Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2006-6-12
pubmed:abstractText
A comparative study of peak shape, elution behavior, elution strength and resolution of seven beta-blockers (acebutolol, alprenolol, labetalol, metoprolol, nadolol, pindolol and propranolol) chromatographed with aqueous-organic mobile phases containing additives such as the ionic liquid (IL) 1-butyl-3-methylimidazolium (BMIM BF(4)) or triethylamine (TEA) is performed using a conventional reversed-phase Kromasil C(18) column and isocratic elution. The efficiencies and asymmetry factors achieved for the group of beta-blockers in the Kromasil C(18) column improve when the cationic modifiers are added to the aqueous-organic mobile phase as competing additives for the silanol active sites. BMIM BF(4) is a significantly better additive compared to TEA. The improvement is more notably for the asymmetry factor, BMIM BF(4) allowing to obtain higher plate numbers than TEA at the same concentration. The effects of both modifiers on elution strength and retention factors are, however, different. TEA decreases the solute retention factors when BMIM BF(4) does not change them significantly. Using other additives taken in the IL family such as 1-butyl-3-methylimidazolium hexafluorophosphate and 1-octyl-3-methylimidazolium tetrafluoroborate (OMIM BF(4)), it is shown that the silanol screening effect is always observed, due to the IL cation, when it is possible to increase or to decrease the solute retention factors playing with the hydrophobic nature or chaotropic character of its anion.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0021-9673
pubmed:author
pubmed:issnType
Print
pubmed:day
30
pubmed:volume
1119
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
202-8
pubmed:dateRevised
2009-1-15
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
Ionic liquids versus triethylamine as mobile phase additives in the analysis of beta-blockers.
pubmed:affiliation
Laboratoire des Sciences Analytiques, Université Claude Bernard-Lyon 1, Villeurbanne, France.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't