TY - JOUR
T1 - Development of high performance and facile to pack molecularly imprinted particles for aqueous applications
AU - Oliveira, D.
AU - Freitas, A.
AU - Kadhirvel, P.
AU - Dias, R. C. S.
AU - Costa, M. R. P. F. N.
N1 - Funding Information:
The authors thank FCT and FEDER under Programme COMPETE (Project PEst-C/EQB/LA0020/2013), QREN, ON2 and FEDER (Project NORTE-07-0162-FEDER-000050) and QREN, ON2 and FEDER (Project NORTE-07-0124-FEDER – 0000014 – Polymer Reaction Engineering). This research was also financed by FCT and FEDER through COMPETE 2020 (Project UID/EQU/50020/2013 – POCI-01-0145-FEDER-006984).
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/7/15
Y1 - 2016/7/15
N2 - Different kinds of molecularly imprinted particles were synthesized and compared, aiming at the development of materials combining high molecular recognition capabilities and facile use as column packing materials for chromatographic aqueous applications. Solution, inverse-suspension and precipitation polymerization were considered and two different model molecules (5-fluorouracil and caffeine) were used to highlight the effect of the interaction between the template molecule and the functional monomer on imprinting efficiency. Particles synthesized through the proposed inverse-suspension process exhibit facile use for packing columns, allow the stable running of chromatographic systems and present a high performance in drug uptake and release in aqueous media. Frontal analysis measurements highlight these key features of the synthesized particles. Drug sorption capabilities of 0.890 μmol/g and 5.774 μmol/g were measured for 5-fluorouracil and caffeine, respectively, using frontal analysis with eluents containing the target molecules at concentration 0.1 mM. Due to the lower amount of solvent required than with precipitation polymerization, the developed inverse-suspension process presents high synthesis yields, which can be exploited for the large-scale manufacture and commercialization of molecularly imprinted materials. The combined features of the particles makes possible their direct use in bioseparations or in the development of assays and pharmacokinetic studies concerning the presence of drugs in biological fluids.
AB - Different kinds of molecularly imprinted particles were synthesized and compared, aiming at the development of materials combining high molecular recognition capabilities and facile use as column packing materials for chromatographic aqueous applications. Solution, inverse-suspension and precipitation polymerization were considered and two different model molecules (5-fluorouracil and caffeine) were used to highlight the effect of the interaction between the template molecule and the functional monomer on imprinting efficiency. Particles synthesized through the proposed inverse-suspension process exhibit facile use for packing columns, allow the stable running of chromatographic systems and present a high performance in drug uptake and release in aqueous media. Frontal analysis measurements highlight these key features of the synthesized particles. Drug sorption capabilities of 0.890 μmol/g and 5.774 μmol/g were measured for 5-fluorouracil and caffeine, respectively, using frontal analysis with eluents containing the target molecules at concentration 0.1 mM. Due to the lower amount of solvent required than with precipitation polymerization, the developed inverse-suspension process presents high synthesis yields, which can be exploited for the large-scale manufacture and commercialization of molecularly imprinted materials. The combined features of the particles makes possible their direct use in bioseparations or in the development of assays and pharmacokinetic studies concerning the presence of drugs in biological fluids.
KW - Adsorption
KW - Biomedical
KW - Chromatography
KW - Drug release
KW - Frontal analysis
KW - Molecular imprinting
UR - http://www.scopus.com/inward/record.url?scp=84963704158&partnerID=8YFLogxK
U2 - 10.1016/j.bej.2016.03.009
DO - 10.1016/j.bej.2016.03.009
M3 - Article
AN - SCOPUS:84963704158
SN - 1369-703X
VL - 111
SP - 87
EP - 99
JO - Biochemical Engineering Journal
JF - Biochemical Engineering Journal
ER -