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Ultrashort Nanotube Blocked Large-Inner-Diameter Multi-Walled Carbon Nanotubes Based Drug Delivery System for Tumor Targeted Therapy

机译:基于超短纳米管的大直径内壁多壁碳纳米管封闭药物输送系统,用于肿瘤靶向治疗

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摘要

The drug loading efficiency, drug release profile, and cellular uptake are critical aspects of any drug delivery system to accomplish delivery objectives. To improve the efficacy of carbon nanotubes based drug delivery system, the highly purified Folic acid (FA)-conjugated large-innerdiameter multi-walled carbon nanotubes (LID-MWCNTs) were employed to establish a novel cisplatin (CDDP)-loaded drug delivery system. Ultra-purified nanotubes with open ends and sidewall defects were fabricated by a multi-step oxidation procedure. Then, FA was attached to external surface of these nanotubes and CDDP was incorporated inside the FA-LID-MWCNT carriers by capillarity and the drug entries were blocked by the ultrashort oxidized LID-MWCNT (UST) nanoparticles. CDDP loading efficiency of the resulted drug delivery system was as high as 70.97%. Meanwhile, the drug delivery system demonstrated a sustained CDDP release profile and an improved cellular uptake. Cytotoxicity test on CAL-27 and MCF-7 cells revealed enhanced inhibition of tumor cell proliferation (IC50 were 4.21 mu M and 3.76 mu M respectively). The FA-conjugated UST-blocked LID-MWCNT based drug delivery system was proved to be a promising strategy to improve the pharmacological activity of CDDP in chemotherapy.
机译:药物装载效率,药物释放曲线和细胞摄取是实现给药目标的任何药物输送系统的关键方面。为了提高基于碳纳米管的药物输送系统的功效,采用高纯度叶酸(FA)-缀合的大直径多壁碳纳米管(LID-MWCNTs)建立了载有顺铂(CDDP)的新型药物输送系统。通过多步氧化工艺制备了具有开口端和侧壁缺陷的超纯化纳米管。然后,将FA附着到这些纳米管的外表面上,并通过毛细管作用将CDDP掺入FA-LID-MWCNT载体内部,并且药物进入被超短氧化LID-MWCNT(UST)纳米颗粒阻塞。最终的药物递送系统的CDDP装载效率高达70.97%。同时,药物递送系统显示出持续的CDDP释放曲线和改善的细胞摄取。对CAL-27和MCF-7细胞的细胞毒性测试显示出对肿瘤细胞增殖的抑制作用增强(IC50分别为4.21μM和3.76μM)。基于FA结合的UST-阻断的LID-MWCNT的药物递送系统被证明是提高化学疗法中CDDP的药理活性的有前途的策略。

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