The present disclosure relates generally to systems and methods for testing biological test samples, and more particularly to a test sampling system configured to collect, process, and test biological samples using a test sensor.
Biological samples provide important information about a variety of physiological conditions. For example, stool testing is a diagnostic technique that can be used to identify a variety of markers, such as hemoglobin proteins and markers of inflammatory conditions, among others. Typically, a patient is required to go to a doctor's office and is subject to an invasive test, such as a colonoscopy, to detect potential illnesses and diseases. Accordingly, there is a need for systems for collecting biological samples as well as systems that allow for rapid testing of the collected samples in a convenient and noninvasive manner
The present disclosure is directed to a system for collecting and processing a biological sample and optionally analyzing the processed biological sample to determine whether one or more target analytes are present in the sample. In particular, the present disclosure describes systems and methods for conveniently collecting, processing, and testing a biological sample collected from the user without having to visit a doctor or undergo an invasive procedure. For example, the biological test sample can include or consist of stool, which a user can easily test from home. The disclosed systems and methods identify one or more target analytes (e.g., a particular substance of the test sample under test, such as biological specimens) in the test sample, and present to the user an easily understandable representation of the test results.
In accordance with some embodiments, a test sampling system is provided. In a representative implementation, the test sampling system includes an outer container having first and second ends and a base affixed to the first end. The test sampling system includes a motorized mixer affixed to the base, and an inner container having first and second ends. The inner container is sized to be received within the outer container via the second end thereof. The first end of the inner container has a membrane layer thereacross, the membrane layer being pierceable by the mixer when the inner container is received by the outer container to bring the mixer into contact with a test sample in the inner container. The test sampling system includes a test sensor configured for contact with the test sample. The test sampling system further includes one or more processors for (i) receiving signals from the test sensor following actuation of the mixer to cause mixing of the sample and (ii) analyzing the sample based on the signals.
In some embodiments, the test sample includes a stool sample and a buffer solution. The one or more processors are configured to analyze the test sample only after the mixer has imparted a uniform consistency thereto. In some embodiments, the uniform consistency corresponds to a threshold viscosity.
In some embodiments, the test sensor can detect proteins or fragments of proteins. In some embodiments, the test sensor can detect different forms of nucleic acid (including but not limited to DNA, mRNA, micro-RNA, siRNA). In some embodiments, the test sensor can detect nucleic acid via amplification of specific nucleic acid sequence, or via detection of specific nucleic acid sequences, for instance through hybridization to an oligonucleotide or through a catalytically inactive CRISPR complex with a sgRNA having an oligonucleotide sequence that is complementary with a DNA sequence of interest. In some embodiments, isothermal DNA amplification can be employed to amplify the DNA and hence facilitate genetic screening for biomarkers. In some embodiments, the test sensor is an immuno-assay. In some embodiments, the test sensor can be one of a FET-type device, or electrochemical-type device. In some embodiments, the test sensor is pre-calibrated. In some embodiments, the outer container includes a cavity, and the test sensor is disposed within the cavity. In some embodiments, the test sensor is integral with the one or more processors. In some embodiments, the one or more processors are disposed within the outer container or the base. In some embodiments, the test sampling system includes a display disposed on the outer container or the base. The display, responsive to the one or more processors, presents results of the analysis.
In some embodiments, the outer container further includes a channel and a shield that is disposed adjacent to the channel. In some embodiments, the test sampling system further includes a filter coupled to a channel of the outer container such that unprocessed test sample is prevented from entering the channel. The shield may be configured to prevent the test sample from entering the channel before it is processed. In some embodiments, the shield is mechanically coupled to the motorized mixer such that a position of the shield is changed from a closed position to an open position based on the actuation of the mixer. In some embodiments, the motor is actuated in a first direction to process the test sample and actuated in a second direction to move the processed test sample though a channel of the outer container. In some embodiments, the mixer includes at least two prongs and/or at least two blades.
In some embodiments, the sampling system further includes a lid including a seal housing a buffer solution. In some embodiments, mechanical coupling of the lid to the second end of at least one of the outer container or the inner container causes the seal to break and release the buffer solution into the test sample. In some embodiments, the test sampling system includes a seal adjacent to the membrane layer of the inner container and a buffer solution between the membrane layer and the seal such that, when the outer container receives the inner container, the mixer pierces the membrane layer and seal to release the buffer solution into the test sample.
In accordance with another embodiment, a test sampling system is provided. In this embodiment, the test sampling system includes a base supporting a motor that is coupled to a shaft. The motor is configured to actuate the shaft around a longitudinal axis. The test sampling system includes an outer container including a first end and a second end opposite the first end, the second end configured to receive an inner container and the first end configured to couple to the base. The first end includes an aperture configured to receive a portion of the shaft and a channel configured to receive a processed test sample. The test sampling system includes a mixer configured to couple to the portion of the shaft received via the first end of the outer container. The test sampling system includes an inner container including a first end and a second end opposite the first end, the second end configured to receive a test sample from a user and the first end including a membrane layer. The membrane layer is configured to be pierced by the mixer when the inner container is received by the outer container such that the mixer contacts at least a portion of the test sample. Upon activation of the motor, the mixer in contact with at least the portion of the test sample is actuated to generate the processed test sample based, at least in part, on the test sample and a buffer solution applied to the test sample via the inner container or the outer container, the processed test sample including a uniform consistency. The test sampling system further includes a test sensor fluidically coupled to the channel. The test sensor is configured to receive a portion of the processed test sample and generate information based thereon. The information includes data identifying one or more substances in the portion of the test sample. The test sampling system also includes one or more processors in communication with the test sensor, the one or more processors configured to receive the information from the test sensor and analyze the test sample based on the information.
In accordance with another embodiment, a method of analyzing a test sample is provided. In various embodiments, the method includes providing an outer container including a motorized mixer. The method includes receiving, within the outer container, an inner container including a sample. The inner container has a membrane layer across a first end thereof, whereby the membrane layer is pierced by the mixer to bring the mixer into contact with the test sample. The method includes causing the mixer to impart a uniform consistency to the test sample and thereupon analyzing the test sample.
In accordance with another embodiment, a method of fabricating a test sampling system is provided. The method of fabricating the test sampling system includes providing an outer container having first and second ends and a base affixed to the first end. The method includes providing a motorized mixer affixed to the base. The method also includes providing an inner container having first and second ends. The inner container is sized to be received within the outer container via the second end thereof. The first end of the inner container has a membrane layer thereacross, the membrane layer being pierceable by the mixer when the inner container is received by the outer container to bring the mixer into contact with a test sample in the inner container. The method includes providing a test sensor configured for contact with the test sample and providing one or more processors. The one or more processors are configured for (i) receiving signals from the test sensor following actuation of the mixer to cause mixing of the sample and (ii) analyzing the sample based on the signals.
Note that the various embodiments described above can be combined with any other embodiments described herein. The features and advantages described in the specification are not all inclusive and, in particular, many additional features and advantages will be apparent to one of ordinary skill in the art in view of the drawings, specification, and claims.
So that the present disclosure can be understood in greater detail, a more particular description may be had by reference to the features of various embodiments, some of which are illustrated in the appended drawings. The appended drawings, however, merely illustrate pertinent features of the present disclosure and are therefore not to be considered limiting, for the description may admit to other effective features as the person of skill in this art will appreciate upon reading this disclosure.
In accordance with common practice, the various features illustrated in the drawings may not be drawn to scale. Accordingly, the dimensions of the various features may be arbitrarily expanded or reduced for clarity. In addition, some of the drawings may not depict all of the components of a given system, method, or device. Finally, like reference numerals may be used to denote like features throughout the specification and figures.
Numerous details are described herein in order to provide a thorough understanding of the example embodiments illustrated in the accompanying drawings. However, some embodiments may be practiced without many of the specific details, and the scope of the claims is only limited by those features and aspects specifically recited in the claims. Furthermore, well-known processes, components, and materials have not been described in exhaustive detail so as to avoid obscuring pertinent aspects of the embodiments described herein.
A test sample, for purposes of this disclosure, includes a stool sample and a buffer solution (e.g., buffer solution 304;
The test sampling system is configured to process the test sample until the test sample obtains a uniform consistency such that the processed test sample can be analyzed by the test sensor 116 and the one or more processors 120 of the test sampling system. In some embodiments, the uniform consistency corresponds to a current draw of test sampling system (e.g., a measured electrical current is below an electrical current threshold, which indicates that a uniform consistency is achieved). Alternatively or additionally, in some embodiments, the uniform consistency corresponds to a threshold viscosity (e.g., a determined viscosity is below a threshold viscosity, which indicates that a uniform consistency is achieved). In some embodiments, a viscosity of the processed test sample is determined based, at least in part, on a current draw of test sampling system. In some embodiments, the test sensor 116 is configured to contact the processed test sample and generate information based thereon. The information includes data identifying one or more substances in the test sample. The one or more processors 120 receive signals (including the generated information) from the test sensor 116 following actuation of the mixer (which causes mixing of the test sample) and analyze the test sample based on the signals. In some embodiments, the test sampling system includes an interface 124 (such as a touch display, one or more buttons, light sources, etc.) disposed on an external portion of the outer container 102 or the base 108.
The interface 124 is configured to present results of the analysis (determined by the test sensor 116 and the one or more processors 120 as discussed below in reference to
A first embodiment 100 of the test sampling system includes two or more prongs 114 coupled to the shaft 112 and the motor 110, and the interface 124 disposed on an external portion of the outer container 102. A second embodiment 150 of the test sampling system includes two or more blades 122 coupled to the shaft 112 and the motor 110, and the interface 124 disposed on an external portion of the base 108.
As shown in exploded view 200, in some embodiments, the motor 110 is coupled to the shield 118. The shield 118 can move from a closed position to an open position based on actuation of the motor 110. In some embodiments, the shaft 112 (which is coupled to or is part of the motor 110) is configured to be received by the outer container 102 via an aperture 202 disposed at the first end of the outer container 102. In some embodiments, the mixer is configured to couple to the portion of the shaft 112 received via the outer container 102. The mixer attached to the portion of the shaft 112 can be swapped by the user. For example, as shown in exploded view 200, the user can switch between the two or more prongs 114 and the two or more or blades 122.
In some embodiments, the shield 118 and the test sensor 116 are disposed within a cavity of the outer container 102. Alternatively, in some embodiments, the test sensor 116 is coupled to the base 108. In some embodiments, the test sensor 116 is integral with the one or more processors 120. The test sensor 116 is fluidically coupled to an opening of the outer container 102 such that, when the shield 118 is in an open position, the test sample contacts a portion of the test sensor 116. The shield 118 is in the open position when the mixer is inactive and in a closed position when the mixer is active. Additional detail information on the opening and closing of the shield 118 is provided below in reference to
As shown in the first view 300, the outer container 102 includes a shield 118 and a test sensor 116. In some embodiments, the shield 118 and the test sensor 116 are disposed within a cavity of the outer container 102. Alternatively, in some embodiments, the test sensor 116 is disposed at an exterior portion of the outer container 102 that is fluidically coupled to a portion of the outer container 102 that contacts a processed test sample. The shield 118 is configured to prevent an unprocessed test sample from contacting the test sensor 116. In some embodiments, one or more processors are disposed within the cavity of the outer container 102. Alternatively, in some embodiments, the one or more processors 120 are disposed at an exterior portion of the outer container 102. In some embodiments, the outer container 102 prevents the test sample from contacting the one or more processors 120.
In some embodiments, the test sampling system includes a lid 302 that is configured to mechanically couple to the outer container 102, the inner container 104 (
In the second view 330, the outer container 102 includes an aperture 202, a channel 306, a filter 308, and a shield guide 310. As described above in reference to
The third view 350 and the fourth view 370 provide different bottom views of the shield guide 310, the shield 118, the test sensor 116, and the aperture 202. As shown in the third view 350 and the fourth view 370, the test sensor 116 can be disposed at an exterior portion of the outer container 102 that is in fluidic contact with a portion of the outer container 102 in contact with a processed test sample (e.g., the channel 306). In some embodiments, when the shield 118 is in the open position, the shield 118 rests in an exterior portion of the outer container 102.
In some embodiments, as described above in reference to
The test sensor 116 receives a portion of the test sample from the inner container 104. For example, the test sensor 116 can be fluidically coupled to a portion of the outer container 102 that makes fluid contact with a processed test sample that enters the outer container 102 when the motorized mixer pierces the membrane layer 106 of the inner container 104 and processes the test sample. In some embodiments, the test sensor 116 can be fluidically coupled to channel 306 of the outer container 102 that makes fluid contact with a processed test sample that enters the outer container 102 when the motorized mixer pierces the membrane layer 106 of the inner container 104 and processes the test sample. In some embodiments, the test sensor 116 is disposed within the outer container 102 or a base 108 (
The test sensor 116, upon receiving the portion of the processed test sample from the outer container 102, generates information (based on the portion of the test sample) including data identifying one or more substances in the portion of the test sample, such as biomarkers associated with colorectal cancer. For example, the test sensor 116 (e.g., an antibody-functionalized graphene layer) can measure, monitored, and analyzed an electrical resistance to determine whether one or more substances with a concentration above a predefined threshold is present in the test sample. For example, a change in the DC resistance of the test sensor 116 above a predefined threshold can be correlated with the detection of one or more substances in the test solution. In some embodiments, the test sensor 116 is one of a FET-type device, a ChemFET-type device, EChemFET-type device, or electrochemical-type device. In some embodiments, the test sensor is an immuno-assay. In some embodiments, isothermal DNA amplification can be employed to amplify the DNA and hence facilitate genetic screening for biomarkers. In some embodiments, the test sensor can detect proteins or fragments of proteins. In some embodiments, the test sensor can detect different forms of nucleic acid (including but not limited to DNA, mRNA, micro-RNA, siRNA). In some embodiments, the test sensor can detect nucleic acid via amplification of specific nucleic acid sequence, or via detection of specific nucleic acid sequences, for instance through hybridization to an oligonucleotide or through a catalytically inactive CRISPR complex with a sgRNA having an oligonucleotide sequence that is complementary with a DNA sequence of interest.
Further details regarding the test sensor 116 and various detection methodologies that can be employed in connection with the test sampling system disclosed herein can be found in the following patents and published applications: U.S. Pat. No. 9,664,674, entitled “Device and Method for Chemical Analysis;” US Pat. Pub. No. 20 19/0079068, entitled “Device and Method for Chemical Analysis;” US Pat. Pub. No. 2019/0284615, entitled “Methods and Devices for Detection of Pathogens;” US Pat. Pub. No. 2020/00 11860, entitled “Functionalized Sensor for Detection of Biomarkers;” U.S. Pat. No. 10,782,285, entitled “Device and Method for Chemical Analysis;” and US Pat. Pub. No. 2020/03 00845, entitled “Methods and Devices for Detection of THC.” The entire contents of each of these publications is hereby incorporated by reference herein.
The test sensor 116 is in communication with the one or more processors 120. The test sensor 116 is configured to provide the one or more processors 120 one or more signals. The one or more signals including the generated information by the test sensors 116. In some embodiments, the test sensor 116 is in communication with the one or more processors 120 via wireless or wired connection. For example, the test sensor 116 can be coupled to the one or more processors 120 via a ribbon cable, USB, or other connecting element. In some embodiments, the test sensor 116 is integral with the one or more processors 120. Alternatively, the test sensor 116 can be communicatively coupled to the one or more processors 206 via Bluetooth or other wireless protocol.
The one or more processors 120 are disposed within a portion of the outer container 102 or the base 108. In some embodiments, the one or more processors 120 are configured to analyze the signals (or generated information) received from the test sensor 116. The one or more processors 120 are configured to determine whether one or more target analytes of interest (e.g., one or more pathogens) are present in the test sample. In general, instructions for analyzing the signals received by the one or more processors 120 can be implemented in hardware, firmware, and/or software using techniques known in the art as informed by the present teachings. In some embodiments, the one or more instructions are stored in a computer memory or computer-readable storage medium coupled to the one or more processors 120.
In some embodiments, the one or more processors 120 are coupled to the printed circuit board (not show) on which electronic circuitry is disposed. The one or more processors 120 and the electric circuitry disposed on the printed circuit board are powered by the internal power source (e.g., batteries) or an external power source (e.g., AC Mains). In some embodiments, the one or more processors 120 are communicatively coupled to the interface 124. In some embodiments, the interface 124 is powered by the internal power source or the external power source.
As described above in reference to
In some embodiments, the motorized mixer is configured to continue to actuate until a test sample is fully processed (e.g., a uniform consistency is imparted on the stool sample and the buffer solution 304 (
In some embodiments, the method 800 includes providing (802) an outer container including a motorized mixer. The method 800 includes receiving (804), within the outer container, an inner container including a sample, the inner container having a membrane layer across a first end thereof, whereby the membrane layer is pierced by the mixer to bring the mixer into contact with the test sample. For example, as shown in
In some embodiments, the top 904 is configured to couple to the collection container 902. The top 904 couples to the collection container 902 such that the contents (i.e., the test sample) of the collection container 902 do not escape the collection container 902 during the processing of the test sample. Additionally, the top 904, when coupled to the collection container 902, reduces or eliminates the chances of the top coming lose or falling from the collection container 902. The motorized top test sampling system 900 provides another test sampling system with less components.
It will be understood that, although the terms “first,” “second,” etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the claims. As used in the description of the embodiments and the appended claims, the singular forms “a,” “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will also be understood that the term “and/or” as used herein refers to and encompasses any and all possible combinations of one or more of the associated listed items. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.
As used herein, the term “if” can be construed to mean “when” or “upon” or “in response to determining” or “in accordance with a determination” or “in response to detecting,” that a stated condition precedent is true, depending on the context. Similarly, the phrase “if it is determined [that a stated condition precedent is true]” or “if [a stated condition precedent is true]” or “when [a stated condition precedent is true]” can be construed to mean “upon determining” or “in response to determining” or “in accordance with a determination” or “upon detecting” or “in response to detecting” that the stated condition precedent is true, depending on the context.
The foregoing description, for purpose of explanation, has been described with reference to specific embodiments. However, the illustrative discussions above are not intended to be exhaustive or to limit the claims to the precise forms disclosed. Many modifications and variations are possible in view of the above teachings. The embodiments were chosen and described in order to best explain principles of operation and practical applications, to thereby enable others skilled in the art.
This application claims priority to U.S. Provisional Patent Application No. 63/285,029, filed Dec. 1, 2021, entitled “Systems and Methods for Processing and Testing Biological Samples,” which is hereby incorporated by reference in their entirety.
Number | Date | Country | |
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63285029 | Dec 2021 | US |