Detailed Information on Publication Record
2014
Separation of oxalate, formate and glycolate in human body fluid samples by capillary electrophoresis with contactless conductometric detection
KUBÁŇ, Petr, Pavol ĎURČ, Miroslava BITTOVÁ and František FORETBasic information
Original name
Separation of oxalate, formate and glycolate in human body fluid samples by capillary electrophoresis with contactless conductometric detection
Authors
KUBÁŇ, Petr (203 Czech Republic, guarantor, belonging to the institution), Pavol ĎURČ (703 Slovakia, belonging to the institution), Miroslava BITTOVÁ (203 Czech Republic, belonging to the institution) and František FORET (203 Czech Republic, belonging to the institution)
Edition
Journal of Chromatography A, Amsterdam, Elsevier, 2014, 0021-9673
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10406 Analytical chemistry
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.169
RIV identification code
RIV/00216224:14310/14:00073642
Organization unit
Faculty of Science
UT WoS
000330256200031
Keywords in English
Capillary electrophoresis; Contactless conductivity detection; Toxic metabolites; Methanol intoxication; Ethylene glycol intoxication; Body fluid samples
Změněno: 4/10/2019 13:22, Mgr. Marie Šípková, DiS.
Abstract
V originále
A new method for rapid determination of toxic metabolites after methanol and ethylene glycol intoxication - oxalate, formate and glycolate in various body fluid samples (blood serum, saliva, urine, exhaled breath condensate) by capillary electrophoresis with contactless conductometric detection was developed. A selective separation of the three target analytes from other constituents present in the analyzed biological matrices was achieved in less than 6 min in a fused silica capillary of 25 mu m I.D. using an electrolyte comprising 50 mM L-histidine and 50 mM 2-(N-morpholino)ethanesulfonic acid at pH 6.1. The only sample preparation was dilution with deionized water. The limits of detection were 0.4, 0.6 and 1.3 mu M and limits of quantitation 1.3, 1.9 and 4.2 mu M for oxalate, formate and glycolate, respectively. The method provides a simple and rapid diagnostic test in suspected intoxication and is able to distinguish the ingested liquid, based on its metabolite trace. The method presents a fast screening tool that can be applicable in clinical practice. (C) 2013 Elsevier B.V. All rights reserved.
Links
ED1.1.00/02.0068, research and development project |
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GA13-21919S, research and development project |
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