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首页> 外文期刊>Advanced Functional Materials >pH-Activated Near-Infrared Fluorescence Nanoprobe Imaging Tumors by Sensing the Acidic Microenvironment
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pH-Activated Near-Infrared Fluorescence Nanoprobe Imaging Tumors by Sensing the Acidic Microenvironment

机译:通过感知酸性微环境的pH值激活的近红外荧光纳米探针成像肿瘤。

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摘要

imaging tumors in their early stages is crucial to increase the surviving rate of cancer patients. Currently most fluorescence probes visualize the neoplasia by targeting the tumor-associated receptor over-expressed on the cancer cell membrane. However, the expression level of these receptors in vivo is hard to predict, which limits their clinical translation. Furthermore, the signal output of these receptor-targeting probes usually stays at a high level, which leads to a strong background signal in normal tissue due to non-specific binding. In contrast to receptors, characteristics of the tumor microenvironment - such as acidosis - are pervasive in almost all solid tumors and can be easily accessed. In this work, a novel biodegradable nanoprobe InNP1 that demonstrates pH-activated near-infrared (NIR) fluorescence in both human glioblastoma U87MC cancer ceils in vitro and the subcutaneous U87MG tumor xenografts in vivo is developed. Bio-distribution, in vivo optical imaging, and autoradiography studies demonstrate that the pH-activated NIR fluorescence is the dominant factor responsible for the high tumorormal tissue (T/N) ratio of InNP1 in vivo. Overall, the work provides a nanoprobe prototype to visualize the solid tumor in vivo with high sensitivity and minimal systemic toxicity by sensing the tumor acidic microenvironment.
机译:对肿瘤进行早期成像对于提高癌症患者的存活率至关重要。当前,大多数荧光探针通过靶向在癌细胞膜上过度表达的肿瘤相关受体来可视化赘生物。但是,这些受体在体内的表达水平很难预测,这限制了它们的临床翻译。此外,这些靶向受体的探针的信号输出通常保持在高水平,由于非特异性结合,在正常组织中导致强烈的背景信号。与受体相反,肿瘤微环境的特征(如酸中毒)在几乎所有实体瘤中普遍存在,并且很容易获得。在这项工作中,开发了一种新型的可生物降解的纳米探针InNP1,该纳米探针在人胶质母细胞瘤U87MC癌症细胞和体内皮下U87MG肿瘤异种移植物中均显示了pH激活的近红外(NIR)荧光。生物分布,体内光学成像和放射自显影研究表明,pH激活的NIR荧光是体内InNP1高肿瘤/正常组织(T / N)比的主要因素。总体而言,这项工作提供了一种纳米探针原型,可通过感测肿瘤的酸性微环境,以高灵敏度和最小的系统毒性可视化体内的实体瘤。

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  • 来源
    《Advanced Functional Materials》 |2010年第14期|P.2222-2230|共9页
  • 作者单位

    School of Pharmacy, Fudan University 826 Zhangheng Rd., Shanghai 201203 (PR China);

    rnDepartment of Radiology, School of Medicine Johns Hopkins University 720 Rutland Ave., Baltimore 21205 (USA);

    rnCancer Hospital, Fudan University 399 Ling-Ling Road, Shanghai 200032 (PR China) Institutes of Biomedical Sciences, Fudan University 138 Yixueyuan Road, Shanghai 200032 (PR China);

    rnDepartment of Gastroenterology, Zhongshan Hospital Affiliated to Fudan University 130 DongAn Rd., Shanghai 200032 (PR China);

    rnSchool of Pharmacy, Fudan University 826 Zhangheng Rd., Shanghai 201203 (PR China);

    rnLaboratory of Molecular Imaging, Department of Radiology Zhongda Hospital, Southeast University 87 Dingjiaqiao Rd., Nanjing 210009 (PR China);

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