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Showing papers by "Tyge Greibrokk published in 2002"


Journal ArticleDOI
TL;DR: A miniaturized temperature-programmed packed capillary liquid chromatographic method with on-column large volume injection and UV detection for the simultaneous determination of the three selective serotonin reuptake inhibitors citalopram, fluoxetine, paroxetines and their metabolites in plasma is presented.

63 citations


Journal Article
TL;DR: In this paper, a miniaturized temperature-programmed packed capillary liquid chromatographic method with on-column large volume injection and UV detection for the simultaneous determination of the three selective serotonin reuptake inhibitors citalopram, fluoxetine, paroxetINE and their metabolites in plasma is presented.

62 citations


Journal ArticleDOI

24 citations


Journal ArticleDOI

18 citations


Journal ArticleDOI
27 Jun 2002-Analyst
TL;DR: A two-valve sub-ambient temperature-promoted reversed-phase packed-capillary liquid-chromatography column-switching system has been tailored for sensitive determination of hydrophobic compounds.
Abstract: A two-valve sub-ambient temperature-promoted reversed-phase packed-capillary liquid-chromatography column-switching system has been tailored for sensitive determination of hydrophobic compounds. Such compounds are not easily dissolved in solvent mixtures of non-eluting properties that traditionally are used for solute enrichment in reversed-phase liquid chromatography. Enrichment-column solute focusing of large sample volumes was promoted by use of sub-ambient temperatures only, allowing the use of sample solvents that were stronger or equal to the mobile phase solvent strength. Subsequent column switching and enrichment-column temperature increment provided efficient low-dispersion back-flushed enrichment-column solute desorption onto the analytical column, where the solute was subjected to temperature-programmed gradient action. The antioxidant, Irganox 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) extracted from low density polyethylene with 100% acetonitrile served as a hydrophobic model compound. The mobile phase consisted of acetonitrile containing 10 mM triethylamine and formic acid, and the 0.25 mm id enrichment-column and analytical column in lengths of 27 and 250 mm, respectively, were packed with 3.5 µm Kromasil C18 particles. Sample volumes of up to 500 µL were successfully focused on the enrichment column at 5 °C using loading flow rates of up to 40 µL min−1 prior to temperature programming to 90 °C. The concentration limit of detection of Irganox 1076 was 6 ng mL−1when using an injection volume of 500 µL. The within-assay precision was in the range 3.5–6.8% (n = 6) while the between-day precision was 7.5% (n = 3) relative standard deviation. The method was linear within the investigated mass range 3–100 ng (R2 = 0.9993).

14 citations