RESUMO
Layered double hydroxides (LDHs) offer unique source of inspiration for design of bone mimetic biomaterials due to their superior mechanical properties, drug delivery capability and regulation cellular behaviors, particularly by divalent metal cations in their structure. Three-dimensional (3D) bioprinting of LDHs holds great promise as a novel strategy thanks to highly tunable physiochemical properties and shear-thinning ability of LDHs, which allow shape fidelity after deposition. Herein, we introduce a straightforward strategy for extrusion bioprinting of cell laden nanocomposite hydrogel bioink of gelatin methacryloyl (GelMA) biopolymer and LDHs nanoparticles. First, we synthesized LDHs by co-precipitation process and systematically examined the effect of LDHs addition on printing parameters such as printing pressure, extrusion rate, printing speed, and finally bioink printability in creating grid-like constructs. The developed hydrogel bioinks provided precise control over extrudability, extrusion uniformity, and structural integrity after deposition. Based on the printability and rheological analysis, the printability could be altered by controlling the concentration of LDHs, and printability was found to be ideal with the addition of 3 wt % LDHs. The addition of LDHs resulted in remarkably enhanced compressive strength from 652 kPa (G-LDH0) to 1168 kPa (G-LDH3). It was shown that the printed nanocomposite hydrogel scaffolds were able to support encapsulated osteoblast survival, spreading, and proliferation in the absence of any osteoinductive factors taking advantage of LDHs. In addition, cells encapsulated in G-LDH3 had a larger cell spreading area and higher cell aspect ratio than those encapsulated in G-LDH0. Altogether, the results demonstrated that the developed GelMA/LDHs nanocomposite hydrogel bioink revealed a high potential for extrusion bioprinting with high structural fidelity to fabricate implantable 3D hydrogel constructs for repair of bone defects.
Assuntos
NanogéisRESUMO
This study investigated the removal of nickel(ii) ions by using two sizes of graphene oxide nanoparticles (GO - 450 nm and GO - 200 nm). The thickness and lateral sheet dimensions of GO are considered to be an important adsorbent and promising method for sufficient removal of metals like nickel, lead, copper, etc. The graphite oxide was prepared by oxidation-reduction reaction (Hummers method), and the final product was labelled as GO - 450 nm. A tip sonicator was used to reduce the size of particles to 200 nm under controlled conditions (time and power of sonication). FTIR spectroscopy shows that both sizes of GO particles contain several types of oxygen groups distributed onto the surface of GO particles. Scanning electron microscopy (SEM) and the statistical analysis confirmed the formation of these two sizes of GO particles. The GO - 200 nm performed better removal of Ni(ii) compared with GO - 450 nm, due to more surfaces being available. The adsorption capacity of GO particles increased drastically from 45 mg g-1 to 75 mg g-1 for GO - 450 nm and GO - 200 nm respectively, these values were carried out after 2 h of incubation. The kinetics of adsorption and several parameters like initial concentration at equilibrium, pH, temperature, and adsorbent dose are controlled and studied by using UV-visible spectroscopy. The results indicated a significant potential of GO - 200 nm as an adsorbent for Ni(ii) ion removal. An additional experiment was performed to estimate the surface area of GO - 450 nm and GO - 200 nm, the results show that the surface areas of GO - 450 nm and GO - 200 nm are 747.8 m2 g-1 and 1052.2 m2 g-1 respectively.
