Simultaneous analysis of substrates,products, and inhibitors of xanthine oxidase by high-pressure liquid chromatography and gas chromatography |
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Authors: | Gerald J. Putterman Badaruddin Shaikh Margarette R. Hallmark Cheryl G. Sawyer Catherine V. Hixson Fulvio Perini |
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Affiliation: | 1. Biological Markers Program, National Cancer Institute, Frederick Cancer Research Center, Frederick, Maryland 21701 USA;2. Carcinogenesis Program, National Cancer Institute, Frederick Cancer Research Center, Frederick, Maryland 21701 USA |
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Abstract: | Procedures are presented for the simultaneous analysis of hypoxanthine, xanthine, allopurinol, oxipurinol, and uric acid in standard mixtures and physiological fluids using gas chromatography (gc) or high-pressure liquid chromatography (hplc). Excellent correlation was obtained between the two methods for hypoxanthine, xanthine, oxipurinol, and uric acid. There are advantages and disadvantages to both methods. hplc requires no prior derivatization, uses isocratic elution with a buffer containing no organic solvent, and has 50- to 100-fold greater sensitivity than gc. Simpler methods of prepurification, readily adapted to clinical laboratories, can be used for hplc analysis. Although substances that are found in some urine samples from cancer patients interfere with hplc, separations by gc are not affected by these substances. |
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