正电子发射断层摄影术
肽
化学
药代动力学
分子成像
Pet成像
体内
对接(动物)
分子探针
肿瘤细胞
结合选择性
配体结合分析
癌症研究
细胞
螯合作用
配体(生物化学)
Spect成像
体外
生物物理学
靶向治疗
分子结合
分子模型
组织分布
受体
临床前影像学
肽合成
作者
Deng Ke Li,Xin Cao,Chao Mu,Zheng Li,Min Chen
标识
DOI:10.1177/10849785251393840
摘要
Objectives: Nectin-4 has been successfully used as a target for tumor therapy. Although several bicyclic peptides and antibodies, Nectin-4 positron emission tomography (PET) probes, have been reported for tumor imaging and expression detection, their production costs or pharmacokinetics still need further improvement. This study developed a novel linear peptide PET probe for rapid examination of Nectin-4-related tumors. Methods: [ 68 Ga]Ga-NOTA-SP was prepared by a one-step chelation reaction, and its quality control was carried out by using radio-high-performance liquid chromatography and thin-layer chromatography. Molecular docking was used to predict the predominant binding of NOTA-SP to Nectin-4. Cell experiments using SW780 cells and PET/computed tomography (CT) imaging, using the SW780 tumor model, were performed to assess the specific binding and targeting ability of [ 68 Ga]Ga-NOTA-SP to Nectin-4. Normal BALB/c mice were used to investigate the plasma concentration–time curves. Results: Under optimal labeling conditions, the labeling efficiency of [ 68 Ga]Ga-NOTA-SP can reach above 95%, with a molar-specific activity of 2.45 MBq/nmol and high in vitro stability. The high specificity of [ 68 Ga]Ga-NOTA-SP to Nectin-4 is demonstrated by molecular docking and cell uptake experiment, showing a binding energy of −5.4 kcal/mol and K d value of 2.483 nM, which was further confirmed by PET-CT imaging. Conclusions: [ 68 Ga]Ga-NOTA-SP using a linear peptide as a vector shows favorable pharmacokinetics and specific targeting ability to Nectin-4, enabling rapid tumor mouse model imaging. It would be a promising PET/CT imaging probe for optimizing Nectin-4-related tumor diagnoses and therapy.
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