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1.
The concentrations of three non-ortho ("coplanar") polychlorinated biphenyls, 3,3',4,4'-tetrachlorobiphenyl (IUPAC PCB 77), 3,3',4,4',5-pentachlorobiphenyl (IUPAC PCB 126), and 3,3',4,4',5,5'-hexachlorobiphenyl (IUPAC PCB 169), were determined in five NIST Standard Reference Materials (SRMs) of environmental and biological interest. The measured levels were approximately between (0.2 to 1.3) ng/g in SRM 1588a (Organics in Cod Liver Oil), (0.3 to 9) ng/g in SRM 1944 (New York/New Jersey Waterway Sediment), (0.2 to 0.4) ng/g in SRM 1945 (Organics in Whale Blubber), (1 to 18) ng/g in SRM 2974 (Organics in Freeze-dried Mussel Tissue [Mytilus edulis]), and (0.1 to 0.4) ng/g in candidate SRM 1946 (Lake Superior Fish Tissue). PCB 169 was present at < 0.1 ng/g in SRMs 1944 and 2974. 相似文献
2.
W. W. Brubaker Jr. M. M. Schantz S. A. Wise 《Analytical and bioanalytical chemistry》2000,367(5):401-406
The concentrations of three non-ortho (“coplanar”) polychlorinated biphenyls, 3,3′,4,4′-tetrachlorobiphenyl (IUPAC PCB 77), 3,3′,4,4′,5-pentachlorobiphenyl (IUPAC PCB 126), and 3,3′,4,4′,5,5′-hexachlorobiphenyl (IUPAC PCB 169), were determined in five NIST Standard Reference Materials (SRMs) of environmental and biological interest. The measured levels were approximately between (0.2 to 1.3) ng/g in SRM 1588?a (Organics in Cod Liver Oil), (0.3 to 9) ng/g in SRM 1944 (New York/New Jersey Waterway Sediment), (0.2 to 0.4) ng/g in SRM 1945 (Organics in Whale Blubber), ¶(1 to 18) ng/g in SRM 2974 (Organics in Freeze-dried Mussel Tissue [Mytilus edulis]), and (0.1 to 0.4) ng/g ¶in candidate SRM 1946 (Lake Superior Fish Tissue). PCB 169 was present at < 0.1 ng/g in SRMs 1944 and 2974. 相似文献
3.
Stapleton HM Keller JM Schantz MM Kucklick JR Leigh SD Wise SA 《Analytical and bioanalytical chemistry》2007,387(7):2365-2379
Standard reference materials (SRMs) are valuable tools in developing and validating analytical methods to improve quality
assurance standards. The National Institute of Standards and Technology (NIST) has a long history of providing environmental
SRMs with certified concentrations of organic and inorganic contaminants. Here we report on new certified and reference concentrations
for 27 polybrominated diphenyl ether (PBDE) congeners in seven different SRMs: cod-liver oil, whale blubber, fish tissue (two
materials), mussel tissue and sediment (two materials). PBDEs were measured in these SRMs, with the lowest concentrations
measured in mussel tissue (SRM 1974b) and the highest in sediment collected from the New York/New Jersey Waterway (SRM 1944).
Comparing the relative PBDE congener concentrations within the samples, we found the biota SRMs contained primarily tetrabrominated
and pentabrominated diphenyl ethers, whereas the sediment SRMs contained primarily decabromodiphenyl ether (BDE 209). The
cod-liver oil (SRM 1588b) and whale blubber (SRM 1945) materials were also found to contain measurable concentrations of two
methoxylated PBDEs (MeO-BDEs). Certified and reference concentrations are reported for 12 PBDE congeners measured in the biota
SRMs and reference values are available for two MeO-BDEs. Results from a sediment interlaboratory comparison PBDE exercise
are available for the two sediment SRMs (1941b and 1944). 相似文献
4.
Poster DL Schantz MM Kucklick JR Lopez de Alda MJ Porter BJ Pugh R Wise SA 《Analytical and bioanalytical chemistry》2004,378(5):1213-1231
Three new mussel tissue standard reference materials (SRMs) have been developed by the National Institute of Standards and Technology (NIST) for the determination of the concentrations of organic contaminants. The most recently prepared material, SRM 1974b, is a fresh frozen tissue homogenate prepared from mussels (Mytilus edulis) collected in Boston Harbor, Massachusetts. The other two materials, SRMs 2977 and 2978, are freeze-dried tissue homogenates prepared from mussels collected in Guanabara Bay, Brazil and Raritan Bay, New Jersey, respectively. All three new mussel tissue SRMs complement the current suite of marine natural-matrix SRMs available from NIST that are characterized for a wide range of contaminants (organic and inorganic). SRM 1974b has been developed to replace its predecessor SRM 1974a, Organics in Mussel Tissue, for which the supply is depleted. Similarly, SRMs 2977 and 2978 were developed to replace a previously available (supply depleted) freeze-dried version of SRM 1974a, SRM 2974, Organics in Freeze-Dried Mussel Tissue. SRM 1974b is the third in a series of fresh frozen mussel tissue homogenate SRMs prepared from mussels collected in Boston Harbor starting in 1988. SRM 1974b has certified concentration values for 22 polycyclic aromatic hydrocarbons (PAHs), 31 polychlorinated biphenyl congeners (PCBs), and 7 chlorinated pesticides. Reference values are provided for additional constituents: 16 PAHs, 8 PCBs plus total PCBs, 6 pesticides, total extractable organics, methylmercury, and 11 trace elements. PAH concentrations range from about 2 ng g–1 dry mass (cyclopenta[cd]pyrene) to 180 ng g–1 dry mass (pyrene). PCB concentrations range from about 2 ng g–1 dry mass (PCB 157) to 120 ng g–1 dry mass (PCB 153). The reference value for total PCBs in SRM 1974b is (2020 ± 420) ng g–1 dry mass. Pesticide concentrations range from about 4 ng g–1 dry mass (4,4-DDT) to 40 ng g–1 dry mass (4,4-DDE). SRM 2977 has certified values for 14 PAHs, 25 PCB congeners, 7 pesticides, 6 trace elements, and methylmercury. Reference values for 16 additional PAHs and 9 inorganic constituents are provided, and information values are given for 23 additional trace elements. SRM 2978 has certified and reference concentrations for 41 and 22 organic compounds, respectively, and contains contaminant levels similar to those of SRM 1974b. Organic contaminant levels in SRM 2977 (mussels from Guanabara Bay, Brazil) are typically a factor of 2 to 4 lower than those in SRM 1974b and SRM 2978. The organic contaminant concentrations in each new mussel tissue SRM are presented and compared in this paper. In addition, a chronological review of contaminant concentrations associated with mussels collected in Boston Harbor is discussed as well as a stability assessment of SRM 1974a.Electronic Supplementary Material Supplementary material is available in the online version of this article at . A link in the frame on the left on that page takes you directly to the supplementary material. 相似文献
5.
Stacy S. Vander Pol John R. Kucklick Stefan D. Leigh Barbara J. Porter Michele M. Schantz 《Analytical and bioanalytical chemistry》2010,397(2):483-492
Toxaphene is a complex technical mixture that has been found ubiquitously in the environment but has caused issues for analysis,
especially of individual congeners. This paper reports the elution order of 26 major toxaphene congeners on three gas chromatographic
columns. The three different stationary phases generally had similar elution orders for the toxaphene congeners, but fewer
co-elutions occurred on a low-bleed, low-polarity column. These congeners (except for two that co-eluted and were not added
to the calibration mixture) were examined in air particulate matter standard reference materials (SRMs), 1648a, 1649a, and
1649b as well as SRM 3067 toxaphene in methanol for assignment of reference values. SRM 3067 had mass fractions an order of
magnitude greater than the air particulate SRMs, which ranged from 0.568 ± 0.018 ng g−1 dry mass (B9-2006 in SRM 1648a) to 12.9 ± 0.20 ng g−1 dry mass (B9-715 (P 58) in SRM 1649a). The three air particulate SRMs all had different mass fractions and proportions of
congeners relative to the sum of the toxaphene congeners. SRM 3067 may be useful as a technical mixture toxaphene congener
calibrant. SRMs 1648a and 1649b will serve as reference materials for the analysis of 21 (three congeners were not included
due to values below the detection limit or a potential polychlorinated biphenyl co-elution) toxaphene congeners in atmospheric
particulate samples. 相似文献
6.
Stapleton HM Harner T Shoeib M Keller JM Schantz MM Leigh SD Wise SA 《Analytical and bioanalytical chemistry》2006,384(3):791-800
Polybrominated diphenyl ethers (PBDEs) have been measured for the first time in three different indoor dust Standard Reference
Materials (SRMs) prepared by the National Institute of Standards and Technology (NIST). Two of these, SRM 2583 (Trace Elements
in Indoor Dust) and SRM 2584 (Trace Elements in Indoor Dust), have been certified previously for lead and other inorganic
constituents. A third, SRM 2585 (Organics in Indoor Dust), is a new indoor dust reference material prepared by NIST which
will be certified for various organic compounds (polycyclic aromatic hydrocarbons, pesticides and polychlorinated biphenyls)
in 2005 including certified concentrations for 16 individual PBDE congeners and reference values for an additional three PBDE
congeners. Dust SRMs were analyzed for 30 PBDE congeners using high-resolution gas chromatography combined with low-resolution
mass spectrometry operated in both negative chemical ionization (GC/ECNI–MS) and electron impact ionization (GC/EI–MS) modes.
Sensitivity was an order of magnitude higher using GC/ECNI–MS relative to GC/EI–MS. These SRMs have been characterized and
compared to the three PBDE commercial products (pentaBDE, octaBDE and decaBDE). PentaBDE and DecaBDE were present in all three
SRMs and were the dominant commercial products, making up approximately 33% and 58%, respectively. Recent studies suggest
that house dust may be a leading source of human exposure to PBDEs. These SRMs are the first reference materials with certified
concentrations for PBDEs, which will aid in validating future measurements of PBDEs in house dust and other similar matrices.
Electronic Supplementary Material Supplementary material is available for this article at http://dx.doi.org/ 10.1007/s00216-005-0227-y 相似文献
7.
John R. Kucklick Michele M. Schantz Rebecca S. Pugh Barbara J. Porter Dianne L. Poster Paul R. Becker Teri K. Rowles Stefan Leigh Stephen A. Wise 《Analytical and bioanalytical chemistry》2010,397(2):423-432
The National Institute of Standards and Technology (NIST) has a diverse collection of control materials derived from marine
mammal blubber, fat, and serum. Standard Reference Material (SRM) 1945 Organics in Whale Blubber was recertified for polychlorinated
biphenyl (PCB) congeners, organochlorine pesticides, and polybrominated diphenyl ether (PBDE) congeners. SRM 1945 has also
been assigned mass fraction values for compounds not frequently determined in marine samples including toxaphene congeners,
coplanar PCBs, and methoxylated PBDE congeners which are natural products. NIST also has assigned mass fraction values, as
a result of interlaboratory comparison exercises, for PCB congeners, organochlorine pesticides, PBDE congeners, and fatty
acids in six homogenate materials produced from marine mammal blubber or serum. The materials are available from NIST upon
request; however, the supply is very limited for some of the materials. The materials include those obtained from pilot whale
blubber (Homogenates III and IV), Blainville’s beaked whale blubber (Homogenate VII), polar bear fat (Homogenate VI), and
California sea lion serum (Marine Mammal Control Material-1 Serum) and blubber (Homogenate V). 相似文献
8.
Synthetic musk fragrances have been measured in water, air, sediments, sewage sludge, and biota worldwide. As the study of
the environmental fate and impacts of these compounds progresses, the need for Standard Reference Materials (SRMs) for these
compounds to facilitate analytical method improvement and interlaboratory comparisons becomes increasingly important. The
National Institute of Standards and Technology (NIST) issues environmental matrix SRMs with certified concentrations for a
variety of persistent organic pollutants including polycyclic aromatic hydrocarbons (PAHs), chlorinated pesticides, and polychlorinated
biphenyl congeners (PCBs). Until now synthetic musk fragrance concentrations have not been reported in NIST SRMs. The objective
of this study was to provide reference values for several commonly detected synthetic musk fragrances in several NIST natural
matrix SRMs. In this study five polycyclic musk fragrances [HHCB (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-γ-2-benzopyran), AHTN (7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene), ADBI (4-acetyl-1,1-dimethyl-6-tert-butylindane), AHMI (6-acetyl-1,1,2,3,3,5-hexamethylindane), and ATII (5-acetyl-1,1,2,6-tetramethyl-3-isopropylindane] and
two nitro musk fragrances [musk xylene (1-tert-butyl-3,5-dimethyl-2,4,6-trinitrobenzene) and musk ketone (4-tert-butyl-3,5-dinitro-2,6-dimethylacetophenone)] were measured in selected environmental SRMs. Gas chromatography–electron impact
mass spectrometry (GC/EI-MS) was used for all analyses. HHCB was the most frequently detected synthetic musk fragrance and
was detected in SRM 2585 Organic Contaminants in House Dust, SRM 2781 Domestic Sludge, SRM 1974b Organics in Mussel Tissue
(Mytilus edulis), and SRM 1947 Lake Michigan Fish Tissue. It was not detected in SRM 1946 Lake Superior Fish Tissue or SRM 1945 Organics
in Whale Blubber. Concentrations of HHCB in these SRMs ranged from 1.12 ng/g in SRM 1947 to 92,901 ng/g in SRM 2781. All of
the polycyclic musk fragrances were detected in SRM 2781 and all of the target compounds were detected in SRM 2585.
Electronic supplementary material Supplementary material is available for this article at and is accessible to authorized users. 相似文献
9.
Barbara R. Hillery James E. Girard Michele M. Schantz Stephen A. Wise 《Journal of separation science》1995,18(2):89-96
A novel p,p-cyanobiphenyl stationary phase (p-cyanobiphenyl, p-allyloxy methylpolysiloxane) has been evaluated for the GC investigation of polychlorinated biphenyls (PCBs). Several PCB congeners which coelute on the phases typically used for PCB analysis (e.g. 5% phenyl methylpolysiloxane) are separated on the p,p-cyanobiphenyl phase, including the hexachlorobiphenyl congeners PCB 163, PCB 164, and PCB 138. In this work, a p,p-cyanobiphenyl stationary phase was used to measure selected PCB congeners in two Standard Reference Materials (SRMs) available from the National Institute of Standards and Technology (NIST), and two Certified Reference Materials (CRMs) available from the Community Bureau of Reference (BCR). The materials analyzed were SRM 1588, Organics in Cod Liver Oil; SRM 1945, Organics in Whale Blubber; CRM 349, Chlorobiphenyls in Cod Liver Oil; and CRM 350, Chlorobiphenyls in Mackerel Oil. Concentrations are reported for several PCB congeners which coelute on the 5% phenyl methylpolysiloxane, including PCB 163 and PCB 164. 相似文献
10.
Comparison of methods for the gas-chromatographic determination of PCB congeners and chlorinated pesticides in marine reference materials 总被引:1,自引:0,他引:1
Michele M. Schantz Reenie M. Parris Joachim Kurz Karlheinz Ballschmiter Stephen A. Wise 《Fresenius' Journal of Analytical Chemistry》1993,346(6-9):766-778
Summary Three gas-chromatographic (GC) columns with different selectivity (DB-5, DB-1701, and C-18) and two different GC detectors (electron-capture and mass-spectrometric) were used to analyze three Standard Reference Materials (SRMs), which are available from the National Institute of Standards and Technology (NIST), and two Certified Reference Materials (CRMs), which are available from the Community Bureau of Reference (BCR), for polychlorinated biphenyl (PCB) congeners and chlorinated pesticides. The materials analyzed were: SRM 1588, Organics in Cod Liver Oil; SRM 1941, Organics in Marine Sediment; SRM 1974, Organics in Mussel Tissue (Mytilus edulis); CRM 349, Chlorobiphenyls in Cod Liver Oil; and CRM 350, Chlorobiphenyls in Mackerel Oil. Results from these different methods are compared, and concentrations for additional PCB congeners and chlorinated pesticides in these reference materials, which have not been measured previously, are reported.Dedicated to Professor Dr. Wilhelm Fresenius on the occasion of his 80th birthday 相似文献
11.
Xue Li Jun Huang Wang Zhang Shubo Deng Siwen Wang 《International journal of environmental analytical chemistry》2013,93(12):1135-1150
A rapid and reliable analytical method based on pressurised solvent extraction (PSE) and GC-NCI-MS was developed for the determination of 41 different PBDEs in soil. All PBDEs, including mono- to hepta-BDEs (sum of 39 congeners), one nona-BDE and deca-BDE, were efficiently extracted from soil samples using the extraction technology of PSE. The extract was then cleaned up on a florisil column. Satisfactory separation of 41 PBDE congeners was obtained on a 15-m DB-5MS capillary column, saving the use of another 30-m column specific for the separation of mono- to hepta-BDEs. PBDEs were identified and quantified by GC-MS in negative chemical ionisation (NCI) mode, and further confirmed in semi electron impact (SEI) mode when the ion source was also NCI. The method detection limits ranged from 0.01 to 0.03?ng?g?1?dw for mono- to hepta-BDEs, 1.43?ng?g?1?dw for the nona-BDE and 0.20?ng?g?1?dw for deca-BDE. The applicability of the method was tested in soil samples collected from an e-waste recycling site at Guiyu. Twenty-one PBDEs (mono- to deca-) were detected, and eighteen congeners were quantified. The concentration range of PBDEs was 0.78–436?ng?g?1?dw. BDE-47, BDE-99, BDE-153, BDE-183, BDE-206 and BDE-209 were the dominant congeners, and BDE-209 accounted for 62% of the total PBDEs. The congener profiles of PBDEs in soil samples were similar to those in three commercial PBDE products (Penta-, Octa- and Deca-BDE), and Deca-BDE product was the most important contributor. 相似文献
12.
Determination of polybrominated diphenyl ethers in marine biological tissues using microwave-assisted extraction 总被引:4,自引:0,他引:4
Growing concern on the environmental impact of polybrominated diphenyl ethers (PBDEs) has created the need for rapid and quality assured analytical methods to quantify PBDEs in a spectrum of matrix types. This study presents the first validated method for the quantification of major PBDE congeners (47, 99 and 100) in marine biological tissues using microwave-assisted extraction (MAE). The recovery of polychlorinated biphenyls and various organochlorine pesticides has also been ascertained. Analytical accuracy, precision, limits of detection and cleanup efficiency were evaluated for PBDE congeners, and empirical data justifies the use of MAE for the extraction and analysis of PBDEs in biological matrices. MAE was also compared to Soxhlet extraction efficiency for PBDEs in the standard reference materials SRM2978 and SRM1588a and gave comparable results (<15% variation). 相似文献
13.
O. Roots V. Zitko H. Kiviranta P. Rantakokko P. Ruokojärvi 《Russian Journal of General Chemistry》2010,80(13):2721-2730
Concentrations of polybrominated diphenyl ethers (PBDEs) in Baltic Sea herring Clupea harengus membras L. collected from Estonian coastal waters are reported. In the period 2006–2008 the total PBDE concentrations (ΣPBDE, sum
of 15 congeners) in Baltic herring varied between 0.57 and 4.08 ng g−1 fresh weight. Highest ΣPBDE concentrations were in a 2007 sample from the mouth of the Gulf of Finland and in a 2007 sample
from the Gulf of Riga. The former contained a high concentration of BDE 209 (16.3 ng g−1) and in the latter this congener was the second most abundant. It is not clear whether the BDE 209 concentration in the Gulf
of Finland sample is not an artefact and this value was not included in the above range. The PBDE concentrations increased
with the age of herring are similar to those reported in [1] in fish collected in the Bothnian Sea in 2002 and did not increase
between 2002 and 2008. The majority of concentrations in herring from the Estonian coastal zone was <1.0 ng g−1 fresh weight. The PBDE congener profiles varied regionally as well as with age of the fish. The main congeners were mostly
the BDEs 47, 99, and 100. Some of the variations probably caused by measurement artefacts. 相似文献
14.
Eight polybrominated diphenyl ether (PBDE) congeners of primary interest to the US EPA were separated using reverse-phase
liquid chromatography on an octadecylsilane column. BDE-28, BDE-47, BDE-99, BDE-100, BDE-153, BDE-154, BDE-183, and BDE-209
were baseline-resolved under isocratic conditions in 92:8 methanol/water (v/v). Negative-ion atmospheric pressure photoionization
(NI-APPI) with a toluene dopant produced precursor ions corresponding to [M–Br+O]– for the eight congeners studied. Each congener was quantified by tandem mass spectrometry through a unique multiple reaction
monitoring (MRM) transition. On-column limits of detection were between 2.4 and 27.8 pg for the eight congeners studied, with
an intra-day method precision of 9%. The LC/NI-APPI/MS/MS method was validated for the analysis of the eight PBDE congeners
in NIST SRM 2585 (Organics in House Dust). Pressurized liquid extraction (PLE) with subsequent LC/NI-APPI/MS/MS analysis afforded
quantitative recovery for all eight PBDE congeners with recoveries ranging from 92.7 to 113%. The liquid-phase separation
of the LC/NI-APPI/MS/MS method is not prone to the thermal degradation issues that plague splitless GC based analyses of highly
brominated PBDEs such as BDE-209. 相似文献
15.
Regueiro J Llompart M Garcia-Jares C Cela R 《Analytical and bioanalytical chemistry》2007,388(5-6):1095-1107
Gas chromatographic analysis of polybrominated diphenyl ethers (PBDEs) has been evaluated in an attempt to achieve better
control of the separation process, especially for highly substituted congeners. Use of a narrow-bore capillary column enabled
adequate determination of tetra, penta, hexa, hepta, octa, nona and decaBDE congeners in only one chromatographic run while
maintaining resolution power similar to that of conventional columns. A micro electron-capture detector (GC–μECD) was used.
Chromatographic conditions were optimized by multifactorial experimental design, with the objective of obtaining not only
high sensitivity but also good precision. In this way two different approaches to maximizing response and minimizing variability
were tested, and are fully discussed. These optimum chromatographic conditions were then used to determine PBDEs extracted
from domestic dust samples by microwave-assisted solvent extraction (MASE). Quantitative recovery (90–108%) was achieved for
all the PBDEs and method precision (RSD < 13%) was satisfactory. Accuracy was tested by use of the standard reference material
SRM 2585, and sub-ng g−1 limits of detection were obtained for all compounds except BDE-209 (1.44 ng g−1). Finally, several samples of house dust were analysed by use of the proposed method and all the target PBDEs were detected
in all the samples. BDE-209 was the predominant congener. Amounts varied from 58 to 1615 ng g−1 and the average contribution to the total PBDE burden of 52%. The main congeners of the octaBDE mixture (BDE-183, BDE-197,
BDE-207 and BDE-196) also made an important contribution (29%) to the total. These are the first data about the presence of
these compounds in European house-dust samples. Finally, the sum of the main congeners in the pentaBDE commercial mixture
(BDE-47, BDE-99, and BDE-100) contributed 14% to the total.
Figure Polybrominated diphenyl ethers in House Dust 相似文献
16.
Two new marine sediment standard reference materials (SRMs) for the determination of organic contaminants 总被引:3,自引:0,他引:3
Wise SA Poster DL Schantz MM Kucklick JR Sander LC Lopez de Alda M Schubert P Parris RM Porter BJ 《Analytical and bioanalytical chemistry》2004,378(5):1251-1264
Two new marine sediment standard reference materials (SRMs), SRM 1941b Organics in Marine Sediment and SRM 1944 New York/New Jersey Waterway Sediment, have been recently issued by the National Institute of Standards and Technology (NIST) for the determination of organic contaminants including polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyl (PCB) congeners, and chlorinated pesticides. Both sediment SRMs were analyzed using multiple analytical methods including gas chromatography/mass spectrometry (GC/MS) on columns with different selectivity, reversed-phase liquid chromatography with fluorescence detection (for PAHs only), and GC with electron capture detection (for PCBs and pesticides only). SRM 1941b has certified concentrations for 24 PAHs, 29 PCB congeners, and 7 pesticides, and SRM 1944 has certified concentrations for 24 PAHs, 29 PCB congeners, and 4 pesticides. Reference concentrations are also provided for an additional 58 (SRM 1941b) and 39 (SRM 1944) PAHs, PCB congeners, and pesticides. SRM 1944, which was collected from multiple sites within New York/New Jersey coastal waterways, has contaminant concentrations that are generally a factor of 10–20 greater than SRM 1941b, which was collected in the Baltimore (Maryland) harbor. These two SRMs represent the most extensively characterized marine sediment certified reference materials available for the determination of organic contaminants.Electronic Supplementary Material Supplementary material is available in the online version of this article at . A link in the frame on the left on that page takes you directly to the supplementary material. 相似文献
17.
Michele M. Schantz Gauthier Eppe Jean-François Focant Coreen Hamilton N. Alan Heckert Rebecca M. Heltsley Dale Hoover Jennifer M. Keller Stefan D. Leigh Donald G. Patterson Jr Adam L. Pintar Katherine E. Sharpless Andreas Sjödin Wayman E. Turner Stacy S. Vander Pol Stephen A. Wise 《Analytical and bioanalytical chemistry》2013,405(4):1203-1211
Four new Standard Reference Materials (SRMs) have been developed to assist in the quality assurance of chemical contaminant measurements required for human biomonitoring studies, SRM 1953 Organic Contaminants in Non-Fortified Human Milk, SRM 1954 Organic Contaminants in Fortified Human Milk, SRM 1957 Organic Contaminants in Non-Fortified Human Serum, and SRM 1958 Organic Contaminants in Fortified Human Serum. These materials were developed as part of a collaboration between the National Institute of Standards and Technology (NIST) and the Centers for Disease Control and Prevention (CDC) with both agencies contributing data used in the certification of mass fraction values for a wide range of organic contaminants including polychlorinated biphenyl (PCB) congeners, chlorinated pesticides, polybrominated diphenyl ether (PBDE) congeners, and polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners. The certified mass fractions of the organic contaminants in unfortified samples, SRM 1953 and SRM 1957, ranged from 12 ng/kg to 2200 ng/kg with the exception of 4,4′-DDE in SRM 1953 at 7400 ng/kg with expanded uncertainties generally <14 %. This agreement suggests that there were no significant biases existing among the multiple methods used for analysis. Figure
Comparison of Concentrations of Selected Compounds in Human Serum and Human Milk Standard Reference Materials (SRMs) 相似文献
18.
Standard reference materials for foods and dietary supplements 总被引:1,自引:0,他引:1
Sharpless KE Thomas JB Christopher SJ Greenberg RR Sander LC Schantz MM Welch MJ Wise SA 《Analytical and bioanalytical chemistry》2007,389(1):171-178
Well-characterized certified reference materials are needed by laboratories in the food testing, dietary supplement, and nutrition
communities to facilitate compliance with labeling laws and improve the accuracy of information provided on product labels,
so that consumers can make good 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) worked to develop a series 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 1947 Lake Michigan Fish Tissue, SRM 2383 Baby Food Composite,
SRM 2384 Baking Chocolate, SRM 2385 Slurried Spinach, and SRM 2387 Peanut Butter. With the enactment of the Dietary Supplement
Health and Education Act of 1994, NIST has been working to develop suites of dietary supplement SRMs characterized for active
and marker compounds and for toxic elements and pesticides, where appropriate. An updated SRM 1588b Organics in Cod Liver
Oil, a suite of ephedra-containing materials (SRMs 3240–3245), a carrot extract in oil (SRM 3276), and a suite of ginkgo-containing
materials (SRMs 3246–3248) are available. Several other materials are currently in preparation. Dietary supplements are sometimes
provided in forms that are food-like; for these, values may also be assigned for nutrients, for example SRM 3244 Ephedra-Containing
Protein Powder. Both the food-matrix and dietary supplement reference materials are intended primarily for validation of analytical
methods. They may also be used as “primary control materials” in assignment of values to in-house (secondary) control materials
to confirm accuracy and to establish measurement traceability to NIST. 相似文献
19.
A multi-class, multi-residue method for the analysis of 13 novel flame retardants, 18 representative pesticides, 14 polychlorinated biphenyl (PCB) congeners, 16 polycyclic aromatic hydrocarbons (PAHs), and 7 polybrominated diphenyl ether (PBDE) congeners in catfish muscle was developed and evaluated using fast low pressure gas chromatography triple quadrupole tandem mass spectrometry (LP-GC/MS–MS). The method was based on a QuEChERS (quick, easy, cheap, effective, rugged, safe) extraction with acetonitrile and dispersive solid-phase extraction (d-SPE) clean-up with zirconium-based sorbent prior to LP-GC/MS–MS analysis. The developed method was evaluated at 4 spiking levels and further validated by analysis of NIST Standard Reference Materials (SRMs) 1974B and 1947. Sample preparation for a batch of 10 homogenized samples took about 1 h/analyst, and LP-GC/MS–MS analysis provided fast separation of multiple analytes within 9 min achieving high throughput. With the use of isotopically labeled internal standards, recoveries of all but one analyte were between 70 and 120% with relative standard deviations less than 20% (n = 5). The measured values for both SRMs agreed with certified/reference values (72–119% accuracy) for the majority of analytes. The detection limits were 0.1–0.5 ng g−1 for PCBs, 0.5–10 ng g−1 for PBDEs, 0.5–5 ng g−1 for select pesticides and PAHs and 1–10 ng g−1 for flame retardants. The developed method was successfully applied for analysis of catfish samples from the market. 相似文献
20.
Ioannis Dosis Maria Athanasiadou Ioannis Athanassiadis Xanthippos Karamanlis 《International journal of environmental analytical chemistry》2013,93(12):1151-1165
Polybrominated diphenyl ether (PBDE) concentrations were determined in marine sediment samples collected from 7 different locations around Thermaikos Gulf in north Greece. PBDEs were detected in all sampling sites and their average total concentration (ΣPBDEs) ranged from 0.26 to 4.92?ng?g?1?d.w. Concentrations were an order of magnitude higher in locations outlining the inner part of the Gulf, which were also closer to industrial areas, sewage treatment plant discharges, the city's harbour and landfill area. These findings suggest pollution in the aquatic ecosystem from industrial and urban activities in the area. Congener profiles exhibit predominance of BDE-209, while concentrations of other PBDE congeners were usually lower, when compared to similar studies from other countries globally, indicating that Thermaikos Gulf is among the low-polluted areas. Statistical analysis showed significant differences among the higher polluted sampling stations. Statistically significant differences also existed between sampling stations with high and low PBDE concentrations. Correlations between congeners suggested local contamination sources; however, specific point sources of pollution were not established. 相似文献