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  • Column liquid chromatography  (1,216)
  • Springer  (1,216)
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  • 1
    Electronic Resource
    Electronic Resource
    The effect of pH on the high pH anion-exchange chromatography elution of monosaccharides (1999)
    Springer
    Chromatographia 49 (1999), S. 699-702 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Anion-exchange chromatography ; High ph elvents ; Monosaccharides ; Carbopac PA-100
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary We have studied the elution behaviour of six common monosaccharides, fucose, galactosamine, glucosamine, galactose, glucose and mannose, on the CarboPac PA-100 column. The relative elution positions of galactose, glucose and mannose were dependent on the sodium hydroxide concentrations, a phenomenon which was likely to be the result of differential ionisation of the hydroxyl groups at ring positions two and four. The optimal resolution of the monosaccharides studied was achieved by elution with 30 mM sodium hydroxide with no appreciable loss in sensitivity at this low concentration.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02466915
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  • 2
    Electronic Resource
    Electronic Resource
    High performance liquid chromatography method for the determination of meropenem in human plasma (1999)
    Springer
    Chromatographia 49 (1999), S. 253-255 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Meropenem in human plasma ; Solid phase extraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary This paper describes an HPLC method for the determination of meropenem in human plasma. The method uses solid phase extraction (SPE) of the samples and has good sensitivity, precision and accuracy. The limit of quantification in plasma samples is 0.02 μg mL−1. Calibration curves were linear over a large dynamic range, namely within 0.02–50 μg mL−1. The method was applied to the determination of meropenem levels in patients receiving meropenem, as a single dose or at steady state.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467552
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  • 3
    Electronic Resource
    Electronic Resource
    FMOC-Cl as derivatizing agent for the analysis of amino acids and dipeptides by the absolute analysis method (1999)
    Springer
    Chromatographia 49 (1999), S. 317-320 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Amino acids ; FMOC derivatives ; Oligopeptides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary One classical method for quantitation of amino acids in proteins is hydrolysis of the proteins and determination of the free amino acids. Although the drastic experimental conditions necessary for complete hydrolysis always cause degradation of some of the amino acids, if mild hydrolysis conditions are used, a mixture of amino acids and oligopeptides is obtained. If these conditions are adequately tuned, the oligopeptides are almost exclusively dipeptides. For this reason we have initiated a study to find a derivatizing agent suitable for the analysis of amino acids and dipeptides by an absolute method of quantitation already tested for amino acids. FMOC-Cl was found to be a suitable derivatizing agent for this purpose.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467563
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  • 4
    Electronic Resource
    Electronic Resource
    Potentiometric detection of monovalent anions separated by ion chromatography using all solid-state contact PVC matrix membrane electrode (1999)
    Springer
    Chromatographia 49 (1999), S. 338-342 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion chromatography ; Monovalent anions determination ; Potentiometric detection ; Ion selective PVC-matrix electrode
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An all solid-state contact tubular PVC-matrix membrane electrode has been applied for potentiometric detection of inorganic and organic monovalent anions using phosphate and hydrogen phosphate eluents at low concentrations. This is a “monovalent detection method” as the selectivity of the electrode towards monovalent anions results in some other anions being undetected unless the concentration of those other anions is higher than 10−3 mol dm−3 in the sample solution injected. It takes only eight minutes to complete the separation with a good resolution. Theoretical and practical considerations are discussed, and in particular, sensitivity, linearity, detection limit and dynamic behaviour are presented. The use of an all solid-state contact bromide-selective electrode as a detector offers so far the best simultaneous sensitivity toward all anions when compared with other detection methods. Determination of Cl− and NO3 − ions in river, rain and drinking water samples without any further sample preconcentration has been successfully achieved. The detection limit is sub-ppb for most of anions in a 20 μL injection volume.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467567
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  • 5
    Electronic Resource
    Electronic Resource
    A system for predicting the retentions of O-alkyl, n-(1-methylthioethylideneamino) phosphoramidates on RP-HPLC (1999)
    Springer
    Chromatographia 49 (1999), S. 444-448 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; O-alkyl, O-(1-methylthioethylideneamino) phosphoramidates ; Quantitative structure-retention relationship (QSRR) ; Reversed-phase LC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary By using factor analysis, cluster analysis and multiple linear regression methods, two parameters, FHF and ECCR, were selected from eight solute-related structure parameters as showing the best correlation with retention data. The relationship between the retention data (k) and these two structure parameters were established for ten O-alkyl, O-(1-methylthioethylideneamino) phosphoramidate compounds under the experimental conditions studied. Retention data (k) for six other compounds that have a high correlation with structure parameters were predicted using these QSRR equations. The system was evaluated by comparing the experimentalk values with the predicted ones. Good agreement was obtained between the experimental and predictedk values.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467621
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  • 6
    Electronic Resource
    Electronic Resource
    Determination of flupoxam residues in soil by high performance liquid chromatography (1999)
    Springer
    Chromatographia 49 (1999), S. 535-538 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Solid phase extraction ; Herbicides in soil ; Flupoxam
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary High-performance liquid chromatography with UV detection was used to determine the residues of flupoxam (a new herbicide) in soils. Soil samples were extracted with aqueous methanol. The soil extracts were cleaned up and concentrated using two solid phase extraction columns: a polymeric stationary phase based on a polystyrene-divinylbenzene resin (Lichrolut EN) and alumina. Recovery experiments were performed at ppb levels in spiked soil samples. The recovery was 76±1.7% for flupoxam in the range 5–100 μg kg−1 of soil. Limit of determination was 3 μg kg−1.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467754
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  • 7
    Electronic Resource
    Electronic Resource
    Analysis of doxorubicin in cell culture media and human plasma using solid phase extraction and HPLC (1999)
    Springer
    Chromatographia 49 (1999), S. 557-561 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Solid phase extraction ; Doxorubicin ; Cell culture media ; Human plasma ; Fluorescence detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Doxorubicin is an antineoplastic antibiotic isolated fromStreptomyces peucetius var.cesius clinically used in the treatment of tumors such as lung or breast, Hodgkin's disease and various types of leukemias. The main goal of this study was to develop a simple and sensitive HPLC method with fluorescence detection for the quantitation of doxorubicin in cell culture media collected during an in vitro studies and in human plasma. Solid phase extraction (C2 silica) was applied. The experiment established five-point standard curve (1 ng mL−1 to 100 ng mL−1). The standard curves prepared in blank cell tissue media were linear over the range of doxorubicin assayed and had a mean correlation coefficient of 0.9973±9.43×10−4 and slope 0.02545±1.85×10−3. The standard curves prepared in human plasma were linear and had mean correlation coefficient of 0.997 and slope 0.01885±5.19×10−4. The limit of quantitation for doxorubicin in both specimens was arbitrarily established to be 1 ng mL−1. Intra-day variabilities were determined using 3–4 replicates of control solutions of doxorubicin (3 ng mL−1 and 30 ng mL−1) in blank plasma and cell culture media. Inter-day variabilities were determined over a four day period analyzing replicates of controls. All precision and accuracy values fell within the acceptable range.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467759
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  • 8
    Electronic Resource
    Electronic Resource
    Indirect liquid chromatographic determination of malathion based on copper(II) dimethyldithiophosphate complex formation (1996)
    Springer
    Chromatographia 42 (1996), S. 680-682 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Cu(II) dimethyldithiophosphate complex ; Malathion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A high-performance liquid chromatographic method has been developed for the quantitative determination of the organophosphorus pesticide malathion. The method is based on alkaline hydrolysis of malathion to dimthyldithiophosphate (DDTP) which is complexed with copper(II) and extracted in chlorofrom. The complex is injected onto a Hypersil ODS or Licrosorb sicolumn and eluted with acetonitrile:methanol:water (80∶10∶10 v:v:v) or chloroform. Detection is at 245 or 260 nm. A linear calibration curve was obtained for 24–240 μg ml−1 DDTP and a detection limit of 2.4–4.8 ng DDTP per injection. The method was applied to the analysis of malathion in commerical products after spraying on leaves. Extrction efficiency of malathion from leaves in acetone-water was also evlauted.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02267701
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  • 9
    Electronic Resource
    Electronic Resource
    LC-separation of derivatized DL-amino acids by aminopropylsilica-bonded Marfey's reagent and analog (1996)
    Springer
    Chromatographia 42 (1996), S. 683-689 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chiral stationary phase ; Enantionary phase ; Enantiomer separation ; Amino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Two chiral stationary phases (CSP-1 and CSP-2)) were synthesized by covalent bonding of aminopropylsilica (APS) to (a) 1-fluoro-2,4-dinitrophenyl-5-L-alanine amide (Marfey's reagent), followed by end-capping of underivatized amino groups of APS with trifluoroacetic anhydride (CSP-1), and (b) by reaction of APS with 1-fluoro-2,4-dinitrophenyl-5-L-phenylalaninetert. butyl ester, followed by cleavage of the tert. butyl ester by trifluoroacetic acid and end-capping of underivatized amino groups of APS withn-butyryl chloride (CSP-2). Both CSPs were found to be suitable for the chiral resolution of 2,4-dinitrophenyl and 3,5-dinitrobenzoyl-DL-amino acid esters by liquid chromatography using mixtures ofn-hexane andiso-propanol as eluents. Racemic 2,2,2-trifluoro-1-(9-anthryl)ethanol was also resolved on CSP-2.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02267702
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  • 10
    Electronic Resource
    Electronic Resource
    Gas and liquid chromatography and enzyme linked immuno sorbent assay in pesticide monitoring of surface water from the western mediterranean (Comunidad Valenciana, Spain) (1996)
    Springer
    Chromatographia 42 (1996), S. 151-158 
    Details
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Column liquid chromatography ; Pesticide residues ; Surface water analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A monitoring programme based on gas chromatography (NPD, ECD) using MSD for confirmatory purposes and coupled-column liquid chromatography was applied to the analysis of pesticide residues in surface water from a predominantly agricultural area of Spain (Comunidad Valenciana). Samples analysed by means of enzyme-linked immunosorbent assay gave similar results to those obtained by GC (MSD) for the determination of total triazines. The test employed had the advantages of a simple test procedure, short analysis time and high confirmatory value. Nevertheless, the multiresidue character, accuracy and unequivocal identification of individual pesticide residues of GC (MSD) make this technique the most appropriate for environmental monitoring programmes. In this monitoring programme about 200 samples were analysed between 1993–1994. 27 different pesticides were detected in 91 of these samples. The pesticides more frequently detected were dimethoate, methidathion, endosulfan A and B, endosulfan sulphate and pirimicarb. The highest concentrations found were 39.9 μg L−1 of dimethoate, 10.6 of pirimicarb and 10.6 of methidathion.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02269645
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