Abstract:The innate ability of poly(N-isopropylacrylamide) (PNIPAAm) thermo-responsive hydrogel to copolymerize and to graft synthetic polymers and biomolecules, in conjunction with the highly controlled methods of radical polymerization which are now available, have expedited the widespread number of papers published in the last decade-especially in the biomedical field. Therefore, PNIPAAm-based hydrogels are extensively investigated for applications on the controlled delivery of active molecules, in self-healing materials, tissue engineering, regenerative medicine, or in the smart encapsulation of cells. The most promising polymers for biodegradability enhancement of PNIPAAm hydrogels are probably poly(ethylene glycol) (PEG) and/or poly(ε-caprolactone) (PCL), whereas the biocompatibility is mostly achieved with biopolymers. Ultimately, advances in three-dimensional bioprinting technology would contribute to the design of new devices and medical tools with thermal stimuli response needs, fabricated with PNIPAAm hydrogels.

No abstract

No abstract

Ultrathin films of poly[N-(2-cyanoethyl)pyrrole] and poly(N-methylpyrrole) and their composites with Au nanoparticles were used for the electrochemical detection of small concentrations (10 mM-100 μM) of dopamine, a neurotransmitter related with neurological disorders. Results indicated that Au nanoparticles improve the sensing abilities of the two polymers, even though they are not essential to obtain effective and fast responses toward the presence of dopamine. Furthermore, although both polymers have been found to be highly sensitive to low concentrations of dopamine, the response of poly[N-(2-cyanoethyl)pyrrole] is better and more effective than the response of poly(N-methylpyrrole). Experimental results were corroborated with quantum mechanical calculations on model systems, which also indicated that the interaction of oxidized dopamine with poly[N-(2-cyanoethyl)pyrrole] is stronger than that with poly(N-methylpyrrole). This behavior has been attributed to two different factors: (i) the flexibility of the cyanoethyl groups, which allows maximize the number of attractive van der Waals interactions, and (ii) the dipole of the cyano group, which interacts favorably with the dipole of the CO bonds of oxidized dopamine. Finally, theoretical results were used to propose an atomistic model that explains the interaction behavior between the oxidized dopamine and the conducting polymers.

This work reports a comprehensive study about cell adhesion and proliferation on the surface of different electroactive substrates formed by pi-conjugated polymers. Biological assays were performed considering four different cellular lines: two epithelial and two fibroblasts. On the other hand, the electroactivity of the three conducting systems was determined in physiological conditions. Results indicate that the three substrates behave as a cellular matrix, even though compatibility with cells is larger for PPy and the 3-layered system. Furthermore, the three polymeric systems are electro-compatible with the cellular monolayers.