Ultrathin Selective Molecularly Imprinted Polymer Microdots Obtained by Evanescent Wave Photopolymerization
Source abstract
Abstract
The fabrication of ultrathin selective molecularly imprinted polymer (MIP) microdots using polymerization by evanescent waves (PEW) is demonstrated for the first time. A specific prepolymerization mixture exhibiting suitable photosentivity at 405 nm was developed, containing in particular the visible-light photoinitiator bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide. PEW allows for nanometric resolution of the MIP dots in the z-scale. Within a few seconds, it is possible to generate molecularly imprinted microdots with sub-100 nm thickness. The amino acid Z -( l )-phenylalanine was used as model imprinting template, and the fluorescent dansyl-phenylalanine was employed as a fluorescently labeled derivative for the recognition tests. The MIP microdots showed specific molecular recognition for ( l )-phenylalanine derivatives and were able to discriminate dansyl-( l )-phenylalanine from dansyl-( d )-phenylalanine.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Analytical chemistry methods development · Microfluidic and Capillary Electrophoresis Applications · Mass Spectrometry Techniques and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Compiègne University of Technology, UMR CNRS 6022, BP20529, Compiègne, 60205, France
School of Chemistry, University of East Anglia, Norwich NR4 7TJ, United Kingdom
Mulhouse Institute for Material Sciences, CNRS LRC 7228, BP2488, Mulhouse, 68057, France
References (23)
Show source-provided references
1. Haupt K. · Anal. Chem. · 2003 · 75 · 37610.1021/ac031385h ↗
2. Zimmerman S. · Chem. Commun. · 2004 · 2004 · 510.1039/B304720B ↗
3. Haupt K. · Chem. Rev · 2000 · 100 · 249510.1021/cr990099w ↗
4. Bertsch A. · J. Photochem. Photobiol., A · 1997 · 107 · 27510.1016/S1010-6030(96)04585-6 ↗
5. Conrad I. · Adv. Mater. · 2003 · 15 · 154110.1002/adma.200304602 ↗
6. Henry O. · Biosens. Bioelectron. · 2008 · 23 · 176910.1016/j.bios.2008.02.010 ↗
7. Guillon S. · Lab Chip · 2009 · 9 · 298710.1039/b905608d ↗
8. Voicu R. · Langmuir · 2007 · 23 · 545210.1021/la063562q ↗
9. Lalo H. · Lab Chip · 2010 · 10 · 131610.1039/b924315a ↗
10. Vandevelde F. · Langmuir · 2007 · 23 · 649010.1021/la700320n ↗
11. Belmont A. · Appl. Phys. Lett. · 2007 · 90 · 19310110.1063/1.2730753 ↗
12. Deeb C. · ACS Nano · 2010 · 4 · 457910.1021/nn101017b ↗
13. Ecoffet C. · Adv. Mater. · 1998 · 10 · 41110.1002/(SICI)1521-4095(199803)10:5<411::AID-ADMA411>3.0.CO;2-P ↗
14. Triger C. · J. Phys. D: Appl. Phys. · 2003 · 36 · 255310.1088/0022-3727/36/20/020 ↗
15. Soppera O. · Proc. SPIE · 2007 · 6647 · 6647OI
16. Ramstroem O. · J. Org. Chem. · 1993 · 58 · 756210.1021/jo00078a041 ↗
17. Decker C. · Polymer · 2001 · 42 · 755110.1016/S0032-3861(01)00221-X ↗
18. Szablan Z. · Macromolecules · 2007 · 40 · 682010.1021/ma070626a ↗
19. Decker C. · Polym. Mat. Sci. Eng · 1986 · 55 · 552
20. Soppera O. · J. Polym. Sci., Part A: Polym. Chem. · 2008 · 46 · 378310.1002/pola.22727 ↗
21. Schmidt R. · Chem. Mater. · 2005 · 17 · 100710.1021/cm048392m ↗
22. Espanet A. · J. Polym. Sci., Part A: Polym. Chem. · 1999 · 37 · 207510.1002/(SICI)1099-0518(19990701)37:13<2075::AID-POLA22>3.0.CO;2-F ↗
23. Croutxé-Barghorn C. · Eur. Phys. J.: Appl. Phys. · 2001 · 13 · 31