2014
DOI: 10.1039/c4an00687a
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A novel biosensor array with a wheel-like pattern for glucose, lactate and choline based on electrochemiluminescence imaging

Abstract: Electrochemiluminescence (ECL) imaging provides a superior approach to achieve array detection because of its ability for ultrasensitive multiplex analysis. In this paper, we reported a novel ECL imaging biosensor array modified with an enzyme/carbon nanotubes/chitosan composite film for the determination of glucose, choline and lactate. The biosensor array was constructed by integrating a patterned indium tin oxide (ITO) glass plate with six perforated poly(dimethylsiloxane) (PDMS) covers. ECL is generated by… Show more

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Cited by 61 publications
(23 citation statements)
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“…Novel ECL labels, including quantum dots with different emission wavelengths, have been used for multiplex ECL protein assays [14,15]. Multiplex enzyme assays for the multiplex imaging of glucose, choline, and lactate on carbon nanotubes functionalised with chitosan and specific enzymes have been reported [16]. Six individually addressable areas were created with a PDMS mask, and a CCD camera was used to detect the ECL signal generated upon interaction of luminol with hydrogen peroxide formed via the enzymatic reactions.…”
Section: Introductionmentioning
confidence: 99%
“…Novel ECL labels, including quantum dots with different emission wavelengths, have been used for multiplex ECL protein assays [14,15]. Multiplex enzyme assays for the multiplex imaging of glucose, choline, and lactate on carbon nanotubes functionalised with chitosan and specific enzymes have been reported [16]. Six individually addressable areas were created with a PDMS mask, and a CCD camera was used to detect the ECL signal generated upon interaction of luminol with hydrogen peroxide formed via the enzymatic reactions.…”
Section: Introductionmentioning
confidence: 99%
“…The other detection method is based on the CCD fluorescence scanner. Both fluorescence intensity and fluorescence position of each reaction point could be collected by a CCD camera, whereas the relevant biological information could be obtained through the relevant software analysis [4,5,6]. Moreover, the detection methods of fluorescent labeling are proven complex and difficult to be labeled, which is time-consuming and laborious, whereas the fluorescent markers are significantly expensive, resulting in high costs.…”
Section: Introductionmentioning
confidence: 99%
“…This allows analysis of the sequence and quantities of target molecules by detection of the intensity distribution of the hybridization signal [5]. Up to now, commercial biological microarray detection has been done by fluorescence and isotope labeling techniques [6,7,8]. However, there are some problems in the detection methods of fluorescent labeling: conventional microarray and sequencing technologies often require several hours of manual operation to complete the labeling process, complex labeling is time-consuming, which leads to high costs, poor reproducibility, and difficulty of use in clinics.…”
Section: Introductionmentioning
confidence: 99%