Separation and determination of 11 marker pteridines in human urine by liquid chromatography and fluorimetric detection

✍ Scribed by Alicia M. de Llanos; Anunciación Espinosa-Mansilla; Florentina Cañada-Cañada; Arsenio M. de la Peña

• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 301 KB
• Volume: 34
• Category: Article
• ISSN: 1615-9306
• DOI: 10.1002/jssc.201000900

✦ Synopsis

Abstract

A simple liquid chromatographic method has been developed to achieve the complete separation and determination of a wide range of pteridinic compounds and creatinine (CREA) in urine samples, in just one run. The influences of mobile phase composition and buffer pH have been studied. The optimized mobile phase was composed of a Tris‐HCl buffer (15 mmol/L) at pH 6.10 solution (eluent A) and a Tris‐HCl buffer (15 mmol/L) at pH 6.40 solution (eluent B), in gradient mode. Analytes were determined by fluorimetric detection, exciting at 272 nm, and measuring the fluorescence emission at three wavelengths, 410, 445 and 465 nm. CREA, as a reference of metabolites excretion in urine, was determined by photometric detection at 230 nm. Pteridines detection limits varied from 0.2 to 6.1 ng/mL, and 0.2 g/mL for CREA. Calculated precision values expressed as RSD (%) varied from 1.1 to 5.9. Two different oxidation procedures for urine samples were optimized. The neopterin/biopterin ratios found were 0.98 and 0.86 for adults and children, respectively, by means of the alkaline iodide/iodine oxidation and 0.45 and 0.57 using neutral KMnO~4~ oxidation.