首页> 外文OA文献 >Polymer-coated NaYF4:Yb3+, Er3+ upconversion nanoparticles for charge-dependent cellular imaging
【2h】

Polymer-coated NaYF4:Yb3+, Er3+ upconversion nanoparticles for charge-dependent cellular imaging

机译:聚合物包覆的NaYF4:Yb3 +,Er3 +上转换纳米粒子用于电荷依赖性细胞成像

摘要

Lanthanide-doped upconversion nanoparticles (UCNPs) are considered promising novel near-infrared (NIR) bioimaging agents with the characteristics of high contrast and high penetration depth. However, the interactions between charged UCNPs and mammalian cells have not been thoroughly studied, and the corresponding intracellular uptake pathways remain unclear. Herein, our research work involved the use of a hydrothermal method to synthesize polyvinylpyrrolidone-coated UCNPs (UCNP-PVP), and then a ligand exchange reaction was performed on UCNP-PVP, with the help of polyethylenimine (PEI) and poly(acrylic acid) (PAA), to generate UCNP-PEI and UCNP-PAA. These polymer-coated UCNPs demonstrated good dispersibility in aqueous medium, had the same elemental composition and crystal phase, shared similar TEM and dynamic light scattering (DLS) size distribution, and exhibited similar upconversion luminescence efficiency. However, the positively charged UCNP-PEI evinced greatly enhanced cellular uptake in comparison with its neutral or negative counterparts, as shown by multiphoton confocal microscopy and inductively coupled plasma mass spectrometry (ICP-MS) measurements. Meanwhile, we found that cationic UCNP-PEI can be effectively internalized mainly through the clathrin endocytic mechanism, as revealed by colocalization, chemical, and genetic inhibitor studies. This study elucidates the role of the surface polymer coatings in governing UCNP-cell interactions, and it is the first report on the endocytic mechanism of positively charged lanthanide-doped UCNPs. Furthermore, this study provides important guidance for the development of UCNPs as specific intracellular nanoprobes, allowing us to control the UCNP-cell interactions by tuning surface properties.
机译:镧系元素掺杂的上转换纳米粒子(UCNPs)被认为是具有高对比度和高穿透深度特征的有前途的新型近红外(NIR)生物成像剂。但是,带电荷的UCNPs与哺乳动物细胞之间的相互作用尚未得到彻底研究,并且相应的细胞内摄取途径仍不清楚。在这里,我们的研究工作涉及使用水热法合成聚乙烯吡咯烷酮包覆的UCNPs(UCNP-PVP),然后在聚乙烯亚胺(PEI)和聚丙烯酸的帮助下对UCNP-PVP进行配体交换反应。 )(PAA),以生成UCNP-PEI和UCNP-PAA。这些聚合物包覆的UCNP在水介质中显示出良好的分散性,具有相同的元素组成和晶相,具有相似的TEM和动态光散射(DLS)尺寸分布,并具有相似的上转换发光效率。但是,带正电的UCNP-PEI与中性或负性对应物相比,极大地提高了细胞摄取,如多光子共聚焦显微镜和电感耦合等离子体质谱(ICP-MS)测量所示。同时,我们发现阳离子UCNP-PEI可以通过网格蛋白内吞机制被有效地内在化,正如共定位,化学和遗传抑制剂研究所揭示的那样。这项研究阐明了表面聚合物涂层在控制UCNP-细胞相互作用中的作用,这是关于正电荷掺杂镧系元素的UCNPs内吞机理的首次报道。此外,这项研究为作为特定的细胞内纳米探针的UCNPs的发展提供了重要的指导,使我们能够通过调节表面性质来控制UCNP-细胞的相互作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号