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首页> 外文期刊>RSC Advances >Mini-review: fluorescence imaging in cancer cells using dye-doped nanoparticles
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Mini-review: fluorescence imaging in cancer cells using dye-doped nanoparticles

机译:迷你评价:使用染料掺杂纳米颗粒的癌细胞中的荧光成像

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摘要

Fluorescence imaging has gained increased attention over the past two decades as a viable means to detect a variety of cancers. Fluorescence imaging has the potential to provide physicians with high resolution images with enhanced contrast, which will allow them to be able to better diagnose and treat patients with cancer. Early detection and treatment are key to eradicating cancer in a patient, and fluorescence imaging has the ability to identify non-advanced, even pre-cancerous, tumors where imaging based on white light or radiation overlooked them. Several fluorescent dyes have been identified as possible fluorophores for enhanced fluorescence imaging, such as cyanine, squaraine, porphyrin, phthalocyanine, and borondipyrromethane dyes. These dyes have high fluorescence quantum yields, which provides a high target to background ratio; however, these dyes are often plagued by low water solubility. This low solubility can be ameliorated by conjugating or covalently attaching these dyes to polymeric crosslinked micelles, polymersomes, or polymer-core nanoparticles. These particle & dye systems then can become platforms on which secondary components can be attached to enhance the systems functionality. For example, dyes attached to these nanocarriers can target tumors through passive targeting; however, active targeting can be achieved by further modifying these nanocarriers with ligands that have a binding affinity for receptors overexpressed in tumor cells, cell surface receptors located on the tumor cell membrane, or endothelium. Fluorescence activation of the probes is another promising technology for the early detection of cancer. Activation requires that there be a change in fluorescence, whether it be an emission wavelength change or a fluorescence "on/off" signal when in the presence of some external stimuli. Activation increases the target to background ratio and enhances the contrast of the obtained image. This review serves to highlight the recent developments of (1) improved fluorescent dyes for the detection of cancer, with a specific focus on dyes that are being coupled to nanocarriers; (2) dye & nanocarrier systems that target, both actively and passively, tumors, and (3) fluorescence activation of these fluorophore systems for better image quality.
机译:过去二十年来荧光成像作为检测各种癌症的可行方法,荧光成像已经增加。荧光成像具有具有具有增强对比度的高分辨率图像的医生,这将使它们能够更好地诊断和治疗癌症患者。早期的检测和治疗是在患者中消除癌症的关键,荧光成像具有鉴定非先进,甚至癌症的能力,其中基于白光或辐射的成像俯视它们。已经鉴定了几种荧光染料作为增强荧光成像的可能荧光团,例如青色素,Squaraine,卟啉,酞菁和硼烷哌甲烷染料。这些染料具有高荧光量子产率,其为背景比提供高靶标;然而,这些染料通常通过低水溶性血液困扰。通过将这些染料与聚合物交联的胶束,聚合物或聚合物 - 核心纳米颗粒缀合或共价将这些染料缀合或共价将该低溶解度可以改善。然后,这些粒子和染料系统可以成为可以连接辅助部件的平台,以增强系统功能。例如,附着于这些纳米载体的染料可以通过被动靶向靶向肿瘤;然而,通过进一步改性这些纳米载体的配体可以通过对肿瘤细胞中过表达的受体具有结合亲和力的配体,位于肿瘤细胞膜或内皮细胞的细胞表面受体来实现活性靶向。探针的荧光激活是早期发现癌症的另一种有希望的技术。激活要求荧光发生变化,在存在一些外部刺激时,是否是发射波长变化或荧光“开/关”信号。激活将目标增加到背景比率并增强所获得的图像的对比度。该综述用于突出(1)近期用于检测癌症的荧光染料的最新发育,特别关注含有纳米载体的染料; (2)染料和纳米载波系统,其靶向,既积极又被动,肿瘤,(3)荧光激活这些荧光团系统,以更好的图像质量。

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  • 来源
    《RSC Advances》 |2016年第70期|共16页
  • 作者单位

    Clemson Univ Dept Mat Sci &

    Engn Ctr Opt Mat Sci &

    Engn Technol Clemson SC 29634 USA;

    Clemson Univ Dept Mat Sci &

    Engn Ctr Opt Mat Sci &

    Engn Technol Clemson SC 29634 USA;

    Clemson Univ Dept Mat Sci &

    Engn Ctr Opt Mat Sci &

    Engn Technol Clemson SC 29634 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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