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Synthesis 68Ga-Radiolabeling and Preliminary In Vivo Assessment of a Depsipeptide-Derived Compound as a Potential PET/CT Infection Imaging Agent

机译:二肽肽衍生化合物作为潜在的PET / CT感染显像剂的合成68Ga放射标记和初步体内评估

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摘要

Noninvasive imaging is a powerful tool for early diagnosis and monitoring of various disease processes, such as infections. An alarming shortage of infection-selective radiopharmaceuticals exists for overcoming the diagnostic limitations with unspecific tracers such as 67/68Ga-citrate or 18F-FDG. We report here TBIA101, an antimicrobial peptide derivative that was conjugated to DOTA and radiolabeled with 68Ga for a subsequent in vitro assessment and in vivo infection imaging using Escherichia coli-bearing mice by targeting bacterial lipopolysaccharides with PET/CT. Following DOTA-conjugation, the compound was verified for its cytotoxic and bacterial binding behaviour and compound stability, followed by 68Gallium-radiolabeling. µPET/CT using 68Ga-DOTA-TBIA101 was employed to detect muscular E. coli-infection in BALB/c mice, as warranted by the in vitro results. 68Ga-DOTA-TBIA101-PET detected E. coli-infected muscle tissue (SUV = 1.3–2.4) > noninfected thighs (P = 0.322) > forearm muscles (P = 0.092) > background (P = 0.021) in the same animal. Normalization of the infected thigh muscle to reference tissue showed a ratio of 3.0 ± 0.8 and a ratio of 2.3 ± 0.6 compared to the identical healthy tissue. The majority of the activity was cleared by renal excretion. The latter findings warrant further preclinical imaging studies of greater depth, as the DOTA-conjugation did not compromise the TBIA101's capacity as targeting vector.
机译:无创成像是早期诊断和监测各种疾病过程(如感染)的强大工具。由于使用非特异性示踪剂(如 67/68 柠檬酸镓或 18 F-FDG)克服了诊断上的局限性,因此存在选择性感染放射性药物的惊人短缺。我们在这里报告TBIA101,这是一种抗菌肽衍生物,已与DOTA偶联,并用 68 Ga进行了放射性标记,用于随后的体外评估和使用带有大肠杆菌的小鼠通过将细菌脂多糖靶向PET /进行体内感染成像CT。 DOTA缀合后,验证该化合物的细胞毒性和细菌结合行为以及化合物稳定性,然后进行 68 Gallium放射性标记。体外实验结果表明,采用 68 Ga-DOTA-TBIA101的µPET / CT技术可检测BALB / c小鼠的肌肉大肠杆菌感染。 68 Ga-DOTA-TBIA101-PET检测到大肠杆菌感染的肌肉组织(SUV = 1.3–2.4)>未感染的大腿(P = 0.322)>前臂肌肉(P = 0.092)>背景(P = 0.021)。与相同的健康组织相比,受感染的大腿肌肉相对于参考组织的正常化显示比率为3.0±0.8,比率为2.3±0.6。大部分活动通过肾脏排泄清除。后一发现需要进一步的临床前成像研究,因为DOTA的结合不会损害TBIA101作为靶向载体的能力。

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