Preparation and characterization of bacterial cellulose/hydroxypropyl chitosan blend as-spun fibers

In the work, N-methylmorpholine-N-oxide monohydrate (NMMO·H₂O) was used as a solvent to solve bacterial cellulose (BC) and hydroxypropyl chitosan (HPCS) together, and regenerated bacterial cellulose (RBC)/HPCS blend as-spun fibers were prepared by blending BC with HPCS via wet-spinning in the Lyocell process. Structure and properties of the blend as-spun fibers were characterized by different techniques, together with the antibacterial activity of the blend as-spun fibers against Staphylococcus aureus. Results revealed that HPCS was mixed with BC very well. The blend as-spun fibers showed a rough and folded surface morphology and an interior pore structure on the cross-section. Compared with pure RBC as-spun fibers, the blend as-spun fibers had lower degree of crystallinity and thermal stability. Although extension at break of the blend as-spun fibers was lower than the pure RBC as-spun fibers, their tensile strength and modulus had been enhanced obviously. The blend as-spun fibers were also found to exhibit excellent antibacterial activities against S. aureus.     

Fabrication of electrospun antimicrobial nanofibers containing metronidazole using nanospider technology

Nanospider technology as a modified electrospinning technique was used for the fabrication of electrospun nanofibers based on poly(vinyl alcohol) (PVA)/poly(ethylene oxide) (PEO) blend as drug delivery system (DDS) for metronidazole (MTZ) as an antimicrobial drug. Electrospun PVA/PEO/MTZ composite nanofibers were stabilized against disintegration in water by heating in oven at 110°C, or by soaking in isopropyl alcohol for 6 hrs. Incorporation of MTZ into electrospun nanofibers was confirmed by SEM, FT-IR spectra and TGA. The drug release results showed that the burst release was suppressed with stabilized electrospun nanofibers compared with non-stabilized ones. Electrospun PVA/PEO/MTZ composite nanofibers exhibited remarkable antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa, Aspergillus niger, Penicillium notatum and Aspergillus flavus which varies with the species of the tested organisms.     

Water-resistant Lignin/Poly(vinyl alcohol) Blend Fibers for Removal of Hexavalent Chromium

Lignin is the second most abundant renewable biomass-derived natural resource that has been used to replace traditional petrochemical-based materials. However, fabricating the lignin component into the various forms required for practical application is still challenging. In this work, we fabricated water-resistant lignin/poly(vinyl alcohol) (PVA) blend fibers by wet spinning and glutaraldehyde crosslinking methods. The effect of the lignin/PVA blend ratio and glutaraldehyde crosslinking process on the physicochemical properties of wet-spun lignin/PVA blend fibers were studied using maximum draw ratios, hydrolytic degradation profiles, and mechanical properties. Furthermore, the hexavalent chromium [Cr(VI)] removal behavior of lignin/PVA blend fibers was investigated according to the effect of pH, initial Cr(VI) concentration, and contact time. The wet-spun lignin/PVA blend fiber achieved excellent water stability through glutaraldehyde crosslinking and exhibited notable Cr(VI) adsorption capacity (350.87 mg/g) and good regeneration ability. These findings demonstrate that glutaraldehyde-crosslinked lignin/PVA blend fibers could be promising adsorbents for the remediation of heavy metal species containing textile wastewater.     

Development of nanofibrous membranes with far-infrared radiation and their antimicrobial properties

This study investigated the incorporation of nanoscale germanium (Ge) and silicon dioxide (SiO₂) particles into poly(vinyl alcohol) (PVA) nanofibers with the aim of developing nanostructures with far-infrared radiation effects and antimicrobial properties for biomedical applications. Composite fibers containing Ge and SiO₂ were fabricated at various concentrations of Ge and/or SiO₂ using electrospinning and layered on polypropylene nonwoven. The morphological properties of the nanocomposite fibers were characterized using a field-emission scanning electron microscope and a transmission electron microscope. The far-infrared emissivity and emissive power of the nanocomposite fibers were examined in the wavelength range of 5-20 μm at 37 °C. The antibacterial properties were quantitatively assessed by measuring the bacterial reductions of Staphylococcus aureus, Klebsiella pneumoniae, and Escherichia coli. Multi-component composite fibers electrospun from 11 wt% PVA solutions containing 0.5 wt% Ge and 1 wt% SiO₂ nanoparticles exhibited a far-infrared emissivity of 0.891 and an emissive power of 3.44·102 W m^?2 with a web area density of 5.55 g m^?2. The same system exhibited a 99.9 % bacterial reduction against both Staphylococcus aureus and Escherichia coli, and showed a 34.8 % reduction of Klebsiella pneumoniae. These results demonstrate that PVA nanofibrous membranes containing Ge and SiO₂ have potential in medical and healthcare applications such as wound healing dressings, skin care masks, and medical textile products.     

Preparation of Cu-BTC/PVA Fibers with Antibacterial Applications

In this study, a metal-organic framework (MOF)/polymer electrospun fiber was prepared. The MOF, copper-1,3,5- benzenetricarboxylate (Cu-BTC), was synthesized using a sonochemical method at 25 °C, with a 1:1:1 mixture of dimethylformamide, ethanol, and deionized water as solvent. The sonication time was shown to have a pronounced effect on the morphology and structure of the Cu-BTC. A square pyramid shape with sides of 100 nm was obtained after 2 h of sonication. Extending the sonication time provided a lower amount of unknown phase and produced a uniform Cu-BTC framework. The Cu-BTC-modified PVA fibers were then fabricated by electrospinning. The effect of the Cu-BTC and PVA concentration was investigated at 25 kV, a flow rate of 10 μl/min, and a working distance of 150 mm. FTIR spectra and FESEM images showed good dispersion of the Cu-BTC on the PVA fiber. The as-prepared Cu-BTC-modified PVA fibers exhibited excellent antibacterial effectiveness against S. aureus.     

Fabrication of Gelatin-Based Electrospun Composite Fibers for Anti-Bacterial Properties and Protein Adsorption

A major goal of biomimetics is the development of chemical compositions and structures that simulate the extracellular matrix. In this study, gelatin-based electrospun composite fibrous membranes were prepared by electrospinning to generate bone scaffold materials. The gelatin-based multicomponent composite fibers were fabricated using co-electrospinning, and the composite fibers of chitosan (CS), gelatin (Gel), hydroxyapatite (HA), and graphene oxide (GO) were successfully fabricated for multi-function characteristics of biomimetic scaffolds. The effect of component concentration on composite fiber morphology, antibacterial properties, and protein adsorption were investigated. Composite fibers exhibited effective antibacterial activity against Staphylococcus aureus and Escherichia coli. The study observed that the composite fibers have higher adsorption capacities of bovine serum albumin (BSA) at pH 5.32–6.00 than at pH 3.90–4.50 or 7.35. The protein adsorption on the surface of the composite fiber increased as the initial BSA concentration increased. The surface of the composite reached adsorption equilibrium at 20 min. These results have specific applications for the development of bone scaffold materials, and broad implications in the field of tissue engineering.     

Effects ofIn Vitro degradation on the weight loss and tensile properties of PLA/LPCL/HPCL blend fibers

PLA/LPCL/HPCL blend fibers composed of poly (lactic acid) (PLA), low molecular weight poly (ɛ-caprolactone) (LPCL), and high molecular weight poly (ɛ-caprolactone) (HPCL) were prepared by melt blending and spinning for bioabsorbable filament sutures. The effects of blending time and blend composition on the X-ray diffraction patterns and tensile properties of PLA/LPCL/HPCL blend fibers were characterized by WAXD and UTM. In addition, the effect ofin vitro degradation on the weight loss and tensile properties of the blend fibers hydrolyzed during immersion in a phosphate buffer solution at pH 7.4 and 37°C for 1–8 weeks was investigated. The peak intensities of PLA/LPCL/HPCL blend fibers in X-ray diffraction patterns decreased with an increase of blending time and LPCL contents in the blend fibers. The weight loss of PLA/LPCL/HPCL blend fibers increased with an increase of blending time, LPCL contents, and hydrolysis time while the tensile strength and modulus of the blend fibers decreased. The tensile strength and modulus of the blend fibers were also found to be increased with an increase of HPCL contents in the blend fibers. The optimum conditions to prepare PLA/LPCL/HPCL blend fibers for bioabsorbable sutures are LPCL contents of 5 wt%, HPCL contents of 35 wt%, and blending time of 30 min. The strength retention of the PLA/LPCL/HPCL blend fiber prepared under optimum conditions was about 93.5% even at hydrolysis time of 2 weeks.     

The effects of boric acid on the rheological behavior of time dependent structure formation in PVA/DMSO solutions

Lots of studies have been carried out to improve the strength of polyvinyl alcohol (PVA) fibers. One of these studies is crosslinking spinning for a good quality fiber. As a crosslinking agent, boric acid (BA, H₃BO₃) was used. PVA can crosslink with BA without adding cation in using dimethyl sulfoxide (DMSO). The effects of BA addition and molecular weight (MW) on the formation of the physical structure in PVA/DMSO solutions were investigated. The results showed that the time dependence of the rheological responses was greatly influenced by the BA addition to the PVA/DMSO solutions. The results also showed that the BA addition to the PVA/DMSO solutions increased the dynamic viscosity (η′), the storage modulus (G′), and the loss modulus (G″) of the PVA/DMSO solutions. Increasing MW of PVA also decreased the time dependence. In addition, the BA addition to the PVA/DMSO solutions decreased the gelation time of the PVA/DMSO solutions. These overall results suggested that the structure formation through specific interactions between PVA molecules and BA resulted in the time dependent changes of the rheological properties of the PVA/DMSO solutions.     

Study of synthesizing energy storage microcapsules in PVA spinning solution and thermal regulating fibers prepared by this solution

Thermal regulating fiber has been a research hotspot worldwide recently. In this paper, the energy storage microcapsules composed of silicon dioxide (SiO₂) as shell and paraffin as core were synthesized in the spinning solution of polyvinyl alcohol (PVA). This solution was used to prepare thermal regulating PVA fibers by wet spinning directly. Orthogonal experiment was conducted to optimize the synthetic conditions of the microcapsules. Chemical structure and morphology of the fibers were characterized by Fourier transform infrared-attenuated total reflectance (FTIR-ATR) and scanning electron microscope (SEM) respectively. The thermal properties of the fibers were studied by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Results present that energy storage microcapsules are successfully synthesized in PVA spinning solution with a mean particle size of 1.39 µm. The fibers containing such microcapsules show a high latent heat storage density of 45.39 J g^?1, which also achieve a relatively better thermal stability.     

Preparation and characterization of PVA/PU blend nanofiber mats by dual-jet electrospinning

A series of blend nanofiber mats comprising poly(vinyl alcohol) (PVA) and polyurethane (PU) were prepared by dual-jet electrospinning in various parameters. Orthogonal experimental design was used to investigate how those parameters affected on fiber diameters and fiber diameter distribution. Altogether three parameters having three levels each were chosen for this study. The chosen parameters were tip-to-collector distance (TCD), voltage and tip-to-tip distance (TTD). Fiber diameters, thermal properties, mechanical properties and hydrophilicity of the blend nanofiber mats were examined by scanning electron microscopy (SEM), thermogravimetric analysis (TGA), tensile test, contact angle and water absorption test, respectively. The results showed that the optimum conditions for PVA/PU blend nanofiber mats fabricated by dual-jet electrospinning were TCD of 20 cm, voltage of 18 kV and TTD of 4 cm. Besides, the thermal stability of PVA/PU blend nanofiber mats had been improved compared with pure nanofibers. Furthermore, the elongation and tensile strength of the blend nanofiber mats were significantly increased compared with pure PVA and pure PU, respectively. And the blend nanofiber mats exhibited well hydrophilicity.     

Fabrication and characterization of silk braided sutures

Silk sutures are already used in surgery. Silk is a natural protein fiber and easily prone to microbial infection hence we have developed novel antimicrobial silk braided sutures. Braided silk sutures were fabricated using a circular braiding machine with a 16 carrier arrangement normally used to produce braided structures. The same structure was used to manufacture braids with three different take-up speed levels obtained by changing the cogwheel ratio on the braiding machine. The influence of braid angle, test parameters such as gauge length and extension rate on tenacity and knot strength of braided silk sutures were studied. Silk sutures fabricated at higher braid angle, tested at shorter gauge length and greater test speed showed lower values of tenacity and knot strength. Chitosan was applied on braided silk sutures to impart antimicrobial characteristics. The Scanning electron microscopy study reveals the absence and presence of chitosan on the surface of untreated and treated sutures respectively. The antimicrobial properties of chitosan and tetracycline hydrochloride drug were tested using Agar diffusion method SN 195920 both when applied independently and collectively on silk sutures against Escherichia coli and Staphylococcus aureus. The combined antimicrobial effect of chitosan and tetracycline hydrochloride drug is very good and can be used to develop antimicrobial silk sutures for providing protection against microbial infections.     

Antimicrobial properties of chitosan nanoparticles: Mode of action and factors affecting activity

The present investigation describes the synthesis and characterization of novel biodegradable nanoparticles based on chitosan for biomedical applications. The presence of primary amine groups in repeating units of chitosan grants it several properties like antibacterial activity, antitumor activity and so on. Chitosan forms nanoparticles spontaneously on the addition of polyanion tripolyphosphate which has greater antimicrobial activity than parent chitosan. In the present study, chitosan nanoparticles (ChNP) were prepared by the ionic gelation method. The physiochemical characteristics of nanoparticles were analyzed using XRD, SEM, FTIR. The antibacterial activity of chitosan nanoparticles against medical pathogens Klebsiella pneumoniae, Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa was evaluated by calculation of minimum inhibitory concentration (MIC) and compared with chitosan and chitin activity. The mode of action and factors affecting antibacterial activity were also analyzed. ChNP compounds exhibited superior antimicrobial activity against all microorganisms in comparison with chitosan and chitin. The antibiofilm activity was studied using crystal violet assay and growth on congo red agar. The study is thus a good demonstration of the applicability of chitosan nanoparticles as an effective antimicrobial agent with antibiofilm activity as well.     

Carbon nanotube/poly(vinyl alcohol) fibers with a sheath-core structure prepared by wet spinning

A method for manufacturing sheath-core structured fibers was developed using wet spinning techniques. The core portion of a fiber was prepared using a carbon nanotube (CNT) solution while the sheath used a fiber-forming polymer such as polyvinyl alcohol (PVA). Preparation methods of CNT solutions were investigated and it was found that dispersivity and concentration played an important role in the formation and spinning of fiber??s core. CNT solution prepared using a surfactant with high molecular weight such as sodium lignosulfonate (SLS) was most effective and the CNT concentration was as high as 30 g/l. Fiber processing conditions were optimized and it was determined that stretching fibers in the coagulation bath was a significant step in the formation of a solid and well structured core. Drawn fibers were so strong and flexible that they could be woven into a fabric for potential use as a pressure sensor. These results are relevant for practical applications, such as the development of large-area fabric sensors. Furthermore, the described procedure to produce sheath-core CNT fibers is scalable as wet spinning methods have been widely used in the fiber industry.     

Synthesis and Characterization of 2-Decenoic Acid Modified Chitosan for Infection Prevention and Tissue Engineering

Chitosan nanofiber membranes are recognized as functional antimicrobial materials, as they can effectively provide a barrier that guides tissue growth and supports healing. Methods to stabilize nanofibers in aqueous solutions include acylation with fatty acids. Modification with fatty acids that also have antimicrobial and biofilm-resistant properties may be particularly beneficial in tissue regeneration applications. This study investigated the ability to customize the fatty acid attachment by acyl chlorides to include antimicrobial 2-decenoic acid. Synthesis of 2-decenoyl chloride was followed by acylation of electrospun chitosan membranes in pyridine. Physicochemical properties were characterized through scanning electron microscopy, FTIR, contact angle, and thermogravimetric analysis. The ability of membranes to resist biofilm formation by S. aureus and P. aeruginosa was evaluated by direct inoculation. Cytocompatibility was evaluated by adding membranes to cultures of NIH3T3 fibroblast cells. Acylation with chlorides stabilized nanofibers in aqueous media without significant swelling of fibers and increased hydrophobicity of the membranes. Acyl-modified membranes reduced both S. aureus and P. aeruginosa bacterial biofilm formation on membrane while also supporting fibroblast growth. Acylated chitosan membranes may be useful as wound dressings, guided regeneration scaffolds, local drug delivery, or filtration.     

Preparation and use of amine-functionalized glycidyl methacrylate-g-poly(ethylene terephthalate) fibers for removal of chromium(VI) from aqueous solution

Poly(ethylene terephthalate) (PET) fibers were grafted with glycidyl methacrylate (GMA) using benzoyl peroxide as initiator. 1,6-diaminohexane (HMDA) was then covalently attached to this GMA grafted PET fibers. Variations of time, temperature, initiator and monomer concentrations were investigated. HMDA-GMA-g-PET fibers were used as a new sorbent for removal of Cr(VI) ions from aqueous solutions through batch adsorption method. Effects of various parameters such as pH, treatment time, and initial ions concentration on the adsorption amount of ions onto reactive fibers were investigated. The adsorption rates of Cr(VI) ions were much higher on the HMDA-GMA-g-PET fiber than on GMA-g-PET and ungrafted PET fiber. Within 60 min, at pH 3, Cr(VI) was removed by 98 % while the initial concentration of ions was at 25 mg/l and by 94 % at 400 mg/l. The Cr(VI) ions adsorbed were easily desorbed by treating with 1M KOH within 10 min.     

Preparation and characterization of nanoscaled poly(vinyl alcohol) fibers via electrospinning

Nanoscaled PVA fibers were prepared by electrospinning. This paper described the electrospinning process, the processing conditions, fiber morphology, and some potential applications of the PVA nano-fibers. PVA fibers with various diameters (50–250 nm) were obtained by changing solution concentration, voltage and tip to collector distance (TCD). The major factor was the concentration of PVA solution which affected the fiber diameter evidently. Increasing the concentration, the fiber diameter was increased, and the amount of beads was reduced even to 0%. The fibers were found be efficiently crosslinked by glyoxal during the curing process. Phosphoric acid was used as a catalyst activator to reduce strength losses during crosslinking. Scanning electron micrograph (SEM) and differential scanning calorimetric (DSC) techniques were employed to characterize the morphology and crosslinking of PVA fibers. It was found that the primary factor which affected the crosslinking density was the content of chemical crosslinking agent.     

Preparation and properties of 2-(2-aminoethoxy) ethyl chitosan/cellulose fiber using N-methylmorpholine-N-oxide process

N-methylmorpholine-N-oxide (NMMO) is used widely in the manufacturing of man-made cellulose fibers and functional lyocell fibers due to its environment-friendly advantage. Although chitosan is known as a natural antibacterial polymer it has poor solubility in neutral to basic medium and the antibacterial activity is shown only in acidic medium. Chitosan’s poor solubility in NMMO is the disadvantage for the production of antibacterial lyocell fibers. This paper investigates a more “NMMO soluble” derivative of chitosan, 2-(2-aminoethoxy) ethyl chitosan (AECS). AECS has greatly improved solubility in NMMO hydrate, and stronger antibacterial activity than chitosan. AECS was introduced to modify the lyocell fiber spun in a co-solution of cellulose and AECS in NMMO hydrate. The physical properties and antibacterial activity of the fibers were examined and the results indicated that the modified lyocell fiber, containing more than 2 wt% of AECS, exhibits good antibacterial activity against E. coli and slightly decreased tensile strength compared with unmodified fibers.     

Antibacterial blend films of cellulose and chitosan prepared from binary ionic liquid system

A new hybrid ionic liquids solvent, 1-allyl-3-methylimidazolium chloride (AMIMCl) and glycine hydrochloride (Gly·HCl) was utilized to dissolve chitosan and fabricate chitosan/cellulose (Cs/Ce) blend films with chitosan proportion varying from 2 to 35 wt.% through solution casting method. FTIR, XRD, TG, SEM and EA were used to evaluate the prepared composites. Besides, the mechanical property and antibacterial activity were also analyzed. The shifting of the characteristic peaks of -NH and C=O for chitosan, similar crystal pattern with low intensity diffraction peaks at 2θ of around 20°, superior thermal stability (increased T_onset) with chitosan ratio below 10 wt.% in the composites suggested that the interactions via hydrogen bonds formed between chitosan and cellulose. Besides, the elemental analysis showed that the actual N% contents from the chitosan in the blend films were roughly equivalent to the theoretical value though the inevitable residue of ionic liquids. Furthermore, the blends not only presented compact structure but also processed high bacterial reduction to E. coli and S. aureus at pH 6.3, which indicated that the Cs/Ce blend films prepared via the Gly·HCl/AMIMCl dissolution method were suitable for production of degradable antibacterial materials.     

Rheological behavior and spinnability of ethylamine hydroxyethyl chitosan/cellulose co-solution in N-methylmorpholine-N-oxide system

In this work, the novel chitosan derivative ethylamine hydroxyethyl chitosan (EHC) was synthesized and blended with cellulose in an aqueous N-methylmorpholine-N-oxide (NMMO) solution in order to fabricate antibacterial chitosan/cellulose fiber. The rheological behaviors of the obtained co-solution in both steady and dynamic states were carefully investigated to determine the spinnability of the co-solution. In steady state, the addition of EHC was found to preserve the power-law flow characteristics of cellulose in the aqueous NMMO solution, while broadening the first Newtonian fluid-flow area. Under dynamic conditions, both Han-plot and viscoelastic analyses indicated the homogeneity of the co-solution. EHC/cellulose antibacterial fibers were successfully spun via the lyocell process using aqueous NMMO as the solvent, confirming the excellent spinnability of the EHC/cellulose co-solution. Scanning electron microscopy was used to observe the morphology of the obtained EHC/cellulose fibers; they were also investigated for antibacterial activity. The obtained EHC/cellulose fiber exhibited good spinning consistency and strong antibacterial activity against Escherichia coli, demonstrating potential applications for the material in antibacterial textiles.     

Preparation of poly(vinyl alcohol)/silver-zeolite composite hydrogels by UV-irradiation

Poly(vinyl alcohol) (PVA)/Ag-zeolite nanocomposite hydrogels were prepared by UV irradiation using PVA solution mixed with Ag-zeolite nanoparticles. Physical properties and changes in morphology of the PVA/Ag-zeolite hydrogels were investigated. The PVA/Ag-zeolite hydrogels were prepared at a PVA concentration of 9 wt% with a UV irradiation distance of 15 cm, where gel fraction and swelling ratio were optimized. Hardness of the PVA/Ag-zeolite hydrogels decreased with increasing amounts of Ag-zeolite, reaching that of soft elastomer when the amount of Ag-zeolite was 5 % by weight. The PVA/Ag-zeolite hydrogels showed strong antimicrobial activities against Staphylococcus aureus and Klebsiella pneumoniae, inducing a reduction of bacteria of over 99.9 % at a Ag-zeolite content of 3 wt%.