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/ ;(F8A 8FFHiIAL Wili &HLY -=-=-------' , --< __-_:_':_j i j j r-_ ----: '-~- -~~---==J. . -----: - Thin Mylar Substrate Figure 15. Thermopile Glucose Sensor (left} With Functional Illustration (right} are Made Using Photolithographic Techniques. This larger device is about 8 mm in length but has approximately 50 micron minimum geometries. (Towe et al.) At ASU the glucose sensor has been constructed on a thin mylar plastic substrate and so can be curved into a cylinder to form a small tube. This tube is then sensitive to glucose concentrations on its outside exposure to the blood stream. Figure 16 shows a photograph and an illustration of a glucose sensor implemented in the form of a catheter. The electrical output signal is routed by wires down the length of the catheter for a remote readout. The device was implanted in a pig over a short duration and the decrease in blood glucose concentrations in response to administration of insulin were recorded and are shown in the right hand panel of Figure 16. lmulin '& E w - !' •' w -• • •! ,_ '"" 'e - .__ Time 10min Figure 16. Photograph and Illustration of the Thermopile Glucose Sensor in a Catheter. Its configuration is shown (left) and its response in detecting changes 1n blood glucose in a pig as a result of insulin administration to the animal. (ASU research.) Towe et al. This glucose sensor approach has been found to have limitations in stability when introduced into tissue or blood. Primarily the problems, as with many sensors, arise from the system chemistry and not as much from the electronic portion of the sensor. The glucose oxidase enzyme slowly decays over time and thus the sensor sensitivity and calibration drifts making it eventually unusable. These problems have no easy solution. Investigators have been working with various forms of blood chemistry sensors for forty years or more. Microfabricated 19 UNCLASSIFIED/ ,<EiOA OEiEil&I.«1k Wili &••LY
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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.