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Rapid Diagnosis of E. Coli using Carbon Nanotube Field Effect Transistor Direct Binding Assay

Published online by Cambridge University Press:  30 March 2012

Woo Jae Park
Affiliation:
Mclean High School, mclean, VA 22101, U.S.A
Sung-Jae Chung
Affiliation:
School of Arts and Sciences, Marymount University, Arlington, VA 22207, U.S.A. Fuzbien Technology Institute, Inc. Rockville, MD 20850, U.S.A.
Man S. Kim
Affiliation:
Fuzbien Technology Institute, Inc. Rockville, MD 20850, U.S.A.
Steingrimur Stefansson
Affiliation:
Fuzbien Technology Institute, Inc. Rockville, MD 20850, U.S.A.
Saeyoung Ahn
Affiliation:
Fuzbien Technology Institute, Inc. Rockville, MD 20850, U.S.A.
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Abstract

Enzyme-Linked Immuno-Sorbent Assay (ELISA), and other methods based on the same principle, are sensitive and specific, but they suffer from several disadvantages, such as their inherent complexity and requirement for multiple reagents, incubation and washing steps and require a relatively large sample size. We have adapted a new carbon nanotube field effect transistors (CNT-FET) based platform to capture Escherichia coli antigens using only the capture anti-body showing good correlation with an established ELISA assay contrived positive and negative specimens were used to test the new CNT-FET platform and results were obtained within three minutes per each sample. The test is easy to perform, rapid, and cost efficient making it a valuable screening tool for E. coli. In this study, we looked at the applicability of using CNT field effect transistor based biosensor as a rapid diagnostic platform for Escherichia coli O157:H7. The CNT-FETs platform detected positive E. coli samples in three minutes using only 2.5 μL of sample volume. This low sample volume required by the CNT-FET platform can be especially advantageous for diagnostic tests constricted by limited amount of samples.

Type
Research Article
Copyright
Copyright © Materials Research Society 2012

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References

REFERENCES

1. Luppa, P.B., Sokoll, L.J. and Chan, D.W., Immunosensors: principles and applications to clinical chemistry. Clin. Chim. Acta, 314 (2001), pp. 126.Google Scholar
2. Wells, M., Advances in optical detection strategies for reporter signal measurements. Curr. Opin. Biotechnol., 17 (2006), pp. 2833.Google Scholar
3. Seydack, M., Nanoparticle labels in immunosensing using optical detection methods. Biosens. Bioelectron., 20 (2005), pp. 24542469.Google Scholar
4. Wang, Y., Tang, Z. and Kotov, N.A., Bioapplication of nanosemiconductors. Mater. Today, 8 (2005), pp. 2031.Google Scholar
5. Gruner, G., Carbon nanotube transistors for biosensing applications. Anal. Bioanal. Chem., 384 (2006), pp. 322335.Google Scholar
6. Star, A., Gabriel, J.C.P., Bradley, K. and Grulner, G., Electronic detection of specific protein binding using nanotube FET devices. Nano Lett., 3 (2003), pp. 459463.Google Scholar
7. Drummond, T. G., Hill, M. G., Barton, J. K., Nature Biotechnol. 21(2003) pp. 11921199.Google Scholar
8. Bange, A., Halsall, H. B., Heineman, W. R., Biosens. Bioelectron. 20(2005), pp.24882503.Google Scholar
9. Lee, M., Im, J., Lee, B. Y., Myung, S., Kang, J., Huang, L., Kwon, Y. K., Hong, S., Nat. Nanotechnol. 1 (2006b), pp. 6671.Google Scholar
10. Kim, J. P., Lee, B. Y., Lee, J., Hong, S., Sim, S. J., Biosens. Bioelectron. 24 (2009), pp. 3723378.Google Scholar
11. Chen, R.J., Zhang, Y., Wang, D. and Dai, H., Noncovalent sidewall functionalization of single-walled carbon nanotubes for protein immobilization. J. Am. Chem. Soc., 123 (2001), pp. 38383839.Google Scholar
12. Dresselhaus, M. S., Eklund, P. C., 1996. Science of Fullerenes and Carbon Nanotubes: Their Properties and Applications. Academic Press, New York.Google Scholar
13. Drummond, T. G., Hill, M. G., Barton, J. K., Nature Biotechnol. 21 (2003), pp.11921199.Google Scholar
14. Kim, J. P., Lee, B. Y., Lee, J., Hong, S., Sim, S. J., Analytical Biochemistry, 381(2) (2008) pp. 193198.Google Scholar