journal article·2013-04

Preparation and characterization of molecularly imprinted organic–inorganic hybrid materials by sol–gel processing for selective recognition of ibuprofen

Ling Zhou, Yanyue Kong, Shian Zhong, Xiaorun Zhou

Publisher page

Abstract

This work adopted semi-covalent imprinting to prepare molecularly imprinted polymers (MIP) with ibuprofen, a non-steroidal anti-inflammatory drug, as template by sol–gel processing, which is characterized by both the high affinity of covalent binding and the mild operation conditions of non-covalent rebinding. A functional monomer, which was used to synthesize the monomer-imprinted molecule complex, was prepared by multi-step synthesis for the first time. MIP was characterized by Fourier transform IR spectrum and nitrogen adsorption. Thin-layer chromatography separation was used to evaluate the specific molecular recognition ability of MIP. In addition, dynamic and thermodynamic studies on MIP imprinting ibuprofen were undertaken. The results of equilibrium rebinding experiments showed that MIP exhibited good adsorption capacity for ibuprofen. Scatchard analysis illustrated that the template-polymer system shows only one-site binding behavior with a dissociation constant of 1.84 mmol L−1. Dynamic adsorption exhibited pseudo-second-order kinetics. The positive value of ΔHθ and the negative values of ΔGθ demonstrated that the binding system for MIP is endothermic and spontaneous.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Analytical chemistry methods development · Molecular Sensors and Ion Detection · Analytical Chemistry and Chromatography

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (36)

Show source-provided references
1. El-Sheikh AH, Al-Quse RW, El-Barghouthi MI, Al-Masri FS (2010) Talanta 83:66710.1016/j.talanta.2010.10.022 ↗
2. Tamayo FG, Turiel E, Martín-Esteban A (2007) J Chromatogr A 1152:3210.1016/j.chroma.2006.08.095 ↗
3. Zhu GF, Fan J, Gao YB, Gao X, Wang J (2011) J. Talanta 84:112410.1016/j.talanta.2011.03.015 ↗
4. Zorita S, Boyd B, Jönsson S, Yilmaz E, Svensson C, Mathiasson L, Bergström S (2008) Anal Chim Acta 626:14710.1016/j.aca.2008.07.051 ↗
5. Beltran A, Marcé RM, Cormack PAG, Borrull F (2009) J Chromatogr A 1216:224810.1016/j.chroma.2009.01.024 ↗
6. Jiang H, Adamsa CD, Koffskey W (2005) J Chromatogr A 1064:21910.1016/j.chroma.2004.12.047 ↗
7. Belmont AS, Jaeger S, Knopp D, Niessner R, Gauglitz G, Haupt K (2007) Biosens Bioelectron 22:326710.1016/j.bios.2007.01.023 ↗
8. Sun H, Fung YS (2006) Anal Chim Acta 576:6710.1016/j.aca.2006.04.058 ↗
9. Pietrzyk A, Kutner W, Chitta R, Zandler ME, D’Souza F, Sannicolò F, Mussini PR (2009) Anal Chem 81:1006110.1021/ac9020352 ↗
10. Holthoff EL, Bright FV (2007) Acc Chem Res 40:75610.1021/ar700087t ↗
11. Volkmann A, Brüggemann O (2006) React Funct Polym 66:172510.1016/j.reactfunctpolym.2006.07.007 ↗
12. Visnjevski A, Schomäcker R, Yilmaz E, Brüggemann O (2005) Catal Commun 6:60110.1016/j.catcom.2005.06.001 ↗
13. Aït-Haddou H, Leeder SM, Gagné MR (2004) Inorg Chim Acta 357:385410.1016/j.ica.2004.04.017 ↗
14. Díaz-Díaz G, Diñeiro Y, Menéndez MI, Blanco-López MC, Lobo-Castañón MJ, Miranda-Ordieres AJ, Tuñón-Blanco P (2011) Polymer 52:246810.1016/j.polymer.2011.04.004 ↗
15. Li Y, Yang HH, You QH, Zhuang ZX, Wang XR (2006) Anal Chem 78:31710.1021/ac050802i ↗
16. Chen PY, Nien PC, Wu CT, Wu TH, Lin CW, Ho KC (2009) Anal Chim Acta 643:3810.1016/j.aca.2009.04.004 ↗
17. Sellergren B, Allender CJ (2005) Adv Drug Deliv Rev 57:173310.1016/j.addr.2005.07.010 ↗
18. Suedee R, Bodhibukkana C, Tangthong N, Amnuaikit C, Kaewnopparat S, Srichana T (2008) J Controlled Release 129:17010.1016/j.jconrel.2008.05.001 ↗
19. Hillberg AL, Brain KR, Allender CJ (2005) Adv Drug Deliv Rev 57:1875
20. Ebelmen M (1846) Ann Chim Phys 16:129
21. Graham T (1864) J Chem Soc 17:318–32710.1039/JS8641700318 ↗
22. Sellergren B (ed) (2001) Molecularly Imprinted Polymers: Man-Made Mimics of Antibodies and Their Application in Analytical Chemistry, Elsevier, p 23
23. Marx S, Liron Z (2001) Chem Mater 13:362410.1021/cm000983z ↗
24. Leung MKP, Chow CF, Lam MHW (2001) J Mater Chem 11:298510.1039/b103182c ↗
25. Lin CI, Joseph AK, Chang CK, Wang YC, Lee YD (2003) Anal Chim Acta 481:17510.1016/S0003-2670(03)00095-3 ↗
26. Yang HH, Zhang SQ, Yang W, Chen XL, Zhuang ZX, Xu JG, Wang XR (2004) J Am Chem Soc 126:405410.1021/ja0389570 ↗
27. Chang YS, Ko TH, Hsu TJ, Syu MJ (2009) Anal Chem 81:209810.1021/ac802168w ↗
28. Fernández-González A, Laíño RB, Diaz-García ME, Guardia L, Viale A (2004) J Chromatogr B 804:24710.1016/j.jchromb.2003.12.030 ↗
29. Cacho C, Turiel E, Ayala AD, Pérez-Conde C (2006) J Chromatogr A 1114:25510.1016/j.chroma.2006.02.051 ↗
30. Azizian S (2004) J Colloid Interf Sci 276:4710.1016/j.jcis.2004.03.048 ↗
31. Ho YS, McKay G (2000) Water Res 34:73510.1016/S0043-1354(99)00232-8 ↗
32. Ho YS, Wase DAJ, Forster CF (1996) Environ Technol 17:7110.1080/09593331708616362 ↗
33. Ho YS, McKay G (1998) Adsorp Sci Technol 16:24310.1177/026361749801600401 ↗
34. Ho YS, Ng JCY, McKay G (2001) Sep Sci Technol 36:24110.1081/SS-100001077 ↗
35. Ho YS, McKay G (1999) Process Biochem 34:45110.1016/S0032-9592(98)00112-5 ↗
36. Ho YS, McKay G (1999) Resour Conserv Recycl 25:17110.1016/S0921-3449(98)00053-6 ↗