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1.
Sánchez-Prado L Llompart M Lores M Fernández-Alvarez M García-Jares C Cela R 《Analytical and bioanalytical chemistry》2006,384(7-8):1548-1557
In this study the photoinduced degradation of triclosan has been investigated by photo-solid-phase microextraction (photo-SPME). In photo-SPME, photodegradation is carried out on the SPME fibre containing the target compound. Triclosan was extracted from aqueous solutions by use of polydimethylsiloxane SPME fibres and these were subsequently exposed to UV irradiation (power 8 W, wavelength 254 nm) for different times (from 2 to 60 min). The photodegradation kinetics of triclosan were investigated, the photoproducts generated were tentatively identified, and the photochemical behaviour of these products was studied by use of this on-fibre approach followed by gas chromatographic–mass spectrometric analysis. Eight photoproducts were tentatively identified, including chlorinated phenols, chlorohydroxydiphenyl ethers, 2,8-dichlorodibenzo-p-dioxin, and a possible dichlorodibenzodioxin isomer or dichlorohydroxydibenzofuran. The main photodegradation mechanisms were postulated and photodegradation pathways proposed. The effect of pH on triclosan degradation and on triclosan-to-dioxin conversion was also investigated. Triclosan degradation occurred, and generation of 2,8-dichlorodibenzo-p-dioxin was confirmed, throughout the pH range studied (from 3 to 9).
相似文献
2.
Various toxicological and metabolic interactions have been reported to exist between arsenic and selenium. In the present
study, synthetic seleno-arsenic compounds, potentially suitable for probing metabolic interactions between these two elements,
were prepared and tentatively characterized by using high-performance liquid chromatography (HPLC)–electrospray tandem mass
spectrometry and HPLC–inductively coupled plasma mass spectrometry. In analogy to the recently identified thio-arsenic species,
which can be prepared from their corresponding oxo-arsenic species via reaction with H2S, the seleno-arsenic compounds were also derived from oxo-arsenic compounds via reaction with H2Se.
Figure H2Se bubbled into solutions containing oxo‐arsenosugars converts them into their seleno‐arsenosugar analogues. 相似文献
3.
Harir M Frommberger M Gaspar A Martens D Kettrup A El Azzouzi M Schmitt-Kopplin P 《Analytical and bioanalytical chemistry》2007,389(5):1459-1467
The photodecomposition of imazamox, a herbicide of the imidazolinone family, was investigated in pure water. The main photoproducts
from the photolysis were followed over time by liquid chromatography mass spectrometry and structures were proposed from exact
mass determinations obtained by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry. The method
comprised exact mass determination with better than 0.2 ppm mass accuracy and a corresponding structural visualization taking
care of respective isotopes with an adapted van Krevelen diagram that enabled a systematic approach to the characterisation
of the elementary composition of each photoproduct. By taking advantage of the high resolving power of FT-ICR MS to make precise
formula assignments, the derived 2D van Krevelen diagram (O/C; H/C; m/z) enabled one to structurally differentiate the formed photoproducts and to propose a degradation pathway for imazamox.
Figure Overview of applied method to analyse the photolysis process of imazamox herbicide 相似文献
4.
Webb A 《Analytical and bioanalytical chemistry》2007,388(3):525-528
Figure Schematic diagram of a typical arrangement used for hyphenating chemical microseparations (e.g. capillary HPLC, CE, or CEC)
with microcoil NMR detection 相似文献
5.
How to confirm identified toxicants in effect-directed analysis 总被引:1,自引:0,他引:1
Brack W Schmitt-Jansen M Machala M Brix R Barceló D Schymanski E Streck G Schulze T 《Analytical and bioanalytical chemistry》2008,390(8):1959-1973
Due to the production and use of a multitude of chemicals in modern society, waters, sediments, soils and biota may be contaminated
with numerous known and unknown chemicals that may cause adverse effects on ecosystems and human health. Effect-directed analysis
(EDA), combining biotesting, fractionation and chemical analysis, helps to identify hazardous compounds in complex environmental
mixtures. Confirmation of tentatively identified toxicants will help to avoid artefacts and to establish reliable cause–effect
relationships. A tiered approach to confirmation is suggested in the present paper. The first tier focuses on the analytical
confirmation of tentatively identified structures. If straightforward confirmation with neat standards for GC–MS or LC–MS
is not available, it is suggested that a lines-of-evidence approach is used that combines spectral library information with
computer-based structure generation and prediction of retention behaviour in different chromatographic systems using quantitative
structure–retention relationships (QSRR). In the second tier, the identified toxicants need to be confirmed as being the cause
of the measured effects. Candidate components of toxic fractions may be selected based, for example, on structural alerts.
Quantitative effect confirmation is based on joint effect models. Joint effect prediction on the basis of full concentration–response
plots and careful selection of the appropriate model are suggested as a means to improve confirmation quality. Confirmation
according to the Toxicity Identification Evaluation (TIE) concept of the US EPA and novel tools of hazard identification help
to confirm the relevance of identified compounds to populations and communities under realistic exposure conditions. Promising
tools include bioavailability-directed extraction and dosing techniques, biomarker approaches and the concept of pollution-induced
community tolerance (PICT).
Figure Toxicity confirmation in EDA as a tiered approach 相似文献
6.
The derivatization of cysteine-containing peptides with benzoquinone compounds is rapid, quantitative and specific in acidic
media. The conversion of cysteines into hydrophobic benzoquinone-adducted residues in peptides is used here to alter the chromatographic
properties of cysteinyl peptides during liquid chromatography separation. The benzoquinone derivatization is shown to allow
the accurate selection of cysteine-containing peptides of bovine serum albumin tryptic digest by diagonal reversed-phase chromatography,
which consists of one primary and a series of secondary identical liquid chromatographic separations, before and after a cysteinyl-targeted
modification of the peptides by benzoquinone compounds.
Figure Diagonal chromatographic selection of cysteinyl peptides modified with benzoquinones
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
7.
Lee JO So HM Jeon EK Chang H Won K Kim YH 《Analytical and bioanalytical chemistry》2008,390(4):1023-1032
Recent advances in nanotechnology have enabled the development of nanoscale sensors that outperform conventional biosensors.
This review summarizes the nanoscale biosensors that use aptamers as molecular recognition elements. The advantages of aptamers
over antibodies as sensors are highlighted. These advantages are especially apparent with electrical sensors such as electrochemical
sensors or those using field-effect transistors.
Figure Feeling proteins with aptamer-functionalized carbon nanotubes 相似文献
8.
Natalini B Sardella R Camaioni E Gioiello A Pellicciari R 《Analytical and bioanalytical chemistry》2007,388(8):1681-1688
The discovery that bile acids are involved in the modulation of nuclear steroid receptors has prompted renewed interest in
this field of research. Due to the nature of research in this field, a technique that enables simple and effective assessment
of the hydrophobic/hydrophilic balance, thus improving and speeding up evaluations of the biological profiles of these compounds,
is greatly needed. In this context, both CMC value determination and RP-HPLC mobility evaluation were explored as possible
approaches. While the CMC was calculated using the noninvasive conductimetric method, the RP-HPLC mobility was assessed by
measuring the retention factor at several mobile phase compositions and extrapolating back to the pure aqueous mobile phase.
The correlation of the CMC with the derived chromatographic hydrophobic index ϕ
0 was satisfactory.
Figure Experimental versus predicted pCMC values 相似文献
9.
10.
Ortner K Sivanandam VN Buchberger W Müller N 《Analytical and bioanalytical chemistry》2007,388(1):173-177
Enzymatically cleaved glycans from sub-milligram quantities of erythropoietin (EPO) and ovalbumin have been analyzed, without
further purification, by two-dimensional diffusion-ordered nuclear magnetic resonance spectroscopy. At NMR sample concentrations
below 50 μmol L−1 the major components of the oligosaccharide fractions could be distinguished by their anomeric proton chemical shift and
their size-dependent diffusion coefficients.
Figure
1H NMR diffusion decay curves of anomeric protons in the EPO glycan fraction 相似文献
11.
12.
Surmeian A Diplasu C Groza A Ganciu M Belenguer P Tempez A Chapon P 《Analytical and bioanalytical chemistry》2007,388(8):1625-1629
A high-current pulsed hollow cathode discharge was used to study the role of atomic and ionic metastables involved in ionization
plasma processes. We observed the enhancement of the spectral emission lines of noble gas ions in the afterglow. A study of
the processes that involve atomic and ionic metastables is of great interest since it should lead to a better understanding
of and enhanced control over the ionization mechanisms crucial to analytical glow discharge mass spectrometry (GDMS) analysis.
Figure Time profile of Ti, Ti+, and Ne+ spectral lines 相似文献
13.
Schaffer B Grogger W Kothleitner G Hofer F 《Analytical and bioanalytical chemistry》2008,390(6):1439-1445
In this work we show how energy-filtered imaging can be used to obtain spectrum images of electron energy-loss spectrometric
data. Focus is placed on improved energy resolution within these data sets. Using two multilayer samples (GaN/AlN and InP/InAs),
we demonstrate the advantages of spectrum-imaging and its extended mapping capabilities. Plasmon-ratio maps are used to quickly
create high-contrast material maps with high signal-to-noise ratio, ratio-contrast plots are used to gain optimum settings
for the ratio maps, and plasmon-position maps are used to map small shifts of the energy position of bulk plasmon peaks.
Figure Scheme of EELS SI and derived plasman-position map 相似文献
14.
Cordes DB Miller A Gamsey S Singaram B 《Analytical and bioanalytical chemistry》2007,387(8):2767-2773
The simultaneous use of several fluorescent reporter dyes in a multicomponent boronic acid-based glucose sensing system is
reported. In one application, two dyes with widely different emission wavelengths are used to report changes in glucose concentration.
A third glucose-insensitive dye was then added to act as a reference dye and provide for a ratiometric correction to the two
reporter dye signals. The inclusion of such a reference dye reduces errors arising from sources such as fluctuations in lamp
intensity and sample dilution.
The simultaneous use of multiple fluorescent reporter dyes 相似文献
15.
X-ray absorption fine structure (EXAFS) spectroscopy spectra were collected for three brominated persistent pollutants: 6-bromo-2,4,5-trichlorophenol
(BrTriClP), pentabromophenol (PentaBrP) and 3,3′,5,5′-tetrabromobisphenol A (TBBA). The substances were selected to be symmetrical
(BrTriClP and TBBA) or asymmetrical (PentaBrP) with respect to the atomic Br positions and to differ in the number of bromine
and other halide atoms, as well as their relative positions. The asymmetrical PentaBrP was modelled with special detail as
not all bromine atoms have identical coordination environments. The studied substances displayed unique EXAFS spectra, which
could be used to determine the molecular structure in fair detail. We conclude that EXAFS spectroscopy is a suitable technique
for molecular characterization of the comparatively complex molecules within the class of compounds of brominated organic
persistent pollutants. A detailed understanding of the EXAFS spectra of the pure compounds opens up possibilities to study
the interactions with soil and sediment matrices by means of EXAFS spectroscopy.
Figure Brominated organic persistent pollutants are characterized by EXAFS spectroscopy 相似文献
16.
Astel A Tsakovski S Simeonov V Reisenhofer E Piselli S Barbieri P 《Analytical and bioanalytical chemistry》2008,390(5):1283-1292
The present study deals with the application of self-organizing maps (SOM) and multiway principal-components analysis to classify,
model, and interpret a large monitoring data set for surface water quality. The chemometric methods applied made it possible
to reveal specific quality patterns of the chemical and biological parameters used to monitor the water quality (relation
between water temperature, turbidity, hardness, colibacteria), seasonal impacts during the long period of observation and
the relative independence on the spatial location of the sampling sites (water supply sources for the City of Trieste).
Figure The schematic procedure for surface water pollution estimation supported by neural network-based classification and multivariate factor
analysis 相似文献
17.
Ma X Zhu T Xu H Li G Zheng J Liu A Zhang J Du H 《Analytical and bioanalytical chemistry》2008,390(4):1133-1137
A chemical prototype sensor was constructed based on nanofiber-structured TiO2 and highly sensitive quartz resonators. The gas-sensing behavior of this new sensor to selected simulant warfare agents was
investigated at room temperature. Results showed rapid response and good reversibility of this sensor when used with high-purity
nitrogen. This provides a simple approach to preparation of materials needed as chemical sensors for selected organic volatiles
or warfare agents.
Figure Sensing behavior of TiO2 nanofiber sensor to chemical vapors 相似文献
18.
An impurity-profiling method for 3,4-methylenedioxymethamphetamine (MDMA) is presented. The impurities of interest were extracted
by solid-phase extraction (SPE) on Bakerbond C18 spe columns from a weakly alkaline solution (pH 8.5). Development of the extraction conditions covered selection of the buffer
for dissolution of the sample and the volume of the eluent used to elute the impurities. An important part of the studies
was to optimise the separation conditions, and the simplex method was used for this purpose. Cluster analysis was applied
for comparison of samples and its grouping. The developed method was based on the areas of 33 selected peaks corresponding
to MDMA impurities. All examined samples were correctly classified into clusters corresponding to the synthetic route.
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19.
Goryacheva IY Basova EY Van Peteghem C Eremin SA Pussemier L Motte JC De Saeger S 《Analytical and bioanalytical chemistry》2008,390(2):723-727
A rapid easy-to-use immunoassay was optimised for the non-instrumental detection of ochratoxin A (OTA) in beer. The analytical
method involves preconcentration on the immunoaffinity layer inside a column followed by direct competitive ELISA detection
in the same layer. The visual cut-off value, i.e. the lowest OTA concentration resulting in no colour development, was 0.2 μg
L-1. Assay validation was performed using samples spiked with OTA. Thirty-seven naturally contaminated samples were screened
with the gel-based method developed and no false-negative results were obtained. The method described offers a simple, rapid
and cost-effective screening tool, thus contributing to better health protection of consumers.
Figure Gel-based immunoassay of spiked beer samples. 相似文献
20.
An intercomparison to establish the performance of routine laboratories in the determination of polybrominated flame retardants
in polymers was organised. Commercial poly(ethyleneterephthalate) was fortified with technical pentabromodiphenyl ether, octabromodiphenyl
ether and decabromodiphenyl ether mixtures and with a decabromobiphenyl technical mixture at 0.4–0.8 g/kg. Homogeneity and
stability of the total Br content in the material was confirmed. Thirty-seven laboratories from Europe, Asia and the Americas
submitted results. Relative repeatability standard deviations for individual congeners ranged from 7 to 17%. Relative between-laboratory
standard deviations ranged from 22 to 61%. No significant influence of a common standard, application of a standard method
or method parameters could be identified. The quality and uncertainty of the results of this study are significantly worse
than those reported in the environmental field and indicate a clear need for a learning process among the laboratories involved.
Figure Mandel’s h (between labs): critical level: 1.91 相似文献