{"title":"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。","authors":"Xinlin Zhong, , , Junjie Yan*, , , Chen Su, , , Xinyu Wang, , , Donghui Pan, , , Yuping Xu, , , Lizhen Wang, , , Chongyang Chen, , and , Min Yang*, ","doi":"10.1021/acs.molpharmaceut.5c00333","DOIUrl":null,"url":null,"abstract":"<p >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 (<sup>18</sup>F) is widely used in clinical practice because of its moderate half-life and high-quality imaging properties. However, traditional <sup>18</sup>F-labeling methods often require a laborious procedure and harsh conditions, which may compromise the structural integrity and biological functions. Developing mild and efficient <sup>18</sup>F-labeling strategies is therefore critical for advancing biomolecular PET tracers. In this study, we developed a novel clickable <sup>18</sup>F-labeled synthon, 1-ethynyl-3-([<sup>18</sup>F]trifluoromethyl)-5-(trifluoromethyl)benzene ([<sup>18</sup>F]<b>1</b>), prepared via an <sup>18</sup>F/<sup>19</sup>F isotope exchange reaction (RCY = 17.2 ± 3.9%). [<sup>18</sup>F]<b>1</b> 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 [<sup>18</sup>F]<b>5a</b> and [<sup>18</sup>F]<b>5b</b>, peaking at 30 min postinjection. Tumor accumulation for [<sup>18</sup>F]<b>5a</b> 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 [<sup>18</sup>F]<b>5b</b> 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[<sup>18</sup>F]<b>5b</b> 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.</p>","PeriodicalId":52,"journal":{"name":"Molecular Pharmaceutics","volume":"22 10","pages":"5860–5869"},"PeriodicalIF":4.5000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Novel Arene Trifluoromethyl-Based 18F-Labeling Strategy for Enhanced Biomolecular Tracer Development in PET Imaging\",\"authors\":\"Xinlin Zhong, , , Junjie Yan*, , , Chen Su, , , Xinyu Wang, , , Donghui Pan, , , Yuping Xu, , , Lizhen Wang, , , Chongyang Chen, , and , Min Yang*, \",\"doi\":\"10.1021/acs.molpharmaceut.5c00333\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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 (<sup>18</sup>F) is widely used in clinical practice because of its moderate half-life and high-quality imaging properties. However, traditional <sup>18</sup>F-labeling methods often require a laborious procedure and harsh conditions, which may compromise the structural integrity and biological functions. Developing mild and efficient <sup>18</sup>F-labeling strategies is therefore critical for advancing biomolecular PET tracers. In this study, we developed a novel clickable <sup>18</sup>F-labeled synthon, 1-ethynyl-3-([<sup>18</sup>F]trifluoromethyl)-5-(trifluoromethyl)benzene ([<sup>18</sup>F]<b>1</b>), prepared via an <sup>18</sup>F/<sup>19</sup>F isotope exchange reaction (RCY = 17.2 ± 3.9%). [<sup>18</sup>F]<b>1</b> 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 [<sup>18</sup>F]<b>5a</b> and [<sup>18</sup>F]<b>5b</b>, peaking at 30 min postinjection. Tumor accumulation for [<sup>18</sup>F]<b>5a</b> 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 [<sup>18</sup>F]<b>5b</b> 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[<sup>18</sup>F]<b>5b</b> 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.</p>\",\"PeriodicalId\":52,\"journal\":{\"name\":\"Molecular Pharmaceutics\",\"volume\":\"22 10\",\"pages\":\"5860–5869\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-08-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Pharmaceutics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.molpharmaceut.5c00333\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Pharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.molpharmaceut.5c00333","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
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.
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.