4.7 Article

Self-validating lab-on-a-chip for monitoring enzyme-catalyzed biological reactions

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 237, 期 -, 页码 16-23

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2016.06.059

关键词

Lab-on-a-chip; Integrated dual detection; Photonics; Electrochemistry; Biofunctionalization; Microfluidics

资金

  1. European Research Council under the European Community's Seventh Framework Programme (FP7)/ERC grant [209243]
  2. Volkswagen Foundation
  3. Generalitat de Catalunya [20145GR1645]
  4. Ramon y Cajal program from Spanish Government

向作者/读者索取更多资源

This paper reports on a miniaturized and highly integrated lab-on-a-chip (LoC) combining both optical and electrochemical transduction modes for self-validating determination of biological analytes that undergo enzyme-catalyzed-reactions. This LoC monolithically integrates a biofunctionalized microfluidic mixer, also working as bioreactor, together with a measurement chamber, both fabricated in polydimethylsiloxane (PDMS) and applied for enzyme-mediated detection of glucose in continuous flow regime. The measurement chamber combines a multiple internal reflection (MIR) photonic cuvette and a tailor-made electrochemical cell, where gold electrode areas are defined by a silicon oxide passivation layer. Having separated mixing/reaction and measurement chambers greatly facilitates the functionalization process during the microsystem fabrication and the further calibration/rinsing steps carried out during the microsystem performance. A cascade bi-enzymatic reaction involving glucose oxidase (GOx) and horseradish peroxidase (HRP) together with azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS) mediator is applied to carry out the glucose dual detection. The optical and electrochemical properties of the ABTS enable simultaneous absorbance and amperometric measurements, without cross-talk. The system requires low sample volumes below 15 mu L and presents tunable analytical properties that can be adjusted by varying the flow rate. Linear ranges extending up to 1.6 mM and 2 mM glucose and limits of detection of 0.23 +/- 0.02 mM and 0.064 +/- 0.001 mM are achieved with the optical and electrochemical detection approaches, respectively, when operating simultaneously at 10 mu L/min flow rate. The high degree of integration results in a minimization of dead volumes, reagent consumption and response time, providing with a high performance self-validating structure ideal for biomedical applications. (C) 2016 Elsevier B.V. All rights reserved.

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