4.5 Article

Bicomponent Microneedle Array Biosensor for Minimally-Invasive Glutamate Monitoring

Journal

ELECTROANALYSIS
Volume 23, Issue 10, Pages 2302-2309

Publisher

WILEY-BLACKWELL
DOI: 10.1002/elan.201100361

Keywords

Amperometry; Biosensors; Glutamate; Microneedle; Poly(o-phenylenediamine)

Funding

  1. Office of Naval Research [N00014-08-1-1202]
  2. National Science Foundation [0547491]
  3. Sandia National Laboratories
  4. United States Department of Energy's National Nuclear Security Administration [DE-SC0004937, DE-AC04-94AL85000]
  5. Mexican government
  6. National Natural Science Foundation of China [20805020]
  7. Chinese Ministry of Education [109079]
  8. Directorate For Engineering
  9. Div Of Civil, Mechanical, & Manufact Inn [0547491] Funding Source: National Science Foundation
  10. Div Of Chem, Bioeng, Env, & Transp Sys
  11. Directorate For Engineering [1066531] Funding Source: National Science Foundation
  12. U.S. Department of Energy (DOE) [DE-SC0004937] Funding Source: U.S. Department of Energy (DOE)

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This article describes the design of a new and attractive minimally-invasive bicomponent microneedle sensing device for the electrochemical monitoring of the excitatory neurotransmitter glutamate and glucose. The new device architecture relies on the close integration of solid and hollow microneedles into a single biosensor array device containing multiple microcavities. Such microcavities facilitate the electropolymeric entrapment of the recognition enzyme within each microrecess. The resulting microneedle biosensor array can be employed as a minimally-invasive on-body transdermal patch, obviating the extraction/sampling of the biological fluid, thereby simplifying device requirements. The new concept is demonstrated for the electropolymeric entrapment of glutamate oxidase and glucose oxidase within a poly(o-phenylenediamine) (PPD) thin film. The PPD-based enzyme entrapment methodology enables the effective rejection of coexisting electroactive interferents without compromising the sensitivity or response time of the device. The resulting microneedle-based glutamate and glucose biosensors thus exhibit high selectivity, sensitivity, speed, and stability in both buffer and undiluted human serum. High-fidelity glutamate measurements down to the 10 mu M level are obtained in serum. The attractive recess design also serves to protect the enzyme layer upon insertion into the skin. This simple, yet robust microneedle design is well-suited for diverse biosensing applications in which real-time metabolite monitoring is a core requirement.

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