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首页> 外文期刊>Nuclearmedicine >Biodistribution and dosimetry of 195mPt-cisplatin in normal volunteers: Imaging agent for single photon emission computed tomography [Biodistribution und dosimetrie von 195mPt-cisplatin bei gesunden probanden bildgebendes radionuklid für die einzelphotonen-emissionscomputertomographie]
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Biodistribution and dosimetry of 195mPt-cisplatin in normal volunteers: Imaging agent for single photon emission computed tomography [Biodistribution und dosimetrie von 195mPt-cisplatin bei gesunden probanden bildgebendes radionuklid für die einzelphotonen-emissionscomputertomographie]

机译:正常志愿者中195mPt-顺铂的生物分布和剂量测定:单光子发射计算机体层摄影术成像剂。

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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 bio distribution 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).
机译:195mPt-顺铂被认为是用于优化接受顺铂化疗的患者剂量的有前景的成像剂。方法:我们研究了195mPt-顺铂在人体中的全身分布和辐射剂量。在五个对象中的每一个中,静脉内注射112.4 MBq 195mPt-顺铂后至144 h进行全身扫描。在注射后直至144小时的不同时间采集血样。注射后长达114小时收集尿液,以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特定于器官的几何平均数拟合到相应图像上作为注射后时间的函数来生成时间/活动曲线。应用OLINDA软件包来计算各个器官的吸收辐射剂量。结果:在头5小时内,大部分活动(32±4%)从尿液中排出。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,肾脏接受最高剂量(平均剂量为2.68±1.5 mG​​y / MBq),其次是脾脏(平均剂量为1.6±0.8 mGy / MBq),其次是肝脏(平均剂量为1.45±0.38 mGy / MBq)。 / MBq)。成人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,可用于the膜上方病理的早期和延迟成像。获得的ED为0.185±0.034mSv / MBq。肾脏接受最高的器官剂量(2.68±1.5 mG​​y / MBq)。

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