Electrophoresis-enhanced localized surface plasmon resonance sensing based on nanocup array for thrombin detection

被引:21
作者
Li, Shuang [1 ,2 ]
Zhang, Diming [1 ]
Zhang, Qian [1 ]
Lu, Yanli [1 ]
Li, Nantao [1 ]
Chen, Qunwei [3 ]
Liu, Qingjun [1 ,2 ]
机构
[1] Zhejiang Univ, Educ Minist, Dept Biomed Engn, Key Lab Biomed Engn,Biosensor Natl Special Lab, Hangzhou 310027, Zhejiang, Peoples R China
[2] Fujian Univ Tradit Chinese Med, Collaborat Innovat Ctr Hlth Management, Fuzhou 350108, Peoples R China
[3] Zhejiang Chinese Med Univ, Hangzhou 310053, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Localized surface plasmon resonance (LSPR); Electrophoresis; Nanocup array; Thrombin; Biosensor; ROLLING CIRCLE AMPLIFICATION; ULTRASENSITIVE DETECTION; SENSITIVE DETECTION; BIOSENSOR; NANOPARTICLES; SENSORS; SPECTROSCOPY; APTASENSOR; APTAMERS; CAPTURE;
D O I
10.1016/j.snb.2016.03.134
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Based on the special electrical and optical properties resulted from periodic nanostructure, localized surface plasmon resonance (LSPR) sensors have been widely used for various chemical and biological detections. Utilizing uniform alignment nanocups, an electrophoresis-enhanced LSPR sensor was designed for sensitive thrombin detection. The nanocup array was composed of nano-scaled funnel shaped cups with nanoparticles along the side walls. Through self-assembly, polyethylene glycol, thrombin-specific peptide, and bovine serum albumin were successively immobilized on the nanocup array. The results demonstrated that the synchronous implementation of electrophoresis and LSPR measurement could lead to obvious peak shifts in optical transmission spectra for detecting thrombin. The detection limit was as low as 10(-11)M. With the high sensitivity and well linearity, the electrophoresis enhanced LSPR sensing offered a novel design perspective for chemical and biological sensors with specific modifications on the nanosensor surfaces. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:219 / 225
页数:7
相关论文
共 44 条
[1]   Stimuli responsive polymers for biomedical applications [J].
Alarcón, CDH ;
Pennadam, S ;
Alexander, C .
CHEMICAL SOCIETY REVIEWS, 2005, 34 (03) :276-285
[2]   Biosensing with plasmonic nanosensors [J].
Anker, Jeffrey N. ;
Hall, W. Paige ;
Lyandres, Olga ;
Shah, Nilam C. ;
Zhao, Jing ;
Van Duyne, Richard P. .
NATURE MATERIALS, 2008, 7 (06) :442-453
[3]   Terminal attachment of polyethylene glycol (PEG) chains to a gold electrode surface. Cyclic voltammetry applied to the quantitative characterization of the flexibility of the attached PEG chains and of their penetration by mobile PEG chains [J].
Anne, A ;
Demaille, C ;
Moiroux, J .
MACROMOLECULES, 2002, 35 (14) :5578-5586
[4]  
Audrey S., 2012, Am. J. Anal. Chem., V2012
[5]   Dielectrophoresis-Enhanced Plasmonic Sensing with Gold Nanohole Arrays [J].
Barik, Avijit ;
Otto, Lauren M. ;
Yoo, Daehan ;
Jose, Jincy ;
Johnson, Timothy W. ;
Oh, Sang-Hyun .
NANO LETTERS, 2014, 14 (04) :2006-2012
[6]   Surface Modifications of Microprojection Arrays for Improved Biomarker Capture in the Skin of Live Mice [J].
Bhargav, Aarshi ;
Muller, David A. ;
Kendall, Mark A. F. ;
Corrie, Simon R. .
ACS APPLIED MATERIALS & INTERFACES, 2012, 4 (05) :2483-2489
[7]   A Novel Photoelectrochemical Biosensor for Tyrosinase and Thrombin Detection [J].
Chen, Jiexia ;
Liu, Yifan ;
Zhao, Guang-Chao .
SENSORS, 2016, 16 (01)
[8]   A multifunctional label-free electrochemical impedance biosensor for Hg2+, adenosine triphosphate and thrombin [J].
Chen, Lifen ;
Chen, Zhong-Ning .
TALANTA, 2015, 132 :664-668
[9]  
Choi Y, 2009, NAT NANOTECHNOL, V4, P742, DOI [10.1038/NNANO.2009.258, 10.1038/nnano.2009.258]
[10]   Electrochemical Crystallization of Plasmonic Nanostructures [J].
Dahlin, Andreas B. ;
Sannomiya, Takumi ;
Zahn, Raphael ;
Sotiriou, Georgios A. ;
Voeroes, Janos .
NANO LETTERS, 2011, 11 (03) :1337-1343