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New Phase Transfer Catalysts for Fluorine-18 Radiolabelling 氟-18放射性标记的新型相转移催化剂
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109167
Zélie Faudemer, Rémi Pelletier, Simon Specklin, Bertrand Kuhnast
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引用次数: 0
CCR8-targeting radioimmunotherapy enhances anti-CTLA-4 immunotherapy through expansion of anti-tumor macrophages, T cells and NK cells in colorectal cancer models ccr8靶向放射免疫治疗通过在结直肠癌模型中扩增抗肿瘤巨噬细胞、T细胞和NK细胞来增强抗ctla -4免疫治疗
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109163
Connor Frank, Kevin Allen, Rubin Jiao, Mackenzie Malo, Ekaterina Dadachova
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引用次数: 0
[18F]FDG-PET provides insights into the liver-brain axis and confirms SUVgluc as a surrogate for MRGlu in a mouse model of liver fibrosis [18F]FDG-PET提供了对肝-脑轴的深入研究,并证实了SUVgluc在小鼠肝纤维化模型中可以替代MRGlu
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-09-04 DOI: 10.1016/j.nucmedbio.2025.109095
Thomas Wanek , Mari Teuter , Asha Balakrishnan , Tobias L. Ross , Frank M. Bengel , Michael Ott , Marion Bankstahl , Jens P. Bankstahl

Purpose

The liver-brain axis regulates metabolic homeostasis, with glucose metabolism playing a key role. Liver dysfunction, such as fibrosis, may impact brain metabolism and consequently, brain function. Positron emission tomography (PET) imaging provides a non-invasive approach to study glucose metabolism in both organs. A recent longitudinal PET/CT study utilizing 2-deoxy-2-[18F]-fluoro-d-glucose ([18F]FDG) amongst other radiotracers revealed significant metabolic changes in the liver in a mouse model of liver fibrosis. Here, we retrospectively analyzed those data to quantify potential associated changes in brain glucose metabolism.

Procedures

Eleven male C57BL/6N mice underwent repeated PET imaging with [18F]FDG at baseline, pre-fibrosis, fibrosis, and remission stages. Cerebral glucose metabolism was assessed using standardized uptake value (SUV), blood glucose-corrected SUV (SUVgluc), and kinetic modeling (Patlak and two-tissue compartment models) for calculation of the glucose metabolic rate (MRGlu).

Results

Both SUVgluc and MRGlu significantly decreased during pre-fibrosis and fibrosis on whole brain level and recovered at remission. SUVgluc statistical parametric mapping identified multiple brain areas with reduced glucose metabolism, which was confirmed by regional analysis showing progressive reduction in SUVgluc. Correlation analyses confirmed SUVgluc as a reliable surrogate for MRGlu, unlike uncorrected SUV. Liver [18F]FDG uptake increased during fibrosis and normalized at remission, mirroring changes in blood glucose concentrations.

Conclusions

[18F]FDG PET imaging revealed that liver fibrosis alters glucose metabolism in both liver and brain, emphasizing the potential of molecular imaging for future assessment of metabolic interaction between liver and brain. [18F]FDG uptake in terms of SUVgluc strongly correlated with MRGlu from kinetic modeling, supporting its utility as a valid surrogate parameter to quantify cerebral glucose metabolism in mice.
目的肝脑轴调节代谢稳态,其中葡萄糖代谢起关键作用。肝功能障碍,如肝纤维化,可能影响脑代谢,从而影响脑功能。正电子发射断层扫描(PET)成像提供了一种非侵入性的方法来研究两个器官的葡萄糖代谢。最近一项利用2-脱氧-2-[18F]-氟-d-葡萄糖([18F]FDG)等放射性示踪剂的纵向PET/CT研究显示,在肝纤维化小鼠模型中肝脏发生了显著的代谢变化。在这里,我们回顾性地分析了这些数据,以量化脑葡萄糖代谢的潜在相关变化。11只雄性C57BL/6N小鼠在基线、纤维化前、纤维化和缓解期用[18F]FDG重复PET成像。采用标准化摄取值(SUV)、血糖校正SUV (SUVgluc)和动力学模型(Patlak和两组织室模型)评估脑葡萄糖代谢,计算葡萄糖代谢率(MRGlu)。结果suvglu和MRGlu在纤维化前和全脑水平均显著降低,缓解后恢复。SUVgluc统计参数映射发现了多个糖代谢降低的脑区,区域分析证实了这一点,显示SUVgluc呈进行性降低。相关分析证实,与未校正的SUV不同,SUVgluc是MRGlu的可靠替代品。肝脏[18F]FDG摄取在纤维化期间增加,缓解后恢复正常,反映了血糖浓度的变化。结论[18F]FDG PET成像显示肝纤维化改变了肝和脑的葡萄糖代谢,强调了分子成像在未来评估肝和脑代谢相互作用方面的潜力。[18F]动力学模型显示,以suvglu表示的FDG摄取与MRGlu密切相关,支持其作为量化小鼠脑糖代谢的有效替代参数的效用。
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引用次数: 0
Estimation of the binding potential of the PET ligand [18F]FEDAC to translocator protein 18 kDa (TSPO) in the brain of experimental stroke model rats 脑卒中模型大鼠脑内PET配体FEDAC与转运蛋白18kda (TSPO)结合电位的估计[18F]
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-05 DOI: 10.1016/j.nucmedbio.2025.109579
Tomoteru Yamasaki , Yiding Zhang , Wakana Mori , Katsushi Kumata , Hidekatsu Wakizaka , Daisuke Arashi , Yusuke Kurihara , Masanao Ogawa , Nobuki Nengaki , Masayuki Fujinaga , Ming-Rong Zhang

Purpose

Translocator protein 18 kDa (TSPO) is a biomarker for neuroinflammation, and [18F]FEDAC was developed as a clinically usable radioligand for its imaging. Here, quantitative PET analyses of [18F]FEDAC in the brain of transient middle cerebral artery occlusion (tMCAO) rats were conducted for the first time.

Methods

Quantitative PET analysis was performed on rats subjected to tMCAO, with blood sampling also conducted as part of the study. To estimate the kinetic parameters of [18F]FEDAC, two-tissue compartment model (2TCM) and simplified reference tissue model (SRTM) analyses were conducted.

Results

The input rate (K1) and distribution volume (VT) (a macroparameter consisting of the K1k4 rate constants from 2TCM analysis) of [18F]FEDAC in the ipsilateral area of tMCAO rats were 0.38 ± 0.19 mL/cm3/min and 5.4 ± 2.7 mL/cm3, respectively, which are roughly twice as high as those in the contralateral area. These results strongly suggest that ipsilateral binding potential (BPND), a quantitative index derived from the VT ratio with respect to the reference region, depends not only on the binding of [18F]FEDAC to TSPO, but also on increases in the input rate from blood. Therefore, in SRTM analyses, we corrected apparent BPND using R1, an index for probe delivery. In validation studies, SRTM analysis with the corrected BPND (corBPND), using the cerebellum as a reference, showed a high correlation with direct BPND (k3/k4) in 2TCM analyses.

Conclusion

The acquisition of quantitative PET images of TSPO distribution in the tMCAO rat brain was successfully achieved by scaling with corBPND.
目的转位蛋白18kda (TSPO)是神经炎症的生物标志物,[18F]FEDAC被开发为临床可用的放射配体用于其成像。本文首次对短暂性大脑中动脉闭塞(tMCAO)大鼠脑内[18F]FEDAC进行定量PET分析。方法对大鼠进行定量PET分析,并采血。为了估计[18F]FEDAC的动力学参数,我们进行了双组织室模型(2TCM)和简化参比组织模型(SRTM)分析。结果[18F]FEDAC在tMCAO大鼠同侧区的输入速率(K1)和分布体积(VT)分别为0.38±0.19 mL/cm3/min和5.4±2.7 mL/cm3,约为对侧区的2倍。这些结果强烈表明,同侧结合电位(BPND),一个由相对于参考区域的VT比率得出的定量指标,不仅取决于[18F]FEDAC与TSPO的结合,还取决于血液输入率的增加。因此,在SRTM分析中,我们使用R1(探针传递的指标)校正了明显的BPND。在验证研究中,以小脑为参照,SRTM分析与校正后的BPND (corBPND)在2个中医分析中显示与直接BPND (k3/k4)高度相关。结论corBPND标度法可成功获取TSPO分布的定量PET图像。
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引用次数: 0
Evaluating mRNA Delivery Using Nuclear Medicine 利用核医学评估mRNA传递
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109117
James Humphries , Andrea Witjaksono , Abishek Poudel , Karine Mardon , Mary-anne Migotto , Seth Cheetham , Christopher Howard , Kristofer Thurecht
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引用次数: 0
Imaging with Nanobody-based bimodal PET/fluorescence tracers for improved clinical decision making 基于纳米体的双峰PET/荧光示踪剂成像改善临床决策
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109148
Jelena Saliën , Sam Floru , Romane Vizier , Jessica Bridoux , Victor Goncalves , Franck Denat , Sophie Hernot
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引用次数: 0
Development and Validation of Blood-Brain Barrier-Penetrating Bispecific Antibodies for Brain ImmunoPET in Alzheimer's Disease and Glioblastoma 用于阿尔茨海默病和胶质母细胞瘤的脑免疫pet血脑屏障穿透双特异性抗体的研制和验证
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109102
Lara Garcia-Varela , Dag Sehlin , Alberto Ouro , Jessica Codesido , María Muñoz , Sahar Roshanbin , Emma Ramos-Docampo , Ximena Aguilar , Noemí Gómez-Lado , Tomás Sobrino , Pablo Aguiar , Stina Syvaenen
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引用次数: 0
Delivery of the Auger Therapeutic [125I]IUdR via Nanocarriers for Treatment of Glioblastoma 纳米载体输送俄格治疗[125I]IUdR治疗胶质母细胞瘤
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109173
Natan Straathof , Qing Tang , Aaraby Nielsen , Katharina Ravn , Vigga Gammelsrød , Amaia Huarte Lorens , Mikkel Andersen , Matthias Herth , Bo Halle , Helge Thisgaard , Andreas Jensen
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引用次数: 0
A cGMP-Compliant Multi-Dose Synthesis of 6-[18F]Fluoro-L-m-tyrosine ([18F]FMT) on the Trasis AllInOne Synthesizer via an Orthogonal RP/Chiral HPLC Purification 基于正交RP/手性高效液相色谱法的Trasis AllInOne多剂量合成6-[18F]氟- l -m-酪氨酸([18F]FMT
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109160
Madelyn Hallisey, Jacob Hooker, Joseph Downey
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引用次数: 0
Ubiquitin-specific protease 14 (USP14): An emerging biomarker for molecular imaging of cancer. 泛素特异性蛋白酶14 (USP14):一种新兴的癌症分子成像生物标志物。
IF 3 4区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2025-11-01 Epub Date: 2025-11-10 DOI: 10.1016/j.nucmedbio.2025.109190
Jenilee Woodfield, Melinda Wuest, Frank Wuest
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引用次数: 0
期刊
Nuclear medicine and biology
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