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99mTc-HYNIC-膜联蛋白V的安全性、生物分布及剂量测定,一种用于人体的新型重组人膜联蛋白V。

Safety, biodistribution, and dosimetry of 99mTc-HYNIC-annexin V, a novel human recombinant annexin V for human application.

作者信息

Kemerink Gerrit J, Liu Xuan, Kieffer Davy, Ceyssens Sarah, Mortelmans Luc, Verbruggen Alfons M, Steinmetz Neil D, Vanderheyden Jean-Luc, Green Allan M, Verbeke Kristin

机构信息

Department of Nuclear Medicine, University Hospital Maastricht, Maastricht, The Netherlands.

出版信息

J Nucl Med. 2003 Jun;44(6):947-52.

Abstract

UNLABELLED

99mTc-hydrazinonicotinamido (HYNIC)-annexin V is a novel tracer for in vivo imaging of apoptosis. The present study on humans was performed to investigate the safety of (99m)Tc-HYNIC-annexin V and to quantify the biodistribution and radiation dose.

METHODS

Six healthy, male volunteers participated in the study. A dual-head gamma camera was used to acquire conjugate anterior and posterior views. Imaging started with a transmission scan using a (57)Co-flood source to obtain a map of the local thickness of the volunteer. Approximately 250 MBq of (99m)Tc-HYNIC-annexin V were injected intravenously, directly followed by a 30-min dynamic study. Whole-body scans were obtained at about 30 min, 3 h, 6 h, and 24 h after injection. Organ uptake was determined after correction for background, scatter, and attenuation. The MIRDOSE3.1 program was used to calculate organ-absorbed doses and effective dose. Signs of adverse effects were investigated by monitoring renal and liver function, hematology, blood coagulation, and vital signs (blood pressure, pulse, respiration rate, temperature, and electrocardiogram).

RESULTS

The kidneys accumulated 49.7 +/- 8.1 percentage injected dose (%ID) at 3 h after injection; the liver, 13.1 +/- 1.0 %ID; the red marrow, 9.2 +/- 1.8 %ID; and the spleen, 4.6 +/- 1.6 %ID. More than 90% of the blood activity was cleared with a half-life of 24 +/- 3 min. The biologic half-life of the activity registered over the total body was long (69 +/- 7 h). Excretion of the activity was almost exclusively through the urine (22.5 +/- 3.5 %ID at 24 h), and hardly any activity was seen in the bowel or feces. Absorbed doses were found to be 196 +/- 31 micro Gy/MBq for the kidneys, 41 +/- 12 micro Gy/MBq for the spleen, 16.9 +/- 1.3 micro Gy/MBq for the liver, and 8.4 +/- 0.9 micro Gy/MBq for the red marrow. The effective dose was 11.0 +/- 0.8 micro Sv/MBq, or 2.8 +/- 0.2 mSv for the average injected activity of 250 MBq. No adverse effects were observed.

CONCLUSION

(99m)Tc-HYNIC-annexin V is a safe radiopharmaceutical, having a favorable biodistribution for imaging of apoptosis in the abdominal as well as thoracic area with an acceptable radiation dose.

摘要

未标记

99mTc-肼基烟酰胺(HYNIC)-膜联蛋白V是一种用于细胞凋亡体内成像的新型示踪剂。本研究针对人类进行,旨在调查99mTc-HYNIC-膜联蛋白V的安全性,并对其生物分布和辐射剂量进行量化。

方法

六名健康男性志愿者参与了本研究。使用双头伽马相机采集前后位联合图像。成像首先使用57Co泛源进行透射扫描,以获取志愿者局部厚度的图谱。静脉注射约250 MBq的99mTc-HYNIC-膜联蛋白V,随后立即进行30分钟的动态研究。在注射后约30分钟、3小时、6小时和24小时进行全身扫描。在对背景、散射和衰减进行校正后确定器官摄取情况。使用MIRDOSE3.1程序计算器官吸收剂量和有效剂量。通过监测肾功能、肝功能、血液学、凝血功能和生命体征(血压、脉搏、呼吸频率、体温和心电图)来调查不良反应迹象。

结果

注射后3小时,肾脏摄取量为49.7±8.1%注射剂量(%ID);肝脏为13.1±1.0 %ID;红骨髓为9.2±1.8 %ID;脾脏为4.6±1.6 %ID。超过90%的血液放射性以24±3分钟的半衰期清除。全身放射性的生物半衰期较长(69±7小时)。放射性几乎完全通过尿液排出(24小时时为22.5±3.5 %ID),肠道或粪便中几乎未见放射性。发现肾脏的吸收剂量为196±31微戈瑞/MBq,脾脏为41±12微戈瑞/MBq,肝脏为16.9±1.3微戈瑞/MBq,红骨髓为8.4±0.9微戈瑞/MBq。有效剂量为11.0±0.8微希沃特/MBq,对于平均注射活度250 MBq,有效剂量为2.8±0.2毫希沃特。未观察到不良反应。

结论

99mTc-HYNIC-膜联蛋白V是一种安全的放射性药物,在腹部和胸部区域用于细胞凋亡成像具有良好的生物分布,且辐射剂量可接受。

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