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Functional inks for light-based 3D printing are actively being searched for being able to exploit all the potentialities of additive manufacturing. Herein, a fast visible-light photopolymerization process is showed of conductive PEDOT:PSS hydrogels. For this purpose, a new Type II photoinitiator system (PIS) based on riboflavin (Rf), triethanolamine (TEA), and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is investigated for the visible light photopolymerization of acrylic monomers. PEDOT:PSS has a dual role by accelerating the photoinitiation process and providing conductivity to the obtained hydrogels. Using this PIS, full monomer conversion is achieved in less than 2 min using visible light. First, the PIS mechanism is studied, proposing that electron transfer between the triplet excited state of the dye (3Rf*) and the amine (TEA) is catalyzed by PEDOT:PSS. Second, a series of poly(2-hydroxyethyl acrylate)/PEDOT:PSS hydrogels with different compositions are obtained by photopolymerization. The presence of PEDOT:PSS negatively influences the swelling properties of hydrogels, but significantly increases its mechanical modulus and electrical properties. The new PIS is also tested for 3D printing in a commercially available Digital Light Processing (DLP) 3D printer (405 nm wavelength), obtaining high resolution and 500 µm hole size conductive scaffolds.

New material solutions are searched for the manufacturing and safety of current batteries. Herein, an extrusion printable polymer separator for lithium batteries based on single-ion polymer electrolytes is presented. The polymer electrolytes are based on methacrylic polymeric nanoparticles (NPs) functionalized with a lithium sulfonamide group combined with different organic plasticizers such as sulfolane and carbonates. The synthesis of the polymer NPs is carried out by emulsion copolymerization of methyl methacrylate and lithium sulfonamide methacrylate in the presence of a crosslinker, resulting in particle sizes of less than 30 nm, as shown by electron microscopy. Then polymer electrolytes are prepared by mixing polymer NPs with varying lithium sulfonamide content and different plasticizers such as carbonates and sulfolane. The polymer electrolytes show ionic conductivities between 2.9 × 10−4 and 2.3 × 10−5 S cm−1 at 85 °C with the highest values for the small-sized NPs with the highest lithium content. As a proof-of-concept application, layer-by-layer printing of a sulfolane-based polymer electrolyte is evaluated via direct ink writing directly onto classic battery electrodes. The electrochemical characterization of the printed solid electrolyte indicates favorable properties, ionic conductivity, lithium transfer number, electrochemical stability window, and cyclability in lithium symmetrical cells, to be used in lithium batteries.

Biodegradation of polyesters driven by enzymes is considered as one of the most effective way of degradation of these materials, as a way to control plastics accumulation in the environment. In this study, we present two different strategies to tune the enzymatic degradation of PBS films triggered by a lipase from Pseudomonas cepacia. Firstly, the kinetics of enzymatic degradation of PBS films was regulated by applying multilayer coats of polysaccharide alginate and chitosan (Alg/Chi) films. Secondly, self-degradable PBS films were prepared by embedding lipase-filled alginate particles. For comparison purposes, a detailed enzymatic degradation study of neat PBS films exposed to a lipase from P. cepacia in solution was made to determine the main experimental parameters influencing their degradation in solution. The results showed that an increase in enzyme concentration increased the degradation extent and rate of neat PBS films. At a fixed enzyme concentration, stirring of the solution containing the enzyme and the PBS also increased the biodegradation rate. In the case of the PBS films coated with a different number of Alg/Chi layers by spray-assisted LbL and subjected to enzymatic degradation experiments in solution, the extent of degradation was found to be dependent on the number of protective coating layers. Therefore, the Alg/Chi biobased coating constitutes an effective barrier to the diffusion of the lipase, thus proving its effectiveness in modulating the enzymatic activity as a function of coating thickness. In the case of self-degradable PBS containing lipase-embedded alginate beads (employed to protect the enzyme during high-temperature processing), only limited biodegradation was observed as the amount of encapsulated enzyme employed was too small. Nonetheless, these results are promising, as the enzymatic activity –indicative of the degradation capacity of the enzyme– determined for all these samples was about 2 orders of magnitude lower than that of p

Eutectogels are an emerging family of soft ionic materials alternative to ionic liquid gels and organogels, offering fresh perspectives for designing functional dynamic platforms in water-free environments. Herein, the first example of mixed ionic and electronic conducting supramolecular eutectogel composites is reported. A fluorescent glutamic acid-derived low-molecular-weight gelator (LMWG) was found to self-assemble into nanofibrillar networks in deep eutectic solvents (DES)/poly(3,4-ethylenedioxythiophene) (PEDOT): chondroitin sulfate dispersions. These dynamic materials displayed excellent injectability and self-healing properties, high ionic conductivity (up to 10−2 S cm−1), good biocompatibility, and fluorescence imaging ability. This set of features turns the mixed conducting supramolecular eutectogels into promising adaptive materials for bioimaging and electrostimulation applications.

Biodegradation of polyesters driven by enzymes is considered as one of the most effective way of degradation of these materials, as a way to control plastics accumulation in the environment. In this study, we present two different strategies to tune the enzymatic degradation of PBS films triggered by a lipase from Pseudomonas cepacia. Firstly, the kinetics of enzymatic degradation of PBS films was regulated by applying multilayer coats of polysaccharide alginate and chitosan (Alg/Chi) films. Secondly, self-degradable PBS films were prepared by embedding lipase-filled alginate particles. For comparison purposes, a detailed enzymatic degradation study of neat PBS films exposed to a lipase from P. cepacia in solution was made to determine the main experimental parameters influencing their degradation in solution. The results showed that an increase in enzyme concentration increased the degradation extent and rate of neat PBS films. At a fixed enzyme concentration, stirring of the solution containing the enzyme and the PBS also increased the biodegradation rate. In the case of the PBS films coated with a different number of Alg/Chi layers by spray-assisted LbL and subjected to enzymatic degradation experiments in solution, the extent of degradation was found to be dependent on the number of protective coating layers. Therefore, the Alg/Chi biobased coating constitutes an effective barrier to the diffusion of the lipase, thus proving its effectiveness in modulating the enzymatic activity as a function of coating thickness. In the case of self-degradable PBS containing lipase-embedded alginate beads (employed to protect the enzyme during high-temperature processing), only limited biodegradation was observed as the amount of encapsulated enzyme employed was too small. Nonetheless, these results are promising, as the enzymatic activity –indicative of the degradation capacity of the enzyme– determined for all these samples was about 2 orders of magnitude lower than that of p

Underwater recording remains a critical challenge in bioelectronics because traditional flexible electrodes can not fulfill essential requirements such as stability and steady conductivity in aquatic environments. Herein, we show the use of elastic gels made of hydrophobic natural deep eutectic solvents as water-resistant electrodes. These eutectogels are designed with tailorable mechanical properties via one-step photopolymerization of acrylic monomers in different eutectic mixtures composed of fatty acids and menthol. The low viscosity of the eutectics turns the formulations into suitable inks for 3D printing, allowing fast manufacturing of complex objects. Furthermore, the hydrophobic nature of the building blocks endows the eutectogels with excellent stability and low water uptake. The obtained flexible eutectogel electrodes can record real-time electromyography (EMG) signals with low interference in the air and underwater.

Deep Eutectic Solvents (DES) are a new class of ionic conductive compounds attracting significant attention as greener alternatives to costly ionic liquids. Herein, we developed novel mixed ionic-electronic conducting materials by simple mixing of poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT:PSS) and various DES as additives. The DES addition induces the supramolecular assembly and gelification of PEDOT:PSS triggered by extensive hydrogen bonding and charge stabilization. The DES gels also known as eutectogels feature boost the mixed ionic-electronic conductivity of PEDOT:PSS up to 368 S·cm-1, unveiling great potential as flexible bioelectronics. All the PEDOT:PSS/DES gels showed shear-thinning behavior and viscosity values ranging from 100 to 1000 Pa·s. The eutectogels show good injectability with almost instantaneous elastic recovery, making them ideal materials for direct ink writing (DIW). As proof of that, PEDOT:PSS/DES (choline chloride: lactic acid) was 3D printed in different patterns, annealed at high temperature, and assembled into adhesive electrodes. This way tattoos-like electrodes, denoted as Eutecta2 were fabricated and placed in-vivo on the forearm and the thumb of human volunteers for electromyography measurements. Eutecta2 hexagonal patterns showed excellent conformability, and their signal-to-noise ratio (SNR) was higher than Ag/AgCl commercial electrodes for thumb motion measurements. Furthermore, forearm motion was measured after 14 days with similar values of SNR, demonstrating long-term stability and reusability. All in all, our findings revealed that DES could be used as inexpensive and safe additives to direct the self-assembly of PEDOT: PSS into supramolecular eutectogels inks for flexible bioelectronics.

[EN] Natural deep eutectics solvents (NADES), owing to their high solvation capacity and nontoxicity, are actively being sought for many technological applications. Herein, we report a series of novel NADES based on choline chloride and plant-derived polyphenols. Most of the obtained phenolic NADES have a wide liquid range and high thermal stability above 150 degrees C. Among them, small-sized polyphenols, like pyrogallol, vanillyl alcohol, or gentisic acid, lead to low-viscosity liquids with ionic conductivities in the order of 10(-3) S cm(-1) at room temperature. Interestingly, polyphenols possess valuable properties as therapeutic agents, antioxidants, adhesives, or redox-active compounds, among others. Thus, we evaluated the potential of these novel NADES for two applications: bioadhesives and corrosion protection. The mixture of choline chloridevanillyl alcohol (2:3 mol ratio) and gelatin resulted in a highly adhesive viscoelastic liquid (adhesive stress approximate to 135 kPa), affording shear thinning behavior. Furthermore, choline chloride-tannic acid (20:1) showed an extraordinary ability to coordinate iron ions, reaching excellent corrosion inhibitive efficiencies in mild steel protection.

Eutectogels are a new class of soft ion conductive materials that are attracting attention as an alternative to conventional hydrogels and costly ionic liquid gels to build wearable sensors and bioelectrodes. Herein, the first example of mixed ionic and electronic conductive eutectogels showing high adhesion, flexibility, nonvolatility, and reversible low-temperature gel transition for 3D printing manufacturing is reporting. The eutectogels consist of choline chloride/glycerol deep eutectic solvent, poly(3,4-ethylenedioxythiophene): lignin sulfonate, and gelatin as the biocompatible polymer matrix. These soft materials are flexible and stretchable, show high ionic and electronic conductivities of 7.3 and 8.7 mS cm−1, respectively, and have high adhesion energy. Due to this unique combination of properties, they could be applied as strain sensors to precisely detect physical movements. Furthermore, these soft mixed ionic electronic conductors possess excellent capacity as conformal electrodes to record epidermal physiological signals, such as electrocardiograms and electromyograms, over a long time.

3D conductive materials such as polymers and hydrogels that interface between biology and electronics are actively being researched for the fabrication of bioelectronic devices. In this work, short-time (5 s) photopolymerizable conductive inks based on poly(3,4-ethylenedioxythiophene) (PEDOT):polystyrene sulfonate (PSS) dispersed in an aqueous matrix formed by a vinyl resin, poly(ethylene glycol) diacrylate (PEGDA) with different molecular weights (M-n = 250, 575, and 700 Da), ethylene glycol (EG), and a photoinitiator have been optimized. These inks can be processed by Digital Light 3D Printing (DLP) leading to flexible and shape-defined conductive hydrogels and dry conductive PEDOTs, whose printability resolution increases with PEGDA molecular weight. Besides, the printed conductive PEDOT-based hydrogels are able to swell in water, exhibiting soft mechanical properties (Young's modulus of similar to 3 MPa) similar to those of skin tissues and good conductivity values (10(-2) S cm(-1)) for biosensing. Finally, the printed conductive hydrogels were tested as bioelectrodes for human electrocardiography (ECG) and electromyography (EMG) recordings, showing a long-term activity, up to 2 weeks, and enhanced detection signals compared to commercial Ag/AgCl medical electrodes for health monitoring.

Unformatted postprint, Mixed conducting polymer electrodes built from poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) (PEDOT:PSS) are attracting a great deal of interest in healthcare monitoring. However, the widespread application of this organic conductor in wearable devices is seriously restricted by toxic additives used to enhance its electrical conductivity. Herein, we explored a family of biocompatible ionic liquids (ILs), based on the cholinium cation and different carboxylated anions, as dopants and gelators for PEDOT:PSS to formulate safe bioelectrodes for long-term cutaneous recording. We examined the effect of the IL anion on the ionic-electronic conductivities and physicochemical properties of these soft conductors. Among the different ILs tested, cholinium lactate ([Ch][Lac]) afforded the greatest increase in the materials' electronic conductivity (≈30 S/cm vs. 0.2 S/cm for non-formulated PEDOT:PSS). Moreover, the PEDOT:PSS/IL mixtures formed gels due to supramolecular intereactions. The gels showed a rheological behavior associated to gels with excellent injectability properties. Finally, the performance of PEDOT:PSS/[Ch][Lac] as biocompatible electrodes for electrocardiogram recording is discussed. All in all, the obtained results unveil the effectiveness of cholinum-based ILs as non-toxic dopants of PEDOT:PSS, paving the way to explore novel bioderived electrolytes.

Unformatted postprint, Conducting polymers (CPs) have been attracting great attention in the development of (bio)electronic devices. Most of current devices are rigid 2D systems and possess uncontrollable geometries and architectures that lead to poor mechanical properties presenting ion/electronic diffusion limitations. The goal of the article is to provide an overview about the additive manufacturing (AM) of conducting polymers, which is of paramount importance for the design of future wearable 3D (bio)electronic devices. Among different 3D printing AM techniques, inkjet, extrusion, electrohydrodynamic and light-based printing have been mainly used. This review article collects examples of 3D printing of conducting polymers such as poly(3,4-ethylene-dioxythiophene) (PEDOT), polypyrrole (PPy) and polyaniline (PANi). It also shows examples of AM of these polymers combined with other polymers and/or conducting fillers such as carbon nanotubes, graphene and silver nanowires. Afterwards, the foremost application of CPs processed by 3D printing techniques in the biomedical and energy fields, i.e., wearable electronics, sensors, soft robotics for human motion, or health monitoring devices, among others, will be discussed.

Natural polymers are of great interest in the biomedical field due to their intrinsic properties such as biodegradability, biocompatibility, and non-toxicity. Layer-by-layer (LbL) assembly of natural polymers is a versatile, simple, efficient, reproducible, and flexible bottom-up technique for the development of nanostructured materials in a controlled manner. The multiple morphological and structural advantages of LbL compared to traditional coating methods (i.e., precise control over the thickness and compositions at the nanoscale, simplicity, versatility, suitability, and flexibility to coat surfaces with irregular shapes and sizes), make LbL one of the most useful techniques for building up advanced multilayer polymer structures for application in several fields, e.g., biomedicine, energy, and optics. This review article collects the main advances concerning multilayer assembly of natural polymers employing the most used LbL techniques (i.e., dipping, spray, and spin coating) leading to multilayer polymer structures and the influence of several variables (i.e., pH, molar mass, and method of preparation) in this LbL assembly process. Finally, the employment of these multilayer biopolymer films as platforms for tissue engineering, drug delivery, and thermal therapies will be discussed.

Conducting polymers (CPs) have been attracting great attention in the development of (bio)electronic devices. Most of the current devices are rigid two-dimensional systems and possess uncontrollable geometries and architectures that lead to poor mechanical properties presenting ion/electronic diffusion limitations. The goal of the article is to provide an overview about the additive manufacturing (AM) of conducting polymers, which is of paramount importance for the design of future wearable three-dimensional (3D) (bio)electronic devices. Among different 3D printing AM techniques, inkjet, extrusion, electrohydrodynamic, and light-based printing have been mainly used. This review article collects examples of 3D printing of conducting polymers such as poly(3,4-ethylene-dioxythiophene), polypyrrole, and polyaniline. It also shows examples of AM of these polymers combined with other polymers and/or conducting fillers such as carbon nanotubes, graphene, and silver nanowires. Afterward, the foremost applications of CPs processed by 3D printing techniques in the biomedical and energy fields, that is, wearable electronics, sensors, soft robotics for human motion, or health monitoring devices, among others, will be discussed.

Alginate/Fe hydrogels were fabricated on hyaluronic acid (HA) and poly(allylamine hydrochloride) (PAH) multilayers to yield photoresponsive nanometer-scale hydrogels. Light irradiation of the resulting hydrogels induced the photoreduction of >hard> Fe to >soft> Fe cations, leading to changes in the mechanical properties of the hydrogels related to their cross-linking behavior. The buildup and the phototriggered response of the supported alginate hydrogels were followed in situ with a quartz crystal microbalance (QCM) using an open cell allowing light irradiation from an LED source on top of the hydrogel. The results were correlated to the release profiles of folic acid, employed herein as a drug model, obtained from light-irradiated supported iron alginate hydrogels.

Herein, multilayer polysaccharide films were proposed and characterized as biomaterials for the local and controlled release of an antitumoral drug. To that aim, multilayer films of alginate (Alg) and chitosan (Chi) were built up through spray assisted layer-by-layer (LbL) technique employing an automatic equipment. A specific drug against breast cancer, tamoxifen (TMX), was incorporated in different intermediate positions of the multilayer Alg/Chi films. Our findings highlight that Alg/Chi multilayer films can be employed for sustained and local TMX delivery and their therapeutic effect can be modulated and optimized by the number of bilayers deposited over the loaded tamoxifen, the quantity of tamoxifen loaded in several intermediate positions and the total area of the film.

El objetivo de esta tesis es el desarrollo de sistemas poliméricos multicapa basados en polímeros naturales mediante la técnica capa a capa (layer-by-layer, LbL) para aplicaciones en terapias de hipertermia magnética local y administración controlada de fármacos. Los capítulos uno y dos reúnen una introducción general y objetivos junto con el estado del arte que muestra una revisión bibliográfica sobre los principales temas desarrollados durante la tesis doctoral. Del estado del arte se puede concluir que: el ensamblado LbL de polímeros naturales suscita un gran interés hoy en día debido a las potenciales aplicaciones de estos sistemas, sobre todo en el área de biomedicina. Además, la mayoría de los materiales obtenidos a partir del ensamblado de polímeros naturales se han obtenido mediante técnicas de inmersión LbL. La deposición LbL asistida por spray es una técnica rápida y sencilla para fabricar materiales nanoestructurados y ha sido menos explorada dejando un campo abierto para la investigación en esta tesis. El tercer capítulo de la tesis se centra en la descripción de los materiales de partida utilizados así como en las técnicas de caracterización más relevantes empleadas en esta tesis. El estudio del ensamblado LbL de dos sistemas poliméricos, alginato/quitosano (Alg/Chi) y ácido hialurónico/poli(hidrocloruro de alilamina) (HA/PAH) se describe en el capítulo cuatro. Del análisis del espesor de los filmes en función del número de capas depositadas se pudo concluir que el espesor de los filmes (Alg/Chi) crecía de forma lineal mientras que el crecimiento de los filmes HA/PAH era exponencial. Además, el crecimiento de los filmes Alg/Chi fabricados mediante spray LbL era mucho mayor que el correspondiente a los filmes fabricados mediante inmersión LbL. Se ha desarrollado además un sistema nanoestratificado derivado de los filmes HA/PAH mediante la incorporación de una capa de gel formada por alginato entrecruzado con iones hierro II con potenciales aplicaciones c, The objective of the present PhD work is the development of multilayer polymer systems based on natural polymers through layer-by-layer (LbL) assembly for applications in magnetic hyperthermia therapies and controlled drug delivery. The first part of this thesis provides a general introduction and objectives together with a state-of-the-art which collects a literature review about the main topics related to this thesis (Chapters 1 and 2). From this state-of-the-art, it is possible to conclude that: LbL assembly of natural polymers constitutes an area of intensive research nowadays, due to the potential applications of these materials mainly on the biomedical field. In addition, most of the studies regarding LbL of natural polymers deal with dipping LbL. Spray assisted LbL is a simple and saving-time technique to fabricate nanostructured materials and it has been much less explored leaving a broad field open to research in this thesis. The third chapter is focused on the description of materials and the most relevant characterization techniques used in this thesis. The study of the LbL assembly of two different systems based on natural polymers, alginate/chitosan (Alg/Chi) and hyaluronic acid/poly(allylamine hydrochloride) (HA/PAH) is described in the fourth chapter. From the determination of the thickness of (Alg/Chi) films as a function of the number of deposited layers, a linear growth was observed up to 5 bilayers whereas (HA/PAH) films presented an exponential growth. The growth of Alg/Chi films built up through spray LbL was much higher than that obtained when films were constructed by dipping LbL. A nanostratified system was obtained from the HA/PAH multilayer structure by incorporation of a gel-like layer formed by alginate crosslinked with iron II ions to be employed as a light-responsive drug delivery system in the future...

Nanomechanical properties of alginate/chitosan (Alg/Chi) multilayer films, obtained through spray assisted layer-by-layer assembly, were studied by means of PeakForce quantitative nanomechanical mapping atomic force microscopy (PF-QNM AFM). Prepared at two different alginate concentrations (1.0 and 2.5 mg/mL) and a fixed chitosan concentration (1.0 mg/mL), Alg/Chi films have an exponential growth in thickness with a transition to a linear growth toward a plateau by increasing the number of deposited bilayers. Height, elastic modulus, deformation, and adhesion maps were simultaneously recorded depending on the number of deposited bilayers. The elastic modulus of Alg/Chi films was found to be related to the mechanism of growth in contrast to the adhesion and deformation. A comparison of the nanomechanical properties obtained for non-cross-linked and thermally cross-linked Alg/Chi films revealed an increase of the elastic modulus after cross-linking regardless alginate concentration. The incorporation of iron oxide nanoparticles (NPs), during the spray preparation of the films, gave rise to nanocomposite Alg/Chi films with increased elastic moduli with the number of incorporated NPs layers. Deformation maps of the films strongly suggested the presence of empty spaces associated with the method of preparation. Finally, adhesion measurements point out to a significant role of NPs on the increase of the adhesion values found for nanocomposite films.

Here we present results on the deswelling behavior of semi-interpenetrating polymer hydrogels of sodium alginate and poly(N-isopropylacrylamide) (PNI-PAAm) containing iron oxide nanoparticles by means of Xray photon correlation spectroscopy (XPCS). The experiments were carried out as a function of temperature starting from temperatures below the low critical solution temperature (LCST) of the materials to temperatures above their LCST. The hydrogels present a hyper-diffusive dynamics of similar nature as that found for the freeze-dried aerogels which has been attributed to their characteristic porous structure. The dynamics of the swollen samples is faster than that of the freeze-dried ones suggesting that water has an effect in accelerating the dynamics of the hydrogels. XPCS has been used to characterize the deswelling process as a function of temperature. Deswelling times for the different samples correlate well with the corresponding relaxation times of the relaxation processes measured by XPCS. (Graph Presented)