一种新的基于芳烃三氟甲基的18f标记策略,用于增强PET成像中生物分子示踪剂的开发。

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Xinlin Zhong, , , Junjie Yan*, , , Chen Su, , , Xinyu Wang, , , Donghui Pan, , , Yuping Xu, , , Lizhen Wang, , , Chongyang Chen, , and , Min Yang*, 
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引用次数: 0

摘要

生物活性分子,如碳水化合物、肽和蛋白质,由于其强大的靶标亲和力和生物相容性,是正电子发射断层扫描(PET)成像的有吸引力的候选者。在现有的放射性核素中,氟-18 (18F)因其半衰期适中和高质量的成像特性而广泛应用于临床实践。然而,传统的18f标记方法通常需要费力的程序和苛刻的条件,这可能会损害结构完整性和生物学功能。因此,开发温和有效的18f标记策略对于推进生物分子PET示踪剂至关重要。在本研究中,我们通过18F/19F同位素交换反应(RCY = 17.2±3.9%)制备了一种新的可点击18F标记的合成物,1-乙基-3-([18F]三氟甲基)-5-(三氟甲基)苯([18F]1)。[18F]1在铜(I)催化叠氮化物-炔环加成(CuAAC)偶联中表现出优异的性能,能够在温和条件下快速和化学选择性地标记叠氮化物修饰的葡萄糖衍生物、精氨酸-甘氨酸- asp (RGD)和环RGD (cRGD)肽以及磷脂。U87 MG、4T1和BT474异种移植模型的PET成像显示[18F]5a和[18F]5b的肿瘤摄取良好,在注射后30分钟达到峰值。在U87 MG、4T1和BT474模型中,[18F]5a的肿瘤积累量分别达到3.11±0.21、2.40±0.17和1.95±0.09% ID/g,而[18F]5b在同一时间点的肿瘤积累量更高,分别达到5.19±0.42、4.90±0.97和2.05±0.11% ID/g,这与cRGD具有较强的结合亲和力相一致。肿瘤与肌肉的比值良好,[18F]5b在4T1模型中达到4.32±0.39。在U87肿瘤中的阻断研究证实了高结合特异性,摄取降低到约1% ID/g。这种基于同位素交换的CuAAC标记策略简化了PET示踪剂的合成,保持了生物分子的完整性,并为分子成像和预靶向应用提供了一个通用的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Novel Arene Trifluoromethyl-Based 18F-Labeling Strategy for Enhanced Biomolecular Tracer Development in PET Imaging

A Novel Arene Trifluoromethyl-Based 18F-Labeling Strategy for Enhanced Biomolecular Tracer Development in PET Imaging

Biologically active molecules, such as carbohydrates, peptides, and proteins, are attractive candidates for positron emission tomography (PET) imaging because of their strong target affinity and biocompatibility. Among available radionuclides, fluorine-18 (18F) is widely used in clinical practice because of its moderate half-life and high-quality imaging properties. However, traditional 18F-labeling methods often require a laborious procedure and harsh conditions, which may compromise the structural integrity and biological functions. Developing mild and efficient 18F-labeling strategies is therefore critical for advancing biomolecular PET tracers. In this study, we developed a novel clickable 18F-labeled synthon, 1-ethynyl-3-([18F]trifluoromethyl)-5-(trifluoromethyl)benzene ([18F]1), prepared via an 18F/19F isotope exchange reaction (RCY = 17.2 ± 3.9%). [18F]1 exhibited excellent performance in copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) conjugation, enabling rapid and chemoselective labeling of azide-modified glucose derivatives, Arg-Gly-Asp (RGD) and cyclic RGD (cRGD) peptides, and phospholipids under mild conditions. PET imaging in U87 MG, 4T1, and BT474 xenograft models showed favorable tumor uptake for both [18F]5a and [18F]5b, peaking at 30 min postinjection. Tumor accumulation for [18F]5a reached 3.11 ± 0.21, 2.40 ± 0.17, and 1.95 ± 0.09% ID/g in U87 MG, 4T1, and BT474 models, respectively, while [18F]5b achieved higher values of 5.19 ± 0.42, 4.90 ± 0.97, and 2.05 ± 0.11% ID/g at the same time point─consistent with the superior binding affinity of cRGD. Tumor-to-muscle ratios were favorable, with[18F]5b reaching 4.32 ± 0.39 in the 4T1 model. Blocking studies in U87 tumors confirmed high binding specificity, with uptake reduced to approximately 1% ID/g. This isotope exchange-based CuAAC labeling strategy streamlines PET tracer synthesis, preserves biomolecule integrity, and offers a versatile platform for molecular imaging and pretargeting applications.

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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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