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As spider silks have extraordinary mechanical properties, the design of high-performance artificial silk fibers has been one of the focuses in the field of biomimetic fibers. Cellulose nanofibers (CNFs) have considerable potential being an effective reinforcing agent in biocompatible composites because of their high aspect ratio, good stiffness of the crystalline regions, and biocompatibility. In this study, regenerated silk fibroin (RSF)/CNF hybrid fibers were dry-spun through a microfluidic chip, which mimicked the shape of spider’s major ampullate gland. The results showed that the presence of CNF can substantially enhance the mechanical properties of RSF. In specific, the breaking strength of the RSF/CNF fibers with 0.1 wt % CNF was increased to 486 ± 106 MPa with a maximum value of 686 MPa, significantly higher than that of silk fibers from silkworm. The enhancement could be attributed to higher orientation of crystalline and mesophase contents, higher crystallinity, and hydrogen bonds linked between RSF and CNF. This study outlined a simple and environmentally friendly pathway to generate artificial silks with high-performance properties.

The flax and equivalent proportion of poly(l‐lactic acid)/poly(d‐lactic acid) (PLLA/PDLA) were melt compounded and injection molded to prepare flax‐reinforced polylactide stereocomplex (sc‐PLA) bio‐composite, and the effect of alkali treatment on the structure and properties of flax as well as the flax/sc‐PLA composite was investigated. SEM and FTIR results showed hemicellulose in flax was almost completely removed after alkali treatment and the treated flax (ALK‐flax) bundles were more separated with a cleaner surface than untreated flax (UN‐flax). DSC results showed homo‐crystallites (hc, Tm = 160–170°C) and stereocomplex crystallites (sc, Tm ∼210°C) coexisted in sc‐PLA and flax/sc‐PLA composites. Compared with sc‐PLA, the total crystallinity and sc‐crystallinity of flax/sc‐PLA composite increased regardless of whether the flax were treated with alkali, whereas ALK‐flax/sc‐PLA composite showed a little higher crystallinity than UN‐flax/sc‐PLA composite. TGA results confirmed ALK‐flax/sc‐PLA composite had a higher thermal degradation temperature than UN‐flax/sc‐PLA composite. The mechanical tests indicated although the mechanical properties of sc‐PLA increased significantly by reinforcing with flax, the ALK‐flax/sc‐PLA composite showed little lower mechanical properties than UN‐flax/sc‐PLA composite. The alkali treatment of flax had no obvious influence on the Vicat softening temperature (VST) of flax/sc‐PLA composites, a higher heat resistance with VST at ∼155°C could be obtained for flax/sc‐PLA composite. POLYM. ENG. SCI., 55:2553–2558, 2015. © 2015 Society of Plastics Engineers

A novel biomaterial ink consisting of regenerated silk fibroin (SF) and 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized bacterial cellulose (OBC) nanofibrils was developed for 3D printing lung tissue scaffold. Silk fibroin backbones were cross-linked using horseradish peroxide/H 2 O 2 to form printed hydrogel scaffolds. OBC with a concentration of 7wt% increased the viscosity of inks during the printing process and further improved the shape fidelity of the scaffolds. Rheological measurements and image analyses were performed to evaluate inks printability and print shape fidelity. Three-dimensional construct with ten layers could be printed with ink of 1SF-2OBC (SF/OBC = 1/2, w/w). The composite hydrogel of 1SF-1OBC (SF/OBC = 1/1, w/w) printed at 25 °C exhibited a significantly improved compressive strength of 267 ± 13 kPa and a compressive stiffness of 325 ± 14 kPa at 30% strain, respectively. The optimized printing parameters for 1SF-1OBC were 0.3 bar of printing pressure, 45 mm/s of printing speed and 410 μm of nozzle diameter. Furthermore, OBC nanofibrils could be induced to align along the print lines over 60% degree of orientation, which were analyzed by SEM and X-ray diffraction. The orientation of OBC nanofibrils along print lines provided physical cues for guiding the orientation of lung epithelial stem cells, which maintained the ability to proliferate and kept epithelial phenotype after 7 days’ culture. The 3D printed SF-OBC scaffolds are promising for applications in lung tissue engineering. Electronic supplementary material The online version of this article (10.1007/s10570-020-03526-7) contains supplementary material, which is available to authorized users.

SummaryThe enantiomers poly(D-lactic acid) (PDLA) and poly(L-lactic acid) (PLLA) were alternately adsorbed directly on calcium carbonate (CaCO3) templates and on poly(styrene sulfonate) (PSS) and poly(allylamine hydrochloride) (PAH) multilayer precursors in order to fabricate a novel layer-by-layer (LBL) assembly. A single layer of poly(L-lysine) (PLL) was used as a linker between the (PDLA/PLLA)n stereocomplex and the cores with and without the polymeric (PSS/PAH)n/PLL multilayer precursor (PEM). Nuclear magnetic resonance (NMR) and gel permeation chromatography (GPC) were used to characterize the chemical composition and molecular weight of poly(lactic acid) polymers. Both multilayer structures, with and without polymeric precursor, were firstly fabricated and characterized on planar supports. A quartz crystal microbalance (QCM), attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and ellipsometry were used to evaluate the thickness and mass of the multilayers. Then, hollow, spherical microcapsules were obtained by the removal of the CaCO3 sacrificial template. The chemical composition of the obtained microcapsules was confirmed by differential scanning calorimetry (DSC) and wide X-ray diffraction (WXRD) analyses. The microcapsule morphology was evaluated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) measurements. The experimental results confirm the successful fabrication of this innovative system, and its full biocompatibility makes it worthy of further characterization as a promising drug carrier for sustained release.

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The UV-excitable fluorescent poly(lactic acid) (PLA) fibers were spun by the traditional melt spinning process, and the effects of the fluorescent powder content (w(FP)) and draw ratio (DR) on the structure and properties of the fluorescent PLA fibers were investigated, respectively. The results showed that the emission spectra of fluorescent PLA fibers were peaked at 530 nm after UV excitation, indicating the PLA fibers would emit green light under UV light. With the increasing of w(FP), the relative fluorescence intensity of PLA fibers increased gradually, whereas more and larger protrusions were formed on the fiber surface due to the agglomeration of fluorescent powder, both the crystallinity and mechanical properties of fluorescent PLA fiber showed the decreasing trend with the increase of w(FP). With the increase of DR, the tensile strength of fluorescent PLA fibers increased gradually, whereas the relative fluorescence intensity of PLA fibers increased firstly and then decreased, and the highest fluorescence intensity was obtained when the

Three kinds of Lyocell fibers with different cross-sections including circular, H-shape, and Y-shape (abbreviated as O-, H-, and Y-Lyocell) were prepared by a dry-jet wet spinning method. The effects of cross-sectional shape on structure and properties of Lyocell fibers were evaluated. The results showed H-Lyocell and Y-Lyocell exhibited triangular and dumbbell cross-sections, respectively, due to die swell. Both non-roundness factor and crystallinity of different cross-sectional Lyocell fibers were in the order of H-Lyocell [ Y-Lyocell [ O-Lyocell. All cross-sectional Lyocell fibers showed similar values of fineness and tensile strength. The profiled Lyocell fibers were superior to circular Lyocell fibers in terms of luster, dyeing properties, and moisture regain. The dye uptake and fixation rate of Lyocell fibers were influenced by shape in the order H-Lyocell [ Y-Lyocell [ O-Lyocell; while for luster and moisture regain the order was Y-Lyocell [ H-Lyocell [ O-Lyocell. Profiled Lyocell fibers are expected to open broader prospects in different textile or composite fields due to their various advantages versus conventional circular Lyocell fibers.