Yao Liu, Siyu Han, Panpan Gu, Bai Wang, Shiyan Tian, Xiaoxu Xu, Chunmei Yang, Shujun Liu, Jianshe Hu
{"title":"柔性可穿戴生物传感器从聚(离子液体)实时信号监测。","authors":"Yao Liu, Siyu Han, Panpan Gu, Bai Wang, Shiyan Tian, Xiaoxu Xu, Chunmei Yang, Shujun Liu, Jianshe Hu","doi":"10.3389/fbioe.2025.1610197","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Modern wearable electronics demand materials that are simultaneously stretchable, conductive, and environmentally robust. Hydrogels meet some of these requirements but dehydrate or freeze easily. To overcome these limitations, we prepared a poly-ionic-liquid (PIL) ionogel that integrates high elasticity with stable ionic conductivity, aiming to enable reliable, skin-compatible strain and biopotential sensing.</p><p><strong>Methods: </strong>1-Vinyl-3-butyl-imidazolium hexafluorophosphate and 1-butyl-3-methyl-imidazolium hexafluorophosphate were mixed at optimized mass ratios, followed by N,N'-methylenebis-acrylamide (cross-linker) and Irgacure-2959 (photoinitiator). The homogeneous precursor was UV-cured for 6 min to obtain a PIL ionogel (PIL-1 - PIL-4 series). Structural, thermal, mechanical, rheological, adhesive, and electrical characteristics were analysed by FT-IR, SEM, TGA/DSC, uniaxial tensile testing, rheometry, 90° peel tests, and real-time resistance measurements. Applications were evaluated by attaching the gel to human joints and by recording EMG/ECG signals.</p><p><strong>Results: </strong>The UV one-step process yielded a dense multi-cross-linked network that combined covalent and ionic interactions. The optimised sample (PIL-2) showed a fracture stress of ∼390 kPa with 320% elongation, sustaining a 500 g load without failure. It retained mass and softness after 30 days and adhered strongly (up to 90° peel strength >4 N) to glass, metals, and skin-even underwater. Electrical tests gave a gauge factor of 1.94 (0-100%), 3.98 (100-200%), and 4.04 (200-320%), with 400 ms response and 500 ms recovery. The gel monitored finger (30°/90°), wrist, and elbow motions reproducibly, functioned as a bioelectrode capturing stable EMG/ECG with clear PQRST waves, and reliably transmitted Morse code via hand gestures.</p><p><strong>Discussion: </strong>The solvent-free PIL ionogel couples mechanical toughness, wide-range elasticity, and stable ionic pathways, outperforming water-rich hydrogels in thermal/long-term stability. Its strong, humidity-tolerant adhesion eliminates extra fixatives, while rapid, high-gain strain transduction and low-impedance skin contact enable multimodal biosensing. These attributes position the material for next-generation flexible electronics, real-time health monitoring, and gesture-based human-machine interfaces.</p>","PeriodicalId":12444,"journal":{"name":"Frontiers in Bioengineering and Biotechnology","volume":"13 ","pages":"1610197"},"PeriodicalIF":4.8000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12133815/pdf/","citationCount":"0","resultStr":"{\"title\":\"Flexible wearable biosensors from poly (ionic liquid) for real-time signal monitoring.\",\"authors\":\"Yao Liu, Siyu Han, Panpan Gu, Bai Wang, Shiyan Tian, Xiaoxu Xu, Chunmei Yang, Shujun Liu, Jianshe Hu\",\"doi\":\"10.3389/fbioe.2025.1610197\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Modern wearable electronics demand materials that are simultaneously stretchable, conductive, and environmentally robust. Hydrogels meet some of these requirements but dehydrate or freeze easily. To overcome these limitations, we prepared a poly-ionic-liquid (PIL) ionogel that integrates high elasticity with stable ionic conductivity, aiming to enable reliable, skin-compatible strain and biopotential sensing.</p><p><strong>Methods: </strong>1-Vinyl-3-butyl-imidazolium hexafluorophosphate and 1-butyl-3-methyl-imidazolium hexafluorophosphate were mixed at optimized mass ratios, followed by N,N'-methylenebis-acrylamide (cross-linker) and Irgacure-2959 (photoinitiator). The homogeneous precursor was UV-cured for 6 min to obtain a PIL ionogel (PIL-1 - PIL-4 series). Structural, thermal, mechanical, rheological, adhesive, and electrical characteristics were analysed by FT-IR, SEM, TGA/DSC, uniaxial tensile testing, rheometry, 90° peel tests, and real-time resistance measurements. Applications were evaluated by attaching the gel to human joints and by recording EMG/ECG signals.</p><p><strong>Results: </strong>The UV one-step process yielded a dense multi-cross-linked network that combined covalent and ionic interactions. The optimised sample (PIL-2) showed a fracture stress of ∼390 kPa with 320% elongation, sustaining a 500 g load without failure. It retained mass and softness after 30 days and adhered strongly (up to 90° peel strength >4 N) to glass, metals, and skin-even underwater. Electrical tests gave a gauge factor of 1.94 (0-100%), 3.98 (100-200%), and 4.04 (200-320%), with 400 ms response and 500 ms recovery. The gel monitored finger (30°/90°), wrist, and elbow motions reproducibly, functioned as a bioelectrode capturing stable EMG/ECG with clear PQRST waves, and reliably transmitted Morse code via hand gestures.</p><p><strong>Discussion: </strong>The solvent-free PIL ionogel couples mechanical toughness, wide-range elasticity, and stable ionic pathways, outperforming water-rich hydrogels in thermal/long-term stability. Its strong, humidity-tolerant adhesion eliminates extra fixatives, while rapid, high-gain strain transduction and low-impedance skin contact enable multimodal biosensing. 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Flexible wearable biosensors from poly (ionic liquid) for real-time signal monitoring.
Introduction: Modern wearable electronics demand materials that are simultaneously stretchable, conductive, and environmentally robust. Hydrogels meet some of these requirements but dehydrate or freeze easily. To overcome these limitations, we prepared a poly-ionic-liquid (PIL) ionogel that integrates high elasticity with stable ionic conductivity, aiming to enable reliable, skin-compatible strain and biopotential sensing.
Methods: 1-Vinyl-3-butyl-imidazolium hexafluorophosphate and 1-butyl-3-methyl-imidazolium hexafluorophosphate were mixed at optimized mass ratios, followed by N,N'-methylenebis-acrylamide (cross-linker) and Irgacure-2959 (photoinitiator). The homogeneous precursor was UV-cured for 6 min to obtain a PIL ionogel (PIL-1 - PIL-4 series). Structural, thermal, mechanical, rheological, adhesive, and electrical characteristics were analysed by FT-IR, SEM, TGA/DSC, uniaxial tensile testing, rheometry, 90° peel tests, and real-time resistance measurements. Applications were evaluated by attaching the gel to human joints and by recording EMG/ECG signals.
Results: The UV one-step process yielded a dense multi-cross-linked network that combined covalent and ionic interactions. The optimised sample (PIL-2) showed a fracture stress of ∼390 kPa with 320% elongation, sustaining a 500 g load without failure. It retained mass and softness after 30 days and adhered strongly (up to 90° peel strength >4 N) to glass, metals, and skin-even underwater. Electrical tests gave a gauge factor of 1.94 (0-100%), 3.98 (100-200%), and 4.04 (200-320%), with 400 ms response and 500 ms recovery. The gel monitored finger (30°/90°), wrist, and elbow motions reproducibly, functioned as a bioelectrode capturing stable EMG/ECG with clear PQRST waves, and reliably transmitted Morse code via hand gestures.
Discussion: The solvent-free PIL ionogel couples mechanical toughness, wide-range elasticity, and stable ionic pathways, outperforming water-rich hydrogels in thermal/long-term stability. Its strong, humidity-tolerant adhesion eliminates extra fixatives, while rapid, high-gain strain transduction and low-impedance skin contact enable multimodal biosensing. These attributes position the material for next-generation flexible electronics, real-time health monitoring, and gesture-based human-machine interfaces.
期刊介绍:
The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs.
In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.