journal article·2014-06-11

Melamine Functionalized Silver Nanoparticles as the Probe for Electrochemical Sensing of Clenbuterol

Peng Miao, Kun Han, Haixuan Sun, Jian Yin, Jing Zhao, Bidou Wang, Yuguo Tang

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Abstract

Clenbuterol, a member of β-agonist family, has now been a serious threat to human health due to its illegal usage in the livestock feeding. Herein, we describe the application of melamine functionalized silver nanoparticles (M-AgNPs) as the electrochemical probe for simple, fast, highly sensitive and selective detection of clenbuterol. Generally, AgNPs are prepared and functionalized by melamine. After interacting with melamine modified gold electrode in the presence of clenbuterol, M-AgNPs can be immobilized on the surface of the electrode via the hydrogen-bonding interactions between clenbuterol and melamine. This sandwich structure permits sensitive and selective detection of clenbuterol. Since M-AgNPs can provide a couple of well-defined sharp silver stripping peaks, which stands for a highly characteristic solid-state Ag/AgCl reaction, a rather low detection limit of 10 pM can be achieved. The detection range is from 10 pM to 100 nM, which is quite wide. This developed biosensor can potentially be used for clenbuterol detection in biological fluids in the presence of various interferences.
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Research context

OpenAlex topics: Pharmacological Effects and Assays · Mass Spectrometry Techniques and Applications · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, China

University of Chinese Academy of Sciences, Beijing 100049, China

Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Science, Jilin 130033, China

Laboratory of Biosensing Technology, School of Life Sciences, Shanghai University, Shanghai 200444, China

References (38)

Show source-provided references
1. Crescenzi C. · Anal. Chem. · 2001 · 73 · 217110.1021/ac0014360 ↗
2. Watkins L. E. · J. Anim. Sci. · 1990 · 68 · 358810.2527/1990.68113588x ↗
3. Brambilla G. · Toxicol. Lett. · 2000 · 114 · 4710.1016/S0378-4274(99)00270-2 ↗
4. He P. L. · Anal. Chem. · 2011 · 83 · 698810.1021/ac200769f ↗
5. Zhang X. F. · Biosens. Bioelectron. · 2012 · 34 · 11210.1016/j.bios.2012.01.026 ↗
6. Zhu G. C. · Anal. Chim. Acta · 2011 · 697 · 6110.1016/j.aca.2011.04.031 ↗
7. Bai J. · Analyst · 2012 · 137 · 434910.1039/c2an35473j ↗
8. Liu G. · Biosens. Bioelectron. · 2011 · 28 · 30810.1016/j.bios.2011.07.037 ↗
9. Guy P. A. · J. Chromatogr. B · 1999 · 736 · 20910.1016/S0378-4347(99)00466-1 ↗
10. Traynor I. M. · Anal. Chim. Acta · 2003 · 483 · 18710.1016/S0003-2670(03)00256-3 ↗
11. Ruta J. · J. Chromatogr. A · 2010 · 1217 · 823010.1016/j.chroma.2010.10.106 ↗
12. Yu Z. Q. · J. Am. Chem. Soc. · 2013 · 135 · 288310.1021/ja311090e ↗
13. Yu Z. Q. · Anal. Biochem. · 2010 · 397 · 19710.1016/j.ab.2009.10.030 ↗
14. Brovelli S. · Nat. Commun. · 2011 · 2 · 28010.1038/ncomms1281 ↗
15. Moghimi N. · Anal. Chem. · 2013 · 85 · 597410.1021/ac400785h ↗
16. Chen Y. · Adv. Mater. · 2013 · 25 · 310010.1002/adma.201204685 ↗
17. Yuan L. F. · Analyst · 2013 · 138 · 53910.1039/C2AN36145K ↗
18. Boudebbouze S. · Chem. Commun. · 2013 · 49 · 715010.1039/c3cc42838a ↗
19. Cao Y. · Biosens. Bioelectron. · 2010 · 25 · 103210.1016/j.bios.2009.09.021 ↗
20. Miao P. · Anal. Bioanal. Chem. · 2011 · 399 · 240710.1007/s00216-010-4642-3 ↗
21. He Y. · Chem. Commun. · 2011 · 47 · 1069210.1039/c1cc14389a ↗
22. Chen Y. · Chem. Commun. · 2004 · 280410.1039/b411181h ↗
23. Kim Y. P. · Angew. Chem., Int. Ed. · 2007 · 46 · 681610.1002/anie.200701418 ↗
24. Xu H. · Anal. Chem. · 2009 · 81 · 66910.1021/ac8020592 ↗
25. Miao P. · Electrochem. Commun. · 2009 · 11 · 190410.1016/j.elecom.2009.08.013 ↗
26. Miao P. · Biosens. Bioelectron. · 2013 · 49 · 2010.1016/j.bios.2013.04.038 ↗
27. Mehrgardi M. A. · Biosens. Bioelectron. · 2011 · 26 · 430810.1016/j.bios.2011.04.020 ↗
28. Zhang C. · Nat. Mater. · 2013 · 12 · 74110.1038/nmat3647 ↗
29. Bo B. · Talanta · 2013 · 113 · 3610.1016/j.talanta.2013.03.056 ↗
30. Doty R. C. · Chem. Mater. · 2005 · 17 · 463010.1021/cm0508017 ↗
31. Zhou Y. · Talanta · 2012 · 97 · 33110.1016/j.talanta.2012.04.041 ↗
32. Chi H. · Analyst · 2010 · 135 · 107010.1039/c000285b ↗
33. Ai K. L. · J. Am. Chem. Soc. · 2009 · 131 · 949610.1021/ja9037017 ↗
34. Wisner J. A. · Angew. Chem., Int. Ed. · 2001 · 40 · 360610.1002/1521-3773(20011001)40:19<3606::AID-ANIE3606>3.0.CO;2-O ↗
35. Zhang J. · Small · 2009 · 5 · 141410.1002/smll.200900073 ↗
36. Yi S. · Org. Biomol. Chem. · 2013 · 11 · 28710.1039/C2OB26834E ↗
37. Yi S. · Chem. Commun. · 2011 · 47 · 550010.1039/C1CC11212K ↗
38. Gaichore R. R. · J. Appl. Electrochem. · 2012 · 42 · 97910.1007/s10800-012-0466-5 ↗