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18F-氟代赤藓红硝基咪唑在癌症研究中的辐射剂量测定

18F-Fluoroerythronitroimidazole radiation dosimetry in cancer studies.

作者信息

Tolvanen Tuula, Lehtiö Kaisa, Kulmala Jarmo, Oikonen Vesa, Eskola Olli, Bergman Jörgen, Minn Heikki

机构信息

Turku PET Centre, Turku University Central Hospital, Turku, Finland.

出版信息

J Nucl Med. 2002 Dec;43(12):1674-80.

Abstract

UNLABELLED

18F-Fluoroerythronitromidazole (FETNIM) is a new promising PET tracer for imaging tumor hypoxia. Accurate radiation dosimetry is important for estimating absorbed radiation doses to patients and for calculating the allowable injected dose.

METHODS

Radiation absorbed doses were estimated from PET scans obtained on cancer patients on the basis of the MIRD procedure. Dynamic acquisition data was obtained from the thorax, abdomen, and head and neck regions. The tracer was injected intravenously and mean injected activity was 366 MBq (range, 288-385 MBq). Arterial blood was continuously assayed over dynamic PET imaging. The bladder wall dose was evaluated from the voided urine activity measurements.

RESULTS

The effective dose to a 70-kg adult was 0.015 or 0.019 mSv/MBq, calculated on 2- or 4-h voiding intervals, respectively. The critical organ proved to be the urinary bladder wall, with a highest absorbed dose of 0.062 or 0.127 mGy/MBq depending on the voiding schedule as described above. Absorbed doses in all other organs were at least 5-fold smaller than the bladder wall doses.

CONCLUSION

With an injected activity of 370 MBq (18)F-FETNIM, the radiation doses are generally comparable with those of other related radionuclide imaging procedures. Specifically, in comparison with (18)F-fluoromisonidazole, the absorbed doses of (18)F-FETNIM are equal. However, special attention should be given to adequate hydration and voiding to limit the relatively high exposure of the critical organ, bladder wall, to (18)F-FETNIM.

摘要

未标记

18F-氟代赤藓红硝基咪唑(FETNIM)是一种用于肿瘤缺氧成像的新型有前景的正电子发射断层显像(PET)示踪剂。准确的辐射剂量测定对于估计患者吸收的辐射剂量以及计算允许的注射剂量很重要。

方法

根据医学内照射剂量(MIRD)程序,从癌症患者的PET扫描中估计辐射吸收剂量。动态采集数据来自胸部、腹部以及头颈部区域。示踪剂通过静脉注射,平均注射活度为366 MBq(范围为288 - 385 MBq)。在动态PET成像过程中持续检测动脉血。通过测量排尿后的尿液活度来评估膀胱壁剂量。

结果

对于一名70千克的成年人,分别根据2小时或4小时的排尿间隔计算,有效剂量为0.015或0.019 mSv/MBq。关键器官被证明是膀胱壁,根据上述排尿时间表,最高吸收剂量为0.062或0.127 mGy/MBq。所有其他器官的吸收剂量至少比膀胱壁剂量小5倍。

结论

注射活度为370 MBq的18F-FETNIM,其辐射剂量总体上与其他相关放射性核素成像程序的剂量相当。具体而言,与18F-氟代米索硝唑相比,18F-FETNIM的吸收剂量相等。然而,应特别注意充分补水和排尿,以限制关键器官膀胱壁对18F-FETNIM的相对高暴露。

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