Coaxial Nanofibers Research Articles

A methylprednisolone-loaded and core-shell nanofiber-covered stent-graft to prevent inflammation and reduce degradation in aortic dissection

BackgroundStent-graft-induced inflammation is an independent risk factor for adverse aortic remodeling in aortic dissection. In this context, we asked that whether a methylprednisolone-loaded stent-graft could reduce inflammation and degradation.MethodsFirst, a coaxial electrospinning technique was used to create a core-shell film with methylprednisolone encapsulated in the inner of poly (L-lactide-co-caprolactone) nanofibers for controllable drug release. Second, an in vitro study was conducted to evaluate the biocompatibility of the nanofiber meshes. Third, the porcine aortic dissection model was developed to investigate the therapeutic effects of the methylprednisolone-loaded stent-graft.ResultsThe results demonstrated that the nanofiber-coated film with a methylprednisolone-poly-caprolactone core layer and a poly (L-lactide-co-caprolactone) shell layer could effectively sustain drug release in vitro. In vivo study showed that the methylprednisolone-loaded stent-graft could reduce degradtion of aortic dissection by regulating inflammation.ConclusionsOverall, the controllable drug release by coaxial nanofiber is a promising approach to alleviate aortic inflammation and promote aortic remodeling after stent-graft implantation.

Preparation of Linalool/Polycaprolactone Coaxial Electrospinning Film and Application in Preserving Salmon Slices.

A linalool/polycaprolactone (LL/PCL) antibacterial film was prepared by using a coaxial electrospinning process, and its physical and chemical properties were characterized. The antibacterial film was formed into an active antibacterial gasket, and its effect on salmon preservation was analyzed. The results show that the LL/PCL nanofiber membrane had a well-developed microstructure, and the fiber surface was smooth and uniform. The diameter of the fibers in the PCL membrane without the core material (linalool) was 113.92 ± 23.74 nm. In contrast, the diameter of the coaxial nanofiber membrane with linalool increased, and the diameter of the LL/PCL membranes with 20% and 40% linalool was 220.62 ± 44.01 and 232.22 ± 56.27 nm, respectively. The hydrophobicity and water vapor permeability were enhanced, whereas the tensile strength and elongation at break decreased slightly, while the thermal stability did not differ significantly with the incorporation of linalool. Analysis of the sustained release of linalool showed that the LL/PCL coaxial fiber membranes could release linalool into the reaction system for a long time. The LL/PCL nanofiber film was used to create an antibacterial active gasket for salmon preservation experiments. Sensory evaluation and analyses of the total bacterial count, total volatile basic nitrogen (TVB-N), thiobarbituric acid reactive substances (TBARS), pH, texture (hardness, elasticity, chewiness, and viscoelasticity), water distribution change, and aroma using an electronic nose were used to determine the quality of salmon. It was found that food-grade tinfoil and the PCL gasket had no significant effect on the freshness of salmon, while the active antibacterial gasket samples containing linalool could decrease the rate of decay salmon and effectively prolong the shelf-life of salmon by releasing linalool.

Natural protein-based electrospun nanofibers for advanced healthcare applications: progress and challenges.

Electrospinning is an electrostatic fiber fabrication technique that operates by the application of a strong electric field on polymer solution or melts. It is used to fabricate fibers whose size lies in the range of few microns to the nanometer range. Historic development of electrospinning has evinced attention due to its outstanding attributes such as small diameter, excellent pore inter-connectivity, high porosity, and high surface-to-volume ratio. This review aims to highlight the theory behind electrospinning and the machine setup with a detailed discussion about the processing parameters. It discusses the latest innovations in natural protein-based electrospun nanofibers for health care applications. Various plant- and animal-based proteins have been discussed with detailed sample preparation and corresponding processing parameters. The usage of these electrospun nanofibers in regenerative medicine and drug delivery has also been discussed. Some technical innovations in electrospinning techniques such as emulsion electrospinning and coaxial electrospinning have been highlighted. Coaxial electrospun core-shell nanofibers have the potential to be utilized as an advanced nano-architecture for sustained release targeted delivery as well as for regenerative medicine. Healthcare applications of nanofibers formed via emulsion and coaxial electrospinning have been discussed briefly. Electrospun nanofibers have still much scope for commercialization on large scale. Some of the available wound-dressing materials have been discussed in brief.

Highly oriented poly (m‐phenyleneisophthalamide)/polyacrylonitrile based coaxial nanofibers integrated with electrospunpolyacrylonitrile‐silvernanoparticle: Application in air filtration of particulate and microbial contaminants

AbstractOn account of increasing attention paid to global air quality problem, air filter media with low‐pressure drop, good strength, and excellent removal efficiency towards pathogens have gradually become a research hotspot. Polymeric electrospun nanofibrous membranes with large surface area to volume ratio, and adjustable porous structure, have attracted increased attention in air filtration applications. In this work, as an innovative extension of classical electrospinning procedure, coaxial electrospinning is used to produce high‐strength fiber with core–sheath structures. The as‐produced poly(m‐phenylene isophthalamide) (PMIA: as the core)/polyacrylonitrile (PAN: as the shell) based coaxial nanofibers integrated with a layer of electrospun PAN–silver nanoparticle membrane, can filter both particulate matter and microbes. Significantly, poly(m‐phenylene isophthalamide)/PAN membrane will exhibit uniform axial alignment of nanofibers, which can effectively improve mechanical strength of filter media along the orientation direction. Benefiting from structural features including the presence of anti‐microbial agent, the developed composite polymeric filter membrane exhibits very low pressure drop (24.52 Pa), 99% filtration efficiency, 9.809 MPa tensile strength and good anti‐microbial activity against Gram‐positiveBacillus subtilisand Gram‐negativeEscherichia coli. Besides, this work provides a versatile platform for exploring coaxial nanofibrous membrane in air filtration application, since it is still in emerging and immature phase.

Synergistic Effect of Co-Delivering Ciprofloxacin and Tetracycline Hydrochloride for Promoted Wound Healing by Utilizing Coaxial PCL/Gelatin Nanofiber Membrane.

Combining multiple drugs or biologically active substances for wound healing could not only resist the formation of multidrug resistant pathogens, but also achieve better therapeutic effects. Herein, the hydrophobic fluoroquinolone antibiotic ciprofloxacin (CIP) and the hydrophilic broad-spectrum antibiotic tetracycline hydrochloride (TH) were introduced into the coaxial polycaprolactone/gelatin (PCL/GEL) nanofiber mat with CIP loaded into the PCL (core layer) and TH loaded into the GEL (shell layer), developing antibacterial wound dressing with the co-delivering of the two antibiotics (PCL-CIP/GEL-TH). The nanostructure, physical properties, drug release, antibacterial property, and in vitro cytotoxicity were investigated accordingly. The results revealed that the CIP shows a long-lasting release of five days, reaching the releasing rate of 80.71%, while the cumulative drug release of TH reached 83.51% with a rapid release behavior of 12 h. The in vitro antibacterial activity demonstrated that the coaxial nanofiber mesh possesses strong antibacterial activity against E. coli and S. aureus. In addition, the coaxial mats showed superior biocompatibility toward human skin fibroblast cells (hSFCs). This study indicates that the developed PCL-CIP/GEL-TH nanofiber membranes hold enormous potential as wound dressing materials.

Electrospun Tio2 Coaxial Nanofibers as a Multifunctional Interlayer for High-Performance Lithium-Sulfur Battery in a Wide Temperature Range

Electrospun Tio2 Coaxial Nanofibers as a Multifunctional Interlayer for High-Performance Lithium-Sulfur Battery in a Wide Temperature Range

Effect of Solution Miscibility on the Morphology of Coaxial Electrospun Cellulose Acetate Nanofibers.

Coaxial electrospinning (co-electrospinning) technique has greatly expanded the universality of fabricating core-shell polymer nanofibers. However, the effect of solution miscibility on the morphology of co-electrospun products remains unclear. Herein, different cellulose acetate (CA) solutions with high solution miscibility but distinctly different electrospinnability were used to survey the effect of solution miscibility on the co-electrospinning process. The structural characterizations show that co-electrospun products are composed of nanofibers with and without the core-shell structure. This indicates that partial solution mixing occurred during the co-electrospinning process instead of absolute no-mixing or complete mixing. Importantly, the solution miscibility also shows a significant influence on the product morphology. In particular, the transformation from nanofibers to microparticles was realized with the increase of core-to-shell flow ratio during the co-electrospinning of core electrosprayable CA/dimethylacetamide (DMAc) solution and shell electrospinnable CA/acetone-DMAc (2/1, v/v) solution. Results show that the solution miscibility exerts a significant effect on not only the formation of core-shell structure but also the product morphology. This work provides a new insight for the in-depth understanding of the co-electrospinning process.

Gold Nanoparticles-Loaded Polyvinylpyrrolidone/Ethylcellulose Coaxial Electrospun Nanofibers with Enhanced Osteogenic Capability for Bone Tissue Regeneration

Biomaterial-based scaffolds fabricated by electrospinning technique are promising platforms for bone tissue engineering. However, the current scaffolds have some limitations in terms of poor osteogenic bioactivities. In this study, citrate-stabilized gold-nanoparticles (GNPs) were encapsulated into polyvinylpyrrolidone/ethylcellulose scaffolds fabricated by coaxial electrospinning technique. Three types of GNPs-loaded electrospun scaffolds (P/E-0.5, P/E-1, and P/E-1.5) were prepared by changing the feeding GNPs. The morphological and physicochemical properties of these GNPs-incorporated electrospun scaffolds were comprehensively characterized. The results demonstrated that GNPs were successfully encapsulated into electrospun scaffolds, and their addition barely affected the morphology but improved the porosity and mechanical properties. In vitro studies revealed that GNPs-incorporated electrospun scaffolds showed excellent biocompatibility and osteogenic bioactivities, wherein the alkaline phosphatase activity, mineralized nodule formation, and the osteogenic-related genes expression were enhanced in GNPs-incorporated electrospun scaffolds compared to the neat P/E electrospun nanofibers. Then, the GNPs-incorporated electrospun scaffolds were surgically implanted into the defect area of the rat skull bone to test their in vivo bone repairing effect. It was observed that GNPs-incorporated scaffolds rapidly accelerated bone regeneration in vivo. Taken together, GNPs-incorporated coaxial electrospun nanofibers might be considered as promising scaffolds in the field of bone tissue regeneration.

Fabrication of Mesoporous Silica Nanoparticle-Incorporated Coaxial Nanofiber for Evaluating the In Vitro Osteogenic Potential.

The most important role of tissue engineering is to develop a biomaterial with a property that mimics the extracellular matrix (ECM) by enhancing the lineage-specific proliferation and differentiation with favorable regeneration property to aid in new tissue formation. Thus, to develop an ideal scaffold for bone repair, we have fabricated a composite nanofiber by the coaxial electrospinning technique. The coaxial electrospun nanofiber contains the core layer, consisting of polyvinyl alcohol (PVA) blended with oregano extract and mesoporous silica nanoparticles (PVA-OE-MSNPs), and the shell layer, consisting of poly-ε-caprolactone blended with collagen and hydroxyapatite (PCL-collagen-HAP). We evaluated the physicochemical properties of the nanofibers using X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR). In vitro biocompatibility, cell adhesion, cell viability, and osteogenic potential were evaluated by 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenlytetrazolium bromide (MTT), calcein AM, and alkaline phosphatase (ALP) activity and Alizarin Red staining in NIH 3T3/MG-63 cells. The results showed that the nanoparticle-incorporated coaxial nanofiber was observed with bead-free, continuous, and uniform fiber morphology with a mean diameter in the range of 310 ± 125nm. From the biochemical studies, it is observed that the incorporation of nanofiber with HAP and MSNPs shows good swelling property with ideal porosity, biodegradation, and enhanced biomineralization property. In vitro results showed that the scaffolds with nanoparticles have higher cell adhesion, cell viability, ALP activity, and mineralization potential. Thus, the fabricated nanofiber could be an appropriate implantable biomaterial for bone tissue engineering.

Adsorption and sustained release of doxorubicin from N-carboxymethyl chitosan/polyvinyl alcohol/poly(ε-caprolactone) composite and core-shell nanofibers

The core-shell nanofibers, produced by the coaxial electrospinning method, are good candidates for delivery of anticancer drugs due to their continuous release without initial burst release. In this work, the N-carboxymethyl chitosan (N-CMCS)-polyvinyl alcohol (PVA)/poly(ε-caprolactone) (PCL) composite and core-shell nanofibers were prepared by two-nozzle and coaxial electrospinning techniques, respectively. Doxorubicin (DOX) as an anticancer drug was loaded into the N-CMCS/PVA/PCL nanofibers fabricated by two-nozzle and coaxial electrospinning. The performance of nanofibers was compared for the adsorption and controlled release of DOX against MCF-7 breast cancer cells death in vitro. The produced fibers were characterized using FTIR, SEM, and TEM analysis. Drug encapsulation efficiency, drug content, and drug release studies were evaluated. The DOX molecules were released from coaxial nanofibers without burst release under extended-release during 20, and 10 days under pH values of 7.4 and 5.5, respectively. The initial burst release at the first hours following by the sustained release of DOX was achieved for composite nanofibers during 11 and 3 days under physiological and acidic pH, respectively. The maximum monolayer sorption capacities of N-CMCS/PVA/PCL composite and core-shell nanofibers for DOX sorption were 74.31 and 40.74 mg g−1, respectively at optimum pH of 8, equilibrium times of 60 min (composite nanofibers) and 120 min (core-shell nanofibers). The maximum MCF-7 breast cancer cells death was about 57% in the presence of DOX loaded-coaxial nanofibers after 7 days. The obtained results demonstrated the high potential of coaxial nanofibers compared with composite nanofibers for drug delivery of anticancer drugs.

Effect of PEO crystallization on dielectric response of PVDF/PEO@IL coaxial electrospinning nanofiber films

AbstractIn this study, core‐shell structured nanofibers (P/E/@IL), in which the blend of poly(ethylene oxide) (PEO) and ionic liquid (IL) acted as core and poly(vinylidene fluoride) (PVDF) acted as shell layer, were prepared by coaxial electrospinning in order to explore the effect of PEO crystallization on the ionic conductivity and dielectric property. For comparison, the blended spinning fibers of PVDF, PEO, and IL (abbreviated as P/E/IL) were also fabricated. It can be observed that the incorporation of IL dramatically improves the dielectric constant () of P/E/@IL composites. However, the tan δ also exhibits a sharp increase with increasing content of IL due to the ion conduction, whereas compared with blended films, the PEO and IL in the core layer exhibit a more positive effect on suppressing the tan δ of film via PEO crystallization. Through melting the PEO lamellae in core, it can be found that the ion conduction as well as tan δ were enhanced. Based on these results, it is confirmed that the ion transport stemmed from IL was suppressed by the PEO lamellae. As the content of IL reached up to 20 wt%, tan δ of the composites with PEO lamellae was reduced to half of P/E/IL spinning fibers.

Preparation and characterization of conductive nerve guide conduit filled with dual drug-loaded nanofibers

Peripheral nerve injury (PNI) has become one of the common clinical diseases. How to promote the regeneration and function recovery of the damaged peripheral nerve has been the focus of attention in the medical field. Evidence suggests that the longitudinal filling of oriented fibers in nerve guide conduit (NGC) is especially beneficial to the repair of long gap PNI. In this study, polypyrrole (PPy) nanospheres (PNSs) were prepared by the soft-templating method, and mixed with poly (lactic acid) (PLA) to prepare conductive PNSs/PLA NGC, and the optimal ratio of PNSs was 4.5%. PLA and vascular endothelial growth factor (VEGF) as shell, chitosan (CS) and paeoniflorin (PF) as core, oriented coaxial nanofibers were obtained and then filled into PNSs/PLA NGC. The composite NGC has excellent mechanical properties, electrical conductivity, hydrophilic properties, and degradation properties. Besides, the successive release of VEGF and PF can play a synergistic role in promoting nerve regeneration. In vitro experiments showed that the composite NGC was nontoxic and suitable for the adhesion and proliferation of nerve cells. In addition, PNSs combined with electrical stimulation (ES) can significantly promote the differentiation and proliferation of nerve cells, which is conducive to nerve regeneration. These positive results indicate that the composite NGC is a promising candidate in the repair of long gap PNI.

Strain-Mediated Magneto-Electric Effects in Coaxial Nanofibers of Y/W-Type Hexagonal Ferrites and Ferroelectrics

Nanofibers of Y- or W-type hexagonal ferrites and core–shell fibers of hexagonal ferrites and ferroelectric lead zirconate titanate (PZT) or barium titanate (BTO) were synthesized by electrospinning. The fibers were found to be free of impurity phases, and the core–shell structure was confirmed by electron and scanning probe microscopy. The values of magnetization of pure hexagonal ferrite fibers compared well with bulk ferrite values. The coaxial fibers showed good ferroelectric polarization, with a maximum value of 0.85 μC/cm2 and 2.44 μC/cm2 for fibers with BTO core–Co2W shell and PZT core–Ni2Y shell structures, respectively. The magnetization, however, was much smaller than that for bulk hexaferrites. Magneto-electric (ME) coupling strength was characterized by measuring the ME voltage coefficient (MEVC) for magnetic field-assembled films of coaxial fibers. Among the fibers with Y-type, films with Zn2Y showed a higher MEVC than films with Ni2Y, and fibers with Co2W had a higher MEVC than that of those with Zn2W. The highest MEVC of 20.3 mV/cm Oe was measured for Co2W–PZT fibers. A very large ME response was measured in all of the films, even in the absence of an external magnetic bias field. The fibers studied here have the potential for use in magnetic sensors and high-frequency device applications.

A baicalin-loaded coaxial nanofiber scaffold regulated inflammation and osteoclast differentiation for vascularized bone regeneration

We demonstrate a simple, effective and feasible method to address the shrinkage of Poly (lactic-co-glycolic acid) (PLGA) through a core-shell structure fiber strategy. The results revealed that introducing size-stable poly-caprolactone (PCL) as the core fiber significantly improved the PLGA-based fibrous scaffold's dimensional maintenance. We further utilized fish collagen to modify the PLGA shell layer (PFC) of coaxial fibers and loaded baicalin (BA) into the PCL core layer (PCL-BA) to endow fibrous scaffold with more functional biological cues. The PFC/PCL-BA fibrous scaffold promoted the osteogenic differentiation of bone mesenchymal stem cells and stimulated the RAW264.7 cells to polarize into a pro-reparative phenotype. Importantly, the in vivo study demonstrated that the PFC/PCL-BA scaffold could regulate inflammation and osteoclast differentiation, favor neovascularization and bone formation. This work tactfully combined PLGA and PCL to establish a drug release platform based on the core-shell fibrous scaffold for vascularized bone regeneration.

Fabrication and characterization of polylactic acid coaxial antibacterial nanofibers embedded with cinnamaldehyde/tea polyphenol with food packaging potential

Polylactic acid (PLA) is a promising food packaging material with biocompatible, nontoxic and biodegradable. In order to reduce the deterioration of aquatic products caused by microorganisms, PLA coaxial nanofiber films with cinnamaldehyde (CMA), tea polyphenol (TP) and its composite as core materials were prepared by using coaxial electrospinning technology. Its microscopic morphology and structure were characterized separately, and its thermal stability, wettability and mechanical properties were determined. The antibacterial activity and antibacterial mechanism of nanofiber films were studied with Shewanella putrefaciens (S. putrefaciens) which is the dominant spoilage of aquatic products as the target of action. The results show that the CMA/TP (m/m = 2:5)-PLA coaxial nanofibers have small diameter, uniform distribution, smooth surface, no pores and fracture. At the same time, the film has strong hydrophobicity, good thermal stability and mechanical properties. Its antibacterial performance is better than that of single-core nanofiber films, which effectively destroys the cell membrane of S. putrefaciens, increases the permeability of cell membrane, and interferes with the synthesis and expression of its protein. The coaxial nanofiber films with CMA, TP and its composite as core material can be used as a fresh-keeping material with antibacterial properties, and has potential application value in the field of food preservation.

In vitro and in vivo biological assessment of dual drug-loaded coaxial nanofibers for the treatment of corneal abrasion

The treatment of corneal abrasion currently involves the topical administration of antibiotics, with moxifloxacin HCl (0.5% w/v) eye drops being one of the most widely used treatments. Our previous work (Tawfik et al., 2020) involved the development of coaxial poly-lactic-co-glycolic acid (PLGA) and polyvinylpyrrolidone (PVP) nanofibers loaded with the antibiotic moxifloxacin HCl and the anti-scarring agent pirfenidone in the core (PVP) and shell (PLGA) respectively, with a view to the system comprising an ocular insert for the combination therapy of corneal abrasion. In this study, we examine the antimicrobial, anti-scarring and pharmacokinetic properties of the fibers alongside consideration of their toxicity and propensity for irritation. Minimum inhibitory concentration and zone of inhibition studies against S. aureus and P. aeruginosa were performed, while fibroblast cell viability and α-smooth muscle actin (α-SMA, a biomarker for scar formation) were measured using MTT and Western Blot assays, respectively. Pharmacokinetic studies and efficacy against infection were performed using a rabbit model, while ocular irritancy was assessed using the Draize test. The studies demonstrated that the antimicrobial activity of the moxifloxacin HCl was preserved following encapsulation into the nanofibers, while the downregulation of α-SMA was demonstrated using concentrations below the IC20 values (concentration required to decrease corneal fibroblast viability by no more than 20%). The pharmacokinetic study showed retention and sustained release of the moxifloxacin HCl over a 24-hour period, in contrast to equivalent eye drops which required four times daily dosing. Evidence of low level (according to the MMTS scale) irritation was detected for the nanofiber systems. Overall, the study has demonstrated that the dual drug-loaded nanofiber system shows potential for once daily dosing as an ocular insert for the treatment of corneal abrasion.

Antibacterial Porous Coaxial Drug-Carrying Nanofibers for Sustained Drug-Releasing Applications.

The phenomenon of drug burst release is the main problem in the field of drug delivery systems, as it means that a good therapeutic effect cannot be acheived. Nanofibers developed by electrospinning technology have large specific surface areas, high porosity, and easily controlled morphology. They are being considered as potential carriers for sustained drug release. In this paper, we obtained polycaprolactone (PCL)/polylactic acid (PLA) core-shell porous drug-carrying nanofibers by using coaxial electrospinning technology and the nonsolvent-induced phase separation method. Roxithromycin (ROX), a kind of antibacterial agent, was encapsulated in the core layer. The morphology, composition, and thermal properties of the resultant nanofibers were characterized by scanning electron microscopy (SEM), attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, differential scanning calorimetry (DSC) and thermogravimetry analysis (TGA). Besides this, the in vitro drug release profile was investigated; it showed that the release rate of the prepared coaxial porous nanofibers with two different pore sizes was 30.10 ± 3.51% and 35.04 ± 1.98% in the first 30 min, and became 92.66 ± 3.13% and 88.94 ± 1.58% after 14 days. Compared with the coaxial nonporous nanofibers and nanofibers prepared by uniaxial electrospinning with or without pores, the prepared coaxial porous nanofibers revealed that the burst release was mitigated and the dissolution rate of the hydrophobic drugs was increased. The further antimicrobial activity demonstrated that the inhibition zone diameter of the coaxial nanofibers with two different pore sizes was 1.70 ± 0.10 cm and 1.73 ± 0.23 cm, exhibiting a good antibacterial effect against Staphylococcus aureus. Therefore, the prepared nanofibers with the coaxial porous structures could serve as promising drug delivery systems.

Comparative Analysis of Electrospun Uniaxial and Coaxial Nanofibers Properties

Coaxial electrospinning, which is a modified electrospinning technique involving an arrangement of multiple solution feed systems, enable the production of multilayered nanofibers. In this study, multilayered nanofibers of polyamide 6 (core) / polycaprolactone (shell) containing silver nanoparticles in the core were produced by coaxial electrospinning method. UV-Visible spectra showed that the size of nanoparticles were about 10 nm and the content of nanoparticles were observed to be proportional to the precursor content added to the solvent. The obtained multilayered nanofibers were characterized in terms of morphology, chemical structure, and silver release properties. The multilayered nanofiber structure was confirmed by the selective dissolution and removal of shell layer. The increase in the PCL content of the multilayered nanofibers with the increase in the flow rate of the shell solution was confirmed by FTIR. The silver release profiles of the nanofibers were observed to be dependent on the nanofiber configuration, and silver content. Shell thickness was also an important parameter affecting the silver release properties for multilayered nanofibers.

Coaxial electrospun PVA/PCL nanofibers with dual release of tea polyphenols and ε-poly (L-lysine) as antioxidant and antibacterial wound dressing materials

Preparing wound dressing with dual-delivery of antioxidant and antibacterial agents is highly desirable in clinical wound treatment. Herein, a series of coaxial nanofiber membranes loaded with antioxidant tea polyphenols (TP) in the core and antibacterial ε-poly (L-lysine) (ε-PL) in the shell layer were successfully fabricated by coaxial electrospinning. The physicochemical characterizations by transmission electron microscopy, inverted fluorescence microscopy and fourier transform infrared spectroscopy confirmed the formation of core-shell structure. The results of in vitro drug release indicated that ε-PL exhibited a fast release profile while TP released in a sustained manner, which is favorable to the achievement of quick bacteria inhibition in the initial phase as well as long-term antioxidant activity during wound healing. The antioxidant activity of coaxial nanofibers was found to be increased with the increment of TP content and incubation time. The antibacterial assays against Escherichia coli and Staphylococcus aureus demonstrated that the incorporation of ε-PL in the coaxial nanofibers led to strong antibacterial activity. Additionally, all the coaxial nanofibers possessed good cytocompatibility. Therefore, the prepared coaxial nanofibers simultaneously incorporated with ε-PL and TP are promising as potential wound dressing materials.

Dual drug delivery of vancomycin and imipenem/cilastatin by coaxial nanofibers for treatment of diabetic foot ulcer infections

Diabetic foot ulcer infections are the main causes of hospitalization in diabetics. The present study aimed to develop vancomycin and imipenem/cilastatin loaded core-shell nanofibers to facilitate the treatment of diabetic foot ulcers. Therefore, novel core-shell nanofibers composed of polyethylene oxide, chitosan, and vancomycin in shell and polyvinylpyrrolidone, gelatin, and imipenem/cilastatin in core compartments were prepared using the electrospinning technique. The nanofibers were characterized using scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, tensile test, and drug release. The antibacterial activity of drug-loaded nanofibers in different drugs concentrations was evaluated against Methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli, and Pseudomonas aeruginosa by disk diffusion method. Furthermore, the cytotoxicity of fibers was investigated by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide assay. The obtained results showed that the prepared nanofibers were smooth having a core-shell structure with almost no cytotoxicity. The nanofibrous mats exhibited significant antibacterial activity against S. aureus and MRSA with the inhibition zones of 2.9 and 2.5 cm and gram-negative bacteria species of E. coli and P. aeruginosa with the inhibition zones of 1.9 and 2.8 cm, respectively. With respect to the significant antibacterial activities of these nanofibrous mats, they might be used as suitable drug delivery devices not only for diabetic foot ulcer infections but also for other chronic wounds.