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R. Cunha, A. Sebastião, J. Ribeiro (1989)
Separation of adenosine triphosphate and its degradation products in innervated muscle of the frog by reverse phase high-performance liquid chromatographyChromatographia, 28
A. Krstulović, P. Brown, D. Rosie (1977)
Identification of nucleosides and bases in serum and plasma samples by reverse-phase high performance liquid chromatography.Analytical chemistry, 49 14
J. Idström, B. Soussi, E. Wanag, A. Bylund‐Fellenius (1990)
Analysis of purine nucleotides in muscle tissue by HPLC.Scandinavian journal of clinical and laboratory investigation, 50 5
A. Krstulović, R. Hartwick, P. Brown (1978)
Use of UV scanning techniques in the identification of serum constituents separated by high-performance liquid chromatography.Journal of chromatography, 158
R. Gayden, B. Watts, R. Beach, C. Benedict (1991)
Quantitation of adenosine, inosine and hypoxanthine in biological samples by microbore-column isocratic high-performance liquid chromatography.Journal of chromatography, 536 1-2
R. Hartwick, A. Krstulović, P. Brown (1979)
Identification and quantitation of nucleosides, bases and other UV-absorbing compounds in serum, using reversed-phase high-performance liquid chromatography : II. Evaluation of human eraJournal of Chromatography A, 186
Tikhonov YuV, A. Pimenov, S. Uzhevko, R. Toguzov (1990)
Ion-pair high-performance liquid chromatography of purine compounds in the small intestinal mucosa of children with coeliac disease.Journal of chromatography, 520
G. Severini, L. Aliberti (1987)
Liquid-chromatographic determination of inosine, xanthine, and hypoxanthine in uremic patients receiving hemodialysis treatment.Clinical chemistry, 33 12
J. Banks, M. Novotny (1989)
Microcolumn liquid chromatography of small nucleic acid constituentsJournal of Chromatography A, 475
R. Berne, R. Curnish, J. Gidday, R. Rubio (1986)
Measurement of Femtomolar Concentrations of AdenosineJournal of Liquid Chromatography & Related Technologies, 9
G. Walter, J. Phillis, Michael O'Reagan (1988)
Determination of rat cerebrospinal fluid concentrations of adenosine, inosine, hypoxanthine, xanthine and uric acid by high performance liquid chromatographyJournal of Pharmacy and Pharmacology, 40
R. Simmonds, R. Harkness (1981)
High-performance liquid chromatographic methods for base and nucleoside analysis in extracellular fluids and in cells.Journal of chromatography, 226 2
R. Hartwick, P. Brown (1976)
Evaluation of microparticle chemically bonded reversed-phase packings in the high-pressure liquid chromatographic analysis of nucleosides and their bases.Journal of chromatography, 126
A. Werner, W. Siems, J. Kowalewski, G. Gerber (1989)
Interrelationships between purine nucleotide degradation and radical formation during intestinal ischaemia and reperfusion: an application of ion-pair high-performance liquid chromatography of nucleotides, nucleosides and nucleobases.Journal of chromatography, 491 1
A. Werner, W. Schneider, W. Siems, T. Grune, C. Schreiter (1989)
Ion-pair reversed phase HPLC determination of nucleotides, nucleosides and nucleobases — Application to nucleotide metabolism in hepatocytesChromatographia, 27
C. Gehrke, K. Kuo, G. Davis, R. Suits, T. Waalkes, E. Borek (1978)
Quantitative high-performance liquid chromatography of nucleosides in biological materials.Journal of chromatography, 150 2
P. Brown (1970)
The rapid separation of nucleotides in cell extracts using high-pressure liquid chromatography.Journal of chromatography, 52 2
K. Miura, M. Okumura, T. Yukimura, K. Yamamoto (1991)
Fluorometric determination of plasma adenosine concentrations using high-performance liquid chromatography.Analytical biochemistry, 196 1
B. Guattari (1989)
Simultaneous quantitative high-performance liquid chromatographic determination of cyclic adenosine 3',5'-monophosphate and adenosine in mouse brain after microwave irradiation: application to isoprenaline effect in vivo.Journal of chromatography, 489 2
An analytical procedure has been developed for the assay of adenosine and some metabolites in brain tissue extracts of rats. This paper reports the extraction method, the technique adopted to avoid enzymatic transformations and the chromatographic conditions for the identification and quantitation of these nucleosides and bases. Peaks in the chromatograms of brain tissue extracts were identified by retention times, absorbance ratios of reference compounds and by enzymatic peak-shift.
Chromatographia – Springer Journals
Published: Dec 1, 1992
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