Zn2+ @Polyvinylpyrrolidone and Urushiol Preparation of Nanofibrous Membranes and Their Synergistic Effect.

In this study, lacquer is gathered from a lacquer tree and rotary evaporation is used to remove impurities to obtain urushiol. Next, 10 mL of anhydrous ethanol serves as the solvent for blending polyvinylpyrrolidone (PVP) at a specified content (0.7 g and 0.2-0.7 g urushiol) to form an electrospinning solution. Electrospinning is carried out with a voltage of 18 kV to prepare PVP/urushiol nanofibrous membranes. At a ratio of 7/4, the PVP/urushiol nanofibrous membranes are not eroded in 98% sulfuric acid and these membranes also demonstrate a 50-60% antibacterial effect against Staphylococcus aureus and Escherichia coli. Moreover, the antibacterial effect can be boosted to 98% with the incorporation of zinc ions. The results indicate that anhydrous ethanol can remove the sensitization of urushiol from PVP/urushiol membranes. Furthermore, animal test results indicate that when rats are in contact with PVP/urushiol anhydrous ethanol for 48 h, their skins are free from dark brown skin allergy. The presence of PVP eliminates the sensitization of urushiol, and the nanofibrous membranes demonstrate low toxicity. Hence, urushiol is the only natural material that enables PVP to withstand 98% sulfuric acid as well as acquire hydrolyzability, thereby qualify PVP as a medical material.

Evaluation of Mechanical Properties of Porous Chitosan/Gelatin/Polycaprolactone Bone Scaffold Prepared by Microwave Foaming Method.

Bone tissue may suffer from bone injury and bone defects due to accidents or diseases. Since the demand for autologous bone and allograft tissue far exceeds the supply, bone scaffolds have taken the lead. The use of bone scaffolds is one of the measures to help heal or regenerate bone tissue. Therefore, a new bone scaffold was proposed in this study, which has a simpler preparation process and stronger performance. This study proposes bone scaffolds with an attempt to use polymers that are synthesized separately with three types of minerals as the filler using the microwave foaming method as follows. A 0.1 wt% of montmorillonite (MMT), zinc oxide (ZnO), or titanium dioxide (TiO2) is added to chitosan (CS)/gelatin mixtures, respectively, after which sodium bicarbonate is added as a foaming agent, thereby forming porous gels. The polymer synthesized from three minerals was used as filler. The following microwave foaming method was adopted: 0.1 wt% MMT, ZnO, or TiO2 was added to the CS/gelatin mixture, and then sodium bicarbonate was added as a foaming agent to form a porous gel. Next, porous gels and polycaprolactone were combined in a self-made mold in order to form bone scaffolds. A stereo microscope is used to observe the morphology of bone scaffolds, after which the pore size analysis, pore connectivity, swell property, porosity, and compressive strength are tested, examining the effects of the mineral type on bone scaffolds. The test results indicate that with MMT being the filler and sodium bicarbonate being the foaming agent, the resulting bone scaffolds yield a porous structure with a pore size between 120 µm and 370 µm. Besides, the incorporation of polycaprolactone also provides samples of 1MCG-P, 2MCG-P, and 5MCG-P with a certain compressive strength of 150-170 MPa. To sum up, the test results substantiate that a combination of the microwave foaming method and MMT generates a porous structure for bone scaffolds (1MCG-P, 2MCG-P, and 5MCG-P), involving a porosity of 38%, an inter-connected porous structure, and the compressive strength that exceeds 150 MPa.

Preparation and Characterization of PEDOT:PSS/TiO2 Micro/Nanofiber-Based Gas Sensors.

In this study, we employed electrospinning technology and in situ polymerization to prepare wearable and highly sensitive PVP/PEDOT:PSS/TiO2 micro/nanofiber gas sensors. PEDOT, PEDOT:PSS, and TiO2 were prepared via in situ polymerization and tested for characteristic peaks using energy-dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FT-IR), then characterized using a scanning electron microscope (SEM), a four-point probe resistance measurement, and a gas sensor test system. The gas sensitivity was 3.46-12.06% when ethanol with a concentration between 12.5 ppm and 6250 ppm was measured; 625 ppm of ethanol was used in the gas sensitivity measurements for the PEDOT/composite conductive woven fabrics, PVP/PEDOT:PSS nanofiber membranes, and PVP/PEDOT:PSS/TiO2 micro/nanofiber gas sensors. The latter exhibited the highest gas sensitivity, which was 5.52% and 2.35% greater than that of the PEDOT/composite conductive woven fabrics and PVP/PEDOT:PSS nanofiber membranes, respectively. In addition, the influence of relative humidity on the performance of the PVP/PEDOT:PSS/TiO2 micro/nanofiber gas sensors was examined. The electrical sensitivity decreased with a decrease in ethanol concentration. The gas sensitivity exhibited a linear relationship with relative humidity lower than 75%; however, when the relative humidity was higher than 75%, the gas sensitivity showed a highly non-linear correlation. The test results indicated that the PVP/PEDOT:PSS/TiO2 micro/nanofiber gas sensors were flexible and highly sensitive to gas, qualifying them for use as a wearable gas sensor platform at room temperature. The proposed gas sensors demonstrated vital functions and an innovative design for the development of a smart wearable device.