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Träfflista för sökning "L773:0003 2670 OR L773:1873 4324 srt2:(2005-2009)"

Sökning: L773:0003 2670 OR L773:1873 4324 > (2005-2009)

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1.
  • Ahlström, Lars-Henric, et al. (författare)
  • Application of standard addition methodology for the determination of banned azo dyes in different leather types
  • 2005
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 1873-4324 .- 0003-2670. ; 552:1-2, s. 76-80
  • Tidskriftsartikel (refereegranskat)abstract
    • An analytical procedure based on microwave-assisted extraction (MAE) and standard addition was applied for the determination of banned azo dyes in bovine, sheep, and goat leather. Standard addition at four different concentration levels was performed using azo dyes, dissolved either in methanol or water. All dyes were determined indirectly by measuring their corresponding harmful aromatic amines, formed after reduction by use of sodium dithionite. Comparing found amounts of amines with theoretical target values allowed an assessment of accuracy. The recoveries were also compared with those obtained for non-spiked samples using external standard calibration. The standard addition approaches provided much better accuracy than external standard calibration, with recoveries close to 100% for most amines. Since there was no great difference in recoveries when using methanol or water as solvent, preparation of the dyes in methanol might be preferred because of the faster evaporation of the solvent after spiking. (c) 2005 Elsevier B.V. All rights reserved.
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2.
  • Ali, Hassan, et al. (författare)
  • Vibrational spectroscopic characterisation of salmeterol xinafoate polymorphs and a preliminary investigation of their transformation using simultaneous in situ portable Raman spectroscopy and differential scanning calorimetry
  • 2008
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 0003-2670 .- 1873-4324. ; 620:1-2, s. 103-12
  • Tidskriftsartikel (refereegranskat)abstract
    • Knowledge and control of the polymorphic phases of chemical compounds are important aspects of drug development in the pharmaceutical industry. Salmeterol xinafoate, a long acting beta-adrenergic receptor agonist, exists in two polymorphic Forms, I and II. Raman and near infrared spectra were obtained of these polymorphs at selected wavelengths in the range of 488-1064 nm; significant differences in the Raman and near-infrared spectra were apparent and key spectral marker bands have been identified for the vibrational spectroscopic characterisation of the individual polymorphs which were also characterised with X ray diffractometry. The solid-state transition of salmeterol xinafoate polymorphs was studied using simultaneous in situ portable Raman spectroscopy and differential scanning calorimetry isothermally between transitions. This method assisted in the unambiguous characterisation of the two polymorphic forms by providing a simultaneous probe of both the thermal and vibrational data. The study demonstrates the value of a rapid in situ analysis of a drug polymorph which can be of potential value for at-line in-process control
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3.
  • Ali Malik, Muhammad, et al. (författare)
  • Imaging fingerprinting of excitation emission matrices
  • 2009
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 0003-2670 .- 1873-4324. ; 635:2, s. 196-201
  • Tidskriftsartikel (refereegranskat)abstract
    • The spectral fingerprinting of the excitation emission matrix (EEM) of fluorescent substances is demonstrated using polychromatic light sources and tri-chromatic image detectors. A model of the measured fingerprints explaining their features and classification performance, based on the polychromatic excitation of the indicators is proposed.Substantial amount of spectral information is retained in the fingerprints as corroborated by multivariate analysis and experimental conditions that favor such situation are identified.In average, for five different substances, the model shows a fitting goodness measured by the Pearsons r coefficient and the root mean square deviation of 0.8541 and 0.0247 respectively, while principal component classification patterns satisfactorily compare with the EEM spectroscopy classification and respectively explain 96% and 93% of the information in the fist two principal components.The measurements can be performed using regular computer screens as illumination and web cameras as detectors, which constitute ubiquitous and affordable platforms compatible with distributed evaluations, in contrast to regular instrumentation for EEM measurements.
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5.
  • Alimelli, Adriano, et al. (författare)
  • Fish freshness detection by a computer screen photoassisted based gas sensor array
  • 2007
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 0003-2670 .- 1873-4324. ; 582:2, s. 320-328
  • Tidskriftsartikel (refereegranskat)abstract
    • In the last years a large number of different measurement methodologies were applied to measure the freshness of fishes. Among them the connection between freshness and headspace composition has been considered by gas chromatographic analysis and from the last two decades by a number of sensors and biosensors aimed at measuring some characteristic indicators (usually amines). More recently also the so-called artificial olfaction systems gathering together many non-specific sensors have shown a certain capability to transduce the global composition of the fish headspace capturing the differences between fresh and spoiled products. One of the main objectives related to the introduction of sensor systems with respect to the analytical methods is the claimed possibility to distribute the freshness control since sensors are expected to be "portable" and "simple". In spite of these objectives, until now sensor systems did not result in any tool that may be broadly distributed. In this paper, we present a chemical sensor array where the optical features of layers of chemicals, sensitive to volatile compounds typical of spoilage processes in fish, are interrogated by a very simple platform based on a computer screen and a web cam. An array of metalloporphyrins is here used to classify fillets of thawed fishes according to their storage days and to monitor the spoilage in filleted anchovies for a time of 8 h. Results indicate a complete identification of the storage days of thawed fillets and a determination of the storage time of anchovies held at room temperature with a root mean square error of validation of about 30 min. The optical system produces a sort of spectral fingerprint containing information about both the absorbance and the emission of the sensitive layer. The system here illustrated, based on computer peripherals, can be easily scaled to any device endowed with a programmable screen and a camera such as cellular phones offering for the first time the possibility to fulfil the sensor expectation of diffused and efficient analytical capabilities. © 2006 Elsevier B.V. All rights reserved.
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7.
  • Astuti, Yeni, et al. (författare)
  • Direct spectroelectrochemistry of peroxidases immobilised on mesoporous metal oxide electrodes : Towards reagentless hydrogen peroxide sensing
  • 2009
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 0003-2670 .- 1873-4324. ; 648:1, s. 2-6
  • Tidskriftsartikel (refereegranskat)abstract
    • In this paper, we employ two peroxidases (horseradish peroxidase, HRP and cytochrome c peroxidase, CcP) to demonstrate their ability to retain their redox and biological functions after their immobilisation on mesoporous TiO2 and SnO2 electrodes. We will also demonstrate the use of HRP immobilised on the metal oxide electrodes for the development of reagentless optical and electrochemical biosensors for the detection of hydrogen peroxide (H2O2) with low detection limit of 0.04 and 1 mu M, respectively. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.
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8.
  • Beni, Valerio, et al. (författare)
  • Development of a portable electroanalytical system for the stripping voltammetry of metals : Determination of copper in acetic acid soil extracts
  • 2005
  • Ingår i: Analytica Chimica Acta. - : Elsevier. - 0003-2670 .- 1873-4324. ; 552:1-2, s. 190-200
  • Tidskriftsartikel (refereegranskat)abstract
    • The development, characterisation and evaluation of a prototype portable electrochemical trace metal analyser are presented. The instrumentis a battery-powered microcontroller-based potentiostat, which implements anodic stripping voltammetry (ASV) at suitable sensor electrodes.It is capable of operating away from the laboratory, in the absence of an external power source and is usable by low-skilled personnel. Thedistinguishing feature of the instrument is its custom software, which enables sample pre-screening, data processing and sample dilution andstandard additions calculations to be carried out. The instrument has been evaluated by application of a methodology for the detection ofcopper in acetic acid soil extracts, both in the laboratory and in the field. Underpotential deposition staircase anodic stripping voltammetry(UPD-SCASV) of the copper at gold disk electrodes was used as a test method. There was good agreement between the instrument resultsand those from laboratory-based reference analytical methods for analyses carried out both in the laboratory and in the field.
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9.
  • Bergström, Staffan, et al. (författare)
  • Extracting syringe for extraction of phthalate esters in aqueous environmental samples
  • 2007
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 1873-4324 .- 0003-2670. ; 594:2, s. 240-247
  • Tidskriftsartikel (refereegranskat)abstract
    • The use of the extracting syringe (ESy), a fully automated membrane-based extraction technique, for analysis of phthalate esters in complex aqueous samples has been investigated. The ESy, working as an autosampler that combines the extraction process and injection into the gas chromatograph (GC) in one single step, is placed on top of the GC equipped with a flame ionisation detector. The aqueous samples are loaded in a tray and automatically extracted by employing microporous membrane liquid-liquid extraction principle. After the extraction, the extract is directly injected into the GC's programmable temperature vaporisation injector. Six different phthalate esters were used as model compounds. Four extraction solvents were tested and the addition of sample organic modifier was examined. Toluene was the optimal solvent to use for extraction. Due to the large variation in polarity of phthalate esters, 50% methanol as organic modifier had to be added to the samples so as to extract the most nonpolar phthalate esters; di-2-ethylhexylphthalate and di-n-octylphthalate, whereas the other four relatively polar phthalate esters were extracted from unmodified samples. No significant difference between extraction of river water, leachate water from a landfill and reagent water was noted, except for minor deviations. The extraction time was 20 min for extraction of a 1-mL sample, resulting in a good linearity for all aqueous media investigated, good enrichment factors (54-110 folds) and low LOD values (0.2-10 ng mL(-1)) and relative standard deviation (%R.S.D.; 0.9-3.7%).
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10.
  • Carlsson, Jenny, 1977-, et al. (författare)
  • Biosensor discrimination of meat juice from various animals using a lectin panel and ellipsometry
  • 2005
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 0003-2670 .- 1873-4324. ; 547:2, s. 229-236
  • Tidskriftsartikel (refereegranskat)abstract
    • In this work, simple microcontact printed gold-wafers were used to make a lectin panel for investigation and discrimination of different meat juices from fresh meat of cattle, chicken, pig, cod, turkey and lamb. Seven different lectins were thus attached to gold surfaces using the streptavidin–biotin method. Lectins recognize and bind specifically to carbohydrate structures present on different proteins. The biorecognition was evaluated with null ellipsometry and the data obtained was related to an internal standard of lactoferrin. The data was evaluated with multivariate data analysis techniques to identify possible discrimination or grouping of data. Scanning ellipsometry was used for visualization of the binding pattern of the lectins and the meat juice proteins. The two-dimensional images obtained could be used to visualize the protein distribution, furthermore, to exclude anomalies. The results showed that the different meat juices from the six different species: cattle, chicken, pig, cod, turkey and lamb could be discriminated from each other. The results showed to be more repetitive for the mammalian meat juices. Using a simple model based on an artificial neuronal net, it was also possible to classify meat juices from the mammals investigated.
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