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     Juliana R. Dias, et. al.
           In direct contact assays no statistical significance was   pro ducible nanofiber meshes from materials with
           observed between control and samples, meaning that   distinct characteristics. The system was used to pro-
           the structures, when in contact with cells, does not   duce nanofibers from two distinct polymers, using
           induce any toxicity. Regarding indirect contact assay,   two different solvents, demonstrating its versatility
           no leachables delivered from the samples to the medium   of the new reassembled apparatus. The fabrication of
           presented toxicity.                                 gelatin meshes is particularly relevant; as like other
                                                               natural polymers, it is a material very sensitive to the
           4. Conclusions                                      environmental conditions, in particular the relative
           This paper introduces a solution electrospinning sys-  humidity. Keeping the processing parameters stable is
           tem developed to produce electrospun meshes for     key to obtain high quality and reproducible meshes,
           applications in tissue engineering and more specifically   i.e., with no beads, resulting in filaments with constant
           for wound dressing applications. For the fabrication of   diameter and in meshes with high porosity between
           the electrospinning system non-conductive materials   pores. Meshes did not show any presence of remaining
           (cork and polymers) were used to replace metallic   solvents, which can be correlated to the lack of toxicity
           ones, allowing to obtain a feasible and versatile   detected through the biological assays.
           laboratory-scale apparatus with ability to produce re-  The two selected materials are particularly relevant
           Figure 5. Characterization of PCL and gelatin electrospun meshes selected for further analysis. (A) Fiber morphology with 1000×
           and 5000× magnifications of PCL meshes; (B) Fiber morphology with 1000× and 5000× magnifications of gelatin meshes crosslinked
           with BDDGE; (C) Comparison between PCL and gelatin average fiber diameter; (D) FTIR spectra of PCL and crosslinked gelatin and
           (E) Influence of the purpose electrospinning system on fiber deposition over the collector in comparison with initial one comprising a
           significant metallic components.
                                       International Journal of Bioprinting (2017)–Volume 3, Issue 2       127





