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A nanoparticle-based strategy for the imaging of a broad range of tumours by nonlinear amplification of microenvironment signals

机译:一种基于纳米粒子的策略,通过微环境信号的非线性放大来成像多种肿瘤

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摘要

Stimuli-responsive nanomaterials are increasingly important in a variety of applications such as biosensing, molecular imaging, drug delivery and tissue engineering. For cancer detection, a paramount challenge still exists in the search for methods that can illuminate tumours universally regardless of their genotypes and phenotypes. Here we capitalized on the acidic, angiogenic tumour microenvironment to achieve the detection of tumour tissues in a wide variety of mouse cancer models. This was accomplished using ultra pH-sensitive fluorescent nanoprobes that have tunable, exponential fluorescence activation on encountering subtle, physiologically relevant pH transitions. These nanoprobes were silent in the circulation, and then strongly activated (>300-fold) in response to the neovasculature or to the low extracellular pH in tumours. Thus, we have established non-toxic, fluorescent nanoreporters that can nonlinearly amplify tumour microenvironmental signals, permitting the identification of tumour tissue independently of histological type or driver mutation, and detection of acute treatment responses much more rapidly than conventional imaging approaches.
机译:响应性纳米材料在各种应用中越来越重要,例如生物传感,分子成像,药物递送和组织工程。对于癌症检测,寻找能够普遍照亮肿瘤而不管其基因型和表型的方法仍然是最重要的挑战。在这里,我们利用酸性,血管生成性肿瘤微环境,以实现在多种小鼠癌症模型中检测肿瘤组织。这是通过使用超pH敏感的荧光纳米探针完成的,该探针在遇到微妙的生理相关pH跃迁时具有可调的指数荧光激活。这些纳米探针在循环中保持沉默,然后响应肿瘤中的新血管系统或细胞外pH值低而被强烈激活(> 300倍)。因此,我们已经建立了无毒的荧光纳米报告,它们可以非线性地放大肿瘤微环境信号,与组织学类型或驱动程序突变无关地识别肿瘤组织,并比常规成像方法更快地检测急性治疗反应。

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  • 来源
    《Nature Materials》 |2014年第2期|204-212|共9页
  • 作者单位

    Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Department of Otolaryngology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

    Department of Pharmacology, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390, USA;

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