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  • 1
    ISSN: 1612-1112
    Keywords: Coupled-column liquid chromatography ; Affinity chromatography ; Restricted access material ; Nonporous microparticulate silica ; Catecholamines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A coupled-column LC-method for fast, direct and routine quantitation of free parent catecholamines norepinephrine, epinephrine and dopamine in human urine has been developed. Direct injection of untreated samples followed by system-integrated, sample cleanup was achieved using a restricted-access affinity precolumn packed with a boronic acid-modified, copolymer support. Analytes were selectively extracted from the urine matrix at an alkaline pH by covalent affinity bonding. Desorption and transfer of the catecholamines to a nonporous, microparticulate-silica analytical column was by changing the pH of the mobile phase to an acidic value. Separation was by ion-pair RP-HPLC under aqueous conditions without addition of organic modifier. Analytes were detected by their natural fluorescence. Limits of quantitation were 5.57, 1.75 and 36.81 pmol for norepinephrine, epinephrine and dopamine, respectively. Urine levels could be quantified with a precision of about 2%. Mean recoveries of norepinephrine, epinephrine and dopamine were 98.18, 102.0 and 101.12%. Using a nonporous packing in the analytical column, analytical times and solvent consumption were reduced considerably compared to conventional porous silica columns.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 25 (1988), S. 199-204 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Column switching ; Catecholamines ; Urine ; Serum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary We developed an automated, two-column HPLC-method that can be used routinely to quantify the catecholamines norepinephrine and epinephrine in body fluids. The method is based on a new, laboratory-prepared SEC-HPAC column material, on the application of a microprocessor-controlled column-switching technique, and on the use of an integrated reaction system for postcolumn derivatization and trihydroxyindol-fluorescence monitoring. It allows the direct injection (upto 500 μl) of an appropriate biological fluid and distinguishes on its integrated sample-processing mode, its practicability, its chemoselectivity and-specivity, its detection limit (2 pg), its within- and between-run precision and its speed of analysis.
    Type of Medium: Electronic Resource
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