Analyte detection device and method for detecting analytes

Abstract

The present invention provides devices and methods for analyte detection. [Solution] The apparatus includes a radiation source for irradiating a sample; a receiver for receiving an optical Raman spectrum of radiation returned from the sample in response to received radiation from the radiation source, wherein the receiver includes a plurality of different types of analytical devices each positioned to receive a selected portion of the received optical spectrum returned from the sample.

Description

Technical Field

[0001] The present invention relates to an analyte detection device and a method for detecting an analyte.

Background Art

[0002] The use of Raman spectroscopy for the transdermal in vivo measurement of glucose or other analytes present in the skin is known. In our co-pending international application WO-A-2016 / 034448, the use of a confocal detection device having at least one component expected to measure the glucose concentration in interstitial fluid by irradiating the skin of a user with light radiation and then detecting and measuring the Raman scattered radiation from the sample is described. This device functions well and provides a non-invasive method of measuring the blood glucose level (correlated with the blood glucose level) in the interstitial fluid of a user.

[0003] The most well-known systems that use Raman spectroscopy to measure or determine analyte concentration are often bulky and stationary. In the field of blood glucose measurement using Raman spectroscopy, miniaturization is desirable because, when provided in a suitably miniaturized form, the device is convenient and easy for use by diabetic patients who often need to determine their blood glucose value several times a day (directly or otherwise).

[0004] WO2012019102 discloses a portable Raman diagnostic system. This system relates to the selection of a specific filter combination that can provide information about a multivariate calibration for extracting analyte concentration in a biological system. The system of WO2012019102 utilizes a method for selecting the wavelength interval to minimize the size of the test device. Multiple wavelength selection methods, the design of a miniaturized spectroscopic device, and the tools necessary to map from one domain (wavelength selection) to another domain (design parameters) are disclosed.

[0005] In an article by MSWrobel titled "Non-invasive blood glucose monitoring using Raman spectroscopy: prospects for device miniaturization," published as part of the 39th International Microelectronics and Packaging (IMAPS) Poland 2015 conference, the use of multiple photodetectors to detect optical signals of specific wavelengths within the received Raman spectrum is disclosed.

[0006] U.S. Patent Nos. 5,701,005, 7,511,255, 5,424,826, U.S. Patent Publication No. 2006 / 0262303, U.S. Patent Publication No. 2013 / 0289414, and U.S. Patent No. 4,997,281 disclose optical systems including spectrometers and / or photofiltration devices. Many of these are used in systems that rely on Raman spectroscopy to determine information about a sample.

[0007] Other analytes or metabolites for which miniaturized Raman devices are considered useful for concentration measurement include any one or more lactates, fatty acids, urea, carbamides, cholesterol, or hemoglobin. [Overview of the project] [Means for solving the problem]

[0008] According to a first aspect of the present invention, an analyte detection device is provided, comprising: a radiation source for irradiating a sample; a receiver for receiving the optical spectrum of radiation returned from the sample in response to the radiation received from the radiation source, wherein the receiver comprises a plurality of different types of analytical devices, each arranged to receive a selected portion of the received optical spectrum returned from the sample. The optical spectrum of radiation returned from the sample would typically be a Raman spectrum.

[0009] The present invention provides an analyte detection system that includes more than one type of analytical device. This means that different portions of the received spectrum can be supplied to or associated with correspondingly different types of analytical devices, particularly those that may have different levels of resolution and / or signal-to-noise ratio. Thus, portions of the received spectrum considered important for the analyte in question can be associated with a first type of analytical device having high resolution and / or a high signal-to-noise ratio, while portions of the spectrum that do not require much detailed information can be associated with a second type of analytical device that provides lower resolution and a lower signal-to-noise ratio.

[0010] This means that an entire instrument can be provided that delivers sufficiently detailed and adequately leveled data as output for an analyte without requiring multiple high-resolution analytical devices. This also means that the entire instrument can be made smaller and / or less expensive without resulting in output data of unacceptably low quality or resolution. In other words, it is possible to deliver the same level of high-quality data for spectral segments considered important, while the instrument used to deliver it can be made simpler, less expensive, and smaller in physical size.

[0011] In other words, this device has the potential to further miniaturize Raman spectroscopy-based blood glucose monitoring devices. This would be advantageous for diabetic patients or other patients who would benefit from a device that allows them to measure their blood glucose and is conveniently portable.

[0012] In one embodiment, the apparatus includes one or more filtering devices arranged to filter the received light spectrum and direct specified components to specific devices of a plurality of different types of analytical devices.

[0013] The use of a filtration device allows for the easy and efficient separation of the received spectrum into desired components or wavelength regions. This then allows for the direction of each sub-region of the spectrum to a suitable designated analytical device. Thus, the received spectrum is further divided into multiple regions by the filtration element, and each subdivided region is then sent to a specific analytical device.

[0014] In one embodiment, the filtration device includes at least one tunable filtration device. Providing a tunable filtration device allows for selective configuration of the apparatus, and thus it can be tuned to analyze a desired analyte. Each analyte being investigated has its own Raman spectrum, and therefore the region of interest within the entire received spectrum may differ.

[0015] In one embodiment, the tunable filtration element includes a filtration element that is tunable by a change in the angle of incidence (AOI) on the filtration device. In another embodiment, the tunable filtration element includes a filtration element (linear variable filter) that is tunable by the substitution of the filter. In such a filter, the transmission window is shifted relative to the side of the filter. In yet another embodiment, an acoustically-optically (electrically) tunable filter is used. In some embodiments, any combination of different types of filtration elements can be used.

[0016] A further example is a filtering element in which the refractive index of a crystal is periodically modulated by high-frequency sound waves generated by a piezoelectric transducer. In such a device, the frequency of the wave generated by the voltage transducer determines the refractive index modulation period, which in turn determines the wavelength of the diffracted light.

[0017] In one embodiment, the different analytical device includes at least one CCD-based spectrometer.

[0018] In one embodiment, the different analytical device includes at least one CMOS-based spectrometer.

[0019] According to a second aspect of the present invention, there is provided a method for detecting an analyte, the method comprising irradiating a sample with light radiation; receiving the optical spectrum of the radiation returned from the sample in response to the received radiation from the light source; and selectively correlating different portions of the received spectrum with different analysis devices. The optical spectrum of the radiation returned from the sample will typically be a Raman spectrum.

[0020] In one embodiment, the method includes filtering the received spectrum into two or more components and correlating the first component with a first analysis device and the second component with a second analysis device.

[0021] In one embodiment, the first analysis device is a CCD-based spectrometer.

[0022] In one embodiment, the second analysis device is a CMOS-based spectrometer.

[0023] Embodiments of the present invention will now be described in detail, reference being made to the accompanying drawings:

Brief Description of the Drawings

[0024] [Figure 1] A schematic diagram of the Raman shift spectrum of an irradiated skin sample. [Figure 2] A schematic diagram of a device for analyte detection. [Figure 3] A schematic diagram of a filtering structure used in the device of FIG. 2.

Modes for Carrying Out the Invention

[0025] As is well known, the basis of a spectroscopic setup is a light source, such as a laser, used to illuminate the sample. Light from the light source interacts with the sample and often results in changes to the light that passes through the sample, is irradiated by the sample, is reflected by the sample, and / or is scattered by the sample. By recovering the altered light and analyzing its spectral distribution, information about the interaction between the incident light and the sample can be obtained. Therefore, information about the molecular components within the sample can be obtained.

[0026] One mode of interaction between incident light and molecular components is Raman scattering, where there is an energy exchange between the molecule and the photons of the incident light. The frequency (i.e., the spectral distribution of the Raman scattered light) differs from the spectral distribution of the incident light and uniquely reflects the specific vibrational levels of the molecule; therefore, this spectrum is a fingerprint spectrum. This can be used to identify the molecular composition of the substance being sought and / or the concentration of specific molecules in the substance.

[0027] The spectrum returned from the sample can be called a received light spectrum because it is received by a receiver, and this spectrum can then be processed or analyzed to obtain information about the sample.

[0028] Our concurrent continuation application WO-A-2016 / 034448 describes an optical configuration and arrangement from which results can be obtained by identifying the depth within a sample from which the detected radiation is analyzed. Indeed, as described, WO-A-2016 / 034448 teaches that ensuring that the Raman scattered light recovered for measurement originates from a specific depth or near a specific depth within the skin can bring several advantages.

[0029] The entire contents of WO-A-2016 / 034448 (including, but not limited to, specific aspects relating to the depth within the sample derived from the collected data, and the optical and physical configuration of the interface or lens between the sample and the device) are incorporated herein by reference.

[0030] The spectral distribution of a received light spectrum is typically measured using a spectrophotometer. A spectrophotometer is an optical device that works by separating a ray of light directed towards the optical device into components of different frequencies, and then measuring the intensity of these components using an analytical device (such as a CCD detector or CCD array).

[0031] Figure 1 shows the Raman spectrum obtained from the sample. The data is obtained from a Raman spectroscopic study of the thenar eminence region of the subject. The thenar eminence region of the subject was irradiated with light, and the detected spectrum 1 is shown in Figure 1. Figure 1 also includes the Raman glucose spectrum 2, which allows the glucose concentration in the test region to be determined using the Raman spectrum obtained from the sample. Since the thenar eminence Raman spectrum includes contributions from any molecule present in the test region, the actual glucose concentration needs to be determined from this spectrum.

[0032] Note that the glucose spectrum includes four main intensity-enhancing regions labeled A-D and enclosed by boxes 3-6. Therefore, these regions in the thenar spectrum 1 will contain a relatively higher level of information regarding glucose concentration in the sampled region than other parts of spectrum 1.

[0033] It is recognized that if the output from a spectrometer is positioned to resolve, for example, the parts of the spectrum that require higher levels of sensitivity / low noise than others, it is possible to obtain a high-quality signal while minimizing the need for expensive CCD detectors.

[0034] Identify spectral patterns A–D, where the most significant changes are attributed to glucose content. Then, analyze the entire spectrum, modifying the details, and in particular, investigate only the regions that most significantly contribute from the contents of the analyte being investigated with a high level of detail. This means that other spectral regions, if any, can be analyzed using simpler and less expensive analytical mechanisms.

[0035] Methods with higher resolution and sensitivity can be assigned to spectral portions containing a higher level of information, while methods with lower resolution and sensitivity can be assigned to spectral portions containing less information, thus significantly reducing the complexity of the measurement setup.

[0036] Figure 2 shows a schematic diagram of an apparatus for measuring glucose concentration subcutaneously and in vivo using Raman spectroscopy. While the detection and measurement of glucose levels are described herein, this method and apparatus can be used to measure the concentrations of other analytes of interest.

[0037] Apparatus 7 includes a light source 8, a probe 9, and a detector 10. The detector 10 will be described in more detail below with reference to Figure 3.

[0038] The subject 11 can be tested by engagement of the end of the probe 9 with the skin surface. The mechanism of light transmission from the light source 8 to the subject's skin 11 may be as detailed in WO-A-2016 / 034448, which has already been mentioned above. In fact, there are many known mechanisms for obtaining Raman spectra from subjects in vivo, and any suitable system disclosed in the art can be used for this purpose.

[0039] Figure 2 schematically illustrates how light from the light source 8 is linked to the subject 11 by the probe 9 and then received by the probe 9 for communication with the analysis device 10. The analysis system 10 includes a number of photodetectors with possible dispersion elements, as described below. Each photodetector is selected from a number of different types of photodetectors so that it can detect the received signal at a desired level of resolution and signal-to-noise ratio. At least two different types of photodetectors are present in the system 10, thereby providing detection at at least two corresponding resolutions and / or signal-to-noise ratios.

[0040] For example, in regions A, B, C, and D of the thenar spectrum 1 in Figure 1, a CCD-based spectrometer can be used to resolve spectral portions where high sensitivity and low noise are required, while a CMOS-based spectrometer can be used to resolve spectral portions where high resolution is still required, but a lower signal-to-noise ratio may be acceptable.

[0041] When an 830-nanometer laser is used as the excitation source (i.e., as source 8 in Figure 2), the Raman spectrum will be in the range of 850-985 nanometers, or 283-1900 cm⁻¹. -1 It is measured at [location / location].

[0042] A schematic diagram of the analysis system 10 is shown with reference to Figure 3.

[0043] Light 12 is received as input to the analysis system 10. A plurality of filtration devices 141-144 are provided. Each of the filtration elements 141-144 is arranged to transmit a portion of the light and reflect another portion. Thus, the portions of light 161-164 transmitted by each of the elements 141-144 represent a spectral portion selected according to its frequency. A plurality of analysis devices 181-184 are provided, each arranged to receive the corresponding transmitted or reflected components originating from the filtration elements 141-144 in question as input. Thus, the device has inherent flexibility, as it can select individual analysis devices or detection units 181-184 to yield a desired level of resolution and / or signal-to-noise ratio for the corresponding portions of the spectrum it is arranged to receive.

[0044] For example, filtration elements 141-144 are each dichroic filters. In another example, these elements could be a grid or, in fact, any other wavelength-dependent filtration device. For example, at least two different types of filtration devices could be used (e.g., using both dichroic mirrors and grids for the selection of different parts of the spectrum).

[0045] In one preferred embodiment, one or more analytical devices 181-184 include a dispersion element. This is particularly useful in areas expected to contain data about the analyte under investigation, as dispersing the receiving portion of the spectrum allows for more detailed analysis.

[0046] In Figure 1, boxes 3-6 show spectral regions with high levels of glucose information. Filter elements 141-144 divide the energy into different detectors with varying resolutions and noise floors depending on the frequency or wavelength. As an example, the spectral region shown by boxes A-D, which contains important Raman vibrations related to glucose, is shown with a resolution of 9 cm. -1 It is preferable to detect this using a CCD-based spectrometer.

[0047] The spectral region outside the area indicated by boxes A-D has a resolution sufficient to simply evaluate the signal gradient over frequency intervals (e.g., 25 cm). -1 Detection can be performed using a CMOS-based spectrometer with ) or, if only the average intensity needs to be evaluated, simply using a photodiode. In fact, for areas outside the box where there is little information about glucose, it is possible to omit the detector altogether.

[0048] Therefore, it provides a system that enables selective analysis of different parts of a spectrum, allowing more data to be extracted from the spectral parts most important to the analysis of the problem without inefficiently dedicating the same amount of resources to less important spectral parts. It allows for the completion of the required level of analysis and investigation of the important parts of the spectrum without wasting time, effort, resources, or cost on less important parts. In a given example, the glucose spectrum is shown superimposed on the spectrum derived from the thenar eminence. This allows for the identification of the region of interest in the thenar eminence spectrum. If another metabolite or analyte were investigated, the region of interest would likely be located elsewhere in the spectrum.

[0049] In one example, a spectrometer is used as at least one detection device. For example, in an embodiment that is not limited, wavelength-scaled standing wave integrated Fourier transform spectroscopy (SWIFTS) is used. This SWIFTS technology is detailed in the paper by Le Coarer et al., titled "Standing Wave Integrated Fourier Transform Spectroscopy" (the entire paper is referenced herein), published in August 2007 in Nature Photonics, Vol. 1. More general Fourier transform spectroscopy methods can also be used.

[0050] If the filtering elements can be selectively and reconfigurably tuned, the system can be modified to focus on different parts of the spectrum depending on the metabolite or analyte being investigated. Therefore, during manufacturing, the filtering elements are tuned to the desired frequency so that the system as a whole is configured for the analysis of a specific selected analyte.

[0051] Tunerable filters or filtration devices can be of several different types. An example includes filters that are tunable by a change in the angle of incidence (AOI) relative to the filtration device. In such filters, the transmission window shifts with respect to the perpendicular of the filter along with the AOI. An example is those manufactured by Semrock Inc. (part of IDEX Health and Science, LLC.), which can be found, for example, at https: / / www.semrock.com / versachrome-edge-tunable-filters.aspx.

[0052] Other examples include filters that are tuned by substitution (linear variable filters). In such filters, the transmission window is shifted relative to the side of the filter. Examples include those from Delta Optical Thin Film A / S, which can be found, for example, at http: / / www.deltaopticalthinfilm.com / products / linear-variable-filters / .

[0053] A further example would be an acousto-optically (electrically) tunable filter in which the refractive index of a crystal is periodically modulated by high-frequency sound waves generated by a piezoelectric transducer. In such a device, the frequency of the wave generated by the voltage transducer determines the refractive index modulation period, which in turn determines the wavelength of the diffracted light. Examples include those found, for example, at http: / / www.olympusmicro.com / primer / techniques / confocal / aotfintro.html.

[0054] Referring again to the example in Figure 1, use a dichroic mirror for 0-280cm -1 The light is filtered, and the spectral range is 283 cm². -1 ~1900cm -1 The light passes through. This light then enters another filter / dichroic mirror set that guides the spectral portion to the appropriate spectrometer and / or detector. Thus, the filter stack is arranged to separate the light into clearly defined spectral portions so that different analytical methods can be applied to different parts.

[0055] In the example described, the apparatus is set up to determine the glucose level in a sample using Raman spectroscopy. As already mentioned, the apparatus and method can be used independently of the analyte being measured. Other examples include one or more lactates, fatty acids, urea, carbamides, cholesterol, or hemoglobin. Figure 1, showing the Raman spectrum, has other molecules on it that are known to have Raman peaks or shifts at certain wavelengths. Therefore, if other spectra among these are to be primarily analyzed, the analytical device will be selected to have high resolution and high signal-to-noise ratio, and will be configured to receive a significant single or multiple portion of the spectrum.

[0056] Embodiments of the present invention have been described with particular reference to the examples provided. However, it will be recognized that the described embodiments can be modified and altered within the scope of the present invention.

Claims

1. A glucose detection device, A radiation source for irradiating a sample; A receiver for receiving the optical Raman spectrum of radiation returned from the sample in response to the radiation received from the radiation source. Includes, The spectrum includes one or more spectral portions that are important in glucose and one or more spectral portions that are not important in glucose. The receiver includes a plurality of analytical devices having different performance characteristics, each arranged to receive a portion of the received Raman light spectrum returned from the sample, selected according to the frequency. The glucose detection apparatus comprises an analytical device having different performance characteristics, which includes at least one analytical device having a high signal-to-noise ratio for detecting important spectral portions in glucose, and at least one analytical device having a second performance characteristic that provides a low signal-to-noise ratio for detecting non-important spectral portions in glucose.

2. The apparatus according to claim 1, comprising one or more filtering devices arranged to filter the received light spectrum and direct a specified component to a specific device of a plurality of analytical devices having different performance characteristics.

3. The apparatus according to claim 2, wherein the filtration device comprises at least one synchronous filtration device, and the filtration device is selectively configured to analyze glucose.

4. The apparatus according to claim 3, comprising one or more mechanically synchronized, electrically synchronized, and acoustically synchronized filtration devices as synchronizeable filtration elements.

5. The apparatus according to any one of claims 1 to 4, wherein the different analytical devices include at least one CCD-based spectrometer.

6. The apparatus according to claim 5, wherein the different analytical devices include at least one CMOS-based spectrometer.

7. The apparatus according to claim 6, wherein one or more Fourier wave spectroscopy and standing wave integrated Fourier transform spectroscopy are used.

8. The apparatus according to any one of claims 1 to 7, wherein one or more selected portions of the received Raman light spectrum are associated with a dispersion member.

9. The apparatus according to any one of claims 1 to 8, wherein the apparatus is arranged to determine the concentration of the analyte.

10. The apparatus according to claim 9, wherein the analyte is selected from the group comprising glucose, lactate, fatty acid, urea, carbamide, cholesterol, alcohol, and hemoglobin.

11. The apparatus according to any one of claims 1 to 10, wherein the analytical device having different performance characteristics includes at least one analytical device having high resolution and a high signal-to-noise ratio for detecting important spectral portions in the analyte to be detected, and at least one analytical device having a second performance characteristic that provides low resolution and a low signal-to-noise ratio for detecting non-important spectral portions in the analyte to be detected.

12. The apparatus according to any one of claims 1 to 11, wherein the apparatus is arranged to select a portion of the received Raman light spectrum in which spectral analysis is not performed.

13. A method for detecting an analyte, Irradiating a sample with light radiation; Receiving the optical Raman spectrum of radiation returned from the sample in response to radiation received from a light source, wherein the spectrum includes one or more spectral portions important for glucose and one or more spectral portions not important for glucose; The method involves selectively associating different frequency portions of the received Raman spectrum with different analytical devices, wherein each analytical device includes at least one analytical device having a high signal-to-noise ratio for detecting spectral portions important in glucose, and at least one analytical device having a second performance that provides a low signal-to-noise ratio for detecting spectral portions that are not important in glucose. Methods that include...

14. The method according to claim 13, comprising filtering the received spectrum into two or more components and associating the first component with a first analytical device and the second component with a second analytical device.

15. The method according to claim 14, wherein the first analytical device is a CCD-based spectrometer.

16. The method according to claim 14 or 15, wherein the second analytical device is a CMOS-based spectrometer.

17. The method according to claim 16, wherein one or more Fourier wave spectroscopy and standing wave integrated Fourier transform spectroscopy are used.

18. The method according to any one of claims 13 to 17, wherein one or more selected portions of the received Raman light spectrum are associated with a dispersion member.

19. The method according to any one of claims 13 to 18, comprising determining the concentration of glucose.

20. The method according to any one of claims 13 to 19, wherein the analytical device having different performance characteristics includes at least one analytical device having high resolution and a high signal-to-noise ratio for detecting important spectral portions in the analyte to be detected, and at least one analytical device having a second performance characteristic that provides low resolution and a low signal-to-noise ratio for detecting non-important spectral portions in the analyte to be detected.

21. The method according to any one of claims 13 to 19, comprising selecting a portion of the received Raman light spectrum for which spectral analysis is not performed.

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