ŠEVČÍKOVÁ, Petra, Zdeněk GLATZ and Josef TOMANDL. Determination of homocysteine in human plasma by mekc and in-capillary detection reaction with 2,2-dipyridyldisulfide. Journal of Chromatography A. Netherlands: Elsevier, 2003, vol. 990, (1+2), p. 197-204. ISSN 0021-9606.
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Basic information
Original name Determination of homocysteine in human plasma by mekc and in-capillary detection reaction with 2,2-dipyridyldisulfide
Authors ŠEVČÍKOVÁ, Petra (203 Czech Republic), Zdeněk GLATZ (203 Czech Republic, guarantor, belonging to the institution) and Josef TOMANDL (203 Czech Republic, belonging to the institution).
Edition Journal of Chromatography A, Netherlands, Elsevier, 2003, 0021-9606.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10600 1.6 Biological sciences
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.950
RIV identification code RIV/00216224:14310/03:00007946
Organization unit Faculty of Science
UT WoS 000181647200022
Keywords in English Capillary electrophoresis; on-column derivatization; homocysteine
Tags Capillary electrophoresis, homocysteine, On-Column Derivatization
Changed by Changed by: doc. RNDr. Josef Tomandl, Ph.D., učo 47. Changed: 6/6/2012 08:30.
Abstract
In this paper, we present a new method for homocysteine quantitation in human plasma based on in-capillary reaction of homocysteine with 2,2-dipyridyldisulfide. Homocysteine is in this so called thiol-exchange reaction quantitatively transformed in mixed disulfide concomitantly with formation of equimolar amount of 2-thiopyridone that is further separated by MEKC and determined specifically at 343 nm. The concentration of homocysteine is thus estimated indirectly from the result of 2-thiopyridone determination. The linear detection range for concentration versus peak area for the assay was from 0.03 to 3 mM (correlation coefficient 0.994) with a detection limit of 6 mM and a limit of quantitation 20 mM. The inter-day reproducibility of the peak area and the migration time were 1.37 % and 0.05 %, respectively. The method is simple, relatively rapid and can be easily automated. Moreover the common CE apparatus with UV detector can be used to distinguish between normal and pathological hyperhomocysteinemia plasma samples.
Links
GA203/02/1447, research and development projectName: Kapilární elektrochromatografie v lineárních a planárních mikrostrukturách s využitím polymerních náplní
Investor: Czech Science Foundation, Capillary electrochromatography in linear and planar microstructures using polymer beds
GA203/03/1125, research and development projectName: Využití kapilární zónové elektroforézy pro studium enzymů
Investor: Czech Science Foundation, Application of capillary zone electrophoresis for the study of enzymes
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