WO2004038388A1 - Procede de detection optique de separation d'informations de surface et de profondeur - Google Patents
Procede de detection optique de separation d'informations de surface et de profondeur Download PDFInfo
- Publication number
- WO2004038388A1 WO2004038388A1 PCT/CN2003/000814 CN0300814W WO2004038388A1 WO 2004038388 A1 WO2004038388 A1 WO 2004038388A1 CN 0300814 W CN0300814 W CN 0300814W WO 2004038388 A1 WO2004038388 A1 WO 2004038388A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- light
- sample
- information
- deep
- incident
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/0059—Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/47—Scattering, i.e. diffuse reflection
- G01N21/49—Scattering, i.e. diffuse reflection within a body or fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
- A61B2562/02—Details of sensors specially adapted for in-vivo measurements
- A61B2562/0233—Special features of optical sensors or probes classified in A61B5/00
- A61B2562/0242—Special features of optical sensors or probes classified in A61B5/00 for varying or adjusting the optical path length in the tissue
Definitions
- the invention relates to an optical detection method, in particular to an optical detection method capable of separating the surface layer and deep information of a medium. Background technique
- Optical detection method is currently the most widely used non-destructive information detection method.
- the absorption and scattering characteristics of the medium are different. Therefore, the transmitted or reflected light passing through the medium also carries different Optical characteristics.
- information such as composition, concentration, and particle size in the medium can be obtained. It is based on this principle that optical measurement of substance composition and concentration has been widely used.
- non-invasive measurement of human body components has become the subject of most concern, especially the non-invasive measurement of human blood glucose concentration, and its success will save hundreds of millions of diabetic patients worldwide from having invasive sugar. Pain and discomfort.
- the existing media information detection methods can be divided into: transmission method, diffuse reflection method, and attenuated total reflection (ATR) method.
- transmission method the light source and the detector are respectively on both sides of the site to be inspected, and receive light transmitted through the tissue.
- US Patent No. 4,621,643 (New Jr., et al., 1986) is an example of measuring fingertip pulse and blood oxygen saturation using a transmission method.
- the transmission method receives all the information on the path that the light passes through. Because the tested individuals are very different, even when compared with the same individual, the time difference is also very serious, which limits the detection of trace components in the human body by transmission.
- the diffuse reflection method is that the light source and the detector are located on the same side of the test site, and the signal of the received light comes from the backscattered light component of the tissue.
- the advantage of the diffuse reflection method is that the transmission and reception are on the same side of the measured medium, which reduces the impact of individual differences and location differences.
- the diffuse reflection method generally uses contact measurement to eliminate the influence of light reflected from the surface of the medium, such as US Patent No. 5,028,787 (Rosenthal RD, et al., 1991), US Patent No. 5,070,874 (Barnes RH, et al. ., 1991), and Japanese Patent Laid-Open Publication No.
- Attenuated total reflection (ATR) method uses the principle of total reflection to make the sample and the light beam act multiple times to improve the sensitivity of the output signal to the active components.
- US Patent No. 4,169,676 Karl N., 1979
- Berman et al. US Patent No. 6,430,424, 2002
- the ATR method measures only the information on the surface of the medium, and it requires contact measurement.
- non-contact measurement is the most ideal method for non-invasive detection of medium information.
- the biggest problem brought by non-contact measurement is how to separate the surface and deep information of the medium.
- the influence of the surface information must be eliminated. Otherwise, the surface information and the deep information are aggregated to the receiving end, which will greatly affect the accuracy of the measurement results.
- the influence of the surface information must be eliminated.
- the effects of deep tissues must be eliminated.
- the technical problem to be solved by the present invention is an optical detection method that can separate the surface layer and deep information of a medium.
- Several detection methods for separating the surface and deep information of the medium were proposed, which laid the foundation for non-contact measurement.
- the reflected light contains two components, as shown in Figure 1.
- Research shows (Anderson .R., "The optics of human skin,” J. Invest. Dennatol. 5 77: 13-19, 1981), because the refractive index of skin and air is very different, so there is nearly 4% ⁇ 7% of incident light is reflected at the interface between the two.
- This part of the reflected light conforms to the Fresnel formula and is related to the incident angle of the light, the polarization state, and the relative refractive index of the tissue.
- the polarization state of the partially reflected light is the same as the polarization state of the incident light.
- the polarized light whose light vector is parallel to the incident plane is incident at the Brewster angle (Liang Yingting, Physical Optics, Beijing: Mechanical Industry Press, 1980)
- the specular reflection light component By analyzing the specular reflection light component, the characteristics of the skin surface tissue can be obtained.
- the other component is a backscattered light component.
- 93% to 96% of the incident light enters the tissue. After multiple scattering and absorption in the tissue, due to the scattering effect, part of the light will escape the skin in the form of scattered light later and become a part of the reflected light.
- the light source 1 is irradiated onto the sample tissue 40 through an incident unit 2, and after being processed by the receiving unit 3, the detection is completed by the detector 4.
- the light irradiated on the tissue 40 of the sample to be tested can pass through a probe, but the probe does not directly contact the tissue of the sample to be tested, but a non-contact method.
- the surface and deep information can be separated.
- the incident unit and the receiving unit may be designed according to different methods, which are described below respectively:
- the separation of surface and deep information can be achieved using the device shown in Figure 3.
- the light beam is first polarized by a polarizing plate 5 to convert unpolarized light into linearly polarized light, and then condenses the linearly polarized light on the skin surface of the measured part through the focusing lens 6.
- the receiving Reflected light passing through deep tissues in the optical path and reflected light from the skin surface are collected by the lens 7 and passed through the polarizing plate 8 for analysis, and are collected on the detector 9.
- the polarizing plate 8 is rotated to be orthogonal to the polarizing plate 5.
- the backward reflection light passing through the deep tissue loses the polarization characteristic, it can reach the detector, and the reflected light on the skin surface has polarization maintaining Characteristics, maintaining the original 3 ⁇ 4 polarization state, so it cannot pass through the polarizing plate 8, so that the surface reflection information can be eliminated.
- the polarizing plate 8 In order to receive the information reflected from the surface, the polarizing plate 8 is rotated so as to be parallel to the polarizing plate 5.
- the light received at this time is a combination of surface reflection information and deep information. Because the deep layer information is already obtained in the orthogonal polarization state, the surface reflection information can be obtained by subtracting the deep layer information in the orthogonal polarization state from the reflection information in the parallel polarization state.
- the specular reflection light conforms to Fresnel's theorem, although the surface of the skin is a rough surface, the surface reflection light is composed of a number of tiny specular reflections, and the reflection occurs at the point of incidence of the light on the skin.
- the backscattered light is scattered multiple times in the tissue, and the path is arbitrary. Therefore, the part where the backscattered light exits is at a certain distance from the incident point. Therefore, we use a light blocking method to separate the surface reflected light from the backscattered light through deep tissues.
- a light-shielding plate 10 is used, and the light-shielding plate is an opaque thin plate, which is placed vertically above the measured part as close to the measured part as possible, but not in contact.
- the incident light and the receiving light path are located on both sides of the light blocking plate, and the part of the reflected light that is reflected by the tissue surface is on the same side of the incident light, and is therefore blocked by the light blocking plate.
- the reflected light passing through the deep tissue bypasses the baffle, is reflected on the receiving side, and is collected by the condenser lens 7. Converged on the detector 9. Therefore, the light collected on the detector comes from the reflected light from deep tissues, eliminating the interference of reflected light from the surface.
- a light-shielding plate 39 is used, and a light-shielding thin plate is used.
- the center of the light-shielding plate has a small hole, which is covered above the measured part, as close as possible to the measured part, but not in contact. .
- the incident light point passes through the small hole, and the reflected light emitted through the small hole basically does not include the backscattered light of the deep tissue, but only the surface reflected light, thereby eliminating the interference of the backscattered light of the deep tissue.
- the spatial imaging method uses geometric optics to separate the light reflected from the surface tissue and the light reflected from the deep tissue. ⁇
- the incident unit the incident light is irradiated on the skin surface in a condensed form, because the reflection effect occurs at the light incident point.
- the imaging point of the receiving optical path is avoided by using the imaging relationship.
- the distance of the incident point of light should be greater than 1 dish.
- the stray light is eliminated by the diaphragm 11. Therefore, the light collected on the detector 9 comes from the reflected light from deep tissues, and the surface reflected light cannot enter the detector due to the imaging relationship, thereby eliminating the disturbance of the surface reflected light.
- the distance should be less than lmm. After the stray light is eliminated by the diaphragm 11, the received light is basically the reflected light from the surface tissue.
- the light is first polarized by the polarizing plate 5 so that the incident light is polarized to be parallel to the incident surface, and then converged by the lens 6 and irradiated on the skin, and the incident angle is about the skin surface.
- Brewster Point In the receiving unit, the backscattered light is received by the convergence method, and the imaging point of the convergence light path avoids the incident light point as much as possible.
- the Brewster angle is related to the wavelength of the incident light.
- the Brewster angle of the measuring light path is fixed, and the incident angle is set to be equal to the Brewster angle.
- the Brewster angle of the light path changes with the change of the wavelength, so the incident angle is set to the minimum. Brewster Point. BRIEF DESCRIPTION OF THE DRAWINGS
- Figure 1 Two components in the skin's reflected light
- Figure 2 Principle block diagram of an optical detection method that can separate surface and deep information of a medium
- Figure 3 Schematic diagram of polarization method
- Figure 4 (a): Schematic diagram of eliminating light reflected from the surface of the tissue with a light blocking plate
- Figure 5 (a): Schematic diagram of eliminating reflected light on the surface of the tissue by spatial imaging
- Figure 6 Schematic diagram of Brewster's angle method
- Figure 8 Energy change of reflected light from the lower and deeper tissues at different incident angles for parallel incident polarized light
- Figure 9 Polarization spectrometry experimental setup
- Figure 10 Backscattered light spectrum of skin measured by polarization method
- Figure 12 Experimental device for space measurement spectral measurement
- Figure 13 Spatial imaging method to measure the backscattered light spectrum of the skin. detailed description
- this experiment designs a complete verification experiment method.
- fresh pigskin was used as the experimental sample.
- the light reflection method was used to separate the specularly reflected light component and the backscattered light component in the reflected light.
- the experiment proved that when linearly polarized light is used as the light source, the specular reflection component is maintained.
- the original polarization state, and the backscattered light that has entered the tissue through multiple scattering events will lose its polarization state and become unpolarized light, thereby verifying the realization of the polarization method.
- the experiment also verified the realization principle of the light blocking method and the Brewster angle method.
- the experimental setup is shown in Figure 7: 632.8nm HeNe laser 12 (Model: 1101P, UNIPHASE INC.) It is a light source with an output power of 4mW, and its output light is linearly polarized light with a degree of polarization of 0.995.
- An aperture 14 is provided between the lens 13 and the lens 15 to eliminate stray light caused by the laser.
- the light is focused on the sample through the lenses 13 and 15, and the reflected light is collected by the optical power meter 19 (model: 835) of the company NEWPORT after being collected by the lens 16.
- the probe 18 has a model number of 818 and a response band of 385 to 1100 nm.
- a polarizer 17 is used as a polarizer in front of the probe to detect the polarization state of the reflected light.
- the sample holder can be rotated according to its own central axis in order to adjust the incident angle of the incident light.
- the receiving frame includes a lens 16, a polarizing plate 17, and a detection probe 18 fixed on a circular track centered on the sample frame so that the receiving portion can be on to adjust the receiving angle.
- the experiment used fresh skin of pig's abdomen as a sample, and made it into a sample block of 40x40mm and thickness of 10mm.
- the degree of polarization is a parameter used to quantitatively analyze the polarized and non-polarized components in a beam. Generally defined as
- FIG. 4 (b) The design parameters of the light-blocking sheet 39 are: thickness 0.2nm, center hole 1.5 ⁇ .
- the light blocking method uses Figure 4 (a). A light blocking plate 10 is placed on the surface of the sample so that the specular reflection light cannot enter the detector.
- the light received by the optical power meter is partially polarized light with a degree of polarization of 0.52.
- the degree of polarization of the light beam after shielding the backscattered light of deep tissues Increased by 75% to 0.91.
- the surface reflected light is linearly polarized light, and its polarization The state is parallel to the polarization state of the incident light. This proves that it is feasible to separate the reflected light from the surface and the deep tissue from the polarization method.
- the light-blocking plate 10 was used in this experiment, and the degree of polarization of the received light was essentially zero (P ⁇ 0.03), indicating the feasibility of using the light-blocking method to eliminate surface-reflected light. .
- a light blocking plate 39 is used, and the polarization degree of the received light is 0.91, which also verifies the feasibility of using the light blocking method to eliminate deep reflected light. Therefore, this experiment verifies the feasibility of using the light-blocking method to separate surface reflected light and deep tissue reflected light.
- FIG. 8 shows the experimental results. From the theoretical analysis and experimental results, it can be seen at the same time: Although the skin is a complex surface, the component of the reflected light on the surface conforms to the Fresnel formula. When polarized light with a light vector parallel to the incident surface enters the sample surface There is also a Brewster angle, which is about 56 °. At this time, the surface reflected light component is substantially zero. The backscattered light passing through deep tissues is basically unaffected by the Brewster angle. Therefore, this experiment verifies the feasibility of using Brewster's angle method to separate surface reflected light and deep tissue reflected light.
- non-contact measurement devices for the detection of human and in vivo components are constructed for different principles of separation of surface and deep information, especially non-invasive measurement devices for blood glucose in humans.
- These devices use near-infrared spectroscopy, and the near-infrared wavelength range is 0.8 to 2.5 ⁇ m. It contains the absorption peak of water 6900 ⁇ , the combined absorption band of sugar 4710, 4400, 4300 cm ' 1 , the first-order frequency doubling absorption band of sugar 6200, 5920, 5775 cm " 1 , the second-order frequency doubling of sugar Absorption band 960 ⁇ 1200 cni-
- Example 2 Example of polarization method
- the polarization method is used to eliminate light reflected on the surface of the tissue, and non-contact spectral measurement of components in the human body is achieved, especially non-invasive measurement of human blood glucose.
- the measurement device is shown in Figure 9.
- the subject of the experiment is the palm of a volunteer.
- the spectrum measurement is performed by FT spectrometer 20 (Spectrum GX FTIR spectrometer, Perkin-Elmer Inc.).
- a 250W bromine tungsten lamp is used as the external light source 32, which is input to In FT, the light is transmitted to the reflector 21 after being split by FT, and then coupled to the near-infrared light guide fiber 23 through a converging lens 22.
- the light output from the fiber is converged to the palm 41 of the measured part through the lens 24 and the polarizer 34 on.
- the reflected light is coupled into the light guide fiber 30 by the lens 27, the polarizing plates 35 and 28, and is converged by the lens 31 to the FT detector.
- 25 and 29 are rotatable adjusting brackets, which are used to adjust the angle of incidence and reception.
- the polarizing plate 34 converts incident light into linearly polarized light, and the polarization state is parallel to the incident surface.
- a polarizer 35 is used at the receiving end, and its polarization state is perpendicular to the incident surface to eliminate surface reflection light.
- the measurement device was used to perform spectrum measurement on the palm 41, and the incident angle was 45 degrees during the measurement.
- the spectrum is shown in Fig. 10. It can be seen from the spectrum that the energy is close to zero at 6900 cm- 1 wave number. This is because water has a strong absorption peak here. Reflected light from deep tissues appears to have almost zero energy in the spectrum due to water absorption. Therefore, it can be explained that the received light is also backscattered light from deep tissues. Thus, the separation of surface reflected light and deep reflected light is achieved.
- Example 3 Example of a light blocking method
- the light method is used to eliminate the light reflected on the surface of the tissue, thereby realizing non-contact spectral measurement of human body components, especially non-invasive measurement of human blood glucose.
- the measurement device is shown in Figure 11.
- the system uses AOTF as the spectroscopic device 42.
- the system light source 32 uses a 250W tungsten halogen lamp and is incident on the AOTF crystal through the lens 33.
- the AOTF crystal is driven by an RF driving module 37 controlled by a computer 38, and performs spectroscopic scanning on the input light.
- the separated light is coupled to the light guide fiber 23 through the converging lens 22, and then converged to the measured part (the palm 41) through the lens 24.
- the light blocking plate 26 eliminates the surface reflected light, and the reflected light inside the tissue is coupled to the light guide fiber 30 by the lenses 27 and 28, and then converged by the transparent lens 31 to the near-infrared photodetector 35. Finally, it is sampled into the computer 38 by the A / D converter 36.
- the near-infrared photodetector can be an InGaAs detector or a PbS detector. Rotate the mounts 25 and 29 to adjust the angle of incidence and reception.
- the measurement device was used to perform spectrum measurement on the same part of the palm of the same volunteer. Its spectrum is similar to Figure 10, so it can be explained that most of the received light comes from backscattered light from deep tissue. Thus, the separation of surface reflected light and deep reflected light is achieved.
- Example 4 Example of space imaging method
- the space imaging method is used to eliminate the reflected light on the surface of the tissue, and the non-contact spectrum of the components in the human body is realized. Measurement, especially non-invasive measurement of human blood glucose.
- the measurement device is shown in Figure 12, and its core component is also an FT spectrometer. Unlike the polarization method, a polarizer is eliminated in the measurement device, and a diaphragm 44 is used in the receiving unit to eliminate the interference of stray light.
- the distance between the incident point and the receiving imaging point must be greater than 1 mm. .
- the measurement device was used to perform spectrum measurement on the palm 41, and the incident angle was 45 degrees during the measurement. Its spectrum is shown in Figure 13. It can be seen from the spectrum that the received light is all backscattered light from deep tissues. Thus, the separation of surface reflected light and deep reflected light is achieved.
- Example 5 Example of the Brewster Angle Method
- the Brewster angle method is used to eliminate reflected light on the surface of the tissue, and non-contact spectral measurement of components in the human body is achieved, especially non-invasive measurement of human blood glucose.
- the Brewster's angle measurement device is basically similar to the polarization measurement device, except that the receiving end no longer needs a polarizer. Because the Brewster angle is a function of the wavelength of the light wave, the angle of incidence should be adjusted to be slightly less than 56 degrees in this measurement device to meet the maximum Brewster angle for all wavelengths.
- the measurement device was used to perform spectrum measurement on the same part of the palm of the same volunteer. Its spectrum is similar to that in Figure 13, so it can be explained that most of the received light comes from backscattered light from deep tissues. Thus, the separation of surface reflected light and deep reflected light is achieved.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Pathology (AREA)
- Biophysics (AREA)
- Biomedical Technology (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Analytical Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Heart & Thoracic Surgery (AREA)
- Medical Informatics (AREA)
- Molecular Biology (AREA)
- Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003272848A AU2003272848A1 (en) | 2002-09-29 | 2003-09-24 | An optical detection method for separating surface and deepness |
US10/528,522 US20060092418A1 (en) | 2002-09-29 | 2003-09-24 | Optical detection method for separating surface and deepness |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB02129271XA CN100483106C (zh) | 2002-09-29 | 2002-09-29 | 可分离介质表层与深层信息的光学检测方法 |
CN02129271.X | 2002-09-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004038388A1 true WO2004038388A1 (fr) | 2004-05-06 |
Family
ID=32097473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2003/000814 WO2004038388A1 (fr) | 2002-09-29 | 2003-09-24 | Procede de detection optique de separation d'informations de surface et de profondeur |
Country Status (4)
Country | Link |
---|---|
US (1) | US20060092418A1 (zh) |
CN (1) | CN100483106C (zh) |
AU (1) | AU2003272848A1 (zh) |
WO (1) | WO2004038388A1 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007119199A1 (en) | 2006-04-18 | 2007-10-25 | Koninklijke Philips Electronics N.V. | Optical measurement device |
WO2007119202A1 (en) * | 2006-04-18 | 2007-10-25 | Koninklijke Philips Electronics N.V. | Optical measurement device |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4559995B2 (ja) * | 2006-03-30 | 2010-10-13 | 株式会社東芝 | 腫瘍検査装置 |
SG177951A1 (en) * | 2007-01-05 | 2012-02-28 | Myskin Inc | System, device and method for dermal imaging |
AU2013201634B2 (en) * | 2007-01-05 | 2015-05-07 | Myskin, Inc. | System, device and method for dermal imaging |
US20090245603A1 (en) * | 2007-01-05 | 2009-10-01 | Djuro Koruga | System and method for analysis of light-matter interaction based on spectral convolution |
US20100185064A1 (en) * | 2007-01-05 | 2010-07-22 | Jadran Bandic | Skin analysis methods |
WO2010059537A1 (en) * | 2008-11-19 | 2010-05-27 | Siemens Healthcare Diagnostics Inc. | Polarized optics for optical diagnostic device |
CA2791624A1 (en) | 2010-02-26 | 2011-09-01 | Myskin, Inc. | Analytic methods of tissue evaluation |
US9265457B2 (en) * | 2010-06-03 | 2016-02-23 | Koninklijke Philips N.V. | Apparatus and method for measuring a tissue analyte such as bilirubin using the Brewster's angle |
US8780362B2 (en) | 2011-05-19 | 2014-07-15 | Covidien Lp | Methods utilizing triangulation in metrology systems for in-situ surgical applications |
US9113822B2 (en) | 2011-10-27 | 2015-08-25 | Covidien Lp | Collimated beam metrology systems for in-situ surgical applications |
EP2703773B1 (de) * | 2012-08-28 | 2014-12-24 | Texmag GmbH Vertriebsgesellschaft | Sensor zum Erfassen einer laufenden Warenbahn |
US9351643B2 (en) | 2013-03-12 | 2016-05-31 | Covidien Lp | Systems and methods for optical measurement for in-situ surgical applications |
JP6323227B2 (ja) * | 2013-12-16 | 2018-05-16 | ソニー株式会社 | 画像解析装置、画像解析方法、およびプログラム、並びに照明装置 |
JP6660634B2 (ja) * | 2015-01-29 | 2020-03-11 | 国立大学法人 香川大学 | 分光測定装置および分光測定方法 |
CN106551690A (zh) | 2015-09-30 | 2017-04-05 | 齐心 | 一种生命体征测量装置及方法 |
CN106932343A (zh) * | 2015-12-31 | 2017-07-07 | 富泰华工业(深圳)有限公司 | 检测材质的装置及方法 |
CN106290208A (zh) * | 2016-07-28 | 2017-01-04 | 青岛海纳光电环保有限公司 | 一种臭氧浓度测定装置 |
EP3384831A1 (en) * | 2017-04-05 | 2018-10-10 | Koninklijke Philips N.V. | Skin gloss measurement using brewster's angle |
CN109141643B (zh) * | 2018-09-28 | 2024-01-30 | 福建师范大学 | 一种宽带信号光偏振成份比测量装置及方法 |
CN111513728B (zh) * | 2020-04-23 | 2022-07-29 | 中国科学院上海技术物理研究所 | 一种多技术融合的无创血糖检测装置及测量方法 |
CN113156557B (zh) * | 2021-04-30 | 2023-02-21 | 浙江光珀智能科技有限公司 | 一种光学面罩及光学*** |
CN115963068B (zh) * | 2023-03-16 | 2023-05-05 | 北京心联光电科技有限公司 | 皮肤组织成分含量的测定方法及装置 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5676143A (en) * | 1992-11-09 | 1997-10-14 | Boehringer Mannheim Gmbh | Apparatus for analytical determination of glucose in a biological matrix |
CN1184936A (zh) * | 1996-11-26 | 1998-06-17 | 松下电工株式会社 | 一种用于非侵入地测量受验者血中葡萄糖浓度的装置 |
CN1224163A (zh) * | 1997-11-21 | 1999-07-28 | 株式会社京都第一科学 | 非接触非侵入式测量方法及测量装置 |
US6025597A (en) * | 1995-10-17 | 2000-02-15 | Optiscan Biomedical Corporation | Non-invasive infrared absorption spectrometer for measuring glucose or other constituents in a human or other body |
JP2000074829A (ja) * | 1998-09-02 | 2000-03-14 | Mitsui Chemicals Inc | グルコースセンサー |
JP2001299727A (ja) * | 2000-04-25 | 2001-10-30 | Matsushita Electric Works Ltd | 生体中のグルコース濃度の測定装置 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2606991A1 (de) * | 1976-02-20 | 1977-08-25 | Nils Dr Med Kaiser | Geraet zur bestimmung des gehaltes von stoffwechselprodukten im blut |
US4621643A (en) * | 1982-09-02 | 1986-11-11 | Nellcor Incorporated | Calibrated optical oximeter probe |
JPH0827235B2 (ja) * | 1987-11-17 | 1996-03-21 | 倉敷紡績株式会社 | 糖類濃度の分光学的測定法 |
US5028787A (en) * | 1989-01-19 | 1991-07-02 | Futrex, Inc. | Non-invasive measurement of blood glucose |
US5070874A (en) * | 1990-01-30 | 1991-12-10 | Biocontrol Technology, Inc. | Non-invasive determination of glucose concentration in body of patients |
SE512871C2 (sv) * | 1992-08-20 | 2000-05-29 | Santen Oy | Oftalmologisk beredning innehållande pilokarpin och ytterligare medel för behandling av okular hypertension |
DE4242232C2 (de) * | 1992-12-15 | 1998-12-10 | Burkhard Kuhls | Vorrichtung und Verfahren zur nicht-invasiven Konzentrationsbestimmung polarisierender Stoffe im menschlichen Körper |
DE4243142A1 (de) * | 1992-12-19 | 1994-06-23 | Boehringer Mannheim Gmbh | Vorrichtung zur in-vivo-Bestimmung einer optischen Eigenschaft des Kammerwassers des Auges |
US5636633A (en) * | 1995-08-09 | 1997-06-10 | Rio Grande Medical Technologies, Inc. | Diffuse reflectance monitoring apparatus |
US5871442A (en) * | 1996-09-10 | 1999-02-16 | International Diagnostics Technologies, Inc. | Photonic molecular probe |
JPH11151229A (ja) * | 1997-11-21 | 1999-06-08 | Kdk Corp | 非接触非侵襲測定方法及び装置 |
US6662030B2 (en) * | 1998-05-18 | 2003-12-09 | Abbott Laboratories | Non-invasive sensor having controllable temperature feature |
US6424851B1 (en) * | 1998-10-13 | 2002-07-23 | Medoptix, Inc. | Infrared ATR glucose measurement system (II) |
US6687521B2 (en) * | 2000-02-03 | 2004-02-03 | Hamamatsu Photonics K.K. | Noninvasion biological optical measuring instrument, measured portion holding device, and method for manufacturing the same |
WO2002016905A2 (en) * | 2000-08-21 | 2002-02-28 | Euro-Celtique, S.A. | Near infrared blood glucose monitoring system |
US6609015B2 (en) * | 2001-01-18 | 2003-08-19 | Koninklijke Philips Electronics N.V. | Analysis of a composition |
-
2002
- 2002-09-29 CN CNB02129271XA patent/CN100483106C/zh not_active Expired - Fee Related
-
2003
- 2003-09-24 AU AU2003272848A patent/AU2003272848A1/en not_active Abandoned
- 2003-09-24 US US10/528,522 patent/US20060092418A1/en not_active Abandoned
- 2003-09-24 WO PCT/CN2003/000814 patent/WO2004038388A1/zh not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5676143A (en) * | 1992-11-09 | 1997-10-14 | Boehringer Mannheim Gmbh | Apparatus for analytical determination of glucose in a biological matrix |
US6025597A (en) * | 1995-10-17 | 2000-02-15 | Optiscan Biomedical Corporation | Non-invasive infrared absorption spectrometer for measuring glucose or other constituents in a human or other body |
CN1184936A (zh) * | 1996-11-26 | 1998-06-17 | 松下电工株式会社 | 一种用于非侵入地测量受验者血中葡萄糖浓度的装置 |
CN1224163A (zh) * | 1997-11-21 | 1999-07-28 | 株式会社京都第一科学 | 非接触非侵入式测量方法及测量装置 |
JP2000074829A (ja) * | 1998-09-02 | 2000-03-14 | Mitsui Chemicals Inc | グルコースセンサー |
JP2001299727A (ja) * | 2000-04-25 | 2001-10-30 | Matsushita Electric Works Ltd | 生体中のグルコース濃度の測定装置 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007119199A1 (en) | 2006-04-18 | 2007-10-25 | Koninklijke Philips Electronics N.V. | Optical measurement device |
WO2007119202A1 (en) * | 2006-04-18 | 2007-10-25 | Koninklijke Philips Electronics N.V. | Optical measurement device |
US7872754B2 (en) | 2006-04-18 | 2011-01-18 | Koninklijke Philips Electronics N.V. | Optical measurement device |
US7978332B2 (en) | 2006-04-18 | 2011-07-12 | Koninklijke Philips Electronics N.V. | Optical measurement device |
Also Published As
Publication number | Publication date |
---|---|
CN1485605A (zh) | 2004-03-31 |
US20060092418A1 (en) | 2006-05-04 |
AU2003272848A1 (en) | 2004-05-13 |
CN100483106C (zh) | 2009-04-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2004038388A1 (fr) | Procede de detection optique de separation d'informations de surface et de profondeur | |
US9597024B2 (en) | Methods and apparatuses for noninvasive determinations of analytes | |
US5657754A (en) | Apparatus for non-invasive analyses of biological compounds | |
RU2549992C2 (ru) | АППАРАТ ДЛЯ НЕИНВАЗИВНОГО АНАЛИЗА in vivo ПОСРЕДСТВОМ СПЕКТРОСКОПИИ КОМБИНАЦИОННОГО РАССЕЯНИЯ | |
US20110184260A1 (en) | Methods and Apparatuses for Noninvasive Determinations of Analytes | |
US20060178570A1 (en) | Methods and apparatuses for noninvasive determinations of analytes | |
CN101151513A (zh) | 分析物无创检测的方法和装置 | |
Louie et al. | Degree of optical polarization as a tool for detecting melanoma: proof of principle | |
US20120044484A1 (en) | Optical probe for measuring light signals in vivo | |
WO2008083573A1 (fr) | Procédé et dispositif d'imagerie pour lumière polarisée linéaire | |
CN101430275B (zh) | 一种非接触测量溶液浓度的装置及方法 | |
Guo et al. | Angular measurements of light scattered by turbid chiral<? xpp qa?> media using linear Stokes polarimeter | |
Louie et al. | Constructing a portable optical polarimetry probe for in-vivo skin cancer detection | |
WO2015106220A1 (en) | Non-invasive system and method for measuring a substance concentration | |
CN105596011B (zh) | 一种无创血糖检测装置 | |
EP3052010B1 (en) | Probe, system, and method for non-invasive measurement of blood analytes | |
CN109856082A (zh) | 香烟滤嘴中爆珠的检测方法与检测装置 | |
CN102499647B (zh) | 一种多模式低相干散射光谱仪 | |
RU2515410C2 (ru) | Способ неинвазивного измерения концентрации глюкозы в крови и устройство для его осуществления | |
CN205913354U (zh) | 一种无创血糖检测装置 | |
US20150157199A1 (en) | Method and apparatus for scatterometric measurement of human tissue | |
CN113208562A (zh) | 一种基于光检测技术的皮肤含水量检测***及方法 | |
TWI522086B (zh) | 非侵入式葡萄糖監測裝置 | |
CN114486813A (zh) | 一种不同偏振态激光损伤阈值测试的装置与方法 | |
JP2007313286A (ja) | 光学的生体情報測定方法及びその装置 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
ENP | Entry into the national phase |
Ref document number: 2006092418 Country of ref document: US Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 10528522 Country of ref document: US |
|
122 | Ep: pct application non-entry in european phase | ||
WWP | Wipo information: published in national office |
Ref document number: 10528522 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: JP |