In this study, composite nanofibers (SF/PCL/CS) for the application of dressings were prepared with silk fibroin (SF), polycaprolactone (PCL), and chitosan (CS) by electrospinning techniques, and the effect of the fiber diameter was investigated using the three-stage Taguchi experimental design method (L9). Nanofibrous scaffolds were characterized by the combined techniques of scanning electron microscopy (SEM) and transmission electron microscopy (TEM), a cytotoxicity test, proliferation tests, the antimicrobial activity, and the equilibrium water content. A signal-to-noise ratio (S/N) analysis indicated that the contribution followed the order of SF to PCL > flow rate > applied voltage > CS addition, possibly owing to the viscosity and formation of the beaded fiber. The optimum combination for obtaining the smallest fiber diameter (170 nm) with a smooth and uniform distribution was determined to be a ratio of SF to PCL of 1:2, a flow rate of 0.3 mL/hr, and an applied voltage of 25 kV at a needle tip-to-collector distance of 15 cm (position). The viability of these mouse fibroblast L929 cell cultures exceeded 50% within 24 hours, therefore SF/PCL/CS could be considered non-toxic according to the standards. The results proposed that the hydrophilic structure of SF/PCL/CS not only revealed a highly interconnected porous construction but also that it could help cells promote the exchange of nutrients and oxygen. The SF/PCL/CS scaffold showed a high interconnectivity between pores and porosity and water uptake abilities able to provide good conditions for cell infiltration and proliferation. The results from this study suggested that SF/PCL/CS could be suitable for skin tissue engineering.

Toxic organic solvent residues and the active substances of thermal degradation (such as anthocyanin and polyphenols) are always a concern with the liposomes produced by traditional techniques. The present study focuses on a new approach for the microencapsulation of Clitoria ternatea petal (CTP) extracts, which contain anthocyanins, by high-pressure processing (HPP) at room temperature. Thus, a series of CTP liposomes were prepared and their physicochemical properties were analyzed by laser granulometry and by scanning electron microscopy (SEM). The results revealed that the average particle size of the liposomes after HPP treatment increased gradually from 300 MPa to 600 MPa, possibly due to the aggregation of liposomes and damage to the phospholipid bilayers. For the preparation of liposomes by the HPP method at 300 MPa, the mean particle size, polydispersity index (PDI), and encapsulation efficiency were 240.7 nm, 0.37, and 77.8%, respectively. The HPP method provided a number of advantages over conventional methods (magnet stirring and ultrasonication) as it could allow liposome preparation with higher encapsulation efficiency, smaller size, and narrower, more reproducible particle size distribution. Conclusively, microencapsulation in the liposomes was successfully achieved with the fast-adiabatic expansion of HPP.

A typical emulsion contains oil and water phases, and these two phases can be combined by an emulsifier with both lipophilic and hydrophilic groups to form a mixture. If the component of water is more than oil, the mixture is termed as o/w emulsion. The water is called the continuous phase and the oil is called the dispersed phase. Oppositely, if the component of oil is more than water, the mixture is termed as w/o emulsion. The oil is called the continuous phase and the water is called the dispersed phase. Chitosan, which is biocompatible and non-toxic, was modified as an amphoteric emulsifier to replace sodium acrylates copolymer in the preparation of emulsions. Both sodium acrylates copolymer and the modified chitosan were used as emulsifiers, respectively, and the properties of moisturizing, transmittance, the number of bacteria, and emulsion stability were measured. The experimental results showed that the amount of amphoteric chitosan is less than that of sodium acrylate copolymer by 20% under a similar degree of emulsification. The measurement of spatial moisture showed the difference in equilibrium humidity was in the range of 2.05 to 2.20 gH2O/kg dry air, indicating that the moisture retention of the modified chitosan is better. In addition, the calculation of bacterial growth confirmed that the number of bacteria in the amphoteric chitosan emulsion and the sodium acrylate copolymer emulsion were 80 and 560, respectively. The emulsion stability was tested by the separation of oil and water phases in the diluted emulsion and by centrifugal accelerated sedimentation. The results showed that, for both emulsifiers, no separation of the oil and water phases occurred within one hour, and the stability of the modified chitosan emulsion was better. Therefore, the modified chitosan successfully substitutes sodium acrylates copolymer as an emulsifier in the preparation of emulsion.