RESUMO
Elastomeric conductive hybrid hydrogels (ECHs) combining conducting polymers with elastomeric hydrogels have recently attracted interest due to their wide range of applications in bioelectronics such as wearable or implantable sensing devices. However, the conductivity of ECHs is typically compromised when conductive polymers are used as fillers in hydrogel networks because the inherent limitations of ECHs severely restrict their applicability. Here, we significantly improved the electrical conductivity of ECHs by using a bioinspired catechol derivative, dopamine (DA), as the dopant and mediator for the in situ polymerization of conducting polypyrrole (PPy) within the elastomeric hydrogel dual-networks. In general, ECHs prepared by conventional methods tend to form separate island structures of conductive polymers dispersed within porous hydrogel matrices. We found that a continuous conductive PPy network prepared using the DA mediator facilitated fast electron transfer within the ECHs, which showed good elastomeric mechanical properties, excellent biocompatibility and high force- or strain-responsiveness suitable for implantable strain-sensing applications.
Assuntos
Elastômeros/química , Condutividade Elétrica , Hidrogéis/química , Células 3T3 , Animais , Elastômeros/farmacologia , Camundongos , Modelos Moleculares , Conformação MolecularRESUMO
Mimicking soft tissue mechanical properties and the high conductivity required for electrical transmission in the native spinal cord is critical in nerve tissue regeneration scaffold designs. However, fabricating scaffolds of high conductivity, tissue-like mechanical properties, and excellent biocompatibility simultaneously remains a great challenge. Here, a soft, highly conductive, biocompatible conducting polymer hydrogel (CPH) based on a plant-derived polyphenol, tannic acid (TA), cross-linking and doping conducting polypyrrole (PPy) chains is developed to explore its therapeutic efficacy after a spinal cord injury (SCI). The developed hydrogels exhibit an excellent electronic conductivity (0.05-0.18 S/cm) and appropriate mechanical properties (0.3-2.2 kPa), which can be achieved by controlling TA concentration. In vitro, a CPH with a higher conductivity accelerated the differentiation of neural stem cells (NSCs) into neurons while suppressing the development of astrocytes. In vivo, with relatively high conductivity, the CPH can activate endogenous NSC neurogenesis in the lesion area, resulting in significant recovery of locomotor function. Overall, our findings evidence that the CPHs without being combined with any other therapeutic agents have stimulated tissue repair following an SCI and thus have important implications for future biomaterial designs for SCI therapy.