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  • Column liquid chromatography  (174)
  • Springer  (174)
  • American Meteorological Society
  • Periodicals Archive Online (PAO)
  • 1995-1999
  • 1990-1994  (174)
  • 1935-1939
  • 1992  (86)
  • 1991  (88)
Collection
Publisher
  • Springer  (174)
  • American Meteorological Society
  • Periodicals Archive Online (PAO)
  • Wiley-Blackwell  (1)
Years
  • 1995-1999
  • 1990-1994  (174)
  • 1935-1939
Year
  • 1
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Normal phase separations ; Cyanopropyldimethyl silica ; Chloro-added polycyclic aromatic hydrocarbons ; Environmental samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Retention characteristics in normal phase HPLC of highly biologically active chloro-added polycyclic aromatic hydrocarbons (PAHs) were studied. Silica, cyanopropyldimethylsilyl- and aminopropylsilyl- modified stationary phases were investigated. Retention properties of chloroadded PAHs on these phases were shown to be strongly influenced by the number of chloro-additions. This is due to the strong polarity of the methylene carbon at the chloro-addition site. Active silica had a strongly degrading effect on the unstable chloro-added PAHs during separation. Aminopropylsilica did not exhibit sufficient selectivity towards chloro-added PAHs when compared to chlorosubstituted PAHs. Cyanopropyldimethylsilica was shown to be applicable to a group separation of chloro-added and chloro-substituted PAHs. A fast clean-up procedure for chloro-added PAHs in complex samplesis outlined. It involves an initial elimination of more polar substances on a short open column with strongly deactivated silica and a subsequent separation on a cyanopropyldimethylsilyl HPLC column in normal phase mode.
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  • 2
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    Chromatographia 32 (1991), S. 345-349 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Column packings ; Pore size distribution ; Diffusion and adsorption ; Band broadening
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The complex intraparticle structure typical of chromatographic column packings has been analyzed by use of an equivalent network model which emphasizes pore size distribution and connectivity. Special attention is given as to the way in which diffusion and adsorption interact and display modified peak spreading characteristics according to the morphology of the pore space. This study reveals a very significant increase in the column band broadening over that expected from physical adsorption which can arise from particular distributions of pore sizes. This has implications for designing packings which take advantage of the separating power due to adsorption but do not compromise the resolution of the chromatographic system.
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  • 3
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fatty acids and bile acids ; Fluorogenic precolumn derivatization ; 2-Bromoacetyl-6-methoxynaphthalene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The use of 2-bromoacetyl-6-methoxynaphthalene as a fluorogenic labelling reagent in pre-column derivatization for the HPLC separation of biologically active carboxylic acids (fatty acids and bile acids) has been investigated. The compound reacts (30 min. at 70°C) with carboxylic acids to give fluorescent esters that can be separated by reversedphase HPLC and detected at λ ex. 300 nm, λ em. 460 nm. The experimental conditions for the derivatization and chromatographic separation are discussed. Applications to the determination of valproic acid and chenodeoxycholic acid in pharmaceutical formulations are described.
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  • 4
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Valproic acid ; Simultaneous determination of anticonvulsants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The derivatizing procedure of Moody et al. [20] for valproic acid has been simplified and applied to the simultaneous HPLC determination of valproic acid (VPA), barbital (B), primidone (PRM), phenobarbital (PB) and carbamazepine (CBZ) in serum or plasma of epileptic patients. The sample is deproteinized with acetonitrile containing esterification agents and an aliquot of the supernatant is heated to 70°C for 15 min with 4-bromophenacyl bromide. The reaction mixture is analysed on a C18 column at ambient temperature, with gradient elution and with detection at 205 nm. The time required for the chromatographic analysis is 13 min; identification is based on retention time and quantification is by peak area determination with an internal standard. The calibration curves show good linearity in the range 6.25 to 100 mg/L. The detection limits at a signal: noise ratio ≥3, ranged from 1 mg/L for B and CBZ to 2–3 mg/L for PRM, PB and VPA. The method described for the simultaneous determination of the five drugs in the same plasma pool, correlated well with isocratic HPLC methods specific for each drug. The simultaneous procedure described allows a reproducible (CVs≤6.5% within run) and rapid (25 min for sample preparation: 13 min for chromatographic run) therapeutic monitoring of patients treated with VPA and two or more antiepileptic drugs.
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  • 5
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Porous polymer spherical packings ; Vinyl ether ; Alkali resistance ; No abnormal adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Spherical, porous-polymer particles for column packing in high-performance liquid chromatography were prepared by suspension copolymerization of alkylvinyl ether with triethyleneglycol divinyl ether. The hydrophobicity of the packings was easily adjusted by changing the monomer ratio. The packings showed the usual reversed-phase liquid chromatographic properties, but did not sho abnormal retention, tailing and broadening of peaks and irreversible adsorption of ionic and aromatic substances, owing to the lack of ionic or aromatic groups. In addition, the packings were stable in alkaline solutions because of the relative alkali stability of C−O−C bonds as compared with CO−O and Si−O−C bonds in conventional packings.
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  • 6
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Anion exchange ; Indirect photometric and direct conductivity detection ; Naphthalenesulfonate ; Inorganic anions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Indirect photometric and unsuppressed direct conductivity detection modes are examined using naphthalene mono-, di-, and tri-sulfonate as mobile phases for the separation of several anions such as F−, Cl−, NO2 −, Br−, NO3 −, SO4=,I−, and SCN− using a commercial anion exchange column. With all three mobile phases, conductivity detection shows better sensitivities and detection limits than indirect photometry. Conductivity detection is 5 to 16 times more sensitive than indirect photometry for all analytes. Detection limits achieved using these mobile phases are, for example, 0.04 ng and 0.1 ng for chloride ion with conductivity and indirect photometry, respectively. Both detection modes give wide linear ranges extending from at least 100 ppm to the detection limit of each anion which is generally about 0.02 ppm. Sulfur oxide anions such as dithionate and tetrathionate are separated using flow programming with naphthalenetrisulfonate as the mobile phase in less than 20 minutes. With both detection modes, desired chromatographic performance of these three eluents is achieved without pH adjustment of the mobile phase.
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  • 7
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Heat-treated milk ; Milk quality indicators ; 5-Hydroxymethyl-2-furfuraldehyde
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An enhanced method of HPLC for the determination of 5-Hydroxymethyl-2-furfuraldehyde (HMF) in fluid milk was perfected. Its resolving capacity permitted the specific separation of this compound. The real concentration (μmol/l) of HMF was determined and not the HMF value, as in the colorimetric analysis, where an intermediary coloured compound (HMF-TBA) is utilised. The optimum pH condition (pH=4.0–4.2) for the mobile phase to prevent overlapping between the HMF peak and the peaks of the other compound (α and β) that coeluted with the HMF and also the optimum organic solvent content (3% or 7%) were established. This is a sensitive, quick and safe method for the determination of HMF in fluid milk.
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  • 8
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Arsenic compounds ; Polymeric styrene divinylbenzene phase ; Ion-pairing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The resolving power of an ion-pair reversed-phase liquid chromatography method, on a polymeric stationary phase (PRP-1) with an alkaline aqueous mobile phase (pH=9) containing tetrabutylammonium cation as ion-pairing agent, is compared with a traditional ion-pairing system using an octadecyl-modified silica column and a neutral aqueous mobile phase (pH=7.3). This chromatographic system (PRP-1 column) provides a rapid means for the determination of two of the most important arsenic species, arsenobetaine and arsenite. Addition of methanol (5%) to the aqueous mobile phase allows the differentation of arsenobetaine from the system peak when using UV detection.
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  • 9
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Gravity-flow column chromatography ; Provitamin A determination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The provitamin A content of some food samples was determined by methods involving MgO: Hyflosupercel gravityflow column chromatography (GFCC) and reversed phase high performance liquid chromatography (HPLC), the quantitation being done by external standardization (HPLC-ES) or internal standardization (HPLC-IS) with Sudan. The results obtained with α- and β-carotene in carrots, β-carotene and β-cryptoxanthin in papaya and β-carotene in tomato and kale agreed well, showing that any of the these techniques can be used, provided the analysis is done under optimum conditions. Good separation of the different provitamins using GFCC depends on the analyst's skill and visual acuity. HPLC-ES required a constant supply of provitamin standards, thus the varying purity of commercially available standards and the high instability of these compounds could pose grave problems. Due to the stability of Sudan, HPLC-IS appeared to be the method of choice although passage of the extract through a MgO: Hyflosupercel minicolumn was required prior to injection to separate chlorophylls, dihydroxy- and polyoxycarotenoids which would otherwise elute with Sudan. Nonconformity of the Sudan structure to those of the provitamins did not effect the quantitative results. The chromatographic separation, identity and quantification of the provitamins could be more easily established by using HPLC-IS, complemented with GFCC.
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  • 10
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    Chromatographia 33 (1992), S. 103-112 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Gas chromatography ; Chiral separations ; Allethrin ; Cypermethrin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Liquid and gas chromatographic separations of the pyrethroid insecticides allethrin and cypermethrin have been investigated with various achiral and chiral stationary phases. Diastercomeric and enantiomeric selectivity was observed for cypermethrin on a Pirkle-type chiral LC stationary phase, but very strong interactions and therefore long retention times prevented the separation of allethrin on this phase. Trans-allethrin isomers were separated on a chiral β-cyclodextrin RP-HPLC column while cypermethrin showed some difficulties on this phase due to isomerization. Diastereomeric but no enantiomeric selectivity by GC was achieved for cypermethrin with an apolar DB 5 capillary. GC separation of the diastereomers was used to study the selective photodegradation of cypermethrin isomers after forestry applications. Chiral β-cyclodextrin-based GC phases showed some enantioselectivity for cis- and trans-allethrin isomers. A separation of the eight isomers into six partially resolved peaks was achieved by GC with a coupled column consisting of chiral permethylated β-cyclodextrin and DB 1701 as stationary phases. This combination was used to characterize allethrin formulations intended for indoor use and to investigate allethrin products formed by ozonolysis of thin films of the insecticide.
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  • 11
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    Chromatographia 33 (1992), S. 177-185 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Diuretics ; Screening and determination of diuretics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary This critical review of different methods proposed for the determination and screening of diuretics is directed mainly, because of its potential application, towards highperformance liquid chromatography.
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  • 12
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    Chromatographia 33 (1992), S. 218-224 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Peak ; Pattern recognition ; Prediction interval
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary It is still difficult to determine peaks and peak boundaries properly, though peak recognition is very important for the precision of quantitative data. A new computer program overcomes these problems using a method which is adapted from human judgements. The algorithm was developed for HPLC but can also be used in other fields of analytical chemistry.
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  • 13
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Diol silica gels ; Carbohydrates ; Evaporative light scattering detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Bonded silica columns have been evaluated for their ability to separate carbohydrates and polyols. Mobile phases consisting of dichloromethane/methanol produced the best separations in comparison with the acetonitrile/water mixtures commonly used with amino columns. Of all the bonded phases tested, LiChrospher Diol silica provided the best separations, and selectivities were not very different from those obtained on the most popular system using an amino bonded phase and acetonitrile/water as eluent. In addition, diol columns with a dichloromethane/methanol eluent offer excellent stability with no Schiff’s base formation of reducing sugars. Using an evaporative light scattering detector, low limit detection is obtainable (20 ng of glucose from a column) and gradient elution is quite feasible.
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  • 14
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Porous graphitized carbon ; Ring-substituted aniline derivatives ; Electronic interactions ; Principal component analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The retention characteristics of 22 aniline derivatives were determined on a porous, graphitized-carbon column in unbuffered acetonitrile-water and methanol-water mixtures. Each aniline derivative gave symmetrical peaks in each eluent without buffers. Good linear correlations were found between the log k′ and the concentration of the organic component in the eluent. The slope and intercept values differed according to the type of organic modifier and the charcter, number and position of substituents, indicating the different selectivities of methanol and acetonitrile and the good separating power of the column. Multivariate mathematical-statistical calculations proved that the retention of ring-substituted aniline derivatives is mainly governed by electronic parameters and the hydrogen acceptor capacity of substituents.
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  • 15
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion-pairing ; Furosine ; Pyridosine ; Milk
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An ion-pair, reversed-phase, liquid chromatographic procedure using UV detection for quantitation of furosine is described. The standard plot was linear (r〉0.999) over a 5 ng range. An authentic synthesised sample of furosine was used for calibration. Commerical milk samples were analyzed by the described procedure.
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  • 16
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Automated peak detection ; Discrete Fourier transform ; Frequency acquisition and filtering ; Peak detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The principle of automated chromatographic peak detection and analysis software is summarized, and critical steps are systematically studied. As the only parameter to be entered is the acquisition frequency, evaluation of its effect on software performance is discussed. In the case of relatively noisy chromatograms, it is shown experimentally that numerous points per peak have to be taken, leading to quite fast computer acquisition procedures. The use of discrete Fourier transform filtration techniques can modify peak shapes and a comparative study evaluates the relative errors induced in the shapes and characteristics of the chromatographic profiles. Optimisation of filtering conditions is achieved and it is shown that for a filter position only 2% of the Nyquist frequency no deformation occurs in the chromatographic profile. Detection of the start and finish of chromatographic peaks is optimized according to a simple four step iterative procedure. In the case of simulations, the difference between the values used to simulate peaks and those calculated by the software are less than 1%.
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  • 17
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fluoropyrimidine drugs ; Pharmacokinetics of doxifluridine ; Chemotherapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A reversed phase high performance liquid chromatographic method has been developed for the simultaneous determination of the pro-drug 5′-deoxy-5-fluorouridine (5′-dFUR), its metabolite 5-fluorouracil (5-FU) and some fluorinated pyrimidines involved in the metabolic activation process of 5-FU. The method has been used to monitor the bioavailability of 5′-dFUR and 5-FU in patients undergoing anticancer chemotherapy. Serum sample treatment involves addition of internal standard (5-bromouracil), protein precipitation with saturated ammonium sulphate solution and liquid-liquid extraction with ethyl acetate-isopropanol (90 ∶ 10 v/v). Urine is simply diluted with mobile phase and injected. The average recovery from serum (at 0.5 μg/mL level) was 95.0%±1.4 for 5′-dFUR and 86.3%±3.5 for 5-FU. A linear response extending over four decades of concentration was observed. Detection limits in the low ng/ mL range were obtained using a 250 μL sample size and a 20 μL injection volume. Within-day and between-day coefficients of variation were below 4 and 10%, respectively.
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  • 18
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Flow injection analysis ; Combined flow injection/HPLC ; Carbamate pesticides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An integrated flow injection (FI)/HPLC system for the total and individual determination of carbamate pesticides (propoxur, carbofuran and carbaryl) is proposed. The determination is based on the alkaline hydrolysis of the analytes and subsequent coupling with diazotized sulphanilic acid to yield the monitored dyes with or without a prior separation step by HPLC in a C18 column. The calibration curves obtained are linear in the μg/ml range and r.s.d. values are between 0.5 and 3.7% in all instances. Injection of the sample into the FI manifold allows the total pesticide content in the sample to be screened. The manifold thus acts as a post-column reactor/detector of the chromatograph for samples with high overall carbamate content, which are also injected into the HPLC instrument. The performance was checked with contaminated water samples.
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  • 19
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; α1 glycoprotein ; Enantioseparation ; β-blocking agents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The enantioselectivity of the α1 glycoprotein chiral stationary phase, Chiral AGP® has been evaluated for a number of β-blocking agents. A correlation has been found between the retention behaviour on this stationary phase and the hydrophobicity of the compounds. The separation factor α is higher for compounds that are well retained. Retention, and thus α, are also controlled by pH and the percentage of organic modifier in the mobile phase.
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  • 20
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Perfluoroalkylated polymer-gel packings ; Aromatic and fluorine-containing compounds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Porous, perfluoroalkylated polymer-gels for column packings in high-performance liquid chromatography (HPLC) were prepared by suspension polymerization of heptadecafluorodecyl arcylate and ethylene glycol dimethacrylate. The packings showed no abnormal retention for ionic or aromatic compounds, due to the lack of ionic or aromatic groups. In addition, the packings showed no excessive retention for strongly hydrophobic compounds which is often the case with long-chain, alkylated silica gels and polymer gels. This is due to the extremely low surface energy of perfluoroalkyl groups. Therefore, perfluoroalkylated polymer gels enable isocratic HPLC separation of solutes with significantly different hydrophobicity.
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  • 21
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Porous glass ; Surface free energy ; Film pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 22
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    Chromatographia 33 (1992), S. 478-484 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Porous glass adsorbents ; Surface free energy ; Oriented adsorption of hydrocarbons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The relationship between the specific capacity factor (k/S, where k is the capacity and S is the surface area of the sorbent, in m2) in the liquid chromatography of aromatic hydrocarbons and the adsorption energy (-°GA) has been investigated. The previously published results, based on the calculation of the work of adhesion (WSA) from contact angles, were re-examined and a new hypothesis on interactions at interfaces was employed. Direct proportionality has been found between k/S and-°GA, which allows prediction of the chromatographic behavior of adsorbates on sorbents. The surface free energy components were calculated in order to determine-°GA in terms of the work of adhesion. The dispersion component of the surface free energy of glass was obtained from the adsorption isotherm of n-octane and it was found that the hydrocarbon molecules are adsorbed in an oriented position. The contact angles of liquids on the outer surface of porous solids do not yield reliable values of WSA and of the surface free energy components. A higher intermolecular attraction increases WSA and decreases the contact angle in pores.
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  • 23
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Adenosine and some metabolites ; Extraction from brain tissue ; Quantitative determination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An analytical procedure has been developed for the assay of adenosine and some metabolites in brain tissue extracts of rats. This paper reports the extraction method, the technique adopted to avoid enzymatic transformations and the chromatographic conditions for the identification and quantitation of these nucleosides and bases. Peaks in the chromatograms of brain tissue extracts were identified by retention times, absorbance ratios of reference compounds and by enzymatic peak-shift.
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  • 24
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    Chromatographia 34 (1992), S. 573-580 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chemically bonded phases (CBP) ; Surface heterogenity ; Surface purification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The surface chemistry of eight silica-gels with different siliceous matrix structures have been described. The influence of surface impurities on the chemical modification process (coverage density) with monooctadecylsilane has been studied. The surfaces of the adsorbents, before chemical modification, were cleaned by extraction with 20% HCl. Bare and modified materials were characterized using different physico-chemical methods e.g.: SIMS, CP/MAS NMR, porosimetry, pH measurement, elemental analysis and chromatography (GC & HPLC). The presence of trace amounts of different metallic elements creating new adsorption centers on the surfaces of the packings, have been demonstrated. Moreover, it has been shown that washing of silica gel adsorbents increases the coverage density of alkylsilyl ligands and improves the chromatographic properties of prepared packings.
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  • 25
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Zone-electrophoretic sample treatment ; Basic and acidic compounds ; Biological samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A modified valve arrangement for zone-electrophoretic sample treatment (ZEST)-which is coupled on-line with column liquid chromatography — is used to pretreat biological (plasma) samples. Carry-over of plasma proteins depends on the pH of the electrophoresis buffer. The determination of propranolol, metoprolol, cromolyn and salicylic acid demonstrates that both basic and acidic analytes can be isolated from the plasma matrix with high selectivity. Analogous piperazines, with different protein binding properties, were used to study the influence of protein binding on the recovery. It is shown that high protein can cause a decreased recovery.
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  • 26
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    Chromatographia 34 (1992), S. 597-600 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Oxindole alkaloids ; Uncaria tomentosa
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The main oxindole alkaloids from the root bark ofUncaria tomentosa were separated by reversed phase HPLC with an acetonitrile/methanol/phosphate buffer solvent gradient. UV detection was carried out at 245 nm. The chromatographic parameters for the separation of the alkaloids were optimized by studying the impact of the pH value of the mobile phase and the column temperature on the separation efficiency of the analytical system. The best separation was achieved with a mobile phase pH of 6.6 and a column temperature of 15°C. The method developed is suitable for the qualitative characterisation and quantitative determination of oxindole alkaloids in crudeUncaria tomentosa extracts and phytopharmaceuticals.
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  • 27
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Enantiomers of furprofen ; Human plasma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A sensitive and stereoselective liquid chromatographic (HPLC) assay for the S and R enantiomers of furprofen in human plasma has been developed. The assay is based on derivatization with S(−)-1-phenylethylamine with formation of two diastereoisomeric derivatives and on their separation and quantitation using HPLC with uv detection. The method is linear from 25 to 600 ng ml−1 of both enantiomers, with a variation coefficient below 10.8%, and a detection limit of 20 ng ml−1. This procedure is suitable for pharmacokinetic studies.
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  • 28
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Micelle-solute association constants ; Polynuclear aromatic hydrocarbons ; Octanol/water partition coefficients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Sodium dodecyl sulphate, hexadecyltrimethylammonium bromide and polyoxyethylene(23) lauryl ether were investigated as mobile phases in the micellar liquid chromatography of polycyclic aromatic hydrocarbons of environmental concern. A wide range of surfactant concentrations were used and the retention parameters and distribution coefficients calculated. The trends in the retention data for the PAHs are discussed and several conclusions are presented concerning the partition coefficients when these surfactants are present in the mobile phase. Comparisons are made between the structural features of the compounds and their capacity factors, and the octanol/water partition coefficients are correlated with hydrophobicity for the PAHs studied.
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  • 29
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Normal phase separations ; Chloro-substituted polycyclic aromatic hydrocarbons ; Coupled column system ; Environmental samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The retention behaviour of chloro-substituted PAHs on several commercial normal bonded phase HPLC columns has been investigated. Chloro-substitution was shown to generally decrease the retention on stationary phases like amino-, diol- and nitrophenylpropyl-modified silica. Dimethylaminosilica exhibited more complex retention characteristics towards chloro-substituted PAHs. On this stationary phase, the position of the chlorine substituents on the aromatic solute seemed to be of greater importance for retention than on the amino-, nitro- and diolsilica. For some chloro-PAHs, the retention was shown to increase with the number of chloro-substitutions, probably due to the large affinity of the electron-rich nitrogen in the stationary phase for the electron deficient π-system of the chloro-PAHs. Chloro-substituted PAHs were strongly retarded on the electron donating 2-(1-pyrenyl)-ethylsilica (PYE) stationary phase. However, the molecular shape of the chloro-derivatives had a large influence on retention, which was considerably decreased for some nonplanar chloro-derivatives of chrysene and benz(a)anthracene. A two-dimensional back-flush HPLC method, consisting of a combination of a nitrophenylsilica column and a PYE column of matched lengths, was shown to be useful for clean-up of chloro-substituted PAHs in environmental samples.
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  • 30
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Column switching ; Lidocaine ; Horse urine analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A rapid method is described for the determination of lidocaine and its metabolites in horse urine using a column switching technique and HPLC analysis. This procedure offers a sensitive assay without the need for time consuming extractions.
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  • 31
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    Chromatographia 34 (1992), S. 132-136 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Cysteine, cystine ; Phenylthiocarbamyl derivatives ; Protein hydrolyzates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new approach is described, and a novel explanation presented, for the high performance liquid chromatographic analysis of cystine and cysteine as their phenylthiocarbamyl derivatives. PTC cystine and cysteine have been eluted with the same retention times and molar responses, most probably due to electrophilic attack of phenylisothiocyanate on cystine resulting in the scission of the disulfide bond yielding two moles of cysteine. Further, total PTC cystine and cysteine have been measured both in model solutions and in standard protein hydrolyzates (lysozyme, bovine albumin, ribonuclease) with the same linearity as the other ineteen amino acids. The reproducibility of the measurements, at the 250–750 pmole level, proved to be 4.1% (Relative Standard Deviation %) or less.
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  • 32
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    Chromatographia 34 (1992), S. 155-158 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Retention ; Crown ethers ; Actinomycin D ; Metal cation complexation
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    Topics: Chemistry and Pharmacology
    Notes: Summary Retention of crown ethers in reverse-phase HPLC has been determined by their bonding ability with cations present in the eluent. The dependence of retention of crown ethers on cation concentration exhibits an inflection and makes it possible to calculate stability constant for the crown ether-cation complex. It is shown that in 75% MeOH retention of antitumor antibiotic, actinomycin D, depends on [Na+] and not on [K+] at concentrations of K+ from 5×10−7 to 10−1 mol l−1. Hence, actinomycin D may be classified as an ionophore-antibiotic.
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  • 33
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Phenolic compounds ; Optimisation of isocratic separations ; River water samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Isocratic column liquid chromatographic systems with UV absorbance detection at 280 nm have been developed for the separation of 29 phenolics and related compounds. The selectivity was investigated on silica-, carbon- and polymer-based separation columns for the separation of phenolic type of components. The effects of various acetonitrile/buffer mixtures, and pH of the mobile phase, and their impact on the retention of the phenols was assessed. Tables of retention times on the four columns for the 29 phenols with two different acetonitrile/buffer mixtures, together with the retention times at three pHs from 6.5 to 2.3 with varying levels of organic modifier on the LiChrospher RP 18 column are presented. As an application, the analysis of real river water samples from the Ebro river is described using a solid phase extraction step prior to injection into the chromatographic system.
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  • 34
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    Chromatographia 34 (1992), S. 173-176 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Carbon packing materials ; Aromatic compound separation ; Eluent effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The retention volume dependences on the molar volume were found for aromatic compounds using liquid microcolumn chromatography. The contributions of the functional groups in molecules of these compounds to the total retention value were calculated from the capacity factor values. The comparison of capacity factor values for carbon sorbents and octadecyl-silicagel has shown that for several microcolumn separations the carbon sorbent column has a better selectivity and resolution than the octadecyl-silicagel column.
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  • 35
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    Chromatographia 34 (1992), S. 177-181 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Synthesis of bonded stationary phases ; Acceptor ligands ; Normal phases ; PAHs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The synthesis of several electron-acceptor stationary phases has been reviewed the materials evaluated for their capacity to separate polyaromatic hydrocarbons (PAHs). Chemically bonded phases were obtained by the same procedure; the organosilane moiety is monofunctional and the HPLC behaviour is compared under identical conditions. Examples of PAHs separations are given.
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  • 36
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    Chromatographia 34 (1992), S. 182-184 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; C18 bonded phase ; Residual silanol groups ; Metal 5-Br-PADAP complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary If any residual (free) silanol groups remain at the surface of silica gel after bonding treatment, they may affect the retention of solutes since the dissociated groups (≡SiO−) will attract cations. The silanol group effect on the retention of cationic solutes will increase with increasing pH of the mobile phase but the effect will decrease with increasing hydrophobic-ion concentration at the C18 surface because such ions can mask the residual silanol groups. A method for the separation of metal complexes with 2-(5-bromo-2-pyridylazo)-diethylaminephenol (5-Br-PADAP) has been developed. The hydrophobic ion in the MeOH/H2O mobile phase was tetrabutylammonium (TBA).
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  • 37
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    Chromatographia 34 (1992), S. 342-346 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; History of chromatography ; Calcium carbonate stationary phase ; Chlorophyll
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    Topics: Chemistry and Pharmacology
    Notes: Summary Although Michael Tswett is the originator of chromatography, little is known about the performance of his chromatographic systems. His descriptions of the separation of plant pigments are detailed but nevertheless difficult to interprete by today's chromatographic theory. By our own experiments with the system calcium carbonate/benzene it was found that the separation factor of chlorophyll a and b is approx. 1.6 which means that less than 100 theoretical plates are necessary for separation. Tswett's columns with 50 μm particles and 2–3 cm of bed height presumably exceeded this plate number. His separations could have been impaired by mass overload and by a volume flow rate which was two orders of magnitude faster than the optimum.
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  • 38
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Isomeric substituted alkylbenzenes ; Retention and resolution
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    Topics: Chemistry and Pharmacology
    Notes: Summary The retention data of isomeric xylenes, ethyltoluenes and diethylbenzenes, and of mesitylene, benzene, toluene and ethylbenzene were obtained on a reversedphase column using methanol-water and ethanol-water mobile phases at four different temperatures. This database was used to relate the dependence of solute retention and resolution on the polarity of the mobile phase, solute dipole moment, and column temperature. The additivity of the free energy of the transfer of solute molecules or solute segments from the stationary phase to the mobile phase, was examined for the isomeric compounds. For this, the logarithm of the net retention volume was substituted for the free energy. Deviations from the additivity of free energies indicate that the separation of isomeric substituted alkylbenzenes is governed by their differential interactions with both the polar mobile phase and nonpolar stationary phase. Among the disubstituted alkylbenzenes,ortho-isomers favor the mobile phase more andpara-isomers tend to prefer the stationary phase more. Themeta-isomers are found to follow the additivity rule closely. These trends are amplified as the polarity of the mobile phase is increased indicating that these isomers are resolved better in water-rich mobile phases. These findings are substantiated by analogous results from gas-liquid chromatographic retention data, estimation of dipole moment effects, and examination of the entropic and enthalpic contributions to the net retention volume.
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  • 39
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Column switching ; Polycyclic aromatics ; Oil distillates
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    Topics: Chemistry and Pharmacology
    Notes: Summary A selective and sensitive HPLC method for the determination of Benzo[a]pyrene (B[a]p) in oil fractions by means of column switching is described. The diluted oil samples were injected directly onto a silica column with isooctane as eluent. After fast elution of the main part of the sample matrix, the B[a]p containing fraction was transferred on-line to a dinitro-aryl-modified silica column for final separation with isooctane/tetrahydrofuran. A detection limit of 50 ppt B[a]p was found when using fluorescence detection.
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  • 40
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Precipitation chromatography of polymers ; Block copolymers of styrene-butyl methacrylate ; Association phenomena
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    Topics: Chemistry and Pharmacology
    Notes: Summary Block copolymers of styrene andt-butyl methacrylate can be analysed by methanol/tetrahydrofuran gradients on C18 or phenyl bonded phase columns. On both of these columns, retention increases with styrene content of the samples. At 50°C, the retention of PS or a block copolymer containing 45% styrene was longer on the phenyl than the C18 columns. This indicates the contribution of adsorption to retention on phenyl bonded phase columns. Lowering the temperature from 50 to 30°C caused earlier elution of part of the sample from the phenyl phase. On a C18 phase the same drop in temperature improved the shape of the peak, which also started later than at 50°C. This effect of temperature is generally observed in polymer retention due to an adsorption mechanism, whereas increasing retention with decrease in temperature is characteristic of a precipitation mechanism. The block copolymer investigated contained 15% free polystyrene precursor which could not be separated from the block copolymer under the conditions employed. The addition of 20% PS homopolymer with a molecular weight similar to that of the styrene block in the copolymer showed that the polystyrene eluted together with the block copolymer, whereas the addition of PS homopolymer with a much higher molecular weight caused an extra peak at the expected elution time.
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  • 41
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Molecular recognition ; Multidentate phenyl-bonded phases ; PAHs
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    Topics: Chemistry and Pharmacology
    Notes: Summary New multidentate phenyl-bonded phases (MPBPs) were synthesized and evaluated the chromatographic retention behaviour with polycyclic aromatic hydrocarbons as sample probes in high-performance liquid chromatography. The new MPBPs show different retention characteristics from the previously synthesized MPBP, designated TP. Nevertheless, the results indicate that the retention mechanism is still the same as the TP phase: the size and shape of the solute molecule can be recognized by a cavity-like space formed by the methyl groups and phenyl rings of MPBPs.
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  • 42
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    Chromatographia 34 (1992), S. 391-397 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Hydrophobic interaction ; Stationary phases ; Salt effect ; Proteins
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    Topics: Chemistry and Pharmacology
    Notes: Summary Retention and selectivity in hydrophobic interaction chromatography (HIC) depend both on the type of stationary phase and on the mobile phase. In the last few years various high performance packing materials and columns have been introduced for HIC resulting in a range of different retentions and selectivity. We have investigated the effect of the stationary phase on the retention of various proteins. The retention of some solutes of different hydrophobicities were measured on three commercial HIC columns (TSK-Phenyl, Synchropack-Propyl, CAA-HIC) under isocratic conditions using water-methanol mixtures as eluent. The log kw values determined according to the literature were devalues determined according to the literature were dependent on the type and structure of the stationary phase and indicated a much less hydrophobic character for these columns than that obtained for reversed phase columns. Gradient separations were then carried out on a standard protein mixture using ammonium sulfate and sodium citrate to change the gradient time. In order to compare the effect of the stationary phase and the two salts investigated apparent capacity factors (kg) were determined and plotted against the gradient time obtained for the three columns in the two eluent system. It was shown that the type of stationary phase had a significant effect on the retention of proteins. In addition, the effect of the mobile phase composition, i.e. salt type, was considerably different on the various stationary phases. In order to exploit the potential of HIC to modulate selectivity for the separation of proteins, the combined effect of the stationary phase and the type of salt should be taken into account.
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  • 43
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    Chromatographia 34 (1992), S. 431-432 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin-layer chromatography ; Porphyrine ether glycerides
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    Topics: Chemistry and Pharmacology
    Notes: Summary Efficient TLC and HPLC conditions for the separation of a newly synthesized class of compounds, porphyrine ether glycerides, have been established. Supplementary physico-chemical characteristics are given for this group of solutes.
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  • 44
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Flow injection analysis ; Combined methods ; Transition metal ions ; Aqueous samples
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    Topics: Chemistry and Pharmacology
    Notes: Summary An automatic method based on the combination of a flow injection (FI) manifold with a liquid chromatograph has been developed for the enrichment and determination of transition metal ions in water samples. Alternatively, the FI configuration can be used as a screening system for the determination of the total concentration of heavy metals. Two-parameter expressions for calibration graphs involving preconcentration time and concentration of the analytes were established for both the FIA and the integrated FIA/HPLC methods. The preconcentration time depends on the concentration level of the analytes in the samples. The method is linear in the range 2–200 ng/ml, with r.s.d. values between 1.5 and 5.0. It has been applied to the determination of copper, lead, zinc, nickel, cobalt, cadmium and manganese in synthetic water samples.
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  • 45
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Solid phase extraction ; PCBs in cod-liver oil ; GC/MS identification
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    Topics: Chemistry and Pharmacology
    Notes: Summary A group of non-planar PCBs (IUPAC nos. 28, 52, 101, 118, 138, 153, and 180) was identified in a cod-liver oil product by using high resolution gas chromatography-mass spectrometry (HRGC/MS) in electron impact (EI) and negative chemical ionization (NCI) modes. The cod-liver oil samples were prepared either in a cyano column by high performance liquid chromatography (HPLC) or by a solid phase extraction (SPE) clean-up procedure that included e.g. purified charcoal treatment. The two methods of sample preparation were evaluated on the basis of the detectabilities of the congeners. The GC/MS-SIM method allowed quantitative monitoring of congeners nos. 52, 101, 118, 138, 153, and 180 at low concentration levels. Detection limits were 1.2 pg and 130 fg (m/z 292.00) in EI and NCI modes, respectively. The determination levels in EI and NCI were 1.8 pg and 290 fg in HPLC followed by HRGC/MS and 170 pg and 27 pg in SPE followed by HRGC/MS. The linear range was from 5.0 pg/μl to 1.0 ng/μl and from 1.0 pg/μl to 1.0 ng/μl in EI and NCI modes, respectively. In addition, the co-planar PCBs, PCDDs, and PCDFs were also screened and two of the chlorinated furanes were identified by HRGC/MS-NCI after separation from non-planar PCBs by SPE. In this case the only congeners that could be quantified were 2,3,4,7,8-PCDF and 1,2,3,4,6,7,8-HCDF, the detection limit for them being 740 fg (m/z 351.90) with NCI. SPE allows the separation of the planar and non-planar compounds, but LC separation is more effective for separation of the compounds of interest from the matrix. LC clean-up is easier and faster to perform than SPE clean-up.
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  • 46
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Calix[4]arenes ; Host-guest chemistry ; Separation of stereoisomers
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    Topics: Chemistry and Pharmacology
    Notes: Summary A high performance liquid chromatographic procedure on 5 μm RP-18 was developed for the separation of the four possible cis-trans isomers of tetramethyl-calix[4]arenoctol, and of their octaacetates, and their octamethyl ethers.
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  • 47
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Sphingomyelin ; Molecular species separation ; Experimental design and optimization ; Chemometrics
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    Topics: Chemistry and Pharmacology
    Notes: Summary An improved method has been developed for the separation of molecular species of intact sphingomyelins from natural sources (chicken egg yolk, bovine brain, and bovine milk) by high performance liquid chromatography with light-scattering detection. The method was developed and optimized using a novel multivariate optimization strategy.
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  • 48
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    Chromatographia 34 (1992), S. 534-536 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Carbohydrates ; Enzymic hydrolysate ; Waste paper
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    Topics: Chemistry and Pharmacology
    Notes: Summary Waste paper was pretreated with 5M sulfuric acid at 28°C to give a gel-like solution which was then hydrolyzed with cellulase, purified fromTrichoderma viride, to form carbohydrates. The determination of the carbohydrates was accomplished using an aminopropylbonded silica HPLC column and an RI detector. The detection limits were 20 ppm; xylose, glucose, and cellobiose were the major components. Salts from the buffer solution may affect the activity of cellulase. The analysis of carbohydrates can be performed under acid conditions. HPLC analysis of carbohydrates from enzymatic hydrolysis is reliable and successful.
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  • 49
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Size exclusion chromatography ; Styrene-methacrylate polymers ; IR and UV spectroscopy ; Lubricating oils additives
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    Topics: Chemistry and Pharmacology
    Notes: Summary Characterization of a poly(styrene-alkyl methacrylate) viscosity index improver according to its chemical composition distribution and molecular weight distribution was carried out by liquid adsorption chromatography, size exclusion chromatography and infrared and ultraviolet spectrophotometry. The industrial polymer was fractionated by liquid chromatography using silica gel as adsorbent and a mixture of 1,2-dichloroethane and methanol as mobile phase. Each fraction was analyzed by size exclusion chromatography and infrared and ultraviolet spectroscopy. The number average molecular weight ranged from 10000 to 36000 and the weight average molecular weight from 19000 to 264000. The styrene content of the various fractions analysed was between 29.5% and 72.2%.
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  • 50
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Laidlomycin, 26-deoxylaidlomycin
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    Topics: Chemistry and Pharmacology
    Notes: Summary High performance liquid chromatography on an octadecyl silica column has been used to determine laidlomycin: 26-deoxylaidlomycin ratios and to determine the concentration of both compounds by standard addition in samples prepared from fermentation broths ofStreptoverticillium olivoreticuli. A refractive index detector was preferred to an ultraviolet detector owing to the presence of UV-absorbing impurities which could not be completely separated from the substances of interest. Linear relationships were obtained from the calibration data. The coefficient of variation for the estimation of ratio and concentration of the compounds determined was better then 5%. The estimated limit of detection for both substances was about 50μg·ml−1.
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  • 51
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Molecular structure parameters ; Prediction of retention ; Phosphoroamidothiotes
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    Topics: Chemistry and Pharmacology
    Notes: Summary Multi-variable regression analysis between lnkw, c (in retention equation lnk′=lnkw+cCb) and molecular structure parameters, including hydrophobicity, electric effect, field effect and position-specific effect constant, was carried out with O-ethyl, O-aryl and N-isopropyl phosphoroamidothioates as test solutes. With these quantitative relationships, the retention behaviour of these solutes for different mobile phase compositions was predicted. The results showed that there are only 26.7% of total, experimentally measured, capacity factors with relative deviations larger than 5% and only 2.2% with deviations larger than 10%, which means that it is possible to apply the method reported to predict retention values for qualitative purposes for different mobile phase compositions.
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  • 52
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Histamine in wine ; Pre-column derivatization ; Solid phase extraction
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    Topics: Chemistry and Pharmacology
    Notes: Summary A method for determining histamine in wine by precolumn derivatization with PITC (phenylisothiocyanate) with reversed-phase HPLC and UV detection is reported. Histamine can be determined together with the 24 amino acids within 40 min, or separately in a shorter time (less than 4 min) if a prior solid phase extraction clean-up is used.
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  • 53
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Cyclodextrin inclusion complexes ; Structure-retention relationships ; Polycyclic aromatics
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    Topics: Chemistry and Pharmacology
    Notes: Summary The retention behaviour of a group of polycyclic aromatic hydrocarbons having nearly equal ionization potentials but different molecular polarizability values was investigated by reversed-phase HPLC and gas chromatography, using β-cyclodextrin as a selective inclusion reagent. In HPLC, the cyclodextrin was applied as an additive to the ethanolwater binary mobile phase, while in gas chromatography β-cyclodextrin served as the stationary phase coated on an inert support. The relationships between the capacity factors, molecular polarizabilities and the shape parameter of solute molecules is discussed.
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  • 54
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    Chromatographia 31 (1991), S. 67-70 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Cortico-steroids ; Drug adulterants
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    Topics: Chemistry and Pharmacology
    Notes: Summary A sensitive and specific method for quantitation of the steroids betamethasone, prednisolone and cortisone acetate commonly used as adulterants in locally produced herb extracts and in certain homeopathic drugs is described. Reverse-phase liquid chromatography with UV detection has been used.
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  • 55
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    Chromatographia 31 (1991), S. 80-84 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion chromatography ; Poly(vinyl alcohol) gel ; Inorganic anions ; UV detection for IC
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Poly(vinyl alcohol) (PVA) gel shows ionic retention properties for common inorganic anions when an acidic eluent is used. The ionic property of the PVA gel is due to the proton-acceptable nitrogen atoms of the cross-linking agent and the carboxylic residues being comprised in the gel matrix. The extent of the net charge on the gel surface depends on the pH of the eluent. At a pH ranging from 2.3 to 5.3, the PVA gel behaves as a weak anion exchanger with very low ion-exchange capacity. At these conditions four UV-absorbing inorganic anions (bromate, bromide, nitrate, and nitrite) are separated by eluting with aqueous sulfuric acid. Alkyl groups introduced on the gel surface hinder the ionized solute molecules from accessing to the positively charged functional groups on the gel surface. A neutral solute (HNO2) is retained with non-ionic interactions.
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  • 56
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Injection conditions ; Chlorophylls and carotenoids ; Extraction solvents ; Phytoplankton pigments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The RP-HPLC analysis of chlorophylls, their degradation products (chloropigments) and carotenoids is very sensitive to the nature of the injection solvent. The effect of sample-solvent interaction can result in the production of distorted, or even false, peaks that could be erroneously interpreted as “pigment like” or as poor chromatographic resolution. The previously suggested theoretical explantion, based on differences in solvent characteristics as expressed by the Polarity Index (P′) or even by the more precise solvent strength parameter for reversed-phase systems (S) we use, was unsatisfactory. The problem seems more complex, with other parameters such as injection volume and solute concentration or solvent selectivity also playing a role. As a practical consequence, however, suggesions are made for optimum injection conditions. Also, the presence of ion-pairing reagents in the injection solvent is demonstrated to be unnecessary.
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  • 57
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    Chromatographia 31 (1991), S. 129-132 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; End-capping ; Chiral stationary phase ; Enantioselectivity
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    Topics: Chemistry and Pharmacology
    Notes: Summary The effect of end-capping chiral stationary phases (CSP's) derived fromN-(2-naphthyl)alanine undecyl ester has been examined using either trimethylchlorosilane (TMCS), hexamethyldisilazane (HMDS), or bis(trimethylsilyl) trifluoroacetamide (BSTFA) as end-capping reagents. The separation factor (α) and capacity factor (k′) of the enantiomers ofN-(3,5-dinitrobenzoyl)leucine octadecyl amide andN-(3,5-dinitrobenzoyl)alanine butyl ester were evaluated on three columns all packed with material from the same batch of stationary phase. These columns were essentially identical before, but not after end-capping with the above reagents. TMCS and HMDS were found to be superior to BSTFA, which appears to cause a significant loss of bonded phase from the silica surface. It seems that residual silanols affect the retention either by interacting with the analyte or by interacting with strands of stationary phase. End-capping usually increases enantioselectivity, sometimes by decreasing k′ for the first enantiomer and increasing k′ for the second enantiomer. The enhancement in enantioselectivity is greatest in relatively nonpolar mobile phases and occurs to a greater extent for phases having incomplete surface coverages.
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  • 58
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Liquid crystal bonded phase ; Polycyclic aromatics ; Carvone and pulegone
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    Topics: Chemistry and Pharmacology
    Notes: Summary A chromatographic and thermodynamic study of the compound [4-(allyloxy)benzoyl]-4-methoxyphenyl (ABMP) as a model of a chemically bonded liquid crystal stationary phase for HPLC was undertaken. A number of polycyclic aromatic hydrocarbons (PAHs) and two small solutes, carvone and pulegone, were studied under varying solvent and temperature conditions. Plots of log k′ vs. % organic in the mobile phase were not completely linear in all cases. The van't Hoff plots revealed at least one phase transition. The enthalpies of solute transfer from the mobile phase to the ABMP phase were determined for several PAHs. All tests indicate that ABMP possess liquid crystal properties when bonded to particulate silica.
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  • 59
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    Chromatographia 31 (1991), S. 193-205 
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Column liquid chromatography ; Silanol adsorption centres ; Strongly interacting adsorption sites ; Suppression of adsorption activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In this second part of the review heterogeneity of the silica surface is described and evidence is presented for the existence of a low population of strong adsorption sites. Methods of detection and determination of these strongly interacting sites are discussed. The last part of the review is devoted to the suppression of unwanted adsorption activity. Methods of blockage and special methods for the preparation of HPLC packings are described.
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  • 60
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    Chromatographia 31 (1991), S. 277-280 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Simplex optimization ; Narasin in fermentation broth ; Vanillin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A rapid HPLC assay with post-column derivatization has been developed for the determination of narasin in fermentation broth. The reaction of narasin with substituted benzaldehydes was investigated under first order conditions and the rate constants were determined for a variety of substituted benzaldehydes. Vanillin reacted most rapidly to produce a red color. The reaction conditions were optimized to acheive a maximum response with a minimum analysis time.
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  • 61
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ovomucoid stationary phase ; Chiral separations ; Mobile phase effects ; Protein conformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The effects of alcoholic modifiers and pH on the chromatographic properties of an immobilized ovomucoid chiral stationary phase have been investigated using acidic, basic and neutral solutes. A series of primary, secondary and tertiary alcohols and pH's ranging from 3.5 to 6.0 were used in this study. The results indicate that both the shape and the hydrophobicity of the alcoholic modifier affect retention (k') and enantioselectivity (α). In general, an increase in the hydrophobicity of the modifier results in a decrease in k's and α's. However, this is not the case whent-butanol is the modifier, suggesting that the size of the alkyl moiety attached to the carbinol carbon also contributes to the chromatographic results. The pH studies indicated that Coulombic interactions play a role in the retention of the acidic and basic solutes. The results also suggest that in addition to ethanol and 1-propanol,t-butanol should be considered during optimization and that maximum efficiencies may be obtained at pH 5.0.
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  • 62
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Adsorption isotherms ; Immobilized serum albumen ; Chiral stationary phase ; Leucine, N-benzoyl derivative
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    Topics: Chemistry and Pharmacology
    Notes: Summary The saturation capacity of columns packed with bovine serum albumin immobilized on silica has been determined for the N-benzoyl derivative of leucine at different compositions of a 1-propanol/water mobile phase. In all cases it has been found that the equilibrium adsorption data are well accounted for by a biLangmuir isotherm. The experimental data are consistent with the assumption that the column saturation capacity of the chiral selective sites as well as the saturation capacity of the non-selective sites are independent of the 1-propanol concentration in the range 0–10%.
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  • 63
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Bonded phase synthesis ; Alkyl and aryldimethyl phases ; CP/MAS NMR spectroscopy
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    Topics: Chemistry and Pharmacology
    Notes: Summary A comparison of newly synthesized, reversed-phase bonded stationary phases is presented. The materials studied include monomeric n-octyl, n-octadecyl, aryl and n-octyldihydrogeno bonded-phases. Differences in reactivity of the silane functional groups are demonstrated and the high coverage obtained with the hydrogeno-bonded phases is shown. The structures of the bonded phases have been determined by29Si and13C CP/MAS NMR spectroscopy.
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  • 64
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    Chromatographia 31 (1991), S. 347-350 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chemically modified silicas ; Surface states ; n-alkylbenzenes
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    Topics: Chemistry and Pharmacology
    Notes: Summary The thermodynamic behaviour of n-alkylbenzenes on chemically modified silicas in reversed-phase liquid chromatography has been examined in acetonitrile-water and methanol-water systems. Plots of the thermodynamic parameters obtained against the organic solvent compositions indicate an interesting trend which implies that the surface states of the chemically modified silicas under the two eluent systems are different.
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  • 65
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    Chromatographia 31 (1991), S. 362-366 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Particle size distribution ; Stationary phase stress ; Silica gel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A particle size distribution analysis has been completed on three different HPLC column packing materials including silica gel (Si60) and two bonded phases (RP8 and RP18). The stationary phases were subjected to 18 hours stress with 1 N or 3 N KOH and found to have quantitatively different distribution patterns initially, at 13 hours and finally at 18 hours although the average particle diameters for the Si60 and RP8 were the same or higher at 18 hours as initially. Thirteen hoursstress with sodium octanesulfonate, tetrabutylammonium phosphate and ammonium acetate at exaggerated conditions also resulted in distributional changes with the Si60 and RP8 decreasing in average particle diameter when exposed to ammonium acetate and tetrabutylammonium stressing respectively.
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  • 66
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Biogenic amines ; Wine ; Food-related biogenic amines
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    Topics: Chemistry and Pharmacology
    Notes: Summary Methods for the separation of food-related biogenic amines (histamine, tyramine, 2-phenylethylamine and tryptamine) have been developed based on ion-interaction reversed-phase liquid chromatography. Two different interaction reagents have been comparatively used, namely octylamine ortho-phosphate (at wave-lengths of 230, 254 and 280 nm) and octylamine salicylate (at a wavelength of 254 nm). The different elution sequence orders shown by the investigated amines for the two reagents are discussed and compared. The detection limits obtained were 20 ppb for tryptamine (λ =280 nm), 500 ppb for 2-phenylethylamine (λ=254 nm), 400 ppb for tyramine (λ=230 or 280 nm) and 900 ppb for histamine (λ=230 nm). The method was applied to the analysis of a five years old Italian red wine, in which 2-phenylethylamine (at a concentration of 72±3 ppm) and tryptamine (at a concentration of 4.0±0.3 ppm) were found to be present.
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  • 67
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    Chromatographia 31 (1991), S. 387-392 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Retention model ; Self-association of water
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    Topics: Chemistry and Pharmacology
    Notes: Summary An attempt has been made to gain a semi-quantitative insight into the self-association of water molecules through hydrogen bonds. This was only possible with the use of a new solute retention model for the chromatographic systems by considering intermolecular interactions between the constituents of binary mobile phases. Four different sizes of the average associative aqueous multimer were assumed. By comparing measured and calculated retention values, the existence of associated aqueous multimers consisting of 100 aqueous monomer units is postulated as an average multimer structure.
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  • 68
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    Chromatographia 31 (1991), S. 401-410 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion-pair reversed-phase separations ; Nucleotides ; Extraction from cells and tissue ; Retention mechanism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary HPLC methods for the separation of nucleotides, nucleosides and nucleobases by ion-pair reversed-phase are reviewed. The advantages of these are discussed versus anion-exchange and reversed phase separations. Extraction procedures for nucleotide determinations from cells and tissues are pointed out in detail. Extracts from red blood cells, Ehrlich ascites tumour cells, hepatocytes, intestine are used for determination of nucleotide concentrations by the methods described.
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  • 69
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion exchange chromatography ; Quantitative amino acid analysis ; OPA/FMOC precolumn derivatization ; Cheese
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    Topics: Chemistry and Pharmacology
    Notes: Summary An improved HPLC method for the quantitative determination of the amino acids from hydrolysed cheese proteins and peptides is described. Some important improvements to the existing method are suggested. The addition of piperidine-4-carboxylic acid (PICA) as a hydrolysis-resistant internal standard enabled the quantification of secondary amino acids. The following analytical parameters have been determined: repeatability, detection limit and linearity in the measuring range. A statistical comparison with the classical ion chromatographic method gave an excellent correlation for all determined amino acids. Both methods are free of artifacts and systematic errors. Compared with ion chromatography, HPLC shows the following advantages: faster equilibration of the column, shorter retention times, more stable baseline, narrower peaks and more sensitive fluorescence detection. A drawback is the slightly lower repeatability for some amino acids.
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  • 70
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chiral separations ; Amino acids ; Fluorogenic derivatization ; N-(Chloroformyl)-carbazole
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    Topics: Chemistry and Pharmacology
    Notes: Summary A new reagent for fluorescence labelling of amino acids, N-(chloroformyl)-carbazole, has been used in order to achieve high sensitivity of detection as well as good optical resolution. The derivatization reaction is fast and conveniently carried out at room temperature by shaking a buffered aqueous solution of the amino acids with an acetone solution of the reagent. The individual derivatized amino acids are first separated and collected via chromatography on a standard octadecyl-silica column. Each amino acid derivative is then analyzed for enantiomer composition by re-injection on a BSA-silica (Resolvosil®) column using fluorescence detection. For some amino acids (alanine, threonine, phenylalanine, tryptophan) enantiomeric separation factors exceeding α=3 have been obtained. The phosphonic acid analogue of alanine (1-aminoethylphosphonic acid) was also found to be well resolved into its enantiomers.
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  • 71
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    Chromatographia 31 (1991), S. 465-468 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Catechins ; Grape seeds ; Proanthocyanidins ; UV-visible spectroscopy/diode array detection
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    Topics: Chemistry and Pharmacology
    Notes: Summary Reversed-phase, high-performance liquid chromatography coupled to photodiode array detection has been used to analyse catechins and proanthocyanidins extracted from grape seeds. Results show that the ethyl acetate fraction obtained by passing extracts of samples adjusted to pH 7.0 through preconditioned C18 SEP-PAK cartridges contains several catechins and proanthocyanidins. Seven peaks have been assigned to standard catechins and proanthocyanidins on the basis of their retention times and UV spectra. Other peaks which appear in the chromatogram show spectral behaviour similar to that of standard catechins and proanthocyanidins.
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  • 72
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    Chromatographia 31 (1991), S. 478-480 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Orosomucoid ; Complex glycans ; α1 glycoprotein ; Glycopeptides
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    Topics: Chemistry and Pharmacology
    Notes: Summary The glycoforms contained within each glycosylation site of orosomucoid can be separated by reverse-phase HPLC without removal of the associated peptide or chemical derivatization. The chromatographic properties of the glycopeptides are dominated by the peptide portion but modified by the hydrophilicity of the glycan in a regular manner depending on its size. Assignments for known structures are readily made, permitting quantitative assessment of changes in glycoform concentration at individual glycosylation sites.
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  • 73
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Immunoaffinity precolomn ; Oestrogens ; Bioanalysis
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    Topics: Chemistry and Pharmacology
    Notes: Summary An automated liquid chromatographic system is described using immunoaffinity precolumns for sample pretreatment. The system consists of a column-switching unit allowing preconcentration from a large volume of sample (e.g. 15 ml of urine) onto an immunoaffinity precolumn (containing polyclonal antibodies immobilized on Sepharose). After sorption, the analytes are desorbed by a mixture of two cross-reacting solutes, followed by reconcentration on a C-18-bonded silica precolumn, and then separation on a C-18-bonded silica analytical column. Using oestrogen steroids as model compounds and UV absorbance detection, the minimum detectable concentration is ca. 200 ng/l with a repeatability of 6–8%. The total analysis time is 45 min which allows the unattended analysis of 30 samples per day. The features of the sample pretreatment method, especially of the immunoselective desorption, are evaluated and the general applicability of the system is discussed.
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  • 74
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Selenonium and arsonium cations ; AAS detection ; Chromatographic optimization
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    Topics: Chemistry and Pharmacology
    Notes: Summary Optimal mobile phase compositions were determined for the separation of selenonium ions [trimethylselenonium, (2-hydroxyethyl)dimethylselenonium and (2-acetoxyethyl)dimethylselenonium] and, separately, for arsonium ions (tetramethylarsonium, arsenobetaine, and arsenocholine) by HPLC with detection by atomic absorption spectrometry (AAS). Surface response methodologies were used to predict the variations in detector response (peak area), capacity factors, and selectivities as a function of the mobile phase composition. For selenonium analytes, a mixture of triethylammonium and trimethylsulfonium ions in the methanol-1% acetic acid mobile phase provided a compromise between resolving power and chromatographic efficiency. By contrast, optimum chromatography of the arsonium analytes was obtained by replacing onium additives in the mobile phase by picrylsulfonic acid. For both selenonium and arsonium analytes, the dominant interaction with the stationary phase was with residual silanols and improvements to the chromatographic performance of these analytes resulted in appreciable decreases in their limits of detection.
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  • 75
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Flame ionization detection ; Poly(styrene-co-methyl acrylate) ; Poly(methyl acrylate-co-n-butyl acrylate) ; Chemical composition distribution
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    Topics: Chemistry and Pharmacology
    Notes: Summary This investigation is focused on the development of HPLC with subsequent flame ionization detection as a tool to determine the chemical composition distribution of non-or poorly UV absorbing copolymers. Experiments were carried out with poly(styrene-co-methyl acrylate) and poly(methyl acrylate-co-n-butyl acrylate) copolymers. HPLC combined with FID provided useful qualitative information. Quantitative information could be obtained after calibration.
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  • 76
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Non-porous cation exchanger ; Hemoglobin A1C ; pH gradient elution
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    Topics: Chemistry and Pharmacology
    Notes: Summary High-performance ion exchange chromatography on a nonporous cation exchanger was examined for the separation of glycated hemoglobin. A standard sample of human hemoglobin was separated with salt or pH gradient elution. Glycated hemoglobin A1C was well separated from other hemoglobin variants in less than 10 minutes. pH gradient elution gave better resolution than salt gradient elution.
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  • 77
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Restricted access packings ; Packings with surface barriers ; Sample clean-up of biologically active analytes
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    Topics: Chemistry and Pharmacology
    Notes: Summary Various types of, so-called, restricted access packings have been developed for sample clean-up and analysis of biologically active solutes by means of HPLC. The unique feature of these packings is that they prevent the access of matrix components such as protein whilst selectively retaining the drug components and their metabolites. This results from the fact that the particles of the packings possess a surface barrier for large solutes at the external or internal surface area and exhibit a controlled gradient in the chemical surface composition. They are grouped, according to their particle structures, into internal-surface reversed phases (ISRP), shielded hydrophobic phases (SHP), semi-permeable surfaces (SPS), dual zone phases (DZP) and mixed functional phases (MFP). The structural characteristics and the chromatographic properties of these packings are reviewwed, especially with regard to their use in the assaying of drugs.
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  • 78
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Air analysis ; Dansylhydrazones of carbonyl compounds ; Chemiluminescence ; Fluorescence
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    Topics: Chemistry and Pharmacology
    Notes: Summary Sensitive and selective detection of dansylhydrazones of atmospheric carbonyl compounds (aldehydes and ketones) can be achieved using high performance liquid chromatography (HPLC) with fluorescence or chemiluminescence detection. The carbonyl compounds are derivatized by drawing air through small glass cartridges packed with porous glass particles impregnated with dansylhydrazine. After sampling, the contents of the cartridges are analyzed on-line by using a small plug of water (200 μL) to transfer and focus the hydrazone derivatives at the head of a HPLC column. Greatly increased sensitivity over traditional methods derives from 1) analysis of the entire contents of the sampling cartridge, and 2) detection by fluoresence or peroxyoxalate chemilum-inescence. Results are compared for photo-initiated and H2O2-initiated peroxyoxalate chemiluminescence. This novel and practical system enables the detection of sub-ppbv concentrations of formaldehyde, acetaldehyde, acetone and higher carbonyls in air using relatively short sampling times.
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  • 79
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Alkyl bonded phases ; Non-specific selectivity ; Hydro-organic mobile phases ; Retention of alkanoate esters
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    Topics: Chemistry and Pharmacology
    Notes: Summary A thermodynamic equation is derived for the non-specific selectivity of alkyl bonded phases as a function of the mobile phase composition using a displacement mechanism to model the sorption of solvents into the bonded phase. The equation is used to calculate the thermodynamic parameters which characterize the incremental behavior of a hydrophobic group in ethyl alkanoate and methyl perfluoroalkanoate ester solutes chromatographed with water-methanol and water-acetonitrile mobile phases on both octyl and octadecyl bonded phases.
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  • 80
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    Chromatographia 32 (1991), S. 23-26 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Enzyme assay ; Alanine amino transferase
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    Topics: Chemistry and Pharmacology
    Notes: Summary An improved method of alanine-amino transferase determination is proposed. The reaction is carried out with alanine and 2-oxoglutarate as substrates and analysis is by HPLC on a reversed-phase chromatographic system using a C18 column and tetrabutylammonium phosphate in phosphate buffer (pH 7.0)-acetonitrile as mobile phase. The enzyme activity was determined by directly following the formation of pyruvic acid without employing any secondary reaction, which is necessary in the spectrophotometric method. The detection limit of pyruvic acid is 10 pmole μl−1 and the standard deviation for the enzymatic activity of standard solutions is 5.4%. Furthermore under the chromatographic conditions selected it is possible to detect the presence of some intermediate species.
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  • 81
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Furfural ; Hydroxymethylfurfural ; Apple juice
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    Topics: Chemistry and Pharmacology
    Notes: Summary A rapid and sensitive method for determining 2-furaldehyde (FUR) and 5-hydroxymethyl-2-furaldehyde (HMF) in apple juices and juice concentrates has been developed. The method for FUR and HMF involves the solid-liquid extraction of the juice by using a C-18 cartridge prior to reversed-phase separation with detection at 280 nm. The mobile phase was acetonitrile-water (8/92, v/v) at a flow rate of 1.0 ml/min. Recoveries from apple juices and juice concentrates spiked at different levels ranged from 94.1 to 104.0 (FUR) and 94.5 to 100.5 (HMF). The quantification limit for both, FUR and HMF, was 5 ppb.
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  • 82
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    Chromatographia 32 (1991), S. 61-64 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Sample-induced pH gradients ; Separation of proteins
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    Topics: Chemistry and Pharmacology
    Notes: Summary The technique of an internal pH gradient induced by the sample is applied to the separation of proteins by liquid chromatography. Compatibility of the method with microcolumns is demonstrated and examples of separations on different types of sorbents are given.
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  • 83
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Counter-current extraction ; Chiral resolution ; Ofloxacin enantiomers ; Aqueous two-phase system
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    Topics: Chemistry and Pharmacology
    Notes: Summary The partial resolution of some drug enantiomers by counter-current extraction in an aqueous two-phase system using bovine serum albumin (BSA) or ovomucoid (OVM) as chiral discriminator is described. The phase system was prepared with dextran 40, polyethylene glycol and a protein. Ofloxacin (OFLX) enantiomer was well recognized by the BSA system, whereas the enantiomers of carvedilol (β-blocker) and DG-5128 (a new oral hypoglycaemic drug) were hardly recognized by the OVM system. The distribution coefficients of (S)-, (R)- and rac-OFLX varied with pH. Good enantioselectivity for OFLX was obtained at relatively high pH (≥ pH 9). The crude optically enriched OFLX enantiomers were extracted from the aqueous fractions and finally purified by thin-layer chromatography.
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  • 84
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Protein separations ; Peptide separations ; Octadecylalumina
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    Topics: Chemistry and Pharmacology
    Notes: Summary A recently-developed octadecyl-bonded alumina (ODA) stationary phase was evaluated for the separation of peptides and proteins by reversed phase high performance liquid chromatography. Using standard water-acetonitrile mobile phase gradients containing 0.1 % trifluoroacetic acid, the average peak capacity obtained for the separation of a mixture of ribonuclease a, cytochrome c, lysozyme and carbonic anhydrase on an ODA column are similar to that obtained on a widely used octadecylsilane (ODS) column. However, overall chromatographic resolution of the components of this mixture on ODA is inferior to that obtained on ODS. Cytochrome c peak areas were found to be ∼50% smaller on the ODA column than on ODS. On the other hand, both peak capacities and resolutions of octapeptide mixtures were found to be generally superior on the ODA column, and peak areas for a representative octapeptide were found to be virtually identical for both ODA and ODS columns. The differences in the results obtained on the ODA and ODS columns for these separations are attributed to the smaller pore size and unique fused-microplatelet shape of the ODA particles. Comparisons of the separations of the tryptic digest of cytochrome c on the ODS and ODA columns demonstrate that the ODA phase is potentially as useful as ODS for peptide mapping applications.
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  • 85
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Enantiomeric separation ; Chiral stationary phase ; Cellulose triacetate ; Flavanones ; Plant extracts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Flavanones ofArachis hypogaea, Hemizonia increscens, Eriodictyon glutinosum andThymus vulgaris extracts have been stereospecifically analysed by gradient elution on a column of cellulose triacetate supported on silica gel diol. The stereochemistry of naringenin, eriodictyol and homoeriodictyol was in favour of the 2S-configurated flavanones.
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  • 86
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Amino bonded phases ; Hydrogen chloride treatment ; Retention anomalies ; Normal-phase separations
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    Topics: Chemistry and Pharmacology
    Notes: Summary The influence of hydrogen chloride on the retention properties of aminopropyl bonded phases is studied using a series of simple aromatics, phenols and acids. The result of the HCL treatment is to mediate the hydrogen bonding interaction between the solute's polar functional groups and the bound amino groups.
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  • 87
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    Chromatographia 32 (1991), S. 73-78 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion-pair separations ; Dianionic species ; Dionium reagent
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    Topics: Chemistry and Pharmacology
    Notes: Summary Dionium cations, polymethylenebis(tributylphosphonium)s (BuCnBPs), were used as ion-pair reagents for ion-pair chromatography of dianionic species, such as maleate, fumarate, phthalates, and naphthalenedisulfonates. The longer the length of methylene chain connecting the two phosphonium cationic ceterns within BuCnBP, the larger was the retention of these dianionic species. The dionium reagents had a higher retention ability compared to conventional monoonium reagents, and enabled a higher resolution among the dianionic species of structural isomers. The extraction behavior of the dianionic species in a loctanol/water system was also investigated. The retention behavior by the use of BuCnBP was discussed in comparison with the extraction behavior.
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  • 88
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chiral separation ; Chiral crown ethers ; Phenylglycine enantiomers
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    Topics: Chemistry and Pharmacology
    Notes: Summary Previous work has demonstrated the possibility of crcating chiral stationary phases by coating a suitable support material via the mobile phase. The result is a wide variety of chiral phase systems which can be used in liquid chromatogrphy to separate enantiomers by a liquid-solid adsorption mechanism. The present paper demonstrates the potential of this technique for chiral crown ethers incorporating an α-D-mannopyranoside unit using the separation of phenyglycine enantiomers as an example.
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  • 89
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    Chromatographia 32 (1991), S. 85-86 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Antiepileptic drugs ; Optimised separation ; Serum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A fast and easy, iscratic high-performance liquid chromatographic method for the simultaneous determination of primidone, phenobarbital, phenytoin, carbamazepine and thiobutabarbital from serum samples has been developed. The optimal eluent composition is 36% acetonitrile, 24% methanol and 40% phosphate buffer. Using a programmable wavelength detector very low (sub-therapeutic) levels of the drugs can be measured.
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  • 90
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion-pair separation ; Salt concentration ; Charge number of solute ; Gouy-Chapman theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Thermodynamic and numerical treatments have been combined with Gouy-Chapman theory were to show that the effect of the salt concentration on the capacity factor in reversed-phase ion-pair liquid chromatography (RP-IPC) can be expressed as lnk′=A+blnCs. The parameter B is related to the charge number of the solute, and the parameter A is determined by both electrostatic and nonelectrostatic interaction, and can the linearly correlated with logarithm of the capacity factor in RP-HPLC for the solute with one negative charge. It also been observed that the electrostatic interaction is reduced with increasing salt concentration in RP-IPC, and this effect is more remarkable for solutes with more than the one negative charge of sulphonic acids.
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  • 91
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Size-exclusion ; Peptides ; Casein hydrolysate ; FAB-MS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A casein hydrolysate was eluted on a TSK G-2000 SW sizeexclusion high-performance liquid chromatography (SE-HPLC) column using a mobile phase which gives a correlation coefficient of 0.98 for the separation of 20 pure and synthetic peptides and proteins of molecular weight (M. W.) varying from 243.28 (Ala-Pro-Gly) to 43 000 (Ovalbumine) daltons. Further isolation and purification of peptides present in each of the 8 different fractions collected from the SE-HPLC were done by reversed-phase HPLC (RP-HPLC). Peptide experimental M. W. determined from the calibration curve obtained for synthetic or purified peptides was compared to their precise M.W. obtained by fast atom bombardment-mass spectrometry analysis (FAB-MS). The results do not show a separation of this complex hydrolysate by SE-HPLC according to the hydrodynamic volume of its constituents.
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  • 92
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Streaming current ; Specific pore volume and surface area ; Specific weight ; Bed porosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The applicability and precision of the method allowing the determination of several characteristics of the sorbent and its bed from two simple chromatographic retention measurements were tested with porous metal oxides and some other solids. The typical time of one retention experiment is 1–3 minutes. The method was verified with chromatographic solid phases containing both mesopores and macropores. The agreement between the retention volume of the streaming current response, caused by the change in the concentration of the polar component of the binary hydrocarbon-based mobile phase, and the total volume of the liquid in the column is decisive for the applicability of the method. If the influence of the error in the determination of the sorbent's weight in the column and of the column tube's volume are neglected, the external and the total bed porosities and the specific weight of the sorbent can be determined with the relative error of the retention volume measurement. The error of the determination of the specific pore volume and internal bed porosity will be twice as much. The specific surface area can be determined approximately for sorbents with average and large surface areas.
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  • 93
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    Chromatographia 32 (1991), S. 523-526 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Debrisoquine ; Urine ; Phenotype
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An isocratic HPLC method is described. It allows the simultaneous determination of debrisoquine and 4-hydroxydebrisoquine in urine. Sample preparation involves a rapid and simple (one step) liquid-liquid extraction without derivatization. Separation, followed by UV-detection, is carried out on a nitrile column in reversephase mode with a binary, aqueous mobile phase. This rapid assay uses a new internal standard (guabenxane) and allows the determination of urinary concentrations with good precision and appropriate sensitivity.
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  • 94
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ruthenium mixed complexes ; Sulfoxides ; N-Heterocyclic bases ; Hydrophobic properties of aromatic ligand
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The elution behaviour of a series of dichlorobis-(dimethylsulfoxide)bis(N-heterocyclic)ruthenium(II) complexes has been investigated using reversed-phase HPLC. Similar trends as those displayed by the free N-heterocyclic bases have been observed for the complexes, essentially reflecting the hydrophobic properties of the aromatic ligands.
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  • 95
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    Chromatographia 32 (1991), S. 527-537 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Supercritical fluid chromatography ; Supercritical fludi extraction (SFE) ; Explosives ; Cholesterol ; Polymer additives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Extraction with supercritical CO2 is a versatile method for sample clean-up and trace enrichment. The off-line coupling of SFE and HPLC is used to determine various explosives in debris as well as pesticides in soil. In food analysis the metod could be applied to determine cholesterol in noodles quantitatively. Correlations between the retention in RP chromatography and required extraction conditions could the established. The higher the organic modifier concentration in the eluent has to be, the smoother the extraction conditions required. With the non-volatile solutes studied, extraction temperature had no influence on extraction yield and speed. On-line coupling of SFE and capillary SFC is a very convenient and sensitive method for the determination of polymer additives. The coupling device described can also be used for “solventless” injection in capillary SFC.
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  • 96
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    Springer
    Chromatographia 32 (1991), S. 555-558 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Organic acids ; Grape musts ; Direct injection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A simple method for reverse-phase HPLC analysis of organic acids present in must has been developed. It is carried out in isocratic conditions, with a weak dilute acid as eluent and U.V. detection. The aim is to minimize sample preparation merely to filtration: direct injection is proposed as an approach toin vivo conditions.
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  • 97
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    Chromatographia 32 (1991), S. 566-572 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Isocratic Optimization ; Overlapping Resolution mapping method ; Substituted Phenols
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The Overlapping Resolution Mapping (ORM) method has been applied to predict the best mobile phase composition for the separation of eleven substituted phenols. This separation was carried out by HPLC using reversed-phase isocratic elution and UV detection with a diode array detector. The effect of temperature on the separation process was also taken into account. The optimized method was applied to identify phenols in waste and drinking water.
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  • 98
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Multisolvent mobile phase ; Optimization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A computer program is described for the optimization of reversed-phase multisolvent separations. After four initial gradient runs are carried out, calculation will locate a possible optimum with binary systems or select two binary mixtures with respect to both the analysis time and the selectivity. In this latter case, two additional experiments will locate the true optimum on a straight line joining these two binary compositions on the solvent triangle (ternary system). The efficiency of this procedure is demonstrated with an illustrative example.
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  • 99
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Styrene/acrylonitrile polymers ; Gradient elution ; Solubility effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Copoly(styrene/acrylonitrile) samples (S/AN) have been repeatedly separated according to composition by gradient HPLC with alkane hydrocarbons as a starting eluent A and dichloromethane (DCM) or tetrahydrofuran (THF) as a solvent B. In these systems, retention increased with AN content of the copolymers. The chemical nature of the column packings used had almost no influence on the retention of S/AN samples. The present paper shows thatn-pentane andn-heptane, when used in a given volumetric gradient with DCM+20% methanol as a solvent B, lead to identical solution characteristics of S/AN on silica columns. A similar result was obtained on C18 columns withn-heptane or cyclohexane, whereas gradient elution with toluene as a starting eluent caused insufficient resolution. Reversed phase separation of S/AN copolymers could be achieved on polystyrene gel columns through gradients with methanol as a starting eluent and DCM or THF as a solvent B. In both systems, retention decreased with increasing AN content of the copolymers. The elution characteristics were almost linear in the range 0–20 wt% AN. This behaviour can be understood in the context of polymer solubility: in both systems, the solubility borderline of S/AN has a distinct maximum at about 25 wt% AN. Reversed phase separation was achieved at the lefthand slope of these curves where the dissolution of a sample with a higher AN content requires less DCM or THF solvent than the dissolution of copolymers which are poorer in AN. This idea predicts that samples with more than 25 wt% AN should elute later than S/AN whose composition is near to the solubility maximum. This indeed was found with a copolymer containing 36.2 wt% AN.
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  • 100
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Formaldehyde in air ; Dinitrophenyl hydrazine ; Occupational hygiene studies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary This work describes an HPLC method for the determination of formaldehyde concentration in air. Traps containing 20–40 mesh silica gel coated with 2,4-dinitrophenylhydrazine (DNPH) are used. After aspiration of air the traps are eluted with methanol. The hydrazone formed is then separated on a C18 column using a mobile phase of methanolwater (50–50 v/v). The effluent is monitored with a UV detector at 365 nm. To calibrate and to compare this method with that of Niosh 2502 (traps coated with 2 benzylamino ethanol on Chromosorb 102), a mixing chamber that generated atmospheres of known concentration of formaldehyde was used.
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