1. Field of the Invention
The invention relates to methods and devices for indicating that an adequate amount of sample has been collected by a sample collection device.
2. Background Information
Sample collection devices are often used to collect a fluid sample, for example a saliva sample, for performing an assay. Examples of sample collection devices include swabs or absorbent materials which are compressible when wet by a fluid sample. When absorbent materials are used, the fluid sample needs to be removed from the absorbent sample collection material to be applied to an assay device. In some assay devices, such as the devices described in U.S. Pat. No. 6,489,172, the sample collection devices include a sample collection member connected to a handle. The sample collection device is placed in the mouth of a subject and then placed into an assay device. The sample collection member becomes compressible due to the addition of saliva, allowing sample to be extracted from the sample collection member when compressed in the assay device. The collection device allows samples to be collected quickly, but there is no indication that an adequate amount of sample has been collected by the sample collection member.
In some sample collection devices, such as those described in U.S. Pat. No. 7,114,403, a sample collection device include a sample collection member connected to a handle. The sample collection device is placed in the mouth of a subject, and then placed in an extraction device which can collect and store the liquid sample until it is added to an assay device. The extraction device also includes an aperture through which sample can be applied to the assay device.
In other sample collection and testing devices, such as those described in U.S. Pat. No. 6,998,273, the sample collection device and the assay device are provided as a single device. The device contains a movable barrier between the sample collection area and the detection area, which allows for a certain amount of sample to be collected before the sample is applied to the assay device.
Traditional sample collection devices do not provide any indication that an adequate amount of sample has been collected by the device. To obtain an accurate assay result, an adequate amount of sample applied to the assay device. Without any indication of the adequacy of the amount of sample collected, a user may collect an inadequate amount of sample to apply to the assay device, which may result in an inaccurate assay result.
The present invention includes in one embodiment a device for indicating the collection of an adequate amount of fluid. The device includes a handle, an sample collection member located at one end of the handle, at least one electrode in fluid communication with the sample collection member, and at least one signal indicator connected to the at least one electrode, the signal indicator indicating that the adequate amount of fluid has been absorbed by the sample collection member.
In embodiments, the sample collection member includes a groove structure. The at least one electrode may be located on a side of the groove structure. The at least one electrode further comprises a processor.
In embodiments, the signal indicator comprises at least one light-emitting diode. The device may also include an adhesive disk located between the sample collection member and the electrode.
The present invention includes a method of indicating the collection of an adequate amount of fluid may include steps of placing a collection device in the mouth of a user, and observing the signal indicator to determine when the adequate amount of fluid has been absorbed the sample collection member.
The present invention includes devices and methods for the collection of fluid samples, for example a saliva sample, which indicate that an adequate amount of sample has been collected by the sample collection device.
In one embodiment, the invention includes a sample collection device, including a sample collection member for the absorption of a fluid sample, and electronic components for indicating that a sufficient amount of sample has been collected by the sample collection device. In embodiments, the sample is a fluid sample, for example, saliva, urine, blood, or other bodily fluids. The electronic components may include at least one electrode, a processor, and an signal indicator. The at least one electrode can be any conductive electrode conductor. In one embodiment, the device includes one electrode.
In another embodiment, the device includes two or more electrodes which are located at the same depth and distributed evenly across the cross-section of the sample collection device.
In another embodiment, the device includes three or more electrodes which are evenly distributed throughout the cross-section of the sample collection device to allow the electrodes to detect the collected fluid sample equally. In embodiments, the distance between the electrodes is 1-10 mm, preferably 2-5 mm. In embodiments, the depth of electrolyte into the chassis is 1-10 mm, preferably for 1-4 mm.
In embodiments, the sample collection member includes a groove structure. The at least one electrode can be located on a side of a groove. In embodiments, the device contains two electrodes which are located on each side of the groove.
In embodiments, the electronic components include at least one signal indicator. For example, the signal indicator may be any visible light or sound. In embodiments, the signal indicator is comprised of at least one light emitting diode. When an adequate amount of sample contacts the at least one electrode, the signal indicator indicates to a user that the proper amount of sample has been collected. In embodiments, the signal indicator is an audible signal.
In embodiments, the sample collection device includes a handle. The sample collection member is connected to one end of the handle, for example, through a chassis, or through an adhesive disk or ring. The handle may contain a window for viewing a signal indicator. The electronic components, such as wires and the at least one electrodes, may be located in the handle, and may contact the sample collection member at a junction between the sample collection member and the handle.
In embodiments, the sample collection device includes cavity at the junction between the sample collection member and the handle. The signal indicator, for example at least one light-emitting diode, may be located in the cavity. The cavity and/or signal indicator may be covered by a transparent material. The sample collection device may also comprise a hollow rod, the hollow rod in contact with the cavity and located in the handle of the sample collection device. The rod may contain the electronic components of the device, for example, wires and a processor. The rod may include a rod channel.
In embodiments, the device includes a chassis, the chassis including at least one aperture through which the at least electrode may contact the sample collection member. The at least one electrode is in contact with the cavity and the chassis. The chassis may be connected to the handle, for example by adhesive bonding, for example an adhesive ring or disk or adhesive film.
In embodiments, the sample collection device includes an assay device. The assay device may be located, for example, in the handle of the device. In another embodiment, the assay device is in fluid communication with the sample collection member. In another embodiment, the sample is applied to a separate assay device after the sample is collected by the sample collection member.
Testing may be performed to determine the presence, absence or level of at least one substance or material, such as, but not limited to, chemical substances, organic compounds, inorganic compounds, metabolic products, drugs or drug metabolites, organic tissues or organisms, metabolites, nucleic acids, protein or polymer. A test may be performed to determine multiple substances or materials. Further, tests may be performed for immune detection, chemical detection, or enzyme detection.
The present devices and methods can be used to collect samples for analysis in diagnostic and/or laboratory tests to determine the presence, absence, or amount of a material or substance. The sample can be a fluid sample, for example, a liquid sample, i.e. blood, plasma, serum, urine, saliva and various secretions, and can also include solid and semi-solid samples after the sample is pre-treated to form a liquid solution. Samples collected can be used for immune detection, chemical detection, or enzyme detection methods to detect the presence or amount of analyte.
The present devices and methods can be used to detect an analyte. The analyte can be detected in any liquid or liquefied sample, such as urine, saliva, saliva, blood, plasma, or serum. The devices and methods of the present invention may be used to detect, for example, analytes including but not limited human chorionic gonadotropin (HCG), luteinizing hormone (LH), follicle stimulating hormone (FSH), hepatitis C virus (HCV), hepatitis B virus (HBV), hepatitis B surface antigen, HIV, or any drug of abuse. The term “drug of abuse” (“DOA”) is used to describe drugs that are used for non-medical purposes. These drugs are absorbed by the body and broken down into different small molecules, which are present in blood, urine, saliva, sweat and other bodily fluids.
In embodiments, the sample collection device includes a sample collection member. The sample collection member may absorb and store the sample. The sample collection member may be constituted of a material selected from, for example, polyvinyl alcohol (PVA), foam, resin, sodium polyacrylate cross-linked material, acrylic acid-ethylene acid copolymer, acrylonitrile polymer unsaponifiable matters, vinyl alcohol, sponge, filter paper, glass fiber, nonwoven, cellulose acetate, or a combination of one or several of these materials. In a preferred embodiment, the sample collection member is made of polyvinyl alcohol foam. The sample collection member can be any shape, including but not limited to cylinder shaped, rectangular, cone-shaped and any other suitable shape.
In the embodiment shown in
In the embodiment shown in
Another embodiment is shown in
In embodiments, the groove 95 can run through the entire sample collection member 60, and divides the sample collection member 60 equally into two parts. Two electrodes 51 are located in the groove on the left side and the right side. In a preferred embodiment, groove 95 does not completely separate the sample collection member into two parts; preferably, the height of the groove 95 is at least a height H1 and is less than a height H2 as shown in
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Electrodes 200, 201 are located in the cavity 403, the electrodes 200, 201 in contact with both chassis 600 and the second end 102 of sample collection member 100. A signal indicator 205 receives an indicator signal sent through the device. The signal indicator 205 may be at least one light-emitting diode, and can be located on the handle in a window. When sample is collected and the sample reaches the second end 102 of the sample collection member 100, the sample contacts two separate electrodes 200, 201, and the electrodes produce an signal which is send to the processor 204 and then to the signal indicator 205, indicating that an adequate amount of sample has been collected.
In another embodiment, the collection device includes a test element. As shown in
The sample collection device can include a sample collection member in contact with at least a portion of at least one electrode, and a processor connected to electronic components. These electronic components can be connected through a conductor or semiconductor, allowing electronic signals to be transmitted between the various components. The processor can be programmed to control the signal processing and response. For example, when sample is collected in the sample collection member, the sample contacts the electrodes produce an electronic signal. The electronic signal is received by the processor, and is sent to another electronic component, for example, a signal indicator to produce a signal, such as light or sound, which indicates that the amount of sample collected is sufficient, or has reached a pre-set amount. In a preferred embodiment, the sample collection member is in contact with at least two electrodes. In the initial stage of use, a microvoltage is applied between the two electrodes. When the two electrodes are contacted by sample to constitute a current path between the electrodes, a current path is generated by the processor after receiving an electronic signal from the electrodes. The electronic signal is sent to the signal indicator, indicating that the amount of sample collected is sufficient. The signal from the electronic components can travel through a conductor, such as wires connected to the processor. A sufficient or adequate amount of sample refers to the amount of sample required meet pre-set requirements, such as minimum volume or weight requirements set by a laboratory or a diagnostic test manufacturer, such as 1 ml, 5 ml or 1-10 ml. The electrodes can be configured within the sample collection member to achieve a requirement for indicating a certain level of sample. As shown in
Any type of signal indicator can be used to indicate that a sufficient amount of sample has been collected, such as visual signals, audible signals, or any other signal that can be understood by a user. The signal indicator may include at least one light-emitting diode, or a speaker for emitting an audible signal. Identification signal can also be a variety of other forms, i.e. color changes, sound reminders, or light reminders. For example, a specific sound, such as an alarm sound, can be used to indicate to a user that a sufficient amount of sample has been collected. Visual signals can also be used in various ways, for example, by a change in color or brightness of light-emitting diodes.
The collected sample can be applied to a test element 500 of a detection device, as shown in
Sample may be applied to a test strip, i.e. a lateral flow test strip, which can detect one or multiple analytes. Various test components can be used together to detect analyte. Any form of test strip may be used to analyze the sample for a particular analyte, i.e. drugs, drug metabolites, or other markers. The test strips may perform an immunoassay or chemical analysis. The assay can be a competitive assay or a sandwich assay. The test strip contains a sample receiving zone 501, a reagent zone 502, a detection zone 503, a control zone 504, and optionally an absorption area 505. Sample is added to the sample receiving zone and flows downstream to the reagent zone by capillary action, where the sample contacts mobilisable labeled binding agents. The sample continues to flow into the detection zone. The detection zone contains immobilized reagents, such as reagents which specifically bind the analyte. When analyte is present in the sample, the analyte binds with the reagents in the detection zone. The test strip can be made of material such as a nitrocellulose membrane. The test strip can be adhered to a supporting material or a hard surface.
The following examples are intended to illustrate but not limit the invention.
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Although the invention has been described with reference to the above example, it will be understood that modifications and variations are encompassed within the spirit and scope of the invention. Accordingly, the invention is limited only by the following claims.
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Various configurations of the sample collection device were tested to determine the average volume of sample collected and the time required to collect the sample. Each configuration was tested three times. The average results for each configuration is listed in the table below.
Although the invention has been described with reference to the above examples, it will be understood that modifications and variations are encompassed within the spirit and scope of the invention. Accordingly, the invention is limited only by the following claims.
This application claims the benefit of priority under 35 U.S.C. §119(e) of U.S. Ser. No. 61/408,450, filed Oct. 29, 2010, the entire content of which is incorporated herein by reference.
Number | Date | Country | |
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61408450 | Oct 2010 | US |