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果胶接枝磁性氧化石墨烯纳米杂化材料作为一种新型的紫杉醇药物载体。

Pectin-conjugated magnetic graphene oxide nanohybrid as a novel drug carrier for paclitaxel delivery.

机构信息

a Department of Chemistry , Kırıkkale University , Kırıkkale , Turkey.

b Department of Bioengineering , Kırıkkale University , Kırıkkale , Turkey.

出版信息

Artif Cells Nanomed Biotechnol. 2018;46(sup1):264-273. doi: 10.1080/21691401.2017.1421211. Epub 2018 Jan 3.

Abstract

Recent studies have shown that graphene oxide (GO) drug carrier functionalized with biocompatible natural polymers lead to higher loading efficacy and better stability with diminished cellular toxicity. Pectin (PEC) is one of the polysaccharide natural polymers, which has the potential to be used for drug delivery. In this work, we have successfully developed a novel PEC-conjugated magnetic GO nanocarrier for effective delivery of paclitaxel. The structure, surface morphology and thermal stability of the nanohybrid were investigated using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM) and zeta-sizer. Moreover, drug loading and release performance were studied by UV-vis absorption spectra. The cytotoxicity test was also performed by MTT test using L-929 fibroblast normal cell and MCF-7 cancer lines. The prepared nanocarrier showed an improved stability with enhanced drug loading capacity. Additionally, pH-responsive release analysis of the nanohybrid illustrated higher drug release at endosomal pH of cancer cell than that of normal physiological environment. Besides, cytotoxicity test demonstrated the synthesized nanohybrid is biocompatible, having very high relative cell viability. Bearing in mind these findings, the designed multifunctional nanohybrid drug carrier will be a good candidate for cancer drug delivery.

摘要

最近的研究表明,用生物相容性天然聚合物功能化的氧化石墨烯(GO)药物载体可提高载药效率和稳定性,同时降低细胞毒性。果胶(PEC)是一种多糖天然聚合物,具有作为药物递送的潜力。在这项工作中,我们成功地开发了一种新型的 PEC 接枝磁性 GO 纳米载体,用于有效递送紫杉醇。使用傅里叶变换红外光谱(FTIR)、X 射线衍射(XRD)、透射电子显微镜(TEM)和 Zeta 粒度仪研究了纳米杂化物的结构、表面形貌和热稳定性。此外,通过紫外可见吸收光谱研究了载药和释放性能。还通过 L-929 成纤维细胞正常细胞和 MCF-7 癌细胞系的 MTT 试验进行了细胞毒性试验。所制备的纳米载体显示出增强的稳定性和提高的载药能力。此外,纳米杂化物的 pH 响应释放分析表明,在癌细胞的内体 pH 下释放的药物高于正常生理环境。此外,细胞毒性试验表明,所合成的纳米杂化物具有生物相容性,相对细胞活力非常高。鉴于这些发现,设计的多功能纳米杂化物药物载体将是癌症药物递送的良好候选物。

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