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  • Column liquid chromatography  (185)
  • Springer  (185)
  • National Academy of Sciences
  • Periodicals Archive Online (PAO)
  • 1995-1999  (82)
  • 1985-1989  (103)
  • 1980-1984
  • 1995  (82)
  • 1989  (103)
Collection
Keywords
Publisher
  • Springer  (185)
  • National Academy of Sciences
  • Periodicals Archive Online (PAO)
  • Wiley-Blackwell  (1)
Years
  • 1995-1999  (82)
  • 1985-1989  (103)
  • 1980-1984
Year
  • 1
    Electronic Resource
    Electronic Resource
    RPLC retention of 1,ω-di(alkoxy)-polysulphides (1989)
    Springer
    Chromatographia 27 (1989), S. 27-30 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; 1,ω-Di(alkoxy)-polysulphides ; Retention contributions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The reaction of S2Cl2 with alcohols yields products, the reversed-phase liquid chromatograms of which are similar to those of dialkyl-polysulphides RSnR, i.e., they represent homologous series. Four of the products were identified via GC-MS as 1,ω-di(alkoxy)-polysulphides having the general structure ROSnOR. Retention contributions of alkyl groups R and sulphur atoms in the −Sn — chain are not much different from values observed with polysulphides. The effect of oxygen, however, is only about −100 index units per O atom, while in dialkyl ethers values of −500 units have been reported.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02290400
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  • 2
    Electronic Resource
    Electronic Resource
    A practical description of retention in reversed phase chromatography using four parameters (1989)
    Springer
    Chromatographia 27 (1989), S. 5-14 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Retention behaviour ; Column parameters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Retention of small molecules on reversed phase or other hydrophobic stationary phases can be represented by k′ values of members of a homologous series at varying solvent compositions. The evaluation of simple linear relationships leads to the introduction of a set of four parameters that contain all the information about retention behaviour of this homologous series in the binary solvent system chosen. It is possible to extrapolate to a hypothetical non-hydrophobic molecule and a solvent, the polarity of which equals that of the stationary phase, to characterize the properties of the stationary phase — eluent system. In addition, a chromatographic method for determination of the phase ratio of the column is proposed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02290396
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  • 3
    Electronic Resource
    Electronic Resource
    Purification of human chorionic gonadotropin hormone by anion-exchange high-performance liquid chromatography (1989)
    Springer
    Chromatographia 27 (1989), S. 601-604 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Anion exchange separation ; Preparative separations ; Human chorionic gonadotropin hormone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A high-performance liquid chromatography (HPLC) method was developed for the purification of 50mg crude human chorionic gonadotropin (HCG) hormone sample in one chromatographic run on a 250×10 mm SERVA DEAE Poliol-Si-500 column. During the 60-minute linear gradient of 0.05 M sodium sulfate, 0.05 M sodium hydrogen sulfate and 0.05% (v/v) acetonitrile in buffer “B” complete separation was accomplished in 40 min. Identity and purity of the fractions were checked by SDS electrophoretic method. The eluted HCG fractions were dialyzed for 24 hours to remove the buffer salts and liophilized. The activity of the hormone did not decreased significantly during the purification procedure.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02258986
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  • 4
    Electronic Resource
    Electronic Resource
    Oxidation of acetophenone in a high temperature open-tubular capillary column liquid chromatographic system (1995)
    Springer
    Chromatographia 40 (1995), S. 99-101 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; High temperature open-tubular columns ; Solvent make-up ; Acetophenone oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Acetophnone, a substance stable at room temperature, is readily oxidizes in a high temperature open tubular liquid chromatographic system by the residual oxygen in the mobile phase. The oxidation product is less UV absorptive and detection sensitivity decreases greatly. To prevent the oxidation, through degassing of the mobile phase is necessary.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02274615
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  • 5
    Electronic Resource
    Electronic Resource
    The removal of endotoxins from protein solutions using column packings with aminated poly (γ-methyl L-glutamate) spheres (1995)
    Springer
    Chromatographia 40 (1995), S. 33-38 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Endotoxins ; Lipopolysaccharide ; Aminated poly(γ-methyl L-glutamate) ; Bovine serum albumin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method is described for the selective removal of endotoxins from various protein solutions using columns packed with aminated poly (γ-methyl L-glutamate) (PMLG-NH2) spheres. The PMLG-NH2 adsorbents showed a high adsorbing activity for endotoxins which had an ionic strength of μ=0.05–1.0 and pH 5.0–9.0. The endotoxin-adsorbing capacity per millitre of the wet adsorbent increased from 0.40 to 1.35 mg (E. coli O111: B4 LPS) at μ=0.2 and pH 7.0 while the aminogroup content of the adsorbent increased from 0.8 to 3.5 meq g−1. The PMLG-NH2-3.5 has an amino-group content of 3.5 meq g−1. This column packing selectively adsorbed endotoxins, without loss of the protein, from a γ-globulin or cytochromec solution which contained endotoxins at μ=0.05 and pH 7.0. On the other hand, when bovine serum albumin (BSA) was present in solution with endotoxins, both the endotoxins and the BSA were adsorbed by the column. The BSA-adsorbing activity increased with increasing amino-group content of the adsorbent. However, this undesirable adsorption was suppressed with increasing ionic strength of the buffer. As a result, when the packing which had an amino-group content of 1.5 meg g−1 was used in conditions of μ=0.2 and pH 7.0, the endotoxins were removed from a BSA-containing solution without affecting the recovery of the BSA.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02274604
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  • 6
    Electronic Resource
    Electronic Resource
    Analysis of lignin degradation products by capillary electrophoresis (1995)
    Springer
    Chromatographia 40 (1995), S. 51-57 
    Details
    ISSN: 1612-1112
    Keywords: Column electrophoresis ; Column liquid chromatography ; Phenolic lignin degradation compounds ; Sugar degradation products ; Quantitative analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method for the quantitative analysis of phenolic lignin degradation products by capillary electrophoresis (CE) with on-column UV detection has been developed. The liquid biomass solutions contain low molecular hemicellulosic sugars and phenolic lignin degradation products with various degrees of polymerization. Special attention has been paid to the monomeric phenolic components of lignin degradation fragments, e.g. derivatives of phenolic acids, aldehydes, and alcohols. Uncoated fused silica capillaries and borate-phosphate buffer systems at moderate pH conditions were used in order to separate the compounds of interest. To provide validation of the method, the same samples were analyzed independently by HPLC using gradient elution on a RP-C18 column. As sugar degradation fragment, furan-2-carboxylic acid was detected.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02274608
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  • 7
    Electronic Resource
    Electronic Resource
    Liquid chromatography of phenolic compounds in natural water using on-line trace enrichment (1995)
    Springer
    Chromatographia 40 (1995), S. 85-90 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Phenolic compounds ; Ion-pair solid phase extraction ; On-line trace enrichment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Two packing materials, C18 and PLRP-S, are studied for on-line trace enrichment of phenolic compounds in water. Various precolumns of different internal diameter are also tested and the addition of an ion-pair reagent to increase retention and thus, breakthrough volumes of phenolic compounds, is studied. Best results are obtained when a PLRP-S precolumn is coupled on-line with a C18 analytical column and DAD detector. Addition of TBA considerably increases breakthrough volumes. In contrast, when a C18 precolumn is used, breakthrough volumes are lower and it is impossible to determine TCP and PCP, under the experimental conditions used, because of interference of other nonpolar compounds in the samples. The performance of the system is evaluated with river and tap water and the preconcentration of 10 ml of sample in a PLRP-S precolumn involves a linear range between 1 μg 1−1 and 20 μl−1 and limits of determination between 0.5 μg l−1 and 1 μg l−1 are obtained.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02274612
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  • 8
    Electronic Resource
    Electronic Resource
    Screening of water samples for polar organic micropollutants using on-column sample enrichment (1995)
    Springer
    Chromatographia 40 (1995), S. 631-637 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Trace analysis ; Pesticides in tap water ; Aromatic sulphonates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Methodology and instrumentation are described which allow chromatographic screening of water samples under substantially simplified conditions and at reduced cost. A single column is used to accomplish sample extraction, trace enrichment, and separation. The performance of such a system is demonstrated, and the results compared with conventionally used concepts.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02315129
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  • 9
    Electronic Resource
    Electronic Resource
    Analysis of pyrithiones by reversed-phase high-performance liquid chromatography (1995)
    Springer
    Chromatographia 40 (1995), S. 669-673 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Transchelation ; Zinc pyrithione and related compounds ; Antidandruff formulations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An analytical procedure has been developed for the determination of zinc pyrithione in antidandruff formulations. Zinc pyrithione was converted into a stable copper complex and then analysed by reversed-phase HPLC. The proposed method allows the separation of the analyte from related pyrithiones and therefore is able to verify the compliance of cosmetic preparations with current legislation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02315135
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  • 10
    Electronic Resource
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    Marked differences between acetonitrile/water and methanol/water mobile phase systems on the thermodynamic behavior of benzodiazepines in reversed phase liquid chromatography (1995)
    Springer
    Chromatographia 41 (1995), S. 84-87 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Benzodiazepines ; Solvent effects ; ACN clusters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Two different methods were used to determine the separation factor α at different temperatures and the Gibbs-Helmholtz parameters (Δ(ΔH), Δ(ΔS)) of two adjacent benzodiazepines on a chromatogram were obtained from plots of lnα versus 1/T. We first studied each factor (fraction of water ϕ in the ACN/water mixture and column temperatureT), which controls the retention mechanism, and then we examined the simultaneous variation of all these factors. The changes in Δ(ΔH) and Δ(ΔS) in relation to a volume fraction of water ϕ in an ACN/water mixture were examined. In the ACN/water system, Δ(ΔH) was fairly constant in the acetonitrile region of ϕ≤0.52 and appears to be a roughly linear function of ϕ for ϕ≥0.52. In this system Δ(ΔS) is approximately a parabolic function of ϕ with an optimum at ϕ≅0.52. The retention mechanism of ten benzodiazepines was found to be significantly different in the methanol/water and ACN/water mixtures. The separation optimization of these ten benzodiazepines was then considered. A fraction of water of 0.43 in the ACN/water mixture and a column temperature of 44°C gave the most efficient separation conditions in the ACN/water mixture.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02274199
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  • 11
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    HPLC determination of urinary 2,4- and 2,6-toluendiamines as potential degradation products of polyurethane breast implants (1995)
    Springer
    Chromatographia 41 (1995), S. 661-664 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Polyurethane degradation products ; 2,4- and 2,6-toluendiamine ; Urine analysis ; Breast implants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A reversed-phase HPLC method has been developed for the urinary determination of mutagenic 2,4- and 2,6-toluendiamines. These amines are degradation products of polyurethane, a material used to cover textured silicone breast implants. FMOC-Cl was used as fluorescent derivatising agent in order to obtain a limit of detection of 15 ng/ml in urine. Pre-treatment of urine samples was by liquid/liquid extraction and urine specimens of patients after surgury were analysed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02267801
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  • 12
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    HPLC analysis of flavonoids and phenolic acids and aldehydes inEucalyptus spp. (1995)
    Springer
    Chromatographia 41 (1995), S. 657-660 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Polyphenols ; Flavonoids ; Phenolic acids and aldehydes ; Eucalyptus spp.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Standards of the polyphenols occurring in wood, bark and leaf extracts ofEucalyptus spp. (i.e. flavonoids and phenolic acids and aldehydes) have been analyzed by HPLC using reversed phase columns, gradient elution and diode-array detection. The conditions used are reported.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02267800
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  • 13
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    Polymer encapsulated stationary phases with improved efficiency (1995)
    Springer
    Chromatographia 40 (1995), S. 657-661 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed phases ; Polyencapsulated silica ; Polyacrylates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary By copolymerization of silica modified with vinyl groups and acrylic acid esters in suspension highly efficient, polymeric-encapsulated stationary-phases can be prepared. The suspending liquid has to be selected such that the monomers are at least partially adsorbed on the surface and the polymer formed does not precipitate. Under these conditions stationary phases capable of speedy mass transfer can be prepared, where the reduced plate heights are between 2 and 3. The silica surface shielding is optimized so that basic and acidic solutes elute with symmetrical peak.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02315133
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  • 14
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    Determination of D- and L-amino acid residues in peptides with fluorescent chiral tagging reagents by high-performance liquid chromatography (1995)
    Springer
    Chromatographia 40 (1995), S. 645-651 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chiral resolution of amino acids ; Pre-column derivatization ; Fluorescent chiral tagging reagents ; Stereochemical purity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Derivatization of amino acid enantiomers with fluorescent chiral Edman-type reagents, 4-(3-isothiocyanatopyrrolidin-1-yl)-7-nitro-2,1,3-benzoxadiazole [R(−)- and S(+)-NBD-PyNCS] and 4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole [R(−)-and S(+)-DBD-PyNCS], yields corresponding diastereomers separable by reversed-phase HPLC on normal achiral columns. The resolved diastereomers were detected fluorometrically at 530 nm with excitation at 490 nm for the NBD-PyNCS derivatives and at 560 nm with excitation at 450 nm for those derived from DBD-PyNCS reagents. This HPLC-derivatization method was used for evaluation of stereochemical purity for some synthetic commercial peptides. The enantioanalysis was reliable down to 0.05% racemization of the amino acid residues and a quantity of 100 μg peptide sample was usually enough for the analysis. Two acid hydrolysis methods, i.e. the standard procedure with constant-boiling hydrochloric acid (HCl) and a rapid vapor-phase procedure with HCl-trifluoroacetic acid (TFA) mixture, were compared. The later was found to be unsuitable owing to increased racemization of the amino acid residues during the hydrolysis. Judging from the results obtained for proline and leucine residues, most of the tested peptides including biologically active peptides, such as neurotensin, [d-Ala2,d-Leu5]-enkepharin and morphine tolerance peptide, possessed stereochemical purities higher than 98%. Influence of structural features of the peptides on the racemization of the amino acid residues was found to be significant.
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    URL: http://dx.doi.org/10.1007/BF02315131
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  • 15
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    HPLC-continuous-flow fast atom bombardment mass spectrometry (HPLC-CFFAB) — a convenient method for the analysis of bile acids in bile and serum (1995)
    Springer
    Chromatographia 40 (1995), S. 674-679 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Mass spectrometric detection ; Fast atom bombardment ionization ; Serum bile acid ; Rat bile
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In order to analyse bile acids in biological matrices, e.g. rat bile and human serum, high performance liquid chromatography (HPLC) was coupled to continuous-flow fast atom bombardment mass spectrometry (CFFAB-MS). A gradient elution system which had already proved to be well suited for the quantitative determination of conjugated bile acids in bile was modified to allow HPLC-CFFAB-MS-coupling. Due to the sensitivity of this coupling method it is possible to obtain more information about the biliary bile acid pattern and species-specific secondary bile acids. Furthermore, we were able to identify obviously unknown bile acid species in rat bile which most likely classify as mono-oxo and di-oxo-taurocholates (MW 513 Da, 511 Da) and mono-oxo-glycocholates (MW 463 Da). In the present study we show that using this system it is possible to determine both conjugated and unconjugated as well as sulfated bile acids, without time consuming group separation and derivatization, from rat bile and human serum. In addition, it is suggested that the method presented here should be considered for use in routine analysis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02315136
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  • 16
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    Fluorescence enhancement of dansylamino acids by bovine serum albumin as mobile phase additive in microcolumn liquid chromatography (1995)
    Springer
    Chromatographia 40 (1995), S. 159-162 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fluorescence enhancement ; Bovine serum albumin ; Dansylamino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The effects of acetonitrile and bovine serum albumin (BSA) concentrations on the signal intensity and retention behavior of dansylamino acids have been examined by using γ-cyclodextrin-bonded silica gel as the stationary phase in microcolumn liquid chromatography. Fluorescence intensities of dansylamino acids were enhanced by BSA as a mobile phase additive, e.g., detection limits of dansyl derivatives of L-Ala and L-Phe were improved by a factor of 12–18.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02272165
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  • 17
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    A statistical study of the correlation between k′ or log k′ and log Pow for a group of benzene and naphthalene derivatives in micellar liquid chromatography using a C-18 column (1995)
    Springer
    Chromatographia 40 (1995), S. 185-192 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Micellar liquid phases ; Octanol-water partition coefficient ; Benzene and naphthalene derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary It is shown that the logarithm of the capacity factor (log k′) for fifteen benzene and naphthalene derivatives in micellar liquid chromatography with forty nine different mobile phases generally correlates better with the logarithm of the octanol-water partition coefficient (log Pow) than the capacity factor (k′). Optimum conditions are established to obtain the best linear correlations of log k′-log Pow.
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    URL: http://dx.doi.org/10.1007/BF02272169
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  • 18
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    Improvement of selectivity of electrochemical detection for the determination of compounds with chloro aromatic rings (1995)
    Springer
    Chromatographia 40 (1995), S. 247-252 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Photolysis ; Electrochemical detection ; Drugs with chlorinated aromatic rings
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Pharmaceuticals containing a thiazide ring or chlorinated aromatic ring were investigated with respect to enhanced selectivity in determination. Oxidative electrochemical detection coupled with HPLC was used to study the influence of the pH of the mobile phase under conditions of photolysis. To cover a pH range 3.9–12, the employment of a polymer column stable in alkaline media was necessary. The method offers the great advantage of derivatization without chemicals at low operating potentials, thereby providing high selectivity.
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    URL: http://dx.doi.org/10.1007/BF02290353
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  • 19
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    Separation of structural isomers using cyclodextrin-polymers coated on silica beads (1995)
    Springer
    Chromatographia 40 (1995), S. 296-302 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Structural isomer separation ; Cyclodextrin ; Polymers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Several β-cyclodextrin (CD)-bonded stationary phases for high performance liquid chromatography (HPLC) were prepared, based on silica beads coated with a poly(alkylamine), [poly(ethyleneimine)(PEI)]. In order to obtain stationary phases with a high content of CD and maximum accessibility of the CD cavity, the functionalization was carried out after the coating, using the mono-tosyl derivative of CD as the intermediate. The ability of these supports to separate ortho, meta and para isomers of some disubstituted benzene derivatives was examined. The contribution of the amino groups of the polymer and of the CD cavity to the separation process is discussed. The resolution is mainly based on the difference in the stability of the complexes of the various isomers with CD. The influence of the amount of CD on the height of the theoretical plate is also studied.
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    URL: http://dx.doi.org/10.1007/BF02290360
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  • 20
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    A potential application for large diameter pellicular supports in the reversed phase study of ultra high molecular mass polystyrenes (1995)
    Springer
    Chromatographia 40 (1995), S. 307-312 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed phase ; Polystyrene ; Pellicular ; Ultra high molecular mass
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Ultra high molecular mass (〉 7 million dalton) polystyrenes are prone to degradation in size exclusion chromatography. In gradient elution reversed phase HPLC they do not elute visibly on small particle size porous supports. However, large diameter C18 pellicular particles were successfully employed for reversed phase study of ultra high molecular mass (15 million dalton) polystyrenes without polymer degradation during elution. Although retention for the lower molecular mass polystyrenes was lower than on small diameter porous particles, the medium high molecular mass polystyrenes (0.5–1 million dalton) showed similar retention. The addition of small diameter porous particles in small quantities, to the large diameter pellicular particles, increased the amount of retention of the low molecular mass polystyrenes without affecting the higher molecular mass polystyrenes.
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    URL: http://dx.doi.org/10.1007/BF02290362
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  • 21
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    High performance liquid chromatographic determination of methyl ethyl ketone in urine as its 3-methyl-2-benzothiazolinone hydrazone derivative (1995)
    Springer
    Chromatographia 40 (1995), S. 336-340 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Methyl ethyl ketone in urine ; Derivatization ; 3-Methyl-2-benzothiazolinone hydrazone ; Comparison with GC-MS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A HPLC method for the determination of methyl ethyl ketone (MEK) in urine after derivatization with 3-methyl-2-benzothiazolinone hydrazone is proposed. The calibration curve for the ketone was linear, ranging between 0.23–10 mg/L, with a detection limit of 0.025 mg/L. The results were compared to those obtained by GC-MS, coupled to the headspace technique. MEK derivatization and the derivative purification processes were verified with respect to the main variables such as reaction temperature, reagent concentration, probable interferences and enrichment phase. The method is simple and reliable and shows a good sensitivity.
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    URL: http://dx.doi.org/10.1007/BF02290366
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  • 22
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    Liquid chromatographic analysis of sulfornamides in foods (1995)
    Springer
    Chromatographia 40 (1995), S. 382-386 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Sulfonamides in foodstuffs ; Honey ; Milk ; Eggs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A procedure for the simultaneous determination of several sulfonamides in different foods, such as honey, milk and eggs is proposed. The analysis is carried out using reversed phase liquid chromatography with spectrophotometric detection. Optimization of the mobile phase led to good separation and a short analysis time when an initial isocratic step with a 3∶97 acetonitrile: water mixture was used for 5 minutes, followed by a linear gradient up to a 40∶60 mixture over 15 min. The proposed method is suitable for routine quality control analysis to ensure the absence of sulfonamides in foods. Recovery studies yielded good results for all food samples because there were no interferences from the matrices.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02269899
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  • 23
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    Determination of aflatoxins in peanut meal by LC/MS with a particle beam interface (1995)
    Springer
    Chromatographia 40 (1995), S. 411-416 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Particle beam LC/MS interface ; Capillary columns for LC ; Mycotoxins ; Peanut meal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new method for the analysis of aflatoxins in food extracts, based on liquid chromatography/mass spectrometry interfacing, is presented. The chromatographic separation was performed with a reversed phase packed capillary column coupled with a modified particle beam interface capable of handling microliter per minute flow rates. This system allows higher overall sensitivity and easier operation procedures. The method has proved to be particularly suitable for the analysis of the toxins in very complex matrices. The specificity of electron impact ionization allowed positive identification of the aflatoxins with an excellent response linearity for accurate quantitation.
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    URL: http://dx.doi.org/10.1007/BF02269904
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    Retention parameters of some isomeric 2-benzoylbenzoic acids in reversed-phase ion-pair high performance thin-layer and column chromatography (1995)
    Springer
    Chromatographia 40 (1995), S. 453-457 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin-layer chromatography ; Reversed phase ; 2-benzoylbenzoic acids ; Anionic and cationic counter ions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The 2-benzoylbenzoic acid series was investigated by reversed-phase, high-performance, thin-layer and column chromatography using various alkylammonium salts and di(2-ethylhexyl)orthophosphoric acid as polar associating reagents. The effects of the individual substituents on retention were quantified by Δlog k′ and ΔRM values. The compounds investigated differing in molecular structure (hydrophilic and hydrophobic substituents) commonly occurring groups in drugs and biologically active substances provide information on molecular interaction in these ion-pair systems. The combined effects on retention of organic modifier and ion-pair reagent concentration were investigated.
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    URL: http://dx.doi.org/10.1007/BF02269912
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    Determination of D- and L-amino acids in biological samples by two-dimensional column liquid chromatography (1995)
    Springer
    Chromatographia 41 (1995), S. 6-14 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Two-dimensional separation ; D- and L-amino acids ; Enantioseperation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A two-dimensional, column liquid chromatographic system is used for the determination of the D- and L-enantiomers of amino acids in biological samples. Separation of the amino acids is first on ion-exchange column by gradient elution with a sodium citratesodium chloride buffer. Enantioseparation is by subsequent injection of 3 μl heart-cuts of the individual amino acids onto a second column with a chiral crown ether stationary phase. Finally, fluorescence detection is after post-column labelling of the amino acids using ano-phthalaldehyde-2-mercaptoethanol reagent solution. The high separation power and selectivity of the system allow processing of complex samples with hardly any additional treatment and the determination of small quantities of D-amino acids in the presence of excess L-form. Applicability of the system is illustrated by the determination of D- and L-aspartate, serine, glutamate and alanine in various complex biological samples, such as protein hydrolysates, urine and biotechnological and food samples. Data are given on detectability, repeatability and linearity.
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    URL: http://dx.doi.org/10.1007/BF02274188
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    Simultaneous determination of preservatives, sweeteners and antioxidants in foods by paired-ion liquid chromatography (1995)
    Springer
    Chromatographia 41 (1995), S. 43-50 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion pair LC ; Sweeteners, preservatives and antioxidants ; Food additive analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A paired-ion, reversed-phase high-performance liquid chromatographic method was developed for the simultaneous determination of sweeteners (dulcin, saccharin-Na and acesulfame-K), preservatives (sodium dehydroacetate, sorbic acid, salicyclic acid, benzoic acid, succinic acid, methyl-para-hydroxybenzoic acid, ethylpara-hydroxybenzoic acid, n-propyl-para-hydroxybenzoic acid, isopropyl-para-hydroxybenzoic acid, n-butyl-para-hydroxybenzoic acid, and isobutyl-para-hydroxybenzoic acid), and antioxidants (3-tertiary-butyl-4-hydroxyanisole and tertiary-butyl-hydroquinone). A mobile phase of acetonitrile-50 mM aqueous α-hydroxy-isobutyric acid solution (pH 4.5) (2.2 ∶ 3.4 or 2.4 ∶ 3.6, v/v) containing 2.5 mM hexadecyltrimethylammonium bromide and a C18 column with a flow rate at 1.0 mL/min and detection at 233 nm were used. This method was found to be very reproducible with detection limits ranged from 0.15 to 3.00 μg. The retention factor (k) of each additive could be affected by concentrations of hexadecyltrimethylammonium bromide and α-hydroxyisobutyric acid, and pH and ratio of mobile phase. The presence of additives in some food samples was determined.
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    URL: http://dx.doi.org/10.1007/BF02274194
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    Prediction of precision from signal and noise measurement in liquid chromatography: Mathematical relationship between integration domain and precision (1995)
    Springer
    Chromatographia 41 (1995), S. 75-83 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Limit of detection ; Precision ; Uncertainty prediction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The precision of integration over noisy instrumental output for quantitative analysis is studied. A probability theory is developed to predict the relative standard deviation (RSD) of integration results over an integration domain from one-point integation (peak height measurement) to entire area integration in HPLC. Common integration modes of horizontal zero line and oblique zero line are taken into account, but no peak overlap is assumed. The question of the analytical superiority of peak height measurement or integration for quantitation is answered. In the HPLC apparatus used, the minimum RSD of measurements is found in the integration domain of ca. ±0.5 σ for analytes [peaks are approximated by the Gaussian signal of width, σ (standard deviation)]. The RSD of integration measurements is also shown to depend on the stochastic properties of back-ground noise (uncorrelated noise and correlated 1/f type noise). The theoretical conclusion is verified by Monte Carlo simulation and HPLC experiments for some aromatic compounds.
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    URL: http://dx.doi.org/10.1007/BF02274198
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    Ion-pair reversed-phase and low-molecular-weight aqueous gel permeation high-performance liquid chromatography methods for the determination of amoxicillin oligomersa (1995)
    Springer
    Chromatographia 41 (1995), S. 651-656 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion-pair and GPC separations ; Amoxicillin oligomers ; β-Lactam ring polymers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Polymeric substances formed from concentrated sodium amoxicillin in an aqueous solution have been separated using two high-performance liquid chromatographic methods. We used a C18 reversed-phase column with tetrabutylammonium chloride as an ion-pairing agent with an acetonitrile gradient and a TSKgel G2500PWxl column with water as the solvent for gel permeation chromatography. The separated materials, ranging in size from the monomer to the tetramer, have been characterized by functional-group chemical analysis, while the identification of the piperazine-2,5-dione was done using a pure standard. A greater number of peaks which were also better defined were obtained using the ion-pair reversed-phase method, and open and closed beta-lactam ring polymer forms could be distinguished. Using the gel permeation method, only a few monomer, piperazine-2,5-dione, dimer, trimer and combined amoxicillin trimer and tetramer peaks were obtained with water, although those obtained were quite well defined. The data on the time-course of formation of the oligomers and the amoxicillin degradation product were virtually identical by both methods.
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    URL: http://dx.doi.org/10.1007/BF02267799
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    Signal enhancement by on-column fluorimetric detection in gradient elution of dansyl amino acids in liquid chromatography (1995)
    Springer
    Chromatographia 41 (1995), S. 148-152 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; On-column fluorimetric detection ; Gradient elution ; Dansyl amino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Fluorimetric detection in the presence of a stationary phase has been applied to gradient elution of dansyl amino acids in liquid chromatography. A 1.5 mm ID quartz tube packed with the same materials as the separation column was employed for the flow cell. Conventional-size columns were employed. The peak height of analytes increased with increasing retention owing to focusing and environmental effects of the stationary phase, leading to improvements in sensitivity, which was pronounced for analytes eluting late. The lower the gradient, the larger the improvement in sensitivity achieved. Detection limits were improved by a factor of up to 5.1 by fluorimetric detection using the packed flow cell, compared with those achieved using a common empty flow cell.
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    URL: http://dx.doi.org/10.1007/BF02267946
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    A study of the behaviour of some new column materials in the chromatographic analysis of Cinchona alkaloids (1995)
    Springer
    Chromatographia 41 (1995), S. 153-160 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; LC-MS ; Cinchona alkaloids ; New column packing materials
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A major problem in the HPLC analysis of alkaloids is the poor peak shape and consequently low resolution, due to the interactions of the basic alkaloids with the residual acidic silanol groups of most reversed phase materials. The performance of new packing materials specially designed for the separation of basic compounds has been studied using mobile phases without the special additives commonly applied in the analysis of alkaloids. Strongly basic Cinchona alkaloids were used as test compounds. Retention characteristics and selectivities of each material were studied, after mobile phase optimisation for the column. The influence of the major factors (nature and content of the organic modifier, pH value, salt concentration) affecting resolution was studied. The mobile phases were chosen so that they could be used in thermospray LC-MS. The addition of salts to the mobile phase improves separation but in general the modification of the mobile phase gave little change in selectivity. The performance of silicabased C18 material proved superior to the polymer materials tested.
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    URL: http://dx.doi.org/10.1007/BF02267947
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    Energy calculations and computer modeling of chromatographic separations on microcrystalline cellulose triacetate (1989)
    Springer
    Chromatographia 27 (1989), S. 77-81 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Microcrystalline cellulose triacetate ; Molecular modeling ; Computer graphics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Molecular modeling and energy calculations have been used to study the chromatographic separation of aromatic compounds on microcrystalline cellubose triacetate. A linear relationship has been found between the logarithms of the capacity factors and the energy values of the interaction of these compounds with this stationary phase. The interaction energies have been calculated for two different spatial dispositions of the solutes in relation to the sorbent.
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    A chemically bonded liquid crystal as a stationary phase for high performance liquid chromatography. Synthesis on silica via an organochlorosilane pathway (1989)
    Springer
    Chromatographia 27 (1989), S. 559-564 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Liquid crystals ; Synthesis of new bonded phases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A compound which becomes a liquid crystal when bonded to a polysiloxane was reacted with dimethylchlorosilane to produce a reagent suitable for bonding to a silica surface. After the silanization reaction was complete, the product was characterized by elemental analysis, diffuse reflectance Fourier transform Infrared Spectroscopy (DRIFT), CP/MAS carbon-13 NMR and differential scanning calorimetry (DSC). Preliminary chromatographic testing was done by retention index measurements using the alkylarylketone homologous series and by measuring the separation factor, α, for anthracene/phenanthrene at two different mobile phase compositions.
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    Physico-chemical applications of HPLC (1989)
    Springer
    Chromatographia 27 (1989), S. 633-638 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Adsorption isotherms ; Equilibria criteria ; Silica and carbon adsorbents ; Aromatic compounds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Examples of high-performance liquid chromatography (HPLC) are given for the determination of adsorption equilibrium and distribution coefficients, calculation of excess adsorption isotherms from solutions ranging from 10−7 to 10−1 mole fraction, changes in activity coefficient of the component predominantly adsorbed from solution and substitution enthalpy. These examples stem from studies of HPLC and the static adsorption of benzene, anisole and benzaldehyde from solutions in n-heptane on macroporous silica and active carbon at various temperatures. A criterion is suggested for evaluating equilibrium in the HPLC process. The potential of size-exclusion chromatography (SEC) for evaluating the volume and predominant diameter of adsorbed pores as well as pore diffraction are discussed. Prospects for HPLC application to molecularstructural analysis and other purposes are discussed briefly.
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    The use of large polycyclic aromatic hydrocarbons to study retention in non-aqueous reversed-phase HPLC (1989)
    Springer
    Chromatographia 27 (1989), S. 118-122 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed-phase chromatography ; Non-aqueous reversed-phase chromatography ; Polycyclic aromatic hydrocarbons ; Solvent strength
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Elution strengths of 11 common HPLC solvents on a polymeric C18 phase were compared using a marker set of polycyclic aromatic hydrocarbons. Naphthalene, pyrene, benzo[ghi]perylene, and three larger naphthologues of 8, 10, and 12 rings (constituting a “naphthalene zigzag” series) were chosen because they span the solvent strength range up to and including the strongest solvents, tetrahydrofuran (THF) and chlorobenzene. Four pairs of similarly shaped isomers were used to probe solvent selectivity. With the exception of THF, HPLC solvent strength correlated with observed red shifts of fluorescence band maxima in each solvent. For THF, the pure solvent and blended mixtures behaved quite differently.
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    The case of the elusive tm values in HPLC (1989)
    Springer
    Chromatographia 27 (1989), S. 156-158 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Mobile phase retention time ; Capacity factor ; Negative capacity factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Numerous ideas and procedures have been suggested in the literature for the determination of tm, the retention time of a non-retained species, in high-performance liquid chromatography. In some cases chromatograms have been obtained showing sample components eluting prior to the assumed non-retained species. This phenomenon results in apparent negative capacity factors for the species in question. We have proposed a method employing small inorganic anions which results in a limiting value for tm and eliminates apparent negative capacity factors.
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    Equilibrium structures of the Arg-aldehyde moiety upon HPLC of peptides (1989)
    Springer
    Chromatographia 27 (1989), S. 228-232 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed-phase ; 13C n.m.r. ; Arginine-aldehyde peptides ; GYKI-14166
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary High-performance liquid chromatographic and13C n.m.r. spectrometry methods were used for the investigation of peptides containing arginine-aldehyde moiety. Investigation of a model compound, N-benzoyl-Arg-H, showed that in an acidic mobile phase peptides containing the arginine-aldehyde group elute in three characteristic peaks. The components of the peaks were found to be constituents of an equilibrium mixture. The structures of the two components were identified, one as the aldehyde hydrate, the other as the cyclanol derivative. The reactivity of TRIS (HCl) buffer at pH 8.5 with the arginine aldehyde moiety was used for the assignment of the equilibrium structures.
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    Ion-pair reversed phase HPLC determination of nucleotides, nucleosides and nucleobases — Application to nucleotide metabolism in hepatocytes (1989)
    Springer
    Chromatographia 27 (1989), S. 639-643 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed-phase ; Ion-pair ; Recoveries ; Hepatocytes ; Purine compounds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Three groups of metabolites were analyzed in extracts of rat hepatocytes by an HPLC method: (i) nucleotides (ATP, ADP, AMP, GTP, GDP, UTP, UDP, IMP, UMP), (ii) nucleosides and nucleobases (adenosine, adenine, guanosine, inosine, xanthine, hypoxanthine, uridine) and (iii) inhibitors of xanthine oxidoreductase (oxypurinol, allopurinol). Perchloric acid extracts were neutralized with K2CO3/triethanolamine and analyzed at 254 nm by reversed-phase ion-pair high-performance liquid chromatography. The nucleotides and their derivatives were separated with a gradient elution using 10 mM NH4H2PO4/2 mM t-butylammonium-phosphate and acetonitrile. Recovery values were estimated for the extraction procedure used. The method was applied to the investigation of nucleotide metabolism of hepatocytes of starved rats at anoxia and reoxygenation.
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    Preparation of silica-based cation-exchangers for use in ion chromatography (1989)
    Springer
    Chromatographia 27 (1989), S. 316-320 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion chromatography ; Silica-based cation-exchanger ; Trimethylsilyl chlorosulfonate ; Lanthanides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A low exchange-capacity, silica-based cation-exchanger for use in ion chromatography has been synthesized. (p-Trimethylsilyl)benzyl-dimethylchlorosilane (TBDCS) reacts with trimethylsilyl chlorosulfonate (TMCS) to produce a compound sulfonated in the para position of the type ArSO2OSi (CH3)3, which is bonded to 5 μm porous silica beads and hydrolysed to the corresponding arylsulfonic acid. The product is hydrophilic and has a high degree of sulfonation, efficiencies of packed columns reaching about 40,000–50,000 plates per meter for the separation of the Mn2+ ion. The new stationary phase has been applied to the ion chromatography of some organic and inorganic ions. It is notable that 14 lanthanides can be separated by isocratic elution about one hour on a 150×4·6 mm column, with 4 mM ethylenediamine and 6 mM α-hydroxyl-isobutanoic acid (pH 3.67) as mobile phase.
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    Enhanced chemiluminescence detection of some dansyl amino acids in liquid chromatography (1989)
    Springer
    Chromatographia 27 (1989), S. 191-193 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Dansyl amino acids ; Chemiluminescence ; Bis(2,4,6-Trichlorophenyl)oxalate, (TCPO) ; Enhancement of luminescence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The dansylated amino acids alanine, glutamic acid, methionine and norleucine were separated by reversedphase HPLC and detected via chemical excitation using the post-column, TCPO-peroxyoxalate reaction system. Enhancement of the chemiluminescence emission was achieved by including the surfactant Triton X-100 in the eluent.
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    Measurement of elastin hydrolysis by reverse-phase HPLC with on-line post-colum derivatization (1989)
    Springer
    Chromatographia 27 (1989), S. 225-227 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reverse-phase chromatography ; Elastin Hydrolysis measurement ; On-line post-column derivatization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Excessive breakdown of elastin, a structural protein, may be related to aortic disease and emphysema. Since L-valyl-L-proline occurs in high concentrations in elastin, a rapid and sensitive method using HPLC with post-column on-line derivatization was used to measure the dipeptide from swine aortic tissue, and the amount of elastin present was determined. Elastin was extracted by alkaline hydrolysis. After neutralization and filtration, the sample was injected onto a ODS-2 gel column, and the dipeptide was eluted by a linear gradient of 0 to 10% of 1-propanol in 50 mM heptafluorobutyrate, pH 3, at a flow rate of 1 ml/min. The eluent was reacted with fluorescamine at pH 8.6, and fluorescence was detected at an excitation wavelength of 395 nm and a 455 nm cutoff emission filter.
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    Separation and purification of porcine pancreatic enzymes by serial operation of ion-exchange and affinity columns (1989)
    Springer
    Chromatographia 27 (1989), S. 449-454 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion exchange and affinity columns in series ; Porcine pancreatic enzymes ; Trypsin and elastase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In order to separate and purify some of the enzymes contained in porcine pancreas, operation of an ion-exchange column in series with an affinity column has been used. The enzymes dealt with possess very similar molecular weights, isoelectric points and active sites. Hence they are difficult to separate and purify by traditional separation and/or purification methods. CM-Sepharose anion-exchange resin adsorbs elastase and trypsin at low pH (4.5) and desorbs them at high pH (9.0) and high ionic strength. Chitin-CHOM affinity adsorbent adsorbs trypsin at high pH (8.0) and desorbs it at low pH (2.5). By virtue of this complementary relationship two chromatographic columns were connected in series for facilitating the separation and purification of elastase and trypsin from porcine pancreas. The result showed that the specific activities of elastase and trypsin had been increased 16 and 22 fold respectively.
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    Anion exchange behaviour of hydrous titanium oxide and its use for column separations (1989)
    Springer
    Chromatographia 27 (1989), S. 472-474 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Hydrous titanium oxide ; Anion exchange ; Polyvalent anions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Hydrous titanium oxide (HTiO), prepared under varying conditions of precipitation, has been studied for its anion exchange behaviour. Its chemical and thermal stability has been examined. The stoichiometry of uptake for Cl− has been investigated using a36Cl radiotracer and the regeneration power of the exchanger checked. Distribution coefficients for halides and polyvalent anions have been determined and on the basis of sorption data some polyvalent anions have been separated using HTiO columns.
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    An improved HPLC determination of flavonoids in medicinal plant extracts (1989)
    Springer
    Chromatographia 27 (1989), S. 509-512 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Flavonoids ; Crataegus ; Passiflora ; Matricaria ; Ginkgo
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Flavonoids of Crataegus monogyna, Passiflora incarnata, Matricaria chamomilla and Ginkgo biloba extracts have been separated by isocratic elution on C18 columns using eluents based on C3 alcohols, tetrahydrofuran or dioxane. Satisfactory results have been obtained at compared to the low resolution achieved with the customary system acetonitrile-water-acetic acid.
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    Polymer coated stationary phases for liquid chromatography (1989)
    Springer
    Chromatographia 28 (1989), S. 19-23 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Preparation of stationary phases ; Polymer coated stationary phases ; Polymer-octyl bonded phase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Polymethyloctylsiloxane-coated stationary phases have been prepared for liquid chromatography, by thermal reaction. The influence of the reaction conditions on retention and efficiency of test substances with different structures has been discussed. The materials have good stability in both acidic and basic eluents.
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    Chromatography based on membrane separation with vesicular packing material (1989)
    Springer
    Chromatographia 28 (1989), S. 561-564 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Size exclusion ; Vesicular packing material ; Proteins and polymers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new vesicular packing material — prepared from plant cell clusters by purification of the intact cell wall framework —is suitable for chromatography, giving high performance at low pressure gradients. The separation is achieved by dialysis through the cell wall, which is an ultrafilter membrane with an extremely sharp size limit of separation. Almost the whole of the stationary liquid phase is located within the vesicle (empty cell) lumina. In contrast to gel filtration vesicle chromatography gives a practically ideal separation of two size groups with an extremely short fractionation range. The size limit of separation was investigated by chromatography of proteins and other polymers. Group separation of molecules of a polydisperse dextran standard preparation showed that the critical Stokes' diameter for dextran permeation into the stationary liquid phase of the vesicular packing is 5 to 6 nm.
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    Semi-preparative high-performance liquid chromatographic separation of four 1.1-dimethylethyl 4- and 5-bromo-trans-2-methylcyclohexane-1-carboxylate isomers (1989)
    Springer
    Chromatographia 28 (1989), S. 585-587 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Preparative scale separation ; 1,1-Dimethylethyl 4- and 5-bromo-trans-2-methylcyclohexane-1-carboxylate ; Trimedlure-related isomers ; Ceratitis capitata
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A semi-preparative high-performance liquid chromatographic procedure on 5-μm silica was developed for the isolation of gram quantities of four 1,1-dimethylethyl 4- and 5-bromo-trans-2-methylcyclohexane-1-carboxylate isomers (trimedlure-related) for NMR studies and comparative biological evaluation as male medfly,Ceratitis capitata, attractants.
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    URL: http://dx.doi.org/10.1007/BF02260682
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    Simultaneous determination of pseudouridine and creatinine in urine by HPLC with polarographic detection (1989)
    Springer
    Chromatographia 28 (1989), S. 605-609 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Electrochemical detection ; Pseudouridine ; Creatinine ; Urine analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The anodic behaviour of pseudouridine a modified nucleoside proposed as tumoral marker, has been studied at a mercury electrode. A method for its determination in urine samples by liquid chromatography with indirect anodic polarographic detection has been developed. The method is simple, highly selective and permits the direct injection of urine after dilution (1∶20) with mobile phase. Creatinine, which also gave an anodic response on mercury, could be simultaneously determined and used as an “internal standard” for Psi. This allowed the pseudouridine/creatinine ratio determination in a single run on the same specimen and the use of urine samples collected randomly instead of the 24h collection. The within-day RSD% for pseudouridine/ creatinine peak areas ratio was 3.4%.
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    URL: http://dx.doi.org/10.1007/BF02260686
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    Investigations into the chromatographic behaviour of silica gels produced from ester silicates (1989)
    Springer
    Chromatographia 28 (1989), S. 9-14 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ester silicate silica gels ; Behaviour with organic bases ; Silanol groups ; Acidic centres
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Silica gels produced from ester silicates (ES-gels) are excellent chromatographic supports. In comparison with other silica gels the RP-materials obtained from them show little peak tailing even with polar, and, in particular, with basic compounds. Gels produced by various manufacturing processes have been classified by adsorption with methyl pyridinium chloride. ES-gels yield very low methyl pyridinium chloride values and small asymmetry parameters. The results indicate that there are strongly acidic, structurally-related surface centres which cause peak tailing on most commercial gels. It was shown that surface silanols on silica gels do not, in themselves, lead to peak tailing.
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    URL: http://dx.doi.org/10.1007/BF02290374
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    Analysis of preservatives in cosmetics—Methylisothiazolones (1989)
    Springer
    Chromatographia 28 (1989), S. 34-38 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Methylisothiazolones ; Preservatives ; Analysis of cosmetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Antimicrobially active formulations based on 2-methyl-3(2H)-isothiazolone and 5-chloro-2-methyl-3(2H)-isothiazolone (Kathon CG, Euxyl K 100) are incorporated into manufactured cosmetics as preservatives. In this paper we report on the analysis of these active components by means of liquid chromatography. It is conventional for the original methylisothiazolone components in cosmetics to be analyzed by reversed phase high-performance liquid chromatography after column chromatographic separation and flash chromatographic purification. In our new analytical method the methylisothiazolones are converted into the respective β-thiosubstituted acrylamide derivatives, which are ionic substances, with the help of the nucleophilic reagent hydrogensulfite. An ion pair high-performance liquid chromatographic method has been developed for the separation and quantification of these derivatives.
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    URL: http://dx.doi.org/10.1007/BF02290380
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    Nucleotide and aldehyde analysis by HPLC for determination of radical induced damage (1989)
    Springer
    Chromatographia 28 (1989), S. 65-68 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Oxygen radicals ; Nucleotides ; Aldehydes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The analysis of two metabolite groups, nucleotides and aldehydes, is necessary for assessment of oxygen radical metabolism during hypoxia and reoxygenation. Nucleotides and their derivatives were determined by HPLC using gradient elution with 10 mM NH4H2PO4 buffer containing 2 mM t-butylammoniumphosphate and acetonitrile. Aldehydes occuring after lipid peroxidation were analyzed by derivatisation to dinitrophenylhydrazones followed by TLC and HPLC separation with methanol/water on an ODS column.
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    URL: http://dx.doi.org/10.1007/BF02290385
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    High-performance-liquid chromatographic separation of 1,3,5-trizine herbicides (1989)
    Springer
    Chromatographia 28 (1989), S. 209-211 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Triazine herbicides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A number of 11 triazine herbicides and 7 of their corresponding metabolites were separated in a single HPLC run. The separation was achieved on a reversed-phase column using gradient elution with acetonitrile/buffer. Detection was by UV absorption at a wave-length of 220 nm.
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    URL: http://dx.doi.org/10.1007/BF02319649
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    Trace enrichment and HPLC analysis of polycyclic aromatic hydrocarbons in environmental samples, using solid phase extraction in connection with UV/VIS diode-array and fluorescence detection (1989)
    Springer
    Chromatographia 28 (1989), S. 203-208 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Solid phase extraction ; Polycyclic aromatic hydrocarbons ; Diode array and fluorescence detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Both the separation of polycyclic aromatic hydrocarbons (PAH's) on tailor made HPLC phases, and their chromatographic enrichment and quantitative determination are of great interest. Because of the generally low concentrations of PAH's in the environment, and the low limiting values in German legislation for drinking water, methods for selective enrichment and sensitive detection are indispensable. On account of their relatively high amounts in soil, the determination of PAH's is valuable for the assessment of the potential danger to ground water by waste materials. These requirements can be fulfilled by used of solid phase extraction on enrichment columns, and fluorescence or UV/VIS diode array detection. For the detection of PAH's in the picogram range, the wavelengths for excitation and emission were time programmed over the chromatogram. With this feature, it is possible to detect all the individual compounds at the highest sensitivity, over the entire analysis.
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    URL: http://dx.doi.org/10.1007/BF02319648
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    A simple highly reproducible gradient system for micro column HPLC (1989)
    Springer
    Chromatographia 28 (1989), S. 289-292 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Micro-bore and capillary columns ; Gradient techniques
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A gradient delivery system for microbore and open tubular liquid chromatography is described. A gradient mixing vessel of 5–100μl, or 25–1000μl allows the generation of binary gradients with high reproducibility. The suitability of the system for short packed micro bore columns and open tubular columns is demonstrated.
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    URL: http://dx.doi.org/10.1007/BF02260777
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    A high-performance liquid chromatographic method for determination of flecainide in human plasma using fluorescence detection (1989)
    Springer
    Chromatographia 28 (1989), S. 303-306 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Flecainide in plasma ; Fluorescence detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A high performance liquid chromatographic method for the determination of flecainide in serum has been developed. The analysis is performed on a microparticulate silica column. The eluate is monitored by fluorescence detection at an excitation wavelength of 300nm and an emission wavelength of 370nm. No sources of interference were identified and a coefficient of variation of less than 8% was observed on repeated flecainide determinations. The method has a good reproducibility, specificity and accuracy, and can be applied in therapeutic drug monitoring of flecainide in patients.
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    URL: http://dx.doi.org/10.1007/BF02260780
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    Assay for methylnaltrexone in rat brain regions and serum by high-performance liquid chromatography with coulometric electrochemical detection (1989)
    Springer
    Chromatographia 28 (1989), S. 359-363 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Coulometric electrochemical detection ; Methylnaltrexone ; Rat brain and serum analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A simple and sensitive method is described for the determination of methylaltrexone, a quaternary narcotic antagonist, in discrete rat brain regions and serum. Separation and quantitation are performed by reversedphase high-performance liquid chromatography with coulometric electrochemical detection. Perchloric acid extracts of the brain tissue or serum were passed through a normal-phase solid-phase extraction CN column, and methylnaltreexone was subsequently eluted with a mixture of absolute ethanol and 25mM trifluoroacetic acid. Methylnaltrexone gave a linear response over the range of 12.5–100ng in 1.0ml for cerebellar homogenates and 25–200ng in 50μl for serum. The average betweenassay coefficients of variation for methylnaltrexone from 1.0ml of cerebellar homogenate and 50μl of serum were 5.2 and 3.6%, respectively, over the concentration range studied. The within-assay coefficients of variation at 12.5ng/ml cerebellar homogenate and 25ng/50μl for serum were 7.4 and 4.6%, respectively. Analytical recovery of methylanyltrexone, added to cerebellar homogenate and serum samples, were 85 and 89%, respectively. The method was applied to the analysis of methylnaltrexone in discrete rat brain regions and serum after intraperitoneal injection.
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    URL: http://dx.doi.org/10.1007/BF02261014
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    Preparative scale reversed-phase HPLC method for simultaneous separation of carotenoids and carotenoid esters (1989)
    Springer
    Chromatographia 28 (1989), S. 129-132 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Carotenoids ; Paprika, Rose hips, Marigold
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method is described for the preparative HPLC of carotenoids and carotenoid esters using a self-packing axially-compressed column. The reversed-phase system used employs an RP-18 stationary phase and a mobile phase consisting of a mixture of petroleum spirit, acetonitrile, methanol and tetrahydrofuran. The method is demonstrated for paprika fruit, rose hips and marigold flowers.
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    URL: http://dx.doi.org/10.1007/BF02319633
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    The effect of an organic eluent modifier and pH on the separation of wheat-storage proteins: Application to the purification of γ-gliadins ofTriticum monococcum L (1989)
    Springer
    Chromatographia 28 (1989), S. 133-138 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Wheat proteins ; γ-gliadins ; Effect of pH on separation ; Effect of organic modifier on separation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Reversed-phase, high-pressure liquid chromatography has been used to separate similar protein (γ-gliadin) components from 70% ethanol extracts of endosperm flour from two different accessions of the diploid wheatTriticum monococcum L. The effect of acetonitrile as the organic eluent was compared to acetonitrile: 2-propanol (3:1) at two different pH's. Conditions for maximum resolution of the γ-gliadin components were found to be at pH 7.2 with acetonitrile: 2-propanol (3:1) as the eluent. These conditions allowed the components to be obtained in sufficient purity for further charaterization.
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    URL: http://dx.doi.org/10.1007/BF02319634
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    Direct preparative resolution of racemic amino-acids using ligand exchange chromatography (chirallec) (1989)
    Springer
    Chromatographia 28 (1989), S. 337-340 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ligand-exchange ; Preparative racemate resolution ; Amino-acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Preparative resolutions of racemic amino-acids by ligand-exchange chromatography are described. Base-line resolution of multigram quantities of many racemic solutes was obtained using very simple equipment (open tubular column).
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    URL: http://dx.doi.org/10.1007/BF02261011
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    Physico-chemical modelling of solute retention in reversed-phase HPLC with temary mobile phases (1989)
    Springer
    Chromatographia 28 (1989), S. 354-358 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ternary mobile phases ; Solute retention model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In our previous publications we have established a new physico-chemically grounded retention model valid for the adsorption and partition mechanism of retention using multicomponent mobile phases. Moreover, we have demonstrated its practical usefulness for predicting solute retention in several different chromatographic modes (i.e. in TLC, normal-phase and reversed-phase HPLC) employing binary mobile phases. In this paper we give an ultimate check to the physicochemical correctness of our new retention model, using it for the description of solute retention in reversedphase HPLC systems with ternary mobile phases of the B+AB1+AB2 type. The complexity of these mobile phases and of the possible intermolecular interactions among the consitituent solvents was supposed to rigidly scrutinize the premises of the assumed new approach. We have observed a good agreement between the experimental retention parameter for a number of solutes chromatographed with the use of two different mobile phases of the B+AB1+AB2 type, and the retention parameter calculated according to the assumed model. Therefore, we believe to have sufficiently tested our new approach and confirmed its physico-chemical correctness.
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    URL: http://dx.doi.org/10.1007/BF02261013
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    Optical resolution HPLC column packings carrying penicillin sulfoxide nucleus. Part IV. Effect of substituents in the benzyl ester group on the optical resolution efficiency (1989)
    Springer
    Chromatographia 28 (1989), S. 513-515 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Optical resolution ; Polymeric adsorbents ; Penicillin sulfoxide ; Substituent effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Fourteen new vinyl polymers carrying penicillin sulfoxide nucleus, poly (substituted-benzyl 1-oxo-6-metha-crylaminopenicillanate)s, were synthesized in order to investigate the influence of the substituents on the optical resolution capabilities. The resolution efficiency of the high-performance liquid chromatography columns comprising the obtained polymers were examined usingtrans-stilbene oxide and N-acetyl-1-phenethyl-amine. It was found that some columns resolved both racemates, some one, while the others did not separate either. A polymer which has 2,6-dichlorobenzyl moiety was found to resolve both racemates more effectively than the unsubstituted polymer.
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    URL: http://dx.doi.org/10.1007/BF02261073
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    HPLC determination of the phenolic metabolites of phenoxy alkanoic acid herbicides (1989)
    Springer
    Chromatographia 28 (1989), S. 465-468 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chlorinated phenols ; 4-Aminoantipyrine derivatives of phenols ; Metabolites of phenoxy alkanoic acid herbicides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary High performance liquid chromatography (HPLC) has been applied to the separation and determination of o-chlorophenol, 2,4-dichlorophenol, 3,4-dichlorophenol, 2,5-dichlorophenol, and 2,4,5-trichlorophenol in water samples after prior derivatization with 4-aminoantipyrine. These substances are the phenolic decomposition products of the phenoxy-alkanoic acid herbicides: 2,4-dichlorophenoxyacetic acid (2,4-D), 2,4-dichlorophenoxybutyric acid (2,4-DB), and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). An RP-C18 column was used, with gradient elution starting at 50/50 and changing to 70/30 methanol/water (v/v) after 24 min. Detection was carried out at 470 nm where the 4-aminoantipyrilquinonimine derivatives show maximum absorbance. The method was linear over a concentration range of 5–10,000 ppb phenol in the original water sample. By using an enrichment step a detection limit of 2 ppb phenol could be approached. The method was used to study the degree of degradation of the phenoxy acids to phenols under different conditions of temperature, pH, and UV irradiation.
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    Optical resolution of 2-hydroxy acids by high-performance ligand exchange chromatography (1989)
    Springer
    Chromatographia 28 (1989), S. 481-486 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ligand exchange ; Chiral phase ; Optical resolution of 2-hydroxy acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Using an MCl GEL CRS10W column, which was packed with octadecyl silica (ODS) coated with N,N-dioctyl-L-alanine, optical resolution of 2-hydroxy acids was performed. The optical resolution of mandelic acid derivatives and C2 to C5 2-hydroxy acids was carried without any pretreatment. The MCl GEL CRS10W column could resolve amino acids and 2-hydroxy acids. For their selective detection, a post-column method was employed in which the specific color reaction of 2-hydroxy acids with iron(III) ion was utilized. For the analysis of foodstuffs, in which amino acids and 2-hydroxy acids often coexist, the present method was found to be effective in distinguishing between these enantiomers.
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    Isolation and quantitative analysis of hydroxylysine glycosides (1989)
    Springer
    Chromatographia 28 (1989), S. 497-501 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Collagen metabolites ; Amino acid derivatives ; Glycosides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Methods are described for the isolation of galactosyl hydroxylysine and glucosylgalactosyl hydroxylysine from collagen and for the quantitative analysis of these hydroxylysine glycosides. The isolation procedure, based upon gel filtration and preparative ionpaired reversed-phase high-performance liquid chromatography, is simple and rapid in comparison with existing methods, allowing the production of tens of milligrams of each glycoside in a single day. Quantitative analysis of the hydroxylysine glycosides is effected by reversed-phase high-performance liquid chromatography with precolumn derivatization (usingo-phthal-dialdehyde) and fluorescence detection.
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    Optical resolution HPLC column packings carrying penicillin sulfoxide nucleus. Part III. Radical copolymers and their optical resolution efficiency (1989)
    Springer
    Chromatographia 28 (1989), S. 511-512 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Optical resolution ; Polymeric adsorbents ; Penicillin sulfoxide ; Copolymerization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A methacrylamide carrying penicillin sulfoxide skeleton, benzyl 1-oxo-6-methacrylaminopenicillanate, was copolymerized with methyl methacrylate. The optical resolution efficiency of the columns comprising the obtained copolymers was investigated using a high-performance liquid chromatography system. A copolymer incorporated by 27mol% of methyl methacrylate showed higher chirality recognition capability than the homopolymer, which suggests that the introduction of methyl methacrylate contributes to enriching desired penicillin sulfoxide alignment (i. e., tracticity) along the polymer main chain. An estimated penicillin monomer's number-average sequence length in the copolymer was 2.7.
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    Separation of metal acetylacetonates by reversed-phase high-performance liquid chromatography (1989)
    Springer
    Chromatographia 28 (1989), S. 519-522 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed-phase chromatography ; Separation of metal acetylacetonates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Using reversed-phase high-performance liquid chromatography acetylacetonate complexes with trivalent metals such as Al(III), Co(III), Cr(III) and Fe(III) have been examined in columns containing RP-2, RP-8 and RP-18 bonded phases. The mobile phase consisted of acetonitrile/water or methanol/water mixtures with various compositions. As shown the order of elution of the acetylacetonates depends on the type of the column packing and on the nature and concentration of the organic modifier in the mobile phase.
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    Determination of vitamin A in pharmaceutical preparations by high-performance liquid chromatography with diode-array detection (1995)
    Springer
    Chromatographia 40 (1995), S. 143-146 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Diode-array detection ; Retinol acetate ; Pharmaceutical preparations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A very simple high-performance liquid chromatographic method for determination of Vitamin A in pharmaceutical preparations without the need for saponification was developed. A reversed-phase (Nova-Pack C18, 4 μm) column was used with a mobile phase of acetonitrile-tetrahydrofuran-water (55∶37∶8) and a flowrate of 1.5 ml/min. Sample treatment only consisted of the extraction of retinol acetate content from capsules or tablets with methanol. Total extraction was achieved by shaking vigorously with the aid of magnetic stirring for three hours at room temperature. No change of solvent is necessary to introduce the sample in the chromatographic system. This method is suitable for routine quantification of Vitamin A.
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    URL: http://dx.doi.org/10.1007/BF02272162
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    Thermodynamic behavior of mixed benzodiazepines by a new liquid chromatographic method (1995)
    Springer
    Chromatographia 40 (1995), S. 193-196 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chemometric methodology ; Elution order ; Simplex optimization ; Benzodiazepines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Using a rapid chemometric methodology to determine the separation factor, α, at different temperatures, Gibbs Helmholtz parameters (Δ (ΔH), Δ (ΔS), Δ (ΔG)) of two adjacent benodiazepines on a chromatogram were obtained from ln α versus T−1 plots. A temperature dependent reversal of the elution order was studied and the mobile phase composition and column temperature were optimized to obtain the best separation. A flow rate of 0.80 ml min−1 with 52.6% methanol in the methanol-water mixture and a column temperature of 48°C gave the most efficient separation of ten benzodiazepines.
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    Mixed-mode liquid chromatography of aliphatic anionic surfactants with a naphthalenetrisulfonate mobile phase (1995)
    Springer
    Chromatographia 40 (1995), S. 237-246 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Mixed mode stationary phases ; Indirect photometric and fluorometric detection ; Conductimetric detection ; Alkyl-sulphates, and sulphonat-phosphates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Separation of three classes of anionic surfactants (alkyl sulfates, alkanesulfonates, and alkyl phosphates) are achieved on a mixed-mode reversed phase (RP) phenyl/-anion exchange column using a naphthalenetrisulfonate (NTS)-acetonitrile (ACN) mobile phase via indirect photometric, indirect fluorometric, direct or indirect conductivity detection. Mixtures of C5−C18 sulfates, C6−C18 sulfonates, and C1−C4 phosphates (mono- and di-ester) can be separated in less than 20, 24, and 20 min respectively. Although hydrophobic effects are more pronounced in mixed-mode chromatography, equivalent-per-equivalent exchange of analysis and eluent ion is still required for sensitive indirect photometric, fluorometric, or conductivity detection. The detection limits of alkyl sulfates and alkanesulfonates are in the range of 3–15 pmoles which are at least an order of magnitude better than suppressed conductivity detection. The determination of surfactants in a variety of real samples is also presented.
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    Enantiomeric separation of D/L-carnitine using HPLC and CZE after derivatization (1995)
    Springer
    Chromatographia 40 (1995), S. 287-295 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Capillary zone electrophoresis ; Enantioseparation ; Carnitine ; Derivatization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Carnitine is an essential component in tissues of animals, higher plants and many microorganisms. Whereas the L-carnitine enantiomer plays an important role in the metabolism of long chain fatty acids, D-carnitine has a considerable toxic influence on biochemical processes. The analytical separation of D-and L-carnitine depends upon derivatization with UV-or fluorescently active substances, e.g. FMOC and (+)/(−)-FLEC. The separation of diastereomeric (+)- and (−)-FLEC carnitine esters was performed successfully with capillary zone electrophoresis (CZE) and HPLC, after optimization of the derivatization process and of the composition and pH of the buffer, using UV- and fluorescence detection. With HPLC separation a detection limit of the carnitine esters of 5 μmol/l when using fluorescence detection was achieved. With both separation systems baseline resolution and short analysis times could be obtained. The enantiomeric FMOC derivatives could be separated using the electrophoretic system and acidic buffers with high concentrations of an osmotic flow modifier together with γ-cyclodextrine as chiral selector. The applicability of the optimized separation conditions are demonstrated in the analysis of agar culture medium inoculated withPseudomonas putida and of pharmaceutical formulations. In all samples very low amounts of D- or L-carnitine could be determined in the presence of the other enantiomeric form. Problems caused by the impurity of the carnitine standards or the derivatization agent (+)/(−)-FLEC are discussed.
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    URL: http://dx.doi.org/10.1007/BF02290359
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    Retention of fullerenes by octadecyl silica. Correlation with NMR spectra at low temperatures (1995)
    Springer
    Chromatographia 40 (1995), S. 507-512 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fullerenes ; Retention vs NMR spectra ; C18 phases ; Low temperature separations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The temperature effect on the retention of fullerenes in the range 80°C to −70°C in liquid chromatography (LC) has been examined using octadecylsilica stationary phases (ODS). It has been found that the maximum retention temperature lies around −10°C with a highly carbon loaded ODS phase. Solid state CPMAS NMR measurements on the stationary phases indicated that the relaxation time at the 30 ppm methylene signal changes with the temperature and has a minimum relaxation time at the temperature which closely matches the maximum retention temperature observed in chromatography. The interpretation of both NMR spectroscopic and LC chromatographic data are discussed.
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    URL: http://dx.doi.org/10.1007/BF02290260
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    Derivatisation of DL-amino acids by urethane — Protected α-amino acidN-carboxyanhydrides for separation by LC (1995)
    Springer
    Chromatographia 40 (1995), S. 601-606 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Amino acid analysis ; Chirality ; Diastereoisomers ; Dipeptides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Using a robotic autosampler, free DL-amino acids were derivatized with highly reactive, urethane-protected, L-α-amino acidN-carboxyanhydrides (NACs) with structures: Boc-Phe-NCA, Boc-Asn(Trt)-NCA, Fmoc-Lys(Boc)-NCA, Fmoc-Met-NCA, Fmoc-Ala-NCA, Z-Ala-NCA, Z-Val-NCA and Z-Leu-NCA (Boc=tert-butyloxycarbonyl, Trt=trityl, Fmoc=9-(fluor-enylmethyl)oxycarbonyl, Z=benzyloxycarbonyl). Using sodium borate buffer and acetonitrile solvent, derivatization was complete in 3.5 min at room temperature. By selection of an appropriate reagent, the resulting diastereomeric,N-protected dipeptides were separated on an octylsilica stationary phase using mixtures of sodium acetate buffer and acetonitrile as eluents.
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    URL: http://dx.doi.org/10.1007/BF02290275
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    High-performance liquid chromatography of dihydroxyacetone as its bis-2,4-dinitrophenylhydrazone derivative (1995)
    Springer
    Chromatographia 41 (1995), S. 61-65 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Dihydroxyacetone ; 2,4-dinitrophenylhydrazine ; Tanning creams
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A rapid and simple HPLC method for the identification and determination of dihydroxyacetone, a tanning agent widely used in a variety of preparations, is presented. The method consists of the analysis of the formulated products after a derivatization reaction which enhances the response and the detection limit of the chromatographic analysis. The characterization and the elucidation of the spacial geometry of the synthesized derivative are described.
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    URL: http://dx.doi.org/10.1007/BF02274196
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    High performance liquid chromatographic analysis of Patent Blue V in cheese (1995)
    Springer
    Chromatographia 41 (1995), S. 431-434 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin-layer chromatography ; Patent Blue V in cheese
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The HPLC method developed for the analysis of the dye Patent Blue V in extracts from cheese is sufficiently sensitive to detect and measure concentrations above 0.1 ppm with a standard deviation of 3%. The extraction procedure described gives a recovery from cheese of about 80%. The method has been applied to commercial samples of cheese and a concentration of the dye of about 0.12 ppm was measured in one case.
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    URL: http://dx.doi.org/10.1007/BF02318618
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    Modelling and prediction of retention in high-performance liquid chromatography by using neural networks (1995)
    Springer
    Chromatographia 41 (1995), S. 435-444 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Micellar liquid chromatography ; Neural networks ; Retention modelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Multi-layer feed-forward neural networks trained with an error back-propagation algorithm have been used to model retention behaviour of liquid chromatography as a function of the composition of the mobile phases. Conventional hydro-organic and micellar mobile phases were considered. Accurate retention modelling and prediction have been achieved using mobile phases defined by two, three and four parameters. With micellar mobile phases, the parameters involved included the concentrations of surfactant and organic modifier, pH and temperature. It is shown that neural networks provide a competitive tool to model varied inherent nonlinear relationships of retention behaviour with respect to the mobile phase parameters. The soft models defined by the weights of the networks are capable of accommodating all types of linear and nonlinear relationships, neural networks being specially useful when the relationships between retention behaviour and the mobile phase parameters are unknown. However, to train neural networks more experimental points than with hard-modelling methods are required, hence the use of the networks is recommended only for those cases where adequate theoretical or empirical models do not exist.
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    URL: http://dx.doi.org/10.1007/BF02318619
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    Simultaneous assay of four stereoisomers of diltiazem hydrochloride. Application to in vitro chiral inversion studies (1995)
    Springer
    Chromatographia 41 (1995), S. 450-454 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Diltiazem hydrochloride stereoisomers ; Chiralcel OF ; Chiral inversion ; Epimerization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The simultaneous stereospecific assay of four stereoisomers of diltiazem hydrochloride in bulk drug and aqueous solution was developed using HPLC on a Chiralcel OF column. The four isomers were quantitated with good precision by the internal standard method. The chiral inversion of (+)-cis-diltiazem hydrochloride in vitro, stability of its (2S, 3S) configuration in the solid and aqueous states was examined by HPLC. Chiral inversion of (+)-cis-diltiazem hydrochloride was not observed in the solid state, and its (2S, 3S) configuration was stable to heat, humidity and light. Chiral inversion of (+)-cis-diltiazem hydrochloride (2S, 3S) was observed in aqueous solution under UV, but not in aqueous solution stored at 80°C for 5h nor under visible light for 10 h. The (+)-cis-diltiazem hydrochloride (2S, 3S) epimerized to (+)-trans-diltiazem hydrochloride (2R, 3S) with a half-life of 5h in aqueous solution under UV but the reverse chiral inversion of (+)-trans-diltiazem hydrochloride (2R, 3S) to (+)-cis-diltiazem hydrochloride (2S, 3S) was not observed.
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    URL: http://dx.doi.org/10.1007/BF02318621
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    Detoxification of acetonitrile-water wastes from liquid chromatography (1995)
    Springer
    Chromatographia 41 (1995), S. 488-491 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Acetonitrile disposal ; Acetonitrile hydrolysis ; Degradation kinetics ; Waste solvent management
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Acetonitrile is one of the most frequently used solvents in column liquid chromatography. Because of its toxicity, safe disposal of the waste solvent is essential. Combustion in a hazardous waste plant, if available, is recommended. Otherwise the waste can be degraded in the laboratory to acetic acid and ammonia by treatment with sodium hydroxide. The addition of hydrogen peroxide is not necessary. The waste needs to be diluted to 10% acetonitrile in water in order to prevent the formation of a two-phase system on addition of concentrated sodium hydroxide. This reagent must be added in excess; 2.5 mols of sodium hydroxide per mol of acetonitrile are recommended. It was found that the kinetics are of second order, with an activation energy of 89 kJ mol−1 and a frequency factor of 9×109. Therefore even at room temperature degradation is possible, although a hydrolysis time of approximately 15 days is needed under these conditions. At 80°C, where refluxing is not necessary, hydrolysis is complete after, e.g., 2 h, depending on the amount of sodium hydroxide added.
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    URL: http://dx.doi.org/10.1007/BF02318626
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    Retention behaviour of metal complexes with 5-sulphoquinoline-8-ol in reversed-phase ion-pair liquid chromatography (1995)
    Springer
    Chromatographia 41 (1995), S. 532-538 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion-pair LC ; 5-Sulphoquinoline-8-ol ; Metal complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The reversed-phase ion-pair liquid chromatographic behaviour of several metal complexes with 5-sulphoquinoline-8-ol (HQS) on an octadecyl-modified silica column was investigated by using a fluorescence detector. The aluminum complex gave two peaks on the chromatograms when eluents containing phosphate buffer were used. The effects of the pH of the eluent, HQS concentration, the nature of anions in the eluent, and the column temperature on the retention behaviour of the aluminum complex are discussed on the basis of the equilibria and the kinetics of the complexation of the aluminum ion with HQS and anions in the eluent. The equilibrium constant for the interconversion reaction between the two Al(III)-HQS species which correspond to the two peaks observed and the second stepwise formation constant for the Zn(II)-HQS complex were evaluated from the HPLC data obtained.
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    URL: http://dx.doi.org/10.1007/BF02269716
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    Liquid chromatographic determination of aniline and derivatives in environmental waters at nanogram per litre levels using fluorescamine pre-column derivatization (1995)
    Springer
    Chromatographia 41 (1995), S. 568-572 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fluorescamine derivatives ; Aniline and aniline derivatives ; Environmental waters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Fluorescamine (fluram) has been used as a fluorogenic compound for pre-column derivatization of aniline and some derivatives. Anilines were derivatized with fluram in citrate buffer media (pH 5.5) to form pyrrolinones. The highly fluorescence pyrrolinones were isolated and pre-concentrated by solid phase extraction. A reversed phase, Spherisorb RP-8 column and tetrahydrofuran: water:formic acid (42∶56∶2) mobile phase was used for separation. Detection method was by a sensitive fluorimetric method and quantitation was at 395 and 495 nm. The various parameters such as reaction conditions between anilines and fluram, solid phase extraction and chromatographic separation were optimized. Calibrations were linear over the range considered with excellent correlation coefficients (r〉0.999). Relative standard deviations are less than 2.5% and detection limits for aniline,p-toluidine, 4-chloroaniline and 4-bromoaniline were 6, 30, 6 and 8 ng L−1, respectively. This method has been used successfully for the determination of anilines in environmental waters.
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    URL: http://dx.doi.org/10.1007/BF02269721
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    Separation of saponins and determination of quinovic acid 3-O-α-L-rhamnopyranoside fromNauclea diderrichii (de Wild) Merr. Bark by high performance liquid chromatography (1995)
    Springer
    Chromatographia 41 (1995), S. 581-584 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Nauclea diderrichii (de Wild) Merr ; Saponins ; Alkaloid glycoside ; Chrysanthelline A
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A reversed-phase HPLC determination of 11 saponins and an alkaloid glycoside inNauclea diderrichii bark is described. Quantitative analysis of quinovic acid 3-O-α-L-rhamnopyranoside which is one of the main saponins was determined, using Chrysanthelline A as internal standard. The complete separation was achieved in 47 minutes. The method of quantification was validated.
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    URL: http://dx.doi.org/10.1007/BF02269723
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    Quantitative determination of toxic mono- and non-ortho polychlorinated biphenyls in cod liver oil after selective liquid chromatographic separation (1995)
    Springer
    Chromatographia 41 (1995), S. 585-593 
    Details
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Column liquid chromatography ; Polychlorinated biphenyls ; Cod liver oil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary By application of a chromatographic column filled with Supelclean ENVI-Carb/Celite and elution with three solvents of different polarity three PCB fractions were obtained. Fraction A contained poly-ortho PCBs, Fraction B mono-ortho PCBs, and Fraction C non-ortho PCBs. The Supelclean ENVI-Carb/Celite column was used in combination with a sample preparation procedure for pre-cleaning of acid-stable chlorinated hydrocarbons such as DDT and its metabolites, HCH isomers, and regulation-relevant PCB congeners. The method was optimized using standard solutions of 55 PCB congeners, 8 chlorinated pesticides and contaminated cod liver oil samples. The influence of traces of remaining matrix on the elution profile of the organochlorine compounds on Supelclean ENVI-Carb/Celite was observed. Quantitation was carried out by GC-ECD with fused silica capillary columns of different polarity.
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    URL: http://dx.doi.org/10.1007/BF02269724
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    Chromatographic analysis of penstemide and serrulatoloside by high-performance liquid chromatography and gradient thin-layer chromatography (1989)
    Springer
    Chromatographia 27 (1989), S. 24-26 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin-layer chromatography ; Penstemide and serrulatoloside
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Penstemide and serrulatoloside, two iridoids of similar molecular structure, were separated by stepwise gradient TLC in a straight-phase systems (silica-ethyl acetate+isopropanol) and by HPLC in a reversed-phase system (ODS-silica — water+methanol).
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    Preparative medium pressure liquid chromatographic (MPLC) and semipreparative HPLC separation of furocoumarin isomers (1989)
    Springer
    Chromatographia 27 (1989), S. 591-595 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Overpressured layer chromatography ; Furocoumarin isomers ; Preparative separation of plant extracts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Preparative medium pressure liquid chromatography and semi-preparative high performance liquid chromatography on silica were employed for the isolation of eight furocoumarin isomers (iso-bergapten, angelicin, psoralen, bergapten, pimpinellin, sphondin, xanthotoxin and isopimpinellin). The conditions were transposed from analytical on-line overpressured layer chromatography and analytical high performance liquid chromatography, respectively. The retention data of the analytical on-line overpressured layer chromatographic separation and the preparative medium pressure liquid chromatographic isolation show a linear relationship. Using 15 μm TLC silica 60 as stationary phase a dry-packing procedure aas developed for labomatic medium pressure liquid chromatographic glass columns. The efficiency of the preparative separation techniques was demonstrated by the isolation of the investigated furocoumarins from Heraclei mantegazziani radix and from Pimpinellae radix (Balkan quality).
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    Separation of bromo- and iodosubstituted thyronines by high-performance liquid chromatography (1989)
    Springer
    Chromatographia 27 (1989), S. 101-104 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Bromo/iodosubstituted thyronines ; Mobile phase optimization ; Radioimmunoassay detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A reversed-phase high performance liquid chromatographic method on C-18 bonded silica is described for the separation of trisubstituted iodo/bromothyronines, which exert thyroid hormone activity. The composition of the mobile phase has been systematically optimized resulting in a ternary mixture of methanol/acetonitrile/water acidified with trifluoroacetic acid. The applicability of ultraviolet absorption detection, amperometric detection and off-line radioimmunoassay was investigated. The latter method allows detection of the different iodo/bromothyronines down to 40–120 ng/l mobile phase; this sensitivity is high enough for application to thyroid hydrolysates in order to clarify the question as to whether bromine can substitute iodine in the biosynthesis of thyroid hormones.
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    Retention of 1,ω-bis-(dialkylamino)-polysulphides and related compounds in reversed-phase HPLC (1989)
    Springer
    Chromatographia 27 (1989), S. 113-117 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Retention contribution of nitrogen ; Effect on methylene and sulphur chains
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The reaction of secondary amines R2NH with disulfur dichloride S2Cl2 in dichloro methane yields mixtures of bis-dialkylamino polysulphides R2N−Sn−NR2 with sulphur chain lengths varying from ns=2 to 14. The S chains are believed to be non-branched. The compounds form homologous series in each of which sulphur atoms give a constant contribution to retention. The sulphur retention index depends slightly on the carbon number in the terminal alkyl groups R. The presence of nitrogen lowers retention. The index increment of N is ca. −160 units, which is distinctly less negative than values found in alkylamines.
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    LC-MS of enzymatic peptic haemoglobin hydrolysate produced at the pilot-plant level (1989)
    Springer
    Chromatographia 27 (1989), S. 128-134 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Size-exclusion chromatography ; Fast atom bombardment-MS ; Peptic haemoglobin hydrolysate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method is described for the ready identification of any peptide isolated from a complex peptic haemoglobin hydrolysate produced on the pilot-plant scale. A combination of size exclusion and reversed-phase, high-performance liquid chromatography have proved to be a useful strategy for fractionation of such a mixture. This technique enabled pure peptides from the total hydrolysate to be obtained. Amino acid analysis and fast atom bombardment mass spectrometry provided the accurate composition and molecular weight of any isolated peptide. Molecular weights are compared with those deduced from size-exclusion chromatography (SEC) and the usefulness of SEC is discussed. The procedure described in this study will be useful for acquiring a better knowledge of such an hydrolysate and could be extended to other crude protein digests.
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    HPLC determination of catabolic amines in silage using their dansyl derivatives and an electrochemical detector (1989)
    Springer
    Chromatographia 27 (1989), S. 216-220 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Electrochemical detector ; Amines ; Silages ; Feedstuffs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The use of the electrochemical detector (EC) in the high performance liquid chromatography (HPLC) of dansyl derivatives of biogenic amines is reported. Isocratic and gradient elution patterns of synthetic mixtures of putrescine, cadaverine, 1,6-diaminohexane, tryptamine, histamine, tyramine, spermine and spermidine on a reversed phase column are shown. Hydrodynamic voltammograms of standard compounds are presented. The detection limits of the EC are compared with those of ultraviolet and spectrofluorimetric detectors. A chromatographic profile of amines from the proteolytic catabolism of maize silage byClostridia is shown.
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    Retention behaviour of selected flavonoid compounds in NP-HPLC (1989)
    Springer
    Chromatographia 27 (1989), S. 625-627 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Normal phase elution ; Silica and cyano columns ; Flavonoid compounds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary HPLC retention data for a number of flavonoid compounds have been evaluated on normal phase silica and cyano colums according to the Soczewinski-Snyder (S.-S.) model. On the silica phase most of the flavones examined exhibited asymetrical peak shapes indicating strong and mixed retention mechanisms; on the cyano phase the intercept of the S.-S. relationship was independent of any hydroxy substitution pattern or of molecular planarity. A similar behaviour, but with different intercept values, was observed with coumarin and quinone compounds.
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    Rapid reversed-phase chromatographic separation and determination of selenum and tellurium (1989)
    Springer
    Chromatographia 27 (1989), S. 292-296 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Selenium(IV)-tellurium(IV) separation ; Flow-through coulometric detector
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The chromatographic behaviour of selenium and tellurium has been investigated with two different reversed-phase chromatographic methods, using P-350 (methyl-bi-isooctyl phosphate) and TBP (tributyl phosphate) as the stationary phases. HCl, HBr, NaCl and NaBr were employed as mobile phase components in both methods. The results suggested that the separation mechanism corresponds to the formation of TeCl (or TeBr) and P-350H (or TBPH) ion associate. A coulometric flow-through detector was applied to determine Se(IV) and Te(IV). Complete separation and quantitative determination of Se and Te could be achieved in 10 minutes.
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    Preparative HPLC of carotenoids (1989)
    Springer
    Chromatographia 27 (1989), S. 325-327 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Carotenoid ; Xanthophyll ; Broccoli ; Paprika
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method is described for the preparative HPLC of up to 50mg of carotenoid using a self-packing axially-compressed column. Oxygenated carotenoids, xanthophylls, are separated with silica as the stationary phase and acetone/petroleum ether as the mobile phase, while carotenes are separated using magnesium oxide/polyamide as the stationary phase and undiluted petroleum ether as the mobile phase.
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    Applications of HPLC with evaporative light scattering detection in fat and carbohydrate chemistry (1989)
    Springer
    Chromatographia 27 (1989), S. 340-342 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Evaporative light scattering detection ; α, ω-Dicarboxylic and hydroxycarboxylic acids ; Alkylglucosides and glycerides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The advantages of an evaporative light scattering detector in HPLC are demonstrated using the separation of α, ω-dicarboxylic and hydroxycarboxylic acids, alkyl glucosides and mono-, di- and triglycerides as examples. By using this detector reversed phase as well as normal phase gradient HPLC becomes possible for substances with no UV absorption.
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    Selectivity of alkyl-bonded phases in reversed-phase liquid chromatography of hydrophobic compounds (1989)
    Springer
    Chromatographia 27 (1989), S. 371-377 
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    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Alkyl-bonded silica gel ; Enthalpy ; Van der Waals volume
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Starting from silica gel with a purity of 99.999%, octadecyl-(ODS), octyl-(C8) and propyl-(C3) bonded silica gels were synthesized, and end-capped by trimethyl groups. The pore size was 150 Å and the specific surface area was 320 m2/g. The ODS and C8 silica gels were stable in both acidic and basic solutions. The selectivity of these bonded-silica gels was examined from the difference of the retention behavior of alkanes (Al−Al), alkylbenzenes (Ph−Al), alkylalcohols (Al−OH) and polyaromatic hydrocarbons (PAH) in aqueous acetonitrile. On these packings the log k′ values decreased in the order Al−Al〉Ph−Al〉PAH〉Al−OH. Furthermore, the chromatographic behavior of these compounds was measured on polymer-coated octadecyl-bonded silica gel (CAP) and octadecyl-bonded vinyl alcohol copolymer gel (ODP). The selectivity was verified from the value of R* of these compounds: $$R = R_v + R^* $$ where R is the retention time, and Rv is the retention time of an alkane having the same Van der Waals volume as the analyte. The R* values indicated that this ODS had more selectivity than C8 and C3, however R* on C8 showed a very good correlation with R* on C3. Their retention behavior on CAP was similar to that of ODS, however, their capacity ratios measured on CAP were smaller than those on ODS. The ODP has selectivity for the retention of aromatic compounds, because PAHs were retained strongly on this column.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02321286
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  • 92
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    Determination ofAlternaria mycotoxins in foodstuffs by gradient elution liquid chromatography with electrochemical detection (1989)
    Springer
    Chromatographia 27 (1989), S. 425-430 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Alternaria mycotoxins ; Food analysis ; Electrochemical detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The electroactivity of majorAlternaria mycotoxins has been explored in order to devise a liquid chromatographic-electrochemical detection (LC-EC) method for the determination of these toxic metabolites in fungal cultures and in naturally contaminated foodstuffs. Alternariol, alternariol methyl ether, altertoxin-I and altertoxin-II have been found to be electroactive and could be detected at sub-nanogram levels. Advantages and limitations of dual electrode (screen mode) coulometric detection and single electrode amperometric detection are presented and discussed. The feasibility of electrochemical detection in gradient elution liquid chromatography as well as its applicability to the analysis of contaminated foodstuffs is demonstrated.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02319558
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  • 93
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    Automatic measurement of some common herbicides by LC using simultaneous UV detection and electrochemical detection in series (1989)
    Springer
    Chromatographia 27 (1989), S. 431-435 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; UV diode array detection ; Electro chemical detection ; Herbicides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An automated procedure is described for simultaneous UV detection at three different wavelengths and electro chemical detection in series of some residual herbicides. UV spectra of nine compounds of different compound groups are presented. Liquid-liquid extraction with dichloromethane and an enrichment of about one thousandfold has been used. Recovery rates after enrichment and detection limits of four s-triazine, three phenyl urea herbicides, metazachlore and metamitrone in river and drinking water are shown. It is concluded that the herbicides examined can be detected at levels between 10ng l−1 and 50ngl−1, without the necessity of derivatisation or clean-up processes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02319559
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  • 94
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    Size exclusion chromatography on porous fractals (1989)
    Springer
    Chromatographia 27 (1989), S. 257-263 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Size exclusion ; Fractal dimension ; Retention model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Some porous packings used in chromatography have been claimed to be fractals with a scale of sizes a〈l〈L, where a is a molecular size and L is the size of the largest pores. For a fractal porous packing, the excluded volume for molecules in solution in the vicinity of the packing surface is directly related to Df, the fractal dimension of the pore surface (2〈Df〈3). Since retention in size exclusion chromatography is itself directly related to this excluded volume, the fractal nature of the packing provides a model of retention in this technique. According to this model there is a linear relationship between log Rs and log(1-Kd), where Rs is the hydrodynamic radius of the solute macromolecules and Kd the distribution coefficient. The fractal dimension is derived from the slope of this plot. Size exclusion chromatographic retention data have been analyzed according to the model. It is found that some HPLC packings are fractals with fractal dimensions ranging from about 2.15 to 2.6, depending on the material. Such a large range of Df values indicates large variations in the selectivities and domains of applications of the different packings. For some classical gel filtration chromatographic gels, the fractal retention model does not seem to apply.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02260458
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  • 95
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    Simultaneous flow rate and temperature programming based on computer-assisted retention prediction for the separation of PTH-amino acids in reversed-phase microcolumn liquid chromatography (1989)
    Springer
    Chromatographia 27 (1989), S. 417-424 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Micro-columns ; Flow rate and temperature programming ; PTH amino acid derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The separation of phenylthiohydantoin (PTH) amino acid derivatives by flow rate and temperature programming in reversed-phase micro-column liquid chromatography (LC) has been investigated. For both programming modes a microcomputer-assisted retention prediction system (REPRES) was constructed. The performance of this system has been evaluated by comparing actually measured retention data to those predicted. Excellent agreements between those data were found. It is clearly indicated that simultaneous flow rate and temperature programming can improve the separation of PTH-amino acids in reduced analysis time.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02319557
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  • 96
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    HPLC and electrophoresis — Competitors or partners (1989)
    Springer
    Chromatographia 28 (1989), S. 89-91 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Electrophoresis ; Comparison of HPLC and electrophoresis ; Proteins, peptides and amino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Protein structure analysis is an indispensible tool in modern biological research. However, the isolation of a protein or the separation of peptides in a form suitable for sequence analysis is a considerable technical challenge. The two predominant separation methods in protein biochemistry are chromatography and electrophoresis. In this paper the position, advantaged and disadvantages of both HPLC and electrophoresis for the separation of amino acids, peptides and proteins in protein structure analysis are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02290389
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  • 97
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    Evaluation of synthetic procedures for the chemical modification of alumina for HPLC (1989)
    Springer
    Chromatographia 28 (1989), S. 565-568 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; New bonded phases ; Alumina ; Protein separation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Several reactions are tested for the chemical modification of alumina. These include the following: chlorination of the surface hydroxyls followed by reaction with an organolithium compound; chlorination of the surface hydroxyls followed by reaction with a Grignard reagent; chlorination of the surface hydroxyls followed by reaction with an amine; chlorination of the surface hydroxyls followed by reaction with an alcohol; direct reaction of the alumina with an organochloroalane and direct reaction of the alumina with an alcohol. Only the first reaction gave a product which contained enough bonded organic material to be easily detected by FTIR. Preliminary stability tests show that the product of the first reaction retains the bonded organic material when exposed to nonpolar and polar organic solvents as well as aqueous solutions of pH 1.0, 7.0 and 12.0. Chromatographic testing establishes reversed-phase behavior for alkylarylketones as solutes and the bonded phase displays good biocompatibility for a series of protein standards.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02260678
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  • 98
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    Separation of adenosine triphosphate and its degradation products in innervated muscle of the frog by reverse phase high-performance liquid chromatography (1989)
    Springer
    Chromatographia 28 (1989), S. 610-612 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Adenosine phosphates ; Adenosine phosphate degradation products ; Innervated frog muscle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Adenosine mono-, di- and triphosphates, inosine monophosphates, adenosine, inosine and hypoxanthine were separated in a single run by high-performance liquid chromatography with UV detection. AC-18 reversephase column was used. An isocratic elution with 100mM phosphate buffer (KH2PO4) pH6.5 and 1.2% methanol, followed by a 5 minute linear gradient up to 15% methanol after the 10th minute was performed during each run with a flow rate of 1.25ml/min. The time required for each analysis was 25 minutes. The detection limit for each substance ranged from 3 to 5 pmol. All the substances under study were detected in the incubation medium when adenosine triphosphate was exogenously applied to the innervated frog sartorius muscle.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02260687
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  • 99
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    Molecular interactions in liquid adsorption chromatography with mixed mobile phase. Solvation of the chromatographed substance in a ternary mobile phase (1989)
    Springer
    Chromatographia 28 (1989), S. 151-156 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Molecular interactions ; Association effects ; Analyte solvation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The linear Jaroniec equation has been utilized for the description of chromatographic systems in which the test substance molecule is solvated by the solvent molecules. A possibility of the formation of multimolecular solvates in the bulk phase has been confirmed. The measurements were made using liquid adsorption chromatography with ternary mobile phase.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02319638
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  • 100
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    Immobilized enzymes as chromatographic phases for HPLC: The chromatography of free and derivatized amino acids on immobilized trypsin (1989)
    Springer
    Chromatographia 28 (1989), S. 551-555 
    Details
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chiral separations ; Trypsin on silica ; Amino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new HPLC stationary phase was synthesized by the covalent immobilization of the enzyme trypsin (TRYP) on silica. The hydrolytic activity of the immobilized enzyme was 72% of the activity of an equivalent molar amount of free TRYP. The initial chromatographic studies indicate that this phase can be used for chiral separations of enantiomeric O- and N,O-derivatized amino acids which are natural substrates on TRYP and that the stereochemical resolutions are a result of the activity of the enzyme.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02260675
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