TY - JOUR
T1 - Simultaneous determination of purine metabolites, creatinine and pseudouridine in ruminant urine by reversed-phase high-performance liquid chromatography
AU - Shingfield, Kevin John
AU - Offer, N W
N1 - Funding Information:
The authors would like to thank Kenny McIssac, Vesa Toivonen, Mervi Mikkola and Sari Siikjärvi for technical assistance during this work. SAC receives financial support from the Scottish Office Agriculture and Fisheries Department.
PY - 1999/2/19
Y1 - 1999/2/19
N2 - Determination of purine metabolites, pseudouridine and creatinine in both bovine and ovine urine using high-performance liquid chromatography (HPLC) is described. Following dilution and filtration, urine samples were analysed directly. Separation and quantification was achieved using a Spherisorb ODS II C
18 column (250x4.6 mm I.D.) under isocratic conditions. The mobile phase contained 7.5 mM ammonium dihydrogen phosphate, 10 mM sodium 1-heptane sulphonic acid and 1.0 mM triethylamine at pH 3.0. Chromatography was achieved at a flow-rate of 1.0 ml/min and monitoring column effluent at 218 nm. Total analysis time was 60 min. Recovery of all compound standards added to urine was above 96%. In all cases, close spectral matches of compound standards and corresponding identified peaks in ovine and bovine urine were obtained. Lowest detectable concentrations of allantoin, uric acid, xanthine, hypoxanthine, creatinine and pseudouridine were 1.1, 1.0, 1.0, 1.0, 3.0 and 0.4 μmol/l, respectively. Advantages of simultaneous determination of purine metabolites, creatinine and pseudouridine in ruminant urine collected from both sheep and cattle exist over current methods. Copyright (C) 1999 Elsevier Science B.V.
AB - Determination of purine metabolites, pseudouridine and creatinine in both bovine and ovine urine using high-performance liquid chromatography (HPLC) is described. Following dilution and filtration, urine samples were analysed directly. Separation and quantification was achieved using a Spherisorb ODS II C
18 column (250x4.6 mm I.D.) under isocratic conditions. The mobile phase contained 7.5 mM ammonium dihydrogen phosphate, 10 mM sodium 1-heptane sulphonic acid and 1.0 mM triethylamine at pH 3.0. Chromatography was achieved at a flow-rate of 1.0 ml/min and monitoring column effluent at 218 nm. Total analysis time was 60 min. Recovery of all compound standards added to urine was above 96%. In all cases, close spectral matches of compound standards and corresponding identified peaks in ovine and bovine urine were obtained. Lowest detectable concentrations of allantoin, uric acid, xanthine, hypoxanthine, creatinine and pseudouridine were 1.1, 1.0, 1.0, 1.0, 3.0 and 0.4 μmol/l, respectively. Advantages of simultaneous determination of purine metabolites, creatinine and pseudouridine in ruminant urine collected from both sheep and cattle exist over current methods. Copyright (C) 1999 Elsevier Science B.V.
KW - Animals
KW - Cattle
KW - Chromatography, High Pressure Liquid
KW - Creatinine
KW - Pseudouridine
KW - Purines
KW - Reproducibility of Results
KW - Sensitivity and Specificity
KW - Sheep
KW - Spectrophotometry, Ultraviolet
KW - Allantoin
KW - Uric acid
KW - Xanthine
KW - Hypoxanthine
KW - Purine metabolites
UR - http://www.scopus.com/inward/record.url?scp=0033047744&partnerID=8YFLogxK
U2 - 10.1016/S0378-4347(98)00549-0
DO - 10.1016/S0378-4347(98)00549-0
M3 - Article
C2 - 10080636
SN - 1387-2273
VL - 723
SP - 81
EP - 94
JO - Journal of chromatography B: Biomedical Sciences and Applications
JF - Journal of chromatography B: Biomedical Sciences and Applications
IS - 1-2
ER -