H. M. Skip Kingston

The plasma zinc/serum copper ratio as a biomarker in children with autism spectrum disorders.

The frequency of zinc deficiency, copper toxicity and low zinc/copper in children with autism spectrum disorders (ASDs) may indicate decrement in metallothionein system functioning. A retrospective review of plasma zinc, serum copper and zinc/copper was performed on data from 230 children with autistic disorder, pervasive developmental disorder-NOS and Asperger’s syndrome. The entire cohort’s mean zinc level was 77.2 μg dl−1, mean copper level was 131.5 μg dl−1, and mean Zn/Cu was 0.608, which was below the 0.7 cut-off of the lowest 2.5% of healthy children. The plasma zinc/serum copper ratio may be a biomarker of heavy metal, particularly mercury, toxicity in children with ASDs.

Accuracy in species analysis: speciated isotope dilution mass spectrometry (SIDMS) exemplified by the evaluation of chromium species☆

Abstract Speciated isotope dilution mass spectrometry (SIDMS) improves accuracy in the determination of chemical species in samples. It can be used to measure elements in their oxidation states as well as in organometallics or other molecular forms of species. SIDMS compensates for species transformations that occur in many of the steps of sample processing, including sampling process, storage, sample preparation and speciated measurement. It is also a diagnostic tool for identifying the most error prone steps. These combined capabilities provide a new method for establishing standard, legally defensible measurement tool in speciation analysis. Early speciation studies of Cr(VI) and Cr(III) demonstrate the unique advantages of SIDMS. Thus far, SIDMS has corrected up to 80% of the reduction of Cr(VI) to Cr(III). In theory, using SIDMS makes it possible to correct up to 90% species conversion with good precision. This paper describes how to apply the method to chromium and provides examples of the general steps.

Simultaneous extraction of arsenic and selenium species from rice products by microwave-assisted enzymatic extraction and analysis by ion chromatography-inductively coupled plasma-mass spectrometry.

A microwave-assisted enzymatic extraction (MAEE) method was developed for the simultaneous extraction of arsenic (As) and selenium (Se) species in rice products. The total arsenic and selenium content in the enzymatic extracts were determined by inductively coupled plasma mass spectrometry (ICP-MS), while the speciation analysis was performed by ion chromatography coupled to inductively coupled plasma-mass spectrometry (IC-ICP-MS). The main factors affecting the enzymatic extraction process were evaluated in NIST SRM-1568a rice flour. The optimum extraction conditions were 500 mg of sample, 50 mg of protease XIV, and 25 mg of alpha-amylase in aqueous medium during 40 min at 37 degrees C. The extraction recoveries of total As and Se reached 100 +/- 3 and 80 +/- 4%, respectively. The species stability study during the MAEE process did not show transformation of the target species in rice products. The results of As speciation obtained for SRM-1568a were in agreement with previous studies of As speciation performed on the same reference material. The proposed method was applied to the determination of As and Se species in rice and rice-based cereals. Arsenite [As(III)], arsenate [As(V)], dimethylarsinic acid (DMA), and selenomethionine (SeMet) were the predominant species identified in rice products.

Simultaneous determination of arsenic and selenium species in fish tissues using microwave-assisted enzymatic extraction and ion chromatography-inductively coupled plasma mass spectrometry.

A microwave-assisted enzymatic extraction (MAEE) method was developed for the simultaneous extraction of arsenic (As) and selenium (Se) species in fish tissues. The extraction efficiency of total As and Se and the stability of As and Se species were evaluated by analyzing DOLT-3 (dogfish liver). Enzymatic extraction using pronase E/lipase mixture assisted by microwave energy was found to give satisfactory extraction recoveries for As and Se without promoting interspecies conversion. The optimum extraction conditions were found to be 0.2 g of sample, 20 mg pronase E and 5mg lipase in 10 mL of 50 mM phosphate buffer, pH 7.25 at 37 degrees C. The total extraction time was 30 min. The speciation analysis was performed by ion chromatography-inductively coupled plasma mass spectrometry (IC-ICP-MS). The accuracy of the developed extraction procedure was verified by analyzing two reference materials, DOLT-3 and BCR-627. The extraction recoveries in those reference materials ranged between 82 and 94% for As and 57 and 97% for Se. The accuracy of arsenic species measurement was tested by the analysis of BCR 627. The proposed method was applied to determine As and Se species in fish tissues purchased from a local fish market. Arsenobetaine (AsB) and selenomethionine (SeMet) were the major species detected in fish tissues. In the analyzed fish extracts, the sum of As species detected was in good agreement with the total As extracted. However, for Se, the sum of its species was lower than the total Se extracted, revealing the presence of Se-containing peptides or proteins.

Comparison of methods with respect to efficiencies, recoveries, and quantitation of mercury species interconversions in food demonstrated using tuna fish

AbstractEight different analytical extraction procedures commonly used to extract mercury species from biological samples were evaluated by analyzing Tuna Fish Tissue Certified Reference Material (ERM-CE464) certified for the content of total mercury and methylmercury. Speciated isotope dilution mass spectrometry (SIDMS; US Environmental Protection Agency’s method 6800) was utilized to evaluate and effectively compensate for potential errors during measurement and accurately quantify mercury species using all the extraction methods. SIDMS was used to accurately evaluate species transformations during sample pretreatment, preparation and analysis protocols. The extraction methods tested in this paper were based on alkaline extraction with KOH or tetramethylammonium hydroxide; acid leaching with HCl, HNO3 or CH3COOH; extraction with l-cysteine hydrochloride; and enzymatic digestion with protease XIV. Detection of total mercury and mercury species from all extraction methods was carried out by inductively coupled plasma mass spectrometry (ICP-MS) and high-performance liquid chromatography–ICP-MS, respectively. Microwave-assisted extraction and ultrasound-assisted extraction were found to be the most efficient alkaline digestion protocols that caused the lowest levels of transformation of mercury species (6% or less). Extraction with 5 M HCl or enzymatic digestion with protease resulted in the second-highest extraction efficiency, with relatively lower transformation of methylmercury to inorganic mercury (3 and 1.4%, respectively). Despite frequent use of acid leaching for the extraction of mercury species from tuna fish samples, the lowest extraction efficiencies and the highest mercury species transformation were obtained when microwave-assisted extraction with 4 M HNO3 or CH3COOH was used. Transformations as high as 30% were found using some literature protocols; however, all the extractions tested produced accurate quantitation when corrected in accordance with the SIDMS method standardized in the US Environmental Protection Agency’s method 6800. FigureDeterminative CRM Tuna Fish Tissue Methylmercury Calibration vs. Determinative Calculation.

Robust microwave-assisted extraction protocol for determination of total mercury and methylmercury in fish tissues

A rapid and efficient closed vessel microwave-assisted extraction (MAE) method based on acidic leaching was developed and optimized for the extraction of total mercury (Hg), inorganic mercury (Hg(2+)) and methylmercury (CH(3)Hg(+)) from fish tissues. The quantitative extraction of total Hg and mercury species from biological samples was achieved by using 5molL(-1) HCl and 0.25molL(-1) NaCl during 10min at 60 degrees C. Total Hg content was determined using inductively coupled plasma mass spectrometry (ICP-MS). Mercury species were measured by liquid chromatography hyphenated with inductively coupled plasma mass spectrometry (LC-ICP-MS). The method was validated using biological certified reference materials ERM-CE464, DOLT-3, and NIST SRM-1946. The analytical results were in good agreement with the certified reference values of total Hg and CH(3)Hg(+) at a 95% confidence level. Further, accuracy validation using speciated isotope-dilution mass spectrometry (SIDMS, as described in the EPA Method 6800) was carried out. SIDMS was also applied to study and correct for unwanted species transformation reactions during and/or after sample preparation steps. For the studied reference materials, no statistically significant transformation between mercury species was observed during the extraction and determination procedures. The proposed method was successfully applied to fish tissues with good agreement between SIDMS results and external calibration (EC) results. Interspecies transformations in fish tissues were slightly higher than certified reference materials due to differences in matrix composition. Depending on the type of fish tissue, up to 10.24% of Hg(2+) was methylated and up to 1.75% of CH(3)Hg(+) was demethylated to Hg(2+).

Development of a microwave-assisted extraction method and isotopic validation of mercury species in soils and sediments

An efficient and rapid closed vessel microwave-assisted extraction method based on an acidic extractant has been developed to determine inorganic mercury and methylmercury in soils and sediments. Parameters optimized during this study were nitric acid concentration, amount of sample, extraction temperature and irradiation time. The results suggest that the nitric acid concentration and the irradiation temperature are statistically significant both for extraction efficiency and for stability of mercury species. A processed topsoil (Hg < 0.01 ng g−1) spiked with inorganic mercury and methylmercury and SRM 2711 (spiked with methylmercury) were used during the method development. The sample preparation was optimized in a closed-vessel system by heating 1.0 g of sample in 10.0 ml of 4.0 mol l−1 HNO3 for 10 min at 100 °C with magnetic stirring. Analyses of the extracts were carried out by using three types of instruments, Direct Mercury Analyzer-80 (DMA-80), inductively coupled plasma mass spectrometer (ICP-MS) and high-performance liquid chromatograph coupled with inductively coupled plasma mass spectrometer (HPLC-ICP-MS). The results obtained from each of these detection techniques agreed significantly at the 95% confidence level. The method was validated by the analyses of two types of specifically prepared reference soil samples and four certified reference materials (BCR 580, SRM 2704, SRM 2709 and SRM 1941a). The inorganic mercury and methylmercury concentrations found were in good agreement at the 95% confidence level with the certified or “made-to” value. The method was also validated using EPA Method 6800 as a diagnostic tool to check whether interconversion of inorganic mercury to methylmercury or vice versa took place during or after extraction; the amount of such interconversions was found to be statistically negligible. The method is in the process of consideration and adopted by the United States Environmental Protection Agency (US EPA) as a primary mercury species extraction protocol from soils and sediments in EPA draft Method 3200.

Peer Reviewed: Microwave-Enhanced Chemistry

Analytical chemists no longer have to accept the technological mismatch between sample preparation and instrumentation.

A New Method to Assess Mercury Emissions: A Study of Three Coal-Fired Electric-Generating Power Station Configurations

Abstract U.S. Environmental Protection Agency (EPA) Method 7473 for the analysis of mercury (Hg) by thermal decomposition, amalgamation, and atomic absorption spectroscopy has proved successful for use in Hg assessment at coal-fired power stations. In an analysis time of ∼5 min per sample, this instrumental methodology can directly analyze total Hg—with no discrete sample preparation—in the solid matrices associated with a coal-fired power plant, including coal, fly ash, bottom ash, and flue gas desulfurization (FGD) material. This analysis technique was used to investigate Hg capture by coal combustion byproducts (CCBs) in three different coal-fired power plant configurations. Hg capture and associated emissions were estimated by partial mass balance. The station equipped with an FGD system demonstrated 68% capture on FGD material and an emissions estimate of 18% (11 kg/yr) of total Hg input. The power plant equipped with low oxides of nitrogen burners and an electrostatic precipitator (ESP) retained 43% on the fly ash and emitted 57% (51 kg/yr). The station equipped with conventional burners and an ESP retained less than 1% on the fly ash, emitting an estimated 99% (88 kg/yr) of Hg. Estimated Hg emissions demonstrate good agreement with EPA data for the power stations investigated.

Measurement of mercury species in whole blood using speciated isotope dilution methodology integrated with microwave-enhanced solubilization and spike equilibration, headspace-solid-phase microextraction, and GC-ICP-MS analysis.

A biomonitoring method was developed for the determination of inorganic-, methyl-, and ethylmercury (Hg(2+), CH3Hg(+), and C2H5Hg(+), respectively) in whole blood by triple-spiking speciated isotope dilution mass spectrometry (SIDMS) using headspace (HS) solid-phase microextraction (SPME) in combination with gas chromatographic (GC) separation and inductively coupled plasma mass spectrometric (ICP-MS) detection. After spiking the blood sample with isotopically enriched analogues of the analytes ((199)Hg(2+), CH3(200)Hg(+) and C2H5(201)Hg(+)), the endogenous Hg species were solubilized in 2.0 mol L(-1) HNO3 and equilibrated with the spikes using a microwave-enhanced protocol. The microwaved sample was treated with a 1% (w/v) aqueous solution of sodium tetrapropylborate (buffered to pH 5.2), and the propylated Hg species were sampled in the HS using a Carboxen/polydimethylsiloxane-coated SPME fiber. The extracted species were thermally desorbed from the fiber in the GC injection port and determined by GC-ICP-MS. The analytes were quantified, with simultaneous correction for their method-induced transformation, on the basis of the mathematical relationship in triple-spiking SIDMS. The method was validated using a bovine blood standard reference material (SRM 966, Level 2). Analysis of human blood samples demonstrated the accuracy and reproducibility of the method, which can detect the Hg species down to 30 pg g(-1) in blood. The validity of the analytical results found for the blood samples was demonstrated using mass balance by comparing the sum of the concentrations of the individual Hg species with the total Hg in the corresponding samples; the latter was determined by isotope dilution mass spectrometry (IDMS) after decomposing the blood using EPA Method 3052 with single-spiking.