Last data update: Jan 27, 2025. (Total: 48650 publications since 2009)
Records 1-3 (of 3 Records) |
Query Trace: Jones DR[original query] |
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Development and validation of a biomonitoring method to measure As, Cr, and Ni in human urine samples by ICP-UCT-MS
Jones DR , Jarrett JM , Stukes D , Baer A , McMichael M , Wallon K , Xiao G , Jones RL . Int J Hyg Environ Health 2021 234 113713 We developed an inductively coupled plasma mass spectrometry (ICP-MS) method using Universal Cell Technology (UCT) with a PerkinElmer NexION ICP-MS, to measure arsenic (As), chromium (Cr), and nickel (Ni) in human urine samples. The advancements of the UCT allowed us to expand the calibration range to make the method applicable for both low concentrations of biomonitoring applications and high concentrations that may be observed from acute exposures and emergency response. Our method analyzes As and Ni in kinetic energy discrimination (KED) mode with helium (He) gas, and Cr in dynamic reaction cell (DRC) mode with ammonia (NH(3)) gas. The combination of these elements is challenging because a carbon source, ethanol (EtOH), is required for normalization of As ionization in urine samples, which creates a spectral overlap ((40)Ar(12)C(+)) on (52)Cr. This method additionally improved lab efficiency by combining elements from two of our previously published methods(Jarrett et al., 2007; Quarles et al., 2014) allowing us to measure Cr and Ni concentrations in urine samples collected as part of the National Health and Nutrition Examination Survey (NHANES) beginning with the 2017-2018 survey cycle. We present our rigorous validation of the method selectivity and accuracy using National Institute of Standards and Technology (NIST) Standard Reference Materials (SRM), precision using in-house prepared quality control materials, and a discussion of the use of a modified UCT, a BioUCell, to address an ion transmission phenomenon we observed on the NexION 300 platform when using higher elemental concentrations and high cell gas pressures. The rugged method detection limits, calculated from measurements in more than 60 runs, for As, Cr, and Ni are 0.23 μg L-1, 0.19 μg L-1, and 0.31 μg L-1, respectively. |
Assessing the stability of Cd, Mn, Pb, Se, and total Hg in whole human blood by ICP-DRC-MS as a function of temperature and time
Tevis DS , Jarrett JM , Jones DR , Cheng PY , Franklin M , Mullinex N , Caldwell KL , Jones RL . Clin Chim Acta 2018 485 1-6 BACKGROUND: Comprehensive information on the effect of time and temperature storage on the measurement of elements in human, whole blood (WB) by inductively coupled plasma-dynamic reaction cell-mass spectrometry (ICP-DRC-MS) is lacking, particularly for Mn and Se. METHODS: Human WB was spiked at 3 concentration levels, dispensed, and then stored at 5 different temperatures: -70 degrees C, -20 degrees C, 4 degrees C, 23 degrees C, and 37 degrees C. At 3 and 5weeks, and at 2, 4, 6, 8, 10, 12, 36months, samples were analyzed for Pb, Cd, Mn, Se and total Hg, using ICP-DRC-MS. We used a multiple linear regression model including time and temperature as covariates to fit the data with the measurement value as the outcome. We used an equivalence test using ratios to determine if results from the test storage conditions, warmer temperature and longer time, were comparable to the reference storage condition of 3weeks storage time at -70 degrees C. RESULTS: Model estimates for all elements in human WB samples stored in polypropylene cryovials at -70 degrees C were equivalent to estimates from samples stored at 37 degrees C for up to 2months, 23 degrees C up to 10months, and -20 degrees C and 4 degrees C for up to 36months. Model estimates for samples stored for 3weeks at -70 degrees C were equivalent to estimates from samples stored for 2months at -20 degrees C, 4 degrees C, 23 degrees C and 37 degrees C; 10months at -20 degrees C, 4 degrees C, and 23 degrees C; and 36months at -20 degrees C and 4 degrees C. This equivalence was true for all elements and pools except for the low concentration blood pool for Cd. CONCLUSIONS: Storage temperatures of -20 degrees C and 4 degrees C are equivalent to -70 degrees C for stability of Cd, Mn, Pb, Se, and Hg in human whole blood for at least 36months when blood is stored in sealed polypropylene vials. Increasing the sample storage temperature from -70 degrees C to -20 degrees C or 4 degrees C can lead to large energy savings. The best analytical results are obtained when storage time at higher temperature conditions (e.g. 23 degrees C and 37 degrees C) is minimized because recovery of Se and Hg is reduced. Blood samples stored in polypropylene vials also lose volume over time and develop clots at higher temperature conditions (e.g., 23 degrees C and 37 degrees C), making them unacceptable for elemental testing after 10months and 2months, respectively. |
Analysis of whole human blood for Pb, Cd, Hg, Se, and Mn by ICP-DRC-MS for biomonitoring and acute exposures
Jones DR , Jarrett JM , Tevis DS , Franklin M , Mullinix NJ , Wallon KL , Derrick Quarles C Jr , Caldwell KL , Jones RL . Talanta 2017 162 114-122 We improved our inductively coupled plasma mass spectrometry (ICP-MS) whole blood method [1] for determination of lead (Pb), cadmium (Cd), and mercury (Hg) by including manganese (Mn) and selenium (Se), and expanding the calibration range of all analytes. The method is validated on a PerkinElmer (PE) ELAN® DRC II ICP-MS (ICP-DRC-MS) and uses the Dynamic Reaction Cell (DRC) technology to attenuate interfering background ion signals via ion-molecule reactions. Methane gas (CH4) eliminates background signal from 40Ar2 + to permit determination of 80Se+, and oxygen gas (O2) eliminates several polyatomic interferences (e.g. 40Ar15N+, 54Fe1H+) on 55Mn+. Hg sensitivity in DRC mode is a factor of two higher than vented mode when measured under the same DRC conditions as Mn due to collisional focusing of the ion beam. To compensate for the expanded method's longer analysis time (due to DRC mode pause delays), we implemented an SC4-FAST autosampler (ESI Scientific, Omaha, NE), which vacuum loads the sample onto a loop, to keep the sample-to-sample measurement time to less than 5 min, allowing for preparation and analysis of 60 samples in an 8-h work shift. The longer analysis time also resulted in faster breakdown of the hydrocarbon oil in the interface roughing pump. The replacement of the standard roughing pump with a pump using a fluorinated lubricant, Fomblin®, extended the time between pump maintenance. We optimized the diluent and rinse solution components to reduce carryover from high concentration samples and prevent the formation of precipitates. We performed a robust calculation to determine the following limits of detection (LOD) in whole blood: 0.07 µg dL−1 for Pb, 0.10 µg L−1 for Cd, 0.28 μg L−1 for Hg, 0.99 µg L−1 for Mn, and 24.5 µg L−1 for Se. © 2016 |
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