American journal of nuclear medicine and molecular imaging最新文献

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The role of 18F-fluorodeoxyglucose PET/computed tomography in the diagnosis and monitoring of large vessel vasculitides - a review article. 18F-氟脱氧葡萄糖PET/计算机断层扫描在大血管血管炎诊断和监测中的作用——一篇综述文章。
IF 2.5
American journal of nuclear medicine and molecular imaging Pub Date : 2023-08-15 eCollection Date: 2023-01-01
Mahshid Bahrami, Hossein Mohammadi, Hannaneh Mirgaloyebayat, Zahra Mohajeri, Pooya Fazeli, Azad Mojahedi, Ali Afsharirad, Reza Tavakoli, Amirhossein Sadeghian, Sayed Mohammad Amin Nourian
{"title":"The role of 18F-fluorodeoxyglucose PET/computed tomography in the diagnosis and monitoring of large vessel vasculitides - a review article.","authors":"Mahshid Bahrami,&nbsp;Hossein Mohammadi,&nbsp;Hannaneh Mirgaloyebayat,&nbsp;Zahra Mohajeri,&nbsp;Pooya Fazeli,&nbsp;Azad Mojahedi,&nbsp;Ali Afsharirad,&nbsp;Reza Tavakoli,&nbsp;Amirhossein Sadeghian,&nbsp;Sayed Mohammad Amin Nourian","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In the last two decades, advancements in positron emission tomography (PET) technology have increased the diagnostic accuracy of patients with large-vessel vasculitis (LVV). Numerous systematic reviews and meta-analyses have been conducted, and patients suspected of having LVV can be diagnosed earlier with 18F-FDG PET. Two subtypes, giant cell arteritis (GCA) and Takayasu arteritis (TA), will progress when their response to corticosteroids and enhanced immunosuppression is inadequate. In the majority of patients, disease activity cannot be monitored solely through laboratory procedures; consequently, glucose metabolism may be a source of potential biomarkers. In this article, we discuss the current state of 18F-FDG PET/CT imaging standards.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 4","pages":"127-135"},"PeriodicalIF":2.5,"publicationDate":"2023-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509293/pdf/ajnmmi0013-0127.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41108807","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Duodenal-type follicular lymphoma in 18F-FDG PET/CT imaging: a case report. 十二指肠型滤泡性淋巴瘤18F-FDG PET/CT显像1例报告。
IF 2.5
American journal of nuclear medicine and molecular imaging Pub Date : 2023-08-15 eCollection Date: 2023-01-01
Wenpeng Huang, Fangfang Chao, Yushuo Peng, Xiaoyue Zhang, Qi Yang, Lele Song, Liming Li, Lei Kang
{"title":"Duodenal-type follicular lymphoma in <sup>18</sup>F-FDG PET/CT imaging: a case report.","authors":"Wenpeng Huang,&nbsp;Fangfang Chao,&nbsp;Yushuo Peng,&nbsp;Xiaoyue Zhang,&nbsp;Qi Yang,&nbsp;Lele Song,&nbsp;Liming Li,&nbsp;Lei Kang","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Follicular lymphoma (FL) is a subtype of non-Hodgkin lymphoma (NHL) that is typically characterized by a slow-growing course. Duodenal-type follicular lymphoma (D-FL) was recently reclassified as a distinct variant. This subtype exhibits unique clinical and biological characteristics, which set it apart from other forms of FL. We report a case of a 36-year-old male patient with multiple, small, gray polypoid lesions in the descending duodenum which were detected by esophagogastroduodenoscopy. The pathological diagnosis was low-grade D-FL. <sup>18</sup>F-FDG PET/CT was performed for staging and revealed the pancreas and peripheral lymph nodes were involved by FL, with a clinical IV stage. The patient underwent a bone marrow smear cytology, which revealed no bone marrow abnormalities, and excluded bone marrow involvement. He was treated with six cycles of chemotherapy using the R-CHOP regimen and reached complete remission.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 4","pages":"164-170"},"PeriodicalIF":2.5,"publicationDate":"2023-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509290/pdf/ajnmmi0013-0164.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41092161","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of enhanced permeability effect and different linear energy transfer of radionuclides in a prostate cancer xenograft model. 前列腺癌症异种移植物模型中放射性核素的增强渗透效应和不同线性能量转移的评估。
IF 2.5
American journal of nuclear medicine and molecular imaging Pub Date : 2023-08-15 eCollection Date: 2023-01-01
Oskar Vilhelmsson Timmermand, Marcella Safi, Bo Holmqvist, Joanna Strand
{"title":"Evaluation of enhanced permeability effect and different linear energy transfer of radionuclides in a prostate cancer xenograft model.","authors":"Oskar Vilhelmsson Timmermand,&nbsp;Marcella Safi,&nbsp;Bo Holmqvist,&nbsp;Joanna Strand","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>We have previously investigated the biodistribution and therapy effect of a humanized monoclonal antibody targeting free prostate-specific antigen (fPSA) intended for theranostics of hormone-refractory prostate cancer. In the present study, we evaluated the off-target effect and different linear energy transfer (LET) radionuclides without the effect of PSA targeting by using an antibody with the same scaffold as previously used immunoconjugates but with random, non-specific, antigen binding region. This allows us to identify alterations generated by specific targeting and those related to passive bystander effects, such as enhanced permeability and retention (EPR). A control humanized IgG monoclonal antibody (hIgG1) and an isotype control IgG monoclonal antibody were conjugated with the chelator CHX-A\"-DTPA. The immunoconjugate was radiolabeled with either Lutetium-177 ([<sup>177</sup>Lu]Lu) or Indium-111 ([<sup>111</sup>In]In). A biodistribution study in mice carrying LNCaP xenografts, was performed to evaluate the non-specific uptake of [<sup>177</sup>Lu]Lu-hIgG1 in tumors and normal organs. Further, therapy studies of [<sup>177</sup>Lu]Lu and [<sup>111</sup>In]In labeled IgG were performed in BALB/c mice carrying LNCaP xenografts. Tumor tissues of treated xenografts and control were sectioned and immunohistochemically stained for Ki67 and PSA. The highest tumor uptake for the [<sup>177</sup>Lu]Lu-hIgG1 was seen at 72 hours (7.2±2 %IA/g), when comparing the tumor uptake of the fPSA targeting antibody to the non-specific antibody, the non-specific antibody contributes to half of the tumor uptake at 72 h. The liver uptake was 3.1±0.5 %IA/g at 24 h, 2.8±0.5 %IA/g at 72 h and 1.3±0.6 %IA/g at 120 h in LNCaP xenografts, which was approximately three times lower at 24 h and two times lower at 72 h than for the antibody with preserved targeting. Immunohistochemical labeling showed a reduction of PSA expression and a reduction of Ki67 labeled cells in the [<sup>111</sup>In]In treated LNCaP tumors, compared to vehicle and [<sup>177</sup>Lu]Lu treated mice. In conclusion, we found that specific targeting might negatively influence normal organ uptake when targeting secreted antigens. Furthermore, different energy deposition i.e. linear energy transfer of a radionuclide might have diverse effects on receptor expression and cell proliferation in tumors.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 4","pages":"147-155"},"PeriodicalIF":2.5,"publicationDate":"2023-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509292/pdf/ajnmmi0013-0147.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41102703","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Automated radiosynthesis of [18F]FMPEP-d2 for cannabinoid receptor PET imaging. 用于大麻素受体PET成像的[18F]FMPEP-d2的自动放射合成。
IF 2.5
American journal of nuclear medicine and molecular imaging Pub Date : 2023-08-15 eCollection Date: 2023-01-01
Huailei Jiang, Yan Guo, Otto Muzik
{"title":"Automated radiosynthesis of [<sup>18</sup>F]FMPEP-<i>d</i><sub>2</sub> for cannabinoid receptor PET imaging.","authors":"Huailei Jiang,&nbsp;Yan Guo,&nbsp;Otto Muzik","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The cannabinoid subtype 1 receptor (CB1R) is highly expressed in the central nervous system and abnormalities in regional CB1R density are associated with neurodegenerative disorders. The PET tracer [<sup>18</sup>F]FMPEP-<i>d</i><sub>2</sub> is an inverse CB1R agonist which was shown to be suitable for non-invasive PET imaging. In this work, we reported the fully automated radiosynthesis of [<sup>18</sup>F]FMPEP-<i>d</i><sub>2</sub> on a Synthra RNplus research module. In a total synthesis time of 70 min, [<sup>18</sup>F]FMPEP-<i>d</i><sub>2</sub> was obtained in 2.2 ± 0.1 GBq (n = 3) with excellent radiochemical and chemical purity. Quality control test showed that [<sup>18</sup>F]FMPEP-<i>d</i><sub>2</sub> product meets all the release criteria for clinical patient use.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 4","pages":"171-178"},"PeriodicalIF":2.5,"publicationDate":"2023-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509289/pdf/ajnmmi0013-0171.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41095337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stroke and molecular imaging: a focus on FDG-PET. 中风与分子成像:聚焦 FDG-PET。
IF 2.5
American journal of nuclear medicine and molecular imaging Pub Date : 2023-04-25 eCollection Date: 2023-01-01
Cyrus Ayubcha, Aamir Amanullah, Krishna H Patel, Eric Teichner, Saket Gokhale, Ulysses Marquez-Valenzuela, Thomas J Werner, Abass Alavi
{"title":"Stroke and molecular imaging: a focus on FDG-PET.","authors":"Cyrus Ayubcha, Aamir Amanullah, Krishna H Patel, Eric Teichner, Saket Gokhale, Ulysses Marquez-Valenzuela, Thomas J Werner, Abass Alavi","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Stroke is the leading cause of disability worldwide, the second most common cause of dementia and the third leading cause of death. Though the etiology of stroke has been explored extensively, there remains open questions in the scientific and clinical study of stroke. Traditional imaging techniques, such as magnetic resonance imaging and computed tomography, have been applied extensively and remain mainstays in clinical practice. Nevertheless, positron emission tomography has proven to be a powerful molecular imaging tool in exploring the scientific aspects of neurological disease, and stroke remains an area of great interest. This review article examines the role of positron emission tomography in the study of stroke including its contributions to elaborating related pathophysiology and delving into possible clinical applications.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 2","pages":"51-63"},"PeriodicalIF":2.5,"publicationDate":"2023-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193198/pdf/ajnmmi0013-0051.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9503757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Imaging ligands targeting glypican-3 receptor expression in hepatocellular carcinoma. 肝细胞癌中靶向glypian-3受体表达的成像配体。
IF 2.5
American journal of nuclear medicine and molecular imaging Pub Date : 2023-01-26 DOI: 10.18060/26670
Shaun D. Grega, David X. Zheng, Q. Zheng
{"title":"Imaging ligands targeting glypican-3 receptor expression in hepatocellular carcinoma.","authors":"Shaun D. Grega, David X. Zheng, Q. Zheng","doi":"10.18060/26670","DOIUrl":"https://doi.org/10.18060/26670","url":null,"abstract":"Hepatocellular carcinoma (HCC) is the third leading cause of cancer mortality. Early detection of HCC is important since potentially curative therapies exist in the initial stages of HCC; no curative therapies exist for late-stage HCC. However, the initial detection of HCC remains challenging due to the lack of symptoms during the early stage of the disease. Other methods of screening and detecting HCC, including blood serum tests and conventional imaging methods, remain inadequate due to genetic differences between patients and the high background activity of liver tissues. Thus, there is a need for an accurate imaging agent for the diagnosis, staging, and prognosis of HCC. Glypican-3 (GPC3) is an oncofetal receptor responsible for regulating cell division, growth, and survival. GPC3 is a clinically relevant biomarker for imaging and therapeutics, as its expression is HCC tumor-specific and absent from normal and other pathological liver tissues. The development of novel GPC3-targeting imaging agents has encompassed three classes of biomolecules: peptides, antibodies, and aptamers. These biomolecules serve as constructs for diagnostic imaging (demonstrating potential as positron emission tomography [PET], single-photon emission tomography [SPECT], and optical imaging agents) and HCC treatment delivery. More than 20 unique ligands have been identified in the literature as showing specificity for the GPC3 receptor. Although several ligands are currently under clinical investigation as therapies for HCC, clinical translation of GPC3-targeting ligands as imaging agents is lacking. This review highlights the current landscape of ligands targeting GPC3 and describes their promising possibilities as imaging agents for HCC.","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"12 4 1","pages":"113-121"},"PeriodicalIF":2.5,"publicationDate":"2023-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45501803","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A rectal gastrointestinal stromal tumor case accompanied by elevated CEA mimicking rectal carcinoma on 18F-FDG PET/CT. 18F-FDG PET/CT显示1例直肠胃肠道间质瘤伴CEA升高的模拟直肠癌。
IF 2.5
Zihao Tao, Sitong Wu, Zhao Chen, Yongkang Qiu, Lele Song, Qi Yang, Lin Nong, Lei Kang
{"title":"A rectal gastrointestinal stromal tumor case accompanied by elevated CEA mimicking rectal carcinoma on <sup>18</sup>F-FDG PET/CT.","authors":"Zihao Tao,&nbsp;Sitong Wu,&nbsp;Zhao Chen,&nbsp;Yongkang Qiu,&nbsp;Lele Song,&nbsp;Qi Yang,&nbsp;Lin Nong,&nbsp;Lei Kang","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal neoplasm arising from gastrointestinal tract and can be benign or malignant. Rectal GISTs are rare and have poor prognosis. We here reported an older male who presented with features of distending discomfort in the rectum and pain in the anus due to a large rectal tumor. Physical examinations detected a mass in the rectum without blood staining on the gloved finger. Carcinoembryonic antigen (CEA) was found to be slightly elevated and the prostate-specific antigen level was normal. <sup>18</sup>F-FDG PET/CT showed a soft tissue density mass at the bottom of the pelvic, with an unclear boundary to the surroundings with the significantly increased FDG uptake (SUVmax 17.5). Although a rectal carcinoma was suspected based on the finding of PET/CT and CEA, the histopathological examination confirmed the diagnosis of the malignant GIST of the rectum. The patient was then treated with imatinib and on follow-up regularly. In this case, <sup>18</sup>F-FDG PET/CT shows the advantage of visualizing both primary and metastatic lesions and provides valuable information for the diagnosis, staging, evaluation, and prognosis of GIST.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 1","pages":"26-32"},"PeriodicalIF":2.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009467/pdf/ajnmmi0013-0026.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9122048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The diagnostic value of the computed tomography scan and ultrasonography in acute appendicitis. 计算机断层扫描和超声检查对急性阑尾炎的诊断价值。
IF 2.5
Mahshid Bahrami, Hannaneh Mirgaloyebayat, Zahra Mohajeri, Hossein Mohammadi, Samira Amin Afshari, Pooya Fazeli, Dorna Masaeli, Sayed Mohammad Amin Nourian
{"title":"The diagnostic value of the computed tomography scan and ultrasonography in acute appendicitis.","authors":"Mahshid Bahrami,&nbsp;Hannaneh Mirgaloyebayat,&nbsp;Zahra Mohajeri,&nbsp;Hossein Mohammadi,&nbsp;Samira Amin Afshari,&nbsp;Pooya Fazeli,&nbsp;Dorna Masaeli,&nbsp;Sayed Mohammad Amin Nourian","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The most prevalent cause of emergency abdominal surgery is acute appendicitis. Ultrasonography is safe and widely available, although it's operator-dependent and difficult for people with massive bodies. Computed tomography (CT) scans are more accurate than ultrasonography, with a 93 to 98% accuracy rate. The goal of this investigation is to evaluate the diagnostic value of ultrasonography and CT scanning for acute appendicitis. This is a cross-sectional study that was performed on 231 patients with suspected with acute appendicitis. The Alvarado score was initially used to diagnose acute appendicitis. A radiologist performed abdominal ultrasonography on all patients. If the results of the ultrasonography were negative or unclear, a CT scan was performed using oral contrast. Finally, all ultrasonography and CT scan data were reevaluated by an experienced radiologist and compared to the patient's final diagnosis in the case of surgery and pathology results. Comparisons between the two groups were performed. The sensitivity, specificity, and positive and negative predictive value of ultrasonography according to pathology results in patients with low clinical suspicion were 74.9%, 63.4%, 94.3%, and 67.6%, respectively. The sensitivity, specificity, positive and negative predictive value of CT scans based on pathology results were 87.9%, 81.8%, 94.7%, and 79.3%, respectively, in patients with low clinical suspicion. The CT scan results in female patients suspected of appendicitis were completely consistent with the pathology results. The CT scan demonstrated greater specificity and sensitivity in diagnosing acute appendicitis compared to abdominal ultrasonography.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 1","pages":"11-17"},"PeriodicalIF":2.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009470/pdf/ajnmmi0013-0011.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9122049","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A carbon-11 labeled imidazo[1,2-a]pyridine derivative as a new potential PET probe targeting PI3K/mTOR in cancer. 碳-11标记咪唑[1,2- A]吡啶衍生物作为靶向癌症PI3K/mTOR的新型潜在PET探针。
IF 2.5
Wenqing Liu, Wenjie Ma, Min Wang, Zhuangzhuang Wang, Shaun D Grega, Qi-Huang Zheng, Zhidong Xu
{"title":"A carbon-11 labeled imidazo[1,2-<i>a</i>]pyridine derivative as a new potential PET probe targeting PI3K/mTOR in cancer.","authors":"Wenqing Liu,&nbsp;Wenjie Ma,&nbsp;Min Wang,&nbsp;Zhuangzhuang Wang,&nbsp;Shaun D Grega,&nbsp;Qi-Huang Zheng,&nbsp;Zhidong Xu","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The PI3K/Akt/mTOR pathway is frequently dysregulated in cancer due to its central role in cell growth, survival, and proliferation. Overactivation of the PI3K/Akt/mTOR pathway may occur through varying mechanisms including mutations, gene amplification, and upstream signaling events, ultimately resulting in cancer. Therefore, PI3K/Akt/mTOR pathway has emerged as an attractive target for cancer therapy and imaging. A promising approach to inhibit this pathway involves a simultaneous inhibition of both PI3K and mTOR using a dual inhibitor. Recently, a potent dual PI3K/mTOR inhibitor, 2,4-difluoro-<i>N</i>-(2-methoxy-5-(3-(5-(2-(4-methylpiperazin-1-yl)ethyl)-1,3,4-oxadiazol-2-yl)imidazo[1,2-<i>a</i>]pyridin-6-yl)pyridin-3-yl)benzenesulfonamide (<b>7</b>), was discovered and demonstrated excellent kinase selectivity IC<sub>50</sub> (PI3K/mTOR) = 0.20/21 nM; good cellular growth inhibition IC<sub>50</sub> (HCT-116 cell) = 10 nM, modest plasma clearance, and acceptable oral bioavailability. Expanding on this discovery, here we present the synthesis of the carbon-11 labeled imidazo[1,2-<i>a</i>]pyridine derivative 2,4-difluoro-<i>N</i>-(2-methoxy-5-(3-(5-(2-(4-[<sup>11</sup>C]methylpiperazin-1-yl)ethyl)-1,3,4-oxadiazol-2-yl)imidazo[1,2-<i>a</i>]pyridin-6-yl)pyridin-3-yl)benzenesulfonamide (<i>N</i>-[<sup>11</sup>C]<b>7</b>) as a new potential radiotracer for the biomedical imaging technique positron emission tomography (PET) imaging of PI3K/mTOR in cancer. The reference standard <b>7</b> and its <i>N</i>-demethylated precursor, 2,4-difluoro-<i>N</i>-(2-methoxy-5-(3-(5-(2-(piperazin-1-yl)ethyl)-1,3,4-oxadiazol-2-yl)imidazo[1,2-<i>a</i>]pyridin-6-yl)pyridin-3-yl)benzenesulfonamide (<b>11</b>), were synthesized in 7 and 8 steps with 10% and 7% overall chemical yield, respectively. <i>N</i>-[<sup>11</sup>C]<b>7</b> was prepared from <b>11</b> using [<sup>11</sup>C]methyl triflate ([<sup>11</sup>C]CH<sub>3</sub>OTf) through <i>N</i>-<sup>11</sup>C-methylation and isolated by high-performance liquid chromatography (HPLC) and solid-phase extraction (SPE) formulation in 40-50% radiochemical yield decay corrected to end of bombardment (EOB) based on [<sup>11</sup>C]CO<sub>2</sub>. The radiochemical purity was > 99% and the molar activity (A<sub>m</sub>) at EOB was in the range of 296-555 GBq/µmol (n = 5).</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 3","pages":"95-106"},"PeriodicalIF":2.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349286/pdf/ajnmmi0013-0095.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9826144","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multimodality imaging of spleen involvement in Erdheim-Chester disease mimicking splenic hemangioma: a unique case report. 模拟脾血管瘤的Erdheim-Chester病累及脾脏的多模态成像:一个独特的病例报告。
IF 2.5
Wenpeng Huang, Yongkang Qiu, Zhao Chen, Qi Yang, Lin Nong, Lei Kang
{"title":"Multimodality imaging of spleen involvement in Erdheim-Chester disease mimicking splenic hemangioma: a unique case report.","authors":"Wenpeng Huang,&nbsp;Yongkang Qiu,&nbsp;Zhao Chen,&nbsp;Qi Yang,&nbsp;Lin Nong,&nbsp;Lei Kang","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Erdheim-Chester disease (ECD) is a rare and clinically heterogeneous non-Langerhans cell histiocytosis, and its diagnosis relies on established clinical, radiologic, histopathological criteria. ECD can be evaluated by whole-body preoperative imaging methods. Although <sup>18</sup>F-FDG PET/CT shows negative findings in some splenic benign or borderline lesions, such as splenic inflammatory myofibroblastic tumors and hemangioendotheliomas, it can provide value in differentiating some malignant diseases, such as hemangiosarcoma and metastases. Here, we report the CT, MRI, and <sup>18</sup>F-FDG PET/CT imaging performance of an ECD patient who presented with only spleen involvement. Even though some clinical and radiological descriptions can be found in the literature, ECD reports with only splenic involvement mimicking splenic hemangioma as the first presentation are rare, to the best of our knowledge. Histopathology and molecular analysis of this case confirmed the diagnosis of ECD. Clinicians should pay attention to the possibility of ECD occurrence in the spleen, while negative findings on <sup>18</sup>F-FDG PET/CT of the spleen indicated a low risk for high-grade malignant splenic tumors and metastases.</p>","PeriodicalId":7572,"journal":{"name":"American journal of nuclear medicine and molecular imaging","volume":"13 3","pages":"118-125"},"PeriodicalIF":2.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349290/pdf/ajnmmi0013-0118.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9826149","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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