Abstract:Emulsion electrospinning using natural and synthetic polymers, including two dissimilar materials is a promising technique for nanofibers fabrication in a core/shell configuration for tissue engineering, controlled or sustained drug delivery and dressing applications. In this study, we designed and fabricated core/shell nanofibers based on polycaprolactone (PCL) as core material and poly(vinyl alcohol) (PVA)‐gelatin (GEL) blend as shell materials (PCL/PVA‐GEL) to achieve high mechanical properties, good cell g… Show more
“…The decrease in the viscosity of the T4 sample indicates a decrease in the interfacial energy between the droplets due to, for example, coalescence or flocculation. This decrease indirectly indicates that the emulsion started to lose stability [ 47 ]. One hour after preparation, this drop in viscosity is more likely to be due to the decomposition of the micelles than to the miscibility of the water and oil phases or the volume fraction of the water phase.…”
Section: Discussionmentioning
confidence: 99%
“…Akbarzadeh et al obtained PCL/PVA-GEL core/shell nanofibers, which induced adhesion of the L929 fibroblasts. Biological studies showed high cell viability (above 80%) after 24 h and 48 h incubation, spindle-like morphology, and no signs of damage (cells debris) [ 47 ]. Basar et al, who also conducted research on the same type of cells, reported a positive effect of the emulsion electrospun PCL/gelatin fibers containing ketoprofen on the viability ant phenotype of the L929 fibroblasts [ 42 ].…”
Emulsion electrospinning is a method of modifying a fibers’ surface and functional properties by encapsulation of the bioactive molecules. In our studies, bovine serum albumin (BSA) played the role of the modifier, and to protect the protein during the electrospinning process, the W/O (water-in-oil) emulsions were prepared, consisting of polymer and micelles formed from BSA and anionic (sodium dodecyl sulfate–S) or nonionic (Tween 80–T) surfactant. It was found that the micelle size distribution was strongly dependent on the nature and the amount of the surfactant, indicating that a higher concentration of the surfactant results in a higher tendency to form smaller micelles (4–9 µm for S and 8–13 µm for T). The appearance of anionic surfactant micelles reduced the diameter of the fiber (100–700 nm) and the wettability of the nonwoven surface (up to 77°) compared to un-modified PCL polymer fibers (100–900 nm and 130°). The use of a non-ionic surfactant resulted in better loading efficiency of micelles with albumin (about 90%), lower wettability of the nonwoven fabric (about 25°) and the formation of larger fibers (100–1100 nm). X-ray photoelectron spectroscopy (XPS) was used to detect the presence of the protein, and UV-Vis spectrophotometry was used to determine the loading efficiency and the nature of the release. The results showed that the location of the micelles influenced the release profiles of the protein, and the materials modified with micelles with the nonionic surfactant showed no burst release. The release kinetics was characteristic of the zero-order release model compared to anionic surfactants. The selected surfactant concentrations did not adversely affect the biological properties of fibrous substrates, such as high viability and low cytotoxicity of RAW macrophages 264.7.
“…The decrease in the viscosity of the T4 sample indicates a decrease in the interfacial energy between the droplets due to, for example, coalescence or flocculation. This decrease indirectly indicates that the emulsion started to lose stability [ 47 ]. One hour after preparation, this drop in viscosity is more likely to be due to the decomposition of the micelles than to the miscibility of the water and oil phases or the volume fraction of the water phase.…”
Section: Discussionmentioning
confidence: 99%
“…Akbarzadeh et al obtained PCL/PVA-GEL core/shell nanofibers, which induced adhesion of the L929 fibroblasts. Biological studies showed high cell viability (above 80%) after 24 h and 48 h incubation, spindle-like morphology, and no signs of damage (cells debris) [ 47 ]. Basar et al, who also conducted research on the same type of cells, reported a positive effect of the emulsion electrospun PCL/gelatin fibers containing ketoprofen on the viability ant phenotype of the L929 fibroblasts [ 42 ].…”
Emulsion electrospinning is a method of modifying a fibers’ surface and functional properties by encapsulation of the bioactive molecules. In our studies, bovine serum albumin (BSA) played the role of the modifier, and to protect the protein during the electrospinning process, the W/O (water-in-oil) emulsions were prepared, consisting of polymer and micelles formed from BSA and anionic (sodium dodecyl sulfate–S) or nonionic (Tween 80–T) surfactant. It was found that the micelle size distribution was strongly dependent on the nature and the amount of the surfactant, indicating that a higher concentration of the surfactant results in a higher tendency to form smaller micelles (4–9 µm for S and 8–13 µm for T). The appearance of anionic surfactant micelles reduced the diameter of the fiber (100–700 nm) and the wettability of the nonwoven surface (up to 77°) compared to un-modified PCL polymer fibers (100–900 nm and 130°). The use of a non-ionic surfactant resulted in better loading efficiency of micelles with albumin (about 90%), lower wettability of the nonwoven fabric (about 25°) and the formation of larger fibers (100–1100 nm). X-ray photoelectron spectroscopy (XPS) was used to detect the presence of the protein, and UV-Vis spectrophotometry was used to determine the loading efficiency and the nature of the release. The results showed that the location of the micelles influenced the release profiles of the protein, and the materials modified with micelles with the nonionic surfactant showed no burst release. The release kinetics was characteristic of the zero-order release model compared to anionic surfactants. The selected surfactant concentrations did not adversely affect the biological properties of fibrous substrates, such as high viability and low cytotoxicity of RAW macrophages 264.7.
“…The porosity of DPS was determined using the liquid displacement technique [27]. The scaffold (W d , dry weight) was submerged in ethanol for 30 min and the weight of wet samples was calculated W 1 .…”
Skin injuries lead to a large burden of morbidity. Although numerous clinical and scientific strategies have been investigated to repair injured skin, optimal regeneration therapy still poses a considerable obstacle. To address this challenge, the decellularized extracellular matrix-based scaffolds recellularized with stem cells offer significant advancements in skin regeneration and wound healing. Herein, a decellularized human placental sponge (DPS) was fabricated using the decellularization and freeze-drying technique, and then re-cellularized with human adipose-derived mesenchymal cells (MSCs). The biological and biomechanical properties and skin full-thickness wound healing capacity of the stem cells-DPS constructs were investigated in vitro and in vivo. The DPS exhibited a uniform three-dimensional microstructure with an interconnected pore network, 89.21% porosity, a low degradation rate, and good mechanical properties. The DPS and MSCs-DPS constructs were implanted in skin full-thickness wound models in mice. An accelerated wound healing was observed in the wounds implanted with MSCs-DPS construct when compared to DPS and control (wounds with no treatment) during 7 and 21 days post-implantation follow-up. In the MSCs-DPS group, the wound was completely re-epithelialized, the epidermis layer was properly organized, and the dermis and epidermis' bilayer structures were restored after 7 days. Our findings suggest DPS is an excellent carrier for MSCs culture and delivery to skin wounds and now promises to proceed with clinical evaluations.
“…PCL has also been combined with various polymers to create blended fibrous scaffolds with enhanced mechanical properties and cell attachment capabilities. Akbarzadeh et al fabricated a biphasic fibrous matrix composed of PCL, PVA and gelatin which demonstrated fibroblast interaction and enhanced cell proliferation within 24 hours [441] whilst Ghasemkhah et al developed gelatin/PCL scaffolds which proved to be promising protein delivery systems to aid in the tissue regeneration process [442].…”
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