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195mPt-顺铂在正常志愿者体内的生物分布与剂量测定。单光子发射计算机断层扫描成像剂。

Biodistribution and dosimetry of 195mPt-cisplatin in normal volunteers. Imaging agent for single photon emission computed tomography.

作者信息

Sathekge M, Wagener J, Smith S V, Soni N, Marjanovic-Painter B, Zinn C, Van de Wiele C, D'Asseler Y, Perkins G, Zeevaart J R

机构信息

Prof. Dr. Mike Sathekge, University of Pretoria, Steve Biko Academic Hospital Private Bag X169, Pretoria 0001, South-Africa, Tel. 01 23 54 17 94, Fax 01 23 54 12 19, E-mail:

出版信息

Nuklearmedizin. 2013 Dec 13;52(6):222-7. doi: 10.3413/Nukmed-0599-13-06. Epub 2013 Oct 10.

Abstract

UNLABELLED

195mPt-cisplatin is regarded as a promising imaging agent for optimizing dosage in patients receiving cisplatin chemotherapy.

METHODS

We investigated the whole-body distribution and radiation dosimetry of 195mPt-cisplatin in humans. Whole-body scans were obtained up to 144 h after intravenous injection of 112.4 MBq 195mPt-cisplatin in each of five subjects. Blood samples were taken at various times up to 144 h after injection. Urine was collected up to 114 h after injection for calculation of renal clearance and whole-body clearance. Time/activity curves were generated by fitting the organ-specific geometric mean counts, obtained from regions of interest, on the respective images as a function of the time after injection. OLINDA software package was applied to calculate the absorbed radiation dose for various organs.

RESULTS

Most of the activity (32 ± 4%) was excreted in the urine during the first 5 h. The effective clearance half-life derived from extrapolation of the whole-body curve was 40 hours (1.7 days). On average, the highest dose was received by the kidneys (mean dose received 2.68 ± 1.5 mGy/MBq), followed by the spleen (mean dose received 1.6 ± 0.8 mGy/MBq) followed by the liver (mean dose received 1.45 ± 0.38 mGy/MBq). The estimated mean effective dose for the adult subject was 0.185 ± 0.034 mSv/MBq.

CONCLUSION

195mPt-cisplatin proved a safe radiopharmaceutical with a favourable biodistribution for early and delayed imaging of pathology above the diaphragm. The ED obtained was 0.185 ± 0.034 mSv/MBq. The highest organ dose was received by the kidneys (2.68 ± 1.5 mGy/MBq).

摘要

未标记

195mPt - 顺铂被视为一种有前景的成像剂,可用于优化接受顺铂化疗患者的剂量。

方法

我们研究了195mPt - 顺铂在人体中的全身分布和辐射剂量学。对5名受试者每人静脉注射112.4 MBq 195mPt - 顺铂后,在长达144小时内进行全身扫描。在注射后长达144小时的不同时间采集血样。在注射后长达114小时收集尿液,用于计算肾脏清除率和全身清除率。通过将从感兴趣区域获得的器官特异性几何平均计数作为注射后时间的函数,拟合到各自图像上,生成时间/活度曲线。应用OLINDA软件包计算各器官的吸收辐射剂量。

结果

大部分活度(32±4%)在最初5小时内通过尿液排出。由全身曲线外推得出的有效清除半衰期为40小时(1.7天)。平均而言,肾脏接受的剂量最高(平均剂量为2.68±1.5 mGy/MBq),其次是脾脏(平均剂量为1.6±0.8 mGy/MBq),然后是肝脏(平均剂量为1.45±0.38 mGy/MBq)。成年受试者的估计平均有效剂量为0.185±0.034 mSv/MBq。

结论

195mPt - 顺铂被证明是一种安全的放射性药物,具有良好的生物分布,适用于膈上病变的早期和延迟成像。获得的有效剂量为0.185±0.034 mSv/MBq。肾脏接受的器官剂量最高(2.68±1.5 mGy/MBq)。

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