Separation of attogram terpenes by the capillary zone electrophoresis with fluorometric detection
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20933239
DOI
10.1016/j.chroma.2010.09.038
PII: S0021-9673(10)01258-6
Knihovny.cz E-zdroje
- MeSH
- biofilmy * MeSH
- butyráty chemie MeSH
- Candida albicans chemie metabolismus MeSH
- cholesterol chemie MeSH
- elektroforéza kapilární metody MeSH
- ergosterol chemie MeSH
- estron chemie MeSH
- farnesol chemie izolace a purifikace metabolismus MeSH
- fluorometrie metody MeSH
- polymery chemie MeSH
- quorum sensing MeSH
- senzitivita a specificita MeSH
- terpeny chemie izolace a purifikace MeSH
- tetrahydronaftaleny chemie MeSH
- vitamin A chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetyl methyl tetramethyl tetralin MeSH Prohlížeč
- butyráty MeSH
- cholesterol MeSH
- ergosterol MeSH
- estron MeSH
- farnesol MeSH
- polymery MeSH
- terpeny MeSH
- tetrahydronaftaleny MeSH
- vitamin A MeSH
An original method based on capillary zone electrophoresis with fluorimetric detection has been developed for the determination of terpenic compounds. The method is based on the separation of a terpenes dynamically labeled by the non-ionogenic tenside poly(ethylene glycol) pyrenebutanoate, which was used previously for the labeling of biopolymers. The background electrolytes were composed of taurine-Tris buffer (pH 8.4). In addition to the non-ionogenic tenside aceton and poly(ethylene glycol) were used as the additives. The capillary zone electrophoresis with fluorometric detection at the excitation wavelength 335 nm and the emission wavelength 463 nm was successfully applied to the analysis of tonalid, cholesterol, vitamin A, ergosterol, estrone and farnesol at level of 10(-17) mol L(-1). Farnesol, is produced by Candida albicans as an extracellular quorum-sensing molecule that influences expression of a number of virulence factors, especially morphogenesis and biofilm formation. It enables this yeast to cause serious nosocomial infections. The sensitivity of this method was demonstrated on the separation of farnesol directly from the cultivation medium.
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