Patent Application
20190183398
Non-invasive biosensing technologies have enormous potential for numerous applications including athletics, neonatology, pharmacological monitoring, and personal health. Biofluids, such as sweat, provide access to many of the same biomarkers, chemicals, and solutes that are found in blood, which can enable the diagnosis of ailments, health status, toxins, physical exertion, and other physiological attributes in the absence of any physical symptoms. Sweat has many of the same analytes and analyte concentrations as found in blood and interstitial fluid. Interstitial fluid has even more analytes nearer to blood concentrations than sweat does, especially for larger-sized and more hydrophilic analytes (such as proteins).
However, one challenge in using sweat to diagnosis physiological conditions is that the electrical signals from biofluid sensors often have a strong dependence on temperature. For example, ion selective electrode (ISE) sensors, have electrical outputs that are governed by the Nernst equation:
where T represents temperature. For ISEs, increasing temperatures will increase the total potential change between two given concentrations. This increased potential change can improve sensor performance by increasing the total bandwidth of the signal. While increasing temperatures can improve sensor performance, temperature variations, even at higher average temperatures, can compromise sensor performance. In particular, variations in sensor temperatures can have an adverse effect on the accuracy of an ISE sensor's response to a target analyte. Similarly, the output of enzymatic sensors, and other sensor modalities is based upon temperature-dependent, kinetic reaction rates. In particular, temperature and temperature variation can have significant effects on electrochemical aptamer-based (EAB) sensors, which are discussed in U.S. Pat. Nos. 7,803,542 and 8,003,374, and U.S. Provisional Application No. 62/523,835, filed Jun. 23, 2017, each of which is hereby incorporated by reference herein in its entirety. For EAB sensors, temperature directly affects the kinetic equilibrium between aptamers and the target analyte concentration in a biofluid sample, and temperature influences structural variations within the aptamer. Accordingly, small changes in temperature will impact the accuracy of single point calibrations by shifting the binding affinity of the aptamer to its target analyte. Likewise, large temperature changes can impact the secondary and tertiary structures of the aptamer, altering the aptamer's pre-capture presentation, and post-capture conformational response to its target analyte.
One solution to the challenge of temperature variation is to add a temperature sensor to a biofluid sensing device, and use the sensor output to correct for temperature-induced errors in the biofluid sensor output signal. For example, integration of a temperature sensor in a sweat sensing device is disclosed in PCT/US13/35092, which is incorporated herein by reference in its entirety. However, for many biofluid sensing applications, simply adding sensors to correct for temperature errors may prove inferior to passively or actively regulating the temperature of the biofluid sensor(s). Furthermore, a temperature sensor may not accurately measure a biofluid sensor temperature without the sensor being thermally isolated from the device wearer's body or the external environment. Accordingly, it is desirable to have biofluid sensing devices which passively or actively regulate the operating temperature of one or more biofluid sensors; as well as simple, yet robust, methods for regulating the operating temperature of one or more sensors in a biofluid sensing device.
The disclosed invention includes a biofluid sensing device capable of passively or actively regulating an operating temperature of one or more sensors. The device includes at least one biofluid sensor in a thermally isolated environment and at least one temperature sensor to measure sensor environment temperature. Some embodiments include at least one thermal component to regulate the sensor temperature by actively adjusting the sensor environment temperature in response to a signal from the temperature sensor. The invention also includes a method of regulating temperature for a biofluid sensing device having at least one sensor for measuring an analyte in the biofluid. The method includes measuring the biofluid sensor environment, and regulating the biofluid sensor environment temperature to within a selected range of the measured sensor temperature. The method further includes maintaining sensor temperature within the selected range of the measured temperature throughout device operation. In some embodiments, the measured temperature is a calibration temperature.
The present disclosure will be further appreciated in light of the following detailed description and drawings in which:
Before continuing with a detailed description of the exemplary embodiments, a variety of definitions should be made, these definitions gaining further appreciation and scope in the detailed description of the embodiments.
As used herein, “interstitial fluid” is a solution that bathes and surrounds tissue cells. The interstitial fluid is found in the spaces between cells. Embodiments of the disclosed invention measure analytes from interstitial fluid found in the skin and, particularly, interstitial fluid found in the dermis. In some cases, where interstitial fluid is emerging from sweat ducts, the interstitial fluid contains some sweat as well, or alternately, sweat may contain some interstitial fluid. As used herein, “mainly interstitial fluid” means fluid that contains by volume less than 50% sweat (i.e., is primarily interstitial fluid). As used herein, “mainly sweat” means fluid that contains by volume 50% or greater of sweat (i.e., may contain some interstitial fluid, but has an equal or greater amount of sweat than interstitial fluid). The percentages of each fluid can be quantified by several methods, such as measuring analyte dilutions in sweat (e.g., some analytes are dilute in sweat but not in interstitial fluid), or by measuring and comparing sample generation rates and their respective contributions to the total fluid volume (e.g., compare sample generation rates with or without application of reverse iontophoresis; or compare sample generation rates with or without natural or chemically-induced sweat stimulation).
As used herein, “sweat” means a biofluid that is primarily sweat, such as eccrine or apocrine sweat, and may also include mixtures of biofluids such as sweat and blood, or sweat and interstitial fluid, so long as advective transport of the biofluid mixtures (e.g., flow) is primarily driven by sweat.
“Biofluid” means any human biofluid, including, without limitation, sweat, interstitial fluid, blood, plasma, serum, tears, and saliva.
As used herein, “chronological assurance” means the sampling rate or sampling interval that assures measurement(s) of analytes in a biofluid at the rate where measurements can be made of new biofluid analytes emerging from the body. Chronological assurance may also include a determination of the effect of sensor function, potential contamination with previously generated analytes, other fluids, or other measurement contamination sources for the measurement(s). Chronological assurance may have an offset for time delays in the body (e.g., a well-known 5 to 30-minute lag time between analytes in blood emerging in interstitial fluid), but the resulting sampling interval (defined below) is independent of lag time, and furthermore, this lag time is inside the body, and therefore, for chronological assurance as defined above and interpreted herein, this lag time does not apply.
As used herein, “biofluid sampling rate”, “sweat sampling rate”, or simply “sampling rate” means the effective rate at which a new biofluid sample reaches a sensor that measures a property of the fluid or its solutes. Sampling rate is the rate at which new biofluid is refreshed at the one or more sensors, with the new biofluid displacing the old biofluid as the new fluid arrives. In one embodiment, the sampling rate can be estimated based on volume, flow-rate, and time calculations, although it is recognized that some biofluid or solute mixing can occur. Sampling rate directly determines, or is a contributing factor in determining, the chronological assurance. Sampling times and rates are inversely proportional (rates having at least partial units of 1/seconds), therefore a short or small time required to refill sample volume can also be said to have a fast or high sampling rate. The inverse of sampling rate (1/s) could also be interpreted as a “sampling interval”. Sampling rates or intervals are not necessarily regular, discrete, periodic, discontinuous, or subject to other limitations. Like chronological assurance, sampling rate may also include a determination of the effect of potential contamination with previously generated biofluid, previously generated solutes (analytes), other fluids, or other measurement contamination sources for the measurement(s). Sampling rate can also be in part determined from solute generation, transport, advective transport of fluid, diffusion transport of solutes, or other factors that will impact the rate at which new samples will reach a sensor and/or is altered by older sample or solutes or other contamination sources.
As used herein, “measured” can imply an exact or precise quantitative measurement and can include broader meanings such as, for example, measuring a relative amount of change of something. Measured can also imply a binary measurement, such as ‘yes’ or ‘no’ type qualitative measurements.
As used herein, “microfluidic components” are channels or other geometries formed in or by polymers, textiles, paper, or other components known in the art to transport fluid in a deterministic manner.
As used herein, “sweat sample channel” means any component of the disclosed invention that is on or adjacent to a sweat sensing device sweat sample collector and that promotes transport of sweat or its solutes by wicking pressure, advective flow, diffusion, or other method of transport, from the collector, across device sensors and to a sweat sample pump. In some embodiments, the channel function may be performed by a suitably configured sweat collector. A channel may be part of the same component or material that serves other purposes (e.g., a sweat collector or a sweat sample pump), and in such cases, the portion of said component or material that, at least in part, fluidically connects the collector to the pump and conveys sweat to a sensor(s) and that is on or adjacent to the sensor(s), is also a channel as defined herein.
As used herein, the term “analyte-specific sensor” is a sensor specific to an analyte which performs specific chemical recognition of the analyte's presence or concentration (e.g., ion-selective electrodes, enzymatic sensors, electrochemical aptamer-based sensors, etc.). Sensors could also be optical, mechanical, or use other physical/chemical methods which are specific to a single analyte. Further, multiple sensors can each be specific to one of multiple analytes.
Turning now to the drawing figures, in which like numerals refer to like features throughout the views, several exemplary embodiments will be described of a wearable sensing device for measuring at least one analyte in a sweat or other biofluid sample. The sensing device measures samples at chronologically assured sampling rates or intervals. The sensing device embodiments described herein can take on many forms including patches, bands, straps, portions of clothing, wearables, or any suitable mechanism that reliably brings sampling and sensing technology into intimate proximity with a biofluid sample as it is transported to the skin surface. While some sensing device embodiments utilize adhesives to hold the device near the skin, devices could also be held by other mechanisms that hold the device secure against the skin, such as a strap or embedding in a helmet. Embodiments herein depict one or more of the sensors as simple individual elements. However, it should be 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, but which may be included in the device embodiments. 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. Certain embodiments of the disclosed invention show sub-components of what would be sensing devices with more sub-components needed for use of the device in various applications. Where these sub-components would be obvious (such as a battery), for purposes of brevity and of greater focus on inventive aspects, such components are not explicitly shown in the figures or described in the embodiments.
With reference to
The device 100 further includes a polymer substrate 110, which could be made of PET or other suitable material. An adhesive (not shown) may extend between the substrate 110 and the skin 12 to attach the device to the wearer. A protective vapor barrier layer 140 extends about the exterior of the device. Outer layer 140 is shown only in the first embodiment (
The device 100 also includes a passive thermal component comprising one or more layers of a low thermal conductivity material or insulator, as indicated at 170 and 172. The insulators 170, 172 may include any one or more of the following materials: cotton (0.04 W/m-K); an air-filled space, such as a container or silica aerogel (0.02 W/m-K); foam glass or glass wool (0.4 W/m-K); Styrofoam (0.3 W/m-K); a vacuum vessel (<0.01 W/m-K), or other materials. Additionally, the insulators 170, 172 may range in thickness from approximately 0.01 mm to 10 mm, but may be thicker than 10 mm in some embodiments. The insulators 170, 172 thermally isolate the sensors 120, 122, 124, 126 in an environment separate from atmospheric or ambient air. The thermal isolation decreases the temperature variability of the sensors 120, 122, 124, 126, enabling the sensors to operate at a consistent, controlled temperature. While the biofluid sensors 120, 124 and temperature sensors 122, 126 are depicted as being separated by intervening insulator material, the invention is not so limited, and some embodiments include configurations where biofluid sensors and temperature sensors are not separated by insulator material.
An active thermal component, consisting of a heater 180, is provided in thermal communication with the sensors 120, 122, 124, 126. The heater 180 may, for example, be a resistive heater, an infrared light emitting diode, or a thermoelectric module, and is placed in thermal communication with the sensors 120, 122, 124, 126, so that generated heat is transferred to the sensor environment. In at least some embodiments, the heater 180 regulates the temperature of the sensors to within a range of ±5° C. to ±0.1° C. of 40° C. (106° F.). In at least some embodiments, the heater 180 regulates the temperature of the sensors to one of the following temperatures: >37° C.; >39° C.; >41° C.; and >45° C.
The heater 180 enables the sensing device 100 to raise and maintain a sensor temperature above the device wearer's body temperature. Maintaining a high sensor temperature is advantageous for a number of reasons. Certain biofluid sensors, such as ISE sensors, tend to be more accurate at higher temperatures. Other sensor types, such as EAB sensors, provide a stronger response (greater signal change) to analyte concentration changes when operating at higher temperatures. Further, maintaining an elevated sensor temperature can reduce temperature variability, and hence sensor output variability, because maintaining a higher sensor temperature will be relatively easier than maintaining a lower sensor temperature for many device applications. This would apply to situations in which the wearer's body temperature or the external temperature increases during device use, e.g., the wearer begins to exercise after device application, the wearer develops a fever, or the device is applied when the external temperature is at a low point, etc. Therefore, if sensor temperature were lowered rather than raised, temperature-induced variability would likely increase.
In this embodiment, an insulating layer 170 extends between the heater 180 and the skin 12, while a second insulating layer 172 substantially surrounds the sensors 120, 122, 124, 126, thereby thermally isolating the sensors and heater 180 from the external environment. With the sensors located within or between the insulating layers 170, 172, changes in conditions outside of the insulating layers (e.g., changes in skin or body temperature, air temperature, etc.) will not immediately affect the sensors, which will be held at a nearly constant temperature by the low thermal conductivity material. If the wearer is using the device in an environment with high external temperatures, the heater 180 may be used to increase the regulated temperature to a temperature that is appropriate for the application.
With further reference to
In an alternative embodiment, shown in
With reference to
With the addition of a thermoelectric cooler 382, the sensors 320, 322, 324, 326 can be regulated to remain below the body temperature (i.e., below around 99° F. or 30° C.), by transferring a lower temperature from thermoelectric cooler 382 through the thermally conducting material 376. The heater 380 and cooler 382 can be operated in conjunction with each other, or separately controlled in response to a signal from the temperature sensor 322 to maintain a consistent, regulated temperature regardless of increases or decreases in body temperature or ambient air temperatures.
With further reference to
With reference to
To regulate the temperature of the sensors 420, 422, 424, 426, the device 400 further includes one or more thermal components. As shown in
With further reference to embodiments of the disclosed invention, additional or alternate temperature sensors (not shown) may be placed adjacent to skin or adjacent to ambient air to further inform temperature regulation, or to directly measure body temperature or ambient temperature, respectively.
While several exemplary embodiments have been described for regulating the temperature of at least one biofluid sensor, it is anticipated that other materials, elements and configurations may also be used, provided the alternative materials, elements or configurations provide chronological assurance and accurate detection and measurement of one or more analytes in a biofluid sample. Various modifications, alterations, and adaptations to the embodiments described herein may occur to persons skilled in the art with attainment of at least some of the advantages. The disclosed embodiments are therefore intended to include all such modifications, alterations, and adaptations without departing from the scope of the embodiments as set forth herein.
The present application claims priority to PCT/US17/47808, filed Aug. 21, 2017, and U.S. Provisional Application No. 62/377,090, filed Aug. 19, 2016, the disclosures of which are hereby incorporated by reference herein in their entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US17/47808 | 8/21/2017 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62377090 | Aug 2016 | US |
