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Adsorption Capacity and Selectivity of Molecularly Imprinted Polymers towards β-Sitosterol
Corresponding Author(s) : St. Fauziah
Asian Journal of Chemistry,
Vol. 31 No. 11 (2019): Vol 31 Issue 11
Abstract
Molecularly imprinted polymers (MIP) as an adsorbent has been synthesized using β-sitosterol as molecule template on free radical polymerization reaction. The capacity and selectivity of the adsorption from MIP to β-sitosterol was studied in this study. The β-sitosterol concentration in the adsorption-desorption test and the MIP selectivity test were analyzed by UV-visible and HPLC. The MIP obtained from the synthesis results in a high adsorption capacity. Based on the Freundlich adsorption isothermal equation, the adsorption capacity (k) was found to be 1.24 mg/g. The MIP can adsorb 100 % β-sitosterol while cholesterol was only 3 %. The MIP is most selective to β-sitosterol, therefore, has high potential to apply as adsorbent at solid phase extraction method to isolate β-sitosterol from sample extract.
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- S. Otles and C. Kartal, Acta Sci. Pol. Technol. Aliment., 15, 5 (2016); https://doi.org/10.17306/J.AFS.2016.1.1.
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References
S. Otles and C. Kartal, Acta Sci. Pol. Technol. Aliment., 15, 5 (2016); https://doi.org/10.17306/J.AFS.2016.1.1.
T. Zhu, C. Yoon and K. Row, Chin. J. Chem., 29, 1246 (2011); https://doi.org/10.1002/cjoc.201190231.
S. Xu, J. Li and L. Chen, Talanta, 85, 282 (2011); https://doi.org/10.1016/j.talanta.2011.03.060.
H. Surikumaran, S. Mohamad and N. Sarih, Int. J. Mol. Sci., 15, 6111 (2014); https://doi.org/10.3390/ijms15046111.
M.-J. Syu, J.-H. Deng, Y.-M. Nian, T.-C. Chiu and A.-H. Wu, Biomaterials, 26, 4684 (2005); https://doi.org/10.1016/j.biomaterials.2004.11.024.
H.Y. Wang, J.G. Jiang, L.Y. Ma and Y.L. Pang, React. Funct. Polym., 66, 1081 (2006); https://doi.org/10.1016/j.reactfunctpolym.2006.01.022.
H. Yan, R. Wang, Y. Han and S. Liu, J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 900, 18 (2012); https://doi.org/10.1016/j.jchromb.2012.05.021.
J. Rene, P. Adhikar and R.L. Bakal, Asian J. Pharm. Technol. Innov., 3, 75 (2015).
K. Matsumoto, B.D.B. Tiu, A. Kawamura, R.C. Advincula and T. Miyata, Polym. J., 48, 525 (2016); https://doi.org/10.1038/pj.2016.23.
H. Yavuz, V. Karakoc, D. Turkmen, R. Say and A. Denizli, Int. J. Biol. Macromol., 41, 8 (2007); https://doi.org/10.1016/j.ijbiomac.2006.11.011.
L. Chen, X. Wang, W. Lu, X. Wu and J. Li, Chem. Soc. Rev., 45, 2137 (2016); https://doi.org/10.1039/C6CS00061D.
X. Song, J. Li, J. Wang and L. Chen, Talanta, 80, 694 (2009); https://doi.org/10.1016/j.talanta.2009.07.051.
E. Blahova, J. Lehotay and I. Skaèáni, J. Liq. Chromatogr. Relat. Technol., 27, 2715 (2004); https://doi.org/10.1081/JLC-200029276.
M. Li, L. Zhang, Z. Meng, Z. Wang and H. Wu, J. Chromatogr. B Analyt. Technol. Biomed. Life Sci., 878, 2333 (2010); https://doi.org/10.1016/j.jchromb.2010.07.003.
H. Zhang, T. Song, F. Zong, T. Chen and C. Pan, Int. J. Mol. Sci., 9, 998 (2008).
M. Biesaga, A. Jankowska and K. Pyrzynska, Mikrochim. Acta, 150, 317 (2005); https://doi.org/10.1007/s00604-005-0359-y.
R. Weiss, A. Molinelli, M. Jakusch and B. Mizaikoff, Bioseparation, 10, 379 (2001); https://doi.org/10.1023/A:1021554106297.
F. Omidi, M. Behbahani, H. Sadeghi Abandansari, A. Sedighi and S.J. Shahtaheri, J. Environ. Health Sci. Eng., 12, 137 (2014); https://doi.org/10.1186/s40201-014-0137-z.
N.H. Soekamto, St. Fauziah, P. Taba and M.B. Amran, IOP Conf. Series: Mater. Sci. Eng., 188, 012048 (2017); https://doi.org/10.1088/1757-899X/188/1/012048.
R. Walsh, Ph.D. Thesis, Pharmaceutical and Molecular Biotechnology Research Centre Waterford Institute of Technology, Waterford: Ireland (2010).
A. Beltran, F. Borrull, R.M. Marcé and P.A.G. Cormack, TrAC Trends Anal. Chem., 29, 1363 (2010); https://doi.org/10.1016/j.trac.2010.07.020.
Q. Zhu, J. Tang, J. Dai, X. Gu and S. Chen, J. Appl. Polym. Sci., 104, 1551 (2007); https://doi.org/10.1002/app.25564.