Recently developed NIST food related standard reference materials

Summary NIST issues food related, chemical composition standard reference materials for validating food analyses. SRMs certified for inorganic constituents are: Non-Fat Milk Powder (SRM 1549), Oyster Tissue (SRM 1566a), Bovine Liver (SRM 1577a), Wheat Flour (SRM 1567a), Rice Flour (SRM 1568a), and Total Diet (SRM 1548). The certificate of analysis for the total diet SRM also provides a certified concentration for cholesterol. Oyster tissue, a renewal SRM, is certified for 25 elements including 6 (Al, Cl, I, P, S, and V), that had not been certified in the previously issued SRM 1566. The elemental certified concentrations are based on concordant results of two or more independent analytical methods. The chemical compositions of the six food matrix SRMs are tabulated. Three food matrix SRMs certified for organic constituents are: Cholesterol and Fat-Soluble Vitamins in Coconut Oil (SRM 1563), Cholesterol in Whole Egg Powder (SRM 1845) and Organics in Cod Liver Oil (SRM 1588). Serum and urine matrix SRMs are also available that may be useful for metabolic and bioavailability studies.     

Characterization of NIST food-matrix standard reference materials for their vitamin C content

The vitamin C concentrations in three food-matrix Standard Reference Materials (SRMs) from the National Institute of Standards and Technology (NIST) have been determined by liquid chromatography (LC) with absorbance detection. These materials (SRM 1549a Whole Milk Powder, SRM 1849a Infant/Adult Nutritional Formula, and SRM 3233 Fortified Breakfast Cereal) have been characterized to support analytical measurements made by food processors that are required to provide information about their products’ vitamin C content on the labels of products distributed in the United States. The SRMs are primarily intended for use in validating analytical methods for the determination of selected vitamins, elements, fatty acids, and other nutrients in these materials and in similar matrixes. They can also be used for quality assurance in the characterization of test samples or in-house control materials, and for establishing measurement traceability. Within-day precision of the LC method used to measure vitamin C in the food-matrix SRMs characterized in this study ranged from 2.7 % to 6.5 %.     

Comparison of NAA methods to determine medium-lived radionuclides in NIST soil standard reference materials

In order to determine the elemental concentrations of three new soil standard reference materials SRMs 2709, 2710 and 2711 from the National Institute of Standards and Technology (NIST), a comparative study of different medium-lived neutron activation analysis methods was carefully performed. Three irradiation conditions (1-hour thermal, 1-hour epithermal and 5-minute epithermal) and two counting modes (normal and Compton suppression) have been evaluated for following ten elements: As, Au, Cd, Ga, K, La, Mo, Sb, Sm, and W. The results show that the method of 5-minute epithermal and a 1-day decay is the optimum way to analyze Ga, while the addition of the Compton suppression is very beneficial for the determination of K. Using the Compton suppression system in conjunction with the 1-hour epithermal and a 1-week decay, is ideal to determine Au, Cd, Mo and W, while routine 1-hour thermal and a 1-week decay, is adequate to determine As, Sb, Sm and La in concentrations found in soil.     

Selenomethionine contents of NIST wheat reference materials

Values of the total selenium and selenomethionine (Semet) content of four wheat-based reference materials have been obtained by gas chromatography-stable isotope dilution mass spectrometry methods. The total Se method is an established one, and the results obtained with it are consistent with previously-assigned values. The Semet method (previously reported by our laboratory) is based on reaction with CNBr. Our data indicate that the four wheat samples (wheat gluten, durum wheat, hard red spring wheat, and soft winter wheat), though having a 30-fold range in total Se content, all have about 45% of their total Se values in the form of selenomethionine. Investigation of the CNBr-based method suggests that additional experiments are needed to verify that all selenomethionine in the wheat samples is accounted for, but also indicates that the values obtained are within 15% of the true values. As the form in which Se occurs in foods and dietary supplements is important from a nutritional perspective, adding information about Se speciation to total Se values in appropriate reference materials makes these materials more valuable in relevant analytical work.     

A european intercomparison of vegetal standard reference materials,based on INAA and some non nuclear spectrochemical techniques

INAA results obtained on 11 vegetal samples proposed as European reference standards, in nutritional, agricultural and analytical studies are reported. A comparison is also reported with the data obtained by 38 European laboratories, by using spectrochemical methods (ICP atomic absorption, X-ray fluorescence, etc.). The usefulness of Instrumental Neutron Activation Analysis (INAA) is stressed, particularly when more usual methods are not sensitive enough for microelements that are important markers of toxic and pollutant substances. To this class belong lanthanides and other rare elements (Sc, Cs, Rb), which can be used both as fingerprint of soil provenance and for evaluating the homogeneity of the sample.     

Isotope-ratio measurements of lead in NIST standard reference materials by multiple-collector inductively coupled plasma mass spectrometry

The capability of a second-generation Nu Instruments multiple collector inductively coupled plasma mass spectrometer (MC-ICP-MS) has been evaluated for precise and accurate isotope-ratio determinations of lead. Essentially the mass spectrometer is a double-focusing instrument of Nier-Johnson analyzer geometry equipped with a newly designed variable-dispersion ion optical device, enabling the measured ion beams to be focused into a fixed array of Faraday collectors and an ion-counting assembly. NIST SRM Pb 981, 982, and 983 isotopic standards were used. Addition of thallium to the lead standards and subsequent simultaneous measurement of the thallium and lead isotopes enabled correction for mass discrimination, by use of the exponential correction law and 205Tl/203Tl = 2.3875. Six measurements of SRM Pb-982 furnished the results 206Pb/204Pb = 36.7326(68), 207Pb/204Pb = 17.1543(30), 208Pb/204Pb = 36.7249(69), 207Pb/206Pb = 0.46700(1), and 208Pb/206Pb = 0.99979(2); the NIST-certified values were 36.738(37), 17.159(25), 36.744(50), 0.46707(20), and 1.00016(36), respectively. Direct isotope lead analysis in silicates can be performed without any chemical separation. NIST SRM 610 glass was dissolved and introduced into the MC-ICP-MS by means of a micro concentric nebulizer. The ratios observed were in excellent agreement with previously reported data obtained by TIMS and laser ablation MC-ICP-MS, despite the high Ca/Pb concentration ratio (200/1) and the presence of many other elements at levels comparable with that of lead. Approximately 0.2 microg lead are sufficient for isotope analysis with ratio uncertainties between 240 and 530 ppm.     

Certification of a new NIST fly ash standard reference material

In June 1993 the National Institute of Standards and Technology (NIST) released the third version of Constituent Elements in Coal Fly Ash Standard Reference Material (SRM 1633b). This material is intended for quality assurance purposes in evaluating the analytical methods used for the determination of constituent elements in coal fly ash or in materials with similar matrices. It has been certified for 23 major, minor and trace elements using ten different analytical techniques. For an element to be certified in a NIST SRM, its concentration is usually determined by at least two independent analytical techniques. The concentrations of additional 24 elements are provided for information only purposes in the new fly ash. Current plans are to certify the concentrations of a number of rare earths upon completion of additional analytical work now in progress. Homogeneity testing was accomplished using instrumental neutron activation analysis and X-ray fluorescence. This presentation summarizes the preparation of this new material and the analytical results used for certification.     

The determination of the uncertainty of reference materials certified by laboratory intercomparison

A pragmatic method is proposed for the implementation of the Guide to the expression of uncertainty in measurement in the certification of reference materials by laboratory intercomparison. It is based on the establishment of a full uncertainty budget for each laboratory result and the estimation of the impact of various laboratory standard uncertainties and of between-units variability on the certified reference material (CRM) uncertainty.     

Application of standard materials and standard reference materials in the analysis of lead in blood

Summary Valuable information can be obtained at little expenses from quality control samples prepared in-house to monitor the determination of blood lead by atomic absorption spectrophotometry. Commercially manufactured control materials can also be used for this purpose. These materials are compared to standard reference materials which at present are available.The relative standard deviations for analysis of NBS standard reference materials were 15.4–2.8% (range 60–754 g/l) and in agreement with the relative standard deviation estimated for the analytical method. The corresponding figures for BCR control reference materials were lower: 1.1–1.4% (range 134–795 g/l).The average analytical bias demonstrated by analysis of NBS standard reference material and BCR control reference material were 3–6% (range 795–60 g/l) and in agreement with bias estimated by analysis of commercially manufactured and in-house prepared control materials.     

Particle size determination of some IAEA and NIST environmental and biological reference materials

Particle size distributions in fifteen International Atomic Energy Agency (IAEA) and sixteen National Institute of Standards and Technology (NIST) reference materials (RMs) were measured with the basic aim to investigate the potential of these materials to be used as reference or quality control materials in analyses where a small sample mass is required (< 100 mg). Most of the investigated materials are commercially available environmental or biological natural matrix RMs with certified values for trace elements, radionuclides, or organometallic compounds. The laser diffraction technique was used in all measurements. From the point of particle size distribution, materials IAEA-390 (Algae, a set of three materials), IAEA-396m (Urban Dust, 3x air jet milled), NIST-SRM 1515 (Apple Leaves), NIST-SRM 1547 (Peach Leaves), NIST-SRM 1566a (Oyster Tissue), NIST-SRM 1570a (Spinach), NIST-SRM 1573a (Tomato Leaves), and NIST-SRM 1648 (Urban Particulate) can be considered appropriate for small sample mass analysis. However, additional analytical tests are needed to confirm the appropriate homogeneous distribution of chemical composition, the level of heterogeneity for individual elements, at this sample mass level.     

Value assignment of nutrient concentrations in five standard reference materials and six reference materials

A number of food-matrix reference materials (RMs) are available from the National Institute of Standards and Technology (NIST) and from Agriculture Canada through NIST. Most of these materials were originally value-assigned for their elemental composition (major, minor, and trace elements), but no additional nutritional information was provided. Two of the materials were certified for selected organic constituents. Ten of these materials (Standard Reference Material [SRM] 1,563 Cholesterol and Fat-Soluble Vitamins in Coconut Oil [Natural and Fortified], SRM 1,566b Oyster Tissue, SRM 1,570a Spinach Leaves, SRM 1,974a Organics in Mussel Tissue (Mytilus edulis), RM 8,415 Whole Egg Powder, RM 8,418 Wheat Gluten, RM 8,432 Corn Starch, RM 8,433 Corn Bran, RM 8,435 Whole Milk Powder, and RM 8,436 Durum Wheat Flour) were recently distributed by NIST to 4 laboratories with expertise in food analysis for the measurement of proximates (solids, fat, protein, etc.), calories, and total dietary fiber, as appropriate. SRM 1846 Infant Formula was distributed as a quality control sample for the proximates and for analysis for individual fatty acids. Two of the materials (Whole Egg Powder and Whole Milk Powder) were distributed in an earlier interlaboratory comparison exercise in which they were analyzed for several vitamins. Value assignment of analyte concentrations in these 11 SRMs and RMs, based on analyses by the collaborating laboratories, is described in this paper. These materials are intended primarily for validation of analytical methods for the measurement of nutrients in foods of similar composition (based on AOAC INTERNATIONAL's fat-protein-carbohydrate triangle). They may also be used as "primary control materials" in the value assignment of in-house control materials of similar composition. The addition of proximate information for 10 existing reference materials means that RMs are now available from NIST with assigned values for proximates in 6 of the 9 sectors of the AOAC triangle. Five of these materials have values assigned for total dietary fiber-the first such information provided for materials available from NIST.     

中红外光谱透射比标准物质研制

采用物化性质稳定的单晶硅作为基质,以直流磁控溅射方式轻蒸镀不同厚度的镍、铬混合膜层,实现了中红外波段(500~4000 cm^–1)不同透射比标准物质的研制。研制的中红外光谱透射比标准物质其透射比标称值分别为10%和50%,扩展不确定度优于0.008(k=2)。该标准物质具有量值稳定、光谱平坦等特点,可用于各类傅里叶变换红外光谱设备的透射比校准。     

Long-term stability of hydrocarbons in NIST gas standard reference material (SRM) 1800

A gas standard reference material (SRM) containing fifteen hydrocarbons in nitrogen at a nominal 5 nmol mol(-1) was issued in 1993. The certification period for SRM 1800 was assigned as 2 years, because of limited stability data. Over a period of 10 years reanalysis of the lot standard (a sample chosen from the SRM lot to which all other lot samples are compared), SRM samples remaining in stock for sale, and SRMs returned to the National Institute of Standards and Technology (NIST) for recertification, were compared with primary standards to assess the stability of the hydrocarbons. New primary standards were periodically introduced into the original primary standard suite to assess the stability and consistency of the primary standards. Over this ten-year period 11 SRM 1800 samples were reanalyzed, resulting in 210 amount-of-substance fraction (concentration) determinations performed for quality-assurance purposes. Of these measurements 209 (99.5%) agreed within the original 95% confidence interval of the +/-4% expanded uncertainty, demonstrating the stability of the standards. There was also agreement to within +/-2% of the original concentration for 204 (97%) of the measurements. This is well within the original +/-4% expanded uncertainty assigned to the hydrocarbon concentrations at the approximate 95% confidence interval demonstrating stability. These results will enable the expiry date to be increased for future restock issues of SRM 1800.     

Development and certification of green tea-containing standard reference materials

A suite of three green tea-containing Standard Reference Materials (SRMs) has been issued by the National Institute of Standards and Technology (NIST): SRM 3254 Camellia sinensis (Green Tea) Leaves, SRM 3255 Camellia sinensis (Green Tea) Extract, and SRM 3256 Green Tea-Containing Solid Oral Dosage Form. The materials are characterized for catechins, xanthine alkaloids, theanine, and toxic elements. As many as five methods were used in assigning certified and reference values to the constituents, with measurements carried out at NIST and at collaborating laboratories. The materials are intended for use in the development and validation of new analytical methods, and for use as control materials as a component in the support of claims of metrological traceability.     

Filling the AOAC triangle with food-matrix standard reference materials

Well-characterized reference materials are needed by laboratories in the food testing and nutrition communities to facilitate compliance with nutritional labeling laws, to provide traceability for food exports needed for acceptance in many foreign markets, and to improve the accuracy of nutrition information that is provided to assist consumers in making sound dietary choices. As a result of the enactment of the Nutrition Labeling and Education Act of 1990 and the Infant Formula Act of 1980, the National Institute of Standards and Technology (NIST) has developed a suite of food-matrix Standard Reference Materials (SRMs) characterized for nutrient concentrations. These include SRM 1544 Fatty Acids and Cholesterol in a Frozen Diet Composite, SRM 1546 Meat Homogenate, SRM 1548a Typical Diet, SRM 1566b Oyster Tissue, SRM 1846 Infant Formula, SRM 1946 Lake Superior Fish Tissue, SRM 2383 Baby Food Composite, SRM 2384 Baking Chocolate, SRM 2385 Spinach, and SRM 2387 Peanut Butter. Many of these materials were developed at the request of the food industry to populate a nine-sectored fat-protein-carbohydrate triangle developed by AOAC International. With the completion of SRM 2387, SRMs representing each sector of the triangle are now available. These food-matrix reference materials are intended primarily for validation of analytical methods for the measurement of proximates, fatty acids, vitamins, minerals, and so on in foods of similar composition. They may also be used as "primary control materials" in the value-assignment of in-house, secondary, control materials to confirm accuracy as well as to establish traceability to NIST.     

Analysis of standard reference materials by absolute INAA

Three standard reference materials were analyzed by a method of absolute INAA. Two different light water pool-type reactors were used to produce equivalent analytical results even though the epithermal to thermal flux ratio in one reactor was higher than that in the other by a factor of two.     

Certification of standard reference materials containing bitter orange

A suite of three dietary supplement standard reference materials (SRMs) containing bitter orange has been developed, and the levels of five alkaloids and caffeine have been measured by multiple analytical methods. Synephrine, octopamine, tyramine, N-methyltyramine, hordenine, total alkaloids, and caffeine were determined by as many as six analytical methods, with measurements performed at the National Institute of Standards and Technology and at two collaborating laboratories. The methods offer substantial independence, with two types of extractions, two separation methods, and four detection methods. Excellent agreement was obtained among the measurements, with data reproducibility for most methods and analytes better than 5% relative standard deviation. The bitter-orange-containing dietary supplement SRMs are intended primarily for use as measurement controls and for use in the development and validation of analytical methods. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Thermal behavior study of biodiesel standard reference materials

Quality control of fuel-related properties of biodiesel, such as thermal stability, is needed to obtain consistent engine performance by fuel users, since biodiesel is susceptible to auto-oxidation when exposed to air, light, and temperature during storage. In this work two pure standard reference materials of biodiesels produced from soy oil and animal feedstocks were studied. Differential scanning calorimetry and thermogravimetry measurements were performed and the analysis of the results revealed small temperature variations in the thermal events among the two standards, these differences are due mainly to their chemical composition, been highly influenced by the amounts of unsaturated esters.     

Iodine in different food articles and standard reference materials

Summary The greater part of essential iodine enters living organisms via the food chain. Nevertheless, quantitative data on its concentration in diets, food articles and also in available SRMs are very poor and scarce. This and WHO recommendations on daily allowances of iodine for man via food articles caused an added demand for accurate and reliable determination of iodine in these samples. From this point of view the purpose of the present was to analyse and to establish the concentration levels of total iodine in some food articles, diets, SRMs and candidate reference materials by the use of rapid radiochemical separation, developed in our laboratory. The results were checked by the analysis of SRMs with available certified values for iodine and good agreement is evident.