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[11C]MeAIB的人体辐射剂量测定,一种用于系统A氨基酸转运成像的新型示踪剂。

Human radiation dosimetry of [11C]MeAIB, a new tracer for imaging of system A amino acid transport.

作者信息

Tolvanen Tuula, Någren Kjell, Yu Meixiang, Sutinen Eija, Havu-Aurén Katja, Jyrkkiö Sirkku, Asola Markku, Kotoneva Eira, Nuutila Pirjo, Minn Heikki

机构信息

Turku PET Centre, Turku University Hospital, P.O. Box 52, 20521, Turku, Finland.

出版信息

Eur J Nucl Med Mol Imaging. 2006 Oct;33(10):1178-84. doi: 10.1007/s00259-006-0096-4. Epub 2006 May 24.

Abstract

PURPOSE

[N-methyl-11C]alpha-methylaminoisobutyric acid ([11C]MeAIB) is a promising positron emission tomography (PET) tracer for imaging hormonally regulated system A amino acid transport. Uptake of [11C]MeAIB is totally specific for amino acid transport since [11C]MeAIB is metabolically stable both extra- and intracellularly. The aim of this study was to measure cumulated radioactivity in different organs and estimate the absorbed radiation doses to humans with the Medical Internal Radiation Dosimetry (MIRD) method.

METHODS

Radiation absorbed doses were calculated from PET images for 25 volunteers. Dynamic acquisition data were obtained for the thoracic, abdominal, femoral and head and neck regions. The median dose of intravenously injected [11C]MeAIB was 422+/-35 MBq, with a range of 295-493 MBq. After PET imaging the radioactivity in voided urine was measured. Experimental human data were used for residence time estimates. Radiation doses were calculated with commonly used software.

RESULTS

The effective dose for a 70-kg adult was 0.004 mSv/MBq, corresponding to a 1.72 mSv effective dose from the PET study with injection of 430 MBq [11C]MeAIB. The highest absorbed doses were in the pancreas (0.018 mGy/MBq), kidneys (0.017 mGy/MBq), intestine (0.014 mGy/MBq), liver (0.008 mGy/MBq) and stomach (0.005 mGy/MBq). Only 0.57% of injected activity was excreted to urine within 1 h after injection.

CONCLUSION

Biodistribution of [11C]MeAIB in the abdominal region reflected the high activity of the transportation of amino acids via system A and these organs also had the highest radiation doses. An effective dose of 0.004 mSv/MBq is fully justified when [11C]MeAIB PET is performed to study system A activity in vivo.

摘要

目的

[N-甲基-11C]α-甲基氨基异丁酸([11C]MeAIB)是一种用于对激素调节的系统A氨基酸转运进行成像的有前景的正电子发射断层扫描(PET)示踪剂。[11C]MeAIB的摄取对氨基酸转运具有完全特异性,因为[11C]MeAIB在细胞外和细胞内代谢均稳定。本研究的目的是用医学内照射剂量学(MIRD)方法测量不同器官中的累积放射性,并估算人体吸收的辐射剂量。

方法

根据25名志愿者的PET图像计算辐射吸收剂量。获取胸部、腹部、股骨以及头颈部区域的动态采集数据。静脉注射[11C]MeAIB的中位剂量为422±35 MBq,范围为295 - 493 MBq。PET成像后测量排尿中的放射性。使用实验性人体数据估算驻留时间。用常用软件计算辐射剂量。

结果

70千克成年人的有效剂量为0.004 mSv/MBq,相当于注射430 MBq [11C]MeAIB的PET研究产生的1.72 mSv有效剂量。吸收剂量最高的器官是胰腺(0.018 mGy/MBq)、肾脏(0.017 mGy/MBq)、肠道(0.014 mGy/MBq)、肝脏(0.008 mGy/MBq)和胃(0.005 mGy/MBq)。注射后1小时内仅0.57%的注入活度排泄到尿液中。

结论

[11C]MeAIB在腹部区域的生物分布反映了通过系统A进行的氨基酸高活性转运,并且这些器官的辐射剂量也最高。当进行[11C]MeAIB PET以研究体内系统A活性时,0.004 mSv/MBq的有效剂量是完全合理的。

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