用于细菌感染PET成像的新型68ga标记泛素29-41复合物的合成及生物学评价

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Yuhao Jiang, Qianna Wang, Xiaojiang Duan, Junhong Feng, Guangxing Yin, Peiwen Han, Qing Ruan, Ziqing Zhao, Jianyong Jiang, Junbo Zhang
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引用次数: 0

摘要

在临床实践中,细菌感染的持续挑战需要开发能够区分感染和炎症过程的精确诊断工具。本研究介绍了一种新型PET示踪剂[68Ga]Ga-NOTA-UBI 29-41的开发和评价,该示踪剂专为特异性细菌感染成像而设计。该示踪剂通过68ga标记nota偶联泛素29-41衍生物合成,在生理盐水和小鼠血清中均表现出优异的放射化学性能和良好的体外稳定性。体外结合试验证实了金黄色葡萄球菌的特异性靶向性,而小鼠模型的体内研究显示,感染肌肉组织的摄取明显高于炎症肌肉组织(p < 0.01)。微pet成像进一步证实了示踪剂在感染部位选择性积累的能力,药代动力学分析显示主要的肾脏清除和快速血液清除动力学。这些发现共同证明了[68Ga]Ga-NOTA-UBI 29-41作为一种临床可翻译的药物的潜力,可以准确区分细菌感染和无菌炎症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Biological Evaluation of a Novel 68Ga-Labeled Ubiquicidin 29-41 Complex for PET Imaging of Bacterial Infections.

The persistent challenge of bacterial infections in clinical practice necessitates the development of precise diagnostic tools capable of differentiating infectious and inflammatory processes. This study presents the development and evaluation of [68Ga]Ga-NOTA-UBI 29-41, a novel PET radiotracer designed for specific bacterial infection imaging. The tracer was synthesized through 68Ga-labeling of a NOTA-conjugated ubiquicidin 29-41 derivative, demonstrating excellent radiochemical properties and good in vitro stability in both saline and mouse serum. In vitro binding assays confirmed specific targeting of Staphylococcus aureus, while in vivo studies in mice models revealed significantly higher uptake in infected versus inflamed muscle tissue (p < 0.01). MicroPET imaging further validated the tracer's ability to selectively accumulate at infection sites, with pharmacokinetic analysis showing predominant renal clearance and rapid blood clearance kinetics. These findings collectively demonstrate the potential of [68Ga]Ga-NOTA-UBI 29-41 as a clinically translatable agent for accurate discrimination between bacterial infections and sterile inflammation.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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