Neopterin, a pyrazinopyrimidine compound, serves as a marker of cellular immune system activation, and it can be used as a prognostic predictor for certain types of diseases. We propose a new simple HPLC method to measure serum neopterin with highly sensitive fluorimetric detection. After TCA serum protein precipitation, the supernatant was diluted five times, injected into a C-18 reversed-phase column and eluted at a flow rate of 1.5 mL/min by an isocratic water-acetonitrile (99:1) mobile phase. The natural fluorescence of the molecule was detected at excitation wavelength 353 nm and emission 438 nm. In these conditions the neopterin retention time was about 4 min. Our proposed method was compared with a validated chromatographic separation, and the obtained data of the serum neopterin from 35 healthy volunteers were analysed by Passing-Bablok regression and Bland-Altman test. Neopterin measurement in healthy subjects was also employed to investigate on its potential relationships with plasma thiols levels. Copyright (C) 2004 John Wiley Sons, Ltd.
A new HPLC method for serum neopterin measurement and relationships with plasma thiols levels in healthy subjects / Carru, Ciriaco; Zinellu, Angelo; Sotgia, S; Serra, R; Usai, Mf; Pintus, Gianfranco; Pes, Giovanni Mario; Deiana, Luca. - In: BIOMEDICAL CHROMATOGRAPHY. - ISSN 0269-3879. - 18:6(2004), pp. 360-366. [10.1002/bmc.325]
A new HPLC method for serum neopterin measurement and relationships with plasma thiols levels in healthy subjects
CARRU, Ciriaco;ZINELLU, Angelo;Sotgia S;PINTUS, Gianfranco;PES, Giovanni Mario;DEIANA, Luca
2004-01-01
Abstract
Neopterin, a pyrazinopyrimidine compound, serves as a marker of cellular immune system activation, and it can be used as a prognostic predictor for certain types of diseases. We propose a new simple HPLC method to measure serum neopterin with highly sensitive fluorimetric detection. After TCA serum protein precipitation, the supernatant was diluted five times, injected into a C-18 reversed-phase column and eluted at a flow rate of 1.5 mL/min by an isocratic water-acetonitrile (99:1) mobile phase. The natural fluorescence of the molecule was detected at excitation wavelength 353 nm and emission 438 nm. In these conditions the neopterin retention time was about 4 min. Our proposed method was compared with a validated chromatographic separation, and the obtained data of the serum neopterin from 35 healthy volunteers were analysed by Passing-Bablok regression and Bland-Altman test. Neopterin measurement in healthy subjects was also employed to investigate on its potential relationships with plasma thiols levels. Copyright (C) 2004 John Wiley Sons, Ltd.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.