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1.
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
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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
5.
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
6.
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
7.
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
8.
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
9.
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
10.
The integration of a range of technologies including microfluidics, surface-enhanced Raman scattering and confocal microspectroscopy
has been successfully used to characterize in situ single living CHO (Chinese hamster ovary) cells with a high degree of spatial (in three dimensions) and temporal (1 s per spectrum) resolution. Following the introduction of a continuous flow of ionomycin, the real time spectral response
from the cell was monitored during the agonist-evoked Ca2+ flux process. The methodology described has the potential to be used for the study of the cellular dynamics of a range of
signalling processes.
Figure Spectral mapping of a single CHO cell 相似文献
11.
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
12.
Pérez Pavón JL García Pinto C Guerrero Peña A Moreno Cordero B 《Analytical and bioanalytical chemistry》2008,391(2):599-607
In the present work we report the results obtained with a methodology based on direct coupling of a headspace generator to
a mass spectrometer for the identification of different types of petroleum crudes in polluted soils. With no prior treatment,
the samples are subjected to the headspace generation process and the volatiles generated are introduced directly into the
mass spectrometer, thereby obtaining a fingerprint of volatiles in the sample analysed. The mass spectrum corresponding to
the mass/charge ratios (m/z) contains the information related to the composition of the headspace and is used as the analytical signal for the characterization
of the samples. The signals obtained for the different samples were treated by chemometric techniques to obtain the desired
information. The main advantage of the proposed methodology is that no prior chromatographic separation and no sample manipulation
are required. The method is rapid, simple and, in view of the results, highly promising for the implementation of a new approach
for oil spill identification in soils.
Figure PCA score plots illustrate clear discrimination of types of crude oil in polluted soil samples (e.g. results are shown for
vertisol) 相似文献
13.
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.
相似文献
14.
Covalent adduction of the model protein apomyoglobin by 4-hydroxy-2-nonenal, a reactive end-product of lipid peroxidation,
was characterized by nanoelectrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (FTICR). The
high mass resolving power and mass measurement accuracy of the instrument facilitated a detailed compositional analysis of
the complex reaction product without the need for deconvolution and transformation to clearly show the pattern of adduction
and component molecular weights. Our study has also demonstrated the value of electron capture dissociation over collision-induced
dissociation for the tandem mass spectrometric determination of site modification for the 4-hydroxy-2-nonenal adduct of oxidized
insulin B chain as an example.
Figure FTICR allowed characterization of 4-hydroxy-2-nonenal (HNE)-modified apomyoglobin (an expanded spectrum of the +15 charge
state is shown) 相似文献
15.
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
16.
Berchmans S Vergheese TM Kavitha AL Veerakumar M Yegnaraman V 《Analytical and bioanalytical chemistry》2008,390(3):939-946
The present work describes, for the first time, in situ electrochemical preparation of dendrimer-encapsulated Cu nanoparticles
using a self-assembled monolayer of fourth-generation amine-terminated polyamidoamine (PAMAM) dendrimer as the template. Atomic
force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) studies of the modified surface confirmed the presence of
Cu nanoparticles entrapped in dendrimer film. Au electrode modified with a monolayer of the dendrimer enables preconcentration
and subsequent voltammetric detection of Cu2+ at picomolar concentrations. Further, Cu nanoparticles in the dendrimer monolayer could be electrochemically derivatised
to Cu hexacyanoferrate, which exhibits specific crystal planes, unlike the random distribution of crystal planes in bulk-formed
Cu hexacyanoferrate, which is another catalytically active material for sensor applications.
Figure Electrochemical preparation of copper–dendrimer nanocomposite 相似文献
17.
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
18.
Purification methods for proteomics samples are of crucial concern for improving the quality of the sample delivered to the
mass spectrometer. They constitute the link between the mass spectrometer and protein processing and peptide isolation steps
that usually require solvents, buffers, or detergents completely incompatible with MS-analysis conditions. This work describes
three new clean-up procedures using synthetic membranes and polymer media and compares them with standard procedures. The
efficiency of each of the purification procedures was studied via application to four standards and two membrane proteins.
This work highlights the importance of versatility in sample preparation, especially for MS-based proteomic investigations.
Figure PMF spectra obtained after MALDI-TOF measurements of bovine mitochondrial complex III (A) and complex IV (B) in-solution digests, with and without purification 相似文献
19.
We report a simple method that combines dialysis, as a purification method, with the multielement capability of ICP to determine
the titanium-to-transferrin mole ratio at physiological pH, under buffer conditions. The method, by means of which titanium
and transferrin are determined simultaneously, enabled us to assess the binding capacities of different titanocene complexes.
Figure Titanocene dichloride 相似文献
20.
We have developed an iterative procedure for predicting the retention times of polycyclic aromatic hydrocarbons (PAHs) and
n-alkanes during separations by temperature-programmed gas chromatography. The procedure is based on estimates of two thermodynamic
properties for each analyte (the differences in enthalpy and entropy associated with movements between the stationary and
mobile phases) derived from data acquired experimentally in separations under isothermal conditions at temperatures spanning
the range covered by the temperature programs in ten-degree increments. The columns used for this purpose were capillary columns
containing polydimethylsiloxane-based stationary phases with three degrees of phenyl substitution (0%, 5%, and 50%). Predicted
values were mostly within 1% of experimentally determined values, implying that the method is stable and precise.
Figure Predicted values were mostly within 1 % of experimentally determined values, thus implying that the method is stable and precise 相似文献