Arrays of electrochemical sensors that include specially coated (as described below) gold electrodes on flexible polyimide sheets have been fabricated and tested in a continuing effort to develop biocompatible, surgically implantable electrochemical-sensor arrays for continuous measurement of concentrations of analytes that play major roles in human and animal metabolism. The effort thus far has been oriented particularly toward developing sensors for monitoring one analyte — glucose — to enable improved treatment of diabetic patients. It is planned to extend this effort to the fabrication and testing of sensors for monitoring lactate and pyruvate and, eventually, to implement the concept of a single array that contains sensors for monitoring glucose, lactate, and pyruvate.
Implantable sensors for monitoring glucose have been under investigation for nearly three decades, with mixed and promising results. In the electrochemical- monitoring approach followed in the present development, cyclic voltammetry, amperometry, square-wave voltammetry, or a combination of these techniques is used to measure the rate of catalytic oxidation of glucose by the enzyme glucose oxidase (GOX) in a reaction mediated by poly[vinyl pyridine Os(bipyridine)2Cl] co ethylamine (POs EA), which is an osmium-based polycationic redox polymer. To ensure biocompatibility, the GOX is entrapped in a poly(ethylene glycol) diacrylate (PEG-DA) hydrogel that has previously been demonstrated to be biocompatible.
The upper part of the figure depicts a typical sensor array; the lower part of the figure depicts some essential features of the fabrication of the array. Fabrication begins with the formation of microdisk electrodes and associated conductors in gold film on a flexible polyimide sheet by use of established deposition and photolithography techniques. The microdisk electrodes are functionalized with a monolayer of 11 mercaptoundecanoic acid (MUA) then coated with POs-EA, which adheres by strong electrostatic attraction to the MUA. The POS-EA layer is further coated with a mixture comprising PEG-DA, a solution containing GOX, and a photopolymerization initiator. Exposure to ultraviolet light causes cross-linking of the PEG-DA to form the PEG-DA hydrogel that encapsulates GOX.
In tests of a five-element array of individually electrically addressable sensors like the one shown in the figure, no cross-talk between adjacent electrodes was observed. It was found that when sampled together, the electrodes behaved as one large electrode with peak current equivalent to the sum of the currents of the individual electrodes — a characteristic that is especially important for diagnosis of failure of one of the sensors in an array. In other tests, an array was shown to exhibit the desired linear sensitivity to the concentration of glucose in the range of biological interest.
This work was done by Michael V. Pishko of Pennsylvania State University for the Army Research Laboratory. For more information, download the Technical Support Package (free white paper) at www.defensetechbriefs.com/tsp under the Bio-Medical category. ARL-0017
This Brief includes a Technical Support Package (TSP).
Implantable Electrochemical Sensors for Metabolic Monitoring
(reference ARL-0017) is currently available for download from the TSP library.
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