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A Broad Nanoparticle-Based Strategy for Tumor Imaging by Nonlinear Amplification of Microenvironment Signals

机译:通过基于微环境信号的非线性放大的肿瘤成像的基于纳米粒子的广泛策略。

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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 search of methods that can illuminate tumors universally regardless of their genotypes and phenotypes. Here we capitalized on the acidic, angiogenic tumor microenvironment to achieve broad detection of tumor tissues in a wide variety of mouse cancer models. This was accomplished using ultra-pH sensitive fluorescent nanoprobes that have tunable, exponential fluorescence activation upon encountering subtle, physiologically relevant pH transitions. These nanoprobes were silent in the circulation, then dramatically activated (>300 fold) in response to neovasculature or to the low extracellular pH in tumors. Thus, we have established non-toxic, fluorescent nanoreporters that can non-linearly amplify tumor microenvironmental signals, permitting identification of tumor 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。对于癌症检测而言,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,以在多种小鼠癌症模型中实现对肿瘤组织的广泛检测。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的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沉默,然后响应新脉管系统或肿瘤中低的细胞外pH而被显着激活(> 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,允许独立于组织学类型或驱动程序突变来鉴定肿瘤组织,并比常规成像方法更快地检测急性治疗反应。

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