首页> 外文期刊>Clinical nuclear medicine >Safety, Biodistribution, and Dosimetry of 123I-6-Deoxy-6-Iodo-D-Glucose, a Tracer of Glucose Transport, in Healthy and Diabetic Volunteers
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Safety, Biodistribution, and Dosimetry of 123I-6-Deoxy-6-Iodo-D-Glucose, a Tracer of Glucose Transport, in Healthy and Diabetic Volunteers

机译:123i-6-脱氧-6-Iodo-D-葡萄糖,葡萄糖运输的示踪剂,健康和糖尿病志愿者,安全性,生物分布和剂量测定法

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Purpose Insulin resistance is a key feature of the metabolic syndrome and type 2 diabetes, in which noninvasive assessment is not currently allowed by any methodology. We previously validated an iodinated tracer of glucose transport (6DIG) and a new methodology for the in vivo quantification of cardiac insulin resistance in rodents. The aim of this study was to investigate the safety, biodistribution, and radiation dosimetry of this method using I-123-6DIG in 5 healthy and 6 diabetic volunteers. Methods The collection of adverse effects (AEs) and medical supervision of vital parameters and biological variables allowed the safety evaluation. Biodistribution was studied by sequentially acquiring whole-body images at 1, 2, 4, 8, and 24 hours postinjection. The total number of disintegrations in each organ normalized to the injected activity was calculated as the area under the time-activity curves. Dosimetry calculations were performed using OLINDA/EXM. Results No major adverse events were observed. The average dose corresponding to the 2 injections of I-123-6DIG used in the protocol was 182.1 +/- 7.5 MBq. A fast blood clearance of I-123-6DIG was observed. The main route of elimination was urinary, with greater than 50% of urine activity over 24 hours. No blood or urine metabolite was detected. I-123-6DIG accumulation mostly occurred in elimination organs such as kidneys and liver. Mean radiation dosimetry calculations indicated an effective whole-body absorbed dose of 3.35 +/- 0.57 mSv for the whole procedure. Conclusions I-123-6DIG was well tolerated in human with a dosimetry profile comparable to that of other commonly used iodinated tracers, thereby allowing further clinical development of the tracer.
机译:目的胰岛素抵抗是代谢综合征和2型糖尿病的关键特征,其中任何方法都不允许非侵入性评估。我们以前经过验证了葡萄糖传输(6dig)的碘化型示踪剂和啮齿动物中心脏胰岛素抵抗的体内含有新方法。本研究的目的是研究这种方法的安全性,生物分布和辐射剂量,在5个健康和6个糖尿病志愿者中使用I-123-6dig。方法采集不利影响(AES)和生命参数的医学监督和生物变量允许安全评估。通过在1,2,4,8和24小时发布假射的全身图像来研究生物分布。计算为注射活性的每个器官中的崩解总数作为时间活性曲线下的区域计算。使用Olinda / EXM进行剂量测定计算。结果未观察到主要不良事件。对应于在方案中使用的I-123-6dig的2个注射的平均剂量为182.1 +/- 7.5 MBQ。观察到I-123-6dig的快速清除。主要的消除途径是尿,超过24小时的尿液活动的50%。未检测到血液或尿液代谢物。 I-123-6dig积累主要发生在肾脏和肝脏等消除器官中。平均辐射剂量测定计算表明整个程序的有效全身吸收剂量为3.35 +/- 0.57msV。结论I-123-6dig在人中具有良好的耐受剂量型,所述剂量分布与其他常用的碘化碘型示踪剂相当,从而允许示踪剂的进一步临床开发。

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