Table of Contents
ISRN Materials Science
Volume 2012 (2012), Article ID 861643, 6 pages
http://dx.doi.org/10.5402/2012/861643
Research Article

Characteristics of Molecularly Imprinted Polymer Thin Layer for Bisphenol A and Response of the MIP-Modified Sensor

1Department of Bioinformatics, Graduate School of Engineering, Soka University, 1-236 Tangi, Hachioji, Tokyo 192-8577, Japan
2Health Technology Research Center, National Institute of Advanced Industrial Science and Technology, 1-8-31 Midorigaoka, Ikeda, Osaka 563-8577, Japan
3RIKEN Quantitative Biology Center, 6-2-3 Furuedai, Suita, Osaka 565-0874, Japan

Received 1 September 2011; Accepted 12 October 2011

Academic Editor: J. Gruber

Copyright © 2012 Izumi Kubo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. C. A. Richter, L. S. Birnbaum, F. Farabollini et al., “In vivo effects of bisphenol A in laboratory rodent studies,” Reproductive Toxicology, vol. 24, no. 2, pp. 199–224, 2007. View at Publisher · View at Google Scholar · View at Scopus
  2. K. Kubo, O. Arai, M. Omura, R. Watanabe, R. Ogata, and S. Aou, “Low dose effects of bisphenol A on sexual differentiation of the brain and behavior in rats,” Neuroscience Research, vol. 45, no. 3, pp. 345–356, 2003. View at Publisher · View at Google Scholar · View at Scopus
  3. B. S. Rubin, J. R. Lenkowski, C. M. Schaeberle, L. N. Vandenberg, P. M. Ronsheim, and A. M. Soto, “Evidence of altered brain sexual differentiation in mice exposed perinatally to low, environmentally relevant levels of bisphenol A,” Endocrinology, vol. 147, no. 8, pp. 3681–3691, 2006. View at Publisher · View at Google Scholar · View at Scopus
  4. S. Tando, K. Itoh, T. Yaoi, J. Ikeda, Y. Fujiwara, and S. Fushiki, “Effects of pre- and neonatal exposure to bisphenol A on murine brain development,” Brain and Development, vol. 29, no. 6, pp. 352–356, 2007. View at Publisher · View at Google Scholar · View at Scopus
  5. S. Porrini, V. Belloni, D. D. Seta, F. Farabollini, G. Giannelli, and F. Dessì-Fulgheri, “Early exposure to a low dose of bisphenol A affects socio-sexual behavior of juvenile female rats,” Brain Research Bulletin, vol. 65, no. 3, pp. 261–266, 2005. View at Publisher · View at Google Scholar · View at Scopus
  6. F. Dessì-Fulgheri, S. Porrini, and F. Farabollini, “Effects of perinatal exposure to bisphenol A on play behavior of female and male juvenile rats,” Environmental Health Perspectives, vol. 110, supplement 3, pp. 403–407, 2002. View at Google Scholar
  7. K. Kawai, T. Nozaki, H. Nishikata, S. Aou, M. Takii, and C. Kubo, “Aggressive behavior and serum testosterone concentration during the maturation process of male mice: the effects of fetal exposure to bisphenol A,” Environmental Health Perspectives, vol. 111, no. 2, pp. 175–178, 2003. View at Google Scholar · View at Scopus
  8. M. Alizadeh, F. Ota, K. Hosoi, M. Kato, T. Sakai, and M. A. Satter, “Altered allergic cytokine and antibody response in mice treated with Bisphenol A,” Journal of Medical Investigation, vol. 53, no. 1-2, pp. 70–80, 2006. View at Publisher · View at Google Scholar · View at Scopus
  9. M. Goto, Y. Takano-Ishikawa, H. Ono, M. Yoshida, K. Yamaki, and H. Shinmoto, “Orally administered bisphenol A disturbed antigen specific immunoresponses in the naïve condition,” Bioscience, Biotechnology and Biochemistry, vol. 71, no. 9, pp. 2136–2143, 2007. View at Publisher · View at Google Scholar
  10. H. Yan, M. Takamoto, and K. Sugane, “Exposure to bisphenol A prenatally or in adulthood promotes TH2 cytokine production associated with reduction of CD4+CD25+ regulatory T cells,” Environmental Health Perspectives, vol. 116, no. 4, pp. 514–519, 2008. View at Publisher · View at Google Scholar · View at Scopus
  11. Y. Ikezuki, O. Tsutsumi, Y. Takai, Y. Kamei, and Y. Taketani, “Determination of bisphenol A concentrations in human biological fluids reveals significant early prenatal exposure,” Human Reproduction, vol. 17, no. 11, pp. 2839–2841, 2002. View at Google Scholar · View at Scopus
  12. S. Takayanagi, T. Tokunaga, X. Liu, H. Okada, A. Matsushima, and Y. Shimohigashi, “Endocrine disruptor bisphenol A strongly binds to human estrogen-related receptor γ (ERRγ) with high constitutive activity,” Toxicology Letters, vol. 167, no. 2, pp. 95–105, 2006. View at Publisher · View at Google Scholar · View at Scopus
  13. J. M. Braun, K. Yolton, K. N. Dietrich et al., “Prenatal bisphenol A exposure and early childhood behavior,” Environmental Health Perspectives, vol. 117, no. 12, pp. 1945–1952, 2009. View at Publisher · View at Google Scholar · View at Scopus
  14. L. F. Doherty, J. G. Bromer, Y. Zhou, T. S. Aldad, and H. S. Taylor, “In utero exposure to diethylstilbestrol (DES) or bisphenol-A (BPA) increases EZH2 expression in the mammary gland: an epigenetic mechanism linking endocrine disruptors to breast cancer,” Hormones and Cancer, vol. 1, no. 3, pp. 146–155, 2010. View at Publisher · View at Google Scholar · View at Scopus
  15. J. E. Biles, K. D. White, T. P. McNeal, and T. H. Begley, “Determination of the diglycidyl ether of bisphenol A and its derivatives in canned foods,” Journal of Agricultural and Food Chemistry, vol. 47, no. 5, pp. 1965–1969, 1999. View at Publisher · View at Google Scholar
  16. R. Pulgar, M. F. Olea-Serrano, A. Novillo-Fertrell et al., “Determination of bisphenol A and related aromatic compounds released from Bis-GMA-based composites and sealants by high performance liquid chromatography,” Environmental Health Perspectives, vol. 108, no. 1, pp. 21–27, 2000. View at Google Scholar · View at Scopus
  17. J. Sajiki, K. Takahashi, and J. Yonekubo, “Sensitive method for the determination of bisphenol-A in serum using two systems of high-performance liquid chromatography,” Journal of Chromatography B, vol. 736, no. 1-2, pp. 255–261, 1999. View at Publisher · View at Google Scholar · View at Scopus
  18. Y. Sun, M. Irie, N. Kishikawa, M. Wada, N. Kuroda, and K. Nakashima, “Determination of bisphenol A in human breast milk by HPLC with column-switching and fluorescence detection,” Biomedical Chromatography, vol. 18, no. 8, pp. 501–507, 2004. View at Publisher · View at Google Scholar · View at Scopus
  19. S. Moors, M. Blaszkewicz, H. M. Bolt, and G. H. Degen, “Simultaneous determination of daidzein, equol, genistein and bisphenol A in human urine by a fast and simple method using SPE and GC-MS,” Molecular Nutrition and Food Research, vol. 51, no. 7, pp. 787–798, 2007. View at Publisher · View at Google Scholar · View at Scopus
  20. N. Rastkari, R. Ahmadkhaniha, M. Yunesiana, L. J. Baleh, and A. Mesdaghiniaa, “Sensitive determination of bisphenol a and bisphenol f in canned food using a solid-phase microextraction fibre coated with single-walled carbon nanotubes before gc/ms,” Food Additives and Contaminants, vol. 27, no. 10, pp. 1460–1468, 2010. View at Publisher · View at Google Scholar
  21. H. Kuramitz, Y. Nakata, M. Kawasaki, and S. Tanaka, “Electrochemical oxidation of bisphenol A. Application to the removal of bisphenol A using a carbon fiber electrode,” Chemosphere, vol. 45, no. 1, pp. 37–43, 2001. View at Publisher · View at Google Scholar · View at Scopus
  22. H. Sanbe and J. Haginaka, “Uniformly sized molecularly imprinted polymers for bisphenol A and β-estradiol: retention and molecular recognition properties in hydro-organic mobile phases,” Journal of Pharmaceutical and Biomedical Analysis, vol. 30, no. 6, pp. 1835–1844, 2003. View at Publisher · View at Google Scholar
  23. I. Kubo, N. Yokota, Y. Nakane, and Y. Fuchiwaki, “The establishment of bisphenol A (BPA) sensing system utilizing molecularly imprinted polymer receptor and electrochemical determination,” International Journal of Electrochemistry, vol. 2011, Article ID 534936, 4 pages, 2011. View at Publisher · View at Google Scholar
  24. R. Shoji, T. Takeuchi, and I. Kubo, “Atrazine sensor based on molecularly imprinted polymer-modified gold electrode,” Analytical Chemistry, vol. 75, no. 18, pp. 4882–4886, 2003. View at Publisher · View at Google Scholar · View at Scopus
  25. Y. Fuchiwaki, R. Shoji, I. Kubo, and H. Suzuki, “6-Chloro-N,N-diethyl-1,3,5-triazine-2,4-diamine (simazine) electrochemical sensing chip based on biomimetic recognition utilizing a molecularly imprinted polymer layer on a gold chip,” Analytical Letters, vol. 41, no. 8, pp. 1398–1407, 2008. View at Publisher · View at Google Scholar · View at Scopus
  26. Y. Fuchiwaki, N. Sasaki, and I. Kubo, “Development of an electrochemical sensing system for 6-chloro-n,n-diethyl- 1,3,5-triazine-2,4-diamine (CAT) utilizing an amalgamated gold electrode and artificial sensor receptor,” Electrochemistry, vol. 75, no. 9, pp. 709–714, 2007. View at Google Scholar · View at Scopus
  27. J. Matsui, Y. Miyoshi, O. Doblhoff-Dier, and T. Takeuchi, “A molecularly imprinted synthetic polymer receptor selective for atrazine,” Analytical Chemistry, vol. 67, no. 23, pp. 4404–4408, 1995. View at Google Scholar · View at Scopus
  28. T. A. Sergeyeva, S. A. Piletsky, A. A. Brovko, E. A. Slinchenko, L. M. Sergeeva, and A. V. El'skaya, “Selective recognition of atrazine by molecularly imprinted polymer membranes. Development of conductometric sensor for herbicides detection,” Analytica Chimica Acta, vol. 392, no. 2-3, pp. 105–111, 1999. View at Publisher · View at Google Scholar · View at Scopus
  29. C. Luo, M. Liu, Y. Mo, J. Qu, and Y. Feng, “Thickness-shear mode acoustic sensor for atrazine using molecularly imprinted polymer as recognition element,” Analytica Chimica Acta, vol. 428, no. 1, pp. 143–148, 2001. View at Publisher · View at Google Scholar · View at Scopus
  30. T. Panasyuk-Delaney, V. M. Mirsky, M. Ulbricht, and O. S. Wolfbeis, “Impedometric herbicide chemosensors based on molecularly imprinted polymers,” Analytica Chimica Acta, vol. 435, no. 1, pp. 157–162, 2001. View at Publisher · View at Google Scholar · View at Scopus