Mayank
Garg†
*a,
Arpana
Parihar†
*b and
Md. Saifur
Rahman
a
aDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA. E-mail: mayankgarg93@tamu.edu
bIndustrial Waste Utilization, Nano and Biomaterials, CSIR-Advanced Materials and Processes Research Institute (AMPRI), Hoshangabad Road, Bhopal, Madhya Pradesh, India. E-mail: arpana_parihar@yahoo.com
First published on 11th December 2023
Due to people's hectic and intense working schedules, health as a priority is often pushed to the sidelines. This is more problematic for people with some health conditions, which require regular monitoring of vitals. Therefore, the development of smart diagnostics is a clinical challenge towards which, a lot of research is being carried out. This primarily includes the development of wearable sensors. These sensors can be worn by individuals for the monitoring of various biomarkers in different bio-fluids. Primary research is being carried out to make them sensitive, reliable, robust, and non/minimally invasive. Since the intended wearable sensor is to be used for continuous monitoring of the individuals, all the components required for the sensing must be on the same platform. This generally includes the sensing platform, microfluidic channels, and its electronic or optical components. The goal of the current review is to highlight the state-of-the-art integrated wearable sensors, describing their important components, methods of manufacturing, and applications of these sensors and discuss the challenges being faced while designing and scaling up these sensors. The contents of this review will help design and develop novel integrated wearable sensors that are expected to revolutionize the field of personalized healthcare.
In this regard, wearable sensors become the key players.2 Wearable sensors are non/minimally invasive analytical devices capable of providing point-of-care systems for the continuous and regular monitoring of individuals’ physiological as well as biological markers.3 Unlike conventional point-of-care devices, wearable sensors can utilize easy-to-sample bio-fluids such as saliva, tears, and sweat for the detection of clinically important biomarkers. This combined with continuous or regular monitoring can help in timely intervention and preventative measures. Since these devices are autonomous, lightweight, and compact, their impact is barely noticed by the user in their daily life. As the data is transmitted wirelessly, this provides mobility and accessibility to the users/patients wearing these devices. This is particularly useful when monitoring neonates and elderly people. The wearable devices can be modified to provide personalized healthcare. The large amount of data obtained through these devices can be used to train machine learning algorithms, which can be helpful for decision-making through artificial intelligence. Though expensive currently, over time, these wearable devices will prove to be cost-effective. The concept of a wearable device is not new and has been in existence for a long time. The wearables used during the 1960s provided the foundation for today's next-generation wearable sensors. Fig. 1 shows the components of the wearable sensor, the biomarkers for which sensors are being developed, and the tremendous jump in the number of publications related to the development of wearable sensors over the years. The current wearables are capable of reliable continuous monitoring of an individual's vitals such as temperature, humidity, blood oxygen level, blood pressure, EEG, ECG, and many biomarkers of clinical relevance.4–9 Apart from the sensing aspect, wearables also play an important role in the thermal management of the human body.10,11 The electrochemistry-based transducer is the most reliable and flexible option available for the design of wearable sensors because of its sensitivity, ease of fabrication, no moving parts, mechanical robustness, and resistance to other conditions.12 This transducer is the most widely used and trusted option for a biosensor.
Most of the research involving the development of wearable biosensors has been primarily limited to the fabrication and testing of the sensing platform i.e., the development of a sensing surface for a particular physiological or biological marker. For instance, though a wearable sensor for cortisol has been developed, it still requires the use of an external potentiostat for the read-out.13–17 There are many such examples. This essentially is against the concept of a wearable sensor. An ideal integrated wearable sensor should have the sensing platform and the associated electronics in a small and compact form that can be easily worn by the user.
The current review article is an attempt to stress the need for integration by briefly discussing the fabrication aspects of integrated wearable sensors using additive manufacturing technologies, the design and fabrication of multiplexed wearable sensors, and various microfluidic-based applications of wearable sensors. Other than these, the review article will also discuss wearable multifunctional flexible sensors, strain sensors, pressure, and thermal sensors along with some discussion on the implantable sensors. This review will highlight the commercially available integrated wearable sensors and report the challenges encountered while designing and fabricating integrated wearable sensors. It will also provide future insights into the field of integrated wearable sensors.
Interactions between a target and a bio-recognition element are the guiding principle while designing a sensing platform. The targets present in the bio-fluid are transported to the sensing surface, where the interactions with the bio-recognition element cause a change in the electrical signal, thereby enabling their detection. The electrochemistry-based transducer is the most reliable and flexible option available for the design of a wearable sensor because of its sensitivity, ease of fabrication, no moving parts, mechanical robustness, and resistance to other conditions.12 This transducer is the most widely used and trusted option for a biosensor. The electrical changes can be amperometric (change in current), voltammetric (change in potential), or impedimetric (change in impedance or resistance). For a typical biosensing surface, the surface of the electrode is modified with a bio-recognition element, which can be an antibody, aptamer, enzyme, peptide, or molecularly imprinted polymers (MIPs).21–24 Using bio-recognition elements is challenging since these need to adapt to the extreme conditions that are generally faced by wearable sensors. Of these elements, the use of an antibody or enzyme is less encouraged since these are the most vulnerable entities outside their physiological conditions. Nowadays, the use of peptides and MIPs is quite prominent since these are almost resistant to physiological conditions. As wearable sensors are intended for continuous monitoring of various biomarkers, the regeneration capability and biocompatibility of these recognition elements also need to be considered. It has been observed that biosensors targeting redox-active molecules are easily regenerated compared to non-redox-active molecules, such as proteins.25 As a wearable biosensor is intended for continuous and long-term usage, the regeneration of the sensing element also needs attention. In an ideal situation, the sensing elements do not need to be replaced. The prolonged exposure of the complex media to the bio-recognition elements reduces their efficiency and therefore they need to be replaced. Since the regeneration of these elements is not possible in wearable conditions, this becomes a bottleneck. MIPs are an attractive alternative to solve this problem since these can be easily regenerated.26 For instance, Gao's group showed the regeneration of a wearable metabolite and nutrient sensor based on MIPs. The sensor was regenerated by the application of an electrical potential for a very short time (less than 30 seconds). During the regeneration step, the electrode's surface gets altered so that it releases the bound analyte and becomes refreshed.27
For the fabrication of a sensor, a substrate is first modified with one of the above-mentioned bio-recognition elements. Since most of the wearable sensors developed are electrochemical transduction-based, the substrate is an electrode.25,28,29 The successful modification of the substrate is a critical part of biosensor design. The electrodes chosen should allow efficient and easy modification with the bio-recognition element, should not get fouled, be bio-compatible, and provide excellent electron mobility for the detection of various biomarkers of interest. These electrode surfaces are then functionalized to immobilize the bio-recognition elements. The use of nanomaterials is quite prominent for the development of electrode materials. Nanomaterials have proven their potential over a long time. They allow for a high surface-to-volume ratio, good electrical and optical properties, and allow efficient immobilization of the bio-recognition elements.30–35 In some cases, the catalytic activity of the nanomaterials has been utilized for the signal generation of electrically active metabolites such as amino acids, ions, or other analytes.
Another component of the sensing platform is the substrate or the platform itself. The wearable sensor should be conformal to the human skin and also the platform on which the sensor is to be fabricated must be flexible and soft. In this regard, many different materials have been explored. For instance, the use of PDMS is quite prominent since it is easy to handle, can be molded into any shape, microfluidic channels can be built on it and is soft on the skin and flexible. For instance, Singh et al. used a PDMS-based platform for the fabrication of a sweat sensor for cortisol. The gold electrode was deposited on the PDMS and microfluidic channels were also created in the PDMS to allow for the transport of sweat to the sensing chamber.36 Polyimide is another low-cost substrate for sensor fabrication. Though this material is not as soft as PDMS, a modified polyimide (PI) surface can be used directly as an electrode material. For instance, the Gao group has demonstrated that the PI surface can be altered using lasers to produce laser-induced graphene, which can then be used as an electrode material. The work reported the use of this Laser Induced Graphene (LIG) electrode for the detection of cortisol in sweat and serum.37
Various electrical components are required to make a wearable sensor work. The foremost is the battery to power up the sensing surface, integrated circuits, and read-out devices. For a typical sweat-based sensor, the induction of sweat through iontophoresis also requires power. The other important component is the integrated circuits (ICs), which manage the power delivery, potentiostat, data acquisition, and transmission.38,39 Various filters are also used in an integrated wearable sensor to eliminate any noise and unwanted signals coming due to external factors or motion artifacts. The electrical components are also responsible for the data transmission onto a smartphone using Bluetooth. The electronic component of a wearable biosensor is fabricated on a solid PCB or sometimes on flexible substrates depending on the intended application.40
The limiting factor for a wearable biosensor is the power supply. Since these sensors are intended for continuous measurements and data transmission, they consume a lot of power. To date, most of the devices developed have an external battery to power them. However, an idealistic situation is that the sensors can power themselves. Self-powered wearable biosensors are next-generation wearable sensors, wherein the sensors rely on energy harvesting from bio-fluids.41 Interested readers can refer to the detailed analysis of various self-powered devices by different researchers.41–45 A notable work is the development of a battery-free powered wearable sensor based on zinc oxide nanowires.46 The work reported the modification of zinc oxide nanowires with lactate oxidase. The flow of sweat on the nanoarrays caused a generation of DC electrical signal which corresponds to the lactate concentration in the sweat. The generation of an electrical double layer by the nanowires creates a potential difference.
The healthcare data generated by the wearable sensor is generally continuously transmitted to a smartphone a laptop or a server for processing. Since the amount of data generated is quite complex, various mathematical models are required to apprehend the data, so that the user can easily understand it. To achieve fast and accurate processing of the data, various models, and cloud computing have been utilized.47–51
The i3DP technique has been found to be the most commercially viable among the 3D printing methods.58 To fabricate the microfluidic channel on a submillimeter scale, the i3DP approach has been widely taken. Typically, the i3DP approach relies on the continuous or drop-on-demand (DoD) mode.59 For fabricating the micrometer scale of microfluidic devices, i3DP has become very demanding. Gowers et al. (2015) demonstrated a 3D-printed microfluidic device that can continuously monitor human tissue metabolite levels.60 A needle-type biosensor integrated with regulatory-certified (FDA) clinical microdialysis probes through the use of a probe outlet holder, is shown in Fig. 2.60 This novel and innovative structure minimizes the extra connection tubing and adaptors, thus miniaturizing the device size. Typically, to substitute the micro vial, the microfluidic device is inserted into the probe outlet holder. To mimic the configuration of the micro vial, an L-shaped 3D-printed microfluidic chip was fabricated. The L-shaped design renders a miniaturized microfluidic chip.
Fig. 2 A microfluidic system that measures lactate and glucose levels in dialysate during cycling.60 Copyright 2015 American Chemical Society. |
Furthermore, fused deposition modeling (FDM) 3D printing has been widely used to fabricate elastomer-based microfluidic devices due to its low cost.61 The FDM involves feeding and melting polymer filaments into a heated metal cylinder that ends with a nozzle and extrudes them.62 Wei et al. (2022) demonstrated a novel precision-controlled 3D-printed tailored microfluidic channel using malt syrup (Fig. 3a).54 The fabricated flexible microfluidic model combined with an encapsulated microfluidic channel layer for collecting sweat and a pH sweat sensor for sensing pH, as shown in Fig. 3a. The design involves several steps starting with the 3D printing of the sugar filament mold, encapsulation of the fabricated microfluidic channels, incorporation of the pH sensor, and encapsulation of the system. Microfluidic devices were mounted on the skin to collect sweat and analyze it as a proof of concept (Fig. 3b). As shown in Fig. 3c, the microfluidic device showed a good performance as its measured pH values matched the pH values of the commercial pH meter.
Fig. 3 (a) Steps (i, ii, and iii) involving manufacturing the microfluidic device and integration, (b) Photograph of the microfluidic chip onto the forehead for sweat collection, and (c) comparison of the real-time results between the commercial pH meter and the developed sweat pH sensor. Adapted with permission from ref. 54. Copyright 2022 Elsevier. |
Though 3D printed microfluidic devices have many advantages still, their resolution is yet to be comparable with the devices made with the conventional lithography technique.58 In addition to the device's resolution, some other issues include a lack of compatible materials, the roughness of the device's surface, layer-by-layer finish, and conformability with the skin.63
However, most available wearable sensors are incapable of detecting and integrating the signals from several analytes. There is a need for multiplexed sensors to monitor glucose, sodium lactate, potassium, and other body metabolites simultaneously in a real-time manner. There is undoubtedly a pressing need to create innovative, multi-analyte detection ability, simple-to-use wearable sensor devices. In this context, a completely integrated wireless multiplexed wearable sensing technology was fabricated by Semionatto et al. in 2017 which is capable of monitoring sweat electrolytes and metabolites in a real-time manner.67 This electrochemical sensor was screen-printed with PET stickers attached to the nose pads on each side of the eyeglasses. The wearable sensor was developed by combining a potentiometric potassium ion-selective electrode and an amperometric lactate biosensor into the two nose-bridge pads of the spectacles and connecting them to an electronic backbone mounted on the arms of the spectacles (Fig. 4IA and IB). This amperometric and potentiometric sensor was printed on two circuit boards (PCBs) mounted on the arms of the eyeglass. The potentiometric and amperometric measurement capabilities of the lactate and potassium sensors, as well as wireless data transfer, were connected to each of the PCBs. This sensor can be connected wirelessly to a host device, such as a smartphone, smartwatch, or laptop, using this controller's built-in Bluetooth low energy (BLE) feature. The lactate eyeglasses biosensor is based on the amperometric monitoring of the hydrogen peroxide product and the lactate oxidase-mediated oxidation of lactate to pyruvate and H2O2 (Fig. 4(IC)). Fig. 4(ID) shows the construction and functionalization of the lactate biosensor for the nose-bridge pad. A limit of detection (LOD) of 0.39 mM (CLk = 3) and a linear range of detection up to 10 mM lactate were obtained. Open-circuit potential measurements were used to assess the analytical performance of the potassium sensor, which provides a LOD of 10−3.9 M. The lactate and potassium electrodes were each linked to a PCB that was positioned on each of the arms of the eyeglass to form the integrated MAG multiplex device (Fig. 4(IIA)). Using the wireless boards, in vitro data calibration curves were produced through an experimental arrangement which is depicted in Fig. 4(IIB). The potassium sensor's potential-time response to an increase in concentration of potassium chloride from 0.01 to 10 mM as shown in Fig. 4(IIC). The response of the lactate sensor while increasing the concentration of lactate from 0 to 10 mM is shown in Fig. 4(IID). Before on-body tests, each sensor was calibrated. During the body test, the sweat's potassium and lactate levels were monitored using a sensor as shown in Fig. 4(IIIAa,a′) and (IIIAb,b′). While exercising, potassium and lactate levels in sweat were detected at the same time, the lactate PCB was repeatedly turned on and off, and simultaneously the potassium level was continuously measured. This ON/OFF process of the lactate sensor caused no interference in the potassium response, suggesting low cross-talk and effective integration of a multiplex wireless sensor into the spectacles. Also, the cross-talk experiment indicates a quick return to the formerly recorded signal and a quick and reliable response. The body glucose level in sweat concerning the time profile is shown in Fig. 4(IIICa,a′). The glucose sensor calibration curve was established by measuring the blood glucose (126 mg dl−1) using a commercial glucose meter for comparison purposes (Fig. 4(IIE)). This led to an estimate of the sweat glucose level of 0.2 mM (Fig. 4C), which follows the anticipated sweat-blood glucose association. Wireless signal transduction was demonstrated coupled with sweat lactate and potassium levels measurement simultaneously with no potential cross-talk. Expanding the complete integrated “Lab-on-a-Glass” wireless multiplexed wearable sensor device to simultaneously monitor more sweat electrolytes and metabolites is a simple approach and this system could be further enhanced by adding temperature and pH microsensors integrated with fluidics to regulate the flow of sweat. This non-invasive wearable device can bridge current gaps in wearable sensor platforms, which is needed for continuous health care monitoring and assessable remote diagnostics, and offers an appealing alternative to other sweat-sensing devices.
Fig. 4 (I) (A) screen-printed interchangeable sticker sensors. (B) Printed MAG eyeglasses combined with a wireless circuit board. (C) Electrochemical sensor on a nose pad with a potassium and lactate sensor associated with recognition and transduction steps. (D) Screen printing process steps for lactate and potassium sensor. (II) (A) MAG device with amperometric and potentiometric PCBs. (B) In vitro measurement setup of the device. (C) Potassium sensor response. (D) Lactate sensor response curve. (E) Glucose sensor response curve. Inset: Calibration plot for lactate, potassium, and glucose respectively. (III) (A) Wireless measurement of sweat potassium (a,a′) and lactate (b,b′) while cycling. (B) Stationary cycling bike with volunteer wearing the MAG device. (C) Measurement of glucose (a,a′) and control with no sensor (b,b′) during exercise using the device. Adapted with permission from ref. 67. Copyright 2017 Royal Society of Chemistry. |
Fig. 5 (I) (a) The manufacturing procedure for strain sensors made of an ultrasensitive graphite nanoflake/nitrile elastomer composite. (b) The tensile strains revealed the good stretchability of the strain sensor. (c) An SEM picture of the conductive network made up of graphite nanoflakes. (d) A magnified SEM picture of (c). (e) A cross-sectional optical image of the graphite nanoflake/nitrile elastomer nanocomposite strain sensors. (II) (a) Strain sensors are robust and resilient, and lightweight and can be placed on leaves. (b) Various shapes of a graphite nanoflake/nitrile elastomer nanocomposite. (c) Graphite nanoflake/nitrile elastomer nanocomposite strain sensors are tough and can be stretched, bent, and twisted. Adapted with permission from ref. 69 Copyright 2022 Royal Society of Chemistry. (III) (a) A setup of the wireless strain sensor. (b) Images of the sensor comprise a portable power source, controller, with a ZigBee receiver, and strain sensor. (c) Signal responses of finger-bending were captured using the sensor system. (d) A tester holding a circuit board and a power source while wearing a sensor on their elbow joint and observing a computer display of electrical signals. (e) A tester who was moving outdoors 50 meters to the ZigBee module. (f) Response signals from the arm bending sensor. (IV) the G/CB/Ni-2 strain sensor monitors motion in a real-time manner. Reaction signals include (a) wrist pulse, (b) blinking, (c) tensing, (d) swallowing, (e) bending of fingers, and (f) wrist movement. A picture of the sensor that is fastened to the wrist shown in insets (b)–(f). Photos of the matching human gestures are included as (g) walking, running, and jumping reaction signals. An image of the sensor mounted over the knee joint is shown in the inset in (g). (h) A picture of a sensor that was fastened to the tester's biceps muscle. (i) Reaction signals when lifting dumbbells of various weights. Adapted with permission from ref. 70 Copyright 2020 Royal Society of Chemistry. |
In another study, Sun et al. (2020) fabricated a flexible, waterproof, and extremely sensitive Internet of Things (IoT) integrated strain sensor by drop-coating graphene (G), carbon black (CB), and polydimethylsiloxane (PDMS) into the 3D framework of a commercial Ni sponge.70 The sensor comprises a G/CB/Ni-2 strain sensor, a ZigBee module, an STM32 controller, and a portable power source as shown in Fig. 5IIIa. The STM32 controller was used to interpret the electrical data from the G/CB/Ni-2 strain sensor before transmitting it in real-time to a computer via the ZigBee module. This allowed the device to monitor human motions wirelessly and remotely. The self-compiled Python program was then used to further store and analyze the data before finally displaying the results on the computer screen. A 5 V portable power source supplied power to the wireless strain sensor via a USB interface. Fig. 5IIIb depicts a picture of the entire system. The ZigBee transmitter and controller were mounted on the circuit board, the controller and strain sensor were attached to the tester's forefinger using 3M tape, and the ZigBee receiver was linked to the PC. The sensor system's electrical response was captured (Fig. 5IIIc). The subject wearing the sensor and holding the circuit board and portable power supply was roughly 10–15 m distant from the PC as depicted in Fig. 5IIId. The distance between the tester and the computer, as shown in Fig. 5IIIIe, was roughly 50 meters. The electrical response seen on the PC screen remained stable and exhibited nearly no change when the subject moved slowly away from the ZigBee (Fig. 5IIIf). Fig. 5(IV) shows the real-time response of motions using this strain sensor. The GF of 138 at 16% strain and prolonged stability of the sensor revealed that it is very sensitive, flexible, and stable. The G/CB/Ni sensor can measure muscular strength as well as accurately track minute human movements like blinking, pulse, and swallowing. This strain sensor also has good waterproof properties, making it safe to use for tracking human motions in humid environments and on water. The flexibility, high sensitivity, and waterproofness of the G/CB/Ni strain sensor make it ideal for use in outdoor motion monitoring, personal rehabilitation training, and healthcare management.
Fig. 6 (I) Illustration of the TDM/PDM/polyacrylate hybrid hydrogel preparation process. (II) Early warning system to track the human temperature. (b) Thermal images were captured using an infrared thermal camera while the hybrid hydrogel was being heated. (c) The hybrid hydrogel's resistance change ratio (DR/R0) at 25, 38, 65, and 95 °C. (d) During heating and chilling cycles, the resistance change ratio (ΔR/R0) of the TDM/PDM/polyacrylate hybrid hydrogel. (e) The hybrid hydrogel's sensing capabilities at 38 °C. (III) (a) Chameleons in various forms mending their discolored damaged skin. (b) The hybrid hydrogel's visible self-healing mechanism. (c) and (d) Properties of the repaired hybrid hydrogel in terms of twisting and stretching. (e) The hybrid hydrogel's stain-resistance characteristics. (f) The hybrid hydrogel's stretching and twisting characteristics following repair. (g) A picture of the fixed TCP/PCP/polyacrylate hybrid hydrogel shining an LED bulb. Adapted with permission from ref. 71 Copyright 2023 Royal Society of Chemistry. |
Fig. 7 (I) (a) Steps of fabrication of PMB pressure wearable sensors. (b) Images of the MXene nanosheets taken with an AFM and (c) TEM images; the inset displays the SAED pattern. (d) The MXene solution, (e) the BCF foam, (f) the MB foam, and (g) the MB foam on a flower. (h) The XRD spectra of Ti3AlC2 powders, MXene nanosheets, BCF foam, and MB foam, and (i) FTIR. (j) MXene nanosheets, MB foam, and BCF XPS spectra. (II) The use of the PMB pressure sensor in soft robotics and the sensing of human movement. RCR responses of the sensors to detect significant motions such as (a) gripping and (b) lifting heavy objects. (c) RCR sensor responses are used to track minute movements. RCR sensor responses in challenging conditions, such as (d) detecting finger touches in water, (e) observing finger bending at a low temperature of 20 °C, and (f) sensing gripping motion at a high temperature of 60 °C. Adapted with permission from ref. 72. Copyright 2022 American Chemical Society. |
Fig. 8 (I) Characterizations of the TCNF/CNT fibers and their scalable production. (a) Diagrams for the hybrid LC spinning technique-based continuous manufacture of TCNF/CNT fiber. (b) Picture of the bobbin-collected TCNF/CNT (20) fiber. (c) The image shows the hybrid schlieren LC texture of TCNF/CNT (20) at 30 mg mL−1 taken with polarised optical microscopy (POM). (d) The relationship between the TCNF/CNT fiber's mechanical characteristics and the CNT content. (e) A picture of the weights that the single fibers were able to lift. (f) TCNF/CNT (20) fiber SEM pictures at low and high magnifications. (g) The TCNF/CNT (20) fiber's isothermal adsorption/desorption plot and BET surface area. (II) TCNF/CNT fibers have good mechanical flexibility, making them ideal for wearable sensors. (a) SEM pictures of the TCNF/CNT (20) fibers that have been merged with sensing apparatus in knotted, flat, single-, and double-twisted forms. (b) The maximum (ΔR/Rb) of the flat, knotted, single- and double-twisted TCNF/CNT (20) wearable sensors in the NO2 concentration range of 0.125–5 ppm. (c) Images of a TCNF/CNT fiber woven into standard fabrics, including photos, schematics, and SEM pictures. (d) The woven TCNF/CNT fiber's real-time NO2-sensing performance with common wearable textiles. Adapted with permission from ref. 73. Copyright 2019 American Chemical Society. |
Integrating carbon nanotubes (CNTs) into nano cellulose enabled Cho et al. (2019) to mass-produce sensing fibers with high mechanical qualities and sensing capabilities without requiring extra effort.73 To facilitate liquid-crystal characteristics, nano cellulose obtained from tunicate (TCNF) was homogeneously mixed with single-walled CNTs. Composite fibers (TCNF/CNT) are continuously created by wet spinning in aligned directions. The TCNF/CNT can be adequately concentrated during the LC phase to use the common wet-spinning method for constant fiber synthesis (Fig. 8Ia). The mechanical characteristics of the TCNF/CNT fiber, the weights lifted by single fibers, the TCNF/CNT image, the polarized optical microscopic image, the SEM image, and the isothermal adsorption/desorption plot are shown in Fig. 8Ib–g. As shown by SEM pictures and the time-dependent NO2 sensing response of the intertwined TCNF/CNT fiber, TCNF/CNT fibers have high mechanical flexibilities and good sensing abilities as wearable sensors (Fig. 8IIa–d). Excellent gas (NO2) sensing efficiency with great selectivity and high sensitivity is confirmed by the TCNF/CNT fibers. The TCNF/CNT fibers can also withstand difficult distortions while preserving their inherent sensing qualities, and they can be seamlessly incorporated with traditional fabrics utilizing a direct weaving process. The ability to run this wearable sensor fiber manufacturing approach at extremely low process costs is also advantageous. For the manufacturing of one meter of TCNF/CNT fiber, the process cost of synthesis is around 0.00403 $ per meter. This scalable, meter-scale production of functional composite fibers is anticipated to offer a framework for the mass manufacture of adaptable wearable sensors.
Real-time continuous sweat biomarker investigations are a prerequisite for health care and for this purpose the development of cost-effective microfluidic devices with quick sample collection and multiplexed analyte identification capabilities is crucial.75 Vinoth et al. (2021) recently fabricated a printed microfluidic-based wearable device for multiplexed high-throughput electrochemical analysis of sweat samples.76 For this, an array of electrodes printed over a flexible polyimide layer and an insulator film to create leakage-free closed, fluid paths to direct sweat samples to the sensing electrodes allows for the one-step production of numerous identical patterns on affordable substrates (Fig. 9(IA)). The fabrication of roll-to-roll several uniform patterns using the screen-printing technique is used to create a carbon-based master mould. After the carbon ink is generated using a thermoplastic elastomer called SBS binder, it is screen-printed with the appropriate fluidic channel arrangement onto a clear polyester substrate (Fig. 9(IB)). The application of a relatively high weight percentage (45%) of SBS binder increases the pattern strength, and ink adhesion, and evades the development of cracks or delamination when multiple fluidic channels are peeled off. By employing carbon black as a filler, the ink's viscosity can be controlled and used to create printed tracks with excellent resolution. These printed carbon tracks that are tightly glued to the substrate enable the recycling and repeated fabrication of a silicone elastomer-based microfluidic multichannel. Additionally, because of the binder's capacity to stretch, it has the constructive flexibility needed to withstand the mechanical stress involved in removing the preserved channel layer from the mould surface. A variety of master moulds created on the polyester layer and a variety of printed sensing electrodes on a polyimide substrate are shown in Fig. 9(IC) and (D), respectively. When the silicone elastomer layer covering the master is peeled off, the cured layer has carved microfluidic channels on the inner surface due to the mould design. These flexible, microfluidic tubes are incorporated into the flexible electrodes to flow the samples to the surface of the transducer and to catch sweat in real-time while exercising.
Fig. 9 (I) Process of a printed microfluidic device. (A) The microfluidic patch's several layers, and (B) the silicone rubber-based microfluidic channels from the screen-printed carbon master is shown schematically. (C) The optical pictures display a variety of printed carbon masters and (D) multiarray electrodes. (E) Pictures of a skin-interfaced, completely integrated microfluidic sensor and (F) a multiarray electrode with four sensing chambers in close-up. (G) Diagram of the design of a tiny PCB with multiplexed analysis and wireless mode of data transmission capabilities. (II) Analysing sweat on the body. (A) The OCP responses for Na-ISE are shown when a nearby amperometric sensor is subjected to a constant voltage of about 170 mV for one second. (B) An optical picture of the portable circuit board. (C) Using the tiny circuit board, measurements of the potentiometric and amperometric responses are simultaneous. (D) Optical pictures displaying the integrated microfluidic wearable sensor on the underarm and (E) upper back areas. For two participants, multiplexed sensor responses were recorded in the (D′, D′′) underarm and (E′, E′′) upper back regions. Adapted with permission from ref. 76. Copyright 2021 American Chemical Society. (III) (A) The stages involved in making the 3D-printed e-ring. (B) Images of the 3D-printed e-ring that display its flexibility, dimensions, and connection to the mobile and small potentiostat. Adapted with permission from ref. 77. Copyright 2021 American Chemical Society. |
Fig. 9(IE) shows a flexible sensor patch that can easily integrate onto human skin, collect sweat samples in real-time, and conduct electrochemical analysis. The electrochemically active region is exposed to the sweat samples through the microfluidic channels placed on the printed electrode Fig. 9(IF). The tiny PCB can fully remove cross-signal interference from nearby electrodes for multiplexed sweat biomarker monitoring. The key components on the PCB for supporting synchronized measurements on one channel of amperometry and 3 channels of potentiometry, are shown in Fig. 9(IG). It is noted that the quick potential deactivation also introduces noise into OCP signals, and retrieving the start OCP levels requires about 60 s. Fig. 9(IIA). This issue was solved by a mini potentiostat which collected interference-free real-time responses from sweat biomarkers Fig. 9(IIB). Fig. 9IIC shows that amperometric lactate signals were recorded at a fixed polarization potential of 170 mV, and the Na+, K+, and pH sensors displayed stable OCP responses. By analyzing sweat from the underarm Fig. 9(IID) and upper back Fig. 9(IIE) regions, it is possible to better understand the geographical dependence on sweat secretion and its biomarker makeup. Fig. 9(IID′,D′′) displays the outcomes of the on-body test performed at the underarm for 2 subjects. Fig. 9(IIE′,E′′) shows the on-body evaluation results for both subjects in the upper back position. The technology enables recurrent pattern transfer from the same master and provides low-cost simple patterning of the master for building soft microfluidic devices. This wearable platform made use of surface functionalization and surface treatment advantages to achieve leakage-free fluidic system construction with an increased sampling rate. The fluidic chamber's easy integration into the printed active sensor region reduces the need for sample volume. Additionally, the physically separated individual sensors prevent electrode components and reaction product interferents from combining. They are excellent candidates for wearable sensing applications due to their high levels of selectivity, sensitivity, long-term stability, carryover efficiency, and reproducibility. Pumpless fluidic systems are made possible by the autonomous fluid flow through capillary action, which also allows real-time fluid flow and assessment. Additionally, a miniaturized electronic circuit board with an in situ signal recorder and wireless components was interfaced with the printed microfluidic patch to enable real-time interpretation of sweat biomarkers.
A smartphone-addressable 3D-printed electrochemical ring for nonenzymatic self-monitoring of glucose in sweat sample perspiration was developed by Katseli et al. in 2021.77 The wearable component, an electrochemical ring (e-ring), was created using a dual extruder 3D printer in a single step (Fig. 9III). The 3D-printed e-ring is made up of three integrated printed electrodes from the conductive carbon-loaded filament and connected to the inside of the green cylindrical holder made of TPU (Fig. 9IIIA). TPU is a material that is often used in the medical sector and has great mechanical characteristics including durability and flexibility. It was chosen to print the holder so that the e-ring would have the right amount of flexibility for optimal finger-fitting (Fig. 9IIIB). The tool allows non-invasive detection of glucose in sweat without interference from other electroactive molecules in the concentration range of 12.5–400 mM and is mechanically robust during bending. The 3D-printed e-ring can be used as a model for internally produced wearable sensors since it fills the gap between current wearable fabrication/sensing technologies and the much-needed real-time glucose self-measurement. The e-ring has an appealing electroanalytical efficiency for sweat glucose measurement because of the utilization of catalytic glucose sensing on gold which is different to the enzymatic sensing approach, in terms of having good sensitivity, selectivity, repeatability, and stability. The e-ring can be used in future research to conduct a more thorough analysis of the relationship between human perspiration and blood glucose levels.
One of the pioneering works in the field of wearable sensors is the development of fully integrated wearable sensors for the simultaneous detection of glucose, lactate, sodium, potassium ions, and skin temperature (to calibrate the response of the sensors).4 The work demonstrated the use of a flexible sensor array for the above-mentioned analytes connected with a wireless circuit board transmitting the data directly to the smartphone. The developed sensor was used for the on-body real-time sweat analysis of subjects during stationary cycling. Gao group reported in 2022 the development of an integrated wearable sensor for the detection of essential amino acids and vitamins.27 The work reported the use of a MIP towards the analyte creating a highly selective electrode surface. The sensor platform also had electrodes for the in-situ induction of sweat, which can also be analyzed for stationary subjects. The integrated system also had a flexible potentiostat and accompanied circuitry for data analysis and wireless transmission. The sensor was also made in a smartwatch configuration wherein the sensor was placed inside a watch with an opening for the sweat through the wrist. After sweat analysis, the screen on the watch gave a read-out corresponding to the analyte concentration. The same group recently reported the development of a flexible wearable bioelectronic system to monitor the analytes during wound healing and release drugs to the infected wound.78 The multiplexed sensor was developed for uric acid, lactate, glucose, ammonium, pH, and temperature sensing.
The microneedle-based wearable sensor is another wearable platform for the continuous monitoring of biomarkers in the interstitial fluid.79 Since it samples the bio-fluid inside the body, it gives a more detailed account of the biomarkers of interest.80 Tehrani et al, demonstrated the development of a wearable microneedle-based sensor for the sensing of glucose, lactate, and alcohol content in the interstitial fluid.81 Continuous monitoring of these biomarkers is of significant interest since these are related to various illnesses. Fig. 10I shows the developed wearable sensor along with the exploded view of the sensor construction. The sensor construction shows the presence of three working electrodes. The electrodes were modified with glucose oxidase, lactate oxidase, and alcohol oxidase. The in vivo testing of the sensor showed its sensing performance during cycling, eating, and drinking. Cheng et al., reported the development of a touch-based and wearable microneedle-based glucose sensor.82 The authors in this work tried to address the issue of low flux and inconsistency during the reverse iontophoresis approach that is generally used for glucose sensing. The authors proposed using a microneedles-based skin penetration system, which was then used for the reverse iontophoresis-based extraction. The authors showed that this system improved the glucose extraction flux by 1.6 times. Fig. 10II(a) and (b) show the sensor construction. The sensor shows the presence of microneedles for the sample extraction. The electrodes were modified with glucose oxidase for glucose sensing and the data generated was transmitted wirelessly to a smartphone. The determination of ions also helps in the determination of various illnesses in the human body. In this regard, Huang et al. developed a stainless steel-based microneedle patch for the simultaneous sensing of calcium, potassium, and sodium ions.83 The stainless-steel microneedles were modified differently for the detection of different ions as shown in Fig. 10III(a) and (b). A layer of gold was first deposited electrochemically on the microneedles, followed by the deposition of PEDOT:PSS polymer. These microneedles were then modified with calcium, potassium, and sodium selective membranes for the detection of calcium, potassium, and sodium respectively.
Fig. 10 (I) (a) A wearable integrated microneedle-based sensor, and (b) an enlarged view of the sensor construction.81 Copyright 2022 Nature Biomedical Engineering. (II) (a) An integrated microneedle-based sensor transmitting data wirelessly, and (b) an enlarged view of the various components of the wearable sensor.82 Copyright 2022 Elsevier. (III) (a) and (b) A stainless steel-based microneedle patch for the simultaneous detection of calcium, potassium, and sodium ions.83 Copyright 2023 Nature. |
The development of goods that are simple to incorporate into a person's lifestyle is necessary for wearable sensor technology to gain widespread acceptance. Sweat analysis has been carried out using most wearable chemical sensors in conjunction with flexible, durable, temporary tattoo-like devices, skin patches, headbands, spectacles, or wristbands. Recent research has also investigated smart bandages for wound healing, mouthguards, diagnostic devices for saliva monitoring, and eyeglasses, and contact lenses for tear assays as additional devices and accessories for human body biomarker sensing applications.95 Sensors integrated into the textiles allow for efficient sweat collection and can present unique opportunities for real-time biomarker monitoring.96 These not only provide a platform for sensing analytes but can also be used for the generation of human motion-induced triboelectric charges, which in turn block microbes.97 Combining the strengths of the fashion trend and wearable sensors to create wearable fashion accessories will result in a wider adoption of wearable sensor technology that can urgently address the need for disease diagnostics and real-time health monitoring. Some of the commercially available wearable sensors are listed in Table 1.
S. No | Product name | Company | Analyte, Sample | Wearable Platform | Monitoring Technique | Price | FDA Approval | Ref. |
---|---|---|---|---|---|---|---|---|
1 | Lingo sensor | Abbott | Track both glucose and ketone, lactate, and alcohol levels | Skin | Optical colorimetery | $420 | Yes | 98 |
2 | Biosensor BX100 | Philips | Deterioration detection solution | Patch | Image-guided therapy | Yes | 99 | |
3 | Lifetemp | Isansys lifecare | Body temperature | Armpit | Silicone gel adhesive | 100 | ||
4 | Paediatric sensors | Isansys lifecare | Heart rate, pulse rate and respiratory rate | Patches | Remote accessibility | 100 | ||
5 | 3150 WristOx | Isansys lifecare | Robustness and reliability | Wrist-worn | PPG waveform | $739 | 100 | |
6 | Sensit smart | PalmSens | Capable of EIS up to 200 kHz | Skin | Screen printed electrodes | 101 | ||
8 | Fitbit smart watch | Fitbit versa | Heart rate monitor | Wrist watch | Electrochemical device | $179.95 | Yes | 102 |
9 | Fingertip SpO2 sensor AMD-DS-NM0002–4 | Amydi-med Electronics | SpO2 sensor | Fingertip, multi-position, foot, toe | Transflectance, reflectance | $3 | Yes | 103 |
10 | Vios chest sensor | Vios | ECG, heart rate, respiratory rate, SpO2, pulse rate, posture, and activity | Chest | Medico electrode | Yes | 104 |
Fig. 11 Futuristic applications of integrated wearable sensors in personalized healthcare [Figure created using icons from Biorender and MS Office]. |
Footnote |
† Equal contribution for the first authorship. |
This journal is © The Royal Society of Chemistry 2024 |