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首页> 外文期刊>Journal of magnetism and magnetic materials >β-cyclodextrin functionalized poly (5-amidoisophthalicacid) grafted Fe_3O_4 magnetic nanoparticles: A novel biocompatible nanocomposite for targeted docetaxel delivery
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β-cyclodextrin functionalized poly (5-amidoisophthalicacid) grafted Fe_3O_4 magnetic nanoparticles: A novel biocompatible nanocomposite for targeted docetaxel delivery

机译:β-环糊精官能化的聚(5-氨基间苯二甲酸)接枝的Fe_3O_4磁性纳米粒子:一种新型的生物相容性纳米复合材料,用于靶向多西他赛的递送

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摘要

Thiol-lactam initiated radical polymerization (TLIRP) was successfully employed to prepare poly-N- 5-acrylamidoisophthalicacid grafted onto Fe_3O_4 magnetic nanoparticles (MNPs@PAIP).β-Cyclodextrin (CD) was then conjugated to the carboxylic groups of the prepared MNPs via carbodiimide activation. Subsequently, tumor-targeting folic acid (FA) was attached to the hydroxyl groups of CD on the surface of the latter MNPs to increase the site-specific intracellular delivery. The prepared MNPs were fully characterized by FTIR, VSM, TGA, XRD, FE-SEM and TEM. Docetaxel (DTX) as hydrophobic anticancer drug was loaded via host-guest inclusion complexation with CD and the release profile of the system was studied at different pH. The effect of MNPs on the cell viability was evaluated for the human embryonic kidney normal cell line (HEK293) as well as HeLa and MDA-MB-231 cancerous cell lines and the results did not show any apparent cytotoxic effect In comparison, DTX loaded MNPs reduced the growth of HeLa and MDA-MB-231 cells more than free DTX. Intracellular uptake ability of DTX loaded MNPs was also studied using fluorescent microscopy and showed cellular uptake about 90% after 4 h treatment.
机译:成功地利用硫醇-内酰胺引发的自由基聚合(TLIRP)制备了接枝到Fe_3O_4磁性纳米粒子(MNPs @ PAIP)上的聚N-5-丙烯酰胺基间苯二甲酸,然后将β-环糊精(CD)通过以下方法与制备的MNPs的羧基共轭:碳二亚胺活化。随后,将靶向肿瘤的叶酸(FA)连接到后者MNP表面上CD的羟基上,以增加位点特异性细胞内递送。 FTIR,VSM,TGA,XRD,FE-SEM和TEM对制备的MNP进行了全面表征。多西他赛(DTX)作为疏水性抗癌药物通过宿主-客体与CD的包合作用负载,并在不同pH下研究了该系统的释放特性。评估了人类胚胎肾正常细胞系(HEK293)以及HeLa和MDA-MB-231癌细胞系MNP对细胞活力的影响,结果未显示任何明显的细胞毒性作用。与游离DTX相比,降低了HeLa和MDA-MB-231细胞的生长。还使用荧光显微镜研究了载有DTX的MNP的细胞内摄取能力,并显示4小时处理后细胞摄取约90%。

著录项

  • 来源
    《Journal of magnetism and magnetic materials》 |2016年第11期|451-459|共9页
  • 作者单位

    Department of Chemistry, University of Zanjan, P.O. Box 45195-313, Zanjan, Iran;

    Department of Pharmaceutical Biomaterials and Medical Biomaterials Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran,Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran;

    Department of Tissue Engineering, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran;

    Department of Chemistry, University of Zanjan, P.O. Box 45195-313, Zanjan, Iran;

    Department of Nanotechnology, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran;

    Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran;

    Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran;

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  • 正文语种 eng
  • 中图分类
  • 关键词

    Targeted drug delivery; β-Cyclodextrin; Docetaxel; Superparamagnetic iron oxide;

    机译:有针对性的药物输送;β-环糊精;多西他赛;超顺磁性氧化铁;

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