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Crosslinking Density in Imprinting Polymerization
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The crosslinking density of a material determines its physical properties, such as the porosity of the material. In imprinting polymerizations, the porosity determines access to internal binding sites and thus the capacity of the imprinted material. This entry is about effect of the commonly used crosslinking density in imprinting polymerization for a variety of applications.

  • molecularly imprinted polymer
  • MIP
  • crosslinking density
  • specific binding
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Subjects: Polymer Science
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Update Time: 30 Sep 2021

1. Introduction

Imprinting polymerization is an exciting technique: By just adding one additional step to the synthesis of a common polymer, a material can be made specific to a chemical. Basically, that chemical, the template, is added to the synthesis solution. The monomers will surround the template automatically and form the strongest bonds possible, since thermodynamically that happens to be the lowest energy state and thus is preferred. The monomers will then be polymerized and crosslinked, and with that the three dimensional structure with the strongest bonds to the template will be conserved. The additional step is to remove the template. This results in a pocket ideal for rebinding the template [1].

How useful specific binding is can be seen in biochemistry. A cell contains a large number of compounds and intermediates, but despite that, enzymes choose one specific compound to react without any side products, simply by providing a very specific binding site. In organic chemistry that is only possible in very few cases with complicated, many-step syntheses resulting in low yields. Another example are antibodies that recognize one specific compound on the surface of pathogenic bacteria to then destroy those bacteria and thus prevent a possible deadly infection. Imprinting polymerization promises specific binding to allow for analogous applications in technology.

Early proof-of-concept for the specific binding with imprinting polymerization came from Mosbach’s group [2][3]. One of the earliest applications that implemented molecularly imprinted polymers (MIPs) was the separation of chiral compounds using chiral solid phases in column chromatography [4][5]. At this point, MIPs are used in many different applications. Broadly, they can be grouped into two categories: Detection and sensing for a variety of compounds, from contaminants to proteins in cells [6][7][8][9][10][11][12][13][14][15][16][17][18] and extraction and purification of compounds from environmental and biological samples [19][20][21][22][23][24][25].

The crosslinking density of a material determines its physical properties, such as the porosity of the material. In imprinting polymerizations, the porosity determines access to internal binding sites and thus the capacity of the imprinted material. The aim of this work is to analyze the effect of the commonly used crosslinking density in imprinting polymerization for a variety of applications. This will be accomplished by selecting current examples of imprinting polymerization and correlating the details of their syntheses with MIP capacity and polymer science data. This will not be a comprehensive review of imprinting polymerization. In fact, only a small number of studies of the vast imprinting polymerization literature will be used.

2. Common Syntheses for Imprinting Polymerizations

Imprinting polymerization generally uses a similar synthesis: A “functional monomer” is selected that is effective in binding the template, the “structural monomer”, which is the crosslinker, is chosen to match the polarity needed for the reaction and possibly also to bind to the template. A solution with the template and monomers is given time to bind to each other, then the initiator is added to the mixture and the polymer is formed. After isolating the polymer, the template is removed [1]. This results in specific binding sites that allow for the specific binding that differentiates imprinted polymers from non-imprinted resins [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26].

Most commonly, imprinting polymerization is based on non-covalent forces, but covalent and semi-covalent imprinting has also been reported [27]. There are variations in where the imprinting occurs (bulk imprinting or surface imprinting [28]), as well as what materials are used (polymeric materials, inorganic materials [29] or hybrid materials [30][31]). In this work, the focus is on either bulk or surface imprinting in polymeric materials.

Looking at bulk imprinting of polymeric materials in more detail, the ratio between the template, functional monomer, and crosslinker is important [32]. The amount of functional monomer is directly related to the amount of template since there has to be sufficient functional monomer to interact with all of the template molecules. The crosslinker then fixes the three-dimensional structure that binds the template most effectively. An effective ratio between template:functional monomer:crosslinker has been identified as 1:4:20 [32]. This has been used in the following syntheses as the starting point for optimization of the system and the application in question [33].

Surface imprinting was developed due to two common problems that were found with bulk imprinting, the difficulty to remove all templates after MIP synthesis, and the difficulty to access internal binding sites [34]. In surface imprinting, the MIP is commonly prepared as a coating onto a hard particle. The starting ratio of template:functional monomer:crosslinker is also 1:4:20 [34].

3. The Effect of Porogen and Crosslinking on Imprinted Materials

In this work, specifically the ratio between the functional monomer and crosslinker is highlighted since that determines the physical properties of the resulting MIP. That ratio also determines the number of accessible binding sites. Table 1 lists the ratio and the total capacity for a variety of examples in recent literature. A large majority is based on the 1:5 ratio described in the preceding section.

Table 1. Functional monomer ratio and total capacity for MIPs for a variety of applications cited in selected recent literature.
Monomer:Crosslinker Molar Ratio Template
Crosslinker
Maximum
Capacity
(mg/g)
Comments Reference
1:2.7 UO22+
EGDMA 2
125 Bulk imprinting
BET A2 670 m2/g, pore vol. 1.439 mL/g, avg. pore Ø 2.2 nm 1
Adsorption dependent on pH, initial conc., regeneration
[35]
1:5 Cu(II)
Pentaerythrol triacrylate 3
2.16 Bulk imprinting
BET A2 6.7 m2/g, pore vol. 0.0088 mL/g, avg. pore Ø 5.2 nm 1
[36]
1:4.5 Extracellular matrix peptides
Pentaerythrol triacrylate 3
49.55 Bulk imprinting
Most templates trapped
[37]
1:3, 1:5 Serotonin reuptake inhibitors
EGDMA 2
27.3 Bulk imprinting
BET A2 193.8 m2/g, pore vol. 0.37 mL/g, pore Ø 7.7 nm 1
[38]
1:3, 1:4, 1:5 Sarafloxacin
EGDMA 2
58.6 Bulk imprinting
Several functional monomers
More crosslinking, less capacity
[39]
1:4 to 1:20 Sialic acid
EGDMA 2
24.7 Bulk imprinting
Specialized acrylates
1:4 highest capacity
[40]
1:2.5 Sulfonylurea pesticides
Divinylbenzene
1.6 Bulk imprinting
BET A2: 409.7 m2/g 1
[41]
1:4 2-(3,4-dimethoxyphenyl)ethylamine
Trimethylopropane trimethacrylate 3
24.5 Bulk imprinting
Optimized crosslinker and porogen
[42]
1:0.38 Atrazine
EGDMA 2
3.45 Bulk Imprinting
Investigating porogen
BET A2 237.5 m2/g, pore vol. 0.0268 mL/g, pore Ø 0.57 nm 1
[43]
1:5 4-Hydroxy-3-nitrophenylacetic acid
EGDMA 2
0.106 Bulk Imprinting
Porogen, pore structure, and sorption investigation
[44]
1:5 Chloramphenicol
EGDMA 2
64.3 Surface imprinting, hollow
rods 1–3 μm long, Ø 50–180 nm 1
[45]
1:4.5 Peptide
EDMA 4
76.9 Surface imprinting, hollow [46]
1:1.2 Cytidine
EGDMA 2
33.39 Surface imprinting, magnetic MIP
BET A2: 980 m2/g 1
[47]
1:2.5, 1:5 Cd(NO3)2
EGDMA2
32 Membrane
Less crosslinking, more adsorption
Less imprinting molecule, less adsorption
[48]
1:1 Acteoside
EGDMA2
62.83 Surface imprinting, membrane [49]
1:1.3 Cd(NO3)2
Ethylene diamine
250.7 Surface imprinting
Surface crosslinking only
BET: A2 192.2 m2/g, pore vol. 0.052 cm3/g, pore Ø 113 nm 1
[50]
1: 0.68 Sulfa-methoxasole
EGDMA 2
20.0 Surface imprinting, magnetic MIP
Computational study
[51]
1:0.44 Sulfonamides
EDMA 4
0.559 Surface imprinting, magnetic MIP
Hybrid with silicon
[52]
1:4 Pseudohepericin
EDMA 4
450 Hollow particle
Prepared by emulsion polymerization
Inner Ø ca. 30 μm 1
[53]
1:5 Estrogens
EGDMA 2
12.1 Hollow particle
Ca. 250 nm inside Ø 1
[54]
1:5 Celecoxib
EGDMA 2
43.29 Hollow particle [55]
1:0.2 Cr(VI)
Trimethylopropane trimethacrylate 3
66.6 Bulk imprinting
BET: A2 4.78 m2/g, pore vol. 0.00554 cm3/g, pore Ø 2.35 nm 1
[56]
1:0.0079 (S)-Naproxen
EGDMA 2
127 Surface imprinting, magnetic MIP
Enantioselectivity 4:1
[57]
1:2.5 Quinine
Trimethylopropane trimethacrylate 3
15.38 Start with colloidal silica crystal microsphere
Coat MIP on porous crystal, then remove crystal
BET: A2 216 m2/g, pore vol. 0.66 cm3/g, avg pore Ø 12.2 nm
[58]
1:1.05 Artimisin
3-Aminopropyltriethoxysilane
45.89 Start with polydopamine as the core
Coat imprinted Si around by the sol-gel method
Phase inversion, then cast as membrane
[59]
1:0.005 Cd(II)
EGDMA 2
950 Bulk Imprinting
Increased porosity by bubbling N through the reaction
[60]

1 A2: Surface area; Ø: Diameter. 2 Ethylene glycol dimethacrylate. 3 Trifunctional crosslinker. 4 Ethylene dimethacrylate.

It is common to use porogens to increase the surface area and with that the capacity of the imprinted polymers [42–44,61–65]. Most porogens are solvents or solvent mixtures. The solubility of the template, monomer(s), and crosslinker is one of the major factors determining the surface area [44,63,65]. Using a solvent or co-solvent that is a non-solvent can lead to phase separation. If the phase separation leads to precipitation of the complex or the polymer, that generally leads to reduced surface area [42,44,63]. If the non-solvent creates an emulsion, that can lead to cracks or pores, which often increase the surface area [42]. An effective way to increase the surface area is to use a solid porogen, usually a salt particle that can later be dissolved and washed out [61,62]. Insoluble polymers have been reported as porogens, as well [61].

When more crosslinkers than monomers are used, each repeating unit of a polymer chain is connected to its neighbors as well as to a repeating unit of a different polymer chain. That allows for minimal free volume between each polymer chain, likely with a lot of interspersed crystalline regions. That means that only imprinting sites on the surface are accessible for binding, and trapped templates will not be able to be removed.

This demonstrates another problem that internal imprinted sites have in an MIP: For a template to be able to reach the site, there has to be a continuous channel to that site, as well as a flow of solvent with the template to be able to move into the site and rebind. Especially with water as the solvent, the amount of water around a solute molecule has to be large for an aqueous solution to be free-flowing [61]. Water has shown to be very viscous due to its extensive hydrogen bonding, and around hydrophilic compounds water can be strongly bound or even crystalline [61].

Which brings up another point: The kinetics of reaching binding sites that are on the surface vs. inside a particle. Templates that bind to surface sites can bind quickly, since the binding sites are readily accessible. Templates that bind to internal sites have to move through a viscous solvent in likely bent channels to reach the binding sites. Therefore, the kinetics of binding to internal sites will always be slower than the kinetics of binding to surface sites. And yet, most studies using bulk imprinting report linear binding kinetics.

The combined evidence from polymer science suggests that when more crosslinkers than functional monomers are used, the inside of the particle is extremely dense and the internal binding sites will not be accessible. Essentially, bulk polymerization and surface polymerization will result in the same outcome, as the data in Table 1 also suggested. In fact, one has to go to very low crosslinking densities (0.5 to 5% of crosslinker) to create materials with accessible internal binding sites.

References

  1. Ramstrom, O. Synthesis and selection of functional and structural monomers. In Molecularly Imprinted Materials, Science and Technology; Yan, M., Ramstrom, O., Eds.; Marcel Dekker: New York, NY, USA, 2005; pp. 181–224.
  2. Arshady, R.; Mosbach, K. Synthesis of substrate-selective polymers by host-guest polymerization. Makromol. Chem. 1981, 182, 687.
  3. Vlatikis, G.; Andersson, I.; Muller, R.; Mosbach, K. Drug assay using antibody mimics made by molecular imprinting. Nature 1993, 261, 645.
  4. Szumski, M.; Buszewski, B. Molecularly imprinted polymers: A new tool for separation of steroid isomers. J. Sep. Sci. 2004, 27, 837–842.
  5. Technical Guide to Chiral HPLC Separations. Available online: http://phx.phenomenex.com/lib/ChiralGuide.pdf (accessed on 29 June 2021).
  6. Soufi, G.J.; Iravani, S.; Varma, R.S. Molecularly imprinted polymers for the detection of viruses: Challenges and opportunities. Analyst 2021, 146, 3087–3100.
  7. Villa, C.S.; Sanchez, L.T.; Ayala Valencia, G.; Ahmed, S.; Gutierrez, T.J. Molecularly imprinted polymers for food applications: A review. Trends Food Sci. Technol. 2021, 111, 642–669.
  8. Wang, X.; Chen, G.; Zhang, P.; Jia, Q. Advances in epitope molecularly imprinted polymers for protein detection: A review. Anal. Methods 2021, 13, 1660–1671.
  9. Abass, A.M.; Rzaij, J.M. A review on: Molecularly imprinting polymers by ion selective electrodes for determination of drugs. J. Chem. Rev. 2020, 2, 148–156.
  10. Romanholo, P.V.V.; Razzina, C.A.; Raymundo-Pereira, P.A.; Prado, T.M.; Machado, S.A.S.; Sgobbi, L.F. Biomimetic electrochemical sensors: New horizon’s and challenges in biosensing applications. Biosens. Bioelectron. 2021, 185, 113242.
  11. Herrera-Chacon, A.; Ceto, X.; del Valle, M. Molecularly-imprinted polymers–towards electrochemical sensors and electronic tongues. Anal. Bioanal. Chem. 2021, 1–24.
  12. Gao, M.; Gao, Y.; Chen, G.; Huang, X.; Xu, X.; Lv, J.; Wang, J.; Xu, D.; Liu, G. Recent advances and future trends in the detection of contaminants by molecularly imprinted polymers in food samples. Front. Chem. 2020, 8, 616326.
  13. Arreguin-Campus, R.; Jimenez-Monroy, K.L.; Dilien, H.; Cleij, T.J.; van Grinsven, B.; Eersels, K. Imprinted polymers as synthetic receptors in sensors for food safety. Biosensors 2021, 11, 46.
  14. Appell, M.; Mueller, A. Mycotoxin analysis using imprinted materials technology: Recent developments. J. AOAC Int. 2016, 99, 861–864.
  15. BelBruno, J.J. Molecularly imprinted polymers. Chem. Rev. 2019, 119, 94–119.
  16. Ramanavicius, S.; Jagminas, A.; Ramanavicius, A. Advances in molecularly imprinted polymers based affinity sensors (Review). Polymers 2021, 13, 974.
  17. Janczura, M.; Lulinski, P.; Sobiech, M. Imprinting technology for effective sorbent fabrication: Current state-of-the-art and future prospects. Materials 2021, 14, 1850.
  18. Leibl, N.; Haupt, K.; Gonzato, C.; Duma, L. Molecularly imprinted polymers for chemical sensing: A tutorial review. Chemosensors 2021, 9, 123.
  19. Hu, T.; Chen, R.; Wang, Q.; He, C.; Liu, S. Recent advances and applications of molecularly imprinted polymers in solid-phase extraction for real sample analysis. J. Sep. Sci. 2021, 44, 274–309.
  20. Aylaz, G.; Kuhn, J.; Lau, E.C.H.T.; Yeung, C.-C.; Al Roy, V.; Duman, M.; You, H.H.P. Recent developments on magnetic molecular imprinted polymers (MMIPS) for sensing, capturing, and monitoring pharmaceutical and agricultural pollutants. J. Chem. Technol. Biotechnol. 2021, 96, 1151–1160.
  21. Torres-Cartas, S.; Catala-Icardo, M.; Meseguer-Lloret, S.; Simo-Alfonso, E.F.; Herrero-Martinez, J.M. Recent advances in molecularly imprinted membranes for sample treatment and separation. Separations 2020, 7, 69.
  22. Arabi, M.; Ostovan, A.; Bagheri, A.R.; Guo, X.; Wang, L.; Li, J.; Wang, X.; Li, B.; Chen, L. Strategies of molecular imprinting-based solid-phase extraction prior to chromatographic analysis. Trends Anal. Chem. 2020, 128, 115923.
  23. Iresh Fernando, P.U.A.; Glascott, M.W.; Pokrzywinski, K.; Fernando, B.M.; Kosgei, G.K.; Moores, L.C. Analytical methods incorporating molecularly imprinted polymers (mips) for the quantification of microcystins: A review. Crit. Rev. Anal. Chem. 2021, 1–15.
  24. Lanza, F.; Sellergren, B. The application of molecula imprinting technology to solid phase extraction. Chromatographia 2001, 53, 599–611.
  25. Sellergren, B. Separation of enantiomers using molecularly imprinted polymers. In Chiral Separation Techniques, 3rd ed.; Subramanian, G., Ed.; Wiley-VCH Verlag: Weinheim, Germany, 2007; pp. 399–431.
  26. Ndunda, E.N. Moleculalarly imprinted polymers–a closer look at the control polymer used in determining the imprinting effect: A mini review. J. Mol. Recogn. 2020, 33, e2855.
  27. Jamieson, O.; Mecozzi, F.; Crapnell, R.D.; Battell, W.; Hudson, A.; Novakovic, K.; Sachdeva, A.; Confarotta, F.; Herdes, C.; Banks, C.E.; et al. Approaches to the rational design of molecularly imprinted polymers developed for the selective extraction and detection of antibiotics in environmental and food samples. Phys. Status Solidi A 2021, 2100021.
  28. Dong, C.; Shi, H.; Han, Y.; Yang, Y.; Wang, R.; Men, J. Molecularly imprinted polymers by the surface imprinting technique. Eur. Polym. J. 2021, 145, 110231.
  29. Lofgreen, J.E.; Ozin, G.A. Controlling morphology and porosity to improve performance of molecularly imprinted sol-gel silica. Chem. Soc. Rev. 2014, 43, 911–933.
  30. Rico-Yuste, A.; Carrasco, S. Molecularly imprinted polymer-based hybrid materials for the development of optical sensors. Polymers 2019, 11, 1173.
  31. Fresco-Cala, B.; Batista, A.D.; Cardenas, S. Molecularly imprinted polymer micro- and nano-particles: A review. Molecules 2020, 25, 4740.
  32. Yilmaz, E.; Schmidt, R.H.; Mosbach, K. The noncovalent approach. In Molecularly Imprinted Materials, Science and Technology; Yan, M., Ramstrom, O., Eds.; Marcel Dekker: New York, NY, USA, 2005; pp. 25–58.
  33. Lanza, F.; Dirion, B.; Sellergren, B. Combinatorial approaches to molecular imprinting. In Molecularly Imprinted Materials, Science and Technology; Yan, M., Ramstrom, O., Eds.; Marcel Dekker: New York, NY, USA, 2005; pp. 225–248.
  34. Cunliffe, D.; Alexander, C. Surface imprinting. In Molecularly Imprinted Materials, Science and Technology; Yan, M., Ramstrom, O., Eds.; Marcel Dekker: New York, NY, USA, 2005; pp. 249–284.
  35. Liu, J.; Chen, M.; Cui, H. Synthesis of ion-imprinted materials with amidoxime groups for enhanced UO22+ adsorption. Inorgan. Chim. Acta 2020, 517, 120196.
  36. Chaipuang, A.; Phungpanya, C.; Thongpoon, C.; Watla-iad, K.; Inkaew, P.; Machan, T.; Suwantong, O. Effect of ethylene diamine tetra-acetic acid and functional monomers on the structure and adsorption properties of copper(II) ion-imprinted polymers. Polym. Adv. Technol. 2021, 32, 3000–3007.
  37. Rosellini, E.; Madeddu, D.; Barbani, N.; Frati, C.; Graiano, G.; Falco, A.; Lagrasta, C.; Quaini, F.; Cascone, M.G. Development of biomimetic alginate/gelatin/elastin sponges with recognition properties toward bioactive peptides for cardiac tissue engineering. Biomimetics 2020, 5, 67.
  38. Gornik, T.; Shinde, S.; Lamovsek, L.; Koblar, M.; Heath, E.; Sellergren, B.; Kosjek, T. Molecularly imprinted polymers for the removal of antidepressants from contaminated wastewater. Polymers 2020, 13, 120.
  39. Cai, T.; Zhou, Y.; Liu, H.; Li, J.; Wang, X.; Zhao, S.; Gong, B. Preparation of monodisperse, restricted-access, media-molecularly imprinted polymers using bi-functional monomers for solid-phase extraction of sarafloxacin from complex samples. J. Chromatogr. A 2021, 1642, 462009.
  40. Mavliutova, L.; Verduci, E.; Shinde, S.A.; Sellergren, B. Combinatorial design of a sialic acid-imprinted binding site. ACS Omega 2021, 6, 1229–1237.
  41. Feng, G.; Sun, J.; Wang, M.; Wang, M.; Li, Z.; Wang, S.; Zheng, L.; Wang, J.; She, X.; El-Aty, A.M.A. Preparation of molecularly imprinted polymer with class-specific recognition for determination of 29 sulfonylurea herbicides in agro-products. J. Chromatogr. A 2021, 1647, 462143.
  42. Lulinski, P.; Maciewska, D. Impact of functional monomers, cross-linkers and porogens on morphology and recognition properties of 2-(3,4-dimethoxyphenyl)ethylamine imprinted polymers. Mater. Sci. Eng. C 2011, 31, 281–289.
  43. Lah, N.F.C.; Ahmad, A.L.; Low, S.C.; Shoparwe, N.F. The role of porogen-polymer complexation in atrazine imprinted polymer to work as an electrochemical sensor in water. J. Environ. Chem. Eng. 2019, 7, 103500.
  44. Janczure, M.; Sobiech, M.; Lulinski, P. Insight into the morphology, pore structure and sorption properties of 4-hydroxy-3-nitrophenylacetic acid imprinted poly(acrylic acid-co-ethylene glycol dimethacrylate) sorbent. Polym. Test. 2021, 93, 106983.
  45. Xie, A.; Dai, J.; Chen, X.; Zou, T.; He, J.; Chang, Z.; Li, C.; Yan, Y. Hollow imprinted polymer nanorods with a tunable shell using hallosyte nanotubes as a sacrificial template for selective recognition and separation of chloramphenicol. RSC Adv. 2016, 6, 51014–51023.
  46. Tang, A.; Duan, L.; Liu, M.; Dong, X. An epitope imprinted polymer with affinity for kininogen fragments prepared by metal coordination interaction for cancer biomarker analysis. J. Mater. Chem. B 2016, 4, 7464–7471.
  47. Öngün, E.; Akgönüllü, S.; Yavuz, H.; Denizli, A. Synthesis of molecularly imprinted magnetic nanoparticles for selective cytindine adsorption. Sep. Sci. Plus 2021, 4, 147–156.
  48. Xi, Y.; Shi, H.; Liu, R.; Yin, X.; Yang, L.; Huang, M.; Luo, X. Insights in ion imprinted membrane with a delayed permeation mechanism for enhancing Cd2+ selective separation. J. Hazard. Mater. 2021, 416, 125772.
  49. Zhao, X.; Cheng, Y.; Xu, H.; Hao, Y.; Lv, Y.; Li, X. Design and preparation of molecularly imprinted membranes for selective separation of acteosides. Front. Chem. 2020, 8, 775.
  50. An, F.-Q.; Li, H.-F.; Guo, X.-D.; Gao, B.-J.; Hu, T.-P.; Gao, J.-F. Novel ionic surface imprinting technology: Design and application for selectively recognizing heavy metal ions. RSC Adv. 2019, 9, 2431–2440.
  51. Lamaoui, A.; Palacios-Santander, J.M.; Amine, A.; Cubiliana-Aguilera, L. Fast microwave-assisted synthesis of magnetic molecularly imprinted polymer of sulfamethoxazole. Talanta 2021, 232, 122439.
  52. Zhao, X.; Lu, L.; Zhu, M.; Liu, H.; He, J.; Zheng, F. Development of hydrophilic magnetic molecularly imprinted polymers for the dispersive solid-phase extraction of sulfonamides from animal-derived samples before HPLC detection. J. Sep. Sci. 2021, 44, 2399–2407.
  53. Florea, A.-M.; Iordache, T.-V.; Branger, C.; Brisset, H.; Zaharia, A.; Radu, A.-L.; Hubea, G.; Sarbu, A. One-step preparation of molecularly imprinted hollow beads for pseudohypericin separation from Hypericum perforatum L. extracts. Eur. Polym. J. 2018, 100, 48–56.
  54. Chen, W.; Xue, M.; Xue, F.; Mu, X.; Xu, Z.; Meng, Z.; Zhu, G.; Shea, K.J. Molecularly imprinted hollow spheres for the solid phase extraction of estrogens. Talanta 2015, 140, 68–72.
  55. Ansari, S. Application of hollow porous molecularly imprinted polymers using K2Ti4O9 coupled with spe-hplc for the determination of celecoxib in human urine samples: Optimization by central composite design (CCD). Anal. Methods 2017, 9, 3200.
  56. Fang, L.; Ding, L.; Ren, W.; Hu, H.; Huang, Y.; Shao, P.; Yang, L.; Shi, H.; Ren, Z.; Han, K.; et al. High exposure effect of the adsorption site significantly enhanced the adsorption capacity and removal rate: A case of adsorption of hexavalent chromium by quaternary ammonium polymers (QAP). J. Hazard. Mater. 2021, 416, 125829.
  57. Goyal, G.; Bhakta, S.; Mishra, P. Surface molecularly imprinted biomimetic magnetic nanoparticles for enantioseparation. Appl. Nano Mater. 2019, 2, 6747–6756.
  58. Lin, Y.; Liu, Y.; Rui, L.; Ou, J.; Wu, Q.; He, J. Template-directed preparation of three-dimensionally ordered macroporous molecularly imprinted microspheres for selective recognition and separation of quinine from cinchona extract. J. Polym. Res. 2021, 28, 179.
  59. Wu, Y.; Lin, R.; Ma, F.; Jiang, Z. Membrane-associated molecularly imprinted surfaces with tailor-made SiO2@polydopamine-based recognition sites for selective separation of artemisin. Coll. Surf. A 2021, 622, 126645.
  60. Perera, R.; Ashraf, S.; Mueller, A. The binding of metal ions to molecularly-imprinted polymers. Water Sci. Technol. 2017, 75, 1643–1650.
  61. Hatakeyama, T.; Hatakeyama, H. Thermal Properties of Green Polymers and Biocomposites; Kluwer Academic Publishers: Dordrecht, The Netherlands, 2010.
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Subjects: Polymer Science
Contributor :
View Times: 41
Revisions: 2 times (View History)
Update Time: 30 Sep 2021
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    Mueller, A. Crosslinking Density in Imprinting Polymerization. Encyclopedia. Available online: https://encyclopedia.pub/entry/14756 (accessed on 01 July 2022).
    Mueller A. Crosslinking Density in Imprinting Polymerization. Encyclopedia. Available at: https://encyclopedia.pub/entry/14756. Accessed July 01, 2022.
    Mueller, Anja. "Crosslinking Density in Imprinting Polymerization," Encyclopedia, https://encyclopedia.pub/entry/14756 (accessed July 01, 2022).
    Mueller, A. (2021, September 29). Crosslinking Density in Imprinting Polymerization. In Encyclopedia. https://encyclopedia.pub/entry/14756
    Mueller, Anja. ''Crosslinking Density in Imprinting Polymerization.'' Encyclopedia. Web. 29 September, 2021.
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