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Hierarchical porous carbon arrays (HPCAs) are facilely produced by directly carbonizing Carex meyeriana through a self-activated and self-template process. The morphology analysis and nitrogen sorption measurements reveal that the obtained HPCAs have a large specific surface area and unique hierarchical pore structure comprising macropore channel arrays and micropores and mesopores developed on the wall of macropore channels. The HPCA electrodes are subsequently prepared by depositing HPCAs to the fluorine-doped tin oxide conductive substrate. Electrochemical tests demonstrate that the HPCA electrode shows a superior electrocatalytic activity for the regeneration of the I–/I3– electrolyte. The superior electrocatalytic activity of HPCA electrodes is mainly due to the combined effect of unique hierarchical pore architecture and large surface area, which facilitates the electrolyte diffusion and provides the abundant effective electrocatalytic active sites. Under 1 sun illumination, the HPCA electrode-based dye-sensitized solar cell displays a gratifying conversion efficiency of 6.45%, which is close to that based on commonly used Pt electrodes.

To meet the increased performance and cost requirements of commercial supercapacitor, a N and O self-doped hierarchical porous carbon is fabricated via a green and simple self-activation route utilizing leaves of wild hollyhock as raw materials. Comparing to commercial activated carbon, the reported material exhibits some marked merits, such as simple and green fabrication process, low cost, and superior capacitance performance. The specific surface area of the obtained N and O co-doped hierarchical porous carbon arrives 954 m2 g−1, and the content of the self-doped nitrogen and oxygen reaches 2.64 at.% and 7.38 at.%, respectively. The specific capacitance of the obtained material reaches 226 F g−1 while the specific capacitance of the symmetric supercapacitor arrives 47.3 F g−1. Meanwhile, more than 90.3% of initial specific capacitance is kept under a current density of 20 A g−1, and no arresting degradation is observed for capacitance after 5000 times cycle, perfectly demonstrating the excellent cycle and rate capability of the obtained material. The obtained N and O co-doped hierarchical porous carbon are expected to be an ideal substitution for commercial activated carbon.

The construction of a biomaterial matrix with biological properties is of great importance to developing functional materials for clinical use. However, the site-specific immobilization of growth factors to endow materials with bioactivities has been a challenge to date. Considering the wide existence of glycosylation in mammalian proteins or recombinant proteins, we establish a bioaffinity-based protein immobilization strategy (bioanchoring method) utilizing the native sugar-lectin interaction between concanavalin A (Con A) and the oligosaccharide chain on glycosylated bone morphogenetic protein-2 (GBMP-2). The interaction realizes the site-specific immobilization of GBMP-2 to a substrate modified with Con A while preserving its bioactivity in a sustained and highly efficient way, as evidenced by its enhanced ability to induce osteodifferentiation compared with that of the soluble GBMP-2. Moreover, the surface with Con A-bioanchored GBMP-2 can be reused to stimulate multiple batches of C2C12 cells to differentiate almost to the same degree. Even after 4 month storage at 4 °C in phosphate-buffered saline (PBS), the Con A-bioanchored GBMP-2 still maintains the bioactivity to stimulate the differentiation of C2C12 cells. Furthermore, the ectopic ossification test proves the in vivo bioactivity of bioanchored GBMP-2. Overall, our results demonstrate that the tag-free and site (i.e., sugar chain)-specific protein immobilization strategy represents a simple and generic alternative, which is promising to apply for other glycoprotein immobilization and application. It should be noted that although the lectin we utilized can only bind to d-mannose/d-glucose, the diversity of the lectin family assures that a specific lectin could be offered for other sugar types, thus expanding the applicable scope further.

Microbial disinfection associated with medical device surfaces has been an increasing need, and surface modification strategies such as antibacterial coatings have gained great interest. Here, we report the development of polydopamine-ferrocene (PDA-Fc)-functionalized TiO2 nanorods (Ti-Nd-PDA-Fc) as a context-dependent antibacterial system on implant to combat bacterial infection and hinder biofilm formation. In this work, two synergistic antimicrobial mechanisms of the PDA-Fc coating are proposed. First, the PDA-Fc coating is redox-active and can be locally activated to release antibacterial reactive oxygen species (ROS), especially ·OH in response to the acidic microenvironment induced by bacteria colonization and host immune responses. The results demonstrate that redox-based antimicrobial activity of Ti-Nd-PDA-Fc offers antibacterial efficacy of over 95 and 92% against methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli), respectively. Second, the photothermal effect of PDA can enhance the antibacterial capability upon near-infrared (NIR) irradiation, with over 99% killing efficacy against MRSA and E. coli, and even suppress the formation of biofilm through both localized hyperthermia and enhanced ·OH generation. Additionally, Ti-Nd-PDA-Fc is biocompatible when tested with model pre-osteoblast MC-3T3 E1 cells and promotes cell adhesion and spreading presumably due to its nanotopographical features. The MRSA-infected wound model also indicates that Ti-Nd-PDA-Fc with NIR irradiation can effectively eliminate bacterial infection and suppress host inflammatory responses. We believe that this study demonstrates a simple means to create biocompatible redox-active coatings that confer context-dependent antibacterial activities to implant surfaces.

Casticin has wide-ranging functional activities, but its water solubility is poor in food products. Here, a nanoemulsion stabilized by Maillard whey protein isolate conjugates (MWPI) was fabricated to encapsulate casticin. The nanoemulsion, with an average diameter of 200 nm, possessed the capability to load 700 μg/g casticin. MWPI-stabilized nanoemulsion showed better stability than that of the WPI nanoemulsion during 4 weeks of storage. Both the inhibition effects of the casticin-loaded nanoemulsion on cancer cells and the process of cellular uptake were studied. Results revealed that the casticin-loaded nanoemulsion had better inhibitory activity in HepG2 and MCF-7 cells than free casticin. Cellular uptake of the nanoemulsion displayed a time-dependent manner. After the nanoemulsion passed into HepG2 and MCF-7 cells, it would locate in the lysosome but not in the nucleus. The main pathway for the nanoemulsion to enter HepG2 cells was pinocytosis, whereas, it entered MCF-7 predominantly through the clathrin-mediated pit. This work implies that MWPI-stabilized nanoemulsions could be utilized as an effective delivery system to load casticin and have the potential to be applied in the food and pharmaceutical industries.

Hemp fiber, as a kind of renewable textile fiber, has evoked much interest due to its excellent properties in various fields. It has been investigated in just one step to finish the process of chemo-enzymatic degumming and modification of hemp fiber, which is done in acetic acidsodium acetate buffer solution containing laccase (6.0 g), hemicellulase (0.3 g) and 2,2,6,6-tetramethylpiperidine-1-oxyl radical (0.3 g) under a mild condition (pH 5, 50C). The degumming effects of different batches of raw hemp fibers were also discussed. We found that the residual rate, fineness, length and tensile strength of degummed fiber were 15–27%, 9.00–24.00 dtex, 14.00–19.00 cm and 3.8–5.1 cN/dtex, respectively. Meanwhile, some of the oxidized functional groups were introduced into degummed fiber, which improved the moisture absorption and water retention value of the hemp fiber. The hemp fiber treated by this process could be further improved and then applied in the textile industry.

In this study, we found an environmentally friendly system in the degumming of hemp fiber without using a strong acid and alkali. The chemo-enzymatic modification and degumming of hemp fiber used an acetic acid–sodium acetate buffer solution containing laccase, hemicellulase and 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO) under a mild condition (pH = 5, T = 50℃). Through comparing and analyzing the physical and chemical properties of fiber products under different treatments, we found the method involving treatment with TEMPO/laccase/hemicellulase not only greatly removed most of the gum attached on the surface of the raw hemp fiber, but also introduced surface-active aldehyde and carboxyl groups into the fiber. The performances of the hemp fibers with different treatments were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray diffraction. We also found the product was finer, with a lower content of non-cellulosic components and it had better water uptake properties (moisture sorption and water retention value), which has potential application values in textile industries.

Open wounds and burns are prone to infection and there remains considerable interest in developing safe and effective mechanisms to confer antimicrobial activities to wound dressings. We report a biomimetic wound dressing for the in situ and sustained generation of reactive oxygen species (ROS). Specifically, we fabricate a catechol-modified chitosan film that mimics features of the melanin capsule generated during an insect immune response to infection. We use an electrochemical reverse engineering approach to demonstrate that this catechol-chitosan film possesses redox-activities and can be repeatedly oxidized and reduced. In vitro tests demonstrate that this film catalyzes the transfer of electrons from physiological reductant ascorbate to O 2 for sustained ROS generation, and confers ascorbate-dependent antimicrobial activities. In vivo antimicrobial experiment with a rat subcutaneous model indicates the catechol-chitosan film at reduced state inhibits the bacterial growth and alleviates the infection of the incisions. Open wound healing tests with a mouse model indicate that the catechol-chitosan film suppresses the bacterial population at the wound site, induces less inflammation and promotes wound healing. We envision this biomimetic approach for the sustained, localized and in situ generation of ROS could provide new opportunities for wound management by protecting against pathogen infection and potentially even enlisting ROS-mediated wound healing mechanisms.

Ultra-high density large-sized Al:ZnO sputtering targets were prepared by hot isostatic pressing(HIP). Studies were conducted on the characteristics of the microstructure of the targets and the photoelectric properties of the deposited film prepared by medium-frequency magnetron sputtering. Experiments showed that, compared to 98% density target, HIP process had no apparent influence on the change of grain dimension of the targets. However, a reduction of the quantity and size of the porosities in the target matrix was recognized and led to an improvement in the uniformity of resistance and thickness and IR transmittance of the deposited film. In this paper, the favorable machining allowance associated to the thickness of the HIPed targets, due to the oxygen-loss layer, was suggested by developing the empirical formula.

All-inorganic CsPbIBr2 perovskite has been regarded as a promising candidate for perovskite solar cells (PSCs) considering its suitable bandgap and high stability. However, the poor quality of CsPbIBr2 film greatly impedes the performance improvement of CsPbIBr2-based PSCs. Herein, we report a facile strategy to improve the quality of CsPbIBr2 perovskite film by introducing cellulose acetate (CA) into the perovskite precursor solution. The interaction between the oxygen functional groups of CA and Pb2+ and the increase of the precursor viscosity induced by CA addition can slow down the crystallization rate of CsPbIBr2 perovskite, which allows the perovskite films have enough time to form high-quality crystal structure. By optimizing the amount of CA (the optimal amount of CA is 2.5 wt%), a high-quality CsPbIBr2 perovskite film with high crystallinity, large grain size, and smooth surface is obtained. As consequence, the carbon-based PSC with a structure of FTO/TiO2/perovskite/carbon using the CsPbIBr2 perovskite film with 2.5 wt% CA achieves a champion efficiency of 7.52%, which is increased by 40.8% compared with the cell based on pure CsPbIBr2 perovskite film. In addition, the PSC based on CsPbIBr2 film with CA exhibits an excellent long-term stability under both ambient condition and high-humidity environment.

Reported herein is a chiral resolution polysulfone membrane prepared via mussel-inspired chemistry. Polysulfone membranes were modified with dopamine, which underwent in situ polymerization on the membrane substrate, and β-cyclodextrin was used as a chiral selector. The preparation conditions were optimized and the resultant membrane obtained under these conditions showed desirable water permeability (~ 24.0 L/(m 2 ·h·bar)) and surface hydrophilicity (contact angle is lower than 37.1 ± 3.4°). The polydopamine layer exhibited desirable stability in a series of aqueous solutions with pH values ranging from 4.0–6.0 or in isopropanol for less than an hour (detachment ratio was lower than 1.2%). Characterization of the surface morphology and XPS elemental analysis revealed that the membrane surface was fully coated by polydopamine and a β-cyclodextrin monolayer formed on the surface of the polydopamine coating. The grafting density of β-cyclodextrin calculated from the XPS results was ~ 11.5 mg/m 2 . The optimal pH value for the resolution of D - or L -tryptophan feed solution was 5.90 and a low concentration of the feed solution provided a high resolution efficiency. The enantiomeric excess (e.e.) value of the membrane for Trp racemic mixture achieved to ~ 3.2% with the feed solution of tryptophan racemic mixture was 5 × 10 − 5 mol/L and the operating pressure was 0.1 MPa. After 3 times of isopropanol-washed regeneration processes, the e.e. value was still stable around to ~ 3%. The mussel-inspired chemically modified membrane exhibited the same mechanical properties as the purely polysulfone-based membrane. The methods and results provided in this paper may facilitate the large-scale production of chiral resolution membranes or other chiral separation membranes with higher performance.

A novel multifunctional amphiphilic graft copolymer has been synthesized consisting of a biodegradable poly(l-aspartic acid) backbone that was decorated by water-soluble poly(ethylene glycol) (PEG) and pH-responsive poly(N,N-diethylaminoethyl methacrylate) (PDEAEMA) side-chains as well as thiol pendant groups. This graft copolymer together with doxorubicin (DOX) formed micelles in water at pH = 10.0 with PDEAEMA and DOX acting as the core and PEG serving as the micellar corona. Upon oxidation, the thiol groups dimerized to form disulfide bonds, thus “locking in” the micellar structure. These crosslinked micelles expanded as the pH was decreased from 7.4 to 5.0 or upon the addition, at pH = 7.4, of glutathione (GSH), a thiol-containing oligopeptide that is present in cancerous cells and cleaves disulfide bonds. At pH = 5.0, GSH addition triggered the disassembly of the micelles. The expansion and disassembly of the micelles have been determined via in vitro experiments to evaluate their DOX release behavior. More importantly, the graft copolymer micelles could enter cells by means of endocytosis and deliver DOX to the nuclei of ovarian cancer BEL-7402 cells. Thus, this polymer and its micelles are promising candidates for drug delivery applications. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 1536–1546

Considerable interest has been devoted to developing nanoscale biomass materials as adsorbents for wastewater treatment. A facile route was proposed to prepare cellulose-based composite nanofibers via electrospinning of cellulose acetate with organically modified montmorillonite, followed by deacetylation. The composite nanofibers are suitable for metal adsorption given their reasonably high selectivity in removing Cr 6+ ions from aqueous solution. The effects of experimental parameters, including solution pH, temperature, and contact time, on the removal of Cr 6+ ions were determined in a batch system to optimize the adsorption conditions. Results from this study may provide a promising biosorbent that can be used as an emerging material in large-scale adsorption of heavy metal ions.

Photothermal therapy (PTT) that utilizes phSUPPotothermal conversion agents (PTC) to ablate tumor under NIR light irradiation has attracted increasing attention due to its excellent therapeutic efficacy and improved target selectivity. Herein, a novel core-shell nanoparticle based on disulfide-crosslinked poly(methacrylic acid) (PMAA) layer coated polydopamine (PDA) particle has been successfully synthesized by precipitation polymerization. For these PDA@PMAA composite nanoparticles, PDA core exhibits high photothermal efficacy, meanwhile, the redox-labile PMAA shell serves as carriers to encapsulate anticancer drugs and selectively release them. Due to the characteristic of the disulfide bond, PMAA shell occurs at selective degradation as well as controlled drug release upon entering cancer cells. Moreover, the DOX-loaded PDA@PMAA nanoparticles demonstrated a synergistic effect, which shows a significantly improved inhibition effect against cancer cells by the combination of photothermal therapy and traditional chemotherapy with low drug dosage and short laser irradiation in an in vitro study. Electronic supplementary material The online version of this article (10.1186/s11671-019-3027-6) contains supplementary material, which is available to authorized users.

Polydopamine (PDA) is a bioinspired material and coating that offers diverse functional activities (e.g., photothermal, antioxidant, and antimicrobial) for a broad range of applications. Although PDA is reported to be redox active, the association between PDA's redox state and its functional performance has been difficult to discern because of PDA's complex structure and limitations in methods to characterize redox-based functions. Here, we use an electrochemical reverse engineering approach to confirm that PDA is redox-active and can repeatedly accept and donate electrons. We observed that the electron-donating ability of PDA offers the detrimental pro-oxidant effect of donating electrons to O2 to generate reactive oxygen species (ROS) or, alternatively, the beneficial antioxidant effect of quenching oxidative free radicals. Importantly, PDA's electron-donating ability depends on its redox state and is strongly influenced by external factors including metal ion binding as well as near-infrared (NIR) irradiation. Furthermore, we demonstrated that PDA possesses redox state-dependent antimicrobial properties in vitro and in vivo. We envision that clarification of PDA's redox activity will enable better understanding of PDA's context-dependent properties (e.g., antioxidant and pro-oxidant) and provide new insights for further applications of PDA. STATEMENT OF SIGNIFICANCE: We believe this is the first report to characterize the redox activities of polydopamine (PDA) and to relate these redox activities to functional properties important for various proposed applications of PDA. We observed that polydopamine nanoparticles 1) are redox-active; 2) can repeatedly donate and accept electrons; 3) can accept electrons from reducing agents (e.g., ascorbate), donate electrons to O2 to generate ROS, and donate electrons to free radicals to quench them; 4) have redox state-dependent electron-donating abilities that are strongly influenced by metal ion binding as well as NIR irradiation; and 5) have redox state-dependent antimicrobial activities.

Membrane separation is recognized as one of the most effective strategies to treat the complicated wastewater system for economic development. However, serious membrane fouling has restricted its further application. Inspired by sphagnum, a 0D/2D heterojunction composite membrane is engineered by depositing graphitic carbon nitride nano/microspheres (CNMS) with plentiful wrinkles onto the polyacrylic acid functionalized carbon nanotubes (CNTs-PAA) membrane through hydrogen bond force. Through coupling unique structure and chemistry properties, the CNTs-PAA/CNMS heterojunction membrane presents superhydrophilicity and underwater superoleophobicity. Furthermore, thanks to the J-type aggregates during the solvothermal process, it is provided with a smaller bandgap (1.77 eV) than the traditional graphitic carbon nitride (g-C3 N4 ) sheets-based membranes (2.4-2.8 eV). This feature endows the CNTs-PAA/CNMS membrane with superior visible-light-driven self-cleaning ability, which can maintain its excellent emulsion separation (with a maximum flux of 5557 ± 331 L m-2 h-1 bar-1 and an efficiency of 98.5 ± 0.6%), photocatalytic degradation (with an efficiency of 99.7 ± 0.2%), and antibacterial (with an efficiency of ≈100%) ability even after cyclic experimental processes. The excellent self-cleaning performance of this all-in-one membrane represents its potential value for water purification.

Uniaxially aligned cellulose nanofibers (CNFs), which are fabricated by electrospinning of cellulose acetate derived from bamboo cellulose (B-CA) followed by deacetylation, were used as reinforcements to make optically transparent composite films. We examined the effects of B-CA concentration and electrospinning parameters (e.g. spinning distance, and collection speed) on fiber morphology and orientation, which act on mechanical-to-optical properties of the CNFs-reinforced composites. Consequently, the resultant composite film exhibits high visible-light transmittance even with high fiber content, as well as improved mechanical properties. The understanding obtained from this study may facilitate the development of novel nanofibrous materials for various optical uses.

A ternary system thermoresponsive hydrogel, poly(N-isopropylacrylamide-co-hydroxyethyl methylacrylate polycaprolactone)/hydroxypropyl cellulose (or P(NIPAAm-co-HEMAPCL)/HPC), was prepared via "alkynyl/azide" click chemistry between the azide modified graft copolymer P(NIPAAm-co-HEMAPCL-N3) and the alkynyl modified HPC (or alkynyl-HPC). The structures of P(NIPAAm-co-HEMAPCL-N3) and alkynyl-HPC were characterized by (1)H NMR, SEC and FT-IR, and the results demonstrated that the mole ratio of the alkynyl and azide functional groups, and the feed ratios of HPC, PCL, and PNIPAAm could be easily adjusted. The incorporation of PCL and HPC dramatically enhanced the compression modulus of the P(NIPAAm-co-HEMAPCL)/HPC hydrogel, which ranged from 500 to 1000 g/cm(2). Due to the immiscibility of HPC and PCL, a heterogeneous and semicontinuous structure was observed via SEM. The incorporation of HPC accelerated the water absorption rate and enhanced the hydrogel's ability to shed water. The swelling-deswelling and compressive properties could also be adjusted by changing the feeding ratio. The hydrogel exhibited reversible swelling-deswelling behavior after three "swelling-deswelling" cycles.

Cellulose acetate derived from bamboo cellulose (B-CA) was prepared via a typical acetylation process and used to fabricate the aligned electrospun nanofibrous membranes (ENMs). A solvent post-treatment by soaking the B-CA ENMs in a mixture solution with different ethanol/acetone volume ratios was also performed to improve the mechanical properties of the membranes. In this study, we showed that this approach can enhance the bonding in the fiber membranes by solvent-induced fusion of inter-fiber junction points and change the degree of molecular orientation of the polymer, which are both considered to have important influences on the mechanical properties of ENMs. The treated membranes exhibited a significant enhancement in mechanical strength while retaining high hydraulic permeability. Increased performances will improve the prospects of ENMs as an emerging material in the filtration space for handling and scale-up manufacturing.

Carbon-based CsPbIBr2 inorganic perovskite solar cells (PSCs) have emerged as one of the most promising photovoltaic devices owing to their excellent stability and simple fabrication process. Nevertheless, the efficiency of state-of-the-art carbon-based CsPbIBr2 PSCs is far from satisfactory due to the poor quality of CsPbIBr2 perovskite film. Herein, we prepare the high-quality CsPbIBr2 perovskite film through a one-step spin-coating method by optimizing both the substrate pre-heating temperature and the post-annealing temperature. The optimization of the substrate pre-heating and post-annealing temperatures greatly improves the coverage and crystallinity of CsPbIBr2 perovskite films, leading to enhanced light harvest and suppressed charge recombination. With the CsPbIBr2 perovskite film prepared at the optimized substrate pre-heating and post-annealing temperatures, the fabricated carbon-based CsPbIBr2 PSC with a simple structure of FTO/TiO2/CsPbIBr2/carbon exhibits a gratifying conversion efficiency of 8.10% with a high open-circuit voltage of 1.27 V. Moreover, the fabricated carbon-based CsPbIBr2 PSC without any encapsulation shows an excellent long-term stability under ambient condition.

Herein, graphene nanoplatelets (GNPs) are incorporated into carbon electrode to fabricate carbon-based CsPbBr3 inorganic PSCs with the FTO/TiO2/CsPbBr3/carbon configuration. Steady-state photoluminescence and electrochemical impedance spectroscopy measurements indicate that the incorporation of GNPs into carbon electrode remarkably enhances the hole extraction and decreases the interfacial charge recombination in carbon-based PSCs compared with unincorporated one. Consequently, the CsPbBr3 PSC with GNP (33.3 wt%)-incorporated electrode exhibits much higher photovoltaic performance than the device with pristine carbon electrode with the efficiency being increased from 4.84% to 6.48%. In addition, the excellent long-term stability of PSC with carbon electrode is also measured under ambient condition.

Electrical signals can be imposed with exquisite spatiotemporal control and provide exciting opportunities to create structure and confer function. Here, we report the use of electrical signals to program the fabrication of a chloramine wound dressing with high antimicrobial activity. This method involves two electrofabrication steps: (i) a cathodic electrodeposition of an aminopolysaccharide chitosan triggered by a localized region of high pH; and (ii) an anodic chlorination of the deposited film in the presence of chloride. This electrofabrication process is completed within several minutes and the chlorinated chitosan can be peeled from the electrode to yield a free-standing film. The presence of active N Cl species in this electrofabricated film was confirmed with chlorination occurring first on the amine groups and then on the amide groups when large anodic charges were used. Electrofabrication is quantitatively controllable as the cathodic input controls film growth during deposition and the anodic input controls film chlorination. In vitro studies demonstrate that the chlorinated chitosan film has antimicrobial activities that depend on the chlorination degree. In vivo studies with a MRSA infected wound healing model indicate that the chlorinated chitosan film inhibited bacterial growth, induced less inflammation, developed reorganized epithelial and dermis structures, and thus promoted wound healing compared to a bare wound or wound treated with unmodified chitosan. These results demonstrate the fabrication of advanced functional materials (i.e., antimicrobial wound dressings) using controllable electrical signals to both organize structure through non-covalent interactions (i.e., induce chitosan’s reversible self-assembly) and to initiate function-conferring covalent modifications (i.e., generate chloramine bonds). Potentially, electrofabrication may provide a simple, low cost and sustainable alternative for materials fabrication. Statement of Significance We believe this work is novel because this is the first report (to our knowledge) that electronic signals enable the fabrication of advanced antimicrobial dressings with controlled structure and biological performance. We believe this work is significant because electrofabrication enables rapid, controllable and sustainable materials construction with reduced adverse environmental impacts while generating high performance materials for healthcare applications. More specifically, we report an electrofbrication of antimicrobial film that can promote wound healing.

Wound dressings play important roles in the management of wounds, and calcium cross-linked alginate (Ca2+-Alg) is a commonly used hydrogel that is adapted for wound treatment. However, conventional methods for fabricating Ca2+-Alg hydrogels can be tedious and difficult to control because of the rapid Ca2+-induced gelation of alginate. In this study, An electrodeposition method was used to rapidly and controllably fabricate Ca2+-Alg films for wound treatment. Several measures of film growth (e.g., thickness and mass) are shown to linearly correlate to the imposed charge transfer at the electrode. Similarly, this charge transfer was also observed to control important physicochemical wound healing properties such as water uptake and retention capacity. Furthermore, a wound healing animal test was performed to evaluate the performance of this electro-fabricated calcium alginate film for wound treatment. This in vivo study demonstrated that wounds dressed with an electro-fabricated Ca2+-Alg film closed faster than that of untreated wounds. Further, the new dermis tissue that formed was composed of reorganized and stratified epithelial layer, with fully developed connective tissue, hair follicle, sebaceous glands as well as aligned collagen. Therefore, our study indicates that this electrofabrication method for the rapid and controlled preparation of alginate film could provide exciting opportunities for wound treatment. More broadly, this study demonstrates the potential of electrochemistry for the fabrication of high performance polymeric materials. Here we report a rapid and controllable fabrication of free-standing alginate films by coupling anodic electrodeposition with subsequent peeling of deposited materials for wound dressing.

In this study, starch with porous structures derived from purple sweet potato was prepared and used as a food-grade polymer for the microencapsulation of olive oil. The optimal reaction conditions for preparing porous starch were determined to improve its adsorption capacity as effective microcapsule-wall materials. Olive oil was then impregnated in microspheres, and loading ratio was optimized by investigating the restrictive factors, including the mass ratio of olive oil to porous starch, as well as the embedding temperature and time. The presence of olive oil in the starch matrix was confirmed by SEM, FTIR, and TGA. Results demonstrated that the porous starch-based microencapsulation exhibit a stable olive oil loading ratio and a significant improvement in oxidative stability compared with free olive oil. The newly-proposed process used in this work was easy to scale up for developing a new and attractive method for oil protection in the food industry.

A stimuli-responsive membrane exhibiting independent pH- and temperature-responsive behavior was fabricated from a blend of commercial polysulfone with a functional amphiphilic binary graft copolymer, namely, polysulfone-graft-(poly(isopropylacrylamide-co-acrylic acid)-random-poly(methyl acrylate)), denoted PSf-g-(P(NIPAAm-co-AA)-r-PMMA). Two graft copolymers with different lengths of P(NIPAAm-co-AA) side chains were designed and enriched on the membrane surface to serve as thermo- and pH-responsive on/off switches. The differences between the dual-responsive behaviors of the two kinds of polymer-blend membranes were studied by water-flux and contact-angle measurements. The PMMA side chains served to securely anchor the graft copolymers to the membrane substrate, and the blended membrane prepared from binary graft copolymer was more stable and exhibited more robust stimuli-responsive behavior than that prepared from mono-graft copolymer PSf-g-P(NIPAAm-co-AA).