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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Oxaliplatin-chitosan nanoparticles induced intrinsic apoptotic signaling pathway: A 'smart' drug delivery system to breast cancer cell therapy
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Oxaliplatin-chitosan nanoparticles induced intrinsic apoptotic signaling pathway: A 'smart' drug delivery system to breast cancer cell therapy

机译:奥沙利铂-壳聚糖纳米颗粒诱导内在的凋亡信号通路:乳腺癌细胞治疗的“智能”药物递送系统

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摘要

This study was to investigate "smart" pH-responsive drug delivery system (DDS) based on chitosan nano-carrier for its potential intelligent controlled release and enhancing chemotherapeutic efficiency of Oxalipaltin. Oxaliplatin was loaded onto chitosan by forming complexes with degradable to construct nano-carrier as a DDS. Oxaliplatin was released from the DDS much more rapidly at pH 4.5 than at pH 7.4, which is a desirable characteristic for tumor-targeted drug delivery. Furthermore, the possible intrinsic apoptotic signaling pathway was explored by Western blot. It was found that expression of Bax, Bik, cytochrome C, caspase-9 and -3 was significantly up-regulated while the Bcl-2 and Sur-vivin were inhibited in breast cancer MCF-7 cells. For instance, nanoparticles inducing apoptosis in caspase-dependent manner indicate that chitosan nanoparticles could act as an efficient DDS importing Oxalipaltin to target cancer cells. These approaches suggest that "smart" Oxaliplatin delivery strategy is a promising approach to cancer therapy.
机译:这项研究旨在研究基于壳聚糖纳米载体的“智能” pH响应药物递送系统(DDS)的潜在智能控制释放和增强奥沙利汀的化学治疗效率。通过形成具有可降解的复合物将奥沙利铂加载到壳聚糖上,以构建纳米载体作为DDS。在pH 4.5时,奥沙利铂从DDS释放的速度比在pH 7.4时释放的快得多,这是靶向肿瘤的药物传递的理想特性。此外,通过蛋白质印迹探索了可能的内在凋亡信号通路。发现在乳腺癌MCF-7细胞中Bax,Bik,细胞色素C,caspase-9和-3的表达显着上调,而Bcl-2和Sur-vivin受到抑制。例如,以胱天蛋白酶依赖性方式诱导细胞凋亡的纳米颗粒表明,壳聚糖纳米颗粒可以作为有效的DDS,将奥沙利帕丁导入靶细胞。这些方法表明“智能”奥沙利铂递送策略是一种有前途的癌症治疗方法。

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