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Validation and Comparison of Two Calibration Methods for the Measurement of Stable Iodine in the Urinary Matrix by ICP-MS:Standard Addition vs.External Calibration 被引量:1
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作者 Geraldine Landon Celine Bouvier-Capely +7 位作者 alexandre legrand Thibaud Sontag Gregory Finance Mailie Saint-Hilaire Francois Rebiere Xavier Millot Valerie Renaud-Salis Michelle Agarande 《American Journal of Analytical Chemistry》 2017年第4期245-263,共19页
Background: In the context of a nuclear reactor accident, thyroid is the main target organ of radioactive iodines. To avoid as much as possible thyroid disorders or even cancer development, it is recommended to admini... Background: In the context of a nuclear reactor accident, thyroid is the main target organ of radioactive iodines. To avoid as much as possible thyroid disorders or even cancer development, it is recommended to administer a single dose of potassium iodide to people at risk of exposure. Nevertheless, the Fukushima Dai-ichi disaster has pointed out many questions about the conditions of stable iodine prophylaxis implementation highlighting the need for reflection further revision of the actual “iodine doctrine”. Therefore, providing useful data is required notably through the implementation of animal experiments to strengthen current knowledge and to edit new recommendations. Methods: Urinary iodine constitutes a very good indicator to investigate the function of thyroid, its interpretation demands reliable analyses. Prior to perform animal experiments, two calibration methods were designed by our lab and compared together (standard addition and external calibration) to assess the urinary concentration of stable iodine in urine by ICP-MS. They were validated based on several key parameters especially linearity, accuracy and limits of detection (LOD) and quantification (LOQ). Results: The results were nicely satisfying. Indeed, both calibration methods have indicated very good coefficients of correlations, accuracies with low expanded relative uncertainties were obtained. The estimated LOD in the sample for standard addition method and external calibration were fully acceptable, 0.39 μg·L-1 and 0.35 μg·L-1, respectively. All performance criteria have been thus fulfilled successfully. The established methods were proven to be accurate, robust and sensitive. Once validated, both calibration methods were applied to rat urine samples and the results of z-score and Wilcoxon W test concluded that there were no statistically significant differences between both methods. 展开更多
关键词 Stable Iodine URINE Standard Addition External Calibration VALIDATION
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Accuracy of Medical Oxygen Flowmeters: A Multicentric Field Study
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作者 Frédéric Duprez Maria Barile +4 位作者 Thierry Bonus Grégory Cuvelier Sandra Ollieuz Shahram Mashayekhi alexandre legrand 《Health》 2014年第15期1978-1983,共6页
The accuracy of 476 oxygen flowmeters was investigated using a thermal mass flowmeter in eight hospitals in France and Belgium. Different oxygen flow rates (2 to 15 l/min) were evaluated at the patient’s bed. When th... The accuracy of 476 oxygen flowmeters was investigated using a thermal mass flowmeter in eight hospitals in France and Belgium. Different oxygen flow rates (2 to 15 l/min) were evaluated at the patient’s bed. When the sample was considered as a whole, the accuracy of delivered flow was acceptable but precision was poor. The variability of the delivered flow between devices was greater when a low flow rate was required. Compensated-pressure oxygen flowmeters for these low rates were more accurate than their non-compensated counterparts. This study emphasizes the need to individually adapt the oxygen flow rate each time a patient has to move from one flowmeter to another. 展开更多
关键词 MEDICAL Device ACCURACY OXYGEN Therapy FLOWMETER
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Operational Protocol for Detection of Contamination by Actinides U,Pu and Am in Urine Using Calixarene Columns:From Mineralization to ICP-MS Measurement
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作者 Celine Bouvier-Capely alexandre legrand +2 位作者 Aurelie Sylvain Annabelle Manoury Francois Rebiere 《American Journal of Analytical Chemistry》 2017年第5期317-333,共17页
Individual monitoring of workers exposed to the risk of intake of actinides requires suitable methods for measuring low level of excreted activity. The current protocols used for actinides analysis in bioassay are usu... Individual monitoring of workers exposed to the risk of intake of actinides requires suitable methods for measuring low level of excreted activity. The current protocols used for actinides analysis in bioassay are usually complicated and highly time consuming. In this work, a protocol based on the microwave digestion of urines followed by the separation of actinides using calix[6]arene-based chromatography columns and their measurement by a quadrupole ICP-MS is developed and validated, for the first time, on urine samples containing the three actinides, U, Pu and Am. With this protocol, the total analysis time is about 2 days, including the mineralization of urine and the chromatographic separation of actinides. Detection limits of actinides in urine are determined and compared to those obtained after “dilute and shoot” ICP-MS analysis or after alpha spectrometry measurement. 展开更多
关键词 ACTINIDES URINE CALIX[6]ARENE Analysis ICP-MS
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