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本文引用的文献

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Uncertainties in internal dose calculations for radiopharmaceuticals.放射性药物内照射剂量计算中的不确定性。
J Nucl Med. 2008 May;49(5):853-60. doi: 10.2967/jnumed.107.048132. Epub 2008 Apr 15.
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Voxel-based mouse and rat models for internal dose calculations.
J Nucl Med. 2006 Apr;47(4):655-9.
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Evaluation of parameters influencing S values in mouse dosimetry.小鼠剂量测定中影响S值的参数评估。
J Nucl Med. 2004 Nov;45(11):1960-5.
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A stylized computational model of the rat for organ dosimetry in support of preclinical evaluations of peptide receptor radionuclide therapy with (90)Y, (111)In, or (177)Lu.一种用于大鼠器官剂量测定的程式化计算模型,以支持用(90)钇、(111)铟或(177)镥进行肽受体放射性核素治疗的临床前评估。
J Nucl Med. 2004 Jul;45(7):1260-9.
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The application of voxel phantoms to the internal dosimetry of radionuclides.体素体模在放射性核素内照射剂量学中的应用。
Radiat Prot Dosimetry. 2003;105(1-4):539-48. doi: 10.1093/oxfordjournals.rpd.a006299.
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Murine S factors for liver, spleen, and kidney.
J Nucl Med. 2003 May;44(5):784-91.
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Decay data for internal and external dose assessment.用于内照射和外照射剂量评估的衰变数据。
Health Phys. 2002 Oct;83(4):471-5. doi: 10.1097/00004032-200210000-00004.
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The GSF family of voxel phantoms.
Phys Med Biol. 2002 Jan 7;47(1):89-106. doi: 10.1088/0031-9155/47/1/307.
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A mouse model for calculating the absorbed beta-particle dose from (131)I- and (90)Y-labeled immunoconjugates, including a method for dealing with heterogeneity in kidney and tumor.一种用于计算来自¹³¹I和⁹⁰Y标记免疫缀合物的β粒子吸收剂量的小鼠模型,包括一种处理肾脏和肿瘤异质性的方法。
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A mouse bone marrow dosimetry model.
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用于剂量评估的雷达现实动物模型系列。

RADAR realistic animal model series for dose assessment.

机构信息

Department of Radiology and Radiological Sciences, Vanderbilt University, Nashville, Tennessee, USA.

出版信息

J Nucl Med. 2010 Mar;51(3):471-6. doi: 10.2967/jnumed.109.070532.

DOI:10.2967/jnumed.109.070532
PMID:20197451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2929767/
Abstract

UNLABELLED

Rodent species are widely used in the testing and approval of new radiopharmaceuticals, necessitating murine phantom models. As more therapy applications are being tested in animal models, calculating accurate dose estimates for the animals themselves becomes important to explain and control potential radiation toxicity or treatment efficacy. Historically, stylized and mathematically based models have been used for establishing doses to small animals. Recently, a series of anatomically realistic human phantoms was developed using body models based on nonuniform rational B-spline. Realistic digital mouse whole-body (MOBY) and rat whole-body (ROBY) phantoms were developed on the basis of the same NURBS technology and were used in this study to facilitate dose calculations in various species of rodents.

METHODS

Voxel-based versions of scaled MOBY and ROBY models were used with the Vanderbilt multinode computing network (Advanced Computing Center for Research and Education), using geometry and tracking radiation transport codes to calculate specific absorbed fractions (SAFs) with internal photon and electron sources. Photon and electron SAFs were then calculated for relevant organs in all models.

RESULTS

The SAF results were compared with values from similar studies found in reference literature. Also, the SAFs were used with standardized decay data to develop dose factors to be used in radiation dose calculations. Representative plots were made of photon electron SAFs, evaluating the traditional assumption that all electron energy is absorbed in the source organs.

CONCLUSION

The organ masses in the MOBY and ROBY models are in reasonable agreement with models presented by other investigators noting that considerable variation can occur between reported masses. Results consistent with those found by other investigators show that absorbed fractions for electrons for organ self-irradiation were significantly less than 1.0 at energies above 0.5 MeV, as expected for many of these small-sized organs, and measurable cross-irradiation was observed for many organ pairs for high-energy electrons (as would be emitted by nuclides such as (32)P, (90)Y, or (188)Re).

摘要

目的

啮齿动物种类广泛用于新放射性药物的测试和批准,因此需要建立鼠类模型。随着更多的治疗应用在动物模型中进行测试,准确计算动物自身的剂量估计变得非常重要,以便解释和控制潜在的辐射毒性或治疗效果。历史上,为小动物建立剂量使用了简化和基于数学的模型。最近,开发了一系列基于非均匀有理 B 样条的体模型的解剖学逼真的人体模型。在此基础上,使用相同的 NURBS 技术开发了逼真的数字鼠整体(MOBY)和鼠整体(ROBY)模型,并在本研究中用于促进各种啮齿动物的剂量计算。

方法

使用比例缩放的 MOBY 和 ROBY 模型的体素版本,结合范德比尔特多节点计算网络(高级计算研究与教育中心),使用几何和跟踪辐射传输代码,计算内部光子和电子源的特定吸收分数(SAF)。然后,为所有模型中的相关器官计算光子和电子 SAF。

结果

将 SAF 结果与参考文献中类似研究的结果进行比较。此外,还使用标准化的衰变数据计算剂量因子,用于辐射剂量计算。制作了光子电子 SAF 的代表性图,评估了所有电子能量都在源器官中吸收的传统假设。

结论

MOBY 和 ROBY 模型中的器官质量与其他研究人员提出的模型基本一致,注意到报告的质量之间可能存在相当大的差异。与其他研究人员发现的结果一致,结果表明,对于许多这些小尺寸的器官,高于 0.5 MeV 的电子自照射的吸收分数明显小于 1.0,对于许多器官对高能电子的交叉照射也可以观察到(如(32)P、(90)Y 或(188)Re 等核素发射的电子)。