Capillary Electrophoresis Immunoassay by Gold Nanoparticles Assisted Signal Generation and Sequential Stacking
Received date: 2016-11-12
Online published: 2017-01-18
Supported by
Project supported by the National Natural Science Foundation of China (No. 21105051).
Brevetoxins (BTXs) are highly toxic biotoxin and can cause human intoxication through food chain. The detection of brevetoxins is very difficult due to lack of optical and electrochemical (EC) signal. In this work, we developed an ultrasensitive capillary electrophoresis (CE) immunoassay and EC method for the determination of BTX-B by gold nanoparticles (AuNPs) assisted signal generation and sequential stacking concentration. The AuNPs were synthesized by sodium citrate reduction of HAuCl4 in water. The AuNPs were conjugated with horseradish peroxidase (HRP) and antibody (Ab) to immobilize the HRP and Ab on the AuNPs surface with the molar ratio of HRP/Ab of 9/1. The Ab conjugated on the AuNPs surface incubated with limited amount of BTX-B in standard solution or shellfish samples to produce immunocomplex on the basis of the noncompetitive immunoreactions. Before sample injection, a NaOH plug with 10 cm height difference for 150 s was hydrodynamically injected into the separation capillary. After incubation for 40 min at room temperature, the immune sample was then electrokinetically injected into the capillary at 10 kV for 330 s. The positively charged analytes migrated rapidly into the capillary and were neutralized and stacked at the boundary between sample and NaOH plug, which led to the first preconcentration. After sample loading, the capillary inlet vial was changed to low-pH buffer solution, and H+ in the buffer solution moved rapidly into the capillary toward cathode across the neutral analytes zone. The neutralized analytes were positively charged again and the injected analytes were further condensed. Next, the formed immunocomplex, unbound HRP-Au-Ab probe and the excess HRP were separated by CE and sensitively detected by EC detection. AuNPs were used as carriers of HRP and Ab in order to carry out EC detection with the EC signals derived from catalytic reaction of the carried HRP to the H2O2/o-aminophenol system. Simultaneously, the EC signal was highly amplified by improving the HRP/Ab molar ratio on the surface of AuNPs. The proposed method by AuNPs assisted signal generation and on-line sequential concentration realized the sensitive and rapid determination of BTX-B in shellfish samples. In the range between 0.1 and 120 ng/mL, the assay allowed quantitative determination of BTX-B and the limit of detection (LOD) was 26 ng/L. The LOD was 365-fold lower than ELISA method. The amplified sensitivity was enhanced by high HRP/Ab ratio at AuNPs surface and sequential preconcentration. The proposed method provides a convenient and sensitive analytical approach for the determination of trace BTX in complex samples.
Zhang Zhaoxiang , Luan Wenxiu , Zhang Chaoying , Liu Yujie . Capillary Electrophoresis Immunoassay by Gold Nanoparticles Assisted Signal Generation and Sequential Stacking[J]. Acta Chimica Sinica, 2017 , 75(4) : 403 -407 . DOI: 10.6023/A16110599
[1] Official Methods of Analysis, 14th ed., Association of Official Analytical Chemists, Arlington, VA, 1984, Section 18.086.
[2] Hua, Y.; Lu, W.; Henry, M. S.; Pierce, R. H.; Cole, R. B. Anal. Chem. 1995, 67, 1815.
[3] Nozawa, A.; Tsuji, K.; Ishida, H. Toxicon 2003, 42, 91.
[4] Wang, Z.; Plakas, S. M.; Said, K. R. E.; Jester, E. L. E.; Granade, H. R.; Dickey, R. W. Toxicon 2004, 43, 455.
[5] Wang, Z.; Ramsdell, J. S. Chem. Res. Toxicol. 2011, 24, 54.
[6] Naar, J.; Bourdelais, A.; Tomas, C.; Kubanek, J.; Whitney, P. L.; Flewelling, L. Environ. Health Perspect. 2002, 110, 179.
[7] Bottein, M.-Y. D.; Fuquay, J. M.; Munday, R.; Selwood, A. I.; Ginkel, R. V.; Miles, C. O.; Loader, J. I.; Wilkins, A. L.; Ramsdell, J. S. Toxicon 2010, 55, 497.
[8] Yang, W. C.; Schmerr, M. J.; Jackman, R.; Bodemer, W.; Yeung, E. S. Anal. Chem. 2005, 77, 4489.
[9] Liu, Y.; Mei, L.; Liu, L.; Peng, L.; Chen, Y.; Ren, S. Anal. Chem. 2011, 83, 1137.
[10] Wang, X.; Song, Y.; Song, M.; Wang, Z.; Li, T.; Wang, H. Anal. Chem. 2009, 81, 7885.
[11] Zhang, X. W.; Zhang, Z. X. Toxicon 2012, 59, 626.
[12] Zhang, X. W.; Zhang, Z. X. J. Food Compos. Anal. 2012, 28, 61.
[13] Zhang, X. W.; Zhang, Z. X. J. Chromatogr. Sci. 2013, 51, 107.
[14] Zhang, Z. X.; Zhang, F.; Liu, Y. Acta Chim. Sinica 2012, 70, 2251(in Chinese). (张召香, 张飞, 刘营, 化学学报, 2012, 70, 2251.)
[15] Liu, X.; Wu, Z.; Zhang, Q.; Zhao, W.; Zong, C.; Gai, H. Anal. Chem. 2016, 88, 2119.
[16] Zhou, G.; Chang, J.; Pu, H.; Shi, K.; Mao, S.; Sui, X.; Ren, R.; Cui, S.; Chen, J. ACS Sens. 2016, 1, 295.
[17] Yang, H.; Fung, S.; Xu, S.; Sutherland, D. P.; Kollmann, T. R.; Liu, M.; Turvey, S. E. ACS Nano 2015, 9, 6774.
[18] Paul, A. M.; Fan, Z.; Sinha, S. S.; Shi, Y.; Le, L.; Bai, F.; Ray, P. C. J. Phys. Chem. C 2015, 119, 23669.
[19] Ma, Z. Y.; Ruan, Y. F.; Xu, F.; Zhao, W. W.; Xu, J. J.; Chen, H. Y. Anal. Chem. 2016, 88, 3864.
[20] Harimech, P. K.; Gerrard, S. R.; El-Sagheer, A. H.; Brown, T.; Kanaras, A. G. J. Am. Chem. Soc. 2015, 137, 9242.
[21] Su, S.; Sun, H.; Cao, W.; Chao, J.; Peng, H.; Zuo, X.; Yuwen, L.; Fan, C.; Wang, L. ACS Appl. Mater. Interfaces 2016, 8, 6826.
[22] Wang, Q.; Zhu, H. Z.; Yang, X. H.; Wang, K. M.; Yang, L. J.; Ding, J. Acta Chim. Sinica 2012, 70, 1483(in Chinese). (王青, 朱红志, 羊小海, 王柯敏, 杨丽娟, 丁静, 化学学报, 2012, 70, 1483.)
[23] Guo, Y.; Li, W. W.; Zheng, M. Y.; Huang, Y. Acta Chim. Sinica 2014, 72, 713(in Chinese). (郭颖, 李午戊, 郑敏燕, 黄怡, 化学学报, 2014, 72, 713.)
[24] Ambrosi, A.; Airò, F.; Merkoci, A. Anal. Chem. 2010, 82, 1151.
[25] Chang, C. W.; Tseng, W. L. Anal. Chem. 2010, 82, 2696.
[26] Chang, C. W.; Chu, S. P.; Tseng, W. L. J. Chromatogr. A 2010, 1217, 7800.
[27] Miao, P.; Ning, L.; Li, X. Anal. Chem. 2013, 85, 7966.
[28] Zhang, Z. X.; Li, X.; Ge, A.; Zhang, F.; Sun, X.; Li, X. Biosens. Bioelectron. 2013, 41, 452.
[29] Bradford, M. M. Anal. Biochem. 1976, 72, 248.
[30] Wang, J.; Huang, W.; Liu, Y.; Cheng, J.; Yang, J. Anal. Chem. 2004, 76, 5393.
/
〈 |
|
〉 |