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    Applications of Long-Wavelength Sources and

    Detectors for Medical Monitoring

    Jonathon T. Olesberg

    Optical Science and Technology Center

    and the Department of Chemistry

    University of Iowa, Iowa City, IA

    There are several exciting possible applications

    of optical sensing for medical monitoring. Optical

    monitoring of body chemistry offers several advantages

    over conventional chemical techniques. Long-wavelength

    semiconductor source and detector technology will likely

    play a key role in making these applications possible and

    practical.

    There are several biochemicals for which

    medical monitoring would be useful, including urea,

    lactate, cholesterol, and creatinine. The best-knownpotential application of non-invasive optical monitoring,

    however, is the measurement of blood glucose for

    individuals with diabetes. Although the importance of

    frequent blood glucose monitoring is clear, and standard

    reagent-based technology for measuring blood glucose is

    well developed, most individuals with diabetes do not

    monitor their blood glucose values nearly as often as they

    should. The primary reasons given for inadequate testing

    are the pain of drawing a sample of blood and the cost of

    the reagent-carrying test strip. Optical measurements can

    do away with both of these factors, allowing the

    measurement to be performed non-invasively and

    reagentlessly.

    Although development of optical blood glucose

    sensors has been pursued aggressively for several years,

    there are still no commercially available instruments. This

    is due to a combination of factors, including an extremely

    high signal-to-noise requirement and the difficulty of

    properly interpreting spectral absorption information. The

    factors required for successful noninvasive biochemical

    monitoring, especially as they relate to the potential

    impact of the development of semiconductor source and

    detector technology in the 2.0-10 m wavelength range,

    will be discussed.

    Biomolecule absorption in the infrared is due to

    interaction of the optical field with vibrational modes of

    the molecule. In this regard, infrared optical sensing is

    much more difficult than the measurement of hemoglobin

    oxygenation in pulse oxymetry, which utilizes electronic

    transitions in the hemoglobin molecule. The most intense

    vibrational interactions are due to bonds involving

    hydrogen atoms, such as, O-H, C-H, and N-H bonds.

    Fundamental vibrational modes exist in the 4-10 m

    wavelength range. Weaker nonlinear combinations of

    fundamental modes exist in the 2.0-2.5 m wavelength

    range, and yet weaker overtones exist in the 1.5-1.8 m

    and 0.8-1.2 m ranges.

    Any measurement in a biological material must

    deal with the presence of water. Water has significant

    absorption throughout the long-wavelength infrared,

    requiring the selection of wavelength bands lying in water

    absorption windows. The dominant water transmission

    windows in the long-wavelength infrared occur between

    2.0-2.5 m, 3.3-5.9 m, and 6.2-11 m.

    Much of the work in noninvasive sensing has

    utilized the shorter wavelength regions (0.8-1.8 m

    wavelength) because of the greater penetration depth of

    water and the abundance of well-developed source and

    detector technology. However, the optical interaction

    strength with glucose is very weak in these ranges. Thefield of biochemical sensing will be greatly aided by

    advances in device technology in the 2.0-2.5 m and

    3-10 m wavelength ranges.

    The requirements for biomolecule sensing in

    aqueous environments are very different from gas

    sensing, where absorption lines are narrow. In an aqueous

    environment, absorption features are broad and highly

    overlapped. Fortunately, though, the exact structure of the

    absorption bands depends on the chemical environment

    surrounding the active bonds. Because of this, the

    absorption spectrum of each chemical species is unique.

    But absorption measurements must be made at several

    wavelengths in order to provide enough degrees of

    freedom to identify glucose in the presence of other

    interfering compounds.

    Much of the present non-invasive chemical

    sensing research is performed using broad-band optical

    sources (e.g., tungsten lamps or glow-bars) and FTIR

    spectrometers. Spectral quality is typically limited by

    detector noise due to the small optical powers provided by

    broad-band sources. In addition, tissue throughput is

    small due to water absorption and tissue scattering: peak

    transmission in the 2.0-2.5 m wavelength range is

    significantly less than 1% per millimeter of tissue.

    Tunable laser sources or arrays of laser diodes caneliminate the low signal limitation, even with modest

    powers (e.g., 10 mW). Unlike gas sensing applications,

    narrow linewidth is not important, but wavelength

    stability (for lasers in an array) or wavelength

    reproducibility (for a tunable system) is critical.

    Successful noninvasive measurements will likely require

    very large (>105) signal-to-noise-ratios, so wavelength

    deviations must be very small.

    Abs. 283, 205th Meeting, 2004 The Electrochemical Society, Inc.