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  • Reversed-phase  (2)
  • L-leucine derivatives  (1)
  • Micro-columns  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 15 (1982), S. 737-742 
    ISSN: 1612-1112
    Keywords: LC ; Reversed-phase ; Chloramphenicol and monosuccinate ester ; Piglet plasma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A method for the determination of chloramphenicol and its monosuccinate ester in piglet plasma is described. It involves precipitation of plasma proteins by addition of methanol to the plasma sample, followed by injection of the supernate onto the column. Chloramphenicol and its ester are separated using a LiChrosorb RP-18 column and phosphate buffer pH 4.9 containing 30% methanol as eluent. Determination of chloramphenicol and its monosuccinate ester in pig plasma was made with a precision of 2.6% and 2.4% (relative standard deviation) at drug levels of 2 and 4 μg·cm−3, respectively. Stability data for the chloramphenicol monosuccinate ester are also presented.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 13 (1980), S. 741-744 
    ISSN: 1612-1112
    Keywords: Miniaturization ; HPLC ; Micro-columns ; 0.67 mm3 micro flow-cell ; Sulphonamides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Methods for the construction of micro-columns equipped with low dead volume end fittings and an easy way to miniaturize a standard flow-cell to a volume of 0.67 mm3 are described. Operation characteristics of the microcolumns were evaluated by plate height versus linear velocity and plate height versus capacity factor plots. The influence of the volume of the flow-cell on the resolution is also demonstrated. An improvement of the resolution factor (RS) from 0.9 to 1.45 between sulphapyridine and sulphamerazine was obtained by using the 0.67 mm3 flow-cell instead of the 12.5 mm3 original flow-cell. The influence of the sample volume on the separation efficiency is also shown.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 14 (1981), S. 529-534 
    ISSN: 1612-1112
    Keywords: HPLC ; Reversed-phase ; L-DOPA, purity of ; L-leucine derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The separation and quantitation of D-DOPA as an impurity in L-DOPA is described. The method involves formation of the diastereomeric derivatives of DOPA with tert-butoxycarbonyl-L-leucine hydroxysuccinimide ester. Separation of the diastereomers was performed by reversed-phase liquid chromatography on LiChrosorb RP-18 and acetonitrile-phosphate buffer with addition of N,N-dimethyloctylamine as the mobile phase. The reproducibility of the method was 5.9% (relative standard deviation) at D-DOPA levels of 0.5% in L-DOPA drug substance.
    Type of Medium: Electronic Resource
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