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健康受试者中大麻素 2 型受体配体 [11C]-NE40 的全身生物分布和辐射剂量学。

Whole-body biodistribution and radiation dosimetry of the cannabinoid type 2 receptor ligand [11C]-NE40 in healthy subjects.

机构信息

Division of Nuclear Medicine, University Hospital Leuven, Herestraat 49, 3000, Leuven, Belgium.

出版信息

Mol Imaging Biol. 2013 Aug;15(4):384-90. doi: 10.1007/s11307-013-0626-y.

Abstract

PURPOSE

The type 2 cannabinoid receptor (CB2R) is part of the human endocannabinoid system and is involved in central and peripheral inflammatory processes. In vivo imaging of the CB2R would allow study of several (neuro)inflammatory disorders. In this study we have investigated the safety and tolerability of [11C]-NE40, a CB2R positron emission tomography (PET) ligand, in healthy human male subjects and determined its biodistribution and radiation dosimetry.

PROCEDURE

Six healthy male subjects (age 20-65 years) underwent a dynamic series of nine whole-body PET/CT scans for up to 140 min, after injection of an average bolus of 286 MBq of [11C]-NE40. Organ absorbed and total effective doses were calculated through OLINDA.

RESULTS

[11C]-NE40 showed high initial uptake in the spleen and a predominant hepatobiliary excretion. In the brain, rapid uptake and swift washout were seen. Organ absorbed doses were largest for the small intestine and liver, with 15.6 and 11.5 μGy/MBq, respectively. The mean effective dose was 3.64±0.81 μSv/MBq. There were no changes with aging observed. No adverse events were encountered.

CONCLUSIONS

This first-in-man study of [11C]-NE40 showed an expected biodistribution compatible with lymphoid tissue uptake and appropriate fast brain kinetics in the healthy human brain, underscoring the potential of this tracer for further application in central and peripheral inflammation imaging. The effective dose is within the typical expected range for 11C ligands.

摘要

目的

2 型大麻素受体(CB2R)是人体内源性大麻素系统的一部分,参与中枢和外周炎症过程。CB2R 的体内成像将允许研究几种(神经)炎症性疾病。在这项研究中,我们研究了 [11C]-NE40(一种 CB2R 正电子发射断层扫描 [PET] 配体)在健康男性人体中的安全性和耐受性,并确定了其生物分布和辐射剂量学。

程序

六名健康男性(年龄 20-65 岁)接受了 9 次全身 PET/CT 动态扫描,每次注射平均 286 MBq [11C]-NE40 后的时间长达 140 分钟。通过 OLINDA 计算器官吸收和总有效剂量。

结果

[11C]-NE40 最初在脾脏中摄取量较高,主要通过肝胆排泄。在大脑中,观察到快速摄取和快速清除。小肠和肝脏的器官吸收剂量最大,分别为 15.6 和 11.5 μGy/MBq。平均有效剂量为 3.64±0.81 μSv/MBq。未观察到随年龄变化。未发生不良反应。

结论

[11C]-NE40 的首次人体研究显示,其预期的生物分布与淋巴组织摄取一致,在健康人类大脑中具有适当的快速脑动力学,这突显了该示踪剂在中枢和外周炎症成像中的潜在应用。有效剂量在 11C 配体的典型预期范围内。

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