Proteins Pre-concentration Using Glycidyl Methacrylate-co-stearyl Methacrylate-co-ethylene Glycol Dimethacrylate Monolith

https://doi.org/10.22146/ijc.49479

Ahmed Ali Alkarimi(1*), Kevin Welham(2)

(1) Department of Chemistry, College of Science, University of Babylon, Hilla 51002, Iraq
(2) Department of Chemistry, Faculty of Science and Engineering, University of Hull, Cottingham Road, Hull HU6 7RX, United Kingdom
(*) Corresponding Author

Abstract


Solid-phase extraction technique is considered as a vital tool in a pre-treatment of different samples. Therefore, it was used as a beneficial and alternative extraction method over the liquid–liquid extraction in diverse applications such as food, environmental, and biological analyses. Glycidyl methacrylate-co-stearyl methacrylate-co-ethylene glycol dimethacrylate (GMA-co-SMA-co-EDMA) monolithic sorbent was prepared as strong cationic-reversed phase sorbent for solid-phase extraction of different proteins. The monolithic sorbent was prepared inside two moulds such as glass microchip device and borosilicate. The morphological properties have been investigated using the Brunauer-Emmett-Teller (BET) model analyzer and scanning electron microscope (SEM), and the formation of the monolithic sorbent was examined using the FT-IR. Eight proteins (cytochrome C, insulin, myoglobin, lysozyme, β-lactoglobulin, trypsin, albumin chicken egg white, and apo-transferrin) with different molecular weight and isoelectric point were investigated for pre-concentration using the SCX/RP sorbent. It was found that the highest extraction recovery was obtained with three proteins cytochrome C, lysozyme, and myoglobin compared with the other proteins. These three proteins were chosen for pre-concentration using the glass microchip. Sorbent performance showed significant results in terms of stability and reproducibility.

Keywords


stearyl methacrylate; solid phase sorbent; glycidyl methacrylate; extraction

Full Text:

Full Text PDF


References

[1] Schley, C., Swart, R., and Huber, C.G., 2006, Capillary scale monolithic trap column for desalting and preconcentration of peptides and proteins in one- and two-dimensional separations, J. Chromatogr. A, 1136 (2), 210–220.

[2] Slabospitskaya, M.Y., Vlakh, E.G., Saprykina, N.N., and Tennikova, T.B., 2009, Synthesis and investigation of a new macroporous monolithic material based on an N‐hydroxyphthalimide ester of acrylic acid‐co‐glycidyl methacrylate‐co‐ethylene dimethacrylate terpolymer, J. Appl. Polym. Sci., 111 (2), 692–700.

[3] Yu, C., Davey, M.H., Svec, F., and Fréchet, M.J., 2001, Monolithic porous polymer for on-chip solid-phase extraction and preconcentration prepared by photoinitiated in situ polymerization within a microfluidic device, Anal. Chem., 73 (21), 5088–5096.

[4] Lingeman, H., and Hoekstra-Oussoren, S.J.F., 1997, Particle-loaded membranes for sample concentration and/or clean-up in bioanalysis, J. Chromatogr. B, 689 (1), 221–237.

[5] Ulrich, S., 2000, Solid-phase microextraction in biomedical analysis, J. Chromatogr. A, 902 (1), 167–194.

[6] Arrua, R.D., Moya, C., Bernardi, E., Zarzur, J., Strumia, M., and Igarzabal, C.I.A., 2010, Preparation of macroporous monoliths based on epoxy-bearing hydrophilic terpolymers and applied for affinity separations, Eur. Polym. J., 46 (4), 663–672.

[7] Armenta, J.M., Gu, B., Humble, P.H., Thulin, C.D., and Lee, M.L., 2005, Design and evaluation of a coupled monolithic pre-concentrator-capillary zone electrophoresis system for the extraction of immunoglobulin G from human serum, J. Chromatogr. A, 1097 (1-2), 171–178.

[8] Wei, Y., Chen, X., Yang, S.C., Lv, Q.H., Ye, F.G., and Zhao, S.L., 2014, Preparation and characterization of polymer solid-phase extraction monolith immobilized metal affinity ligands, Chin. J. Anal. Chem., 42 (4), 495–500.

[9] Płotka-Wasylka, J., Szczepańska, N., de la Guardia, M., and Namieśnik, J., 2016, Modern trends in solid phase extraction: New sorbent media, TrAC, Trends Anal. Chem., 77, 23–43.

[10] Gilart, N., Borrull, F., Fontanals, N., and Marcé, R.M., 2014, Selective materials for solid-phase extraction in environmental analysis, Trends Environ. Anal. Chem., 1, e8–e18.

[11] Andrade-Eiroa, A., Canle, M., Leroy-Cancellieri, V., and Cerdà, V., 2016, Solid-phase extraction of organic compounds: A critical review (Part I), TrAC, Trends Anal. Chem., 80, 641–654.

[12] Arrua, R.D., Strumia, M.C., and Alvarez Igarzabal, C.I., 2009, Macroporous monolithic polymers: Preparation and applications, Materials, 2 (4), 2429–2466.

[13] Oberacher, H., and Huber, C.G., 2002, Capillary monoliths for the analysis of nucleic acids by high-performance liquid chromatography–electrospray ionization mass spectrometry, TrAC, Trends Anal. Chem., 21 (3), 166–174.

[14] Tanaka, N., Nagayama, H., Kobayashi, H., Ikegami, T., Hosoya, K., Ishizuka, N., Minakuchi, H., Nakanishi, K., Cabrera, K., and Lubda, D., 2000, Monolithic silica columns for HPLC, Micro‐HPLC, and CEC, J. High. Resolut. Chromatogr., 23 (1), 111–116.

[15] Trojer, L., Lubbad, H., Bisjak, P., Wieder, W., and Bonn, K., 2007, Comparison between monolithic conventional size, microbore and capillary poly(p-methylstyrene-co-1,2-bis(p-vinylphenyl)ethane) high-performance liquid chromatography columns: Synthesis, application, long-term stability and reproducibility, J. Chromatogr. A, 1146 (2), 216–224.

[16] Jančo, M., Sýkora, D., Svec, F., Fréchet, J.M.J., Schweer, J., and Holm, R., 2000, Rapid determination of molecular parameters of synthetic polymers by precipitation/redissolution high‐performance liquid chromatography using “molded” monolithic column, Journal of Polymer Science Part A: Polymer Chemistry, 38 (15), 2767–2778.

[17] Huck, C.W., and Bonn, G.K., 2000, Recent developments in polymer-based sorbents for solid-phase extraction, J. Chromatogr. A, 885 (1-2), 51–72.

[18] Peterson, D.S., Rohr, T., Svec, F., and Fréchet, J.M., 2003, Dual-function microanalytical device by in situ photolithographic grafting of porous polymer monolith: Integrating solid-phase extraction and enzymatic digestion for peptide mass mapping, Anal. Chem., 75 (20), 5328–5335.

[19] Ueki, Y., Umemura, T., Li, J., Odake, T., and Tsunoda, K., 2004, Preparation and application of methacrylate-based cation-exchange monolithic columns for capillary ion chromatography, Anal. Chem., 76 (23), 7007–7012.

[20] Alzahrani, S., 2012, Investigation of monolithic materials for protein sample preparation, Dissertation, Department of Chemistry, University of Hull, United Kingdom.

[21] Paul, S., and Rånby, B., 1976, Methyl methacrylate (MMA)-glycidyl methacrylate (GMA) copolymers. A novel method to introduce sulfonic acid groups on the polymeric chains, Macromolecules, 9 (2), 337–340.

[22] Safa, K.D., and Nasirtabrizi, M.H., 2006, Ring opening reactions of glycidyl methacrylate copolymers to introduce bulky organosilicon side chain substituents, Polym. Bull., 57 (3), 293–304.

[23] Wang, L., Su, Y., Zheng, L., Chen, W., and Jiang, Z., 2009, Highly efficient antifouling ultrafiltration membranes incorporating zwitterionic poly([3-(methacryloylamino)propyl]-dimethyl(3-sulfopropyl) ammonium hydroxide), J. Membr. Sci., 340 (1-2), 164–170.

[24] Liu, Y., and Laskin, A., 2009, Hygroscopic properties of CH3SO3Na, CH3SO3NH4, (CH3SO3)2Mg, and (CH3SO3)2Ca particles studied by micro-FTIR spectroscopy, J. Phys. Chem. A, 113 (8), 1531–1538.

[25] Refat, M.S., Ismail, L.A., and Adam, A.M.A., 2013, Synthesis and structural characterization of charge-transfer complexes derived from three symmetrically substituted 4,4¢-bis-(1,3,5-triazinylamino)stilbene-2,2¢-disulfonate derivatives with some p-acceptors. Part one: Chloranilic acid, Int. J. Chem. Sci., 11 (4), 1647–1658.

[26] Miyazaki, S., Morisato, K., Ishizuka, N., Minakuchi, H., Shintani, Y., Furuno, M., and Nakanishi, K., 2004, Development of a monolithic silica extraction tip for the analysis of proteins, J. Chromatogr. A, 1043 (1), 19–25.



DOI: https://doi.org/10.22146/ijc.49479

Article Metrics

Abstract views : 2429 | views : 1840


Copyright (c) 2020 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.