Evolution of virulence in Fusarium oxysporum f. sp. vasinfectum using serial passage assays through susceptible cotton.

Fifty strains of Fusarium oxysporum, recovered from rhizosphere soil around native Gossypium species and found to be mildly virulent on cotton (Gossypium hirsutum), were used to assay the propensity for evolution of virulence using serial passage assays through cotton. Only one lineage A strain, 2613, successfully completed 10 successive passages, while all others lost the ability to cause foliar disease symptoms at various stages during this process. Based on 46 amplified fragment length polymorphism (AFLP) markers generated with four EcoRI x MseI primer combinations, mutants were identified in offspring isolates from strain 2613 regardless of whether serial passages occurred in cotton or on water agar, suggesting the occurrence of spontaneous mutations. Significantly increased virulence was observed in the offspring isolates generated on cotton, while no increasing virulence was found in those obtained on water agar, suggesting that the evolution of virulence in F. oxysporum f. sp. vasinfectum is associated with the presence of cotton. No clear correlation was observed between the AFLP mutations and increased virulence in this study.

Radionuclide calibrator comparisons and quality improvement in nuclear medicine.

The traceability of activity measurements performed during the development phase of the radiopharmaceutical and in its clinical application is essential for establishing the comparability of clinical results reported in the nuclear medicine field. This paper presents and discusses the evaluation over time of the quality of activity measurement results obtained in Cuban nuclear medicine, on the basis of statistical samples taken during the radionuclide calibrator comparison program. An attempt is also made to evaluate the role played by such comparisons in quality measurement improvement in nuclear medicine, on the basis of results obtained in a number of countries and published by several authors over a period of time. Specifically, improvements of the measurement performance over time assessed by such exercises were found dissimilar in magnitudes for different countries. Two phases could be distinguished in the improvement process over time. Firstly, a fast improvement can be obtained resulting from the improvement in measurement accuracy of devices. After that, the achievement of new and sustained improvements goes slowly and requires an application of quality assurance programs where the qualification upgrading of personnel become an essential point.

International guidance on the establishment of quality assurance programmes for radioactivity measurement in nuclear medicine.

A new guidance document for the implementation of quality assurance (QA) programmes for nuclear medicine radioactivity measurement, produced by the International Atomic Energy Agency, is described. The proposed programme is based on the principles of ISO 17025 and will enable laboratories, particularly in developing countries, to provide consistent, safe and effective radioactivity measurement services to the nuclear medicine community.

Comparison of strontium-89 solution sources in UK hospitals, 2003.

Concerns have been raised within the nuclear medicine field about the accuracy of measurements of 89Sr. The 85Sr impurity present in the 89Sr solution has a significant effect on the response of radionuclide calibrators used in hospitals. A comparison was conducted between the National Physical Laboratory (NPL) and the UK hospital physics community. Only 58% of the results were within 5% of the NPL value. Work at NPL has resulted in correction factors for the NPL secondary standard radionuclide calibrator and for Capintec calibrators, which will produce a significant improvement in performance.

Some results of a simulated test for administration of activity in nuclear medicine.

This paper describes the results obtained using a simulated test for administration of activity in nuclear medicine between 2002 and 2004. Measurements in the radionuclide calibrator are made during the different stages of the procedure. The test attempts to obtain supplementary information on the quality of the measurement, with the aim of evaluating in a more complete way the accuracy of the administered activity value compared with the prescribed one. The participants' performance has been assessed by means of a statistical analysis of the reported data. Dependences between several attributes of the simulated administration tests results are discussed. Specifically, the proportion of satisfactory results in the 2003-2004 period was found to be higher than in 2002. It reveals an improvement of the activity administration in the Cuban nuclear medicine departments since 2003.

Comparison of radioactivity measurements with radionuclide calibrators in the Republic of Korea.

Recognizing the importance of comparisons of radionuclide calibrators in nuclear medicine and the need to provide access to activity standards that are traceable to the international measurement system, the Korea Food & Drug Administration (KFDA) as a national secondary standard dosimetry laboratory (SSDL), started a comparison program in 2002. The first two comparisons were conducted with (131)I (71 participants) and (99m)Tc (72 participants). The results indicated that only 61% of reported activities for (131)I and 65% for (99m)Tc were within +/-5% of the correct value. These numbers increased to 84% for (131)I and 83% for (99m)Tc when a +/-10% limit was applied. Follow-up action on those calibrators with results outside the +/-10% limits only produced a small improvement. There was also a marked difference in performance between the various calibrator types used. The results have shown that such comparisons are necessary to improve the quality of the measurements and to identify those radionuclide calibrators that are not functioning correctly.

MRA calibration and measurement capabilities--radioactivity.

The practical realisation of the Mutual Recognition Arrangement relies on its two main Appendices, B and C. Appendix B relates to the equivalence of national measurement standards. The dissemination of these standards is achieved by the provision of physical standards and measurement services, where the associated measurement values are traceable to the SI. Appendix C specifies the quantities and ranges for which participating institutes recognise the validity of calibration and measurement certificates issued by other participating institutes and these are detailed in the database devoted to these standards and services, commonly referred to as calibration and measurement capabilities. Each participating institute has the opportunity to submit entries, via its Regional Metrology Organisation (RMO), to the database but, in order for users to be able to make informed choices, it is important that the data are entered to a common standard. The Joint Committee of the RMOs and the Bureau International des Poids et Mesures is responsible for the coordination of data provided by the RMOs. It is for individual RMOs to ensure the correctness of their own entries and to review and comment on those from others. This paper details that process and describes the various entries in the tables. It also addresses some of the remaining issues that still need to be resolved, in particular, the magnitudes of uncertainties and the need for supporting comparisons, both of which still present some significant problems.

Half-life data--a critical review of TECDOC-619 update.

An accurate knowledge of selected nuclear decay data is critical to a wide range of processes involving radionuclides. An IAEA publication in 1991 was dedicated to the evaluation of half-lives and specific gamma-ray emission probabilities for 39 selected radionuclides considered to be important for detector efficiency calibrations. A new exercise was initiated in December 1998 to update this previous evaluation and to include a number of new radionuclides of interest; 62 radionuclides were considered along with specific parent-daughter combinations (to give a total of 64 radionuclides). That work is now being completed and a new set of recommended data is being prepared for publication. A critical comparison of the 1991 and 2003 half-life data suggests that there has not been any significant improvement in the accuracy of the recommended data. The possible reasons for this situation are discussed together with the evaluation procedure and the quality of the available data. Proposals are made for concerted actions that could lead to a significant improvement in these recommended half-life data.

Primary standardisation of 204Tl using the efficiency tracing method.

The electron-capture and beta(-) -emitting radionuclide 204Tl has been known from previous experience to show discrepancies between different methods of standardisation. Source preparation is also difficult due to the complex chemistry of thallium. The Bureau International des Poids et Mesures (BIPM) intercomparison held in 1997, showed discrepancies of up to 10% between measurements of solid sources and liquid scintillation methods. These problems have been the subject of a BIPM CCRI(II) working group since 1999. This paper presents the results from a primary standardisation of a 204Tl solution using 4pibeta-gamma coincidence counting and liquid scintillation counting. The tracer technique was used for the 4pibeta-gamma coincidence counting, where 204Tl was traced with 134Cs and 60Co. The extrapolation to 100% beta-efficiency was performed by three different approaches: foiling, adding carrier and measuring sources of different initial masses. The results showed that tracing with 60Co and using external foiling gave the same result as obtained by liquid scintillation counting. A comparison of the results achieved by the different methods of measurement, tracers and methods for extrapolation is presented and discussed in this paper.

Establishing equivalence for activity standards of short-lived radionuclides using the NPL secondary standard radionuclide calibrator.

Conventional comparison techniques used between National Metrology Institutes are not practicable for short-lived radionuclides because of geographical separations and transport difficulties. The NPL Secondary Standard Radionuclide Calibrator provides an alternative approach and a comparison was conducted with 18F to investigate its feasibility. The exercise was successful and the paper details the protocol used, the quality assurance mechanisms introduced to underpin the comparison and an analysis of the results. It was also demonstrated that this approach could be linked to the BIPM SIR system. Recommendations are presented for the extension of this work to other suitable, short-lived radionuclides.

Secondary standardisation of 95mTc.

The radionuclide 95mTc, which has a half-life of 61(2)days and emits a number of gamma-rays, may be used in radiochemical analysis as a yield tracer for the long-lived fission product 99Tc. In this work, we present (i) the production of 95mTc via an (alpha, 2n) reaction with stable 93Nb (a method which does not result in the production of any 97mTc, 98Tc or 99Tc), (ii) the chemical separation of 95mTc from niobium via coprecipitation, liquid-liquid extraction and liquid chromatography, and (iii) the secondary standardisation of 95mTc with high-resolution gamma-ray spectrometry and an ionisation chamber system.

Syringe calibration factors for the NPL Secondary Standard Radionuclide Calibrator for selected medical radionuclides.

Before a radiopharmaceutical is administered to a patient, its activity needs to be accurately assayed. This is normally done via a radionuclide calibrator, using a glass vial as the calibration device. The radionuclide is then transferred to a syringe and it is now becoming common practice to re-measure the syringe and use this value as the activity administered to the patient. Due to elemental composition and geometrical differences, etc. between the glass vial and the syringe, the calibration factors are different for the two containers and this can lead to an incorrect activity being given to the patient unless a correction is applied for these differences. To reduce the uncertainty on syringe measurements, syringe calibration factors and volume correction factors for the NPL Secondary Standard Radionuclide Calibrator have been derived by NPL for several medically important radionuclides. It was found that the differences between the calibration factors for the syringes and glass vials depend on the energies of the photon emissions from the decay of the radionuclides; the lower the energy, the greater the difference. As expected, large differences were observed for 125I (70%) and only small differences for 131I. However, for radionuclides such as 99mTc and 67Ga, differences of up to 30% have been observed. This work has shown the need for the use of specifically derived syringe calibration factors as well as highlighting the complexity of the problem with regard to syringe types, procurement, etc.

Calibration of the NPL secondary standard radionuclide calibrator for 125I seeds used for prostate brachytherapy. National Physical Laboratory.

In the therapeutic use of radionuclides, by far the most rapid growth in recent years is that of 125I seeds used for the treatment of prostate cancer. Large numbers of these seeds are used in each treatment and there is a need for a simple but accurate means of confirming their dose rates. This mechanism requires a transfer device for which the calibration factors are traceable to national standards. The NPL secondary standard radionuclide calibrator, because of its guaranteed reproducibility and traceable calibration procedure, is ideally suited for this purpose. A series of characterisation measurements have been performed on the NPL radionuclide calibrator in order to estimate the uncertainty levels that can be achieved and these are presented together with the relevant calibration factors for some typical seeds.

NPL secondary standard radionuclide calibrator. Syringe calibration factors for radionuclides used in nuclear medicine. National Physical Laboratory.

The measurement of the activity of a radiopharmaceutical administration to a patient is normally achieved via the use of a radionuclide calibrator. Although these radionuclides are normally measured initially in a standard glass vial, an aliquot of the solution is then usually withdrawn into a syringe prior to the administration. Both for general quality assurance good practice and for additional guarantees for patient safety, a confirmatory measurement of the syringe is almost obligatory Because of the different geometries and elemental compositions between plastic syringes and glass vials, the calibration factors for syringes may well be significantly different from those for the glass containers. The magnitude of these differences depends on the energies of the emitted photons. A variety of syringes typically used in hospital administrations, and covering a range of volumes and manufacturers, were obtained. The results obtained were compared to those for glass vials and show the large errors that can be produced by ignoring these differences in container format.

Standardisation of 11C.

The increasing use of positron emission tomography for medical imaging and the availability of short-lived positron emitters has raised concerns about the accuracy of calibration of secondary standard measurement systems and the viability of using a single long-lived positron emitter as a reference calibration source for all positron emitters. Potential problems arise because the 511 keV quanta arising from positron annihilation are not generally produced at the same point as the original disintegration. In addition, the secondary standard may also be responsive to the associated bremsstrahlung radiation. The magnitude of both effects depends on the positron end-point energy. In order to resolve these problems, it is necessary to produce absolute standards of these positron-emitting radionuclides and the work presented here details the results of such work with 11C.

Standardization and decay data of 237Np.

This paper reports contributions from participants in the EUROMET project (No. 416) which was entitled "237Np research into problems relating to purification, characterization and standardization". Primary standardizations were made by the defined low solid angle, coincidence, 4pi alpha, 2pi alpha and liquid scintillation counting methods. Secondary standardizations were made with calibrated gamma-ray spectrometers. Absolute X-ray, gamma-ray and alpha-particle emission probabilities were also determined. The results for the successful conclusion of both primary and secondary standardization are presented together with the values for alpha-particle and gamma-ray emission probabilities determined in this exercise. Several significant inconsistencies remain with the gamma-ray emission probabilities, and these are highlighted.

Nuclear data used in the analysis of thorium in the workplace.

The analysis of thorium in the workplace can be achieved using a variety of metrological techniques. The uncertainty on the final measured values will include components that arise from the uncertainties in the nuclear data that are used. These data include half-lives, branching ratios and gamma ray emission probabilities. It is important that a common, consistent and reliable data set is used in order to minimise the potential differences between analytical results. With particular reference to the problems associated with thorium analysis, some of the various sources of nuclear data are discussed and a recommended set of data is proposed.

Thorium in the workplace: the preparation and validation of comparison samples for a European-based measurement comparison project.

The quality of any comparison exercise depends critically on the quality. accuracy and fitness for purpose of the comparison samples. The comparisons were designed to move progressively from the testing of the analysis capabilities for relatively simple. aqueous solutions through to the more complex natural matrix materials encountered in the workplace. In each case, it was imperative that the comparison samples were prepared and validated in such a way as to ensure traceability of their activity values to national and international standards of radioactivity, to enable a reasonable estimate to be made of the uncertainty on those values and to ensure homogencity both within and between samples. The processes involved are discussed.

Thorium in the workplace: results from a European-based measurement comparison project.

A Series of comparisons were conducted to test the capabilities of a range of metrological techniques and analytical laboratories engaged in the assay of thorium in the workplace. The results of these exercises are presented together with the decision criteria used to determine whether results are significantly different from the true value. The discussion highlights those aspects which warrant closer and further attention.