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Steady-State Fluorescence Anisotropy Studies of Molecularly Imprinted Polymer Sensors

Published online by Cambridge University Press:  01 February 2011

Yin-Chu Chen
Affiliation:
Biomedical Engineering Department, Oregon Health Science University, Portland, OR
Zheming Wang
Affiliation:
Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA
Mingdi Yan
Affiliation:
Chemistry Department, Portland State University, Portland, OR
Scott A. Prahl
Affiliation:
Biomedical Engineering Department, Oregon Health Science University, Portland, OR
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Abstract

Molecularly imprinted polymers (MIPs) are used as recognition elements in biochemical sensors. In a fluorescence-based MIP sensor system, it can be difficult to distinguish the analyte fluorescence from the fluorescence of the polymer itself. We studied steady-state fluorescence anisotropy of anthracene imprinted in a polymer (polyurethane) matrix. Vertically polarized excitation light was incident on MIP films coated on silicon wafers; vertically and horizontally polarized emission was measured. We compared the fluorescence anisotropy of MIPs with imprinted molecules, MIPs with the imprinted molecules extracted, MIPs with rebound molecules, and non-imprinted control polymers. It is shown that differences in fluorescence anisotropy between the polymers and imprinted fluorescent molecules may provide a means to discriminate the fluorescence of analyte from that of the background polymer.

Type
Research Article
Copyright
Copyright © Materials Research Society 2004

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References

REFERENCES

[1] Haupt, K. and Mosbach, K., Chem. Rev. 100, 2495 (2000).Google Scholar
[2] Kriz, D., Ramstrom, O., and Mosbach, K., Anal. Chem. 69, A345 (1997).Google Scholar
[3] Dickert, F. L., Lieberzeit, P., and Tortschanoff, M., Sens. Actuators, B - Chem. 65, 186 (2000).Google Scholar
[4] Chen, Y.-C., Brazier, J. J., Yan, M., Bargo, P. R., and Prahl, S. A., Sens. Actuators, B - Chem., (accepted for publication).Google Scholar
[5] Aoki, H., Horinaka, J., Ito, S., Yamamoto, M., Katayama, H., Kamigaito, M., and Sawamoto, M., Polym. J. 33, 464 (2001).Google Scholar
[6] Bur, A. J., Vangel, M. G., and Roth, S. C., Polym. Eng. Sci. 41, 1380 (2001).Google Scholar
[7] Sato, N., Sugiura, K., Ito, S., and Yamamoto, M., Langmuir 13, 5685 (1997).Google Scholar
[8] Morrison, M. E., Dorfman, R. C., Clendening, W. D., Kiserow, D. J., Rossky, P. J., and Webber, S. E., J. Phys. Chem. 98, 5534 (1994).Google Scholar
[9] Pokorna, V., Vyprachticky, D., Pecka, J., and Mikes, F., Macromol. Chem. Phys. 202, 155 (2001).Google Scholar
[10] Wandelt, B., Turkewitsch, P., Wysocki, S., and Darling, G. D., Polymer 43, 2777 (2002).Google Scholar
[11] Brazier, J. J., Yan, M., Prahl, S. A., and Chen, Y.-C. in Molecularly Imprinted Materials Sensors and Other Devices, edited by Shea, K. J., Roberts, M. J., and Yan, M., (Mater. Res. Soc. Proc. 723, Pittsburgh, PA, 2002) pp. 115120.Google Scholar
[12] Stenger, D. A., Georger, J. H., Dulcey, C. S., Hickman, J. J., Rudolph, A. S., Nielsen, T. B., McCort, S. M., and Calvert, J. M. J. Am. Chem. Soc. 114, 8435 (1992).Google Scholar
[13] Principles of Fluorescence Spectroscopy, by Lakowicz, Joseph R., (Plenum Publisher, 2nd edition, 1999)Google Scholar