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A thiopyrylium salt for PET/NIR‐II tumor imaging and image‐guided surgery

机译:硫代吡啶鎓盐用于PET / NIR-II肿瘤成像和图像指导手术

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摘要

All tumor imaging modalities have resolution limits below which deeply situated small metastatic foci may not be identified. Moreover, incomplete lesion excision will affect the outcomes of the patients. Scintigraphy is adept in locating lesions, and second near‐infrared window (NIR‐II) imaging may allow precise real‐time tumor delineation. To achieve complete excision of all lesions, multimodality imaging is a promising method for tumor identification and management. Here, a NIR‐II thiopyrylium salt, XB1034, was first synthesized and bound to cetuximab and trans‐cyclooctene (TCO) to produce XB1034‐cetuximab‐TCO. This probe provides excellent sensitivity and high temporal resolution NIR‐II imaging in mice bearing tumors developed from human breast cancer cells MDA‐MB‐231. To enable PET imaging, Ga‐NETA‐tetrazine is subsequently injected into the mice to undergo a bio‐orthogonal reaction with the preinjected XB1034‐cetuximab‐TCO. PET images achieved in the tumor models using the pretargeting strategy are of much higher quality than those obtained using the direct radiolabeling method. Moreover, real‐time NIR‐II imaging allows accurate tumor excision and sentinel lymph node mapping. In conclusion, XB1034 is a promising molecular imaging probe for tumor diagnosis and treatment.
机译:所有肿瘤成像方式均具有分辨率极限,低于该极限,可能无法识别位于深处的小转移灶。此外,不完全的病灶切除会影响患者的预后。闪烁扫描技术可以很好地定位病变,并且第二次近红外窗口(NIR-II)成像可以精确实时地描绘肿瘤。为了完全切除所有病变,多模态成像是一种有希望的肿瘤识别和治疗方法。在这里,首先合成了NIR-II硫代吡啶鎓盐XB1034,并与西妥昔单抗和反式环辛烯(TCO)结合生成XB1034-西妥昔单抗-TCO。该探针在患有从人乳腺癌细胞MDA-MB-231发育而来的肿瘤的小鼠中提供出色的灵敏度和高时间分辨率的NIR-II成像。为了进行PET成像,随后将Ga-NETA-四嗪注射入小鼠体内,使其与预先注射的XB1034-西妥昔单抗-TCO发生生物正交反应。使用预靶向策略在肿瘤模型中获得的PET图像质量比使用直接放射标记法获得的图像高得多。此外,实时NIR-II成像可准确切除肿瘤并标记前哨淋巴结。总之,XB1034是用于肿瘤诊断和治疗的有前途的分子成像探针。

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