Micro-electromembrane extraction across free liquid membranes. Instrumentation and basic principles
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24792701
DOI
10.1016/j.chroma.2014.04.047
PII: S0021-9673(14)00615-3
Knihovny.cz E-zdroje
- Klíčová slova
- Free liquid membranes, Micro-electromembrane extraction, SPADNS, UV–vis spectrophotometry,
- MeSH
- anionty chemie MeSH
- barvicí látky chemie MeSH
- elektroforéza kapilární metody MeSH
- kationty chemie MeSH
- membrány umělé * MeSH
- pentanoly chemie MeSH
- reprodukovatelnost výsledků MeSH
- spektrální analýza MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- anionty MeSH
- barvicí látky MeSH
- kationty MeSH
- membrány umělé * MeSH
- n-pentanol MeSH Prohlížeč
- pentanoly MeSH
A micro-electromembrane extraction (μ-EME) technique using electrically induced transfer of charged analytes across free liquid membranes (FLMs) was presented. A disposable extraction unit was proposed and it was made of a short segment of transparent perfluoroalkoxy tubing, which was successively filled with three liquid plugs serving as acceptor solution, FLM and donor solution. These plugs formed a three-phase extraction system, which was precisely defined, that was stable and required μL to sub-μL volumes of all respective solutions. Basic instrumental set-up and extraction principles of μ-EME were examined using an anionic and a cationic dye, 4,5-dihydroxy-3-(p-sulfophenylazo)-2,7-naphthalene disulfonic acid trisodium salt (SPADNS) and crystal violet, respectively. Transfers of the charged dyes from donor into acceptor solutions across FLMs consisting of 1-pentanol were visualized by a microscope camera and quantitative measurements were performed by UV-vis spectrophotometry. The effects of operational parameters of μ-EME system were comprehensively investigated and experimental measurements were accompanied with theoretical calculations. Extraction recoveries above 60% were achieved for 5min μ-EME of 1mM SPADNS at 100V with repeatability values below 5%. Selectivity of FLMs was additionally examined by capillary electrophoretic analyses of acceptor solutions and the potential of FLMs for μ-EME pretreatment of samples with artificial complex matrices was demonstrated.
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