究仍在进行中。化学治疗剂由于其对DNA修复和/或细胞复制的非特异性作用而导致高全身毒性。传统医学,例如n 羊驼草n(LC)被认为具有抗癌的治疗潜力。本研究集中于阳离子脂质体纳米配方LC(CL-LC)在结肠癌细胞(HCT15)中的靶向药物递送,并与抗结肠癌药物7-乙基-10-羟基喜树碱(SN38)进行比较纳米形式(CL-SN38)。 LC的胶体悬浮液是使用薄膜水化法制备的。使用紫外线,动态光散射,扫描电子显微镜,能量,色散X射线光谱对药物进行了表征。n Invitro 药物释放显示SN38和LC的动力学分别为49%和89%,而CL-SN38和CL-LC的动力学分别为73%和74%持续释放药物。通过实时聚合酶链反应,Bad和p53蛋白的蛋白质印迹分析,研究了Bcl-2,Bax,p53的形态变化,细胞活力,细胞毒性,凋亡,癌症相关基因表达分析。纳米级LC可显着抑制结肠癌细胞的生长并增加其凋亡,表明其对结肠癌细胞具有潜在的抗癌活性。

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