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Standard Reference Material 3280 Multivitamin/ Multielement Tablets was issued by the National Institute of Standards and Technology in 2009, and has certified and reference mass fraction values for 13 vitamins, 26 elements, and two carotenoids. Elements were measured using two or more analytical methods at NIST with additional data contributed by collaborating laboratories. This reference material is expected to serve a dual purpose: to provide quality assurance in support of a database of dietary supplement products and to provide a means for analysts, dietary supplement manufacturers, and researchers to assess the appropriateness and validity of their analytical methods and the accuracy of their results.
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Química Farmacéutica/normas , Suplementos Dietéticos/análisis , Suplementos Dietéticos/normas , Vitaminas/análisis , Carotenoides/análisis , Química Farmacéutica/métodos , Control de Calidad , Estándares de Referencia , Reproducibilidad de los Resultados , Comprimidos , Estados Unidos , Vitaminas/químicaRESUMEN
Perchlorate, an inorganic anion, has recently been recognized as an environmental contaminant by the US Environmental Protection Agency. Urine is the preferred matrix for assessment of human exposure to perchlorate. Although the measurement technique for perchlorate in urine was developed in 2005, the calibration and quality assurance aspects of the metrology infrastructure for perchlorate are still lacking in that there is no certified reference material (CRM) traceable to the International System of Units. To meet the quality assurance needs in biomonitoring measurements of perchlorate and the related anions that affect thyroid health, the National Institute of Standards and Technology (NIST), in collaboration with the Centers for Disease Control and Prevention (CDC), developed Standard Reference Material (SRM) 3668 Mercury, Perchlorate, and Iodide in Frozen Human Urine. SRM 3668 consists of perchlorate, nitrate, thiocyanate, iodine, and mercury in urine at two levels that represent the 50th and 95th percentiles, respectively, of the concentrations (with some adjustments) in the US population. It is the first CRM being certified for perchlorate. Measurements leading to the certification of perchlorate were made collaboratively at NIST and CDC using three methods based on liquid or ion chromatography tandem mass spectrometry. Potential sources of bias were analyzed, and results were compared for the three methods. Perchlorate in SRM 3668 Level I urine was certified to be 2.70 ± 0.21 µg L(-1), and for SRM 3668 Level II urine, the certified value is 13.47 ± 0.96 µg L(-1).
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Cromatografía Liquida/normas , Percloratos/orina , Espectrometría de Masas en Tándem/normas , Orina/química , Cromatografía Liquida/métodos , Exposición a Riesgos Ambientales/análisis , Humanos , Estándares de Referencia , Espectrometría de Masas en Tándem/métodos , Estados UnidosRESUMEN
Exact matching is investigated as a means of improving high-performance inductively coupled plasma optical emission spectrometry (HP-ICP-OES), a technique developed at the National Institute of Standards and Technology (NIST) to enable elemental determinations with relative expanded uncertainty of approximately 0.2% expressed at 95% confidence. "Exact matching" refers to the very careful matching of analyte mass fractions, internal standard mass fractions, and matrix compositions among the calibration and unknown sample solutions prepared for an analysis. Computer spreadsheet modeling results and laboratory data involving 16 pairs of analyte and internal standard wavelengths show that exact matching of analyte and internal standard mass fractions mitigates imprecision and bias that can be caused by even subtle nonlinearity in the ICP-OES instrument response. Laboratory experiments also demonstrate matrix effects caused by small variations in acid composition and by mass fractions of Na less than 4 mg kg(-1), emphasizing the need for exact matching of matrix compositions. HP-ICP-OES analyses performed at NIST with and without exact matching illustrate that exact matching enables relative expanded uncertainties to be halved to approximately 0.1%.
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Standard Reference Material (SRM) 1849 Infant/Adult Nutritional Formula has been issued by the National Institute of Standards and Technology (NIST) as a replacement for SRM 1846 Infant Formula, issued in 1996. Extraction characteristics of SRM 1846 have changed over time, as have NIST's analytical capabilities. While certified mass fraction values were provided for five constituents in SRM 1846 (four vitamins plus iodine), certified mass fraction values for 43 constituents are provided in SRM 1849 (fatty acids, elements, and vitamins) and reference mass fraction values are provided for an additional 43 constituents including amino acids and nucleotides, making it the most extensively characterized food-matrix SRM available from NIST.
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Fórmulas Infantiles/normas , Aminoácidos/análisis , Conducta Cooperativa , Ácidos Grasos/análisis , Humanos , Lactante , Fórmulas Infantiles/química , Estándares de Referencia , Vitaminas/análisisRESUMEN
A heated (approximately 90 degrees C) laminar flow interface has been designed to assist in the development of an argon electrospray sample introduction system for low-flow rate applications using inductively coupled plasma (ICP) spectrometry. Previously, the stability and robustness of the ICP were compromised by the entrainment of air, N2, or gas mixtures (e.g., Ar-N2) from the electrospray source. Also, more concentrated organic solvents (e.g., 50% (v/v) methanol-water), typically introduced by electrospray, could generate carbon deposits that obstruct the entrance lens to an ICP optical emission spectrometer (ICP-OES) or the sampler/skimmer cone interface in an ICP mass spectrometer (ICP-MS), decreasing analyte sensitivity. With the new interface design, a stable spray of 5% (v/v) methanol-water in a pure argon environment is achieved, eliminating the aforementioned problems. The turbulence and the consequent droplet loss caused by high gas velocity around the electrospray capillary are mitigated by the use of a laminar-flow gas with the aid of a flow diffuser. The argon electrospray interface is successfully installed on an ICP-OES and an ICP-MS for the first time.
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An automated sample introduction system, utilizing a demountable direct injection high-efficiency nebulizer (d-DIHEN), is successfully incorporated for the first time with an inductively coupled plasma optical emission spectrometer (ICP-OES) for the measurement of the phosphorus content in acid-digested nucleotides and deoxyribonucleic acid (DNA). With this experimental setup, the solution uptake rate and volume are reduced from 170 to 30 microL min(-1) and from 10 to 2.4 mL, respectively, thereby reducing the required DNA sample mass for solutions containing 3 microg g(-1) P from 300 to 72 microg of DNA, in comparison to previous analyses in our laboratory using a glass concentric nebulizer with cyclonic spray chamber arrangement. The use of direct injection also improves P (I) 213.617 nm sensitivity by a factor of 4 on average. A high-performance (HP) methodology in combination with the previous sample introduction system and ICP-OES provides simultaneous, time-correlated internal standardization and drift correction resulting in relative expanded uncertainties (% U) for the P mass fractions in the range of 0.1-0.4 (95% confidence level) for most of the thymidine 5'-monophosphate (TMP), calf thymus DNA (CTDNA), and plasmid DNA (PLDNA) analyses. The d-DIHEN with HP-ICP-OES methodology allows for the quantification of DNA mass at P mass fractions as low as 0.5 microg g(-1), further reducing the required DNA mass to 12 microg, with small uncertainty (< or = 0.4%). This successful approach will aid in the development and certification of nucleic acid certified reference materials (CRMs), particularly for these samples that are typically limited in volume.
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ADN/análisis , Métodos Analíticos de la Preparación de la Muestra , Animales , ADN/química , Vidrio , Nebulizadores y Vaporizadores , Nucleótidos/análisis , Nucleótidos/química , Fósforo/química , Análisis EspectralRESUMEN
High-performance inductively coupled plasma optical emission spectrometry (HP-ICP-OES) was used to certify the Be mass fraction in National Institute of Standards and Technology (NIST) Standard Reference Material (SRM) 1877 Beryllium Oxide Powder. The certified value and expanded uncertainty expressed at a 95% confidence level is (0.3576 +/- 0.0024) g/g. To obtain best results, the Be mass fractions, Mn (internal standard) mass fractions, and matrix compositions of the calibration solutions were carefully matched to those of the sample solutions for each individual HP-ICP-OES analysis. This "exact matching" approach was used because experience at NIST has shown that it often affords improved accuracy and precision in HP-ICP-OES analysis. NIST has never published these observations. Due to the toxicity of BeO and the difficulty of containing the very fine powder material, sets of solutions for HP-ICP-OES analysis were prepared by laboratories collaborating with NIST who have the experience and equipment needed to work with the material safely. Each laboratory utilized a unique digestion protocol(s). After preparing the sets of solutions, the collaborating laboratories shipped them to NIST for HP-ICP-OES analysis. NIST provided the collaborating laboratories with solution preparation kits and spreadsheets to help establish traceability of the HP-ICP-OES results to the International System of Units (SI) and to allow exact matching to be accomplished. The agreement observed among the four individual Be mass fraction values determined from the sets of solutions prepared by the collaborating laboratories was 0.074% relative (1s of mean). The excellent agreement provides a measure of confidence in the robustness of each of the digestion procedures, as well as in the certified Be mass fraction value. The analytical benefits of using exact matching for this particular certification were investigated. Results show that exactly matching the matrix compositions of the standards to the samples for each HP-ICP-OES analysis was critical to obtaining the excellent agreement observed among the individual Be mass fraction values and also helped to minimize bias and uncertainty in the certified value. Unlike previous NIST studies, exactly matching the Be and Mn mass fractions of the standards to the samples for this particular certification appears to have had little effect on the data.
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Berilio/química , Certificación , Espectrofotometría Atómica/métodos , Berilio/normas , Peso Molecular , Estándares de Referencia , Espectrofotometría Atómica/normasRESUMEN
Owing to the absence of readily available certified particulate reference materials (RMs), most analytical methods used to determine particulate contaminant levels in workplace or other environments are validated using solution RMs, which do not assess the robustness of the digestion step for all forms and sizes of particles in a sample. A library of particulate RMs having a range of chemical forms and particle sizes is needed to support a shift in method evaluation strategies to include both solution and particulate RMs. In support of creating this library, we characterized bulk and physically size separated fractions of beryllium oxide (BeO) particles recovered from the machining fluid sludge of an industrial ceramic products grinding operation. Particles were large agglomerates of compact, crystalline BeO primary particles having diameters on the order of several micrometers. As expected, the particle surface area was independent of sieve size, with a range from 3.61 m(2)/g (53-63-microm fraction) to 4.82 m(2)/g (355-600-microm fraction). The density was near the theoretical value (3.01 g/cm(3)). The data support more detailed characterization of the sludge materials for use as size-selective RMs. This work illustrates an approach that can be used to develop RMs that are difficult to digest.
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Berilio/normas , Técnicas de Química Analítica/métodos , Tamaño de la Partícula , Estándares de Referencia , SolubilidadRESUMEN
The certification of Standard Reference Material (SRM is a registered trademark of NIST) 3103a As Spectrometric Solution is based on the gravimetric preparation value that is verified by inductively coupled plasma optical emission spectrometry (ICP-OES) measurements. A disagreement between the gravimetric and the spectrometric values for a batch of As calibration solutions led to the discovery that the solutions contained a mixture of trivalent and pentavalent As species and that the pentavalent species was approximately 8% more sensitive than the trivalent species with ICP-OES determination. The kinetics of the reaction between As metal and nitric acid were studied, and the results were applied to develop a procedure that would consistently produce single-species pentavalent As standards, which eliminates As speciation as a source of measurement bias in the SRM certification process.
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BACKGROUND: Cyanide (CN) is a lethal toxin. Quantification in blood is necessary to indicate exposure from many sources, including food, combustion byproducts, and terrorist activity. We describe an automated procedure based on isotope-dilution gas chromatography-mass spectrometry (ID GC/MS) for the accurate and rapid determination of CN in whole blood. METHODS: A known amount of isotopically labeled potassium cyanide (K13C15N) was added to 0.5 g of whole blood in a headspace vial. Hydrogen cyanide was generated through the addition of phosphoric acid, and after a 5-min incubation, 0.5 mL of the headspace was injected into the GC/MS at an oven temperature of -15 degrees C. The peak areas from the sample, 1H12C14N+, at m/z 27, and the internal standard, 1H13C15N+, at m/z 29, were measured, and the CN concentration was quantified by ID. The analysis time was 15 min for a single injection. RESULTS: We demonstrated method accuracy by measuring the CN content of unfrozen whole blood samples fortified with a known amount of CN. Intermediate precision was demonstrated by periodic analyses over a 14-month span. Relative expanded uncertainties based on a 95% level of confidence with a coverage factor of 2 at CN concentrations of 0.06, 0.6, and 1.5 microg/g were 8.3%, 5.4%, and 5.3%, respectively. The mean deviation from the known value for all concentrations was <4%. CONCLUSION: The automated ID GC/MS method can accurately and rapidly quantify nanogram per gram to microgram per gram concentrations of CN in blood.
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Cianuros/sangre , Ácido Ascórbico , Radioisótopos de Carbono , Cromatografía de Gases y Espectrometría de Masas , Humanos , Cianuro de Hidrógeno/sangre , Técnicas de Dilución del Indicador , Indicadores y Reactivos , Isótopos de Nitrógeno , Temperatura , IncertidumbreRESUMEN
Homogeneous incorporation of analytes of known isotopic abundance into sol-gel-derived standards that mimic important mineral systems has the potential to contribute significantly to providing solid standard benchmarks for a range of applications. This preliminary study reports on the synthesis of solid glass standards produced via the sol-gel method and their doping with Standard Reference Material (SRM) 981 Common Lead Isotopic Standard and SRM 982 Equal-Atom Lead Isotopic Standard. Custom isotopic materials were also prepared using mixtures of the two isotopic SRMs. Particles from these solid samples were then introduced into an inductively coupled plasma mass spectrometer via laser ablation to determine whether materials of suitable homogeneity could be developed as isotopic reference materials. Preliminary results for Pb isotope ratios show that these solid isotopic reference standards are capable of correcting for instrumental mass bias and laser ablation-induced bias due to fractionation simultaneously. Correction factors generated from the quotient of the certified and measured Pb isotopic ratios in sol-gel disks spiked with SRMs 981 and 982 were successfully applied to produce accurate isotope ratios using comparative control/unknown checks. These correction factors were also used to assign Pb isotopic ratios in NIST SRM 612 Trace Elements in Glass that were in excellent agreement with published measurements, suggesting that tunable matrix sol-gel disks can serve as adequate control matrixes for evaluation of isotope ratios in glass samples.