A high-performance liquid chromatographic method for the determination of pseudouridine and uric acid in native human urine and ultrafiltrated serum
✍ Scribed by Heinrich Topp; Gernot Sander; Gesa Heller-Schöch; Gerhard Schöch
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 471 KB
- Volume
- 150
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
✦ Synopsis
A simple and reliable HPLC method for quantitative determination of pseudouridine and uric acid in human urine and serum using a cation-exchange resin is described. This method is straightfonvard (12 runs of urine samples per day since the sample is only diluted into buffer and then chromatographed), sensitive, and highly reproducible. The column is stable over long periods (-3 months of uninterrupted use at a time; it is thereafter easily restored to the original state). Mean excretion values for pseudouridine (in rmol/mmol creatinine) are 26.4 + 3.1 (I 7 female adults), 23.8 + 2.5 (12 male adults), 164.7 f 32.2 (37 male preterm infants): mean values for uric acid (pmol/mmol creatinine) are, respectively, 310.3 + 90.5, 278.2 f 56.1. and 1108 t 3 14. Human serum is deproteinized by pressure ultrafiltration in microcollodion bags with a nominal exclusion molecular weight of 12.400 and then put directly onto the HPLC column. The complete procedure takes 4 h. 0 1985 Academic PW, 1~.
📜 SIMILAR VOLUMES
A high-performance liquid chromatographic method has been developed for the determination of a-keto acids in human urine and plasma. These acids were prepurified using a column of hydrazide gel and derivatized with o-phenylenediamine into 2-quinoxalinol derivatives, which were extracted into ethyl a
Spironolactone (I), a potassium sparing diuretic, is widely used in the treatment of edema. Metabolic degradation starts with rapid deacetylation, leading to the short lived a-thiol [l]. Subsequent elimination of hydrogen sulfide yields canrenone (II), which exists in enzymatic equilibrium with canr
A reversed-phase high-performance liquid chromatography assay for mangiferin in rat plasma and urine was developed. Rutin was employed as an internal standard. The mobile phase consisted of acetonitrile-water (16:84, v/v) containing 3% acetic acid at a flow rate of 1 mL/min. Detection was at 257 and
A high-performance liquid chromatographic method was developed to determine stobadin pharmacokinetics in dog and man. The relative bioavailability of stobadin dipalmitate compared with dihydrochloride was 46.4 per cent in dog. In man peak serum concentrations ranged from 12 to 289 ng ml-1 after a si