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Functionalized R9–reduced graphene oxide as an efficient nano-carrier for hydrophobic drug delivery

机译:作为疏水药物递送的有效纳米载体的官能化R9-还原的石墨烯氧化物

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Loading of hydrophobic drugs on smart carbon nano-carriers is a challenging issue for developing advanced drug delivery systems. We introduced a novel, stable, functionalized, and targeted graphene-based drug delivery system for smart transportation of hydrophobic agents. For this purpose, the planar size of graphene oxide (GO) sheets was initially engineered using ultra-sonic waves under controlled conditions. The sonication treatment not only tuned the GO sheet sizes, but also led to formation of desired reactive groups, appropriate for developing functionalized and targeted drug carriers. Afterwards, the hydrothermal reaction was simultaneously employed for both grafting R9 peptides and reduction of GO sheets. Therefore, the produced functional structure is an R9–rGO complex with proper stability in physiological solutions and also with a high-performance loading capability of Paclitaxel (PX). The in vitro experiments revealed that the R9–rGO–PX compound was efficiently uptook by Hela cancer cell lines, and reduced the viability of Hela and MCF-7 cells more than 90% after 72 hours. The proposed approach has the advantage of green production of an applicable graphene-based drug delivery system for improving the smart transportation of hydrophobic anti-cancer drugs.
机译:智能碳纳米载体对疏水药的装载是开发先进药物递送系统的挑战性问题。我们介绍了一种新型,稳定,官能化和靶向石墨烯的药物输送系统,用于疏水剂的智能运输。为此目的,最初在受控条件下使用超声波波动设计石墨烯(GO)片材的平面尺寸。超声处理处理不仅调整了去纸张尺寸,而且还导致了适于形成官能化和靶向药物载体的所需反应性基团的形成。然后,同时使用水热反应用于接枝R9肽和去纸的还原。因此,所产生的功能结构是R9-RGO复合物,具有适当的生理溶液稳定性,并且还具有紫杉醇(PX)的高性能负载能力。体外实验表明,R9-rgo-Px化合物通过HeLa癌细胞系有效地抑制了Hela癌细胞系,并在72小时后降低了Hela和MCF-7细胞的活力超过90%。该方法具有适用于适用的石墨烯的药物递送系统的绿色生产优势,用于改善疏水性抗癌药物的智能运输。

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