Transportation vehicle, physiological state detection device, and physiological state detection method applied to transportation vehicle
US-2024374188-A1 · Nov 14, 2024 · US
US2017138860A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017138860-A1 |
| Application number | US-201515322874-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 2, 2015 |
| Priority date | Jul 2, 2014 |
| Publication date | May 18, 2017 |
| Grant date | — |
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Characterizing, identifying, or diagnosing the type and/or nature of a sample or a tissue such as an abnormal growth using a Raman spectrum includes analyzing distinct spectral subintervals within the Raman spectrum in two distinct wavelength ranges, such as FP and HW wavelength ranges, to identify a match with one or more reference markers in one or both wavelength ranges; and from the match characterizing, identifying, or diagnosing the type and/or nature of the sample or tissue. FP and HW Raman spectra can be detected or acquired simultaneously using a single diffraction grating.
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1 . A Raman spectroscopy apparatus comprising: a first illumination source configured for directing illumination into a tissue; a Raman spectrograph configured for simultaneously detecting fingerprint (FP) and high wavenumber (HW) Raman spectra from illumination scattered by the tissue; and a computerized control and analysis module comprising at least one processing unit and a memory storing program instructions executable by the at least one processing unit for analyzing discrete spectral sub-intervals of the detected Raman spectra in FP and HW wavelength ranges to identify a match with one or more reference markers in one or both wavelength ranges. 2 . The apparatus of claim 1 , wherein the Raman spectrograph has a single broadband diffraction grating. 3 . The apparatus of claim 2 , wherein the first illumination source comprises a source of collimated illumination for generating an excitation energy to apply to the tissue, and wherein the apparatus further comprises a probe for transmitting the collimated illumination to the tissue and returning the detected Raman spectra from the tissue to the spectrograph. 4 . The apparatus of claim 3 , wherein the one or more reference markers comprise specific peaks in the detected Raman spectra. 5 . The apparatus of claim 3 , wherein the computerized control and analysis module includes program instructions executable by the at least one processing unit for diagnosing an abnormal growth based upon the match. 6 . The apparatus of claim 3 , wherein the probe comprises a confocal fiber-optic probe. 7 . The apparatus of claim 6 , further comprising an endoscope having an elongate shaft having an instrument channel within which the probe is carried. 8 . The apparatus of claim 3 , wherein the computerized control and analysis module includes program instructions executable by the at least one processing unit for dynamically adjusting a power of the collimated illumination. 9 . The apparatus of claim 3 , wherein the computerized control and analysis module includes program instructions executable by the at least one processing unit for dynamically adjusting a time to which the tissue is exposed to the collimated illumination. 10 . The apparatus of claim 3 , further comprising a calibration apparatus configured for standardizing the probe or the entire Raman apparatus with respect to at least one calibration reference. 11 . The apparatus of claim 3 , further comprising: an additional illumination source configured for outputting additional illumination into the tissue; and a hot mirror filter configured for compensating for illumination interference between the illumination output by the first illumination source and the additional illumination output by the additional illumination source. 12 . A Raman spectroscopy method performed by a Raman spectroscopy apparatus, the method comprising: directing illumination output by a first illumination source into a tissue; simultaneously detecting by way of a probe fingerprint (FP) and high wavenumber (HW) Raman spectra from illumination scattered by the tissue; and analyzing discrete spectral sub-intervals in the detected Raman spectra in both FP and HW wavelength ranges to identify a match with one or more reference markers in one or both wavelength ranges. 13 . The method of claim 12 , wherein simultaneously detecting FP and HW Raman spectra comprises diffracting illumination in both FP and HW wavelength ranges using a single broadband diffraction grating. 14 . The method of claim 12 , further comprising diagnosing the nature of an abnormal growth based upon the match. 15 . The method of claim 12 , wherein the one or more reference markers are specific peaks in the detected Raman spectra. 16 . The method of claim 12 , further comprising dynamically adjusting the power of the illumination. 17 . The method of claim 12 , further comprising dynamically adjusting a time to which the tissue is exposed to the illumination. 18 . The method of claim 12 , further comprising performing a calibration or standardization procedure to standardize the probe or the entire Raman apparatus with respect to at least one calibration reference prior to illuminating the tissue. 19 . The method of claim 12 , further comprising: directing additional illumination into the tissue using an additional illumination source while directing the illumination output by first illumination source into the tissue; and compensating for illumination interference between the illumination output by the first illumination source and the additional illumination output by the additional illumination source using a hot mirror filter.
for receiving instruments · CPC title
for introduction into the body, e.g. by catheters (A61B5/1459 takes precedence) · CPC title
Raman spectrometry; Scattering spectrometry {; Fluorescence spectrometry} · CPC title
Circuits of general importance; Signal processing · CPC title
of calibration, e.g. protocols for calibrating sensors · CPC title
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