Toward an Injectable Continuous Osmotic Glucose Sensor

Author:

Johannessen Erik1,Krushinitskaya Olga1,Sokolov Andrey2,Häfliger Philipp3,Hoogerwerf Arno4,Hinderling Christian5,Kautio Kari6,Lenkkeri Jaakko6,Strömmer Esko6,Kondratyev Vasily6,Tønnessen Tor Inge7,Mollnes Tom Eirik2,Jakobsen Henrik1,Zimmer Even8,Akselsen Bengt8

Affiliation:

1. Vestfold University College, Tønsberg, Norway

2. Institute of Immunology, Oslo University Hospital, Oslo, Norway

3. Institute of Informatics, University of Oslo, Oslo, Norway

4. Swiss Center for Electronics and Microtechnology, Neuchâtel, Switzerland

5. Zurich University of Applied Sciences, Wädenswil, Switzerland

6. VTT Electronics, Oulu, Finland

7. Department of Anesthesia and Intensive Care, Oslo University Hospital, Oslo, Norway

8. Lifecare AS, Bergen, Norway

Abstract

Background: The growing pandemic of diabetes mellitus places a stringent social and economic burden on the society. A tight glycemic control circumvents the detrimental effects, but the prerogative is the development of new more effective tools capable of longterm tracking of blood glucose (BG) in vivo. Such discontinuous sensor technologies will benefit from an unprecedented marked potential as well as reducing the current life expectancy gap of eight years as part of a therapeutic regime. Method: A sensor technology based on osmotic pressure incorporates a reversible competitive affinity assay performing glucose-specific recognition. An absolute change in particles generates a pressure that is proportional to the glucose concentration. An integrated pressure transducer and components developed from the silicon micro- and nanofabrication industry translate this pressure into BG data. Results: An in vitro model based on a 3.6 × 8.7 mm large pill-shaped implant is equipped with a nanoporous membrane holding 4–6 nm large pores. The affinity assay offers a dynamic range of 36–720 mg/dl with a resolution of ±16 mg/dl. An integrated 1 × 1 mm2 large control chip samples the sensor signals for data processing and transmission back to the reader at a total power consumption of 76 μW. Conclusions: Current studies have demonstrated the design, layout, and performance of a prototype osmotic sensor in vitro using an affinity assay solution for up to four weeks. The small physical size conforms to an injectable device, forming the basis of a conceptual monitor that offers a tight glycemic control of BG.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Bioengineering,Endocrinology, Diabetes and Metabolism,Internal Medicine

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