Electrospun biodegradable nanofibers scaffolds for bone tissue engineering

Many polymeric materials have been developed and introduced for bone regeneration. Especially, their nanofibrous forms are mostly applied for artificial extracellular matrices. Polymeric materials in their nanofibrous form show some potent properties such as high surface‐to‐volume ratio, tunable porosity, and ease of surface functionalization. Benefiting from the properties of their main polymer and additives, they can provide new opportunities for cell seeding, proliferation, and new 3D‐tissue formation. This article focuses on most cited polymeric nanofibrous scaffolds fabricated by electrospinning and recent achievements. They were divided into two main categories: natural (collagen, silk, keratin, gelatin, chitosan, and alginate) and synthetic (e.g., polycaprolactone, polylactic acid, and polyglycolic acid) polymers. The role of several additives like hydroxyapatite, bone morphogenetic proteins (BMPs), tricalcium phosphate, and collagen type I in improving the adhesion, differentiation, and tissue formation of stem cells were discussed. Finally, the osteogenic capacity and ability of nanofibrous scaffolds to support the growth of clinically relevant bone tissue were briefly studied. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42883.     

Fabrication and characterization of chitosan/kefiran electrospun nanofibers for tissue engineering applications

Chitosan (CS)-based nanofibrous scaffolds are very promising in tissue engineering applications. However, electrospinning of CS is not possible unless using toxic solvents such as trifluoroacetic acid or by blending with other polymers. In the present study, we investigated CS-based nanofibers' fabrication by blending it with kefiran as a natural polysaccharide. A series of solutions with various CS to kefiran ratios were prepared and underwent electrospinning. The effects of main process parameters, including applied voltage and needle tip-to-collector distance on nanofibers' diameter and morphology, were also studied. Nanofibers containing 80% CS and 20% Kefiran with an average diameter of 81 ± 17 nm were successfully electrospun. Thermogravimetric analysis indicated the presence of both polymers in blend nanofibers. The diameter of CS/kefiran nanofibers increased with enhanced applied voltage, while needle tip-to-collector distance did not significantly affect the mean diameters. Appropriate viability of l929 cells on the obtained scaffolds was demonstrated utilizing Alamar blue assay. Also, cell attachment onto the fiber surface was confirmed by scanning electron microscopy. Results indicated that CS/kefiran nanofibrous scaffolds would be promising for tissue engineering applications.     

Influence of hydroxyapatite and BMP‐2 on bioactivity and bone tissue formation ability of electrospun PLLA nanofibers

An excellent bioactive scaffold material which could induce and promote new bone formation is essential in the bone repair field. In this study, the bioactive material hydroxyapatite (HA) and the bone morphogenetic protein‐2 (BMP‐2) were added to poly‐l‐lactic acid (PLLA) using the electrospinning method. Scanning electron microscopy investigations performed on four different fiber scaffolds, PLLA, PLLA/HA, PLLA/BMP‐2 and PLLA/HA/BMP‐2, revealed that the fibers of all scaffolds are closely interwoven, and the presence of large interconnected voids between the fibers, resulting in a three‐dimensional porous network structure that was similar to the structure of the extracellular matrix of healthy bones. In the MG63 cell culture growth experiments, the composite scaffold material PLLA/HA/BMP‐2 showed a higher bioactivity than the other three scaffold materials. The four scaffold materials were implanted in rabbits’ tibia for 30 and 90 days. The results of the animal experiments indicate that the capability of the PLLA/HA/BMP‐2 composite to induce and promote bone tissue formation was better compared with PLLA/HA or PLLA/BMP‐2, suggesting that PLLA combined with HA/BMP‐2 is a promising material for bone tissue repair. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42249.     

Biocompatible graphene-embedded PCL/PGS-based nanofibrous scaffolds: A potential application for cardiac tissue regeneration

Research in the field of tissue engineering, especially heart tissue engineering, is growing rapidly. Herein, the morphological, chemical, mechanical and biological properties of poly (caprolactone) (PCL)/poly (glycerol sebacate) (PGS) and PCL/PGS/graphene nanofibrous scaffolds are investigated. Initially, PGS pre-polymer is synthesized and characterized by nuclear magnetic resonance and Fourier transform infrared spectroscopies. Then, in order to use the benefits of PGS, this polymer is mixed with PCL. Blending PGS with PCL resulted in the enhancement of ultimate elongation and reduction in the elastic modulus due to the intrinsic properties of PGS. The hydrophobicity of PCL nanofibers is reduced by adding PGS as hydrophilic polymer (105 ± 3° vs. 44 ± 2°). Also, the addition of graphene to the blend nanofibers is balanced the hydrophilicity. Degradation rate of pure PCL nanofibers is very slow but it is increased in the presence of PGS. All nanofibrous scaffolds are biocompatible and non-toxic. The highest cell adhesion (covered area = 0.916 ± 0.032) and biocompatibility (98.79 ± 1%) are related to PCL/PGS loaded with 1% wt of graphene (PCL/PGS/graphene ₁). Thus, this sample can be a good candidate for further examinations of cardiac tissue engineering.     

Composite chitosan/poly(ethylene oxide) electrospun nanofibrous mats as novel wound dressing matrixes for the controlled release of drugs

The aim of this study was to develop novel biomedical electrospun nanofiber mats for controlled drug release, in particular to release a drug directly to an injury site to accelerate wound healing. Here, nanofibers of chitosan (CS), poly(ethylene oxide) (PEO), and a 90 : 10 composite blend, loaded with a fluoroquinolone antibiotic, such as ciprofloxacin hydrochloride (CipHCl) or moxifloxacin hydrochloride (Moxi), were successfully prepared by an electrospinning technique. The morphology of the electrospun nanofibers was investigated by scanning electron microscopy. The functional groups of the electrospun nanofibers before and after crosslinking were characterized by Fourier transform infrared spectroscopy. X‐ray diffraction results indicated an amorphous distribution of the drug inside the nanofiber blend. In vitro drug‐release evaluations showed that the crosslinking could control the rate and period of drug release in wound‐healing applications. The inhibition of bacterial growth for both Escherichia coli and Staphylococcus aureus were achieved on the CipHCl‐ and Moxi‐loaded nanofibers. In addition, both types of CS/PEO and drug‐containing CS/PEO nanofibers showed excellent cytocompatibility in the cytotoxicity assays. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42060.     

Fabrication and characterization of novel nanofibers from cress seed mucilage for food applications

Cress seed mucilage (CSM) as a new source of biomacromolecule has gained attraction in food science due to its biodegradability and biocompatibility. In this research CSM–poly(vinyl alcohol) (PVA) nanofibers were produced under different conditions by electrospinning technique. Viscosity and electrical conductivity of the produced biopolymers were analyzed. The effect of CSM to PVA volume ratio and applied electrical field were evaluated on nanofiber morphology by scanning electron spectroscopy. The optimum nanofibers showed smooth and uniform surfaces with diameter size range of 95–278 nm. The results of Fourier transform infrared spectroscopy of CSM–PVA nanofiber with volume ratio of 60:40 showed characteristic peaks of CSM and PVA. X‐ray diffractometer data clearly revealed the amorphous structure of the electrospun nanofibers. Thermogravimetric and derivative thermogravimetric analysis indicated that thermal stability of electrospun nanofibers increased in comparison to CSM and PVA. The results of this study indicated that CSM can be applied as a new source of biopolymer for production of nanofibers that could be used for different applications such as delivery systems and packaging film fabrication. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45811.     

Fabrication and characterization of double‐network agarose/polyacrylamide nanofibers by electrospinning

This study focused on the preparation of electrospun cross‐linked double‐network (DN) of agarose/polyacrylamide (PAAm) nanofibers. The agarose formed the first‐network that was physical‐linked by the agar helix bundles. After UV‐irradiation, the chemically crosslinked PAAm was formed as the second network. The resulting cross‐linked DN agarose/PAAm nanofibers were characterized by scanning electron microscopy (SEM), contact angle, attenuated total reflectance‐Fourier transform infrared spectroscopy (ATR‐FT‐IR), thermogravimetric analysis (TGA), and tensile test. SEM analysis shows the agarose/PAAM nanofibers present with the thickness of 187 nm. Agarose/PAAm nanofibers were showing FT‐IR spectral peaks at ～1660, 1590, and 1070 cm^?1 indicating the presence of both agarose and polyacrylamide in the crosslinked DN Agarose/PAAm nanofiber sheet, it suggests the strong interaction and good compatibility between the two components. Agarose/PAAm nanofiber sheet was showing thermal stability close to the pure polyacrylamide. From the tensile test study, agarose/PAAm strength improved by 66.66% compared to the pure agarose. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42914.     

Novel electrospun nanofibers incorporating polymeric prodrugs of ketoprofen: Preparation,characterization, and in vitro sustained release

A facile and efficient protocol for the preparation of nanofibers incorporating polymeric ketoprofen prodrugs and polyvinylpyrrolidone was developed. Polymeric ketoprofen prodrugs were constructed by a two‐step chemo‐enzymatic synthetic route, and nanofibers prepared by electrospinning from dimethylformamide/ethanol (1 : 1, v/v) solutions. The morphological characteristics of the fibers were influenced by the concentration of active agent in the spinning solution; average diameters varied from 196 to 370 nm. In vitro release studies indicated that the ketoprofen release rate from the electrospun fibers was significantly higher than that from the pure polymeric prodrugs. Cumulative drug release from the electrospun fibers reached 40–70% after 3 h and 75–100% after 12 h, while the pure polymeric prodrug released only 7–9% of the active agent over 12 h. Functional nanofibers incorporating polymeric prodrugs therefore comprise potentially effective drug delivery systems for sustained release. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1570–1577, 2013     

Fabrication of polymer/drug‐loaded hydroxyapatite particle composite fibers for drug sustained release

The aim of this study is to fabricate polymer/hydroxyapatite (HA) particle composite fibers for drug encapsulation and sustained release. Firstly, drug‐loaded hydroxyapatite particles are synthesized in one step, then by electrospinning of the blends of drug‐loaded hydroxyapatite particles and polymer solution the drug‐loaded polymer/hydroxyapatite particle composite fibers are successfully prepared. Effect of loading ratio of drug‐loaded hydroxyapatite particles in the fibers and pH value of the release medium on the drug release kinetics are both investigated, and the results demonstrate that, as compared with the polymer/drug electrospun fibers, the drug in the polymer/drug‐loaded hydroxyapatite particle composite fibers shows a sustained release manner, and the drug release rate can be regulated by both the loading ratio of drug‐loaded hydroxyapatite particles in the composite fibers and pH value of the buffer solution. The results indicate that the developed drug‐loaded polymer/hydroxyapatite particle composite fibers show great potential in bone regeneration and other related biomedical fields. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42871.     

Fabrication and evaluation of poly(lactic acid), chitosan,and tricalcium phosphate biocomposites for guided bone regeneration

This study presents and evaluates an approach for fabricating poly(lactic acid) (PLA)/chitosan (CS)/tricalcium phosphate (TCP) electrospun scaffolds for guided bone regeneration, a dental procedure that uses membranes to direct and delineate regions of osteogenesis. Biomaterials were pre‐processed using cryomilling, a solid‐state grinding technique that facilitates the generation of powdered biocomposites conducive to electrospinning. X‐ray diffraction (XRD) confirmed the generation of cryomilled blends consisting of PLA, CS, and TCP. Results from the differential scanning calorimetry showed an upward shift in glass transition temperature and an increase in crystallinity with the inclusion of TCP reinforcing the observations from XRD. Murine macrophages were used to confirm the biocompatibility of the cryomilled powders and was evaluated using CellTiter‐Blue (CTB) cell viability assay and brightfield microscopy. Scanning electron microscopy was used to examine the morphology of the fibers produced via electrospinning, while Raman spectroscopy confirmed material homogeneity. In vitro studies with MG‐63 cells validated the capacity of composite scaffolds to encourage proliferation, while Coherent anti‐Stokes Raman scattering and fluorescence microscopies provided visual evidence of cell proliferation. CTB assay revealed that cells maintain viability and metabolic activity at 3 and 7 days after seeding, demonstrating the potential of the biocomposite membranes. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46692.     

Electrospinning of polycaprolactone nanofibers using H2O as benign additive in polycaprolactone/glacial acetic acid solution

Considerable efforts have been devoted to the production of polycaprolactone (PCL) nanofibrous structures by electrospinning. However, some toxic solvents have often been used to achieve bead‐free nanofibers. At present, a benign solvent such as glacial acetic acid (GAC) only leads to beaded or microscale fibers. Therefore a study is done to extend the electrospinnability of the PCL/GAC system by the addition of H₂O. The solution properties of conductivity, viscosity, and surface tension were altered by the addition of H₂O, especially increasing the conductivity and viscosity. These properties essential to electrospinning could remain stable for 6 h when the H₂O content was less than or equal to 9 vol %. Then ultrafine PCL fibers with diameters from 188 to 200 nm, 10 times smaller than when dissolved in pure GAC, were electrospun from solutions of PCL with concentrations in the range of 17 to 20 wt % with H₂O content at 9 vol %. Finally, the crystallinity and crystallite size of the resulting fibers were smaller than that of raw PCL pellets. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45578.     

Electrospinning polycaprolactone dissolved in glacial acetic acid: Fiber production,nonwoven characterization,and In Vitro evaluation

The electrospinning of polycaprolactone (PCL) dissolved in glacial acetic acid and the characterization of the resultant nonwoven fiber mats is reported in this work. For comparison purposes, PCL fiber mats were also obtained by electrospinning the polymer dissolved in chloroform. Given the processing parameters chosen, results show that 14 and 17 wt % PCL solutions are not viscous enough and yield beaded fibers, 20 and 23 wt % solutions give rise to high quality fibers and 26 wt % solutions yield mostly irregular and fused fibers. The nonwoven mats are highly porous, retain the high tensile strain of PCL, and the fibers are semicrystalline. Cells adhere and proliferate equally well on all mats, irrespective of the solvent used in their production. In conclusion, mats obtained by electrospinning PCL dissolved in acetic acid are also a good option to consider when producing scaffolds for tissue engineering. Moreover, acetic acid is miscible with polar solvents, which may allow easier blending of PCL with hydrophilic polymers and therefore achieve the production of electrospun nanofibers with improved properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41068.     

Silver‐nanoparticle‐Incorporated composite nanofibers for potential wound‐dressing applications

The aim of this study was to develop stable and porous poly(ethylene oxide) (PEO)–polycaprolactone blended and silver nanoparticle (Ag NP) incorporated composite nanofiber scaffolds as antibacterial wound dressings. A facile approach for the in situ synthesis of Ag NPs was explored. In this synthesis method, N,N‐dimethylformamide (DMF) was used as a solvent; it also acted as reducing agent for Ag NP formation. The stabilization of Ag NPs in the fibers was accomplished by PEO, which in turn acted as a reducing agent along with DMF. The successful synthesis of crystalline Ag NPs was confirmed by various characterization techniques. Thermogravimetric analysis, wettability, and surface roughness analysis of the nanofibers were done to examine the suitability of the scaffold for wound dressing. The as‐synthesized composite nanofibers possessed good roughness, wettability, and antibacterial potential against recombinant green fluorescent proteins expressing antibiotic‐resistant Escherichia coli. Thus, the nanofiber scaffold fabricated by this approach could serve as an ideal wound dressing. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42473.     

Sulfobetaine-functionalized electrospun poly(ethylene-co-vinyl alcohol) membranes for blood filtration

Functionalization imparting zwitterionic sulfobetaines has been proven as the most versatile method for improving the hemocompatibility of polymers. In this study, we aimed to enhance the hemocompatibility of electrospun poly(ethylene-co-vinyl alcohol) (EVAL) by photografting with a betaine N-(3-sulfopropyl)-N-methacroyloxyethyl-N,N-dimethyl ammonium betaine (SMDB). SMDB was UV-photografted to electrospun EVAL fibroporous membranes to obtain EVAL-g-PSMDB poly[N-(3-sulfopropyl)-N-methacroyloxyethyl-N,N- dimethylammonium betaine] grafted on EVAL with different extents of grafting. The functionalization was confirmed by analysis of the attenuated total reflectance–Fourier transform infrared spectra. The effects of functionalization on the morphology, wettability, mechanical properties, and hemocompatibility of the electrospun EVAL membranes were also studied by scanning electron microscopy, water contact angle measurement, universal testing machine measurement, and in vitro hemocompatibility evaluation, respectively. The findings highlight that SMDB functionalization significantly reduced protein adsorption, hemolysis, and platelet adhesion. Blood cell consumption studies projected that the SMDB-functionalized EVAL was able to capture leukocytes from blood, and hence, this system has the potential to be used as a filter medium for the selective removal of leukocytes from blood. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47057.     

Biphasic,tough composite core/shell PCL/PVA-GEL nanofibers for biomedical application

Emulsion electrospinning using natural and synthetic polymers, including two dissimilar materials is a promising technique for nanofibers fabrication in a core/shell configuration for tissue engineering, controlled or sustained drug delivery and dressing applications. In this study, we designed and fabricated core/shell nanofibers based on polycaprolactone (PCL) as core material and poly(vinyl alcohol) (PVA)-gelatin (GEL) blend as shell materials (PCL/PVA-GEL) to achieve high mechanical properties, good cell growth, and proliferation via emulsion electrospinning. The effect of water to acetic acid ratio in the solvent system (8:2, 7:3, 6:4, 5:5) and also type and concentration (3, 5, 7 w/v %) of surfactant on emulsion stability and nanofibers morphology were investigated. The emulsion containing 2% Tween80 and 1% Span60 as surfactants were selected by considering the stability of emulsion and uniform fiber morphology. In the tensile strength and elongation at break, 53 and 8% increase in the crosslinked wet state of the PCL/PVA-GEL nanofibers compared with PVA-GEL nanofibers were observed respectively. The cell culture results indicated that the PCL/PVA-GEL nanofibers surface has presented suitable interaction with fibroblast cells and cells attached and proliferated well on the fabricated substrate within 24 and 48 hours and also would be a good candidate for biomedical applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48713.     

Nanoporous hollow fibers as a phantom material for the validation of diffusion magnetic resonance imaging

Diffusion-weighted magnetic resonance imaging (MRI) is an emerging noninvasive imaging modality. In this study, highly aligned, uniform, nanoporous, hollow polycaprolactone fibers were successfully synthesized in a single step to mimic the axon bundle structure in human white matter. Their porous nature, morphology, and physicochemical properties were carefully studied with respect to their suitability as a phantom material for brain imaging. The aligned fibrous bundles were then arranged into specific angles (30 and 90°), scanned, and evaluated with high-resolution MRI fiber tractography. Diffusion tensor imaging and the tractography of fibers of five different structures at three temperatures were acquired and compared. Furthermore, an integrated brain phantom created from a combination of agar gel and aligned fibrous bundles was also fabricated and analyzed. The results demonstrate the excellent ability of the fibers to mimic the axonal bundles of brain white matter. The fibrous bundles were well mixed in the common agar phantom while retaining their fibrous configuration; this demonstrated their potential as brain white matter phantoms. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47617.     

Novel bilayer electrospun poly(caprolactone)/ silk fibroin/ strontium carbonate fibrous nanocomposite membrane for guided bone regeneration

In this study, a thin layer with a thickness of about 120 μm of poly(caprolactone) (PCL) was fabricated by electrospinning method. Then, a fibrous nanocomposite composed of PCL/silk fibroin/strontium carbonate (PCL/SF/SrCO₃) was electrospun on the prepared layer. Then, they were characterized. The mechanical properties, water uptake, degradation rate, wettability, porosity, and bioactivity of the electrospun membrane were scrutinized in vitro. Cytotoxicity of the samples was assessed by using osteoblast-like cells (SAOS-2) and L929 fibroblasts. Moreover, the cell adhesion, alkaline phosphatase (ALP) activity, and calcium deposition through alizarin red staining were conducted. Results revealed that the bilayer structure doubled the optimum mechanical properties and the addition of SrCO₃ up to 15%–20% increased ALP activity, calcium deposition, and bioactivity. According to the results, the nanofibrous bilayer membrane containing 20 wt% SrCO₃, 20 wt% SF, and 60 wt% PCL was chosen as the optimum sample. Therefore, this membrane could be applied in guided bone regeneration (GBR).     

静电纺纳米纤维的应用

综述了静电纺纳米纤维在保护性服用材料、传感器、过滤防护材料、高分子纳米模板、纳米复合改性材料、航空航天等方面的应用;详述了在生物医用材料方面的应用;展望了静电纺丝纳米纤维的发展前景;指出应继续研发具有特殊性能的静电纺纳米纤维新产品,扩大其应用领域,最终实现成果产业化。     

Rapid polymer fiber airbrushing: Impact of a device design on the fiber fabrication and matrix quality

Polymer fiber matrixes can be used in a variety of applications, including electronics, tissue engineering, or coatings. Polymer airbrushing (air‐blast spinning) has the potential to overcome some of the limitations of electrospinning and has the advantage of depositing nanofibers directly on various materials. The airbrushing technique has yet to be better evaluated and optimized to achieve a higher fiber reproducibility and bulk material quality. In this study, a gravity‐fed brush (commercial airbrush) and syringe‐pump‐operated brush [custom‐built airbrush (CBA)] were compared to determine the effect of the coaxial brush design on the efficacy of fiber fabrication. At comparable fiber deposition rates, gas pressures, and polymer concentrations, the CBA produced smaller and more uniform fibers with a lower average size of polymer beads. The obtained data suggest that capillary pinching was the dominant mechanism responsible for fiber formation when we used the CBA. The estimated pinching energy was lower for the CBA at the compared polymer concentrations and at a high gas pressure. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42813.     

Flurbiprofen axetil loaded coaxial electrospun poly(vinyl pyrrolidone)–nanopoly(lactic‐co‐glycolic acid) core–shell composite nanofibers: Preparation,characterization, and anti‐adhesion activity

Flurbiprofen axetil (FA)‐loaded coaxial electrospun poly(vinyl pyrrolidone) (PVP)–nanopoly(lactic‐co‐glycolic acid) core–shell composite nanofibers were successfully fabricated by a facile coaxial electrospinning, and an electrospun drug‐loaded system was formed for anti‐adhesion applications. The FA, which is a kind of lipid microsphere nonsteroidal anti‐inflammatory drug, was shown to be successfully adsorbed in the PVP, and the formed poly(lactic‐co‐glycolic acid) (PLGA)/PVP/FA composite nanofibers exhibited a uniform and smooth morphology. The cell viability assay and cell morphology observation revealed that the formed PLGA/PVP/FA composite nanofibers were cytocompatible. Importantly, the loaded FA within the PLGA/PVP coaxial nanofibers showed a sustained‐release profile and anti‐adhesion activity to inhibit the growth of the IEC‐6 and NIH3T3 model cells. With the significantly reduced burst‐release profile, good cytocompatibility, and anti‐adhesion activity, the developed PLGA/PVP/FA composite nanofibers were proposed to be a promising material in the fields of tissue engineering and pharmaceutical science. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41982.