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通过物理加载紫杉醇到聚乙二醇(PEG)-接枝-碳纳米管上以实现有效的癌症治疗。

Delivery of paclitaxel by physically loading onto poly(ethylene glycol) (PEG)-graft-carbon nanotubes for potent cancer therapeutics.

机构信息

Institute of Materials Research and Engineering, A*STAR (Agency for Science, Technology and Research), 3 Research Link, Singapore.

出版信息

Nanotechnology. 2010 Feb 10;21(6):065101. doi: 10.1088/0957-4484/21/6/065101. Epub 2010 Jan 8.

DOI:10.1088/0957-4484/21/6/065101
PMID:20057024
Abstract

UNLABELLED

Physically loading of paclitaxel (PTX) onto carbon nanotubes (CNTs) is achieved through immersion of poly(ethylene glycol) (PEG)-graft-single walled CNTs (PEG-g-SWNTs) or PEG-graft-multi-walled CNTs (PEG-g-MWNTs) in a saturated solution of PTX in methanol. After loading once the loading capacity (LD%) is 26% (w/w) and 36% (w/w) for PEG-g-SWNTs or PEG-g-MWNTs, respectively. With these PTX contents, PTX loaded PEG-g-SWNTs and PTX loaded PEG-g-MWNTs still have good dispersity in aqueous solution and individual CNTs can be observed in TEM images. PTX can be released from PEG-g-CNTs several times faster than from free PTX but still in a sustained profile with less than 40% of PTX being released in 40 days at pH 7 or 5. In vitro cytotoxicity of samples is evaluated in HeLa cells and MCF-7 cells. PEG-g-SWNTs and PEG-g-MWNTs show low cytotoxicity in both cells with insignificant effects on the cell proliferation rates. However, both PTX loaded PEG-g-SWNTs and PTX loaded PEG-g-MWNTs show high efficacy to kill HeLa cells and MCF-7 cells, as reflected by IC(50) lower than free PTX. Therefore, PTX loaded PEG-g-CNTs are promising for cancer therapeutics.

KEYWORDS

carbon nanotubes, poly(ethylene glycol), drug delivery, cancer therapy, nanomedicine.

摘要

未加标签

通过将聚乙二醇(PEG)-接枝单壁碳纳米管(PEG-g-SWNTs)或 PEG-接枝多壁碳纳米管(PEG-g-MWNTs)浸入紫杉醇(PTX)在甲醇中的饱和溶液中,实现了将紫杉醇物理加载到碳纳米管(CNTs)上。负载一次后,PEG-g-SWNTs 或 PEG-g-MWNTs 的负载量(LD%)分别为 26%(w/w)和 36%(w/w)。在这些 PTX 含量下,负载 PTX 的 PEG-g-SWNTs 和负载 PTX 的 PEG-g-MWNTs 在水溶液中仍具有良好的分散性,并且可以在 TEM 图像中观察到单个 CNTs。与游离 PTX 相比,PTX 从 PEG-g-CNTs 中的释放速度快几倍,但仍呈持续释放模式,在 pH7 或 5 下 40 天内释放少于 40%的 PTX。在 HeLa 细胞和 MCF-7 细胞中评估了样品的体外细胞毒性。PEG-g-SWNTs 和 PEG-g-MWNTs 在两种细胞中均显示出低细胞毒性,对细胞增殖率没有明显影响。然而,负载 PTX 的 PEG-g-SWNTs 和负载 PTX 的 PEG-g-MWNTs 对 HeLa 细胞和 MCF-7 细胞均具有高效的杀伤作用,IC(50)低于游离 PTX。因此,负载 PTX 的 PEG-g-CNTs 有望用于癌症治疗。

关键词

碳纳米管、聚乙二醇、药物输送、癌症治疗、纳米医学。

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