Plasma creatinine and creatine quantification by capillary electrophoresis diode array detector
Articolo
Data di Pubblicazione:
2005
Citazione:
Plasma creatinine and creatine quantification by capillary electrophoresis diode array detector / Zinellu, A., Caria, M.A., Tavera, C., Sotgia, S., Chessa, R., Deiana, L., Carru, C.. - In: ANALYTICAL BIOCHEMISTRY. - ISSN 0003-2697. - 342:(2005), pp. 186-193. [10.1016/j.ab.2005.01.045]
Abstract:
Traditional clinical assays for nonprotein nitrogen compounds, such as creatine and creatinine, have focused on the use of
enzymes or chemical reactions that allow measurement of each analyte separately. Most of these assays are mainly directed to urine
quantiWcation, so that their applicability on plasma samples is frequently hard to perform. This work describes a simple free zone
capillary electrophoresis method for the simultaneous measurement of creatinine and creatine in human plasma. The eVect of analytical
parameters such as concentration and pH of Tris–phosphate running buVer and cartridge temperature on resolution, migration
times, peak areas, and eYciency was investigated. Good separation was achieved using a 60.2-cm£75-m uncoated silica capillary,
75mmol/L Tris–phosphate buVer, pH 2.25, at 15 °C, in less than 8min. We compared the present method to a validated capillary
electrophoresis assay, by measuring plasma creatinine in 120 normal subjects. The obtained data were compared by the Passing–
Bablok regression and the Bland–Altman test. Moreover the performance of the developed method was assessed by measuring creatine
and creatinine in 16 volunteers prior to and after a moderate physical exercise.
2005 Elsevier Inc. All rights reserved.
enzymes or chemical reactions that allow measurement of each analyte separately. Most of these assays are mainly directed to urine
quantiWcation, so that their applicability on plasma samples is frequently hard to perform. This work describes a simple free zone
capillary electrophoresis method for the simultaneous measurement of creatinine and creatine in human plasma. The eVect of analytical
parameters such as concentration and pH of Tris–phosphate running buVer and cartridge temperature on resolution, migration
times, peak areas, and eYciency was investigated. Good separation was achieved using a 60.2-cm£75-m uncoated silica capillary,
75mmol/L Tris–phosphate buVer, pH 2.25, at 15 °C, in less than 8min. We compared the present method to a validated capillary
electrophoresis assay, by measuring plasma creatinine in 120 normal subjects. The obtained data were compared by the Passing–
Bablok regression and the Bland–Altman test. Moreover the performance of the developed method was assessed by measuring creatine
and creatinine in 16 volunteers prior to and after a moderate physical exercise.
2005 Elsevier Inc. All rights reserved.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Capillary electrophoresis, Tris–phosphate buVer, Creatinine, Creatine
Elenco autori:
Zinellu, Angelo; Caria, Marcello Alessandro; Tavera, C.; Sotgia, S.; Chessa, R.; Deiana, Luca; Carru, Ciriaco
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