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Review of designing an information processing ware for a diabetic chip
Youssef T AL-Sheikh1, Joseph D Andrade, Jared Millington
1Department of Biomedical Informatics, School of Medicine, University of Utah, Salt Lake City, Utah 84112, USA. youssef.alsheikh@gmail.com
Abstract:
Miniaturization of clinical chemistry analyzers can empower research conducted to better understand, diagnose, manage, and cure diseases such as diabetes. For the last decade, we have been working on the design and development of miniaturized clinical chemistry devices, including a Diabetic Chip (diabetiChip). These devices measure a small array of analytes, are small, portable, fast, easy-to-operate, and inexpensive. The chosen analytical method for the diabetiChip uses bioluminescence, which is highly sensitive and specific, and is based on photon counting and specific enzymatic reactions. Bioluminescent reactions were intentionally chosen for analyzing metabolic reactions because they use some of the central nodes of metabolism, such as adenosine triphosphate. Operations of the diabetiChip's information processing ware are the focus of this paper; we show the feasibility of using a set of kinase-containing enzymatic reactions of a firefly bioluminescence-coupled glucose assay in designing the diabetiChip. We have developed and tested the feasibility of the glucose assay; the assay's analytical detection limits (before sample dilution) were 5-185 microM. Uncertainty associated with reporting a 100 microM concentration was about +/- 5 microM. The results show that an FFL bioluminescent-coupled glucose assay is promising in terms of reducing sample volume and cost. The concept of GlucoFaces in visualizing measurements of the diabetiChip is also discussed.
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