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Photostable Ratiometric Pdot Probe for in Vitro and in Vivo Imaging of Hypochlorous Acid

机译:用于次氯酸体外和体内成像的光稳定比例Pdot探针

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摘要

Developing probes for the detection of reactive oxygen species (ROS), a hallmark of many pathophysiological process, is imperative to both understanding the precise roles of ROS in many life-threatening diseases and optimizing therapeutic interventions. We herein report an all-in-one fluorescent semiconducting polymer based far-red to near-infrared (NIR) Pdot nanoprobe for the ratiometric detection of hypochlorous acid (HOCl). The fabrication takes the advantage of flexible polymer design by incorporating target-sensitive and target-inert fluorophores into a single conjugated polymer to avoid leakage or differential photobleaching problems existed in other nanoprobes. The obtained nanoprobe has improved performance in HOC1 sensing, such as high brightness, ideal far-red to NIR optical window, excellent photostability, self-referenced ratiometric response, fast response, and high selectivity. The dual-emission property allows the sensitive imaging of HOC1 fluctuations produced in living macrophage cells and peritonitis of living mice with high contrast. This study not only provides a powerful and promising nanoprobe to be potentially used in the investigations of in situ HOC1 status of diseases in living systems but also puts forward the design strategy of a new category of ratiometric fluorescent probes facilitating precise and reliable measurement in biological systems.
机译:开发用于检测活性氧物种(ROS)(许多病理生理过程的标志)的探针,对于了解ROS在许多威胁生命的疾病中的确切作用以及优化治疗干预都是必不可少的。我们在此报告了一种基于荧光的多合一荧光半导体聚合物,用于远红外至近红外(NIR)Pdot纳米探针,用于次氯酸(HOCl)的比例检测。通过将目标敏感和目标惰性的荧光团合并到单个共轭聚合物中来避免其他纳米探针中存在的泄漏或差异性光漂白问题,该制造利用了灵活的聚合物设计优势。所获得的纳米探针在HOC1感测方面具有改善的性能,例如高亮度,理想的远红外到NIR光学窗口,出色的光稳定性,自参考比例响应,快速响应和高选择性。双重发射特性允许以高对比度对活巨噬细胞和活小鼠腹膜炎中产生的HOC1波动进行敏感成像。这项研究不仅提供了强大而有前途的纳米探针,可潜在地用于研究生命系统疾病的原位HOC1状况,而且提出了一种新型比例荧光探针的设计策略,该探针有助于在生物系统中进行精确可靠的测量。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第20期|6911-6918|共8页
  • 作者单位

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

    Clinical Research Division and Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, United States;

    Clinical Research Division and Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, United States;

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

    Clinical Research Division and Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, United States,Division of Medical Oncology, University of Washington School of Medicine, Seattle, Washington 98195, United States;

    Department of Chemistry, University of Washington, Seattle, Washington 98195, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:07:59

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