• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
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  • 优先权
    • 专利摘要:
    a nephelometer that measures the turbidity of low volume suspensions using measurements of light transmitted through and/or scattered by the sample. the sample suspension is placed in a bowl arranged in a row adapted to facilitate the measurement of turbidity of low volume samples. the lower portion of the bowl has smaller dimensions, in horizontal cross section, in relation to the top portion. both the top and bottom portions have angled surfaces. the lower, smaller portion of the bowl is analyzed by the nephelometer.
    公开号:BR112017006363B1
    申请号:R112017006363-8
    申请日:2015-09-29
    公开日:2021-06-29
    发明作者:Brian Reuben Langhoff；William Alan Fox；Kerry Lynn Smith
    申请人:Bd Kiestra B.V.；
    IPC主号:
    专利说明:

    RELATED REFERENCE TO RELATED REQUEST
    [001] This application claims the benefit with respect to the filing date of Provisional Application No. 62/056911, filed on September 29, 2014, the descriptive content of which is incorporated by reference in this report. FUNDAMENTALS OF THE INVENTION
    [002] Bacterial cultures show growth, ordinarily, on specialized media plates. The plates generate massive colonies and some isolated colonies. Isolated colonies have the purest form of bacteria because the colony usually develops from a limited amount of bacteria and is isolated from the growth of other bacteria. Testing for the least amount of colonies is generally desired to ensure sample purity. However, current laboratory practices require collecting bacterial samples from media and diluting the samples in tubes containing relatively large volumes of fluid. Obtaining a sufficient concentration of bacterial matter in the fluid suspension requires collecting a large amount of bacterial colonies from the media plate in order to make a suspension. One drawback is that this technique can reduce sample purity.
    [003] One approach is to create a highly concentrated suspension from a low-yield bacterial sample using small fluid volumes (eg 200-500 μL). This is especially important in machine automation when an automated colony capture system is being employed for sample collection and suspension creation. For example, an automated colony picker can be asked to make several passes along the media board in order to capture colonies when generating the hold. Optimized results are obtained if the taker selects from a relatively small amount of colonies (eg 5 or less) in order to create a suspension containing the proper concentration of bacteria. This approach requires a fluid volume of suspension of 300 µL or less. An obstacle is the difficulty in determining the bacterial concentration in a small fluid volume containing a highly concentrated suspension. Therefore, there is a need for a system and methods for accurately determining bacterial concentrations in a small fluid volume, while automatically diluting samples to a desired concentration.
    [004] The bacterial concentration can be determined by measuring the turbidity or "cloudity" of a culture and then carrying this measurement in cell quantities (CFUs). The standard microbiological method of estimating the turbidity of a sample is based on obtaining a quantitative value known as a McFarland value. McFarland values are well known to those skilled in the art and are not described in detail in this report. McFarland standards comprise of solutions of known turbidity that are used for standardization of culture density in microbiological, clinical and other similar laboratories.
    [005] The turbidity of microbiological suspensions is usually determined by an instrument such as a nephelometer or a densitometer. The instruments base their measurements on the physical principles of light scattering resulting from the interaction of light with particles present in a suspension. The turbidity of the samples affects the transmission and scattering of light, and provides conditions by measuring the intensity of light transferred through a sample. A nephelometer is an automatic instrument used to measure the turbidity of a sample by passing light through the sample at an angle and measuring the intensity of the scattered light. Such a measurement is based on the principle that a dilute suspension of small particles will scatter light that is passed through (and not absorbed) by the particles. The amount of scattering is determined by collecting light at an angle of 30 or 90 degrees.
    [006] The nephelometers currently used in laboratories are designed to admit the samples inside a round container/tube. This practice provides acceptable results as long as the tubes or container are cleaned prior to use and positioned within the instrument within the same orientation for each respective sample. For the nephelometer, round tubes have several drawbacks. One understands that the tubes are not disposable, and must be cleaned prior to reuse, at the risk of cross-contamination. Another drawback is that the light paths are more variable through the round tubes making it difficult to obtain a consistent light path from one sample to another and from one tube to another.
    [007] In practically all circumstances, a container presenting a unique configuration is necessary for each sample placed inside the nephelometer to measure the turbidity. The use of containers with different sizes and shapes can provide inconsistent turbidity readings for each sample. Apparatus and methods are necessary and are designed to minimize the variability of measurements between containers, as well as minimizing the effect of diffraction and refraction along with light as it passes through and between different media.
    [008] Furthermore, most nephelometers such as the PhoenixSpec TM (Becton Dickinson) require a cell length of at least one (1) centimeter (cm) in their associated tubes, and are therefore not intended for use with a very small volume of microbiological suspensions, such as, for example, suspensions of around 200 or around 500 micro-liters (μL). In standard test tubes (eg a 15 ml test tube), a suspension as low as around 500 µL may yield cell lengths of less than 1 cm, which may not be suitable for measuring the McFarland value. making use of a commercially available nephelometer. A narrower test tube, for example, can be used to increase the sample elevation close to a detectable level. However, such test tubes are often not used containing nephelometers and/or densitometers because these instruments are designed to house test tubes of specific sizes and configurations. Therefore, there is a need for an apparatus and method that can provide conditions for a quick and accurate measurement of turbidity for suspensions with a volume smaller than around 500 μL, and preferably as low as around 200 μL. In addition, there is a need for an apparatus and methods where the sample can be purified and diluted inside the container for turbidity estimation, where the container is configured to dilute the samples and provide consistent and accurate turbidity measurements for small sample volumes. BRIEF SUMMARY OF THE INVENTION
    [009] The apparatus and bowl (cuvette) described in this report cooperate to provide accurate optical investigation of a small sample volume. Optical inquiry as used by this report consists of transmitting an optical signal along with the sample within an optically transparent bowl. Examples of optical probing include spectrometry and nephelometry. The invention is described in terms of nephelometry but the bowl aspects described in this report are applicable and adaptable to other devices aimed at optical investigation. In one embodiment, the apparatus and methods according to the present invention provide an accurate estimate of McFarland values for a microbiological suspension aimed at sample volumes having a volume of around 100 μL, to around 500 μL, and for all volumes and ranges within that range through the use of electronic detectors/sensors and specialized containers. Small volumes are defined elsewhere in this report. The sensors/detectors and the nephelometer cooperate in providing a uniform light path for all samples that are measured using the detectors/sensors described in this report. The methods described in this report make use of the principles of nephelometry, which measures the amount of light scattered and/or transmitted through a sample to provide a turbidity sample.
    [010] In the methods described, there is the selection of a diameter, volume and orientation of the container inside the nephelometer relative to the light source to provide a sample cell length advantageously for turbidity measurements. According to the modalities described in this report, the biological sample is mixed with a suspension fluid directly inside the container positioned in the automated system or apparatus (ie, the nephelometer) designed to measure the turbidity of the sample. In certain embodiments, a continuous array of receptacles configured for receiving containers (the containers comprising of various sizes, volumes and lengths of cells) is continuously indexed through the apparatus. Because the device is automated, it is convenient for use in various microbiological, clinical and laboratory adjustments.
    [011] The apparatus according to the present invention consists of an array of electronic sensors positioned adjacent to a specialized bowl/container illuminated with light wavelengths selected from an LED or a laser source. The bowl is designed for ascertaining a small sample volume (defined elsewhere in this report) for turbidity measurements. First, there is the preparation of the microbiological suspension. Then, the suspension is introduced into the container. In one embodiment, the apparatus obtains turbidity measurements for samples in small volume containers that concentrate the samples in the area of the container where the sample is ascertained. In some embodiments, the containers have a rectangular or square configuration. For this purpose, the walls of the container are at an angle of ninety degrees to each other. This arrangement allows for more uniform control of wall thicknesses, which reduces the variability of McFarland readings between containers that would arise if wall thickness variations from one container to another are large. In addition, the square shape of the containers allows light to enter the container at a right angle to the plane of the container surface. This reduces the amount of diffraction or refraction of the investigative light as it enters (or exits) the container.
    [012] In the other modalities described in this report, there is a description of an automated nephelometer apparatus featuring a base, a receptacle configured to receive a container, a dispersion detector, a detector for transmitted light, an attenuation filter. light, a light source, and a focusing lens. The nephelometer is adapted to receive a container having a small volume portion from which the nephelometer measurements are taken and a large volume dilution portion provided to enable the suspension to be diluted to the desired concentration. The container that is adapted to be received by the nephelometry apparatus described in this report is assumed to be of an interchangeable character in the form of a “container” or a “bowl”. In one embodiment, the apparatus is configured to receive and process one container at a time. In another embodiment, the apparatus has a sliding channel configured to receive a continuous series of containers disposed on the inside of the linear receptacle. The linear receptacle is configured to present depths that are designed for receiving the receptacles. Containers can receive liquid samples covering a volume ranging from around 200 μL to around 500 μL.
    [013] In one modality, the sample suspension is metered into a simple container and the container is individually ascertained by the nephelometer. After the sample suspension has been processed and McFarland values are obtained, the container is removed from the nephelometer and a new container is placed in the nephelometer for evaluation. In this embodiment, the nephelometer may have one bowl receptacle or multiple bowl receptacles. Each receptacle is configured to perform nephelometry measurements as described in this report. In the modality where the nephelometer receives a series of measuring bowls, there is the provision of a series of bowl receptacles to facilitate the nephelometry measurements of several suspensions in parallel.
    [014] In an alternative embodiment, the bowls are provided in a two-dimensional arrangement. The lower, narrower portion of the bowls extends below the array support. The disposition is positioned on the disposition-support base and inspects each bowl individually. In one modality, the layout is positioned on the base by a robot.
    [015] With respect to the container or bowl, in one modality, the bowl has a narrower lower portion, and a wider upper portion. Optionally, there is a tapered transition portion from the upper wider portion to the lower portion. The lower portion is adapted by the nephelometer for gauging. The upper portion and the lower portion share a common axis. In the illustrated embodiment, both portions are square or rectangular, and therefore both have flat gaskets. In one embodiment, the plane of the pads in the upper portion is parallel to the planes of the pads in the lower portion. In another embodiment, the plane of the bottom pads intersects the plane of the top pads at an angle of 45 degrees. However, the bowls covered in this report need not have a rectangular or square top portion. In other embodiments, the top portion can be round or elliptical, if desired. The base portion (through which the measurements are made) is required to be rectangular or square for the reasons described in this report.
    [016] In one embodiment, the nephelometer incorporates two detectors that simultaneously capture the light that is transmitted and/or scattered from the suspension particles through where the optical signal is transmitted. The side scatter detector is positioned to receive light within a right angle of 90 degrees from the light beam incident on the bowl. The transmitted light detector is positioned to receive light directly from the light source which is transmitted through the bowl and proceeding through the suspension. In some embodiments, the transmitted light detector is positioned perpendicular to the incident light beam. In alternative embodiments, the transmitted light detector is positioned opposite the light source, but at an angle that reduces the effect caused by reflectance refraction and diffraction caused by the detector surface and surrounding structure. A light attenuation filter is positioned between the container and the transmitted light detector in some embodiments. In the example modalities, there is the use of a focusing lens. The focusing lens is positioned directly in front of a light source and is used to focus light along a narrow beam along the light path. In some embodiments, the light beam is collimated through an aperture or a series of apertures (eg, two apertures).
    [017] Several modalities described in this report provide an additional accurate method of measuring the turbidity of a suspension where said suspension has a volume insufficient to be read by most nephelometer or densitometer devices. The methods described in this report obtain the turbidity estimates of a liquid suspension presenting low volumes in the range of around 200 μL to around 500 μL. The methods and apparatus can also be used to measure the turbidity of suspensions of samples with higher volumes. The methods described in this report further allow for automated dilution of the sample suspension inside containers designed in accordance with the present invention. Methods include placing a suspension fluid in a container, adding a suspended biological sample containing microorganisms to the suspension fluid, mixing the sample, and gauging the initial turbidity of the sample. The volume of the initial fluid suspension is preferably around 300 μL or less. This way, if the dilution is necessary, the dilution will not lead to the total volume being presented in excess of around 3.6 mL. That said, the apparatus and methods described in this report are not limited to measuring turbidity only for small volumes. If the turbidity of the initial sample suspension is less than the predetermined desired turbidity, an additional suspension fluid is added using the automated system of the present invention to further dilute the sample and repeat the turbidity measurements for the diluted suspension. Methods of various modalities make it possible to measure McFarland levels of samples for use with methods such as Mass Spectrometry (eg matrix-assisted desorption/ionization laser - time duration mass spectrometer, MALDI-TOF). BRIEF DESCRIPTION OF THE DRAWINGS
    [018] In order to serve specialists with knowledge in the area of interest regarding the execution and use of the present matter in question, reference is made to the attached drawings.
    [019] Fig. 1A illustrates a low-volume simple bowl nephelometer modality.
    [020] Fig. 1B consists of a carved view of the single bowl nephelometer along line 1-1 of Fig. 1A.
    [021] Fig. 2A comprises a view of a series of details of Fig. 1B.
    [022] Fig. 2B consists of a perspective view of a continuous bowl nephelometer.
    [023] Fig. 3 illustrates a row/strip model of multiple linear low volume bowls facing the continuous series bowl nephelometer.
    [024] Fig. 4A illustrates a bowl according to an embodiment of the present invention.
    [025] Fig. 4B illustrates a bowl according to an alternative embodiment of the present invention.
    [026] Fig. 5 illustrates a process flowchart illustrating a modality for a sample preparation process using the nephelometer described in this report.
    [027] Fig. 6 illustrates stacked bowls.
    [028] Fig. 7 consists of an indented view of the transmitted light detection path path for an embodiment of the present invention.
    [029] Fig. 8 is an indented view of the scattered light detector path path for an embodiment of the present invention.
    [030] Fig. 9 consists of a carved view of the modality pertinent to Fig. 7, but illustrating the light source and the transmitted light detector.
    [031] Fig. 10 consists of a perspective view of the nephelometer according to a modality. DETAILED DESCRIPTION
    [032] The modalities described in this report provide automated methods of measuring the turbidity of liquid suspensions making use of containers that are configured to receive and measure low volumes of samples and at the same time accommodating the suspension dilution inside the individual containers. The methods also describe the possibility of measuring the turbidity levels in suspensions presenting insufficient volume to be measured using conventional containers and apparatus. The nephelometry device described in this report is configured for integration with a system where suspension dilution and turbidity measurements are automated.
    [033] All numerical values within the detailed description and claims in this report are modified by the expressions "around" or "approximately" to the indicated value, and take into account experimental errors and variations, which would be expected by experts in the field.
    [034] According to the use given in this report, a "low volume" and/or "small volume" sample refers to a sample having a volume of around 100 μL to around 500 μL and all volumes and ranges within that range (ie, around 100 μL to around 200 μL; around 100 μL to around 300 μL; around 100 μL to around 400 μL; around 200 μL to in around 500 μL; around 200 μL to around 300 μL; around 200 μL to around 400 μL; around 300 μL to around 500 μL, around 300 μL to around 340 μL, around 400 μL to around 500 μL, etc.).
    [035] As used in this report, the term "liquid suspension" and/or "liquid sample" refers to a mixture of soluble and/or insoluble particles and/or solid materials dispersed in a liquid. In some embodiments, the liquid sample consists of a biological sample. Examples of a biological sample are well known to experts in the field and are not described in detail in this report. Representative examples include biological tissue, living fluid, fresh blood, stored blood, etc.
    [036] According to the use given in this report, a "bowl" and/or "micro-bowl" and/or "low volume bowl" and/or "LVC" and/or "sample container" or "container ” consist of a suitable container for admitting the liquid suspension. The container is preferably made of optically clear plastic or glass and is designed to hold a test sample in a specific space and orientation for testing or processing.
    [037] According to the use given in this report, "algorithms" comprise one or more mathematical instructions that are used to manipulate the data values to make a decision based on a mathematical value, thus generating a value more accurate or corrected data representative of the desired output.
    [038] According to the use given in this report, an "amplifier" consists of an electronic circuit that is used to effect a smaller original electronic signal with increasing its amplitude to produce a new proportionally larger signal representative of the original signal. Suitable amplifiers are well known to experts in the field and are not described in detail in this report.
    [039] As used in this report, an "analog to digital converter" or an "A/D converter" consists of an electronic device that is capable of taking a variable electrical signal and transforming it into a number that is representative of the amplitude of the original signal.
    [040] As used in this report, "dilution" means a solution or suspension produced by adding liquid diluent to a concentrated solution or suspension resulting in a new suspension or solution with a uniformly lower concentration of sample in the solution or suspension from the original.
    [041] As used in this report, "laser" or "laser diode" consists of an electronic device that produces a concentrated and focused light beam when an electric current is applied.
    [042] According to the use given in this report, the "light attenuation filter" consists of a device placed in a light path in order to absorb and reduce the amount of light as it passes through the filter resulting in the light that came to pass through the filter with a proportionally lower intensity than the original light source.
    [043] As used in this report, the "light emitting diode" or "LED" consists of an electronic device that emits light of a specific type and orientation when an electrical current is applied.
    [044] According to the use given in this report, "McFarland" consists of a unit for measuring the amount of solid particles dispersed in a liquid or fluid suspension.
    [045] According to the use given in this report, "nephelometer" consists of an instrument capable of measuring the amount of solid particles present in a suspension. As used in this report, “nephelometry” refers to a method whereby the amount of suspended solids in a suspension can be measured.
    [046] According to the use given in this report, "photo-diode" and/or "detector" comprises an electronic device used to measure the intensity of light in a given environment.
    [047] According to the usage given in this report, “saturated” and/or “saturation” comprises the point at which the detector came to reach the maximum amount of output signal it is capable of producing. For example, adding more light to the photodetector beyond the saturation point does not produce any further change in the detector's output signal, reaching its maximum operational capacity.
    [048] As used in this report, "suspension" consists of a solution where solids are evenly distributed in the liquid.
    [049] According to the use given in this report, "turbidity" comprises the measurement of the amount of suspended solids present in a solution (ie, the cloudiness of a liquid sample).
    [050] In the embodiments described below, the apparatus is described in terms of the device that is configured to detect the light that has come to be both transmitted through and scattered by the sample in the bowl. Devices and methods where only the light scattered by the sample and transmitted through the sample, or both come to be measured to determine the turbidity, are taken into account in this report. In some embodiments, an additional photodetector may be provided along the side of the light path to the scattered light detector, the transmitted light detector, or both. In those modalities where the light source consists of an LED, the measurement made by this additional photodetector is used on a control link to adjust the power along the LED and maintain a consistent, repeatable light intensity. The use of such detectors to control the LED output, addressing thermal drift and compensating for any degradation in the signal output, is well known to experts in the field and is not described in detail in this report.
    [051] Fig. 1 illustrates the system of a modality described in this report for measuring the turbidity of a liquid sample using a nephelometer and the principles of nephelometry. The sample system is designed to house a simple bowl 110 that features a suspended fluid 120 positioned on the inside of a nephelometer base 100, as shown in Fig. 1A. The system also includes a light source 120, a focusing lens 170, a side scatter detector 140, a transmitted light detector 150, and a light attenuation filter 160 (FIG. 1B). Bowl 110 containing a sample 120 is positioned near the center of the apparatus and inside the base of the nephelometer 100. Light source 130, scatter detector 140 and transmitted light detector 150 are positioned at 90 degree angles between itself around bowl 110. Positioning scatter detector 140 within close proximity to the bowl containing sample suspension 120 and parallel to the incident light source minimizes the effects of diffraction, refraction and reflection along with scattered light. The transmitted light detector 150 is positioned 180 degrees or in the opposite direction from the light source 130. The detector 150 can also be oriented either perpendicular to the incident light beam or at a different angle to reduce reflectance effects arising from their surfaces. Light attenuation filter 160 is positioned between bowl 110 and transmitted light detector 150. The turbidity gauging system detects scattered and/or transmitted light passing through the tested sample at an angle. Within this configuration, sample suspensions are processed individually within container 110.
    [052] The invention contemplates the use of low volume containers/bowls (or micro-bowls) that are designed to process relatively small amounts of fluid and biological suspensions for use with the low volume nephelometer. In the exemplary embodiments, the bowl is molded from an optically transparent plastic having minimally tapered sides that feature an optically smoothed polish to be conveniently oriented within the nephelometer described in this report. Bowls can be configured as individual units for single use applications. In embodiments where a series of bowls are employed for preparing suspensions, the bowls can be configured for use alongside strips in linear rows for such applications. Alternatively, the bowls can be configured for use with a matrix arrangement designed for simultaneous processing of multiple matrices. In matrix mode, multiple series of suspensions are prepared in parallel. Figures 4A-B illustrate alternative modalities to the low-volume bowl model for use with the nephelometers described in this report. Bowl 110 has a lower portion 410 which has a small volume. The suspension is initially prepared in the small volume portion. Therefore, the suspension is first disposed on the inside of the lower portion 410 of the bowl. Then, a biological sample suspected of containing targeted microorganisms is added, and mixed with the fluid suspension to provide a test sample suspension 120. The turbidity of the suspension in the lower portion 410 is gauged. Light 130 passes through sample suspension 120 which is positioned on the inside of the lower portion 410. The gauging apparatus is configured to gauge the turbidity of the sample in the lower portion 410 of the bowl. Below the lower portion 410 there is a "large particle" collection area 420, which is designed to receive large particles that separate and settle outside the sample suspension, otherwise there would be an adverse interference with the accuracy of the measurements. turbidity effected by the nephelometer. Low volume samples on the other hand have insufficient volume to provide conditions for the particulate contaminants to settle from the portion of suspension ascertained by the nephelometer. For example, light passing through a low volume suspension containing particulate impurities may not differentiate between the suspended sample and the impurities and may provide inaccurate McFarland values which in turn will lead to the sample being processed. unduly. For example, an inaccurate McFarland value can report the wrong dilution. An inaccurate McFarland value can lead to a sample being processed downstream (either by the AST or Maldi standard, for example), whereas if the true McFarland value was known, the sample would not have to be processed again. That is, the true McFarland value would inform the operator that the sample was not suitable for Maldi or AST. Furthermore, the presence of impurities in the sample can interfere with the accuracy of measurements of the concentration of the sample being tested. Bowls, in accordance with the present invention, provide with a separate collection area 420 that is presented on the outside of the direct light path that passes through the lower portion 410. The particulate contaminants accommodate within the collection area 420 and do not remain in the test area of the sample suspension, which occurs in the lower portion 410. The cell extension of the lower portion is in the range of around 5.5 mm and is designed to provide sufficient cell extension for low samples. volume to obtain turbidity measurements. The lower portion is designed to provide sufficient cell extension once the test sample suspension is prepared so that light passes through the samples and is captured by detectors 140 and 150. Preferably, the lower portion 410 is made a highly polished optical material or a material close to exhibiting optical clarity and other optically transmissive materials known to those skilled in the art. Such materials allow light to pass through the walls of the lower portion of the bowl without interference.
    [053] An expert in the field will appreciate that there are three dimensions of model freedom to configure the small-volume portion of the bowl. The dimensions of the small volume largely consist of a matter of model choice. In one embodiment, the dimensions of the small model portion are configured to admit a device (eg, a capture tool) that will introduce the sample into the lower portion of the bowl. For example, and not by way of limitation, the lower portion of the bowl is sized to provide a suitable environment for a 3mm capture tool to be submerged and rotated inside the lower portion so that it does not touch the sides of the bowl , generating scratches and aberrations on the surface that could degrade the optical transparency of the bowl.
    [054] Naturally, the dimensions of the lower portion must accommodate optical inspection of the sample. Specifically, the lower portion of the bowl is sized to work with the light source and detectors of the optical inspection device. The dimensional constraints with the bowl model are therefore a function of the configuration of the device which will optically probe the sample.
    [055] Above the lower portion 410 is the upper portion 400 which is employed to dilute the sample suspension positioned inside the container for further processing in downstream applications. The upper portion 400 has a wider width and length than the lower portion 410. Preferably, the internal dimensions of the container are shaped to accommodate the automated mixing of the biological sample containing a fluid in the suspension for further dilution of the test sample suspension directly inside the container when required. In operation, the in-line vessel model allows for measurement of the turbidity of the sample suspension and, if the target turbidity has not been achieved, for additional sample dilution and repeated turbidity measurements. This configuration allows for real-time sample dilution (ie, as the sample is being investigated). In addition, the aligned container model makes it possible to measure the turbidity of low volume sample suspensions (eg suspensions containing a volume of around 200 μL to around 500 μL), while still presenting the benefits of a larger volume to accommodate the sample dilution.
    [056] In the example embodiments, the container consists of two bowls lined up. The top alignment has an approximately square or rectangular or round perimeter. Basically, the geometric configuration of the top portion consists of a matter of model choice. The bottom alignment has an approximately square perimeter. The bowl “view magnification” from top to bottom because the top alignment is larger (in horizontal cross section) than the bottom. Alternative shapes for the bowl are further contemplated as long as the walls of the bottom portion of the bowl are at an angle to each other (eg, the bowl is not cylindrical, elliptical, etc.). It was determined that positioning the walls of the lower portion of the bowl (ie, the portion received by the nephelometer) within an angle to each other (compared to a round tube) allows for less aberration with the optical signal and better mixing of the test sample. In an illustrated embodiment, the upper portion 400 has been selected to have four sides 430 that are perpendicular to each other, thus defining a square. The lower portion 410 also has four sides 440 that are perpendicular to each other, except the dimensions of the sides 440 which are narrower than the sides 430. The lower, smaller portion 410 is configured to be admitted by the base of the nephelometer and/or by the linear bowl layout. The top of the bowl features a 450 opening for inlet sample and diluent. The side walls 430 and 440, respectively, of the upper and lower portions, are configured as flat surfaces. Without being bound by any particular theory, flat surfaces are believed to minimize the diffraction and refraction of light passing through the surface of the bowl. Furthermore, the square configuration of the bowls/containers allows for light paths passing through and into the sample suspension and container at right angles to the surface plane of the container. This configuration further minimizes the potential for diffraction or refraction of the light source 130 as it enters and leaves the bowl.
    [057] Various bowl configurations are contemplated. In one embodiment, the top portion of the bowl is tapered along with the bottom portion. The corners of the top portion align with the corners of the bottom portion, as seen by straight lines 401 (FIG. 4A). The tapered edges 401 demarcate the transition between the wider upper portion 400 and the narrower lower portion 410. In another embodiment, the edges of the upper portion 400 are offset from the edges of the lower portion 410, in the form of offset edges 402 illustrated in FIG. 4B. For example, edges 402 are offset by 45 degrees from the edges of the top portion. Advantageously, this configuration allows the light source and detectors to be arranged on either side of the bowl when the bowl is positioned inside the base of the nephelometer. The positioning of the bowls with the edges 402 on the inside of the linear array 300 allows for more efficient transport of the bowls through the nephelometer because they can be processed in series and received by the nephelometer and calibrated without further handling of the bowl.
    [058] The bowl/nephelometer assembly for measuring turbidity operates as described in the following modalities. Bowl 110 is positioned inside the base of the nephelometer 100. The bowls are positioned inside the base of the nephelometer either automatically or manually. Referring to FIG. 5, the fluid from the initial suspension (free of micro-organisms) is placed in the inner part of bowl 100. The fluid volume is around 200 μL to around 500 μL. Preferably, the initial fluid volume in the suspension is around 300 µL. More fluid can be added to the bowl if dilution is necessary to obtain specific McFarland values. Next, a biological sample suspected of containing microorganisms is added to bowl 110 and mixed with the fluid in the suspension to yield a test sample suspension. The apparatus described in this report measures the initial turbidity of the test sample and the MacFarland value is recorded. The sample suspension is further diluted by adding more suspension fluid addition if the initial turbidity readings are too high. Dilution is automated in one mode. The upper portion allows the volume of fluid in the suspension to exceed the volume of the lower portion. The device measures the turbidity of the diluted suspension. Once the predetermined McFarland value is obtained, the suspension is either processed by downstream testing, or stored or discarded. The suspension can be diluted as many times as necessary in order to obtain the desired McFarland values.
    [059] A light coming from the source 130 ascertains the suspension 120 (eg the tested sample) disposed in the inner part of the bowl 110. The light reaching the surface (eg the flat side wall of the bowl/container) is referred to in this report as the incident light. The light that is scattered from the particles of suspension 120 is referred to in this report as the scattered light. A portion of the incident light is reflected by the bowl surface. Transmitted or refracted light consists of the portion of the incident light that is transmitted through the surface (eg, the flat sidewall of the bowl/container).
    [060] In operation, transmitted light is received by the transmitted light detector 150. In the example embodiments, the transmitted light detector 150 is positioned along the incident light path to maximize detection of the light transmitted through the suspension. In situations where the detector surface 150 is highly reflective, the detector 150 can be positioned so that the detector surface is located at a slight angle (not 90 degrees) to the axis of the light path. Positioning the detector 150 within an angle optimizes the detection of transmitted light without reflecting the light returned to the suspension 120 or directing light to other portions of the nephelometer. The intensity of light collected by the detector is proportional to the turbidity of the suspension.
    [061] The light attenuation filter 160 is positioned directly in front of the transmitted light detector 150. The filter reduces the intensity of light incident upon the detector by an amount that is proportional to that of the incident beam. In the exemplary embodiments, the filter enables detector 150 to function without saturation and provides sufficient bandwidth with operational intensity to the detector for detecting slight variations in transmitted light intensity.
    [062] The apparatus according to the present invention also measures the amount of scattered light. The scatter detector 140 is positioned with its sensing surface parallel to the incident light path and along one side of the bowl. Portions of light that have passed through the suspension sample are scattered by the suspended particles. Side scatter detector 140 collects some of the scattered light. The amount of scattered light that the detector 140 collects provides a signal that is proportional to the amount of particles in the suspension 120 tested. One way to measure the turbidity of suspension 120 is to process the amount of scattered light collected by the scatter detector 140 through several algorithms, well known in the technical field. Data collected from scatter detector 140 can be combined with data collected from transmission detector 150 in a number of ways. For example, the signals can be physically combined or the detector values manipulated mathematically to combine them in a way to further enhance the accuracy and reliability of the initial signals. The signals or data values may be additively, subtractively, differentially combined, etc., so as to provide a resultant signal representative of the combined signals. When the signals from the detector values are combined in this way, it becomes possible to enhance the resolution and accuracy of the data collected for measuring turbidity. Advantageously, data collected from two separate detectors (scatter and transmittance data) can provide more accurate results for samples with small volumes. Dual gauging is advantageous in those modalities where dispersion gauging is not enough. Although the inventors do not wish to be bound by a particular theory, it is the inventors' view that gauging both transmitted and scattered light leads to more accurate accuracy due to the limited length of the light path through the small volume of the sample.
    [063] In the exemplary embodiments, the dispersion detector 140 and the transmittance detector 150 consist of high efficiency photodiode detectors. However, other detectors with similar characteristics can also be used. Suitable detectors include those that operate across the visible light spectrum from ultra-violet (UV) to infrared (IR). Appropriate detectors can be selected based on their linear response curves, size, reproducibility of results, and the ability to operate/detect light paths under low light conditions and detect instantaneous variations in light intensity with resolution enabled scouting. Examples include photodiodes, photomultiplier tubes, avalanche detectors, solar cells, photoresistors, photosensors, etc. Such detectors are commercially available and well known to those skilled in the art and are not described in detail in this report.
    [064] In the example embodiments, the light source consists of a high-intensity light-emitting diode (LED) or diode laser. Preferably, the LED light frequency is around 650 nm. Preferably, the wavelength of the light in the detector is within the red color range (ie, around 620 to 750 nm). However, the specialist can make use of the inquiry light together with different frequencies of visible light. Optionally, a focusing lens 170 (FIG. 1B) is used to focus light into a narrow beam (for example, a beam that is around 3mm in diameter). The focusing lens 170 is positioned in front of the light source 130. The use of a focusing lens 170 focuses light from the light source 130 within the sample area 410 of the container/bowl and minimizes the amount of light that may be spread from the test area. A specialist in the field is aware that light that is scattered on the outside of the test area (ie the bottom portion 41 of the bowl) makes the dispersion useless for sample turbidity purposes due to the high signal of background. The focused light then passes from the focusing lens 170 (not shown) to the lower portion 410 of the bowl at a perpendicular angle to the bowl trim. The perpendicular angle reduces the unwanted diffraction and refraction that occurs when a beam of light passes from one medium (eg air) to another (eg the sides of a flat bowl surface). The path of the focused light beam is maintained as light transmits through the suspension towards detectors 140 and 150. In modalities where the light source consists of a diode laser, additional lenses may not be needed to focus the light beam. . This is due in part to the properties of the laser providing the focused and collimated light to ascertain suspension. A focusing lens or a series of apertures is employed in those embodiments where the light source comprises an LED and collimation or focusing of the light is desired or required.
    [065] FIG. 3 illustrates the series of receptacles/bowl arrangement for use with an embodiment of the apparatus of the present invention. The array of bowls consists of a strip of arrays of bowls that is moved along the guided channel 220. An LED light source 130 is positioned along one side of the guided channel 220 that guides the strip 300. The strip 300 is fitted. slide with 220 channels. Strip 300 also includes standoffs or other structures 530 (FIG. 6) for convenient stacking, packaging, and shipping. Strip 300 is advanced through the nephelometer and bowl depths 329 are positioned between light source 130 and detectors 140 and 150 (not shown) for processing. After processing is complete, the linear strip 300 can be indexed and advanced to the next bowl continuing with processing for later samples using the same nephelometer. Bowl strip 300 can be stored or disposed of based upon the user's individual needs. In this modality, a simple nephelometer is designed to efficiently process multiple samples without the need to remove individual bowls and replace them with new bowls. Linear Bowl Strip 300 can be designed with various bowl shapes, sizes and configurations. For example, the depths 320 of strip 300 can be designed to be more or less deep, widened, narrowed, larger, shorter, etc. depending on the bowl model. In addition, the depths can be fixed to each other via individual depths or be entered individually at the positioned depths one after the other.
    [066] In one modality, the bowl strips are stackable and can be separated into either individual bowls or a linear strip of bowls, depending on the nephelometer configuration. This mode is illustrated in FIG. 6. These bowls 550 are driven by rack 510. Rack 510 features a flat surface from which the bowls are suspended. The flat surface is braced (not shown) to enable the bowls to be separated into individual bowls or bowl strips. Stackable bowls also feature 530 spacings as described above. Note that to facilitate stacking, the lower portion 540 of bowl 500 is received by the larger, larger portion 550.
    [067] FIG. 2 illustrates a mode where bowls are advanced through the nephelometer in series. The system is designed for use with a series of bowls that are advanced through the nephelometer in a continuous mode. Individual bowls 110 can be positioned directly inside a nephelometer base 100 by positioning the lower portion of the bowl in channel 220, as shown in FIG. 2B. Alternatively, the individual containers 110 may be positioned firstly inside the linear container array 300, and the multiple linear array housing containers 300 (FIG.3A) can be positioned inside the nephelometer via passage through channel 220 After the containers are placed inside the nephelometer base either individually or inside the linear array, the suspension is prepared in the bowl and turbidity measured as described above.
    [068] The system housing a linear container arrangement (FIG. 2) also includes a light source 130, a focusing lens 170, a scatter detector 140, a transmitted light detector 150 and a light attenuation filter 160 (FIG. 1B, as described above). Bowl 110 containing a sample 120 is positioned in the central part of the apparatus and in the inner part of the nephelometer base 100. The light source 130, the scatter detector 140 and the transmitted light detector 150 are positioned at a 90 degree angle between around the bowl 110, as described above. The side scatter detector surface 140 is positioned parallel to the incident beam coming from the light source 130. Positioning the scatter detector 140 within close proximity to the tested sample 120 and parallel to the incident light source minimizes the effects of diffraction, refraction and reflection of scattered light. The transmitted light detector 150 is positioned opposite the light source 130 and incident light from the light source propagates towards the transmitted light detector. Detector 150 can also be positioned either perpendicular to the incident light path or a few degrees off perpendicularity to reduce reflection effects from its surfaces. Light attenuating filter 160 is positioned between bowl 110 and transmitted light detector 150.
    [069] FIG. 7 consists of a cross section of a nephelometer employing the path for light transmitted through the lower portion 540 of the bowl 500. The light source (570, FIG. 9) is received by an opening 575 in a side of the bowl receptacle 580 of the 590 nephelometer. Aperture 575 receives the light source. Sensor 600 (FIG.9) is positioned in an opening 605 directly opposite opening 575, with the lower portion of bowl 540 positioned between these. The nephelometer features a 620 cap.
    [070] FIG. 8 consists of a cross-section of a nephelometer showing the path for light scattered through the lower portion 540 of the bowl 500. The light source (570, FIG. 9) comprises one side of the bowl receptacle 580 of the nephelometer 590. The sensor 630 (FIG. 10) is positioned in an opening 635 orthogonal to light source 570, with the lower portion of bowl 540 positioned between these.
    [071] FIG. 9 consists of a cross section of a nephelometer employing the path for light transmitted through the lower portion 540 of the bowl 500. The light source 570 is admitted by an opening 575 along one side of the bowl receptacle 580 of the nephelometer 590. sensor 600 and bowl 500 there is a light attenuation filter 640 which is positioned on the front of the transmittance detector to lower the light intensity close to a useful level so as not to saturate the sensor. Aperture 575 receives light source 570 and lens 650 for focusing the optical signal. Sensor 600 is positioned in an opening 605 directly opposite opening 575, with the lower portion of bowl 540 positioned between these.
    [072] FIG. 10 is a perspective view of the nephelometer 590 showing an aperture 575 for the light source 570, the aperture 635 for the scattered light sensor, and the aperture 605 for the transmitted light sensor.
    [073] In one modality, the sample is placed inside a bowl and processed individually when placed in a nephelometer. After the sample has been processed and McFarland values are obtained, the bowl is removed from the nephelometer and replaced with a new bowl. In this mode, one or more nephelometers are operated independently. In an alternative embodiment, the nephelometer is configured to provide a continuous series of bowls alongside the nephelometer for gauging. A linear bowl channel 220 receives a strip 300 of individual bowl depths 320 (FIG. 3B). The strip is transported through the nephelometer, interrupted to each bowl to be optically checked for gauging, as described in detail throughout the report.
    [074] The methods for measuring turbidity are automated, according to the present invention. The data collected from the measurements can be further processed to generate meaningful results. In these modes, the signal coming from the detectors is fed to the signal amplifiers. The amplifier output is communicated to the analog-to-digital conversion circuit which releases a digital representation of the input signal which is then processed using various algorithms to determine whether the measured value falls within the target value. If the target value is higher than the target value, then the sample is diluted as described above and turbidity re-measured. Such recalibration can be done manually by an operator or in an automated manner where the bowl is transferred out of the nephelometer for dilution and transported back to the nephelometer for further recalibration. Methods aimed at processing the signal into a useful output are developed using varying dilutions of several biological and non-biological samples and associating McFarland values with suspension concentrations. This data is then used to produce datasets that are further analyzed employing algorithms that correct for linearity and offset the data curves to produce a representative output value for a turbidity value and comparison with the target value. This process is repeated until the desired turbidity is achieved.
    [075] Although the invention has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrations of the principles and applications of the present invention. Therefore, it is understood that numerous modifications can be made to the illustrative embodiments and that other provisions can be devised without departing from the spirit and scope of the present invention, defined in accordance with the appended table of claims.
    权利要求:
    Claims (17)
    [0001]
    1. Apparatus for optical investigation of a sample, CHARACTERIZED by the fact that the method comprises: a light source (130) facing an optical signal; a base (100) having a bowl receptacle (580) so that; at least one of a first light detector (150) for detecting transmitted light positioned in an opening of the base to receive the optical signal transmitted directly through a bowl (110), received by the bowl receptacle (580) where the bowl (110 ) comprising a narrower bottom portion (410) comprising a plurality of flat side walls, each side wall at an angle from an adjacent side wall, and a wider upper portion (400) comprising a plurality of flat side walls, each wall side at an angle from an adjacent side wall, with the wider upper portion (400) having a larger perimeter than the perimeter of the lower narrower portion (410) of the base further adapted to position the bowl (110) so that the light source (130) is positioned to transmit an optical signal transmitted directly through the flat side wall of the narrower lower portion (410) of the bowl or a second light detector (140) for detecting scattered light positioned to receive the optical signal from the light source (130) scattered through the contents of the lower portion of the bowl (410); and a second light detector (140) for detecting scattered light positioned to receive the optical signal from the light source (130) scattered across contents in the lower portion of the bowl (410) the second detector surface positioned approximately parallel to an optical path of an optical source from the first detector; where the light source and at least one of a first light detector and second light detector detectors are disposed in openings (575, 605, 635) in the base (100).
    [0002]
    2. Apparatus according to claim 1, CHARACTERIZED in that it further comprises: a channel (220) configured to advance a linear series of bowls (110, 300), each bowl (110) being advanced in series along a position gauging, where the lower portion of the bowl (410) is adjacent to the light source (130), the first light detector (150) and the second light detector (140) for gauging.
    [0003]
    3. Apparatus, according to claim 2, CHARACTERIZED by the fact that the apparatus consists of a nephelometer (590).
    [0004]
    4. Apparatus according to claim 1, CHARACTERIZED by the fact that the apparatus is configured to receive an arrangement of bowls (300) configured as a strip from which the lower portion of the bowl is suspended.
    [0005]
    5. Apparatus according to claim 1, CHARACTERIZED by the fact that the light source (130) is selected from the group consisting of a laser light source and an LED.
    [0006]
    6. Apparatus, according to claim 1, CHARACTERIZED by the fact that the apparatus consists of a spectrometer.
    [0007]
    7. Apparatus according to claim 1, CHARACTERIZED in that the apparatus consists of a nephelometer (590) in which the second light detector (140) comprises a surface that receives the scattered optical signal in which the second light detector surface light is positioned approximately parallel to the optical path from the light source (130) to the first light detector (150) wherein the first light detector (150) is a transmitted light detector.
    [0008]
    8. Apparatus according to claim 1, characterized in that it further comprises a light attenuation filter (160) positioned between the bowl and the first light detector (150) or the second light detector (140).
    [0009]
    9. Apparatus, according to claim 1, CHARACTERIZED by the fact that it further comprises one of the items between a focusing lens (170), an aperture (575) or a series of apertures positioned intermediately between the light source (130) and the narrower lower portion of the bowl (410) and optionally wherein the focusing lens (170), aperture (575) or series of apertures collimates the light transmitted therethrough.
    [0010]
    10. Apparatus, according to claim 1, CHARACTERIZED by the fact that the first and second detectors (150, 140) are positioned at an angle of 90° to each other.
    [0011]
    11. Apparatus, according to claim 1, CHARACTERIZED by the fact that at least one of the first and second light detectors (150, 140) operate through the visible light spectrum from the ultra-violet (UV) to the infra- red (IR).
    [0012]
    12. Apparatus, according to claim 11, CHARACTERIZED by the fact that the wavelength of light detected by at least one of the first and second light detectors is in the range from around 620 to around 750 nm.
    [0013]
    13. Apparatus, according to claim 1, CHARACTERIZED by the fact that the bowl is optically transparent.
    [0014]
    14. Method for measuring the turbidity of a sample, CHARACTERIZED in that it comprises: provision of a bowl (110) with a sample (120) arranged next to a nephelometric apparatus (590), the bowl (110) comprising a lower portion narrower (410) and a wider upper portion (400), the wider upper portion (400) having a wider perimeter than the perimeter of the narrower lower portion (410), wherein the narrower lower portion and the wider upper portion each comprises a plurality of flat sidewalls, each sidewall at an angle to an adjacent sidewall, the bowl further comprising a tapered portion from the wider upper portion to the lower narrower portion, the bowl (110) having a sample (120) for inspection disposed in at least the lower, narrower portion (410); receiving the bowl on a base (100) which positions the bowl (110) so that a flat side wall of the narrower lower portion of the bowl is positioned in an optical path defined by an opening or series of openings of a light source (130 ) emits light directed towards the lower, narrower portion of the bowl (410); transmitting light from the light source (130) near a lower, narrower portion (410) of the bowl (110); detection, employing at least one of a first detector (150) positioned to receive the optical signal transmitted directly through a sample (120) in the narrower lower portion of the bowl (410) received by the base (110) or a second detector (140 ) positioned to receive an optical signal spread across the sample (120) at the lower, narrower portion of the bowl (410), the second detector (140) having a surface positioned approximately parallel to the optical path from the light source (130) to the first detector (150).
    [0015]
    15. Method according to claim 14, CHARACTERIZED in that the bowl (110) is positioned in an arrangement of bowls (300) and the arrangement of bowls (300) is positioned in the nephelometric apparatus (590) so that the turbidity of the sample (120) disposed in the lower portion (410) of each bowl (110) will be calibrated.
    [0016]
    16. Method according to claim 15, CHARACTERIZED by the fact that the arrangement of bowls (300) consists of a strip.
    [0017]
    17. Method according to claim 14, CHARACTERIZED by the fact that it further comprises the collimation of light directed to the narrower lower portion of the bowl (410).
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    ES2784785T3|2020-09-30|
    JP2017534854A|2017-11-24|
    US10935490B2|2021-03-02|
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    AU2015326540B2|2020-11-26|
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    AU2015326540A1|2017-04-20|
    JP6698640B2|2020-05-27|
    BR112017006363A2|2017-12-19|
    EP3201602A2|2017-08-09|
    US20170307525A1|2017-10-26|
    CA2962365C|2020-05-12|
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    法律状态:
    2020-06-09| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2021-04-13| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2021-06-29| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 29/09/2015, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
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