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Occupational Intakes of Radionuclides Part 1 - ICRP

Occupational Intakes of Radionuclides Part 1 - ICRP

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DRAFT REPORT FOR CONSULTATION<br />

be different and 241 Am lung results may underestimate Pu activity in the lung (e.g.<br />

nitrate aerosols).<br />

6.4 Measurements<br />

6.4.1 Data Collection and Processing<br />

(335) Some types <strong>of</strong> measurement data may need processing before use. Examples<br />

include:<br />

Lung. Generally, the combined activity in lungs and thoracic lymph nodes is<br />

referred to as ‘lung’ activity, and it is this quantity that is calculated by internal<br />

dosimetry s<strong>of</strong>tware. Where estimates <strong>of</strong> lung and lymph activity are given<br />

separately, they should be summed. ‘Chest’ measurements may also include<br />

counts from activity in liver and skeleton for radionuclides that concentrate in<br />

these tissues and their contributions will be needed to be subtracted.<br />

Urine and faecal samples collected over periods less than 24 hours should in<br />

general be normalized to an equivalent 24 hour value. This can be achieved by<br />

multiplying by the ratio <strong>of</strong> the reference 24 hour excretion volume or mass to<br />

the volume or mass <strong>of</strong> the sample. The reference volumes, for males and<br />

females respectively, are: for urine 1.6 litres and 1.2 litres; and for faeces 150 g<br />

and 120 g (<strong>ICRP</strong>, 2002a). For urine sampling, another widely used method is<br />

to normalise to the amount <strong>of</strong> creatinine excreted per day; 1.7 g and 1.0 g for<br />

males and females respectively (<strong>ICRP</strong>, 2002a). If the 24 hour sample is less<br />

than 500 ml for urine or less than 60 g for faeces, then it is doubtful that it has<br />

been collected over a full 24 hour period and normalization should be<br />

considered. Collection <strong>of</strong> faecal samples should preferentially cover a period<br />

<strong>of</strong> about three days, as the transit time through the alimentary tract is subject to<br />

large inter (and intra-) subject variations.<br />

(336) For some radionuclides the collection <strong>of</strong> spot samples are sufficient for<br />

routine sampling, e.g. the monitoring <strong>of</strong> intakes <strong>of</strong> tritiated water.<br />

6.4.2 Single Measurements, Acute <strong>Intakes</strong><br />

Special monitoring<br />

(337) For special or task-related monitoring when the time <strong>of</strong> intake is known, the<br />

intake can be estimated from the measured results using the m(t) values given in<br />

subsequent reports <strong>of</strong> this series. An m(t) value is a value <strong>of</strong> a bioassay quantity<br />

measured at time t after a unit intake <strong>of</strong> a specified radionuclide, sometimes known as<br />

a retention or excretion function. If only a single measurement is made, the intake, I,<br />

can be determined from the measured quantity, M, if the contribution <strong>of</strong> previous<br />

intakes to the measured quantity M is negligible.<br />

I <br />

M<br />

mt<br />

121<br />

(6.1)<br />

(338) The intake should be multiplied by the dose coefficient (eij, for pathway i and<br />

radionuclide j) to obtain the committed effective dose E:<br />

E(50) = eij × I (6.2)

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