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In vivo Off-Resonance Saturation Magnetic Resonance Imaging of αvβ3-Targeted Superparamagnetic Nanoparticles

机译:αvβ3靶向的超顺磁性纳米粒子的体内离共振饱和磁共振成像。

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摘要

Magnetic resonance imaging is a powerful clinical imaging technique that allows for noninvasive tomographic visualization of anatomic structures with high spatial resolution and soft tissue contrast. However, its application in molecular imaging of cancer has been limited by the lack of sensitivity and detection accuracy in depicting the biochemical expression of these diseases. Here, we combine an ultrasensitive design of superparamagnetic polymeric micelles (SPPM) and an off-resonance saturation (ORS) method to enhance the imaging efficacy of tumor biomarkers in vivo. SPPM nanoparticles encoded with cyclic (RGDfK) were able to target the αvβ3-expressing microvasculature in A549 non–small cell lung tumor xenografts in mice. ORS greatly improved tumor detection accuracy over the conventional T2*-weighted method by its ability to turn “ON” the contrast of SPPM. This combination of ORS imaging with a tumor vasculature–targeted, ultrasensitive SPPM design offers new opportunities in molecular imaging of cancer.
机译:磁共振成像是一种强大的临床成像技术,可对具有高空间分辨率和软组织对比度的解剖结构进行无创层析成像。然而,由于在描述这些疾病的生化表达时缺乏敏感性和检测准确性,其在癌症分子成像中的应用受到了限制。在这里,我们结合了超顺磁性高分子胶束(SPPM)和超共振饱和(ORS)方法的超灵敏设计,以增强体内肿瘤生物标记物的成像功效。带有环状(RGDfK)编码的SPPM纳米颗粒能够靶向小鼠A549非小细胞肺肿瘤异种移植物中表达αvβ3的微脉管系统。与传统的T2 *加权方法相比,ORS具有“打开” SPPM对比度的能力,大大提高了肿瘤检测的准确性。 ORS成像与靶向肿瘤脉管系统的超灵敏SPPM设计的结合为癌症分子成像提供了新的机会。

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