Literature DB >> 15534069

Evaluation of parameters influencing S values in mouse dosimetry.

Cecilia Hindorf1, Michael Ljungberg, Sven-Erik Strand.   

Abstract

UNLABELLED: Clinical radionuclide therapy studies are commonly preceded by studies with small animals. Reliable evaluation of therapeutic efficacy must be based on accurate dosimetry. This study was performed to evaluate the influence of the mass of organs, the shape of organs, and the distances between organs on S values for mice.
METHODS: A voxel-based version of a geometric model of a mouse was developed for input in our Monte Carlo program based on EGS4. Simulations were made for each source organ separately to resolve the S values for each organ. For verification purposes, S values were calculated for spheres of different masses and compared with the S values in the MIRDOSE3.1 software and with the S values on the Radiation Dose Assessment Resource Web site. The variation in the mass of the organs was determined from dissected mice. The influence of the shape of an organ was investigated by successive elongation of a sphere into spheroids with a constant mass. The right kidney was moved in the phantom of the mouse to evaluate the effect of organ distances on S values. The absorbed fractions for the mouse model presented here were compared with the results from some previously published models. The radionuclides used were (90)Y, (131)I, (111)In, and (99m)Tc.
RESULTS: The results showed that the organ mass for one animal can differ by up to 33% from the mean mass. If linear interpolation from S value tables is used to obtain an S value for the specific mass of an organ, then the S value can differ by up to 80% from its true value. The corresponding deviation obtained by scaling according to mass is 20%. The shape of an organ was found to be the least important parameter for the S value. The cross-absorbed S value is strongly dependent on the geometry and the emitted radiation. For example, a 9.2-mm movement of the kidney can cause the S value from the liver to the right kidney to decrease to 0.05% of its original value for (90)Y.
CONCLUSION: We conclude that the mass and the shape of organs and their locations relative to each other have considerable effects on mouse dosimetry.

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Year:  2004        PMID: 15534069

Source DB:  PubMed          Journal:  J Nucl Med        ISSN: 0161-5505            Impact factor:   10.057


  10 in total

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3.  Assessment of S values in stylized and voxel-based rat models for positron-emitting radionuclides.

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Review 5.  Preclinical Voxel-Based Dosimetry in Theranostics: a Review.

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7.  Pre-clinical quantitative imaging and mouse-specific dosimetry for 111In-labelled radiotracers.

Authors:  Ana M Denis-Bacelar; Sarah E Cronin; Chiara Da Pieve; Rowena L Paul; Sue A Eccles; Terence J Spinks; Carol Box; Adrian Hall; Jane K Sosabowski; Gabriela Kramer-Marek; Glenn D Flux
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8.  Estimation of Photon Specific Absorbed Fractions in Digimouse Voxel Phantom using Monte Carlo Simulation Code FLUKA.

Authors:  A Sinha; H K Patni; B M Dixit; N K Painuly; N Singh
Journal:  J Biomed Phys Eng       Date:  2016-12-01

9.  Evaluation of Electron Specific Absorbed Fractions in Organs of Digimouse Voxel Phantom Using Monte Carlo Simulation Code FLUKA.

Authors:  A Sinha; N Singh; B M Dixit; N K Painuly; H K Patni; A Yadav
Journal:  J Biomed Phys Eng       Date:  2019-04-01

10.  Quantification of Macrophage-Driven Inflammation During Myocardial Infarction with 18F-LW223, a Novel TSPO Radiotracer with Binding Independent of the rs6971 Human Polymorphism.

Authors:  Mark G MacAskill; Agne Stadulyte; Lewis Williams; Timaeus E F Morgan; Nikki L Sloan; Carlos J Alcaide-Corral; Tashfeen Walton; Catriona Wimberley; Chris-Anne McKenzie; Nick Spath; William Mungall; Ralph BouHaidar; Marc R Dweck; Gillian A Gray; David E Newby; Christophe Lucatelli; Andrew Sutherland; Sally L Pimlott; Adriana A S Tavares
Journal:  J Nucl Med       Date:  2020-08-28       Impact factor: 11.082

  10 in total

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