Polypyrrole (Ppy), as a conductive polymer, is commonly used for nerve tissue engineering because of its good conductivity and non-cytotoxicity. To avoid the inconvenience of Ppy processing, it was coated on electrospun poly(L-lactic acid-co-ε-caprolactone)/silk fibroin (PLCL/SF) nanofibers via the in situ oxidative polymerization of pyrrole monomers in this study. Ppy-coated PLCL/SF membranes were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermogravimetric (TG) analysis. The results confirmed the disposition of Ppy on the PLCL/SF nanofibers, and the nanofibers kept their nanofibrous morphology and thermal stability, in comparison to the untreated ones. The conductivities and water contact angles were evaluated as well, and indicated that the conductivity and hydrophilicity of Ppy-coated nanofibers were increased. Furthermore, this study showed that electrical stimulation (ES) promoted PC12 cell differentiation and axonal extension on Ppy-coated nanofibers. The MTT assay suggested that both Ppy and ES could promote Schwann cell (SC) proliferation. Immunofluorescence staining and real time-qPCR (RT-qPCR) testing demonstrated that ES could induce PC12 cell differentiation even without nerve growth factor (NGF) treatment, and moreover, Ppy coating increased the inducing effects on PC12 cell differentiation. The overall results indicated the promising potential of Ppy-coated PLCL/SF nanofibrous membranes for peripheral nerve repair and regeneration.

Nanofibers of naturally modified polymer such as carboxymethyl cellulose (CMC) blended with poly(vinyl alcohol) (PVA) at different ratios was obtained by electrospinning technique. The blended solutions of CMC and PVA loaded with and without diclofenac sodium (DS) were electrospun using environmentally benign electrospinning technique in the absence of organic solvents. Scanning electron microscopy (SEM), Fourier transform infrared (FTIR), thermogravimetric analysis (TGA) were used to investigate the surface morphology functional groups, as well as the thermal stability of DS loaded CMC/PVA nanofibers mat. The mechanical properties of the as prepared electrospun nanofibers was also evaluated. The entrapment efficiency and the in vitro release of DS loaded CMC/PVA nanofibers were characterized using UV-Vis spectroscopy. The obtained results displayed that the blended nanofibers have shown a smooth morphology, no beads formation when the concentration of CMC was equal or below 5% and beads formation above 5%. FTIR data demonstrated that there were good interactions between CMC and PVA possibly via the formation of hydrogen bonds. The electrospun blended CMC/PVA nanofibers exhibit good mechanical properties. From the in vitro release data, it was found that with the presence of CMC, the release of DS from the nanofibers mats became sustained controlled. Due to the biocompatibility and low cost of the two blended polymers (CMC and PVA), the blended nanofibers system can be considered as one of the promising materials for the preparation of excellent drug carrier.