CROSS-REFERENCE TO RELATED APPLICATIONS This application relates to U.S. Provisional Application Nos. 62/053,388, filed on Sep. 22, 2014, and 62/155,527, filed on May 1, 2015, the disclosures of which are hereby incorporated by reference herein in their entirety.
BACKGROUND OF THE INVENTION Sweat sensing technologies have enormous potential for applications ranging from athletics, to neonatology, to pharmacological monitoring, to personal digital health, to name a few applications. Sweat contains many of the same biomarkers, chemicals, or solutes that are carried in blood and can provide significant information enabling one to diagnose ailments, health status, toxins, performance, and other physiological attributes even in advance of any physical sign. Furthermore, sweat itself, the action of sweating, and other parameters, attributes, solutes, or features on, near, or beneath the skin can be measured to further reveal physiological information.
If sweat has such significant potential as a sensing paradigm, then why has it not emerged beyond decades-old usage in infant chloride assays for Cystic Fibrosis or in illicit drug monitoring patches? In decades of sweat sensing literature, the majority of medical literature utilizes the crude, slow, and inconvenient process of sweat stimulation, collection of a sample, transport of the sample to a lab, and then analysis of the sample by a bench-top machine and a trained expert. This process is so labor intensive, complicated, and costly that in most cases, one would just as well implement a blood draw since it is the gold standard for most forms of high performance biomarker sensing. Hence, sweat sensing has not emerged into its fullest opportunity and capability for biosensing, especially for continuous or repeated biosensing or monitoring. Furthermore, attempts at using sweat to sense “holy grails” such as glucose have not yet succeeded to produce viable commercial products, reducing the publically perceived capability and opportunity space for sweat sensing.
Small, portable, and wearable biosensors are difficult to make so that they are precise and accurate. Such sensors are often generally challenged in their ability to make quality analytical measurements equal to what can be done with a dedicated measurement machine or large lab. This is especially true for sensors integrated in a small patch or wearable device because of the need for miniaturization and lower cost, and because such devices are placed in less controllable environments than many lab or machine settings.
Many of the drawbacks stated above can be resolved by creating novel and advanced interplays of chemicals, materials, sensors, electronics, microfluidics, algorithms, computing, software, systems, and other features or designs, in a manner that affordably, effectively, conveniently, intelligently, or reliably brings sweat sensing technology into intimate proximity with sweat as it is generated. Further, a sweat sensor capable of analytical assurance is needed. With such a new invention, sweat sensing could become a compelling new paradigm as a biosensing platform.
SUMMARY OF THE INVENTION The present invention provides a wearable sweat sensor device capable of analytical assurance. In one embodiment, a sweat sensor device with analytical assurance includes at least one sensor for detecting a first analyte, and at least one calibration medium containing at least the first analyte. When the first analyte in the at least one calibration medium comes into contact with the at least one sensor, the concentration medium provides a calibration of the at least one sensor.
In another embodiment, a method of detecting a solute in sweat includes directing a calibration medium in a device to at least one sensor for detecting the solute in the device, calibrating the at least one sensor, positioning the device on skin, directing sweat to the device, and measuring the solute in the sweat using the device.
In another embodiment, a method of detecting a solute in sweat using a device for detecting the solute in sweat, the device including at least one sensor, includes providing fluidic access to the at least one sensor through an aperture in a first backing element, directing at least one calibration medium to the at least one sensor through the aperture, calibrating the at least one sensor, placing the device on skin, directing sweat to the device, and measuring the solute in the sweat using the device.
BRIEF DESCRIPTION OF THE DRAWINGS The objects and advantages of the present invention will be further appreciated in light of the following detailed descriptions and drawings in which:
FIG. 1A is a cross-sectional view of a device according to an embodiment of the present invention.
FIG. 1B is a cross-sectional view of the device of FIG. 1A during calibration.
FIG. 1C is a cross-sectional view of the device of FIG. 1A positioned on skin.
FIG. 2A is a cross-sectional view of a device and a calibration module according to an embodiment of the present invention.
FIG. 2B is a cross-sectional view of the device and calibration module of FIG. 2A during calibration.
FIG. 2C is a cross-sectional view of a portion of the device of FIG. 2A.
FIG. 3 is a cross-sectional view of a device and a calibration module according to an embodiment of the present invention.
FIG. 4 is a cross-sectional view of a device according to an embodiment of the present invention.
FIG. 5 is a cross-sectional view of a device according to an embodiment of the present invention positioned on skin.
FIG. 6A is a cross-sectional view of a device according to an embodiment of the present invention positioned on skin.
FIG. 6B is a cross-sectional view of the device of FIG. 6A during calibration.
FIG. 6C is a cross-sectional view of a device according to an embodiment of the present invention positioned on skin.
FIG. 7A is a cross-sectional view of a device according to an embodiment of the present invention positioned on skin.
FIG. 7B is a cross-sectional view of the device of FIG. 7A during calibration.
FIG. 7C is a cross-sectional view of the device of FIG. 7A after calibration.
FIG. 8 is a cross-sectional view of a device according to an embodiment of the present invention.
DETAILED DESCRIPTION OF THE INVENTION The present application has specification that builds upon International Application Nos. PCT/US13/35092, filed Apr. 2, 2013, PCT/US14/61083, filed Oct. 17, 2014, PCT/US14/61098, filed Oct. 17, 2014, PCT/US15/32830, filed May 28, 2015, PCT/US15/32843, filed May 28, 2015, PCT/US15/32866, filed May 28, 2015, PCT/US15/32893, filed May 28, 2015, and PCT/US15/40113, filed Jul. 13, 2015, the disclosures of which are hereby incorporated herein by reference in their entirety.
Embodiments of the present invention apply at least to any type of sweat sensor device that measures sweat, sweat generation rate, sweat chronological assurance, sweat solutes, solutes that transfer into sweat from skin, properties of or items on the surface of skin, or properties or items beneath the skin. Embodiments of the present invention further apply to sweat sensing devices that have differing forms including: patches, bands, straps, portions of clothing, wearables, or any suitable mechanism that reliably brings sweat stimulating, sweat collecting, and/or sweat sensing technology into intimate proximity with sweat as it is generated by the body. While certain embodiments of the present invention utilize adhesives to hold the device near the skin, other embodiments include devices held by other mechanisms that hold the device secure against the skin, such as a strap or embedding in a helmet.
Sweat stimulation, or sweat activation, can be achieved by known methods. For example, sweat stimulation can be achieved by simple thermal stimulation, by orally administering a drug, by intradermal injection of drugs such as methylcholine or pilocarpine, and by dermal introduction of such drugs using iontophoresis. Sweat can also be controlled or created by asking the subject using the patch to enact or increase activities or conditions which cause them to sweat. These techniques may be referred to as active control of sweat generation rate.
Certain embodiments of the present invention show sensors as simple individual elements. It is understood that many sensors require two or more electrodes, reference electrodes, or additional supporting technology or features which are not captured in the description herein. Sensors are preferably electrical in nature, but may also include optical, chemical, mechanical, or other known biosensing mechanisms. Sensors can be in duplicate, triplicate, or more, to provide improved data and readings. Sensors may be referred to by what the sensor is sensing, for example: a sweat sensor; an impedance sensor; a sweat volume sensor; a sweat generation rate sensor; and a solute generation rate sensor.
In an aspect of the present invention, a sweat sensor device is capable of providing analytical assurance as described below. Analytical assurance means (but is not limited to) an assurance of the precision, accuracy, or quality of measurements provided by the sweat sensor device. In other words, analytical assurance could further refer to improved confidence in the precision, accuracy, or quality of measurements made.
With reference to FIGS. 1A-1C, a sweat sensor device is designed to be calibrated before use. The sweat sensor device 100 has an adhesive side supported by carrier 150 and carrier 152. Carriers 150, 152 could be a variety of materials. By way of example, carriers 150, 152 could be wax or siliconized paper, such as that used in bandage backings. Carrier 150 is sufficiently sealed against the underside of the device 100 such that it covers and seals the adhesive side of the device 100 with exception to aperture 120a. Aperture 120a allows access to one or more sensors (not shown) via direct access or through microfluidic connections. Carriers 150, 152 are removable from device 100. In the illustrative embodiment, the carrier 152 may be removed without removing the carrier 150.
With reference to FIG. 1B, the carrier 152 of the device 100 may be removed to expose the aperture 120a. A sponge 160, which is permeated with a calibrating solution or medium, is pressed against the device 100 to bring the solution in contact with the sensors of the device 100. Importantly, the carrier 150 shields the rest of the device 100 from the application of the calibrating solution but allows the calibration solution or medium to contact at least one sensor though the aperture 120a. The calibrating solution is provided with pre-determined concentration of solutes or other properties of sweat (e.g., pH). The sponge 160 is held against the device 100 for a period of time adequate to allow the sensors to be calibrated based on measurements of analytes in the solution. The time required for a sensor to be calibrated may vary depending on the sensor stabilization time. The time required for a sensor to stabilize can be, for example, as short as several minutes, to as long as 30 minutes for a nM or pM sensor, or as long as multiple hours for ion-selective electrodes that require wetting periods. Once the sweat sensor device 100 has completed calibration, it is now capable of providing sweat measurements with analytical assurance. Carrier 150 may be subsequently removed, and the device 100 may be applied to skin 12 to be used, as shown in FIG. 1C. The calibration techniques disclosed herein significantly improve the ease with which sensors in patches or wearable devices may be calibrated. Conventional sensor calibration techniques require the sensor to be dipped into a beaker or vial containing a calibration solution. For a sensor in a patch or wearable device, as taught herein, such techniques are generally impractical for commercial usage (e.g. a non-laboratory setting such as a home, or may damage or degrade the sweat sensor device.
A variety of techniques and compositions may be used to calibrate sensors according to methods of the present invention. For instance, a calibration solution may be used where the solution composition is based on properties of skin, contaminants on skin, or other solutes or properties that would affect analytical assurance for a sensor placed on skin. A collected human sweat sample or an artificial sweat sample (e.g., such as one available from Pickering Laboratories) may also be used to calibrate a sensor. Further, the solution could be concentrated, diluted, or spiked with a solute or property of interest. The selected concentration of solutes could be, for example: low enough to confirm the lower limit of detection for the sensor, or could be near or below physiological levels to confirm the accuracy of the sensor. Where a device includes more than one sensor, the concentration of solutes in the applied sponge 160 could be designed to calibrate all of the sensors, one of the sensors, or a subset of the sensors. In an alternate embodiment, sponge 160 can be replaced by any other technique to apply a calibrating solution, including for example using a spray bottle (not shown).
In one embodiment, more than one calibration solution may be applied with similar or different concentrations or properties of sweat to calibrate a sensor. In the embodiment illustrated in FIG. 1B, more than one sponge 160 may be applied in sequence (not shown) to the device 100. When multiple sponges 160 are applied in sequence, the different sponges 160 may have calibration solutions, for example, that increase in concentration, or properties to calibrate sensor response or linearity with change in concentration. Alternatively, the different sponges 160 may have solution concentrations that increase or decrease to determine the rate of response or adaptation of sensors. Determining the sensor response rate improves analytical assurance because some sensors experience a lag between the change in analyte concentration in solution and the change in measured analyte concentration that is caused by the analytes' tendency to adhere to the sensor.
The application of a calibration solution (e.g., using the sponge 160) also allows one to determine other properties such as drift of sensors over time. In one embodiment, a sponge 160 may be applied for a sufficient time such that sensor drift can be determined to improve the analytical assurance for the sensor. For high quality sensors, drift typically is observable only after a period of hours or more.
With reference to FIGS. 2A and 2B, a sweat sensor device 200 is coupled to a calibration module 240. The calibration module 240 includes a housing 250 that defines a reservoir 254. The calibration module 240 acts as a carrier for the device 200 similar to the carrier 150 of FIG. 1A. Housing 250 includes aperture 220a that provides fluidic access from the reservoir 254 to at least one sensor 220 (shown in FIG. 2C) within the device 200. A calibration solution 270 is sealed inside the housing 250 by a membrane 260. On the other side of the membrane 260 (i.e., the side of the reservoir 254 adjacent the aperture 220a) is a gas, inert gas, or fluid 278. The application of pressure (as indicated by arrow 280) to the housing 250 causes the membrane to rupture, as shown in FIG. 2B. In this regard, the calibration module 240 has been activated by the pressure applied in the direction of arrow 280 and the calibration solution 270 comes into contact with one or more sensors of the device 200 near aperture 220a. The pressure may be applied, for example, by a user pressing against the housing 250. In one embodiment, to ensure the sensors are wetted, the calibration module 240 may include a sponge material (not shown) on the side of the membrane 260 adjacent to the aperture 220a. Alternatively, the housing 250 may be designed such that gravity is not a factor in the movement of the calibration solution 270 past the sensor and/or that a shaking motion could be applied to ensure calibration solution 270 comes into contact with one or more sensors of the device 200.
In one embodiment, the device 200 may include a flow restricting element. As illustrated in FIG. 2C, the flow restricting element 290 may be positioned adjacent the aperture 220a between the device 200 and the housing 250. A wicking material 230 surrounds a sensor 220 and the flow restricting element 290. The flow restricting element 290 may be, for example, a flow limiting element (e.g., reduced porosity in a textile), a flow constriction element (e.g., small pore or aperture), or a flow stopping element. In the illustrated embodiment, the restricting element 290 is a polymer film with a flow restriction component, such as a small gap. In this configuration, the gap restricts the flow of sweat from the skin to wicking material 230. The flow restricting element may prevent a sweat pumping element, such as wicking material 230, within the device 200 from being saturated with the calibration solution 270. In other words, the flow restricting element 290 prevents the calibration solution 270 from saturating the sweat pumping capacity of device 200. While the restricting element 290 in FIG. 2C is shown as being part of device 200, other configurations and techniques are capable of being used to restrict the flow of sweat to the device 200. In one embodiment, the flow restricting element 290 could be a component of element 250 shown in FIGS. 2A and 2B. In another embodiment, pumping or wicking elements could be removed or not fluidically connected to sensors during calibration and added or connected after calibration is complete.
With further reference to FIGS. 2A and 2B, in one embodiment, the calibration solution 270 could be a gel and component 278 may be a gel (rather than the gas 278 discussed above). As membrane 260 ruptures, the calibration gel 270 comes in contact with the gel 278. The solutes in the calibration gel 270 will diffuse, rather than flow by advection, through the gel 278 to come into contact with one or more sensors of the device 200 near aperture 220a. The materials for gels 270, 278 could be similar or different gel materials, so long as the diffusion of solutes in gel 270 can occur through the gel 278. This configuration allows for calibration of the sensors over a varying concentration level as the calibration solution diffuses into gel 278. For example, a sensor could be calibrated between a zero concentration level—which is the starting concentration for gel 270—and the maximum concentration of the solutes which results from slow diffusion-based mixing of concentrations between gel 270 and gel 278 where gel 270 contains a concentration of at least one solute to be used for calibration. Although a calibration involving a concentration gradient could be achieved where components 270, 278 are liquids, such a calibration would be less predictable, because fluid mixing is often more chaotic than the diffusion of solutes where components 270, 278 are gels, which are more homogeneous.
With further reference to FIG. 2B, in one embodiment, the rupture of membrane 260 could be caused by removing the housing 250 from the device 200. This may be convenient for use, since the device 200 cannot be adhered onto skin until housing 250 is removed. During the removal of the housing 250, the calibration solution 270 could be quickly (as little as seconds) brought into contact with sensors of the device 200, and the device may be applied to the skin. The calibration of the sensors may continue until sweat from the skin replaces the calibration solution, which is a process that may take at least several minutes, if not much longer. This approach ensures that the user always calibrates the device before use, without any extra steps beyond the expected minimum (i.e., removal of the housing 250) for applying an adhesive patch to the skin. This may be more broadly referred to as calibration which occurs as backing element or material, or housing material, is removed from the adhesive side of a device.
In one aspect of the invention, a calibration module may include more than one calibration solution or medium. With reference to FIG. 3, a device and a calibration module according to another embodiment of the invention are shown. The device 300 and calibration module 340 are similar in construction to those shown in FIGS. 2A and 2B, and similar reference numerals refer to similar features shown and described in connection with FIGS. 2A and 2B, except as otherwise described below. The calibration module 340 includes multiple solutions 370, 372, 374 within the reservoir 354. The solutions 370, 372, 374 could sequentially flow over aperture 320a past the sensors (as indicated by arrow 380) inside calibration module 340. The solutions 370, 372, 374 displace gas 378 as they flow past aperture 320a. The calibration module 340 may include a mechanism for pumping, gating, or introducing fluids as known by those skilled in the art. For example, component 378 could be a sponge material (not shown) that wicks the solutions 370, 372, 374 against the sensor. Further, the device 300 may include an electrowetting gate (not shown) to form a capillary between the solutions 370, 372, 374 and the sponge. It will be recognized that more complex arrangements with mechanical pumps and valves could be also used in other embodiments of the present invention. The solutions 370, 372, 374 may have the same or varying concentrations. In one embodiment, the solutions 370, 372, 374 contain a lowest concentration, a middle concentration, and a highest concentration, respectively, for calibration.
In another aspect of the present invention, a calibration module may include one or more calibration solutions containing more than one solute. Such a configuration allows sensor calibration, while also allowing a determination of any cross-interference between various solutes in, or properties of, sweat. For example, potassium (K+) and ammonium (NH4+) are known to interfere with each other in ion-selective electrode sensors. In one embodiment, a calibration module (e.g., module 340) may include a first solution containing a high concentration of K+ and a low concentration of NH4+. A second solution in the calibration module may contain a low concentration of K+ and a high concentration of NH4+. Further solutions may contain equal concentrations of K+ and NH4+, which could be high, moderate, or low. In this manner, any cross-interference between K+ and NH4+ for a device (e.g., device 300) may be determined.
With reference to FIG. 4, device 400 includes an external introduction port 490, a microfluidic component 480 that moves fluid to or past sensors, and an optional outlet port 492 with absorbing sponge 460. Microfluidic component 480 may be, for example, a 50 micron polymer channel that is 500 microns wide. One or more calibration solutions could be introduced at port 490 while the device 400 is on the skin 12. The calibration solution may be introduced at port 490 using a variety of methods. For example, the calibration solution could be introduced at port 490 by the application of droplets, by using a cartridge, by using a carrier, such as those discussed above, or using another approach. In addition to a calibration solution, a fluid that refreshes the usability of sensors may also be introduced to the device 400 though port 490 and be wicked through the microfluidic component 480 across sensors by sponge 460. In various embodiments, the fluid may change the pH level or cause a sensor probe to release an analyte. In one embodiment, such a refreshing fluid could be introduced to the device 400, followed by the introduction of the calibration fluid. The introduction of a fluid (e.g., a calibration solution) may be followed by a removal of the fluid. For example, in one embodiment, the sponge 460 could be removed after collection of the refreshing fluid and disposed of. The sponge 460 could be a wicking sponge material, a textile, hydrogel, or other material capable of wicking and collecting a fluid.
With reference to FIG. 5, a device 500 includes a first reservoir 530 and a second reservoir 532 that are fluidically coupled by microfluidic component 580. The first reservoir 530 includes a calibrating solution 570, and the second reservoir 532 includes a displaceable gas 578. Microfluidic component 580 is designed to provide access to a sensor (not shown). Calibration of the device 500 using aspects of the present invention could occur before device 500 operation begins, before sweat from skin 12 is sampled, or at times during the use of the device 500 using one more methods of timed microfluidic operation known by those skilled in the art. By way of example, the device 500 may include gates that swell (close) or dissolve (open) after prolonged exposure to a fluid. The gates (not shown) may be formed by a swellable polymer or a soluble salt or sugar, for example. The calibration solution 570 could stay in contact with the sensors for a determined period of time before it is removed. The calibration solution 570 may be removed, for example, by wicking or by pumping. Pumping may be accomplished through gas pressure (not shown) using the release of an internal pressurized gas source or generated gas source (e.g., electrolysis of water). Alternatively, the calibration solution 570 could remain in contact with sensors until it is replaced by sweat.
With reference to FIGS. 6A and 6B, a device 600 is shown which includes a substrate 610 carrying two similar sensors 620, 622 and a membrane 615 that covers the sensor 620. The sensors 620, 622 are similar in that, if one is calibrated, they are similar enough that calibration for one can be used for the others. In one embodiment, the sensors are of the same generation type (e.g. amperometric) but have different analyte targets (e.g. glucose and lactate). In another embodiment, the sensors target the same analyte, and calibration for one sensor will typically best predict the calibration for the second. Device 600 further includes a dry dissolvable calibration medium 670 for one or more analytes between the membrane 615 and the sensor 620. The calibration medium 670 could also be a liquid or a gel. FIG. 6B shows a flow of sweat 690 generated by the skin 12 as indicated by arrows 690a. The water in the sweat 690 penetrates through membrane 615 and dissolves calibration medium 670 to create a calibration solution 670a. Membrane 615 allows water transport through the membrane 615, while delaying or preventing transport of analytes to be sensed from the sweat 690 at least during a calibration between sensors. By way of example, the membrane 615 could be made of a dialysis membrane, Nafion membrane, track-etch membrane, reverse-osmosis membrane, or sealed reference electrodes. In this configuration, sensors 620, 622 can be compared in their readings of an analyte. If the concentration of an analyte in solution 670a is known, then the concentration of the analyte in sweat 690 can be better determined through comparison of the measured signal from sensors 620, 622. In an exemplary embodiment, membrane 615 creates a defined volume around sensor 620 such that the concentration of analytes is predictable (i.e., known amount of dilution as the calibration medium 670 dissolves). For example, a porous polymer or polymer textile could be used which has a finite porous volume in it to fix the volume of calibration solution 670a around the sensor 620. In one embodiment, calibration solution 670a may include a concentration of the analyte that is greater than the concentration of that analyte present in sweat. For example, the calibration solution 670a may include an analyte at a concentration roughly 10 times or more than that found in the sweat that wets the calibration medium 670.
With reference to FIG. 6C, in one embodiment, element 620 of the device 600 represents two or more different sensors 620a and 620b requiring calibration. For example, the first sensor 620a in element 620 could be for detecting cortisol, and often these types of sensors require calibration. Sensor 622 shown in FIG. 6A would, in this example, also be for detecting cortisol and would measure cortisol found in sweat directly. The second sensor 620b in element 620 could be for detecting Na+ (such as an ion-selective electrode or through simple electrical conductance of solution). The dry dissolvable calibration medium 670 includes a known starting concentration of cortisol 672a and Na+ 672b. As water moves through the membrane 615, it dissolves or dilutes the calibration medium 670 to create the calibration solution 270a, in which concentrations of both Na+ and cortisol could be measured. The Na+ sensor 620b may be configured so that it would not need calibration using the calibration solution 270a. For example, sensor 620b may be an ion-selective electrode having a sealed reference electrode (not shown) to allow it to accurately quantify Na+ concentrations. As the Na+ dilutes as the water moves in, the amount of water is also indirectly measured (by measuring Na+), and therefore the amount of dilution of cortisol would be known from the time when the water began moving through the membrane 615 until the water fills the space between the membrane 615 and the sensors 620a, 620b. In summary, the measurement of Na+ would be used to determine the total dilution that has occurred as water moves into the calibrating solution 670a, and therefore the amount of dilution of cortisol in calibrating solution 670a is also known. Therefore a dilution calibration curve could be provided for the first sensor 620a, which would then provide a dilution calibration for sensor 622 as well.
With further reference to FIGS. 6A-6C, in one aspect of the present invention, membrane 615 may act as a binding medium that binds solutes in sweat such that sweat is diluted of one or more analytes before it reaches the calibrating medium. Such a binding medium would be in the sweat flow path between sweat glands and at least one sensor. The binding medium may provide specific binding (e.g., a layer of beads doped with ionophores) or non-specific binding (e.g., cellulose). As a result, the calibration medium 670 would not need to provide a concentration of analyte or analytes greater than that found in real sweat, as the initial sweat which reaches the calibration sensor would be diluted of the analyte to be calibrated. Specific binding materials include beads or other materials those known by those skilled in the art that promote specific absorption.
In another aspect of the present invention, conditions can be provided that denature or alter an analyte in sweat such that its concentration is effectively lowered before reaching a calibration medium. In one embodiment, a binding solute in solution that binds to the analyte in a way similar to how the analyte binds to a probe on the sensor is provided at a location between the sensor and skin. In one embodiment, the binding solute may be present in a wicking textile (not shown) that brings sweat from skin to the sensors. Because the analyte will bind with the binding solute, the sensor probes are prevented from binding with such analytes. For example, the sensor could be an electrochemical aptamer or antibody sensor, and the binding solute could be an aptamer or antibody that is suspended in solution. Those skilled in the art will recognize other techniques that are useful for lowering concentrations of analytes in sweat such that a more pure fluid is provided for the purposes of calibration.
With reference to FIGS. 7A-7C, a device 700 includes a sensor 720 for sensing a first analyte and a sensor 722 for sensing a second analyte, and the device 700 further includes a polymer substrate 710, and calibration mediums 770, 772 for calibrating the first and second sensors 720, 722, respectively. The calibration mediums 770, 772 may be positioned adjacent to the sensors 720, 722 using a variety of techniques. For example, the calibration mediums 770, 772 could be a dry powder placed adjacent to a sensor, held in place by a glue or a dissolvable medium, or held in place by another technique until wetted by sweat. The calibration mediums 770, 772 generally: (1) can rapidly take up sweat and allow wetting of sweat against sensors 720, 722; (2) release a concentration of calibrating analytes into sweat near sensors 720, 722 quickly enough to alter the concentration of said analytes in sweat; (3) maintain calibration concentrations of analytes in sweat long enough for sensor 720, 722 calibration to be performed; and (4) promote a generally fixed fluid volume initially as they uptake sweat such that calibration analyte concentrations are repeatable. In one embodiment, calibration mediums 770, 722 may be made of a material that would rapidly swell to a known volume as it wets but would more slowly dissolve and wash away, therefore allowing adequate time for calibration (discussed further below). With reference to FIG. 7B, once calibration mediums 770, 772 are wetted with sweat 790 generated as shown by arrows 790a, calibration solutions 770a, 772a are formed. Over time, the calibration analytes within calibration solutions 770a, 772a are transported away from sensors 720, 722 by the sweat 790 such that sensing can be performed on new sweat, as shown in FIG. 7C.
Calibration mediums, useful in embodiments of the present invention can be constructed using a variety of methods. With further reference to FIGS. 7A-7C, calibration mediums 770, 772 may release the analytes contained therein initially upon contact with sweat, or at some time thereafter, through time-release techniques. In various embodiments, a calibration medium could be formed from a dissolvable polymer, such as a water soluble polymer or a hydrogel. Exemplary polymers include polyvinylpyrolidone (PVP), polyvinylachohol (PVA), and poly-ethylene oxide. PVP can be used as a dissolvable polymer that can swell with up to 40% water in a humid environment or can be used as a hydrogel if cross-linked using, for example, UV light exposure. Like PVP, PVA can be used as a water dissolvable material or as a hydrogel. Also, such polymers can have a wide range of molecular weights that can affect the rate at which such polymers dissolve. Consider several exemplary embodiments. In one embodiment, a calibration medium of PVP with a known concentration of at least one analyte is coated onto a sensor or is positioned adjacent to a sensor. When wetted or hydrated, the PVP will act as a calibration solution. Such a calibration medium could also contain one or more preservatives. If PVP, or another suitable material, were used as a water dissolvable polymer, its surface would wet quickly with sweat before the PVP appreciably dissolves. Then, before the PVP fully dissolves, the sweat would hydrate the polymer and allow for sensor calibration. Therefore, the polymer itself could provide a predictable volume and dilution of calibrating analytes confined inside the polymer for a period of time (seconds, or minutes) before it fully dissolves. In one embodiment where the device includes a protein-based sensor, such as an electrically active beacon aptamer sensor, the calibrating analyte confined in the polymer could be a protein, such as a cytokine. Initially, as water and ions from sweat permeate the polymer to wet it, the calibrating protein solution would remain at least partially immobilized inside the polymer, and outside proteins in sweat would be at least partially excluded. The calibration medium may be adapted to prevent outside proteins from being absorbed based on the size of the proteins, based on properties such as the solubility or lipophilicity of the proteins. The calibration medium may also include ionophores to allow certain solutes and the water from sweat to electronically activate the sensor while excluding other solutes. Therefore, a predictable dilution or concentration of the calibration medium could be provided long enough to allow sensor calibration (e.g., on the order of seconds or minutes) before the polymer dissolves. In one embodiment, the calibrating analytes may be absorbed by the sensor underneath the polymer, and the sensor will be calibrated when water and salt (i.e., sweat) reaches the sensor, which enables the proper electrical connection needed for a complete sensing circuit. Similarly, hydrogels could be used as calibration mediums as long as a suitable time period for calibration is provided. For example, in one embodiment, the thickness of the hydrogel provides adequate time for the calibrating analyte inside the hydrogel to calibrate the sensor before external analytes in sweat enter the hydrogel and dominate the signal provided from the sensor. It should be recognized that calibration mediums may have alternative configurations. For example, in various embodiments, the calibration medium may be constructed of may be a textile that is coated with analytes or may include multiple layers of polymers or gels having different properties. Additionally, various techniques, such as altering the pH, may be used to remove the calibrating analytes from sensors to prevent interference with measurements of new sweat.
With reference to FIG. 8, a device 800 contains two sensors 820, 822 for example, and two identical calibration mediums 870. Sensors 820, 822 and calibration mediums 870 are enclosed by substrate 810 and seal 817. Seal 817 includes fluidic gates 880, 882. Fluidic gates 880, 882 only allow sweat to reach sensors 820, 822 as determined by the design of the fluidic gates 880, 882 (e.g., based on a dissolution rate of the gate). In one embodiment, when gates 880, 882 allow the passage of fluid, sweat would first enter the space between the membrane 810 and seal 817 and dissolve calibration mediums 870. In this manner, sensors 820, 822 may be calibrated similarly to the calibration methods discussed above. After a period of time (e.g., 30 minutes), the calibration medium 870 would diffuse out through the microfluidic gates 880, 882 as new sweat enters. As the medium 870 diffuses, the analyte concentrations near the sensors 820, 822 would be increasingly dominated by those in new sweat. The device 800 of FIG. 8 is useful when a sensor is to be calibrated and used only when needed. In one embodiment, sensors 820, 822 are one-time use, and the device 800 is configured to perform multiple readings. Where more than one microfluidic gate is used, the gates may be designed to open and close at the same time or at different times. Multiple fluidic gate configurations are possible as known by those skilled in the art, including thermo-capillary, electrowetting, melting of wax barriers, or other known techniques. In one embodiment, a wicking element could also be included (not shown) to bring a continuous flow of sweat to the sensor 820 or 822, and mitigate the need for a calibration medium to diffuse out, thereby decreasing the time required to calibrate the device.
With further reference to FIG. 8, in one embodiment, one or both of gates 880, 882 could be a dissolvable polymer (e.g., PVP or PVA) and seal 817 could be a membrane (e.g., a dialysis membrane) that is permeable to water but highly impermeable to at least one analyte to be calibrated. Therefore, as sweat wets the membrane 817, water moves though the membrane 817 and dissolves calibration medium 870 and creates a calibrating solution for calibrating at least one of the sensors 820, 822. Later, as at least one of the gates 880, 882 dissolves away, sweat including the analytes that were previously excluded by membrane 817 enters through the dissolved gate 880, 882 and begins to be sensed by the now-calibrated sensor 820 or sensor 822. The exact dimensions shown in FIG. 8 are non-limiting and are provided as an example only. For example, in one embodiment, gates 880, 882 could have larger area than membrane 817.
For purpose of clarity, layers and materials in the above-described embodiments of the present invention are illustrated and described as being positioned ‘between’ sweat and sensors and, in some cases, ‘between’ one or more of each layer or material. However, terms such as ‘between’ should not be so narrowly interpreted. The term ‘between’ may also be interpreted to mean ‘in the fluidic pathway of interest’. For example, in one embodiment, a microfluidic channel that is 3 mm long and 300 μm×100 μm in area could be positioned in the pathway (or ‘between’) of flow of sweat from the skin to the sensors and may include any one or more of the features illustrated and discussed for the present invention. Therefore, ‘between’ or other terms should be interpreted within the spirit of the present invention, and alternate embodiments, although not specifically illustrated or described, are included with the present invention so long as they would obviously capture similar purpose or function of the illustrated embodiments.
This has been a description of the present invention along with a preferred method of practicing the present invention, however the invention itself should only be defined by the appended claims.
