Micro and Nanofabrication of Molecularly Imprinted Polymers

被引:19
作者
Bompart, Marc [1 ]
Haupt, Karsten [1 ]
Ayela, Cedric [2 ]
机构
[1] Univ Technol Compiegne, UMR CNRS, F-60205 Compiegne, France
[2] Lab Integrat Mat Syst, F-33405 Talence, France
来源
MOLECULAR IMPRINTING | 2012年 / 325卷
关键词
Biosensor; Lithography; Microbiochip; Microfabrication; Molecularly imprinted polymer; Nanocomposite; Nanofabrication; Nanomaterial; Synthetic receptor; SOLID-PHASE EXTRACTION; EVANESCENT WAVES; SILVER NANOPARTICLES; BIOMIMETIC NETWORKS; SYNTHETIC HOSTS; RECOGNITION; FABRICATION; FILM; SENSORS; DNA;
D O I
10.1007/128_2011_308
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Molecularly imprinted polymers (MIPs) are tailor-made receptors that possess the most important feature of biological antibodies and receptors - specific molecular recognition. They can thus be used in applications where selective binding events are of importance, such as chemical sensors, biosensors and biochips. For the development of microsensors, sensor arrays and microchips based on molecularly imprinted polymers, micro and nanofabrication methods are of great importance since they allow the patterning and structuring of MIPs on transducer surfaces. It has been shown that because of their stability, MIPs can be easily integrated in a number of standard microfabrication processes. Thereby, the possibility of photopolymerizing MIPs is a particular advantage. In addition to specific molecular recognition properties, nanostructured MIPs and MIP nanocomposites allow for additional interesting properties in such sensing materials, for example, amplification of electromagnetic waves by metal nanoparticles, magnetic susceptibility, structural colors in photonic crystals, or others. These materials will therefore find applications in particular for chemical and biochemical detection, monitoring and screening.
引用
收藏
页码:83 / 110
页数:28
相关论文
共 146 条
[61]   Peptide Imprinted Polymer Nanoparticles: A Plastic Antibody [J].
Hoshino, Yu ;
Kodama, Takashi ;
Okahata, Yoshio ;
Shea, Kenneth J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (46) :15242-+
[62]   Photo-lithographically impregnated and molecularly imprinted polymer thin film for biosensor applications [J].
Huang, HC ;
Lin, CI ;
Joseph, AK ;
Lee, YD .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1027 (1-2) :263-268
[63]   A multi-array sensor via the integration of acrylic molecularly imprinted photoresists and ultramicroelectrodes on a glass chip [J].
Huang, Hui-Chi ;
Huang, Sheng-Yu ;
Lin, Chin-I ;
Lee, Yu-Der .
ANALYTICA CHIMICA ACTA, 2007, 582 (01) :137-146
[64]   A fluorescence polarisation molecular imprint sorbent assay for 2,4-D: a non-separation pseudo-immunoassay [J].
Hunt, CE ;
Pasetto, P ;
Ansell, RJ ;
Haupt, K .
CHEMICAL COMMUNICATIONS, 2006, (16) :1754-1756
[65]   NITRATE-SELECTIVE ELECTRODE DEVELOPED BY ELECTROCHEMICALLY MEDIATED IMPRINTING DOPING OF POLYPYRROLE [J].
HUTCHINS, RS ;
BACHAS, LG .
ANALYTICAL CHEMISTRY, 1995, 67 (10) :1654-1660
[66]   Enzymatic nanolithography of a self-assembled oligonucleotide monolayer on gold [J].
Hyun, J ;
Kim, J ;
Craig, SL ;
Chilkoti, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (15) :4770-4771
[67]   Manufacturing of nanochannels with controlled dimensions using protease nanolithography [J].
Ionescu, RE ;
Marks, RS ;
Gheber, LA .
NANO LETTERS, 2005, 5 (05) :821-827
[68]   Regioselective introduction of two boronic acid groups into [60]fullerene using saccharides as imprinting templates [J].
Ishi-i, T ;
Nakashima, K ;
Shinkai, S .
CHEMICAL COMMUNICATIONS, 1998, (09) :1047-1048
[69]   Molecularly imprinted polymers and infrared evanescent wave spectroscopy. A chemical sensors approach [J].
Jakusch, M ;
Janotta, M ;
Mizaikoff, B ;
Mosbach, K ;
Haupt, K .
ANALYTICAL CHEMISTRY, 1999, 71 (20) :4786-4791
[70]   Composites of multiwalled carbon nanotubes and molecularly imprinted polymers for dopamine recognition [J].
Kan, Xianwen ;
Zhao, Yao ;
Geng, Zhirong ;
Wang, Zhilin ;
Zhu, Jun-Jie .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (13) :4849-4854