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Wearable biomimetic electronics have aroused tremendous attention due to their capability to continuously detect and deliver real-time dynamic physiological signals pertaining to the wearer's environment. However, upon close contact with the human skins, a wearable sensor undergoes mechanical strain which inevitably degrades the electrical performance. To address this issue, we demonstrate a universal design approach for stretchable and multiplexed biosensors that can yield unaltered ion sensing performance under variable mechanical tensile strains, which is achieved by introducing a PMMA molecular layer between stretchable substrate and ion sensors. Such design demonstrates reliable multiplexed ion sensing capability and provides high sensitivity (>50 mV/decade), reliable selectivity, as well as wide working range (0.1-100 mM) for sodium, ammonium, potassium and calcium ions in complex sweat biomarkers. Via this introduced PMMA molecular layer, our sensor even exhibits 95 % electrical performance maintained up to 30 % tensile strain, whereas the mechanical tensile property is far superior to original sensor performance. Besides, the sensors were also utilized for real-time monitoring of ions in sweat to validate its biomedical electronics applications. This sensing platform can be easily extended to other biomimetic sensors to enable stable signal acquisition for biomedical electronics.
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http://dx.doi.org/10.1016/j.aca.2023.342083 | DOI Listing |
PLoS One
September 2025
Orthopaedics, Hebei Medical University Third Hospital, Shijiazhuang, China.
Enoxaparin sodium (ES), a low molecular weight heparin derivative, has recently been recognized for its diverse biological activities. In particular, the ability of heparin to modulate inflammation has been utilized to enhance the biocompatibility of bone implant materials. In this study, we utilized poly (methyl methacrylate) (PMMA), a drug loading bone implant material, as a matrix and combined this with enoxaparin sodium (ES) to create enoxaparin sodium PMMA cement (ES-PMMA) to investigate the regulatory effects of ES on inflammatory responses in bone tissue from an animal model.
View Article and Find Full Text PDFSmall
September 2025
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, Lehn Institute of Functional Materials, GBRCE for Functional Molecular Engineering, School of Chemistry, IGCME, Sun Yat-Sen University, Guangzhou, 510275, China.
Methylammonium lead bromide perovskite (MAPbBr) quantum dots (QDs) have emerged as promising candidates for next-generation optoelectronic applications owing to their exceptional photoluminescent properties. However, their practical applications face significant challenges due to inherent instability issues. Herein, a solvent-induced in situ crystallization method is presented to encapsulate MAPbBr QDs within a crosslinked (cl-) polymethyl methacrylate (PMMA) network.
View Article and Find Full Text PDFDalton Trans
September 2025
University of Cologne, Faculty for Mathematics and Natural Sciences, Department of Chemistry and Biochemistry, Institute for Inorganic and Materials Chemistry, Greinstrasse 6, D-50939 Köln, Germany.
In the frame of our research aiming to develop efficient triplet-emitting materials, we are exploring the role of the second coordination sphere in enhancing the rigidity of structures and its controlling aspect over the extents of excited state distortions. We thus synthesised three N^C^N cyclometalated complexes [M(L)Cl] (M = Pt, Pd, and Ni), where the two -positions of the pyridyl moieties in 1,3-di(2-pyridyl)-benzene are benzyl substituted (Bn) forming a tight binding pocket for the metal and the Cl ancillary ligand. The molecular structures from single-crystal X-ray diffraction show a markedly distorted square planar M(II) coordination with values of around 0.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Department of Chemistry and Pharmacy, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058 Erlangen, Germany.
A growing interest towards all-organic electronics emphasized the importance of interfaces between the functional components of such devices. In particular, the interaction between the dielectric and semiconductor plays a critical role in device functionality, with strong dependency of charge carrier accumulation and mobility on semiconductor molecular arrangement. We report on the beneficial adsorption conformation with a nearly upright standing molecular orientation of a 2-tridecyl-[1]benzothieno[3,2-][1]benzothiophene (C-BTBT) semiconductor monolayer deposited on Langmuir-Blodgett-prepared polymethyl methacrylate (PMMA) dielectric films.
View Article and Find Full Text PDFPolymers (Basel)
August 2025
Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.
Poly(methyl methacrylate) (PMMA) and its composites are widely used in industrial applications; therefore, their durability is of great concern. In this study, the photooxidative degradation behavior of nanosilica-filled PMMA composite films and the cooperative effect of mixed solvents containing tetrahydrofuran (THF) and chloroform (TCM), as well as interfacial functional groups, was investigated. The surface functional groups of nanosilica fillers, such as polar, aryl, and alkyl moieties, significantly affect the photodegradation kinetics and pathways for PMMA.
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