Publications by authors named "Thomas W Vetter"

The National Institute of Standards and Technology, which is the national metrology institute of the USA, assigns certified values to the mass fractions of individual elements in single-element solutions, and to the mass fractions of anions in anion solutions, based on gravimetric preparations and instrumental methods of analysis. The instrumental method currently is high-performance inductively coupled plasma optical emission spectroscopy for the single-element solutions, and ion chromatography for the anion solutions. The uncertainty associated with each certified value comprises method-specific components, a component reflecting potential long-term instability that may affect the certified mass fraction during the useful lifetime of the solutions, and a component from between-method differences.

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In recent years, microwave-induced combustion (MIC) has proved to be a robust sample preparation technique for difficult-to-digest samples containing high carbon content, especially for determination of halogens and sulfur. National Institute of Standards and Technology (NIST) has applied the MIC methodology in combination with isotope dilution analysis for sulfur determinations, representing the first-reported combination of this robust sample preparation methodology and high-accuracy quantification approach. Medium-resolution mode sector-field inductively coupled plasma mass spectrometry was invoked to avoid spectral interferences on the sulfur isotopes.

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Article Synopsis
  • A new radiochemical neutron activation analysis (RNAA) method was developed to measure arsenic levels in standard reference materials (SRMs) for blood and urine samples.
  • Samples were freeze-dried, irradiated, and analyzed using gamma-ray spectroscopy after separating arsenic from other materials.
  • The results were standardized with values from other labs, yielding certified arsenic concentrations for several levels in the SRMs, while an information value was assigned for one level due to measurement discrepancies.
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Article Synopsis
  • - The National Institute of Standards and Technology (NIST) and the National Institutes of Health (NIH) created the Standard Reference Material (SRM) 1950 to enhance metabolomics research by providing a reliable reference for metabolite concentrations in human plasma.
  • - SRM 1950 reflects the metabolite profile of adult human plasma, with samples obtained from a diverse group of donors to represent the U.S. population's ethnic composition.
  • - This reference material includes around 100 different analytes such as amino acids and clinical markers, and is the first of its kind specifically designed for the broad applications within the diverse field of metabolomics.
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The potential effect of spectral interference on the accurate measurement of the cadmium (Cd) mass fraction in fortified breakfast cereal and a variety of dietary supplement materials using inductively coupled plasma quadrupole mass spectrometry was studied. The materials were two new standard reference materials (SRMs)--SRM 3233 Fortified Breakfast Cereal and SRM 3532 Calcium Dietary Supplement--as well as several existing materials--SRM 3258 Bitter Orange Fruit, SRM 3259 Bitter Orange Extract, SRM 3260 Bitter Orange-containing Solid Oral Dosage Form, and SRM 3280 Multivitamin/Multielement Tablets. Samples were prepared for analysis using the method of isotope dilution and measured using various operating and sample introduction configurations including standard mode, collision cell with kinetic energy discrimination mode, and standard mode with sample introduction via a desolvating nebulizer system.

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Reference spectra of ammonia from four sources are compared. Low-resolution spectra (i.e.

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An ion exchange-gravimetric method, previously developed as a National Committee for Clinical Laboratory Standards (NCCLS) reference method for the determination of sodium in human serum, has been re-evaluated and improved. Sources of analytical error in this method have been examined more critically and the overall uncertainties decreased. Additionally, greater accuracy and repeatability have been achieved by the application of this definitive method to a sodium chloride reference material.

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