Fast determination of ethylene glycol, 1,2-propylene glycol and glycolic acid in blood serum and urine for emergency and clinical toxicology by GC-FID
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
25159437
DOI
10.1016/j.talanta.2014.07.020
PII: S0039-9140(14)00575-X
Knihovny.cz E-zdroje
- Klíčová slova
- Chloroformate, Experimental design, GC, Glycolic acid, Glycols,
- MeSH
- chromatografie plynová metody MeSH
- ethylenglykol krev otrava moč MeSH
- glykoláty krev otrava moč MeSH
- lidé MeSH
- plamínková ionizace metody MeSH
- propylenglykol krev otrava moč MeSH
- sérum chemie MeSH
- studie případů a kontrol MeSH
- toxikologie metody MeSH
- urgentní zdravotnické služby * MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- ethylenglykol MeSH
- glycolic acid MeSH Prohlížeč
- glykoláty MeSH
- propylenglykol MeSH
A simple, cost effective, and fast gas chromatography method with flame ionization detection (GC-FID) for simultaneous measurement of ethylene glycol, 1,2-propylene glycol and glycolic acid was developed and validated for clinical toxicology purposes. This new method employs a relatively less used class of derivatization agents - alkyl chloroformates, allowing the efficient and rapid derivatization of carboxylic acids within seconds while glycols are simultaneously derivatized by phenylboronic acid. The entire sample preparation procedure is completed within 10 min. To avoid possible interference from naturally occurring endogenous acids and quantitation errors 3-(4-chlorophenyl) propionic acid was chosen as an internal standard. The significant parameters of the derivatization have been found using chemometric procedures and these parameters were optimized using the face-centered central composite design. The calibration dependence of the method was proved to be quadratic in the range of 50-5000 mg mL(-1), with adequate accuracy (92.4-108.7%) and precision (9.4%). The method was successfully applied to quantify the selected compounds in serum of patients from emergency units.
Citace poskytuje Crossref.org