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Enhancement of cytotoxicity of artemisinin toward cancer cells by transferrin-mediated carbon nanotubes nanoparticles

机译:转铁蛋白介导的碳纳米管纳米颗粒增强青蒿素对癌细胞的细胞毒性

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摘要

Artemisinin (ART) is a kind of drug with an endoperoxide bridge which tends to react with Fe2+ to generate radicals for killing cancer cells. However, simultaneous delivery of hydrophobic ART and Fe2+ ions into cancer cells remains a major challenge. In this study, a multi-functional tumor-targeting drug delivery system employing hyaluronic acid-derivatized multi-walled carbon nanotubes (HA-MWCNTs) as drug carriers, transferrin (Tf) as targeting ligand and ART as a model drug for cancer treatment was constructed. This delivery system (HA-MWCNTs/Tf@ART) not only retained optical property of MWCNTs and cytotoxicity of ART but also demonstrated synergistic anti-tumor effect using ART and Tf. Compared with free ART, remarkably enhanced anti-tumor efficacy of this drug vehicle was realized both in cultured MCF-7 cells in vitro and in a tumor-bearing murine model in vivo, due to increased intracellular accumulation of ART and co-delivery of Tf and ART analogs. HA-MWCNTs/Tf@ART with laser irradiation demonstrated the highest inhibition effect compared to the other groups. This result may provide a new way of using promising natural drugs for cancer therapy.
机译:青蒿素(ART)是一种具有内过氧化物桥的药物,该过氧化物趋于与Fe2 +反应生成自由基以杀死癌细胞。然而,将疏水性ART和Fe 2+离子同时递送到癌细胞中仍然是主要挑战。在这项研究中,采用透明质酸衍生的多壁碳纳米管(HA-MWCNTs)作为药物载体,转铁蛋白(Tf)作为靶向配体和ART作为癌症治疗模型药物的多功能肿瘤靶向药物递送系统是建。该递送系统(HA-MWCNTs / Tf @ ART)不仅保留了MWCNT的光学性质和ART的细胞毒性,而且还展示了使用ART和Tf的协同抗肿瘤作用。与游离ART相比,由于ART中细胞内积累的增加和Tf的共同递送,在体外培养的MCF-7细胞和体内荷瘤鼠模型中均实现了这种药物载体的显着增强的抗肿瘤功效。和ART类似物。与其他组相比,激光照射的HA-MWCNTs / Tf @ ART表现出最高的抑制作用。该结果可能提供使用有前景的天然药物进行癌症治疗的新方法。

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