Combined isolation and purification procedures prior to the high-performance liquid chromatographic-ion-trap tandem mass spectrometric determination of estrogens and their conjugates in river sediments.

A fast and sensitive analytical procedure has been developed for the simultaneous separation and determination of alpha-estradiol, beta-estradiol, estriol, estrone and ethynylestradiol and their sulfate, glucuronide and acetate conjugates in river sediments. The procedure includes a microwave-assisted extraction (MAE) with aqueous methanol (25:75, v/v) at 100 degrees C in 10 min, a clean-up on Oasis WAX cartridge and a high-performance liquid chromatography-ion-trap tandem mass spectrometry (HPLC-IT-MS/MS) with electrospray ionization. The recovery for each compounds ranged from 83 to 107% and the repeatability represented as RSDs ranged from 4.9 to 9.6%. The limits of detection (LODs) were down to 1 ng g(-1). The analytical performance of the method was evaluated using determination of free and conjugated estrogens in river sediments.

High-performance liquid chromatographic/ion-trap mass spectrometric speciation of aquatic mercury as its pyrrolidinedithiocarbamate complexes.

Mercury-pyrrolidinedithiocarbamate complexes are first time used for speciation of aquatic mercury with high-performance liquid chromatographic/ion trap-mass spectrometric method utilizing atmospheric pressure chemical ionization (APCI). The separation of the four mercury species was achieved in less than 5 min with a linear gradient profile of aqueous methanol from 70 up to 100% (v/v) in 4th min, isocratic elution at 100% up to 5th min and followed by a negative gradient to 70% in 6th min. The best separation was achieved on a reverse phase Zorbax Eclipse XDB C18 column (50 mm x 2.1 mm i.d., 1.8 microm particle size). The on-column limits of detection (injection volume 1 microL) were 370 pg for methylmercury (MeHg+), 280 pg for ethylmercury (EtHg+), 250 pg for phenylmercury (PhHg+) and 90 pg for inorganic mercury (Hg2+) when the data were collected in selective ion monitoring (SIM) mode. A method of isolation and preconcentration of the mercury species using a "home-made" C18 solid phase extraction (SPE) microcolumns was developed to enhance sensitivity of the method. The preconcentration factor as much as 2500 was achieved with on-column complex formation of mercury-pyrrolidinedithiocarbamate. Methanol (100%) was chosen for elution of preconcentrated mercury species. The method was applied for the determination of mercury species in river water samples.

Sensitive capillary electrophoretic determination of mercury species with amperometric detection at a copper electrode after cation exchange preconcentration.

A capillary electrophoretic method for the separation of four mercury species with amperometric detection was developed. Inorganic Hg2+, methyl-, ethyl-, and phenyl-mercury were complexed with L-cysteine and separated in a counterelectroosmotic mode in an electrolyte solution comprised of 20 mM sodium tetraborate at pH 9.5. Amperometric detection of separated species was achieved at passivated copper electrode under electrocatalytic oxidation conditions. The four mercury species were separated in less than 8 min with LODs ranging from 170 to 450 microg/L. Cation exchange preconcentration was used to decrease the LODs down to 1.7 microg/L.

Total mercury and mercury species in birds and fish in an aquatic ecosystem in the Czech Republic.

Total mercury and mercury species (methylmercury-MeHg, inorganic mercury--Hg(2+)) were determined in the aquatic ecosystem Záhlinice (Czech Republic). Four tissues (muscle, intestines, liver and kidney) of three bird species--cormorant, great crested grebe and Eurasian buzzard, muscle tissues of common carp, grass carp, northern pike, goldfish, common tench, perch and rudd, aquatic plants (reed mace and common reed), sediments and water were analysed. Relative contents of MeHg (of total Hg) were in the range from 71% to 94% and from 15% up to 62% in the muscle and intestines and in liver, respectively, for all birds. Statistically significant differences were found between contents of MeHg in liver tissues of young and adult cormorant populations (F(4.60)=56.71, P<10(-5)). Relative contents of MeHg in muscle tissues of fishes were in the range from 65.1% to 87.9% of total Hg.

Mercury speciation by CE: a review.

CE methods for the speciation of inorganic and organomercury compounds are reviewed. Sample preparation, separation conditions and detection modes are discussed. Efficient separation and sensitive determination of mercury species by CE typically involves complexation with various thiols, chromogenic and other chelating agents; however, some methods do not require complexation. Spectrophotometric detection based on UV-visible absorption is by far the most commonly used. Hyphenated techniques, such as CE/inductively coupled plasma (ICP)-MS, hydride generation coupled to ICP-MS or atomic fluorescence spectrometry and CE/atomic absorption spectrometry are gaining popularity due to their high sensitivity and selectivity. Last, but not least, the potential and applications of electrochemical methods for detection of separated mercury species are outlined.

Ion exchange preconcentration and separation of mercury species by CE with indirect contactless conductometric detection.

Capillary electrophoretic separation of four mercury species (inorganic Hg(2+), methyl-, ethyl-, and phenylmercury) was achieved in less than 8 min with an electrolyte consisting of 150 mM 2-amino-2-methyl-propanol (AMP) at pH 11.6. The analytes were complexed with 0.1% mercaptopropionic acid (MPA), separated in counter-EOF as anionic complexes, and detected by a contactless conductometric detector. Ion exchange preconcentration with on-column formation of MPA-mercury complexes was developed. Preconcentration factors of 25-150 were achieved and LODs in the range of 2.9-6.9 ng/mL were feasible. This method may prove to be applicable as a rapid screening method for mercury speciation in environmental samples.

Uptake of thallium from naturally-contaminated soils into vegetables.

Thallium transfer from naturally (pedogeochemically) contaminated soils into vegetables was studied. Three different types of top-soil (heavy, medium, and light) were used for pot experiments. The soils were collected from areas with low, medium, and high levels of pedogeochemical thallium (0.3, 1.5 and 3.3 mg kg(-1)). The samples of vegetables were collected and analysed. The total content of thallium in soil and the type of soil (heavy, medium and light), plant species and plant variety were found to be the main factors influencing thallium uptake by plants. The uptake of thallium from soils with naturally high pedogeochemical content of this element can be high enough to seriously endanger the food chain. These findings are very important because of the high toxicity of thallium and the absence of threshold limits for thallium in soils, agricultural products, feedstuffs and foodstuffs in most countries, including the Czech Republic.

Liquid chromatographic--cold vapour atomic fluorescence spectrometric determination of mercury species.

Solvent extraction, sonication, and microwave-assisted extractions in the presence of extraction agents (thioacetic acid, citric acid, cysteine, 2-mercaptoethanol, HCl + NaCl, etc.) were tested for the isolation of mercury species. A mixture of 6 M HCl and 0.1 M NaCl was selected as the most suitable extraction agent. The extraction efficiency was about 10% higher and the RSD below 3.3% when microwave-assisted extraction was applied instead of sonication. The liquid chromatography-cold vapour atomic fluorescence spectrometry (LC/CV-AFS) method was optimised and used for separation and determination of inorganic mercury cations and alkylated and arylated mercury species. Isocratic elution at a flow rate of 0.15 mL/min (with a mobile phase containing 0.05% 2-mercaptoethanol (pH = 5) and 7% methanol and with a stepwise increase of methanol content up to 100% MeOH in the 15th min) was used for separation of mercury species on a Hypersil BDS C18 RP column. The limits of detection of the LC/CV-AFS system were estimated as 0.2 microg/L (3%) for MeHg+, 0.07 microg/L (5.3%) for inorganic Hg, 0.06 microg/L (3.4%) for PhHg+, and 0.12 microg/L (4.4%) for EtHg with the corresponding RSDs at 5 microg/L (n = 10) given in parentheses. The concentrations (2-10 mg/kg fresh weight) of total mercury and methylmercury (90-99% of the total mercury) in selected fish obtained by HPLC/CV-AFS were in good agreement (absolute deviations 0.05 mg/kg) but more precise (RSDs <5.4% at 5 mg/L, n = 10) than those determined by GC coupled to an electron capture detector. The RSDs (3.1-8.2% and 4.1-9.0%) of the overall analytical procedure for the determination of total mercury (AMA 254) and methylmercury (HPLC/CV-AFS) were determined for intra-day and inter-day assays, respectively.

Uptake of thallium from artificially and naturally contaminated soils into rape (Brassica napus L.).

An inductively coupled plasma mass spectrometry (ICP/MS) method was used for the evaluation of thallium transfer from naturally (pedogeochemically) and artificially contaminated soils into rape. Two sets of three different types of top soils (heavy, medium, and light) were used for pot experiments. The first set was collected from areas with high levels of pedogeochemical thallium (0.3, 1.5, and 3.3 mg kg(-1) DM). The second set of three soils with naturally low content of thallium was artificially contaminated with thallium sulfate to achieve five levels of contamination (0, 0.4, 2, 4, and 6 mg kg(-1) DM Tl). The soil samples and the samples of winter and spring rape (straw, seeds) from both sets were collected and analyzed. Plant and soil samples from fields were collected at 42 selected sites situated in South Bohemia and in Czech-Moravian Highlands where higher pedogeochemical content of thallium was expected. More intensive transport (better availability) of Tl was observed in the case of artificially contaminated soils. The physicochemical form and the total content of Tl in soil were found to be the main factors influencing its uptake by plants. The concentration of Tl in rapeseeds in the field samplings was mostly 45% of its content in the particular soil. Nevertheless the uptake of Tl from soils with naturally high pedogeochemical content can be high enough to seriously endanger food chains. These findings are very important because of the high toxicity of Tl and the absence of threshold limits for Tl in soils, agricultural products, feedstuffs, and foodstuffs in most countries including the Czech Republic.