Documents / Report
This Defense Intelligence Agency reference document, dated 31 March 2010 (DIA-08-1003-020), was one of a series of advanced technology reports produced in FY 2009 under the Advanced Aerospace Weapon System Applications (AAWSA) program. It surveys biosensors and BioMEMS, covering brain-implanted neuroelectrodes, drug-delivery pumps, implantable glucose sensors, brain-machine interfaces, retinal prostheses, microfluidic lab chips, NASA cell culture systems, and microcantilever sensors. It concludes that the field is expanding rapidly toward nanomechanical systems.
UNCLASSIFIED/ ,tf8A 8FFHIIOI 1155 011! X COMMERCIAL BLOOD GLUCOSE SENSORS The present method of blood glucose monitoring depends on a needle puncture of the skin to withdraw a drop of blood to place on a color changing test strip. The test strip is read by a small handheld reader. Glucose test strips do not have to necessarily be small, but by making the sensor very small the amount of blood required for the test is reduced. The sensors often are made by techniques of photolithography or in some cases by microscale screen printing in order to achieve reproducibility. The skin-puncture test is painful and time consuming, and thus noninvasiveness is the key desired characteristic of glucose sensors. Research is being directed at a noninvasive glucose sensor that is accurate enough to work external to the body and through the skin. Short term (a few days) wearable needle glucose sensors are available from major companies like Medtronic Inc. but fall short of the convenience of a noninvasive sensor. ENZYME-BASED BIOSENSORS The key component in most biosensors is a reactive chemistry on the sensor surface. The sensor chemistry is chosen to give it specificity to only one analyte (such as glucose). The concentration of the analyte is determined by a sensor that can directly measure the analyte reaction products reacting with the sensor surface. For example sensor chemistries to measure glucose are often based on glucose oxidase enzyme which promotes a chemical reaction at the sensor surface. Glucose oxidase enzyme complex structure is seen in Figure 10. Glucose oxidase catalyzes the reaction: glucose + 02 (glucose oxidase) ➔ gluconolactone + H102 + heat (79 kl/mole) Figure 10. Glucose Oxidase Enzymes Like Glucose Oxidase are Large Folded Molecules That Act as Catalysts for a Chemical Reaction (http://www. 1nnovations- report.de/bilder_neu/17279 _gluc.jpg) This reaction of glucose with oxygen (from the air) occurs in the presence of glucose oxidase enzyme. The enzyme itself is a catalyst to the reaction and so is not consumed. Rather it presents favorable conditions and ability to transfer electrons on its molecular structure for glucose and oxygen to come together to react. Figure 10 shows the enzyme structure. Typically in a sensor the enzyme is a large molecule and can be trapped in a porous gel and thus is not able to diffuse away from the sensor surface. Glucose and oxygen, being small molecules, can diffuse through the gel to the enzyme whereby the reaction occurs and the reaction products will diffuse away. The enzyme is unconsumed and the reaction process is continuous as long as glucose is present. 14 UNCLASSIFIED/ ;«F81it 8FFIIIAI!: 1!181! &••1::Y
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Report, from the dia collection. The PDF is mirrored here; the original link is above. 45 pages are in the text index: search them above, or from the library's search.