Gelatin fibers were prepared by electrospinning of gelatin/acetic acid/water ternary mixtures with the aim of studying the feasibility of fabricating gelatin nanofiber mats at room temperature using an alternative benign solvent by significantly reducing the acetic acid concentration. The results showed that gelatin nanofibers can be optimally electrospun with low acetic acid concentration (25% v/v) combined with gelatin concentrations higher than 300 mg/ml. Both gelatin solutions and electrospun gelatin mats (prepared with different acetic acid aqueous solutions) were analyzed by FTIR and DSC techniques in order to determine the chemical and structure changes of the polymer. The electrospun gelatin mats fabricated from solutions with low acetic acid content showed some advantages as the maintenance of the decomposition temperature of the pure gelatin (~230ºC) and the reduction of the acid content on electrospun mats, which allowed to reach a cell viability upper than 90% (analyzed by cell viability test using human dermal fibroblast and embryonic kidney cells). This study has also analyzed the influence of gelatin and acetic acid concentration both on the solution viscosity and the electrospun fiber diameter, obtaining a clear relationship between these parameters.

The development of suitable biomimetic scaffolds is a fundamental requirement of tissue engineering. Although electrospinning has emerged as an effective method for producing such scaffolds of nanometer-sized fibers, the influence of solution characteristics on the morphology of the resulting nanofibers depends on each polymer solution system. In this study, gelatin nanofibers and microfibers were prepared via electrospinning using mixtures of water and acetic acid at different ratios as solvents. The viscosities of gelatin solutions before electrospinning were analyzed and two different behaviors were found as a function of the solvent composition, taking into account classic models of polymer science. A power law relationship between viscosity and gelatin concentration was found for each solvent system, and an empirical model including the influence of acetic acid was obtained for aqueous systems. Moreover, a ternary diagram considering gelatin, water, and acetic acid mass fractions was constructed as a tool to establish the electrospinnability domains in terms of fiber occurrence and morphology. Also, the isodiametric curves were defined in the fibers region. Finally, in order to correlate the diameter of electrospun nanofibers and the electrospinnability zones, the Berry number was used. However, as its only allows the range of electrospinnability to be established for a fixed solvent composition, a new dimensionless parameter (Bemod) was suggested to take into account all the acetic acid aqueous solutions as a single solvent.

. Preparation of electrospun nanofibers from solutions of different gelatin types using a benign solvent mixture composed of water/PBS/ethanol. Polymers for Advanced Technologies, 2016, 27, 382-392 ABSTRACTThe feasibility of using Phosphate Buffer Saline (PBS)/ethanol mixtures as a benign solvent to electrospin three types of gelatin was studied. Gelatins with different chemical properties, such as Bloom, were selected and the effect of the gelatin nature and its concentration on the electrospinnability of the dope solution and on the fiber diameter of the electrospun mats were studied. Viscosity of the gelatin solution, which follows a power law relationship with the gelatin concentration, was found to significantly influence the morphology of the mats and the fiber diameter. It was demonstrated that the PBS/ethanol solvent interacted with the gelatins as a good solvent with a Flory exponent of 0.65. In addition, the effect of the solvent composition on the fiber formation process was evaluated corroborating that the ionic strength of the medium and the PBS/ethanol ratio significantly affected the morphology and the diameter of the electrospun fibers. Chemical structure and thermal stability of the electrospun gelatin mats were characterized by Fourier Transform Infrared Spectroscopy (FTIR) and Differential Scanning Calorimetry (DSC). Finally, cytotoxicity of the electrospun mats was analyzed by the Alamar Blue assay, using human foreskin fibroblasts (BJ-5ta), resulting in a high cell viability (80-90%) regardless the type of gelatin.

The thermosensitive properties of the hydrogel poly(N-isopropylacrylamide) (pNIPAAm) together with the good mechanical properties of lyocell fibres make a combination of the two to be thought of as a smart textile. In the present study the optimal values of various parameters that control the grafting process of pNIPAAm onto lyocell fibres were determined considering the influence of the interaction between them. The copolymerization of pNIPAAm hydrogel onto lyocell fibres was performed in aqueous acidic medium using cerium(IV) as initiator. An experimental design was planned in order to study the effect of the interactions between some variables that affect the kinetics of the graft copolymerization: the cerium(IV) initiator concentration, the N-isopropylacrylamide (NIPAAm) monomer concentration and the liquor fibre-to-bath ratio. The results show that the interaction between the concentrations of NIPAAm and the initiator significantly affects the degree of grafting (DG), the optimum values being 1250 and 12.25 mmol L−1, respectively. In contrast, the liquor ratio parameter shows no significant interaction with the other two variables studied, meaning that it acts independently but showing a proportional relationship with respect to the DG obtained. In addition, the presence of pNIPAAm in the copolymer obtained was confirmed by Fourier transform infrared spectral analysis. Moreover, the water sorption capacity, depending on the temperature, of the lyocell/pNIPAAm copolymer was studied, with an increase being observed when the DG is higher than 60% and also increasing with the temperaturePostprint (published version