Diagnostic procedures imply the administration of activity levels that do not lead to the appearance of radiation deterministic effects; therefore only stochastic risks have to be considered. This means that the stochastic risk associated with exposure to ionizing radiation cannot be assessed for an individual patient. However, the concept of risk associated with a diagnostic procedure is valid for a population of patients, and requires, as a prerequisite, the determination of the absorbed dose, i.e. the energy absorbed per unit mass (in grays) in all irradiated tissues or organs of interest.

In a diagnostic context, determination of absorbed doses (i.e. a dosimetric study) is also required before the introduction of a new radiopharmaceutical to the market in order to obtain marketing authorization from the relevant agency such as the European Medicines Agency (EMA) or the Food and Drug Administration (FDA). This also helps to determine the range of activity to inject for a given procedure. In addition, “good clinical practice” implies injecting the minimum activity compatible with the diagnostic purpose, and assessing the radiation exposure delivered by that amount of activity.

Hence, the purpose of dosimetry within the context of radiation risk assessment for diagnostic nuclear medicine procedures is twofold:

  1. 1.

    Determination of reference levels of irradiation for every new radiopharmaceutical.

    For a new radiopharmaceutical, the determination of reference levels of irradiation and consequently of the risks associated with the administration first requires an accurate determination of the biokinetics of the tracer. This step is usually carried out via quantitative imaging, blood sampling or excreta measurements in a restricted number of patients (or healthy volunteers). Some data are also derived from preclinical experiments in animals. Pharmacokinetics modelling is also often used at this stage. Then, based on the tracer distribution in space and time, radiation dose is calculated using phantoms, i.e. computational models that mimic organ geometry, organ-to-organ distances, and body composition of patients.

  2. 2.

    Provision of absorbed dose estimates for radiopharmaceuticals in routine use.

    The provision of absorbed dose estimates for radiopharmaceuticals in routine use is generally a simple task since it requires only a patient-specific determination of the administered activity (in megabecquerels), a task performed routinely in nuclear medicine departments prior to injection. Then, using precalculated tables (e.g. the ICRP reports [13]) that for a given radiopharmaceutical give the absorbed dose in organs or tissues for a reference model per injected activity (in megabecquerels), it is possible to derive an estimate of the absorbed dose delivered to a reference person. This step implicitly relies on the hypothesis that the kinetic model chosen to establish precalculated tables satisfactorily reflects the average kinetics of the radiopharmaceutical in subjects of interest.

Evaluation of the impact on patients’ health of the administration of small amounts of radioactive substances, or of amounts that are not or are only infrequently repeated, as currently used in diagnostic imaging procedures, relies heavily on a precise and accurate determination of reference levels of irradiation, and it affects the quality of the data used further for routine diagnostic procedures. This impact, however, has not been addressed systematically in a European context. Data on biokinetics and dosimetry of these agents are reported in diverse and widespread sources and are sometimes difficult to access. Therefore, the European Commission addressed this issue in the framework of the FP 7 HEALTH-2009-1.2-6 project PEDDOSE.NET (“Dosimetry and Health Effects of Diagnostic Applications of Radiopharmaceuticals with particular emphasis on the use in children and adolescents"). One of the main objectives of this project is to summarize and evaluate the current knowledge on dosimetry and the corresponding dose-related risks when administering radiopharmaceuticals for diagnostic purposes in children and adults.

The aim of this review is to provide detailed data on biokinetics and dosimetry for diagnostic radiopharmaceuticals in children and adults, and it focuses on assessing how absorbed doses were derived.

Material and methods

Literature on the available biokinetics and dosimetry data was systematically reviewed, mostly using PubMed ( and the secondary literature cited in the articles found. Primarily, we concentrated on radiopharmaceuticals commonly used in Europe.

The following inclusion criteria were used:

  • Publications of official bodies such as the International Commission on Radiological Protection (ICRP) [13]

  • Peer-reviewed journals

  • Special conference proceedings containing detailed descriptions on methodologies in dosimetry

The literature was searched back to the publication date of ICRP 53 (1987) [1] if there were no other data available. In principle the following criteria for inclusion of data as defined by the EANM Dosimetry Committee guidance document on good clinical reporting [4] were used:

  • The quantitative imaging method used: planar, SPECT(/CT) or PET(/CT), and potential corrections (e.g. attenuation and scatter correction). The fewer corrections the authors applied the higher was the likelihood of increased uncertainties in the assessment of residence times.Footnote 1

  • The availability of data on biokinetics, in particular detailed information on residence times and how they were derived. Providing residence times enables a potential recalculation and reassessment of the absorbed doses and hence the effective dose (ED) if needed.

  • Organ masses can differ by more than a factor of 3 [6]. As a SPECT, PET, CT or MRT scan allow the measurement of organ volumes and therefore masses, several studies have assumed uniform distribution of activity and applied a first-order correction by multiplying the activity concentration by the phantom organ weight, resulting in normalized time–activity curves and residence times.

  • Another aspect of importance is the time-points at which the measurements for determining the time–activity curves were made. To obtain a reliable assessment of the area under the curve, a minimum of three data points is recommended (MIRD 16 [7]) and the time between the first and the last measurement should not be too short, otherwise the absorbed dose would be overestimated when using physical decay after the last data point.

  • Information on bladder voiding intervals is also crucial because for some radiopharmaceuticals (e.g. 18F-fluoride) the absorbed dose to the bladder depends very much on the voiding period and the first voiding after injection; therefore, the ED differs between datasets with different voiding intervals.

  • Detailed information on the absorbed doses to the relevant organs and, if available, the way they were calculated (i.e. the computer code and the source of the S-valuesFootnote 2) are essential, especially for a comparison of the results. Scaling the S-values with individual organ masses is useful for patient dosimetry in radionuclide therapy but deviates from the usual approach for the dosimetry of diagnostic procedures. Furthermore, calculation of ED is not based on individual patient data. Calculating ED according to ICRP is based on reference values for the human body and organs [9].

  • The tissue-weighting factors for describing the radiation-related risk changed in 1991 with the publication of ICRP 60 [10]. In this work the ED was introduced. Prior to ICRP 60 the quantity “effective dose equivalent (EDE)” [11] was used. In 2007 the ICRP (ICRP 103 [9]) published a new set of tissue-weighting factors and a new calculation method. Therefore, when comparing EDs one has to know which tissue weighting factors were used.

  • The reliability of dosimetry data is highly dependent on the number of participants in a study. It is important to know the number of volunteers/patients who took part in a dosimetry study because this affects the variability in individual biokinetics.

In this review a summary of the most important findings is given. Details on the available data in the references sorted according to these criteria are given in the Electronic supplementary material in Tables 1.1–1.4 and 2.1–2.6 for adults and in Tables 3.1–3.4 for children. If there were no data available, the corresponding radiopharmaceuticals are not listed in the table. In addition, the reference values for each radiopharmaceutical taken from the latest respective ICRP report [13] are also listed in order to compare these data with the ED or, if not available, EDE values in the cited references.


The investigated PET and non-PET radiopharmaceuticals with and without marketing authorization are displayed in Tables 1 and 2, respectively.

Table 1 PET radiopharmaceuticals considered in this review indicating their European marketing authorization status. No product names are given for radiopharmaceuticals with more than one trademark
Table 2 Non-PET radiopharmaceuticals considered in this review indicating their European marketing authorization status. No product names are given for radiopharmaceuticals with more than one trademark

In the following sections the most important findings of our literature search are summarized. Further details not provided in the text are given in the corresponding tables in the Electronic supplementary material.

PET radiopharmaceuticals

As a whole-body scan with a PET scanner can take 30 min or more (especially with older PET systems) and the uptake of many PET radiopharmaceuticals occurs within 10 min of injection, many studies involving the detailed measurement of time–activity curves are limited to scanning only one organ per subject. Subsequently, the results of many single-organ measurements are merged into a “virtual” subject for a complete biokinetic model and calculation of absorbed doses. If the number of participants is large enough, individual variations should not be important, but the small size of many studies leads to organ data based on few subjects. In these cases the results have to be viewed with care, as ICRP 106 [3] mentions in the section “Uncertainties in absorbed dose estimates” that intersubject variability may introduce considerable variation in accumulated activity. A detailed analysis of uncertainties in internal dose calculations for radiopharmaceuticals has also been given by Stabin [12].

It is desirable that dosimetric publications include the individual residence times, because in combination with administered activities reanalysis of patient data is feasible if new or different dosimetry and calculation methods should become available [4]. Unfortunately, most studies omit the individual data and state only the mean values and standard deviations, which can only provide a rough estimate of intersubject variance.


Acetate is used in the assessment of myocardial oxidative metabolism [13] and in renal, pancreatic and nasopharyngeal disease [3]. More recently 11C-acetate has become an important tracer for imaging prostate cancer [14, 15]. The only human study on quantitative whole-body imaging is that by Seltzer et al. [15] which included six healthy male volunteers. In this detailed study the individual residence times in all the volunteers were determined for the important organs, and the organ doses were calculated for the mean values using MIRDOSE3.1 [16]. The data were compared with data published by the Oak Ridge Institute for Science and Education (ORISE) in 1995 (no detailed citation information available) which were based on a simple three-compartment model in which all activity not measured in the blood or excreted via the breath was assumed to reside in the heart [15]. The experiments were performed in dogs; activity was measured only in the blood and expired air [17].

The latest ICRP report (ICRP 106 [3]) relies on tabulated blood flow data for most human tissues by Leggett and Williams [18]. The study by Seltzer et al. [15], however, was not used in ICRP 106 [3].


Choline is used for the imaging of prostate and brain tumours. Roivainen et al. [19] showed that it is rapidly metabolized and cleared from the blood. Tolvanen et al. [20] performed a complete dosimetric study. They compared data from normal and tumour-bearing rats and from six patients. The rat-derived and human-derived absorbed organ doses differed by up to a factor of approximately 6, while the rat-derived and human-derived ED differed by a factor of approximately 1.5.


Methionine is used in tumour diagnosis. There is only one study on whole-body PET [21] which included five volunteers and gives all relevant information for dosimetry. This study was also used as a basis for the biokinetic model in ICRP 106. However, the ED calculated by ICRP is 60% higher than the one calculated by Deloar et al. [21].

18F-Florbetaben (BAY94)

Florbetaben is specific for beta-amyloid and is therefore used in the diagnosis of Alzheimer’s disease. There is one published study [22] on dosimetry that included only three subjects and partially omitted biokinetic data. While the authors show time–activity curves for several organs, they do not give residence times.


Just like 11C-choline, 18F-choline is primarily used in the detection of prostate cancer and its metastases in bone. Since 2010 it has had marketing authorization only in France under the name IASOcholine®; other European countries will follow soon [23]. Currently it is not known if the biokinetics of 11C- and 18F-labelled choline are different. According to Roivainen et al. [19], 11C-choline is rapidly metabolized into 11C-betaine while DeGrado et al. [24] have speculated that differences in blood clearance can be explained by metabolic trapping of 18F-choline. DeGrado et al. [24] compared animal and human data. As they assumed instantaneous uptake and no biological clearance they probably overestimated the radiation dose. The authors did not provide biokinetic data for individual subjects. A correction for the male organ dose has been published as an erratum [24]. Nosske and Brix [25] developed a biokinetic model based on the available data for humans. They assumed equal biokinetics for 11C- and 18F-choline. Janzen et al. [26] provided extensive data on dosimetry; and in addition they explained their compartment model in detail.

Zankl et al. [27] were mainly interested in comparing the absorbed dose of locally absorbed electrons and electron-specific absorbed fraction values calculated using a Monte-Carlo method in a voxel-based computational phantom. Therefore, the biokinetic data for a single patient were sufficient for the purposes of their study, and they did not give any details about the acquisition of the data.


DOPA is an amino acid analogue which is marketed under the name of IASOdopa® in Austria, Germany and France. It is used in the diagnosis of several neurological and oncological diseases. The organ doses published in the SPC (Summary of Product Characteristics) [28] were taken from addendum 4 to ICRP 53 [29], which has been replaced by ICRP 106 [3]. No pretreatment with carbidopa was assumed in the ICRP 106 report and for the dosimetric data given in the SPC. Different biokinetics after this pretreatment have been reported, especially for the brain and bladder [30]. All the studies mentioned are included in ICRP 106; no newer literature is available.


The uptake of FDG is dependent on glucose metabolism and can be used in the detection of fast-growing cancer cells and inflammation. There are many studies that have included adult subjects, but in most either no whole-body scans were performed [3136] or time–activity curves were fitted to the sum of two exponential functions to three data points only [37, 38]. In two studies [33, 34] the experiments were repeated in the same subjects with small intrasubject variability.

Dowd et al. [32] measured urine activity only and developed a dynamic bladder model. Deloar et al. [37] used MRI to determine organ masses of their subjects and PET for activity distribution. Using these data they calculated residence times and absorbed doses utilizing the MIRD phantom, the Japanese reference man and S-values scaled with the individual organ masses. A dynamic bladder model was not used and they did not provide individual data. This study was used in ICRP 106. In another study by Deloar et al. [38] the authors compared thermoluminescent dosimetry with whole-body PET-based dosimetry and found good agreement. They did not give individual patient data. While both studies by Deloar et al. [37, 38] give an identical ED, they were performed in different subjects and the organ doses vary slightly. The authors of MIRD Dose Estimate Report No. 19 [35] merged the data from four studies in which the biokinetic data for specific organs were determined. This study was used in ICRP 106.

Wu et al. [36] were interested in developing an improved bladder model and therefore imaged only the bladder. They reported absorbed doses to the bladder wall in relation to initial bladder volume and first urine voiding time and individual biokinetic data. Koukouraki et al. [39] studied the pretherapeutic use of FDG and gave the rate constants for a local diagnostic three-compartment model (a blood compartment and two tissue compartments). Khamwan et al. [40] imaged patients in a Thai hospital and developed a dosimetry for Thais. Due to missing biokinetic data and some omitted imaging details, it is difficult to evaluate the results of their study. They used tissue weighting factors from ICRP 103 [9] and the S-values of the MIRD phantom (70 kg reference man) scaled with the subjects’ organ masses.


FET is an amino acid used in imaging lymphomas. Pauleit et al. [41] determined the biokinetics and performed a dosimetric assessment based on blood and urine samples and two whole-body scans. As they did not report details for the determination of the time–activity curves, the results cannot be heavily relied upon.


Sodium fluoride is a bone-seeking pharmaceutical and is therefore used for bone scanning. In 1978 Charkes et al. [42] reported the rate constants for a whole-body five-compartment model, which was used in ICRP 53. Since then further research has only been performed using a diagnostic local three-compartment model first used by Hawkins et al. [43]. The studies working with this model show a wide variation in bone uptake by a factor of up to 10 [44] depending on the location of the bone (usually vertebrae or humerus), hydration and the diseases of the subjects. Fluoride uptake into bone is around 50% in healthy subjects [1], so diseases affecting the whole skeletal system such as osteoporosis might significantly affect dosimetry.

In February 2011 fluoride was approved by the FDA, but the dosimetric data have not been updated and in the official FDA information EDE is still given [45]. In Europe, fluoride is now also available as IASOflu® [46]. In France it was approved as early as 2008. In the French SPC there is no recommendation given for the activity dosage in paediatric nuclear medicine [47].


18F-MISO is used in imaging hypoxia. Graham et al. [48] pooled the organ data obtained from 60 patients with scans differing in field of view and scanning time. They randomly chose a residence time from the pool for each measured source organ, used them to calculate the absorbed doses with S-values from MIRDOSE2 [16], and repeated this 1,000 times using a Monte-Carlo simulation. The resulting median values and 25% and 75% percentiles are presented in a table.


All 68Ga-labelled radiopharmaceuticals mentioned here are peptide analogues that bind to somatostatin receptors, which are often overexpressed in neuroendocrine tumours. Despite its widespread use and ease of distribution (68Ga is eluted from a 68Ge/68Ga radionuclide generator), the literature on 68Ga is sparse. For 68Ga-DOTANOC, a single but well done study is available [49]. Despite an intensive search, no publications dealing with dosimetry for 68Ga-DOTATATE were found. There are data only for 111In-DOTATATE and 177Lu-DOTATATE used in therapy [50]. The pretherapeutic use of 68Ga-DOTATOC has been studied [39], and Hartmann et al. [51] performed a complete dosimetric study of 68Ga-DOTATOC, although the significance of the difference between the reported male and female ED values seems doubtful due to the small number of subjects.

82Rb Generator

82Rb is commercially available as CardioGen-82® (a 82Sr/82Rb generator) and is used in cardiac imaging; it is approved by the FDA. The absorbed organ doses in the SPC [52] are based on studies in rats [53] and only two humans [54]. The ICRP calculations are based on a theoretical model of blood flow and represent “worst case” conditions. Stabin [55] has proposed a revision to the radiation dosimetry of 82Rb. He compared the blood-flow model of the ICRP [1] with a blood-flow model proposed by Leggett and Williams [18] and with the data from the two humans [54]. He analysed the biokinetic data using OLINDA/EXM dose calculation software [56], and concluded that the model of Leggett and Williams is most appropriate for general use. The latter model provided an ED that was smaller than the ICRP’s “worst case condition” by a factor of 2. Senthamizhchelvan et al. studied the biodistribution in ten healthy volunteers at rest [57] and under pharmacological stress [58]. The studies were methodologically correct and well accomplished and provided new results, with the exception of the improper use of ICRP 103 weighting factors (see Discussion). However, in both studies [57, 58], ED values were also calculated using the ICRP 60 weighting factors. The calculated EDs are comparable to those obtained by Stabin [55] using the data of Ryan et al. and Leggett and Williams. However, the ED value calculated using the data of Leggett and Williams is 50% higher than the value calculated by Senthamizhchelvan et al., while the value calculated using the data of Ryan et al. is 30% lower.

Other radiopharmaceuticals


99mTc-antigranulocyte is a monoclonal antibody (BW 250/183) produced in murine cells and used in determining the location of inflammation/infection in peripheral bone in adults with suspected osteomyelitis [59]. It was approved by the EMA in 2010 and is marketed under the name Scintimun®. Published data on biokinetics are available but without residence times for calculating absorbed doses [6062]. The biokinetic study of Buchmann et al. [62] evaluated the suitability of 99mTc-anti-CD66 monoclonal antibody BW 250/183 for myeloablative radioimmunotherapy.

No published dosimetry data were found in peer-reviewed journals for the monoclonal antibody BW 250/183. In the core SPC of IBA Molecular [63] and the core SPC of the EMA [59] data on dosimetry have been included. However, in the SPC of IBA Molecular only the organ doses and the EDE have been given. These data contain no detailed description of the origin of the biokinetic and dosimetric data. The same applies to the data in the core SPC of the EMA.Footnote 3 In this SPC the organ doses were calculated for the reference man and the reference woman separately and then the ED was calculated using the ICRP 103 [9] tissue weighting factors. As noted in the discussion, ICRP 103 should not yet be used for describing the risk of medical procedures in nuclear medicine.


Most commonly, MAA is used in lung perfusion imaging for the diagnosis or exclusion of pulmonary emboli. The biokinetic model adopted by ICRP 53 is the same as that used for iodine-labelled MAA [1], except for the excretion model which is replaced by the model for 99mTc-pertechnetate when a blocking agent has been given. The latest data on quantitative imaging were published in 1983 by Malone et al. [64]. According to ICRP 53 [1], the quantitative data on the metabolism of iodine- and technetium-labelled MAA in the literature show discrepancies.


Pertechnetate is used in imaging the thyroid and salivary glands, and for the diagnosis of Meckel's diverticulum. Biokinetic data are available in ICRP 53 [1], and no newer data have been published. The biokinetic model of ICRP 53 relies on data published in 1965, 1966 and 1969, and on data published in the MIRD Dose Estimate Report No. 8 in 1976 [65], the latter relying on a compartment model proposed by Hays and Berman [66]. Smith et al. [67] calculated organ doses and ED for the well-established MIRD system of mathematical anthropomorphic phantoms and a family of realistic voxel phantoms using the biokinetic data published in ICRP 53 [1], and compared the results.

99mTc-Sestamibi (MIBI)

Sestamibi is mainly used in imaging the myocardium. The latest data found were publications that were used for the biokinetic model in ICRP 80 by Wackers et al. [68] and Leide et al. [69]. In both studies rest and stress tests were conducted. There are significant differences in MIBI uptake in several organs between rest and stress studies; these also differ considerably between individual subjects [69].


Technegas is used in lung ventilation scintigraphy to diagnose pulmonary embolism. It is an aerosol of ultrafine 99mTc-labelled carbon particles with a particle size around 50 nm [70]. A summary of the biokinetics can be found in ICRP 80 [2], according to which a biokinetic model was developed. None of the references in ICRP 80 provide organ doses for organs other than the lung. The organ dose for the lung is reported as 4.5 mSv/37 MBq [71]. This organ dose relies on data published in the “Handbook of radiation doses in nuclear medicine and diagnostic X-ray” [72] to which we were not allowed access, and hence could not assess how this dose was calculated.


Tetrofosmin, marketed as Myoview™, is used in myocardial perfusion imaging and in imaging of the female breast. Biokinetic and dosimetric data are published in the latest ICRP report (ICRP 106) [3]. However, due to a printing error, the values in the ICRP 106 table for the resting subject and the subject under stress are identical. The data in both tables belong to the stress data (personal communication with a member of the ICRP task group). Unfortunately, an erratum has never been published by ICRP. Although the biokinetic data are the same in ICRP 80 and ICRP 106, the absorbed doses to the organs, and hence the ED, are slightly different in the stress studies (probably in the rest study too, but these data are not available). This is due to the fact that the ICRP has changed the phantoms and the source of the S-values used for calculating the doses. For ICRP 53 and ICRP 80 [1, 2], a 70-kg adult male phantom was considered that was described in MIRD Pamphlet No. 5 Revised [73], and which was based on the ICRP 23 [74] reference man. The corresponding S-values used for absorbed dose calculations were taken from MIRD Pamphlet No. 11 [8]. For children the phantoms considered were those developed by Cristy [75].

For ICRP 106 [3], the phantoms considered were those developed by Cristy and Eckerman [76] for both adult male and children. The whole-body mass of the adult phantom of Cristy and Eckerman changed slightly to 73.7 kg. For absorbed dose calculations the published S-values of Stabin and Siegel [77] were used.

The biokinetics are quite similar to those of sestamibi. However, tetrofosmin is cleared more rapidly from the liver and the absolute uptake in the heart is lower. The biokinetic data in ICRP 80 and ICRP 106 are based on publications by Smith et al. [78] and Higley et al. [79]. Both studies were conducted in the same hospitals (multicentre study with two hospitals) and the same number of patients. It is not clear if the patient groups were identical because the injected activity differed between the studies. However, the calculated EDs are the same in both publications. The dosimetric data provided by GE Healthcare in the core SPC [80] are human data; the source of the data, however, is not referenced.


201Tl is used in myocardial perfusion imaging. There are discrepancies in the reported amounts of testicular uptake of 201Tl-chloride [3]: uptake values in the range 0.15–1.1% (percentage uptake at 24 h) have been reported [81]. In a revised dosimetry study, Thomas et al. [81] performed quantitative imaging for the testes only, shielded from the body background. They combined these data with biokinetic data from older publications. With these datasets for the testes the absorbed dose per administered activity calculated in this study is less than 50% of the previously accepted value. These data have also been included in the ICRP 106 [3] data in combination with the data of Krahwinkel et al. [82]. Therefore, a testicular uptake of 0.3% has generally been adopted instead of 0.8% (ICRP 53 [1] and ICRP 80 [2]). That is the reason why the recalculation of the ED performed in ICRP 106 shows a substantial decrease as compared to ICRP 80 (0.14 mSv/MBq vs. 0.22 mSv/MBq).


Sodium Iodide is used in the evaluation of thyroid function and/or morphology. In 2003 a refinement of the ICRP 53 biokinetic model was published by Johansson et al. [83]. In this compartment model the uptakes in the stomach wall and the salivary glands were included resulting in a slight change in the ED compared to the ED reported in ICRP 80 [2].

123I-Ioflupane (123I-FP-CIT)

Ioflupane is a cocaine analogue used in imaging dopamine transporters (DaT). GE Healthcare holds a marketing authorization under the name DaTSCAN™. In 1998 a phase I biodistribution and dosimetry study was published by Booij et al. [84]. The residence times for several source organs were calculated separately for each subject fitting a multicompartment model to the time–activity curves for these organs. Furthermore, the absorbed doses to the organs were calculated for each subject independently and averaged. An erratum has been published containing a correction of the residence time for the gallbladder content; however, this does not affect the value of ED [84]. The manufacturer-provided data published in the SPC [85] include absorbed doses for the target organs and the ED, but there is no reference as to how these data were derived. Comparing the absorbed doses and the ED given in the SPC with the data in the paper by Booij et al. [84] shows that these data were used for the SPC.


Most of the radiopharmaceuticals (except Zevalin) presented in this section are somatostatin derivatives (see the section about 68Ga). There is one study on 111In-DOTA-lanreotide with complete dosimetric data [86] and one on therapy with 90Y [87] comparing DOTA-lanreotide and DOTATOC. For 111In-DOTATATE information is scarce. A single report [88] presents data for blood clearance and calculated absorbed organ doses for 90Y therapy. Two studies on 111In-DOTATOC are available, one with absorbed organ doses and partly omitted biokinetics [89] and the other with residence times determined with a compartment model [90].

111In-DTPAOC (also known as DTPA-octreotide or pentetreotide) is marketed as OctreoScan™. The reports by Bajc et al. [91] and Stabin et al. [92] contain all relevant data for dosimetry. Two other studies [93, 94] have considered only the pretherapeutic use of 111In-DTPAOC and estimated biokinetic data for 90Y-DOTATOC have been published.

Ibritumomab, licensed as Zevalin®, is an antibody that is labelled with either 111In or 86Y for pretherapeutic imaging or 90Y as a therapeutic agent against lymphomas. In the EU Zevalin has marketing authorization only for therapeutic use with 90Y. Two reports by Wiseman et al. [95, 96] present only estimated absorbed organ doses for therapy, while MIRD Dose Estimate Report No. 20 [6] provides complete biokinetic and dosimetric data for 111In-ibritumomab.


67Ga-citrate is used for localization of inflammatory lesions. The only available biokinetic and dosimetric data were published in the MIRD Dose Estimate Report No. 2 in 1973 [97]. These data were used for the biokinetic model in ICRP 53 [1].

Dosimetry data in paediatric nuclear medicine

In the following we present a summary of the few data available for paediatric applications in nuclear medicine diagnostics. Further details are given in the tables in the Electronic supplementary material.

In general ICRP uses the same biokinetic models for children as for adults and paediatric age-dependent mathematical phantoms to calculate absorbed doses in children as there is a lack of specific knowledge. According to ICRP [1], it is assumed that this might lead to an overestimate of the absorbed dose because of shorter biological half-lives in children than in adults; however, the measurements for 99mTc-DMSA and 99mTc-HMPAO in children show that the kinetics are not very different.


Only two publications actually present measured data for paediatric subjects. Ruotsalainen et al. [98] imaged the brain and bladder of newborns with serious neurological symptoms. The residence times of other organs were taken from the literature and scaled according to body and brain mass. Then the S-values of a newborn Cristy-Eckerman phantom [99] were used for calculation of absorbed doses. They found that only 4% to 7% of injected activity is excreted into the bladder while ICRP 106 assumes 24%. Niven and Nahmias [100] examined very low birth weight newborns with suspected lung inflammation. As these patients were on average three times lighter than a full-term newborn, they scaled the S-values of the newborn Cristy-Eckerman phantom with individual organ masses assuming target and source organ were identical. Due to large uncertainties, they were only able to calculate dosimetry for three cases based on assumptions.


The review by Gelfand [101] includes (as do at least two other papers [102, 103]) a table for absorbed doses of 18F-fluoride in children that claims to be derived from ICRP 53, but the organ doses differ by up to 20%. For example, the absorbed dose to the bladder wall of a 1-year-old child is 1.3 mSv/MBq according to Gelfand and 1.1 mSv/MBq according to ICRP 53.


Imaging was performed in 24 children aged from 5 weeks to 14.8 years (15 normal and 9 with renal pathology). The administered activities were scaled according to the EANM 1990 paediatric dosage card [104]. No obvious age dependencies in the biokinetics in children with normal renal function were found; only children younger than 1 year showed a reduced urinary excretion uptake [105]. Therefore the differences between adults and children with normal renal function are relatively small; the adult biokinetic data are a good approximation for all ages [105]. Absorbed dose calculations have also been reported by Smith et al. [106]. Their computer code used paediatric anthropomorphic phantoms representing children of ages 15, 10, 5 and 1 year weighing 55.6, 32.4, 18.6 and 9.9 kg, respectively, and a newborn weighing 3.4 kg. The children were matched to the closest phantom by age and weight. A second approach was also chosen: interpolation between the organ doses calculated with two adjacent phantoms for each child.

99mTc-HMPAO (99mTc-exametazime)

Vestergren et al. [107] evaluated the biokinetics of HMPAO in children. Since it is very difficult to study children, especially very young ones, only three whole-body scans were done (1, 7 and 24 h after injection). For the calculation of the absorbed doses in children the same biokinetic models as used in adults were used, and the age of each patient was rounded to the closest of the ages 0, 1, 5, 10 and 15 years and adult. For most organs no obvious age-dependent differences in the residence times were found. There were differences only in the brain and in the nonspecified organs [107].


The dosimetry data in the publication on paediatric radiation dosimetry by Stabin et al. [108] rely on measured data from only four children at different ages (8 days, and 2.5, 5 and 14 years). The authors emphasized that these data were only preliminary and, therefore, no true age-dependency has been identified.


According to ICRP 53 (relying on data by Gelfand et al. [109]) the absorbed dose to the growing regions of children’s bone is higher by a factor of 2–5 than assumed for the mean absorbed dose in adults and hence the mean absorbed dose in children using the adult biokinetics is not likely to be considerable underestimated.


Compiling data on radiopharmaceutical dosimetry for diagnostic nuclear medicine inevitably leads to the question of up-to-date minimum standards for collecting reliable data for dosimetry. In principle, the steps described in MIRD Pamphlet No. 16 [7], ICRU 67 [110] and the EANM dosimetry guidance document on good dosimetry reporting [4] should be considered. State-of-the-art dosimetry today includes the use of CT systems for attenuation correction, scatter correction, consideration of the duration of the study depending on the biokinetics of the radiopharmaceutical and of bladder voiding intervals, a calculation of residence times including an analysis of the errors associated with the respective calculation method and the appropriate use of phantoms for calculating EDs. As the number of subjects in many biokinetic and dosimetric studies is fewer than 10 the question of the validity of the data for a larger population needs to be addressed. In the scope of the new ICRP recommendations [9] (ICRP 103) gender-specific differences might also need to be considered in the future.

In some cases it was very difficult to find data on biokinetics and dosimetry, especially for radiopharmaceuticals that changed their name during the approval phase. For example, it was not clear at first glance that 123I-Ioflupane and 123I-FP-CIT are identical. The same applies to 99mTc-HMPAO and 99mTc-exametazime. For some radiopharmaceuticals with marketing authorization such as 99mTc-antigranulocyte no peer-reviewed articles containing dosimetry data have been published; thus the quality of the underlying experimental data cannot be assessed. For 18F-fluoride, a more frequently used PET radiopharmaceutical, no whole-body quantitative imaging data are available, and the biokinetic models rely only on compartment models (based on blood and urinary excretion) and/or local quantitative images. For 68Ga-DOTATATE no published data on dosimetry are available.

For some radiopharmaceuticals the biokinetic data were acquired more than 20 years ago (e.g. 67Ga-citrate, 99mTc-DMSA, 99mTc-DTPA, 99mTc-ECD, 99mTc-MAA, 99mTc-pertechnetate, 99mTc-sestamibi, and 18F-fluoride). Due to considerable improvements in nuclear medicine equipment over the years, an improved assessment of the absorbed doses seems warranted and would be of scientific interest. For 201Tl-chloride, a recalculation of the absorbed doses in ICRP 106 [3] following reevaluation of the available data on testicular uptake led to a substantially decreased ED compared to ICRP 80 [2] (11 mSv vs. 17 mSv with an administered activity of 75 MBq).

Dosimetry data for paediatric nuclear medicine applications of radiopharmaceuticals are sparse. In the case of missing paediatric data, the ICRP reports use the biokinetics obtained in adults and paediatric age-dependent mathematical phantoms. As the size and weight of children and adolescents vary considerably and show only a poor correlation with age, the dose coefficients (listed in the ICRP publications) should be adjusted according to weight instead.

The latest publication of the ICRP on absorbed doses for radiopharmaceuticals (ICRP 106) [3] still applies the tissue weighting factors given in ICRP 60 [10]. The 2007 ICRP recommendations (ICRP 103) [9] now clearly demand the use of male and female reference voxel phantoms which were published in ICRP 110 [111]. The new concept demands a determination of the equivalent doses to the organs and tissues of the reference male and the reference female separately. In order to obtain the equivalent doses to the reference person, the gender-specific equivalent doses are averaged; hence the new tissue weighting factors can be applied. Moreover, according to ICRP 103, only the latest ICRP voxel phantoms should be used for the calculations of ED. Applying the new weighting factors to a set of equivalent organ doses previously calculated with a mathematical phantom will therefore not result in a correct ED value due to ICRP 103. Presently, the modified tissue weighting factors and the subsequent calculation of the ED according to the formalism of ICRP 103 cannot be applied to nuclear medicine as the S-values for radiopharmaceuticals using the new recommendations of the ICRP are still missing.

As, in many cases, the dosimetry protocols applied for a given radiopharmaceutical are very heterogeneous with respect to the time-points and bladder voiding, and to the dose assessment after the last data point (e.g. for 18F-choline, 18F-FDG, 99mTc-ECD and 99mTc-HMPAO). Therefore, the development of more uniform protocol templates for diagnostic nuclear medicine dosimetry is required.

In many articles the description of the methodology and the reporting of the results are incomplete so that it is difficult to get information for reassessment of absorbed doses. In future articles the use of the suggestions given by the EANM guidance document on good dosimetry reporting [4] is strongly recommended.


For most diagnostic radiopharmaceuticals dosimetry data are available, although the data collection and calculation methods are heterogeneous. As some of the data were acquired more than 20 years ago, it would be of interest to generate new data on biokinetics and dosimetry in diagnostic nuclear medicine using state-of-the art equipment and more uniform dosimetry protocols. Data for paediatric nuclear medicine are missing in most cases.

As some of the references collected for this review are not easily accessible a major conclusions of this work is that, for easier public access to dosimetry data of diagnostic radiopharmaceuticals, a database containing these data should be created and maintained.