Efficient transport of antioxidant therapeutics across brain-associated barriers remains a major challenge for neuroprotective strategies. Here, we report caffeic acid–functionalized gold nanoparticles (AuNPs–CA) engineered to enhance passive diffusion and provide intrinsic redox activity. Monodisperse ∼ 12 nm AuNPs were synthesized and covalently conjugated with caffeic acid, yielding stable nanoconjugated systems that retained the catechol–quinone redox interconversion essential for antioxidant function. Transport properties were evaluated using a non-cellular, electrospun PMMA–gelatin scaffold designed as a simplified passive-diffusion model that mimics selected structural features of the blood–brain barrier. AuNPs–CA exhibited controlled release of caffeic acid under enzymatic degradation and demonstrated significantly improved diffusion compared to free CA. SH-SY5Y neuronal-like cells showed high viability upon exposure to the nanoconjugated systems and also preserved their normal morphology. Antioxidant assays confirmed strong radical-scavenging activity, indicating that the conjugation strategy maintains the redox functionality of caffeic acid. These findings establish AuNPs–CA as a dual-function nanoplatform that couples enhanced passive diffusion through a simulated barrier with robust neuroprotective properties, supporting their potential utility in future therapeutic approaches targeting oxidative stress–related neurodegenerative conditions.

The rapid growth of the global population has increased the need for efficient fabrication methods and materials to purify polluted water. In this study, we report the fabrication and characterization of reusable and efficient three-dimensional (3D) polydimethylsiloxane (PDMS) sponge composites designed for water treatment applications. By varying the ratios (10/90, 30/70, and 50/50) of large and small sacrificial templates’ particles used in the fabrication method, we tailored the sponge’s morphology and the interconnected pores’ distribution. To achieve an enhanced photocatalytic activity, we incorporated titanium dioxide (TiO2) at different concentrations (1 % TiO2, 5 % TiO2, and 10 % TiO2 w/w) into the PDMS matrix. Scanning electron microscopy (SEM) was used to evaluate the structure of both 3D PDMS and TiO2@PDMS sponges, while energy dispersive X-ray analysis (EDX) and X-ray diffraction (XRD) confirmed the successful incorporation of TiO2 into the sponge framework. The photocatalytic performance of the 3D TiO2@PDMS composites was assessed by monitoring the degradation of Rhodamine B (RhB) under solar light irradiation, and the results were compared to those obtained using reference (TiO2-free) sponges under identical conditions. Very low Ti leaching effect have been evidenced by using Inductively Coupled Plasma−Mass Spectrometry (ICP-MS). The reusability of the sponges was demonstrated through complete bleaching of the 554 nm RhB absorption band after four consecutive degradation cycles.

Monitoring superoxide anion in chronic wounds is critical for understanding oxidative stress and guiding personalized treatment. We present a novel electrochemical biosensor enabling real-time superoxide detection in cell culture, integrating enzymatic selectivity with a biocompatible electrospun membrane for direct tissue contact. The biosensor employs screen-printed electrodes (SPE) modified with electropolymerized poly(3,4-ethylenedioxythiophene) (PEDOT), which enhances enzyme immobilization and signal transduction, with superoxide dismutase (SOD) for enhanced selectivity. The analytical performance of SPE/PEDOT/SOD biosensor was evaluated by fixed potential amperometry at +0.3 V with a sensitivity of 130.3 ± 5.6 μA cm-2·mM-1, and a 1.5 μM detection limit. A cell-based wound model was developed to simulate chronic wound conditions, using an adhesive membrane modified with electrospun Nylon fibers that provided a biocompatible surface for cell adhesion and proliferation. Cells cultured on the membrane were irradiated with UV light to induce superoxide generation, mimicking oxidative stress in chronic wounds. Although the membrane introduced a diffusion barrier that reduced sensitivity by 40 %, it ensured close contact between cells and the electrode surface, enabling accurate in situ quantification of superoxide. Chronoamperometric detection at +0.3 V revealed sharp photocurrent peaks followed by decay, consistent with ROS generation and enzymatic clearance. The PEDOT matrix exhibited a photo-amplifying effect, nearly tripling the sensitivity under UV irradiation. The developed device is suitable for real-time oxidative stress profiling in wound models with potential for ex vivo and in vivo applications.

Paper-based devices hold great promise in biosensing, but the choice of electrode materials influences performance. Here, we report a paper-based electrochemical sensor developed for nucleic acid quantification, in a sandwich-type architecture integrating 3-electrode systems on metallized electrospun polymeric fibers. A 3D-printed hydrophobic barrier on the chromatographic paper defines injection and testing zones. Fluid diffusion through paper and concentration gradients are considered in the design. Electrochemical characterization is performed using 40 mu L of methylene blue solution, which interacts with double-stranded nucleic acids, reducing its redox activity. This interaction mechanism within the paper substrate is confirmed by spectroscopy. The sensor achieves detection of nucleic acids in 3 min with 2 mu L of solution. Real sample analysis is performed for the quantification of PCR-amplified genes with a limit of detection of 1.38 ng mu L-1. The device serves as a promising point-of-care diagnostics tool for the direct quantification of amplified genetic material.

Amyloid beta (Aβ) peptide aggregates are well-established biomarkers for Alzheimer's disease, though the complete etiology of this disorder remains elusive. Developing biointerfaces to elucidate the physiological roles of these peptides is essential. This study investigates the aggregation, fibrillation, and interaction of Aβ peptides with conductive, biocompatible nanostructured materials designed for applications involving neuronal cells. Various conductive, rigid, and flexible surfaces, both functionalized and non-functionalized with Aβ40 fibrils, were fabricated. These included glass substrates and poly(methyl methacrylate) electrospun fiber networks coated with gold via magnetron sputtering. The substrates were also functionalized through physical adsorption with poly-l-lysine and collagen, known to support cell proliferation, as well as with the inverse-Aβ40 peptide and an Amyloid Protein Non-Aβ Component, and the results were compared. The scaffolds were characterized using scanning electron microscopy, X-ray diffraction, atomic force microscopy, contact angle and electrical measurements, while their biological interactions were assessed using MTS assays, fluorescence imaging, and scanning electron microscopy. Fibroblast L929 and neuroblastoma SH-SY5Y cell lines were used as models, with results indicating an elevated cell viability, comparable to the control. The developed nanostructured surfaces are highly promising for integration into advanced neuromorphic engineering devices, as they have proven capable of maintaining their structural integrity when exposed to proteases.

A novel scaffold for in situ electrochemical detection of cell biomarkers was developed using electrospun nanofibers and commercial adhesive polymeric membranes. The electrochemical sensing of cell biomarkers requires the cultivation of the cells on/near the (bio)sensor surface in a manner to preserve an appropriate electroactive available surface and to avoid the surface passivation and sensor damage. This can be achieved by employing biocompatible nanofiber meshes that allow the cells to have a normal behavior and do not alter the electrochemical detection. For a better mechanical stability and ease of handling, nylon 6/6 nanofibers were collected on commercial polymeric membranes, at an optimal fiber density, obtaining a double-layered platform. To demonstrate the functionality of the fabricated scaffold, the screening of cellular stress has been achieved integrating melanoma B16-F10 cells and the (bio)sensor components on the transducer whereas the melanin exocytosis was successfully quantified using a commercial electrode. Either directly on the surface of the (bio)sensor or spatially detached from it, the integration of cell cultures in biosensing platforms based on electrospun nanofibers represents a powerful bioanalytical tool able to provide real-time information about the biomarker release, enzyme activity or inhibition, and monitoring of various cellular events.

Electrospun nanofibres based on poly(styrene sulfonate) doped poly(3,4-ethylenedioxythiophene) (PEDOT:PSS) were fabricated using a straightforward procedure which combines electrospinning, sputtering deposition and electrochemical synthesis. In general, electrospun fibre meshes based on conducting polymers are prepared by mixing the conducting polymer with a carrier polymer or chemically coverage of the fibres. In contrast, freestanding nylon 6/6 nanofibre webs were prepared through electrospinning and were coated by sputtering with gold in order to make them conductive. Further, a PEDOT:PSS layer was electrochemically deposited onto the metalized nanofibre meshes and the synthesis parameters were chosen in such a way to preserve the high active area of the fibres. The prepared material was morphologically characterized and the formation of PEDOT:PSS was also demonstrated. The PEDOT:PSS coated nanofibres revealed remarkable electrical properties (sheet resistance of about 3.5 Omega cm(-2)), similar to those of metalized nanofibres (sheet resistance around 3 Omega cm2). The in vitro studies using L929 fibroblast mouse cells showed that the bioactive material has no cytotoxic effect and allows proliferation. Moreover, after 72 h of incubation, the fibroblasts shrunk their nuclei and spread suggesting that a differentiation in myofibroblast occurs without application of any kind of external stimuli. These results will be helpful for developing efficient materials for wound healing applications that work without energy consumption.

In this work, polyvinylidene fluoride (PVDF) fibres loaded with mineral powders, such as titanium dioxide (TiO2), barium titanate (BaTiO3), and calcium magnesium silicate (CaxMgSi2Oy), were prepared by electrospinning polymeric suspensions containing 20 wt.% PVDF and 3 wt.% powder. The piezoelectric polymer was combined with powders having antibacterial, piezoelectric, or bioactive properties, respectively, in the desire to obtain multifunctional materials compatible with the requirements of the medical field. All powders were characterized in terms of morphology and crystalline structure, which confirmed the nanometric character of TiO2 samples and micrometric one for the other two, as well as the lower crystallite size for TiO2 specimens as against BaTiO3 and CaxMgSi2Oy. The final fibrous scaffolds were homogeneous, composed of individual fibres with a diameter below 1 mu m and decorated with aggregates of inorganic particles, placed either inside the fibres or attached to their surface. The biological evaluation demonstrated the superiority of the composites towards the plain polymer in terms of cell viability.

The importance of multifunctional smart medical devices increases constantly during the last decades, fuelled by socio - economic challenges such as population aging and high costs of the healthcare system. Consequently, numerous research teams are focused on developing such devices with multiple functionalities in terms of both diagnostic and therapeutical approaches.Wearables become ubiquitous since computing and communication devices got smaller and more powerful, new functions being constantly added to consumer products such as smart watches or fitness monitors. Physical or chemical parameters including pulse, blood pressure or oxygen saturation are easily measured. Employing complex architectures based on nanostructures and materials with tailored properties represents an important path in developing a new generation of wearable medical devices which may both monitor chemical parameters (sweat or blood composition) and deliver various therapies. The present report focuses on describing such architectures with the potential of incorporating both health monitoring, transdermal drug delivery and other therapeutic functions in a relatively straightforward manner. As functional elements microscopic fibers are employed as both electrodes for electrochemical sensors, as microscopic heaters for the drug delivery function or, as building blocks for other specific functions. The fibers are fabricated using electrospinning or centrifugal/force spinning and functionalization (e.g. electrical conductivity) is achieved through physical and electrochemical deposition. Therefore, the fibers can be covered with thin metal layers and rendered conductive, oxidic or polymeric layers making them responsive to various stimuli. Heating is achieved in a straightforward manner through Joule effect and the use of a temperature responding hydrogel enables a controlled release of specific drugs while simultaneously improving epidermal permeation. These fiber-based systems can be easily employed on cheap, biocompatible substrates such as paper or textile materials and therefore can be mass produced with reasonable costs leading to a new generation of medical devices with increased functionality.

In this work, polyvinylidene fluoride was obtained in the form of one-dimensional structures with the help of electrospinning technique. Several types of precursor solutions were tested to find the optimal experimental conditions to produce smooth, continuous and beadless fibres, morphologically suitable for the development of piezoelectric scaffolds dedicated to tissue engineering applications. Thus, the influence of solvent type, polymer concentration, as well as electrospinning parameters (feeding rate, spinneret-collector distance, and applied voltage) was assessed and the best situation was the one with a 2:3 ratio between dimethylformamide and acetone, 20 % polymer concentration, 1 mL/h flow, 20 cm distance and 18 kV voltage. In the end, the fibres were loaded with barium titanate commercial particles, as first attempt to produce a piezoelectric composite with potential in the medical field.

The present work reports a new configuration of soft artificial muscle based on a web of metal covered nylon 6/6 micrometric fibers attached to a thin polydimethylsiloxane (PDMS) film. The preparation process is simple and implies the attachment of metalized fiber networks to a PDMS sheet substrate while heating and applying compression. The resulting composite is versatile and can be cut in different shapes as a function of the application sought. When an electric current passes through the metallic web, heat is produced, leading to local dilatation and to subsequent controlled deformation. Because of this, the artificial muscle displays a fast and ample movement (maximum displacement of 0.8 cm) when applying a relatively low voltage (2.2 V), a consequence of the contrast between the thermal expanse coefficients of the PDMS substrate and of the web-like electrode. It was shown that the electrical current producing this effect can originate from both direct electric contacts, and untethered configurations i.e. radio frequency induced. Usually, for thermal activated actuators the heating is produced by using metallic films or conductive carbon-based materials, while here a fast heating/cooling process is obtained by using microfiber-based heaters. This new approach for untethered devices is an interesting path to follow, opening a wide range of applications were autonomous actuation and remote transfer of energy are needed.

The present work reports the synthesis and characterization of polycaprolactone fibers loaded with particulate calcium magnesium silicates, to form composite materials with bioresorbable and bioactive properties. The inorganic powders were achieved through a sol–gel method, starting from the compositions of diopside, akermanite, and merwinite, three mineral phases with suitable features for the field of hard tissue engineering. The fibrous composites were fabricated by electrospinning polymeric solutions with a content of 16% polycaprolactone and 5 or 10% inorganic powder. The physico-chemical evaluation from compositional and morphological points of view was followed by the biological assessment of powder bioactivity and scaffold biocompatibility. SEM investigation highlighted a significant reduction in fiber diameter, from around 3 μm to less than 100 nm after the loading stage, while EDX and FTIR spectra confirmed the existence of embedded mineral entities. The silicate phases were found be highly bioactive after 4 weeks of immersion in SBF, enriching the potential of the polymeric host that provides only biocompatibility and bioresorbability. Moreover, the cellular tests indicated a slight decrease in cell viability over the short-term, a compromise that can be accepted if the overall benefits of such multifunctional composites are considered.

Designing complex electrochemical artificial muscles aims towards novel devices which besides excellent actuation capabilities should also present the ability to self-sense the modification of environmental parameters. In order to improve efficiency, mimicking the structure of natural muscles, synthetic actuators should have a similar fibrillary morphology. The importance of using materials based on fiber building blocks in actuators aimed at soft robotics field was demonstrated in the present report by comparing a fibrillary artificial muscle with one based on a classical film structure. Nylon electrospun fiber meshes and films were covered in the same conditions with a thin polypyrrole (PPy) layer. The fibrillary electrospun web morphology mimics that of natural muscles and the structure performs a fast, ample bending movement in liquid electrolyte when switching an applied electric potential between −0.6 and +0.6 V. Using the same actuation conditions, no movement of a film based artificial muscle was observed. In order to check the sensing ability of both fibrillary and film like electroactive architectures, their response i.e. PPy reaction when potential cycles were applied in different concentrations of LiClO 4 electrolyte were recorded. The obtained results suggest that the ion exchange of the fibrillary artificial muscle is more efficient due to its higher active surface and such devices could work also as dual device (sensor/artificial muscle).

A non-conventional, bioinspired device based on polypyrrole coated electrospun fibrous microstructures, which simultaneously works as artificial muscle and mechanical sensor is reported. Fibrous morphology is preferred due to its high active surface which can improve the actuation/sensing properties, its preparation still being challenging. Thus, a simple fabrication algorithm based on electrospinning, sputtering deposition and electrochemical polymerization produced electroactive aligned ribbon meshes with analogous characteristics as natural muscle fibers. These can simultaneously generate a movement (by applying an electric current/potential) and sense the effort of holding weights (by measuring the potential/current while holding objects up to 21.1 mg). Electroactivity was consisting in a fast bending/curling motion, depending on the fiber strip width. The amplitude of the movement decreases by increasing the load, a behavior similar with natural muscles. Moreover, when different weights were hung on the device, it senses the load modification, demonstrating a sensitivity of about 7 mV/mg for oxidation and − 4 mV/mg for reduction. These results are important since simultaneous actuation and sensitivity are essential for complex activity. Such devices with multiple functionalities can open new possibilities of applications as e.g. smart prosthesis or lifelike robots.

Electrospun polymeric fibers present an emerging alternative for the development of flexible electronics, enabling applications in wearable sensors and biosensors for continuous monitoring, and actuators for tissue engineering. The possibility to prepare sub-micrometric polymeric scaffolds, their processing for increasing the conductivity, their modification with different materials, conductive polymers and biomolecules in order to obtain functional flexible electrodes, allows the development of innovative devices for healthcare, and biomedical applications. In this review, the impact of metallized electrospun polymeric fibers in electrochemical (bio)sensors and actuators is discussed. A relation between their structure and functionality is provided, alongside with an overview of the different methods to obtain functional conductive fibers.

Embedding electronic and optoelectronic devices in common, daily use objects is a fast developing field of research. New architectures are needed for migrating from the classic wafer- based substrates. Novel types of flexible PMMA/Au/Alq3/LiF/Al structures were obtained starting from electrospun polymer fibers. Thus, using an electrospinning process poly (methyl metacrylate) (PMMA) nanofibers were fabricated. A thin Au layer deposition rendered the fiber array conductive, this being further employed as the anode. The next steps consisted of the thermal evaporation of tris(8-hydroxyquinolinato) aluminum (Alq3) and aluminum deposition as the cathode. The Au covered PMMA nanofiber layer had a similar behavior with an indium tin oxide film i.e. low sheet resistance 10.6 Ω/sq and high transparency. The low electrode resistivities allow an electron drift mobility of about 10-6cm2V-1s-1at a low applied field, similar to the counterpart structures based on thin films. Concerning the relaxation processes in these structures, the Cole-Cole plots exhibit a slightly deformed semicircle, indicating a more complex equivalent circuit for the processes between metal electrodes and the active layer. This equivalent circuit includes reactance equivalent processes at the anode, cathode, in the active layer and most probably originates from the roughness of the metallic electrodes.

Arti�cial muscles comprise a bunch of materials, composites and devices performing a similar behavior to biological muscles, since a mechanical actuation is produced while consuming a certain amount of energy. However, in order to mimic the multiple simultaneous functionalities of the natural muscles, i.e. the proprioception, new devices should be designed. A non-conventional, bioinspired device based on polypyrrole coated electrospun �brous microstructures, which works simultaneously as arti�cial muscle and mechanical sensor is reported. A simple fabrication algorithm based on electrospinning, sputtering deposition and electrochemical polymerization produced electroactive aligned ribbon meshes with analogous characteristics as natural muscle �bers. These can simultaneously produce a movement (by applying an electric current/potential) and sense the effort of holding weights (by measuring the potential/current while holding objects up to 24 mg). The amplitude of the movement decreases by increasing the load, a behavior similar with natural muscles. Moreover, when different weights were hanged on the device, it senses the load modi�cation, demonstrating a sensitivity of about 6 mV/mg for oxidation and 3 mV/mg for reduction. These results are important since simultaneous actuation and sensitivity are essential for complex activity. Such devices with multiple functionalities can open new possibilities of applications as smart prosthesis or lifelike robots.

Core–double shell nylon-ZnO/polypyrrole electrospun nanofibers were fabricated by combining three straightforward methods (electrospinning, sol–gel synthesis and electrodeposition). The hybrid fibrous organic–inorganic nanocomposite was obtained starting from freestanding nylon 6/6 nanofibers obtained through electrospinning. Nylon meshes were functionalized with a very thin, continuous ZnO film by a sol–gel process and thermally treated in order to increase its crystallinity. Further, the ZnO coated networks were used as a working electrode for the electrochemical deposition of a very thin, homogenous polypyrrole layer. X-ray diffraction measurements were employed for characterizing the ZnO structures while spectroscopic techniques such as FTIR and Raman were employed for describing the polypyrrole layer. An elemental analysis was performed through X-ray microanalysis, confirming the expected double shell structure. A detailed micromorphological characterization through FESEM and TEM assays evidenced the deposition of both organic and inorganic layers. Highly transparent, flexible due to the presence of the polymer core and embedding a semiconducting heterojunction, such materials can be easily tailored and integrated in functional platforms with a wide range of applications.