In a previous report', we described the high-pressure liquid chromatographic (HPLC) separation and quantitation of isomeric hydroxyanilines involving reversedphase partition chromatography of the mixtures on a C,, column with the mobile phase methanol-water (15%) containing 0.26 M ammonium acetate (
High-pressure liquid chromatographic-reductive electrochemical detection analysis of serum trans-phylloquinone
โ Scribed by Takami Ueno; J.W. Suttie
- Book ID
- 102986905
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 548 KB
- Volume
- 133
- Category
- Article
- ISSN
- 0003-2697
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โฆ Synopsis
A sensitive method for the determination of human serum trans-phylloquinone levels has been developed. Serum samples were extracted with hexane and subjected to preliminary separation on a silica semipreparative HPLC column with an 80% recovery as determined by the addition of [3H]phylloquinone. The portion of the eluate containing trans-phylloquinone was dried and injected into a PBondapak C-18 analytical HPLC column, and the concentration of the vitamin was determined by reductive electrochemical detection utilizing a glassy carbon electrode and an A&A.@ reference electrode. The presumed vitamin peak was confirmed as trans-phylloquinone by rechromatography at different HPLC conditions, hydrodynamic voltamography, and photodegradation. As little as 300 pg/ml trans-phylloquinone could be detected, and normal human serum concentrations were found to be in the range of 1 rig/ml. KEY WORDS: vitamin K, trans-phylloquinone; HPLC, plasma electrochemical potential detection.
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