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

  • Bergoi Ibarlucea
  • , Xavier Munoz-Berbel
  • , Pedro Ortiz
  • , Stephanus Büttgenbach
  • , César Fernández-Sánchez*
  • , Andreu Llobera
  • *Autor correspondiente de este trabajo
  • CSIC
  • Technische Universität Dresden
  • Oxford Nanopore Technologies
  • Technical University of Braunschweig

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

23 Citas (Scopus)

Resumen

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 μL 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 μL/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.

Idioma originalInglés
Páginas (desde-hasta)16-23
Número de páginas8
PublicaciónSensors and Actuators B: Chemical
Volumen237
DOI
EstadoPublicada - 1 dic 2016
Publicado de forma externa

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