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Development of a fast method for simultaneous determination of hippuric acid, mandelic acid, and creatinine in urine by capillary zone electrophoresis using polymer multilayer-coated capillary

This paper reports the development of a fast separation method employing capillary zone electrophoresis for the simultaneous determination of hippuric acid, mandelic acid, and creatinine in samples of urine using a coated capillary. The background electrolyte was composed of 10 mmol L −1 tris(hydrox...

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Published in:Analytical and bioanalytical chemistry 2017-03, Vol.409 (7), p.1943-1950
Main Authors: Vitali, Luciano, Gonçalves, Samantha, Rodrigues, Victor, Fávere, Valfredo T., Micke, Gustavo A.
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cited_by cdi_FETCH-LOGICAL-c476t-1569afde630decc37b24faaee6968b1c5f2c347653315bc0ff01344a6669e90b3
cites cdi_FETCH-LOGICAL-c476t-1569afde630decc37b24faaee6968b1c5f2c347653315bc0ff01344a6669e90b3
container_end_page 1950
container_issue 7
container_start_page 1943
container_title Analytical and bioanalytical chemistry
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creator Vitali, Luciano
Gonçalves, Samantha
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Fávere, Valfredo T.
Micke, Gustavo A.
description This paper reports the development of a fast separation method employing capillary zone electrophoresis for the simultaneous determination of hippuric acid, mandelic acid, and creatinine in samples of urine using a coated capillary. The background electrolyte was composed of 10 mmol L −1 tris(hydroxymethyl)aminomethane and 30 mmol L −1 2-hydroxy-isobutyric acid at pH 3.6. The internal standard was 3,5-dihydroxybenzoic acid. Separations were performed in a fused silica capillary (32 cm total length, 8.5 cm effective length, and 50 μm internal diameter) coated with crosslinked hydroxypropyltrimethyl ammonium chloride chitosan and κ-carrageenan. Direct UV detection was performed at a wavelength of 200 nm. Samples and standards were injected hydrodynamically (−50 mbar, 3 s) using the short-end injection procedure. The electrophoretic system was operated under constant voltage of 30 kV with positive polarity on the injection side. The separation time for hippuric acid, mandelic acid, and creatinine was less than 70 s. The evaluation of some analytical parameters of the method for the three analytes showed good linearity ( R 2  > 0.99), limit of detections of 0.21 to 0.63 mg L −1 , inter-day precision better than 3.0% (peak area), and recovery in the range of 98 to 106%. The method developed was applied in the analysis of the three analytes in urine samples. Graphical Abstract New method using capillary zone electrophoresis for analysis of creatinine, hippuric acid and mandelic acid in urine
doi_str_mv 10.1007/s00216-016-0142-4
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The background electrolyte was composed of 10 mmol L −1 tris(hydroxymethyl)aminomethane and 30 mmol L −1 2-hydroxy-isobutyric acid at pH 3.6. The internal standard was 3,5-dihydroxybenzoic acid. Separations were performed in a fused silica capillary (32 cm total length, 8.5 cm effective length, and 50 μm internal diameter) coated with crosslinked hydroxypropyltrimethyl ammonium chloride chitosan and κ-carrageenan. Direct UV detection was performed at a wavelength of 200 nm. Samples and standards were injected hydrodynamically (−50 mbar, 3 s) using the short-end injection procedure. The electrophoretic system was operated under constant voltage of 30 kV with positive polarity on the injection side. The separation time for hippuric acid, mandelic acid, and creatinine was less than 70 s. The evaluation of some analytical parameters of the method for the three analytes showed good linearity ( R 2  &gt; 0.99), limit of detections of 0.21 to 0.63 mg L −1 , inter-day precision better than 3.0% (peak area), and recovery in the range of 98 to 106%. The method developed was applied in the analysis of the three analytes in urine samples. 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The background electrolyte was composed of 10 mmol L −1 tris(hydroxymethyl)aminomethane and 30 mmol L −1 2-hydroxy-isobutyric acid at pH 3.6. The internal standard was 3,5-dihydroxybenzoic acid. Separations were performed in a fused silica capillary (32 cm total length, 8.5 cm effective length, and 50 μm internal diameter) coated with crosslinked hydroxypropyltrimethyl ammonium chloride chitosan and κ-carrageenan. Direct UV detection was performed at a wavelength of 200 nm. Samples and standards were injected hydrodynamically (−50 mbar, 3 s) using the short-end injection procedure. The electrophoretic system was operated under constant voltage of 30 kV with positive polarity on the injection side. The separation time for hippuric acid, mandelic acid, and creatinine was less than 70 s. 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subjects Acids
Alpha hydroxy acids
Ammonium
Analytical Chemistry
Biochemistry
Blood vessels
Capillary zone
Carboxylic acids
Characterization and Evaluation of Materials
Chemical properties
Chemistry
Chemistry and Materials Science
Chromatography
Creatinine
Creatinine - urine
Electrolytes
Electrophoresis
Electrophoresis, Capillary - methods
Food Science
Hippurates - urine
Injection
Kidney diseases
Laboratory Medicine
Mandelic Acids - urine
Methods
Monitoring/Environmental Analysis
Polymers
Polymers - chemistry
Research Paper
Scientific imaging
Silica
Ultraviolet radiation
Urine
title Development of a fast method for simultaneous determination of hippuric acid, mandelic acid, and creatinine in urine by capillary zone electrophoresis using polymer multilayer-coated capillary
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