hHEPATO-Cy5,一种用于图像引导肝胆外科手术的双模示踪剂。

Daphne D D Rietbergen, Tessa Buckle, Leon J Slof, Maarten P van Meerbeek, Clarize M de Korne, Mick M Welling, Matthias N van Oosterom, Kevin Bauwens, Meta Roestenberg, Julia Kloetzl, Fijs W B van Leeuwen
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引用次数: 0

摘要

肝癌是全球癌症死亡的主要原因。肝脏表层病变的手术切除越来越多地通过荧光染料吲哚菁绿(ICG)的胆汁排泄紊乱来引导。为了将这种方法推广到更深层的病灶,我们开发了一种专用的双模示踪剂,既能促进荧光引导,又能促进放射引导。方法:合成并鉴定了一种由甲基化氰基-5(Cy5)荧光染料和巯基乙酰三丝螯合物(hHEPATO-Cy5)组成的示踪剂。使用荧光胆盐、MitoTracker 染料和甲基化 Cy5 作为对照,在肝细胞培养(二维培养和体外病变模型)中评估了细胞摄取和排泄情况。放射性标记后,对 99mTc-hHEPATO-Cy5 在小鼠体内 24 小时的药代动力学进行了评估(注射剂量百分比和每克组织注射剂量百分比、SPECT/CT 成像和荧光成像)。以 ICG 为参照物,在猪模型中评估了机器人辅助肝胆手术过程中提供实时荧光引导的能力。结果:hHEPATO-Cy5 的独特分子特征可促进肝胆排泄。对肝细胞的体外研究表明,甲基化 Cy5 仍会内化,而 hHEPATO-Cy5 的快速清除(10 分钟)与荧光胆盐类似。在小鼠体内使用 99mTc-hHEPATO-Cy5 发现肝脏积聚,胆汁清除迅速。随着时间的推移,胆囊的计数率降低了 2 个数量级(P = 0.008),这充分体现了胆汁清除的有效性。在猪模型的肝胆外科手术中,hHEPATO-Cy5 可实现与 ICG 相当的荧光病灶识别。结论双模 99mTc-hHEPATO-Cy5 是识别肝脏病变的有效方法。与众不同的是,它有助于克服纯荧光方法的缺点,将其扩展到深度放射引导。
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hHEPATO-Cy5, a Bimodal Tracer for Image-Guided Hepatobiliary Surgery.

Liver cancer is a leading cause of cancer deaths worldwide. Surgical resection of superficial hepatic lesions is increasingly guided by the disrupted bile excretion of the fluorescent dye indocyanine green (ICG). To extend this approach to deeper lesions, a dedicated bimodal tracer that facilitates both fluorescence guidance and radioguidance was developed. Methods: A tracer comprising a methylated cyanine-5 (Cy5) fluorescent dye and a mercaptoacetyltriserine chelate (hHEPATO-Cy5) was synthesized and characterized. Cellular uptake and excretion were evaluated in hepatocyte cultures (2-dimensional culture and in vitro lesion model), using a fluorescent bile salt, MitoTracker dye, and methylated Cy5 as a control. After radiolabeling, the pharmacokinetics of 99mTc-hHEPATO-Cy5 were assessed in mice over 24 h (percentage injected dose and percentage injected dose per gram of tissue, SPECT/CT imaging and fluorescence imaging). The ability to provide real-time fluorescence guidance during robot-assisted hepatobiliary surgery was evaluated in a porcine model using ICG as a reference. Results: The unique molecular signature of hHEPATO-Cy5 promotes hepatobiliary excretion. In vitro studies on hepatocytes showed that where methylated Cy5 remained internalized, hHEPATO-Cy5 showed fast clearance (10 min) similar to that of fluorescent bile salt. In vivo use of 99mTc-hHEPATO-Cy5 in mice revealed liver accumulation and rapid biliary clearance. The effectiveness of bile clearance was best exemplified by the 2-orders-of-magnitude reduction in count rate for the gallbladder (P = 0.008) over time. During hepatobiliary surgery in a porcine model, hHEPATO-Cy5 enabled fluorescence-based lesion identification comparable to that of ICG. Conclusion: The bimodal 99mTc-hHEPATO-Cy5 provides an effective means to identify liver lesions. Uniquely, it helps overcome the shortcomings of fluorescence-only approaches by allowing for an extension to in-depth radioguidance.

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