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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Effects of iron oxide nanoparticles on biological responses and MR imaging properties in human mammary healthy and breast cancer epithelial cells
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Effects of iron oxide nanoparticles on biological responses and MR imaging properties in human mammary healthy and breast cancer epithelial cells

机译:氧化铁纳米颗粒对人乳腺健康和乳腺癌上皮细胞生物学反应和MR成像性能的影响

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Superparamagnetic iron oxide nanoparticles (SPIONs, diameters >50 nm) have received great attention due to their promising use as magnetic resonance imaging (MRI) contrast agents. In this study, we evaluated the cellular uptake and biological responses in vitro of ultrasmall SPIONs (USPIONs, diameters<50 nm). We compared the cellular responses between breast epithelia isolated from healthy and breast cancer donors after exposure to carboxy-terminated USPIONs (10 and 30 nm PEG-coated, 10 and 30 nm non-PEG-coated). The particles were characterized using transmission electron microscopy (TEM), dynamic light scattering (DLS) and gel electrophoresis. Cellular interactions with USPIONs were assessed by confocal microscopy and TEM. Cellular uptake of USPIONs was quantified using ICP-MS. Cell viability was measured by MTT and neutral red uptake assays. T2* weighted MRI scans were performed using a 7T scanner. Results demonstrated that cell association/internalization of USPIONs was size- and surface coating-dependent (PEG vs. non-PEG), and higher cellular uptake of 10 and 30 nm non-coated particles was observed in both cell types compared with PEG-coated particles. Cell uptake for 10 and 30 nm non-coated particles was higher in cancer cells from two of three tested donors compared to healthy cells from three donors. There was no significant cytotoxicity observed for all tested particles. Significantly enhanced MRI contrast was observed following exposure to 10 and 30 nm non-coated particles compared to PEG-coated particles in both cell types. In comparison, cancer cells showed more enhanced MRI signals when compared to normal cells. The data indicate that cell responses following exposure to USPIONs are dependent on particle properties. (c) 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1032-1042, 2016.
机译:超顺磁性氧化铁纳米粒子(SPIONs,直径> 50 nm)因其有望用作磁共振成像(MRI)造影剂而受到广泛关注。在这项研究中,我们评估了超小型SPION(USPION,直径<50 nm)的体外细胞吸收和生物学响应。我们比较了暴露于羧基封端的USPIONs(10和30 nm PEG涂层,10和30 nm非PEG涂层)后从健康和乳腺癌供体中分离出的乳房上皮细胞之间的细胞反应。使用透射电子显微镜(TEM),动态光散射(DLS)和凝胶电泳对颗粒进行表征。通过共聚焦显微镜和TEM评估了与USPIONs的细胞相互作用。使用ICP-MS对USPIONs的细胞摄取进行了定量。通过MTT和中性红摄取测定法测量细胞活力。使用7T扫描仪进行T2 *加权MRI扫描。结果表明,USPIONs的细胞缔合/内在化作用取决于大小和表面涂层(PEG与非PEG),并且与PEG涂层相比,两种细胞类型均观察到更高的10和30 nm非涂层颗粒的细胞吸收粒子。与来自三个供体的健康细胞相比,来自三个测试供体中的两个供体的癌细胞对10和30 nm非涂层颗粒的细胞摄取更高。对于所有测试的颗粒,没有观察到明显的细胞毒性。在两种细胞类型中,与PEG包被的颗粒相比,暴露于10和30 nm非包被的颗粒后观察到MRI对比度明显增强。相比之下,与正常细胞相比,癌细胞显示出更多增强的MRI信号。数据表明,暴露于USPIONs后的细胞反应取决于颗粒性质。 (c)2015 Wiley Periodicals,Inc. J Biomed Mater Res B部分:Appl Biomater,104B:1032-1042,2016。

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