CRMs for quality control of determinations of chemical forms of elements in support to EU legislation

The concern for the control of toxic chemical forms of elements in the environment is reflected by an increasing number of analyses performed by research and routine laboratories. The European Commission has recognised the need to include some of these species in the list of dangerous substances to be monitored, e.g. in the marine environment or in groundwater. However, in most cases, the specifications are far from being sufficient in respect to the chemical forms of the element to be determined. Furthermore, these determinations are in most cases based on multi-step analytical techniques which are often prone to errors (e.g. at the extraction, derivatization or separation steps). Certified reference materials (CRMs) certified for their content in chemical forms of elements are, therefore, necessary to ensure the accuracy of these measurements and hence the respect of the regulations. However, the lack of CRMs for speciation analysis hampers the quality control of determinations which in turn leads to an incomparability of data produced; so far the number of CRMs produced by international organisations, e.g. NIST (USA), NIES (Japan), NRCC (Canada) and BCR (Belgium), is very limited and concerns mainly compounds such as e.g. methyl-mercury and butyltin compounds in biological matrices or sediments. The Standards, Measurements and Testing Programme (formerly BCR) of the European Commission has started a series of projects for the improvement of speciation analysis in environmental matrices, the final aim of which being the production of a variety of environmental CRMs. The existing EU legislation involving chemical forms of elements is presented, the requirements for the preparation of CRMs for speciation analysis are discussed and an update of the most recent CRMs produced within the Standards, Measurements and Testing Programme (SM&T) is given.     

CRMs for quality control of determinations of chemical forms of elements in support to EU legislation

The concern for the control of toxic chemical forms of elements in the environment is reflected by an increasing number of analyses performed by research and routine laboratories. The European Commission has recognised the need to include some of these species in the list of dangerous substances to be monitored, e.g. in the marine environment or in groundwater. However, in most cases, the specifications are far from being sufficient in respect to the chemical forms of the element to be determined. Furthermore, these determinations are in most cases based on multi-step analytical techniques which are often prone to errors (e.g. at the extraction, derivatization or separation steps). Certified reference materials (CRMs) certified for their content in chemical forms of elements are, therefore, necessary to ensure the accuracy of these measurements and hence the respect of the regulations. However, the lack of CRMs for speciation analysis hampers the quality control of determinations which in turn leads to an incomparability of data produced; so far the number of CRMs produced by international organisations, e.g. NIST (USA), NIES (Japan), NRCC (Canada) and BCR (Belgium), is very limited and concerns mainly compounds such as e.g. methyl-mercury and butyltin compounds in biological matrices or sediments. The Standards, Measurements and Testing Programme (formerly BCR) of the European Commission has started a series of projects for the improvement of speciation analysis in environmental matrices, the final aim of which being the production of a variety of environmental CRMs. The existing EU legislation involving chemical forms of elements is presented, the requirements for the preparation of CRMs for speciation analysis are discussed and an update of the most recent CRMs produced within the Standards, Measurements and Testing Programme (SM&T) is given.     

Overview of SM & T (BCR) activities for the quality control of mercury determination in the environment

The aim of the Standards, Measurements and Testing Programme (SM & T) of the European Commission (continuation of the BCR and Measurements and Testing Programmes) is to contribute to the harmonisation and improvement of methods and measurements carried out within the European Union and hence to the comparability of data necessary for e.g. trade activities, monitoring of environment, food and health, etc. R & D projects along these lines are currently funded; in the field of environmental analysis, they consist in most cases in the organisation of interlaboratory studies (intercomparisons and certifications of reference materials) in which laboratories may collaborate to improve the measurement or analysis concerned. Other activities are related to development of new methods and pre-normative research. This paper describes the objectives of the SM & T programme and the main actions undertaken, and gives examples of projects dealing with mercury determination in environmental matrices. Received: 24 September 1996 / Revised: 19 January 1997 / Accepted: 24 January 1997     

Overview of SM & T (BCR) activities for the quality control of mercury determination in the environment

The aim of the Standards, Measurements and Testing Programme (SM & T) of the European Commission (continuation of the BCR and Measurements and Testing Programmes) is to contribute to the harmonisation and improvement of methods and measurements carried out within the European Union and hence to the comparability of data necessary for e.g. trade activities, monitoring of environment, food and health, etc. R & D projects along these lines are currently funded; in the field of environmental analysis, they consist in most cases in the organisation of interlaboratory studies (intercomparisons and certifications of reference materials) in which laboratories may collaborate to improve the measurement or analysis concerned. Other activities are related to development of new methods and pre-normative research. This paper describes the objectives of the SM & T programme and the main actions undertaken, and gives examples of projects dealing with mercury determination in environmental matrices. Received: 24 September 1996 / Revised: 19 January 1997 / Accepted: 24 January 1997     

Certified reference materials for the quality control of environmental analysis within the standards,measurements and testing programme (formerly BCR)

A great number of analyses is performed every year, the results of which are used for many purposes, e.g. the quality of goods and food, the status of quality of the environment or the health of patients. The accuracy of these results is a prerequisite for a good interpretation of the data obtained. One of the most powerful tool for achieving quality control of chemical analysis is to use reference materials (RMs) and certified reference materials (CRMs). These materials are necessary for one or more of the following items: method validation (CRMs), monitoring of the state of statistical control (RMs), samples in inter-comparisons (RMs), etc. The requirements and use of RMs and CRMs in chemical analysis are described, with special emphasis on environmental analysis, and some examples of environmental materials currently in production within the Standards, Measurements and Testing Programme (formerly BCR) of the European Commission are given.     

BCR reference materials for food and agricultural analysis: an overview

Summary The BCR is a research programme of the European Communities having the broad aim of improving accuracy and measurement harmony in areas of concern at Community level. Much of the work is directly relevant to the removal of trading and other obstacles as is necessary for the achievement of a single European market by 1992.The presentation provides an overview of the sector of the programme concerned with Reference Materials (RMs) for food and agricultural analyses.Summarises are given of activities for inorganic, trace organic and nutritional analyses, for calibration of rapid methods (NMR, NIR, XRF and Immuno-assay techniques) and technological measurements (industrial quality of cereals, food colour, water-sorption and detection of fraudulent addition of sugar during wine making by NMR). An alphabetic listing of analytes and properties studied during the programme is given.

---

BCR-Referenzmaterialien für die Lebensmittel- und landwirtschaftliche Analyse — Ein Überblick

     

Planning and certification of new multielemental reference materials for research in antarctica

The adoption of the principles of Good Laboratory Practice (GLP) and the implementation of the ensuing procedures for quality assurance (QA) and quality control (QC) of analytical determinations are nowadays deemed essential to the achievement of sound, credible and comparable experimental information. This is certainly also applicable to research projects currently being carried out in the antarctic continent, in particular as regards investigations on global change phenomena. Worldwide investments made so far in this field do require in fact that reliability of data be optimized so as to allow for a harmonized assessment of ongoing trends. In this context the Italian National Programme for Research in Antarctica has recently launched a project for the preparation of new multielemental certified reference materials (CRMs) to be used for QC of analyses performed on environmentally significant materials. The suitability of CRMs to verify the accuracy of experimental measurements acknowledgedly depends, among others, on the degree of similarity of their matrix composition and analyte levels to those expected for real samples. From this standpoint three CRMs are planned, namely: i) marine sediment certified for Al, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sn and Zn; ii) ocean water certified for Cd, Cr, Cu, Fe, Hg, Mn, Ni and Pb; iii) krill certified for As, Cd, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sn and Zn. Regarding the first two matrices, amounts of ca. 100 kg and ca. 1001, respectively, have been collected during the IX (1993–1994) antarctic expedition, while krill was taken in the course of the X (1994–1995) campaign. The pretreatment of sediment has been accomplished in terms of homogenization, stabilization and characterization of the preliminary ground mass. Approximately 500 bottles, each containing 75 g of material are now ready for distribution to interested laboratories involved in chemical measurements of antarctic matrices, whereas ocean water and krill will follow at a later stage. Finally, depending on circumstances, also the certification of organochlorine compounds in the same materials will be attempted.     

Interlaboratory programme for the quality control of trimethyllead determination in the environment

Determinations of the trimethyllead moiety in environmental samples are carried out by a number of laboratories in Europe. To verify the quality of such determinations, the Measurements and Testing Programme (formerly BCR) of the European Commission organised an interlaboratory exercise which allowed discussion and comparison of the different techniques used so far in lead speciation analyses. In addition, this first step enabled a study of the feasibility of the preparation of candidate reference materials (CRMs) for the determination of the trimethyllead moiety in simulated rainwater to be carried out. The solutions used in this study were carefully prepared and their homogeneity and stability verified. This paper describes the organisation and the results of the intercomparison and discusses the further development of the project.     

Certification of trimethyl‐lead in an urban dust reference material (CRM 605)

In order to control the quality of trimethyl‐lead determination in urban dust, the Standards, Measurements and Testing Programme (formerly BCR) of the European Commission organized interlaboratory studies of which the final aim was to certify a Reference Material. This paper describes the preparation of an urban dust reference material (CRM 605), the homogeneity and stability studies, and the analytical work performed for the certification of the trimethyl‐lead content (7.9 ± 1.2 μg kg⁻¹ by mass). Copyright © 1999 John Wiley & Sons, Ltd.     

Reference material needs in clinical laboratory science

In 1968, clinical chemistry was considered to be the field most in need of certified reference materials (CRMs). While significant progress has been made in this area, new diagnostic assays are continually being developed that create a need for new CRMs. Members of the clinical laboratory community help to identify reference material needs. Professional and governmental organizations, such as IFCC, AACC, NCCLS, CDC, and the national metrological institutes (NMIs), respond to develop protocols and materials. Several measurands are presented as examples. In the late 1950s and early 1960s, in response to a need for standardization of lipid and lipoprotein measurements, CDC developed a reference system that included secondary reference materials. Over the years, the process of preparation of these materials was refined, eventually leading to the development of NCCLS guideline for preparation of commutable frozen serum pools for use as secondary reference materials (C37-A). This protocol was used for the preparation of NIST SRM 1951a (lipids in frozen (liquid) human serum). In the 1980s, a need for a reference material for blood lead was identified. CDC and NIST cooperated to develop SRM 955 (lead in bovine blood). More recently, efforts have been initiated to standardize high-sensitivity C-reactive protein (hsCRP) assays. In this case, a CRM for CRP existed (CRM 470, developed by IFCC and available from IRMM), but at concentrations in the acute phase reactant range and not in the low range needed for hsCRP assays. CDC coordinated a study to evaluate diluted CRM470 and other candidate materials as secondary reference materials for hsCRP assays.Presented at BERM-9—Ninth International Symposium on Biological and Environmental Reference Materials, June 15–19, 2003, Berlin, Germany.     

Method validation and reference materials

For implementation of food and feed legislation, there is a strong need for development and harmonisation of reliable, validated and if possible, robust and simple analytical methods. In addition, precise methods used for measuring the exposure of humans to certain types of food contaminants and residues (natural, man-made or produced during technological treatment) such as, e.g. mycotoxins, acrylamide, pesticides and allergens have to be available, in order to compare results derived from monitoring studies. Methods should be validated (in-house or in a collaborative trial) according to harmonised protocols and good laboratory practice must be in place in order to be compliant with internationally harmonised standards. The way in which this is implemented depends strongly on the analyte, interference within the food matrix and other requirements that need to be met. Food and feed certified reference materials, when matrix matched and containing the appropriate concentration of the certified substance, are an extremely useful tool in validation of measurements.Presented at BERM-9—Ninth International Symposium on Biological and Environmental Reference Materials, 15–19 June 2003, Berlin, Germany.     

Selective Pressurized Liquid Extraction of PCB’s from Food and Feed Samples: Effects of High Lipid Amounts and Lipid Type on Fat Retention

Fat free extraction of polychlorinated biphenyls (PCBs) from fat containing food and feed matrices was achieved by selective pressurized liquid extraction using sulphuric acid impregnated silica inside 100 mL extraction cells on a Dionex ASE300. Data were compared to previous publications where extractions had been performed on a Dionex ASE200, with 33 mL cells and a Dionex ASE300, with 34 mL. In all extractions a high lipid amount of 1,500–3,000 mg was used in the extractions. Seven different fat/fat retainer ratios (FFRs) were tested (0.200, 0.150, 0.100, 0.075, 0.050, 0.040 and 0.025) at 100 and 150 °C using n-heptane as extraction solvent. The FFR ratio differed between triglycerides and fish oil in that fat free extracts were obtained at FFR of 0.050 for fish oil at 150 °C but 0.040 for fish triglycerides. When the extraction temperature was lowered to 100 °C a FFR ratio of 0.050 resulted in fat free extracts for both matrices. These data differ from previous studies, on ASE200 33 mL cells and ASE300 34 mL cells, were both matrices required a FFR of 0.025. The influence on the PCB recovery of these higher amounts of lipids in the extraction cells was tested by spiking triglycerides and fish oil with PCBs and extracting them with FFR-values of 0.025, 0.040 and 0.050. This showed that there was no difference in the PCB recovery and thus allowing a higher amount of lipids in each extraction cell when a FFR ratio of 0.050 could be used. The method was also tested on naturally contaminated cod liver homogenate, naturally contaminated cod liver oil spiked to feed for poultry, as well as certified reference materials (Cod liver oil BCR 349 and Spiked pork fat IRMM 445).     

Efficient production of reference materials of hazardous organics using smart calibration by nuclear magnetic resonance

The accurate quantification of pesticide residues in food is an important factor in assuring the quality of life of our citizens. In general, chromatographic methods are used, which require certified reference materials (CRMs) for each analyte of interest for accurate quantitative analysis. Recently, regulation of pesticides in food, limiting the positive maximum residue (positive list system) has been brought into effect in Japan. Furthermore, ISO/IEC 17025 requires calibration and testing laboratories to program calibrations and measurements traceable to the International System of Units (SI). Accordingly, these laboratories need a suite of CRMs that are traceable to the SI. In order to address these requirements for every analyte of interest in an efficient manner, a new approach to producing SI traceable CRMs is required. Nuclear magnetic resonance (NMR) has been used widely in chemical analysis. One of the well known characteristics of NMR is the proportional relationship between peak area and the number of nuclei contributing to the peak. If accurate relative intensities of peak areas are obtained, this provides an attractive quantitative tool for organic compounds. The area of a signal from an analyte can be measured with respect to another signal originating from a comparator that has been added to the sample solution. The chosen comparator should not react with the analyte or resonate at any chemical shift similar to that of the analyte. This enables us to produce SI traceable CRMs more effectively. In this paper, we demonstrate a new approach for producing CRMs for pesticides using quantitative NMR??an SI traceable quantitative technique.     

Statistical estimation of the influence of mineralization methods on the results of heavy metals determination in cereals by the DPASV method

Summary The Community Bureau of Reference (BCR) has undertaken the development of a range of reference materials designed to meet the principal needs for food analysis and measurement. This work falls within the scope of a general collaborative programme designed to improve measurement accuracy and comparability within Europe.The development of well characterised food reference materials frequently poses serious difficulties, not only with respect to stability and homogeneity, but also for accurate certification. A pre-requisite for accurate certification is a high level of agreement between the collaborating laboratories, preferably when employing methods based on different principles.Especially for trace organic analysis, it is necessary to carry-out preliminary intercomparisons of candidate certification methods in order to identify and eliminate the major sources of error. This process is greatly facilitated if the critical steps such as recovery, clean-up and final determination can be studied separately. The paper describes this approach by reference to three milk-powders which were recently certified for their aflatoxin M₁ content and presents results for bovine muscle, bovine liver and pig kidney CRMs recently certified for toxic and nutritional element.     

Designs of experiment for proficiency testing with a limited number of participants

Metrological designs of experiment for proficiency testing (PT) with a limited number of participants are discussed. The designs are based on development of in-house reference materials (IHRMs) with traceable assigned values and fit-for-purpose uncertainties, used in a PT scheme as the measurement standards. When adequate certified reference materials (CRMs) are available, a comparative approach for IHRM development, using simultaneous analysis of IHRM and CRM test portions in pairs, is proposed for PT objectives. In the case where adequate CRMs are not available – for example, in the field of analysis of unstable aqueous systems – the function of the measurement standard for PT can be fulfilled by a synthetic IHRM prepared gravimetrically using non-adequate, non-aqueous CRMs or pure substances. The CRM or the pure substance is used as a spike for fortification of a natural water sample, while the natural water sample is used as a working IHRM for the spike determination. In this case the traceability chain is longer, since two IHRMs are added for one quantity determination, but it remains unbroken.Presented at the Second International Conference on Metrology –Trends and Applications in Calibration and Testing Laboratories, 4–6 November 2003, Eilat, Israel     

Mineral oil certified reference materials for the determination of polychlorinated biphenyls from the National Metrology Institute of Japan (NMIJ)

Four mineral oil certified reference materials (CRMs), NMIJ CRM 7902-a, CRM 7903-a, CRM 7904-a, and CRM 7905-a, have been issued by the National Metrology Institute of Japan, which is part of the National Institute of Advanced Industrial Science and Technology (NMIJ/AIST), for the determination of polychlorinated biphenyls (PCBs). The raw materials for the CRMs were an insulation oil (CRM 7902-a and CRM 7903-a) and a fuel oil (CRM7904-a and CRM 7905-a). A solution of PCB3, PCB8, and technical PCB products, comprising four types of Kaneclor, was added to the oil matrices. The total PCB concentrations in the PCB-fortified oils (CRM 7902-a and CRM 7904-a) are approximately 6 mg kg⁻¹. In addition, the mineral oils which were not fortified with PCBs were also distributed as CRMs (CRM 7903-a and CRM 7905-a). Characterization of these CRMs was conducted by the NMIJ/AIST, where the mineral oils and the PCB solution were analyzed using multiple analytical methods such as dimethylsulfoxide extraction, normal-phase liquid chromatography, gel permeation chromatography, reversed-phase liquid chromatography, and chromatography using sulfoxide-bonded silica; and/or various capillary columns for gas chromatography, and two ionization modes for mass spectrometry. The target compounds in the mineral oils and those in the PCB solution were determined by one of the primary methods of measurement, isotope dilution–mass spectrometry (ID-MS). Certified values have been provided for 11 PCB congeners (PCB3, 8, 28, 52, 101, 118, 138, 153, 180, 194, and 206) in the CRMs. These CRMs have information values for PCB homologue concentrations determined by using a Japanese official method for determination of PCBs in wastes and densities determined with an oscillational density meter. Because oil samples having arbitrary PCB concentrations between respective property values of the PCB-fortified and nonfortified CRMs can be prepared by gravimetric mixing of the CRM pairs, these CRMs can be used for validation of PCB analyses using various instruments which have different sensitivities. Figure Preparation and certification processes of the mineral oil CRMs (example shown is polychlorinated biphenyls in insulation oil, high/low concentrations) Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Production of certified reference materials for the detection of genetically modified organisms

Certified reference materials (CRMs) are an essenIial tool in the quality assurance of analytical measurements. They are produced, certified, and used in accordance with relevant ISO (International Organization for Standardization) and BCR (Community Bureau of Reference) guidelines. The Institute for Reference Materials and Measurements (IRMM; Geel, Belgium) has produced the first powdery genetically modified organism (GMO) CRMs in cooperation with the Institute for Health and Consumer Protection (Ispra, Italy). Until now, different weight percentages in the range of 0-5% for 4 GMOs in Europe were produced and certified: Bt (Bacillus thuringiensis)-11 and Bt-176 maize, Roundup Ready soybean, and MON810 maize. Bt-11 and Bt-176 maize and Roundup Ready soybean were produced by IRMM on behalf of Fluka Chemie AG (Buchs, Switzerland). Characterization of used base material is the first step in production and is especially important for GMO CRMs. The production of powdery GMO CRMs and methods used for production control are described. Thorough control of homogeneity and stability are essential for certification of reference materials and ensure validity of the certificate for each bottle of a batch throughout a defined shelf-life. Because production of reference materials and their maintenance are very labor- and cost-intensive tasks, the usefulness of new types of GMO CRMs must be estimated carefully.     

Sediment certified reference materials for the determination of polychlorinated biphenyls and organochlorine pesticides from the National Metrology Institute of Japan (NMIJ)

Two marine sediment certified reference materials, NMIJ CRM 7304-a and 7305-a, have been issued by the National Metrology Institute of Japan in the National Institute of Advanced Industrial Science and Technology (NMIJ/AIST) for the determination of polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs). The raw materials of the CRMs were collected from a bay near industrial activity in Japan. Characterization of these CRMs was conducted by NMIJ, where the sediments were analyzed using multiple analytical methods such as pressurized liquid extraction (PLE), microwave-assisted extraction (MAE), saponification, Soxhlet extraction, supercritical fluid extraction (SFE), and ultrasonic extraction; the target compounds were determined by one of the primary methods of measurements, isotope dilution–mass spectrometry (ID-MS). Certified values have been provided for 14 PCB congeners (PCB numbers 3, 15, 28, 31, 70, 101, 105, 138, 153, 170, 180, 194, 206, 209) and 4 OCPs (γ-HCH, 4,4′-DDT, 4,4′-DDE, 4,4′-DDD) in both CRMs. NMIJ CRM 7304-a has concentrations of the contaminants that are a factor of 2–15 greater than in CRM 7305-a. Both CRMs have information values for PCB homolog concentrations determined by collaborative analysis using a Japanese official method for determination of PCBs. The total PCB concentrations in the CRMs are approximately 920 and 86 μg kg⁻¹ dry mass respectively. Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users.