The crystalline morphologies of electrospun random and aligned poly(ε-caprolactone) (PCL) nanofibers, obtained by a plate collector and a two-parallel-conductive-plate collector, respectively, were characterized by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), two-dimensional wide-angle X-ray diffraction (2D WAXD), and polarized Fourier transform infrared (polarized FTIR) spectroscopy. The fiber orientations and diameters of the aligned nanofibers were found to depend on the gap size of the collector, which was much larger than those previously reported, thus easing and improving sample handling and characterization. The degree of crystallinity of the aligned nanofibers was higher than that of their randomly aligned counterparts. The crystallites in the nanofibers were highly oriented along the nanofiber axis, as were the molecular chains. The estimated crystallite size suggested that a single nanofiber was composed of dozens of nanofibrils and that each nanofibril was further composed of crystallites along the nanofiber axis with an amorphous region of extended PCL molecular chains between neighboring crystallites.

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Particulate matter (PM) pollution poses a significant threat to human health. Air filtration is an effective way to eliminate PM pollution. In this study, nanofibers of polycarbonate (PC), a polymer that has been widely used in engineering due to its favorable properties, were obtained using the electrospinning technique and applied to filter PM. The results revealed that the PM is either intercepted by the nanofibers or captured on the surfaces of the fibers by inertial impaction or diffusion. The filtration efficiency of this PC membrane was higher than those of both polyvinyl alcohol (PVA) and polystyrene (PS) membranes with similar fibrous morphologies, suggesting that polarity is the most influential factor shaping the interaction of particles and fiber surfaces. Moreover, fiber diameter and membrane thickness also influence filtration efficiency by varying the odds that particles and fiber surfaces will meet.

Regulating cell migration dynamics is of significance in tissue engineering and regenerative medicine. A 3D scaffold was created to provide various topographies based on a poly­(ε-caprolactone) (PCL) self-induced nanohybrid shish-kebab structure, which consisted of aligned PCL nanofibers and spaced PCL crystal lamellae grown on the fibers. Electrospinning was applied followed by self-induced crystallization. The results resembled natural collagen fibrils in an extracellular matrix. This variable microstructure enabled control of cell adhesion and migration. The kebab size was controlled by initial PCL concentrations. The geometry of cells seeded on the fibers was less elongated, but the adhesion was more polarized with a higher nuclear shape index and faster migration speed. These results could aid in rapid endothelialization in tissue engineering.

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Soft tissue engineering has been seeking ways to mimic the natural extracellular microenvironment that allows cells to migrate and proliferate to regenerate new tissue. Therefore, the reconstruction of soft tissue requires a scaffold possessing the extracellular matrix (ECM)-mimicking fibrous structure and elastic property, which affect the cell functions and tissue regeneration. Herein, an effective method for fabricating nanofibrous hydrogel for soft tissue engineering is demonstrated using gelatin–hydroxyphenylpropionic acid (Gel–HPA) by electrospinning and enzymatic crosslinking. Gel–HPA fibrous hydrogel was prepared by crosslinking the electrospun fibers in ethanol-water solution with an optimized concentration of horseradish peroxidase (HRP) and H2O2. The prepared fibrous hydrogel held the soft and elastic mechanical property of hydrogels and the three-dimensional (3D) fibrous structure of electrospun fibers. It was proven that the hydrogel scaffolds were biocompatible, improving the cellular adhesion, spreading, and proliferation. Moreover, the fibrous hydrogel showed rapid biodegradability and promoted angiogenesis in vivo. Overall, this study represents a novel biomimetic approach to generate Gel–HPA fibrous hydrogel scaffolds which have excellent potential in soft tissue regeneration applications.

This paper provides a method combining eco-friendly supercritical CO2 microcellular foaming and polymer leaching to fabricate small-diameter vascular tissue engineering scaffolds.

Biodegradable and bioabsorbable polymers have drawn considerable attention because of their mechanical properties that mimic human soft tissue. Poly(l-lactide-co-ε-caprolactone) (PLCL), the copolymer of L-lactic (LA) and ε-caprolactone (CL), has been applied in many tissue engineering and regenerative medicine fields. However, both the synthesis of PLCL and the structure-activity relationship of the copolymer need to be further investigated to allow tuning of different mechanical properties. The synthesis conditions of PLCL were optimized to increase the yield and improve the copolymer properties. The synthetic process was evaluated by while varying the molar ratio of the monomers and polymerization time. The mechanical properties of the copolymer were investigated from the macroscopic and microscopic perspectives. Changes in the polymerization time and feed ratio resulted in the difference in the LA and CL content, which, in turn, caused the PLCL to exhibit different properties. The PLCL obtained with a feed ratio of 1:1 (LA:CL) and a polymerization time of 30 h has the best toughness and elasticity. The developed PLCL may have applications in dynamic mechanical environment, such as vascular tissue engineering.