Search Results (21)

Printable piezoelectric materials are emerging as a cornerstone of next-generation sensing, actuation, and energy harvesting technologies, driven by the need for lightweight, flexible, and digitally manufactured transducers. Conventional ceramic piezoelectrics offer exceptional electromechanical performance but require high-temperature sintering and exhibit intrinsic brittleness, limiting their integration with soft or unconventional substrates. Polymeric piezoelectrics, in contrast, provide mechanical compliance and low-temperature processability yet suffer from lower crystallinity, reduced piezoelectric coefficients, and limited thermal stability. These contrasting characteristics have catalyzed the development of functional piezoelectric inks—ceramic, polymeric, and hybrid formulations engineered for additive manufacturing techniques such as direct ink writing, stereolithography, screen printing, and inkjet printing. This review systematically examines the material compositions, dispersion chemistries, printing requirements, thermal treatment pathways, and poling strategies that govern the performance of printed piezoelectric transducers. By comparing ceramic-based, polymer-based, and hybrid systems, we reveal the fundamental trade-offs between printability, crystallinity, mechanical compliance, and electromechanical response, and map how these trade-offs shape device design across wearable electronics, soft robotics, and structural health monitoring. Finally, we highlight emerging approaches—including surface functionalization, low-temperature crystallization, liquid-phase sintering, and engineered ceramic–polymer interfaces—that offer promising routes to bridge the gap between printability and high piezoelectric performance. Full article

Printed biosensors have attracted increasing attention as platforms for rapid, low-cost, and portable diagnostics because they can be fabricated on flexible or rigid substrates using scalable printing techniques. Their performance is strongly influenced by both the printing process and the materials employed, since factors such as ink rheology, particle dispersion, interfacial behavior, and post-processing conditions directly affect device architecture, sensing performance, and manufacturing reliability. This review summarizes recent advances in printed biosensors from the combined perspectives of printing technologies and functional materials. Commonly employed printing techniques, including inkjet, screen, aerosol jet, and roll-to-roll gravure printing, are discussed with emphasis on their processing characteristics and material requirements. The review also examines key material platforms used in printed biosensors, including carbon-based nanomaterials, metal oxides, metal nanoparticles, conductive polymers, dielectric materials, and hybrid composites, highlighting their roles in electrical conductivity, catalytic activity, biomolecule immobilization, mechanical flexibility, and overall analytical performance. Finally, current challenges and emerging research directions are outlined with respect to ink stability, post-processing strategies, sensor reliability, manufacturability, and practical translation. Overall, this review emphasizes that the development of high-performance printed biosensors depends on the synergistic integration of rational material design with optimized printing strategies. Full article

Squid ink has recently garnered considerable attention as a natural melanin source for the development of biocompatible nanomaterials. Although numerous studies have explored the biological and therapeutic applications of squid ink, the fabrication and modification strategies for squid ink-derived nanoparticles (SINPs) have yet to be comprehensively reviewed. This paper provides an integrated overview of current extraction, purification, and functionalization strategies for SINPs, with a particular focus on how functionalization approaches modulate their physicochemical characteristics and biological behaviors. The review begins by outlining the natural mechanisms of melanin formation and summarizing common extraction methods—including centrifugation, ultrasonication, and dialysis. Subsequently, various surface modification and hybridization techniques—including polymer coating, incorporation of metallic elements (e.g., Se and Fe), and loading of photosensitizers—are compared in terms of their contributions to functional enhancement. Finally, the challenges of reproducibility, batch-to-batch variability, and scalable manufacturing are discussed, outlining future directions for the development of squid ink-derived nanomaterials into standardized biomedical platforms. Full article

Decellularization removes immunogenic intracellular components of fish tissues while keeping the extracellular matrix (dECM) structure, mechanical integrity, and bioactivity. Fish-derived dECM retains native bioactive components, exhibiting high biocompatibility, low immunogenicity, and biodegradability, while supporting cell adhesion, proliferation, and tissue regeneration. Due to its abundance, minimal ethical concerns, and low zoonotic risks, fish wastes are emerging as sustainable sources of dECM, offering an eco-friendly alternative to mammalian biomaterials. This review highlights advances in decellularizing fish wastes such as skin, scales, bones, viscera, and swim bladders from species including tilapia, tuna, milkfish, carp, goldfish, and sturgeon. Physical, chemical, biological, and hybrid decellularization methods are assessed for cell removal, ECM preservation, and mechanical performance. Recent advances in polymer-dECM composites, crosslinking, and 3D bioprinting have significantly improved scaffold performance, making fish-derived dECM applicable for healing of wounds, regeneration of bone and cartilage, and repair of soft tissues. Despite its potential, challenges remain in optimizing perfusion rates, temperature variations, and tissue-specific protocols, as well as developing eco-friendly decellularization techniques using biodegradable reagents. Future perspectives include expanding decellularized fish tissue sources, innovating bio-inks for 3D bioprinting, and refining tissue-specific processing methods to maximize the potential of fish-derived dECM in regenerative medicine and tissue engineering. Full article

Additive manufacturing of hydrogel-based scaffolds requires concurrent control of material rheology and extrusion dynamics, especially in multi-material architectures. In this work, we develop a modular multi-material extrusion-based 3D-printing platform that combines a filament-fed extruder for thermoplastic polymers with a piston-driven extruder for viscous gel inks, together with an empirical calibration procedure for gel dosing. The calibration algorithm optimizes the pre-extrusion and retraction displacement (E_Pr/R) based on stepwise extrusion experiments and reduces the discrepancy between theoretical and measured deposited mass for shear-thinning alginate gels to below the prescribed tolerance. The calibrated system is then used to fabricate two representative hybrid constructs: partially crosslinked sodium alginate scaffolds with an internal hollow channel supported by a removable polycaprolactone framework, and self-supporting structures based on a sodium alginate–chitosan polyelectrolyte complex obtained by sequential co-extrusion. The resulting constructs remain mechanically stable after ionic crosslinking and solvent treatment and can subsequently be converted into highly porous scaffolds by freeze- or supercritical drying. The proposed combination of hardware architecture and extrusion calibration enables reproducible multi-material 3D printing of hydrogel–thermoplastic hybrid scaffolds and can be readily adapted to other gel-based inks for tissue engineering applications. Full article

A newly developed series of polylactide (PLA)-based composites filled with hybrid lignin–carbon nanotube (CNTs) particles were studied using thermal and dielectric techniques. The low CNT content (up to 3 wt%) aimed to create conductive networks while enhancing particle–polymer adhesion. For comparison, PLA composites based on lignin and CNTs were also examined. Although infrared spectroscopy showed no significant interactions, calorimetry and dielectric spectroscopy revealed a rigid interfacial PLA layer exhibiting restricted mobility. The interfacial polymer amount was found to increase monotonically with the particle content. The hybrid-filled PLA composites exhibited electrical conductivity, whereas PLA/Lignin and PLA/CNTs remained insulators. The result was indicative of a synergistic effect between lignin and CNTs, leading to lowering of the percolation threshold to 3 wt%, being almost ideal for sustainable conductive printing inks. Despite the addition of lignin and CNTs at different loadings, the glass transition temperature of PLA (60 °C) decreased slightly (softer composites) by 1–2 K in the composites, while the melting temperature remained stable at ~175 °C, favoring efficient processing. Regarding crystallization, which is typically slow in PLA, the hybrid lignin/CNT particles promoted crystal nucleation without increasing the total crystallizable fraction. Overall, these findings highlight the potential of eco-friendly conductive PLA composites for new-generation applications, such as printed electronics. Full article

This article outlines the method of creating electrodes for electrochemical sensors using hybrid nanostructures composed of graphene and conducting polymers with insertion of gold nanoparticles. The technology employed for graphene dispersion and support stabilization was based on the chemical vapor deposition technique followed by electrochemical delamination. The method used to obtain hybrid nanostructures from graphene and conductive polymers was drop-casting, utilizing solutions of P3HT, PANI-EB, and F8T2. Additionally, the insertion of gold nanoparticles utilized an innovative dip-coating technique, with the graphene-conducting polymer frameworks submerged in a HAuCl₄/2-propanol solution and subsequently subjected to controlled heating. The integration of gold nanoparticles differs notably, with P3HT showing the least adhesion of gold nanoparticles, while PANI-EB exhibits the highest. An inkjet printer was employed to create electrodes with metallization accomplished through the use of commercial silver ink. Notable variations in roughness (grain size) result in unique behaviors of these structures, and therefore, any potential differences in the sensitivity of the generated sensing structures can be more thoroughly understood through this spatial arrangement. The electrochemical experiments utilized a diluted sulfuric acid solution at three different scan rates. The oxidation and reduction potentials of the structures seem fairly alike. Nevertheless, a notable difference is seen in the anodic and cathodic current densities, which appear to be largely influenced by the active surface of gold nanoparticles linked to the polymeric grains. The graphene–PANI-EB structure with Au nanoparticles showed the highest responsiveness and will be further evaluated for biomedical applications. Full article

Our research outlines a method for creating chemosensors utilizing hybrid nanostructures derived from TiO₂ ceramic nanotubes alongside conducting polymers, with embedded gold nanoparticles. The method used to create hybrid nanostructures from ceramic nanotubes and conducting polymers was drop-casting. AFM analysis highlighted an increased roughness, particularly for PANI-EB, exhibiting a significantly larger grain size exceeding 3.5 μm, with an increased inclusion of gold and uniform arrangement on the surface. The Rku parameter values being around three suggested that the layers primarily exhibited peaks rather than depressions, showing a Gaussian distribution. A chemiresistor was created by using an ink-jet printer and a multilayer metallization was achieved with commercial silver ink for printed electronics. Based on the experimental calibration curve, which exhibits adequate linearity over a wider range of H₂S concentrations in air up to 1 ppm, the detection limit was established at 0.1 ppm, a threshold appropriate for recognizing oral diseases. The sensor is a simple, affordable, and durable device designed for individual use, offering significant benefits for patients by enabling improved tracking of the syndrome’s advancement or treatment success. Full article

This paper describes the process of producing chemosensors based on hybrid nanostructures obtained from Al₂O₃, as well as ZnO ceramic nanotubes and the following conducting polymers: poly(3-hexylthiophene), polyaniline emeraldine-base (PANI-EB), and poly(3, 4-ethylenedioxythiophene)-polystyrene sulfonate. The process for creating ceramic nanotubes involves three steps: creating polymer fiber nets using poly(methyl methacrylate), depositing ceramic films onto the nanofiber nets using magnetron deposition, and heating the nanotubes to 600 °C to burn off the polymer support completely. The technology for obtaining hybrid nanostructures from ceramic nanotubes and conducting polymers is drop-casting. AFM analysis emphasized a higher roughness, mainly in the case of PANI-EB, for both nanotube types, with a much larger grain size dimension of over 5 μm. The values of the parameter Rku were close or slightly above 3, indicating, in all cases, the formation of layers predominantly characterized by peaks and not by depressions, with a Gaussian distribution. An ink-jet printer was used to generate chemiresistors from ceramic nanotubes and PANI-EB structures, and the metallization was made with commercial copper ink for printed electronics. Calibration curves were experimentally generated for both sensing structures across a wider range of NH₃ concentrations in air, reaching up to 5 ppm. A 0.5 ppm detection limit was established. The curve for the ZnO:PANI-EB structure presented high linearity and lower resistance values. The sensor could be used in medical diagnosis for the analysis of breath ammonia and biomarkers for predicting CKD in stages higher than 1. The threshold value of 1 ppm represents a feasible value for the presented sensor, which can be defined as a simple, low-value and robust device for individual use, beneficial at the patient level. Full article

This paper describes the process of producing chemiresistors based on hybrid nanostructures obtained from graphene and conducting polymers. The technology of graphene presumed the following: dispersion and support stabilization based on the chemical vapor deposition technique; transfer of the graphene to the substrate by spin-coating of polymethyl methacrylate; and thermal treatment and electrochemical delamination. For the process at T = 950 °C, a better settlement of the grains was noticed, with the formation of layers predominantly characterized by peaks and not by depressions. The technology for obtaining hybrid nanostructures from graphene and conducting polymers was drop-casting, with solutions of Poly(3-hexylthiophene (P3HT) and Poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-bithiophene] (F8T2). In the case of F8T2, compared to P3HT, a 10 times larger dimension of grain size and about 7 times larger distances between the peak clusters were noticed. To generate chemiresistors from graphene–polymer structures, an ink-jet printer was used, and the metallization was made with commercial copper ink for printed electronics, leading to a structure of a resistor with an active surface of about 1 cm². Experimental calibration curves were plotted for both sensing structures, for a domain of CH₄ of up to 1000 ppm concentration in air. A linearity of the curve for the low concentration of CH₄ was noticed for the graphene structure with F8T2, presenting a sensitivity of about 6 times higher compared with the graphene structure with P3HT, which makes the sensing structure of graphene with F8T2 more feasible and reliable for the medical application of irritable bowel syndrome evaluation. Full article

The possibility of controlling the porosity and, as a result, the permeability of fibrous non-woven fabrics was studied. Modification of experimental samples was performed on equipment with adjustable heating and compression. It was found that the modification regimes affected the formation of the porous structure. We found that there was a relationship between the permeability coefficient and the porosity coefficient of the materials when the modification speed and temperature were varied. A model is proposed for predicting the permeability for modified material with a given porosity. As the result, a new hybrid composite material with reversible dynamic color characteristics that changed under the influence of ultraviolet and/or thermal exposure was produced. The developed technology consists of: manufacture of the non-woven needle-punched fabrics, surface structuring, material extrusion, additive manufacturing (FFF technology) and the stencil technique of ink-layer adding. In our investigation, we (a) obtained fibrous polymer materials with a porosity gradient in thickness, (b) determined the dependence of the material’s porosity coefficient on the speed and temperature of the modification and (c) developed a model for calculating the porosity coefficient of the materials with specified technological parameters. Full article

The features or actuation behaviors of nature’s creatures provide concepts for the development of biomimetic soft bioactuators/robots with stimuli-responsive capabilities, design convenience, and environmental adaptivity in various fields. Mimosa pudica is a mechanically responsive plant that can convert pressure to the motion of leaves. When the leaves receive pressure, the occurrence of asymmetric turgor in the extensor and flexor sides of the pulvinus from redistributing the water in the pulvinus causes the bending of the pulvinus. Inspired by the actuation of Mimosa pudica, designing soft bioactuators can convert external stimulations to driving forces for the actuation of constructs which has been receiving increased attention and has potential applications in many fields. 4D printing technology has emerged as a new strategy for creating versatile soft bioactuators/robots by integrating printing technologies with stimuli-responsive materials. In this study, we developed a hybrid ink by combining gelatin methacryloyl (GelMA) polymers with iron oxide nanoparticles (IONs). This hybrid ION-GelMA ink exhibits tunable rheology, controllable mechanical properties, magnetic-responsive behaviors, and printability by integrating the internal metal ion-polymeric chain interactions and photo-crosslinking chemistries. This design offers the inks a dual crosslink mechanism combining the advantages of photocrosslinking and ionic crosslinking to rapidly form the construct within 60 s of UV exposure time. In addition, the magnetic-responsive actuation of ION-GelMA constructs can be regulated by different ION concentrations (0–10%). Furthermore, we used the ION-GelMA inks to fabricate a Mimosa pudica-like soft bioactuator through a mold casting method and a direct-ink-writing (DIW) printing technology. Obviously, the pinnule leaf structure of printed constructs presents a continuous reversible shape transformation in an air phase without any liquid as a medium, which can mimic the motion characteristics of natural creatures. At the same time, compared to the model casting process, the DIW printed bioactuators show a more refined and biomimetic transformation shape that closely resembles the movement of the pinnule leaf of Mimosa pudica in response to stimulation. Overall, this study indicates the proof of concept and the potential prospect of magnetic-responsive ION-GelMA inks for the rapid prototyping of biomimetic soft bioactuators/robots with untethered non-contact magneto-actuations. Full article

Smart hinges fabricated using three-dimensional (3D) printing have been accepted in the aerospace, robotics, and biomedical fields since these devices possess a shape memory characteristic. Shape memory polymers (SMPs) are the preferred materials for creating smart hinges due to their ability to achieve programmable complex geometries. However, fabricating SMPs with embedded components remains a challenge due to the constraints of current 3D printing methods and material limitations. This study investigated the use of a hybrid 3D printing method, direct ink writing (DIW), and embedded 3D printing (e-3DP) to print smart hinges with an embedded circuit to act as a strain sensor. The main components of the SMP included tert-Butyl acrylate (tBA) and aliphatic urethane diacrylate (AUD), but this SMP ink had a low viscosity and could not be used for DIW or e-3DP. Fumed silica (FS) was added to the SMP to tune its rheology, and it was shown that the FS concentration significantly affected the rheological properties, dry-out process, filament geometries, and self-supporting capabilities. This study presents a hybrid 3D printing approach for creating smart hinges with internal strain sensors in one step, demonstrating the versatility of DIW/e-3DP. The findings from this work provide a foundational and reliable technical solution to efficiently fabricate functional, self-monitoring, smart devices from SMPs for diverse applications. Full article

Bioprinting is an emerging technology involved in the fabrication of three-dimensional tissue constructs for the repair and regeneration of various tissues and organs. Collagen, a natural protein found abundantly in the extracellular matrix of several tissues, can be extracted from collagen-rich tissues of animals such as sheep, cows, rats, pigs, horses, birds, and marine animals. However, due to the poor printability of collagen bioinks, biocompatible collagen scaffolds that mimic the extracellular matrix (ECM) are difficult to fabricate using bioprinting techniques. Gelatin methacrylate (GelMA), a semi-synthetic polymer with tunable physical and chemical properties, has been found to be a promising biomaterial in various bioprinting applications. The printability of collagen can be improved by combining it with semi-synthetic polymers such as GelMA to develop hybrid hydrogels. Such hybrid hydrogels printed have also been identified to have enhanced mechanical properties. Hybrid GelMA meshes have not previously been prepared with collagen from ovine sources. This study provides a novel comparison between the properties of hybrid meshes with ovine skin and bovine hide collagen. GelMA (8% w/v) was integrated with three different concentrations (0.5%, 1%, and 2%) of bovine and ovine collagen forming hybrid hydrogels inks that were printed into meshes with enhanced properties. The maximum percentage of collagen suitable for integration with GelMA, forming hybrid hydrogels with a stable degradation rate was 1%. The water-soluble nature of ovine collagen promoted faster degradation of the hybrid meshes, although the structural crosslinking was identified to be higher than bovine hybrid meshes. The 1% bovine collagen hybrid meshes stood out in terms of their stable degradation rates. Full article

3D printing is an emerging and powerful technique to create shape-defined three-dimensional structures for tissue engineering applications. Herein, different alginate–cellulose formulations were optimized to be used as printable inks. Alginate (Alg) was chosen as the main component of the scaffold due to its tunable mechanical properties, rapid gelation, and non-toxicity, whereas microcrystalline cellulose (MCC) was added to the hydrogel to modulate its mechanical properties for printing. Additionally, Fmoc-FFY (Fmoc: 9-fluorenylmethoxycarbonyl; F: phenylalanine; Y: tyrosine), a self-assembled peptide that promotes cell adhesion was incorporated into the ink without modifying its rheological properties and shear-thinning behavior. Then, 3D-printed scaffolds made of Alg, 40% of MCC inks and Fmoc-FFY peptide were characterized by scanning electron microscopy and infrared spectroscopy, confirming the morphological microstructure of the hydrogel scaffolds with edged particles of MCC homogeneously distributed within the alginate matrix and the self-assembly of the peptide in a β-sheet conformation. Finally, the cytocompatibility of the scaffolds was tested in contact with the MG63 osteosarcoma cells, confirming the absence of cytotoxic components that may compromise their viability. Interestingly, MG63 cell growth was retarded in the scaffolds containing the peptide, but cells were more likely to promote adhesive interactions with the material rather than with the other cells, indicating the benefits of the peptide in promoting biological functionality to alginate-based biomaterials. Full article