4.7 Article

A microfluidic system utilizing molecularly imprinted polymer films for amperometric detection of morphine

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 121, 期 2, 页码 576-582

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2006.04.111

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molecularly imprinted polymer; microfluidics; micropumps; MEMS; morphine; electrochemical; amperometric detection

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This study reports a microfluidic system for detecting morphine (MO) using a combination of a molecularly imprinted polymer (MIP) and electrochemical sensing techniques. A monomer, called 3,4-ethylenedioxythiophene (EDOT), was used to mix with morphine molecules through an electropolymerization process on a sensing electrode. The modified MIP-PEDOT (poly-ethylenedioxythiophene as the imprinting polymer with MO as the template) electrode was then used for detecting the morphine via the amperometric method. Key components including MIP films, a PDMS (polydimethylsiloxane)-based microchannel, a peristaltic micropump, microvalves and sensing microelectrodes were integrated to form a new microfluidic system for morphine sensing utilizing MEMS (micro-electro-mechanical-systems) technologies. The morphine samples were automatically transported to the MIP-PEDOT sensing electrode using the peristaltic micropump. Then, the morphine was detected using the electrochemical method. Experimental data show that the sensitivity of the MIP-PEDOT morphine sensor is 171.5 mu A/cm(2) MM in detecting morphine concentration ranging from 0.01 to 0.2 mM ata flow rate of 92.3 mu l/min. The novel combination of microfluidics, MIP, and electrochemical sensing technologies provides a promising approach for highly sensitive, highly selective morphine sensing with a low sample consumption rate. More importantly, the whole process can be performed in an automatic format by using the enabling microfluidic technology. A multi-functional electrochemical detection system is feasible using similar microfluidics/MIP/electrochemical technologies. (c) 2006 Elsevier B.V. All rights reserved.

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