An improved method and apparatus for determining noninvasively and in vivo one or more unknown values of a known characteristic, particularly the concentration of an analyte in human tissue. The method includes: (1) irradiating the tissue with infrared energy (400 nm-2400 nm) having at least several wavelengths in a given range of wavelengths so that there is differential absorption of at least some of the wavelengths by the tissue as a function of the wavelengths and the known characteristic, the differential absorption causeing intensity variations of the wavelengths incident from the tissue; (2) providing a first path through the tissue; (3) optimizing the first path for a first sub-region of the range of wavelengths to maximize the differential absorption by at least some of the wavelengths in the first sub-region; (4) providing a second path through the tissue; and (5) optimizing the second path for a second sub-region of the range, to maximize the differential absorption by at least some of the wavelengths in the second sub-region. In the preferred embodiment a third path through the tissue is provided for, which path is optimized for a third sub-region of the range. With this arrangement, spectral variations which are the result of tissue differences (e.g., melanin and temperature) can be reduced. At least one of the paths represents a partial transmission path through the tissue. This partial transmission path may pass through the nail of a finger once and, preferably, twice. Also included are apparatus for: (1) reducing the arterial pulsations within the tissue; and (2) maximizing the blood content i the tissue.
Described is a method which uses spectral data simultaneously collected in a continuous array of discrete wavelength points of the visible spectrum adjacent to the infrared and near infrared part of the light spectrum. The spectral data is collected using a number of detectors with different sensitivity ranges. Some detectors may be sensitive to visible and possibly, to part of the near infrared portion of radiation. Spectral data from die infrared spectrum is collected with the infrared detectors, and are in some embodiments insensitive to the visible links.
A fixture is provided on a set probe and a hole of the set probe communicates with that of the fixture so that a measuring probe consisting of an optical fiber bundle is inserted in the holes. A measured object is irradiated with light from a forward end of the measuring probe, so that outgoing light from the measured object enters the measuring probe. An air pack for coming into contact with the measured object is provided on the forward end of the measuring probe in a position not hindering emission and incidence of light. The air pack is connected with a pressure sensor, so that an indicator reads the pressure. Pressing force of the measuring probe is so adjusted that the pressure is at a constant value which is set for each measured object
A method of and an apparatus for regulating a pressure applied to an area of a living body during a biodata measurement with the use of a biodata measuring apparatus. The apparatus is designed to irradiate with light the area of the living body by means of a detecting probe then held in contact with the area of the living body, then to detect light transmitted through and/or reflected from the area of the living body, and finally to measure a predetermined biodata within the living body on the basis of a spectrum of the transmitted and/or reflected light. The method and the apparatus include pressing, during the biodata measurement, the area of the living body with a predetermined pressure through a soft pressure medium to thereby regulate the pressure applied to the area of the living body to a value equal to the predetermined pressure.
A method and apparatus for photoplethysmographic measurements is disclosed. In this system light from a plurality of emitters is delivered to the tissue-under-test. A subset of one or more of the emitters is known to be quiet light sources with relatively stable output intensity levels and spectral contents. A second subset of one or more emitters is known to be relatively noisy light sources with output intensity levels that fluctuate over time. The use of noisy light sources may be necessary for the photoplethysmographic measurements due to favorable spectral output characteristics such as narrow spectral bandwidth or desirable center wavelengths for the measurement of the hemodynamic parameters or analytes of interest. This invention utilizes the quiet light sources to enable the use of noisy light sources without the loss in accuracy or precision of analyte measurement that would otherwise typically be associated with the use of noisy light sources in the design and use of a photoplethysmographic instrument.
The invention provides a design process that is used in the determination of the pattern of detector and illumination optical fibers at the sampling area of a subject. Information about the system, specifically a monochromator (e.g. to determine the optimal number of fibers at an output slit) and the bundle termination at a detector optics stack (e.g. to determine the optimal number of fibers at the bundle termination), is of critical importance to this design. It is those numbers that determine the ratio and number of illumination to detection fibers, significantly limiting and constraining the solution space. Additional information about the estimated signal and noise in the skin is necessary to maximize the signal-to-noise ratio in the wavelength range of interest. Constraining the fibers to a hexagonal perimeter and prescribing a hex-packed pattern, such that alternating columns contain illumination and detection fibers, yields optimal results. In the preferred embodiment of the invention, two detectors share the totality of the detection fibers at the sampling interface. A third group of detection fibers is used for classification purposes.
