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首页> 外文期刊>Process Biochemistry >Naringenin-loaded nano-structured lipid carrier fortifies oxaliplatin-dependent apoptosis in HT-29 cell line
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Naringenin-loaded nano-structured lipid carrier fortifies oxaliplatin-dependent apoptosis in HT-29 cell line

机译:装有柚皮素的纳米结构脂质载体可增强HT-29细胞系中奥沙利铂依赖性细胞凋亡

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摘要

In the present study, we inspected the role of naringenin-loaded nanostructured lipid carriers (NLCs) in the induction of apoptosis in (HT-29) colon cancer cell in co-administration with oxaliplatin. The cytotoxicity behavior of nanoparticles was investigated by MTT assay and DAPI staining. To understand the molecular mechanism of formulation in induction program cell death, flow cytometric and Real-Time RT-PCR assays were applied. New formulation revealed a mean particle size of 98 +/- 3 nm with homogenous dispersity, which was confirmed by SEM graphs. Naringenin and Oxaliplatin-induced cell death in HT-29 colon cancer by IC50 value of 150 +/- 11.04 NM and 20 +/- 2.25 mu M, respectively. Loading Naringenin into new formulation declined the proportion of cell proliferation of HT-29 colon cancer from 47 +/- 9.1% to 27 +/- 5.3% (p 0.05). Co-administration of naringenin loaded NLCs and oxaliplatin produced markedly increase the population of apoptosis from 31 +/- 2.3% up to 50 +/- 1.2% (p 0.05). Gene expression profile revealed a substantial decrease in anti-apoptotic factors including survivin, cyclin-B1, and Nrf2 along with an increase in pro-apoptotic factor Bid mRNA expression. In conclusion, our data represented that naringenin-loaded NLCs can be introduced as a potential adjuvant to develop the efficacy of chemotherapy and decrease its high dose-dependent side effects.
机译:在本研究中,我们检查了含有柚皮素的纳米结构脂质载体(NLC)在与奥沙利铂共同给药中诱导(HT-29)结肠癌细胞凋亡的作用。通过MTT分析和DAPI染色研究了纳米颗粒的细胞毒性行为。为了解制剂在诱导程序细胞死亡中的分子机制,应用了流式细胞仪和实时RT-PCR分析。新配方显示平均粒径为98 +/- 3 nm,具有均匀的分散性,这已通过SEM图得到证实。柚皮素和奥沙利铂诱导的HT-29结肠癌细胞死亡,IC50值分别为150 +/- 11.04 NM和20 +/- 2.25μM。将Naringenin装入新配方后,HT-29结肠癌的细胞增殖比例从47 +/- 9.1%降低到27 +/- 5.3%(p <0.05)。产生柚皮素的NLC和奥沙利铂的共同给药显着增加了细胞凋亡的数量,从31 +/- 2.3%增加到50 +/- 1.2%(p <0.05)。基因表达谱显示抗凋亡因子(包括生存素,cyclin-B1和Nrf2)显着降低,同时促凋亡因子Bid mRNA表达增加。总之,我们的数据表明,可以将纳瑞宁素负载的NLC作为潜在的佐剂使用,以提高化疗的疗效并降低其高剂量依赖性副作用。

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