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High resolution tumor targeting in living mice by means of multispectral optoacoustic tomography

机译:多光谱光声层析成像技术在活体小鼠中高分辨率靶向肿瘤

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Background Tumor targeting is of high clinical and biological relevance, and major efforts have been made to develop molecular imaging technologies for visualization of the disease markers in tissue. Of particular interest is apoptosis which has a profound role within tumor development and has significant effect on cancer malignancy. Methods Herein, we report on targeting of phosphatidylserine-exposing cells within live tumor allograft models using a synthetic near infrared zinc(II)-dipicolylamine probe. Visualization of the probe biodistribution is performed with whole body multispectral optoacoustic tomography (MSOT) system and subsequently compared to results attained by planar and tomographic fluorescence imaging systems. Results Compared to whole body optical visualization methods, MSOT attains remarkably better imaging capacity by delivering high-resolution scans of both disease morphology and molecular function in real time. Enhanced resolution of MSOT clearly showed that the probe mainly localizes in the vessels surrounding the tumor, suggesting that its tumor selectivity is gained by targeting the phosphatidylserine exposed on the surface of tumor vessels. Conclusions The current study demonstrates the high potential of MSOT to broadly impact the fields of tumor diagnostics and preclinical drug development.
机译:背景技术肿瘤靶向具有高度的临床和生物学相关性,并且已经做出重大努力来开发用于使组织中的疾病标志物可视化的分子成像技术。特别令人感兴趣的是细胞凋亡,其在肿瘤发展中具有深远的作用并且对癌症恶性具有显著作用。方法在本文中,我们报道了使用合成的近红外锌(II)-二甲基吡啶胺探针靶向活肿瘤同种异体移植模型中的磷脂酰丝氨酸暴露细胞。探针生物分布的可视化是通过全身多光谱光声层析成像(MSOT)系统进行的,然后与平面和层析荧光成像系统获得的结果进行比较。结果与全身光学可视化方法相比,MSOT通过实时提供疾病形态和分子功能的高分辨率扫描,可显着提高成像能力。 MSOT的增强分辨率清楚地表明,该探针主要位于肿瘤周围的血管中,这表明,通过靶向暴露于肿瘤血管表面的磷脂酰丝氨酸可以提高其肿瘤选择性。结论当前的研究表明MSOT具有广泛的潜力,可广泛影响肿瘤诊断和临床前药物开发领域。

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