COMPARISON OF POLYMER-COATINGS OF CAPILLARIES FOR CAPILLARY ELECTROPHORESIS WITH RESPECT TO THEIR APPLICABILITY TO MOLECULAR IMPRINTING ANDELECTROCHROMATOGRAPHY
O. Bruggemann et al., COMPARISON OF POLYMER-COATINGS OF CAPILLARIES FOR CAPILLARY ELECTROPHORESIS WITH RESPECT TO THEIR APPLICABILITY TO MOLECULAR IMPRINTING ANDELECTROCHROMATOGRAPHY, Journal of chromatography, 781(1-2), 1997, pp. 43-53
Citations number
19
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
In molecular imprinting (MI), interactive monomers and suitable cross-
linking agents are polymerized in the presence of a template. Once the
template has been removed, the remaining space acts as a highly speci
fic binding site for the template or analogs thereof, due to the uniqu
e three-dimensional arrangement of interaction points. Several steps a
re involved in producing such a polymer coat inside a capillary electr
ophoresis capillary. First, the silanization of the inner surface of t
he capillary with a suitable silane is necessary, to link a monolayer
of unsaturated groups suitable for polymerization to the capillary sur
face. These monomeric groups are then integrated into the three-dimens
ional polymer coat produced in the next step, MI-capillary coatings id
eally are highly porous and of a thickness, delta, which is smaller th
an the inner radius, r, of the capillary in question. Porous polymer n
etworks can be produced by dispersive polymerization using a suitable
solvent (porogen). However, the exact conditions for producing a coati
ng suitable for capillary zone electrophoresis had to be determined ex
perimentally. Seven porogens, namely hexane, toluene, tetrahydrofuran,
acetonitrile, CHCl3, dimethyl sulfoxide and dimethylformamide, and tw
o cross-linkers, namely ethyleneglycoldimethacrylate and divinylbenzen
e, at concentrations of between 5 and 20% (v/v) were investigated. In
about 20% of the combinations, a polymer coat of the desired qualities
was obtained, The applicability of the MI capillaries to specific sep
arations was demonstrated for the separation of a racemic mixture of S
(+)- and R(-)-2-phenylpropionic acid. trans-3-(3-Pyridyl)-acrylic acid
was used as the interactive monomer in this case. (C) 1997 Elsevier S
cience B.V.