Recent developments in biokinetic models and the calculation of internal dose coefficients

Timothy Fell*, A. W. Phipps, G. M. Kendall, G. N. Stradling

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

In most cases the measurement of radioactivity in an environmental or biological sample will be followed by some estimation of dose and possibly risk, either to a population or an individual. This will normally involve the use of a dose coefficient (dose per unit intake value) taken from a compendium. In recent years the calculation of dose coefficients has seen many developments in both biokinetic modelling and computational capabilities. ICRP has recommended new models for the respiratory tract and for the systemic behavior of many of the more important elements. As well as this, a general age-dependent calculation method has been developed which involves an effectively continuous variation of both biokinetic and dosimetric parameters, facilitating more realistic estimation of doses to young people. These new developments were used in work for recent ICRP, IAEA and CEC compendia of dose coefficients for both members of the public (including children) and workers. This paper presents a general overview of the method of calculation of internal doses with particular reference to the actinides. Some of the implications for dose coefficients of the new models are discussed. For example it is shown that compared with data in ICRP Publications 30 and 54: the new respiratory tract model generally predicts lower deposition in systemic tissues per unit intake; the new biokinetic models for actinides allow for burial of material deposited on bone surfaces; age-dependent models generally feature faster turnover of material in young people. All of these factors can lead to substantially different estimates of dose and examples of the new dose coefficients are given to illustrate these differences. During the development of the new models for actinides, human bioassay data were used to validate the model. Thus, one would expect the new models to give reasonable predictions of bioassay quantities. Some examples of the bioassay applications, e.g., excretion data for the plutonium model, are discussed briefly.

Original languageEnglish
Pages (from-to)109-115
Number of pages7
JournalJournal of Radioanalytical and Nuclear Chemistry Articles
Volume226
Issue number1-2
DOIs
Publication statusPublished - 1997

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