Search

Developing biomaterial formulations with specific biochemical characteristics and physical properties suitable for bioprinting of 3D scaffolds is a pivotal challenge in tissue engineering. Therefore, the design of novel bioprintable formulations is a continuously evolving research field. In this work, the authors aim at expanding the library of biomaterial inks by blending two natural biopolymers: pectin and gelatin. Cytocompatible formulations are obtained by combining pectin and gelatin at different ratios and using (3-glycidyloxypropyl)trimethoxysilane (GPTMS) as single crosslinking agent. It is shown that the developed formulations are all suitable for extrusion-based 3D bioprinting. Self-supporting scaffolds with a designed macroporosity and micropores in the bioprinted struts are successfully obtained by combining extrusion-based bioprinting and freeze-drying. The presence of gelatin in these formulations allows for the modulation of porosity, of water uptake and of scaffold stiffness in respect to pure pectin scaffolds. Results demonstrate that these new biomaterial formulations, processed with this specific approach, are promising candidates for the fabrication of tissue-like scaffolds for tissue regeneration.

Poultry feathers are among the most abundant and polluting keratin-rich waste biomasses. In this work, we developed a one-pot microwave-assisted process for eco-friendly keratin extraction from poultry feathers followed by a direct electrospinning (ES) of the raw extract, without further purification, to obtain keratin-based bioplastics. This microwave-assisted keratin extraction (MAE) was conducted in acetic acid 70% v/v. The effects of extraction time, solvent/feathers ratio, and heating mode (MAE vs. conventional heating) on the extraction yield were investigated. The highest keratin yield (26 ± 1% w/w with respect to initial feathers) was obtained after 5 h of MAE. Waste-derived keratin were blended with gelatin to fabricate keratin-based biodegradable and biocompatible bioplastics via ES, using 3-(Glycidyloxypropyl)trimethoxysilane (GPTMS) as a cross-linking agent. A full characterization of their thermal, mechanical, and barrier properties was performed by differential scanning calorimetry, thermogravimetric analysis, uniaxial tensile tests, and water permeability measurements. Their morphology and protein structure were investigated using scanning electron microscopy and attenuated total reflection-infrared spectroscopy. All these characterizations highlighted that the properties of the keratin-based bioplastics can be modulated by changing keratin and GPTMS concentrations. These bioplastics could be applied in areas such as bio-packaging and filtration/purification membranes.

One of the main challenges of the interface-tissue engineering is the regeneration of diseased or damaged interfacial native tissues that are heterogeneous both in composition and in structure. In order to achieve this objective, innovative fabrication techniques have to be investigated. This work describes the design, fabrication, and validation of a novel mixing system to be integrated into a double-extruder bioprinter, based on an ultrasonic probe included into a mixing chamber. To validate the quality and the influence of mixing time, different nanohydroxyapatite–gelatin samples were printed. Mechanical characterization, micro-computed tomography, and thermogravimetric analysis were carried out. Samples obtained from three-dimensional bioprinting using the mixing chamber were compared to samples obtained by deposition of the same final solution obtained by manually operated ultrasound probe, showing no statistical differences. Results obtained from samples characterization allow to consider the proposed mixing system as a promising tool for the fabrication of graduated structures which are increasingly being used in interface-tissue engineering.

Neural tissue engineering has recently emerged as an alternative strategy to repair nerve damage and promote nerve regeneration. It involves the fabrication of scaffolds with properties mimicking those of the natural extracellular matrix for guiding a three-dimensional (3D) neural regeneration. These engineered constructs, in addition to mechanical support, should be also capable of providing proper chemical and electrical stimuli for adhesion, migration, and proliferation of the neural cells. In this study, we developed conductive composite hydrogel films based on gelatin and carbon black (CB) as scaffolds for neural tissue engineering applications. The presented hydrogel constructs were fabricated in the form of films using the solvent casting method after dispersing several concentrations of CB in a 5 % (w/v) gelatin solution along with (3-glycidoxypropyl)trimethoxysilane (GPTMS) as the crosslinking agent at a concentration of 1.84 % (v/v). The CB concentrations of 0.3 %, 0.5 %, 0.7 %, and 0.9 % (w/w) with respect to the gelatin amount were chosen. The morphological, compositional, swelling, dissolution, electrical, mechanical, and wettability properties together were characterized as function of CB content and compared with those of pure gelatin-based hydrogel. Results demonstrated that the incorporation of different quantities of CB relatively reduced the water uptake capability of the films and increased the stability in water of the gelatin matrix. Findings from the mechanical tests revealed that composite hydrogels have a lower elastic modulus with respect to the pure gelatin matrix. Moreover, it was found that the incorporation of incremental CB concentrations kept the wettability surface property unchanged while the electrical characterization of the proposed structures showed a reduction of the electrical impedance. Overall, the study suggests that the composite structures could be used as a potential candidate for fabrication of scaffolds for neural regeneration with tunable electrical and mechanical properties by varying the CB concentration in a finite range.