Preparation and Preliminary Evaluation of a Novel 68Ga-Labeled Linear Peptide PET Probe Targeting Nectin-4.

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Deng Ke Li, Xue Cen Cao, Chao Mu, Zheng Li, Mu Mei Chen
{"title":"Preparation and Preliminary Evaluation of a Novel <sup>68</sup>Ga-Labeled Linear Peptide PET Probe Targeting Nectin-4.","authors":"Deng Ke Li, Xue Cen Cao, Chao Mu, Zheng Li, Mu Mei Chen","doi":"10.1177/10849785251393840","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>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.</p><p><strong>Methods: </strong>[<sup>68</sup>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 [<sup>68</sup>Ga]Ga-NOTA-SP to Nectin-4. Normal BALB/c mice were used to investigate the plasma concentration-time curves.</p><p><strong>Results: </strong>Under optimal labeling conditions, the labeling efficiency of [<sup>68</sup>Ga]Ga-NOTA-SP can reach above 95%, with a molar-specific activity of 2.45 MBq/nmol and high <i>in vitro</i> stability. The high specificity of [<sup>68</sup>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<sub>d</sub> value of 2.483 nM, which was further confirmed by PET-CT imaging.</p><p><strong>Conclusions: </strong>[<sup>68</sup>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.</p>","PeriodicalId":55277,"journal":{"name":"Cancer Biotherapy and Radiopharmaceuticals","volume":" ","pages":"169-177"},"PeriodicalIF":1.7000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Biotherapy and Radiopharmaceuticals","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/10849785251393840","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/11/5 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

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: [68Ga]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 [68Ga]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 [68Ga]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 [68Ga]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 Kd value of 2.483 nM, which was further confirmed by PET-CT imaging.

Conclusions: [68Ga]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.

一种新型靶向Nectin-4的68ga标记线性肽PET探针的制备及初步评价
目的:Nectin-4已被成功地用作肿瘤治疗的靶点。虽然已经报道了几种双环肽和抗体,Nectin-4正电子发射断层扫描(PET)探针用于肿瘤成像和表达检测,但它们的生产成本或药代动力学仍有待进一步改进。本研究开发了一种新型线性肽PET探针,用于快速检测nectin -4相关肿瘤。方法:采用一步螯合法制备[68Ga]Ga-NOTA-SP,采用射频高效液相色谱法和薄层色谱法对其进行质量控制。分子对接预测NOTA-SP与Nectin-4的优势结合。采用SW780细胞和PET/ CT成像,采用SW780肿瘤模型进行细胞实验,评估[68Ga]Ga-NOTA-SP对Nectin-4的特异性结合和靶向能力。以正常BALB/c小鼠为研究对象,观察其血药浓度-时间曲线。结果:在最优标记条件下,[68Ga]Ga-NOTA-SP的标记效率可达95%以上,其摩尔比活性为2.45 MBq/nmol,体外稳定性高。通过分子对接和细胞摄取实验证实了[68Ga]Ga-NOTA-SP对Nectin-4的高特异性,其结合能为-5.4 kcal/mol, Kd值为2.483 nM, PET-CT成像进一步证实了这一点。结论:以线性肽为载体的[68Ga]Ga-NOTA-SP具有良好的药代动力学和对Nectin-4的特异性靶向能力,可实现肿瘤小鼠模型的快速成像。它是一种很有前途的PET/CT成像探针,可用于优化nectin -4相关肿瘤的诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书