Literature DB >> 20838097

The CONRAD approach to biokinetic modeling of DTPA decorporation therapy.

Bastian Breustedt1, Eric Blanchardon, Philippe Bérard, Paul Fritsch, Augusto Giussani, Maria Antonia Lopez, Andrea Luciani, Dietmar Nosske, Jean Piechowski, Jutta Schimmelpfeng, Anne-Laure Sérandour.   

Abstract

Diethylene Triamine Pentaacetic Acid (DTPA) is used for decorporation of plutonium because it is known to be able to enhance its urinary excretion for several days after treatment by forming stable Pu-DTPA complexes. The decorporation prevents accumulation in organs and results in a dosimetric benefit, which is difficult to quantify from bioassay data using existing models. The development of a biokinetic model describing the mechanisms of actinide decorporation by administration of DTPA was initiated as a task in the European COordinated Network on RAdiation Dosimetry (CONRAD). The systemic biokinetic model from Leggett et al. and the biokinetic model for DTPA compounds of International Commission on Radiological Protection Publication 53 were the starting points. A new model for biokinetics of administered DTPA based on physiological interpretation of 14C-labeled DTPA studies from literature was proposed by the group. Plutonium and DTPA biokinetics were modeled separately. The systems were connected by means of a second order kinetics process describing the chelation process of plutonium atoms and DTPA molecules to Pu-DTPA complexes. It was assumed that chelation only occurs in the blood and in systemic compartment ST0 (representing rapid turnover soft tissues), and that Pu-DTPA complexes and administered forms of DTPA share the same biokinetic behavior. First applications of the CONRAD approach showed that the enhancement of plutonium urinary excretion after administration of DTPA was strongly influenced by the chelation rate constant. Setting it to a high value resulted in a good fit to the observed data. However, the model was not yet satisfactory since the effects of repeated DTPA administration in a short time period cannot be predicted in a realistic way. In order to introduce more physiological knowledge into the model several questions still have to be answered. Further detailed studies of human contamination cases and experimental data will be needed in order to address these issues. The work is now continued within the European Radiation Dosimetry Group, EURADOS.

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Year:  2010        PMID: 20838097     DOI: 10.1097/HP.0b013e3181bfba02

Source DB:  PubMed          Journal:  Health Phys        ISSN: 0017-9078            Impact factor:   1.316


  3 in total

1.  EURADOS strategic research agenda: vision for dosimetry of ionising radiation.

Authors:  W Rühm; E Fantuzzi; R Harrison; H Schuhmacher; F Vanhavere; J Alves; J F Bottollier Depois; P Fattibene; Ž Knežević; M A Lopez; S Mayer; S Miljanić; S Neumaier; P Olko; H Stadtmann; R Tanner; C Woda
Journal:  Radiat Prot Dosimetry       Date:  2015-03-09       Impact factor: 0.972

2.  The Incorporation of Radionuclides After Wounding by a "Dirty Bomb": The Impact of Time for Decorporation Efficacy and a Model for Cases of Disseminated Fragmentation Wounds.

Authors:  Alexis Rump; Daniela Stricklin; Andreas Lamkowski; Stefan Eder; Michael Abend; Matthias Port
Journal:  Adv Wound Care (New Rochelle)       Date:  2017-01-01       Impact factor: 4.730

3.  Managing Internal Radiation Contamination Following an Emergency: Identification of Gaps and Priorities.

Authors:  Chunsheng Li; Armin Ansari; George Etherington; Jean-Rene Jourdain; Boris Kukhta; Osamu Kurihara; Maria Antonia Lopez; Florence Ménétrier; Arlene Alves Dos Reis; Stephen Solomon; Jiangfeng Zhang; Zhanat Carr
Journal:  Radiat Prot Dosimetry       Date:  2016-08-12       Impact factor: 0.972

  3 in total

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