Antibacterial antiadhesion membranes from silver‐nanoparticle‐doped electrospun poly(L‐lactide) nanofibers

Electrospun fibrous membranes have been used frequently in biomedical applications, but their simultaneous use as antibacterial agents and in the prevention of cell adhesion on repaired tendons after injury has not been investigated. In this study, silver‐nanoparticle (SN)‐loaded poly(L ‐lactide) (PLLA) fibrous membranes were prepared by the electrospinning of SNs into PLLA fibers. Micrograph results showed that these membranes were composed of electrospun fibers and that the fibers were incorporated with SNs. From the results of X‐ray diffraction and thermogravimetry, we concluded that the SNs were physically mixed into the fibers at the desired content. The mechanical properties were not significantly changed. The preliminary antibacterial effects on Staphylococcus epidermidis and Staphylococcus aureus and the synergistic antiproliferative effects of the SN‐loaded PLLA fibrous membranes were observed. Taken together, these results demonstrate that SNs can be directly loaded onto a biodegradable PLLA fibrous membrane via electrospinning to achieve proper material properties with preliminary potential as antibacterial antiadhesion barriers for tendon injury. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Prevention of Intra-Abdominal Adhesion by Bi-Layer Electrospun Membrane

The aim of this study was to compare the anti-adhesion efficacy of a bi-layer electrospun fibrous membrane consisting of hyaluronic acid-loaded poly(ɛ-caprolactone) (PCL) fibrous membrane as the inner layer and PCL fibrous membrane as the outer layer with a single-layer PCL electrospun fibrous membrane in a rat cecum abrasion model. The rat model utilized a cecal abrasion and abdominal wall insult surgical protocol. The bi-layer and PCL membranes were applied between the cecum and the abdominal wall, respectively. Control animals did not receive any treatment. After postoperative day 14, a visual semiquantitative grading scale was used to grade the extent of adhesion. Histological analysis was performed to reveal the features of adhesion tissues. Bi-layer membrane treated animals showed significantly lower adhesion scores than control animals (p < 0.05) and a lower adhesion score compared with the PCL membrane. Histological analysis of the bi-layer membrane treated rat rarely demonstrated tissue adhesion while that of the PCL membrane treated rat and control rat showed loose and dense adhesion tissues, respectively. Bi-layer membrane can efficiently prevent adhesion formation in abdominal cavity and showed a significantly decreased adhesion tissue formation compared with the control.     

Functional Hyaluronic Acid-Polylactic Acid/Silver Nanoparticles Core-Sheath Nanofiber Membranes for Prevention of Post-Operative Tendon Adhesion

In this study, we prepared core-sheath nanofiber membranes (CSNFMs) with silver nanoparticles (Ag NPs) embedding in the polylactic acid (PLA) nanofiber sheath and hyaluronic acid (HA) in the nanofiber core. The PLA/Ag NPs sheath provides mechanical support as well as anti-bacterial and anti-inflammatory properties. The controlled release of HA from the core could exert anti-adhesion effects to promote tendon sliding while reducing fibroblast attachment. From the microfibrous structural nature of CSNFMs, they function as barrier membranes to reduce fibroblast penetration without hampering nutrient transports to prevent post-operative peritendinous adhesion. As the anti-adhesion efficacy will depend on release rate of HA from the core as well as Ag NP from the sheath, we fabricated CSNFMs of comparable fiber diameter, but with thick (Tk) or thin (Tn) sheath. Similar CSNFMs with thick (Tk⁺) and thin (Tn⁺) sheath but with embedded Ag NPs in the sheath were also prepared. The physico-chemical properties of the barrier membranes were characterized in details, together with their biological response including cell penetration, cell attachment and proliferation, and cytotoxicity. Peritendinous anti-adhesion models in rabbits were used to test the efficacy of CSNFMs as anti-adhesion barriers, from gross observation, histology, and biomechanical tests. Overall, the CSNFM with thin-sheath and Ag NPs (Tn⁺) shows antibacterial activity with low cytotoxicity, prevents fibroblast penetration, and exerts the highest efficacy in reducing fibroblast attachment in vitro. From in vivo studies, the Tn⁺ membrane also shows significant improvement in preventing peritendinous adhesions as well as anti-inflammatory efficacy, compared with Tk and Tn CSNFMs and a commercial adhesion barrier film (SurgiWrap^®) made from PLA.     

Synthesis and Characterization of Biocompatible Poly(ethylene glycol)-b-Poly(L-lactide) and Study on Their Electrospun Scaffolds

A series of multiblock copolymer, Poly(L-lactide)-b-Poly(ethylene glycol) (PLLA-b-PEG) were synthesized and characterized by Fourier transform infrared spectra, differential scanning calorimetry and wide angle X-ray diffraction. PLLA-b-PEG fibrous scaffolds were prepared by electrospinning. The morphology of the fibers was affected by the solution concentration and different weight ratio of PLLA/PEG. In comparison with the electrospun PLLA membrane, the electrospun fibrous membranes of PLLA-b-PEG demonstrated an enhanced water absorption percentage and reductive water contact angle. The electrospun PLLA-b-PEG with weight ratio 90/10 and 75/25 fibrous membranes exhibited good flexibility and deformability to be beneficial for tissue engineering scaffolds.     

Electrospun poly(L‐lactide)/poly(ε‐caprolactone) blend fibers and their cellular response to adipose‐derived stem cells

Polymer blending is one of the most effective methods for providing new, desirable biocomposites for tissue‐engineering applications. In this study, electrospun poly(L ‐lactide)/poly(ε‐caprolactone) (PLLA/PCL) blend fibrous membranes with defect‐free morphology and uniform diameter were optimally prepared by a 1 : 1 ratio of PLLA/PCL blend under a solution concentration of 10 wt %, an applied voltage of 20 kV, and a tip‐to‐collector distance of 15 cm. The fibrous membranes also showed a porous structure and high ductility. Because of the rapid solidification of polymer solution during electrospinning, the crystallinity of electrospun PLLA/PCL blend fibers was much lower than that of the PLLA/PCL blend cast film. To obtain an initial understanding of biocompatibility, adipose‐derived stem cells (ADSCs) were used as seed cells to assess the cellular response, including morphology, proliferation, viability, attachment, and multilineage differentiation on the PLLA/PCL blend fibrous scaffold. Because of the good biocompatibility and nontoxic effect on ADSCs, the PLLA/PCL blend electrospun fibrous membrane provided a high‐performance scaffold for feasible application in tissue engineering using ADSCs. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

A novel carrier of radionuclide based on surface modified poly(lactide-co-glycolide) nanofibrous membrane

Electrospun nanofibrous membrane is an approved drug carrier. However, the radionuclide carrier used an electrospun membrane is rare. In this study, Poly(lactide-co-glycolide)(PLGA) nanofibrous nonwovens were prepared through electrospinning technology, and then surface modification of the nonwoven was performed to stably conjugate the radioisotope with the fibrous membrane. A novel PLGA nanofibrous nonwoven conjugated with radioactive yttrium ⁹⁰Y for tumor internal radiotherapy was prepared for the first time. Evaluation of the stability of the radioisotope indicated that the leakage of ⁹⁰Y from the PLGA membranes can be neglected after 24 h incubation in saline. The retention of ⁹⁰Y on the PLGA membrane was 75% when five half lives of ⁹⁰Y expired and the vast majority of radioactive decay had occurred. This labeled nanofibrous membrane function as a novel radio-medical appliance with excellent surface hydrophilic and mechanical properties that can be directly implanted into the lesions not only to locally kill the cancerous cells but also to play the anti-adhesion role at where surgical procedures have been made to remove the tumor tissue.     

Multi-Layer Electrospun Membrane Mimicking Tendon Sheath for Prevention of Tendon Adhesions

Defect of the tendon sheath after tendon injury is a main reason for tendon adhesions, but it is a daunting challenge for the biomimetic substitute of the tendon sheath after injury due to its multi-layer membrane-like structure and complex biologic functions. In this study, a multi-layer membrane with celecoxib-loaded poly(l-lactic acid)-polyethylene glycol (PELA) electrospun fibrous membrane as the outer layer, hyaluronic acid (HA) gel as middle layer, and PELA electrospun fibrous membrane as the inner layer was designed. The anti-adhesion efficacy of this multi-layer membrane was compared with a single-layer use in rabbit flexor digitorum profundus tendon model. The surface morphology showed that both PELA fibers and celecoxib-loaded PELA fibers in multi-layer membrane were uniform in size, randomly arrayed, very porous, and smooth without beads. Multi-layer membrane group had fewer peritendinous adhesions and better gliding than the PELA membrane group and control group in gross and histological observation. The similar mechanical characteristic and collagen expression of tendon repair site in the three groups indicated that the multi-layer membrane did not impair tendon healing. Taken together, our results demonstrated that such a biomimetic multi-layer sheath could be used as a potential strategy in clinics for promoting tendon gliding and preventing adhesion without poor tendon healing.     

Durable adhesives based on electrospun poly(vinylidene fluoride) fibers

Herein, the fabrication of poly(vinylidene fluoride) (PVDF) fibrous membrane using electrospinning is reported and its use for dry‐adhesive applications is demonstrated. The shear and normal adhesion performance of the samples was investigated using an Instron tensile tester and an atomic force microscope (AFM) respectively. For shear adhesion measurements, the electrospun membrane was finger pressed on to a glass slide and pulled in shear mode using a tensile tester. The thickness of the electrospun membrane was varied and the effect of thickness on shear adhesion was investigated. The shear adhesion strength increased when the thickness of the samples was reduced. Shear adhesion strength of a 200 µm thick sample was determined to be approximately 0.165 N/cm. For normal adhesion measurements, a flat tipless cantilever was used to indent the sample and then retract back to measure the pull‐off force. High shear adhesion strength and normal pull‐off force recorded are attributed to the fine size of the fibers that conform to the asperities present on the surfaces of the glass slide and the AFM cantilever. The durability of the adhesive was also verified by repeating the AFM adhesion measurements over 1000 consecutive attachment–detachment cycles. The pull‐off force was seen to be constant over 1000 attachment–detachment cycles. Our results indicate that these electrospun fibrous membranes can potentially be used as reusable dry‐adhesives. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44393.     

Processing and properties of hydrophilic electrospun polylactic acid/beta‐tricalcium phosphate membrane for dental applications

Typical electrospun polylactic acid (PLA) membranes revealing potential hydrophobicity and inflammation from acid release during degradation are major drawbacks as an ideal guided tissue regeneration (GTR) barrier. This study investigated the in vitro degradation properties of electrospun PLA/beta‐tricalcium phosphate (β‐TCP) membranes treated by polyethylene oxide dip‐coating process. After surface modification, the membranes revealed good wettability in contact angle measurement. The addition of β‐TCP can render good pH buffering properties for electrospun PLA membranes during the in vitro degradation test. The mechanical properties of the hybrid membrane showed no significant difference in suture pullout force at a dried or wetted state. For cell adhesion and proliferation, the membranes with hydrophilicity can enhance the cell attachment at early stage. Overall, these results show that electrospinning combined with dip coating is a feasible processing technology for producing hydrophilic fibrous GTR membranes. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers.     

Preparation of hydrophilic poly(l-lactide) electrospun fibrous scaffolds modified with chitosan for enhanced cell biocompatibility

The methods of co-electrospinning and surface hydrolysis have been used for improving hydrophilicity of Poly(l-lactide) (PLLA), while most of them resulted in high shrinkage and changed mechanical properties of bulk polymers. In this study, we modify PLLA electrospun scaffolds by grafting chitosan by aminolysis technology. The results showed that the amount of grafted chitosan on fibrous scaffolds could be adjusted by controlling aminolysis time, and the hydrophilicity of scaffolds was dependent on the amount of grafted chitosan. Water contact angle of scaffolds were changed from 138.3° to 0°. Characteristic analysis of scaffolds indicated that aminolysis method did not affect the porous structure. The density of the modified scaffolds was between 0.48 and 0.54 g/cm³ and the tensile strength was between 3.24 and 3.45 MPa, which were statistically not different as compared to unmodified scaffolds (P > 0.05). The statistical analysis of the cell culture results showed that the cell proliferation on chitosan modified PLLA scaffolds were significantly improved as compared to that on the unmodified PLLA scaffolds (P < 0.05). All of results suggest that the aminolysis method is a convenient and effective mild chemical treatment method to improve hydrophilicity and cell biocompatibility of PLLA electrospun fibrous scaffolds for tissue engineering without sacrificing other properties.     

Effect of different preparation methods on structure and properties of chitosan/poly-lactic acid blend porous membrane

Two kinds of blend solutions were used to prepare chitosan (CS)/poly-l-lactic acid (PLLA) blend membranes by the immersion precipitation phase inversion method. CS/PLLA blend membrane was fabricated by mixing CS-acetic acid solution and PLLA-dioxane solution, chitosan powder (CSP)/PLLA blend membrane was fabricated by mixing CSP and PLLA-dioxane solution. The membrane structure and properties were characterized by Scanning Electron Microscope, Wide Angle X-ray Diffraction, porosity, water vapor transmission rate and swelling property. The results showed that CS content in CSP/PLLA blend membrane was nearly 70 times higher than in CS/PLLA blend membrane. Two types of blend membranes took on an unsymmetrical structure with a skin layer, a microvoid sub-layer and a porous bottom surface. But CSP/PLLA blend membrane exhibited a porous skin layer, while the skin layer of CS/PLLA blend membrane was impact. The WAXD analysis revealed that PLLA and CS were amorphous in CS/PLLA blend membrane, while there were PLLA and CS crystalline in CSP/PLLA membrane, which resulted in the higher initial modulus of CSP/PLLA blend membrane. The porosity, WVTR and equilibrium swelling (Q _eq ) of CSP/PLLA blend membrane were higher than that of CS/PLLA blend membrane, especially Q _eq . The swelling kinetics results showed that in the initial swelling, water molecules diffusion followed Non-Fickian diffusion for CS/PLLA blend membrane swelling, and the swelling of CSP/PLLA blend membrane fitted with the relaxation diffusion model. The swelling kinetics studies for whole swelling revealed that the swelling degree and the initial swelling rate of CSP/PLLA membrane were significantly higher than that of CS/PLLA membrane, although the total swelling rate of CSP/PLLA blend membrane decreased lightly.     

Electrochemical studies of electrospun organic/inorganic hybrid nanocomposite fibrous polymer electrolyte for lithium battery

Poly(vinylidene fluoride-co-hexafluoropropylene) P(VdF-co-HFP)/magnesium aluminate (MgAl₂O₄) hybrid fibrous nanocomposite polymer electrolyte membranes were newly prepared by electrospinning method. The as-prepared electrospun pure and nanocomposite fibrous polymer membranes with various MgAl₂O₄ filler contents were characterized by X ray diffraction, differential scanning calorimetry and scanning electron microscopy techniques. The fibrous nanocomposite polymer electrolytes were prepared by soaking the electrospun membranes in 1 M LiPF₆ in EC:DEC (1:1, v/v). The fibrous nanocomposite polymer electrolyte membrane with 5 wt.% of MgAl₂O₄ show high electrolyte uptake, enhanced ionic conductivity is found to be 2.80 × 10⁻³ S cm⁻¹ at room temperature and good electrochemical stability window higher than 4.5 V. Electrochemical performance of commercial celgard 2320, fibrous pure and nanocomposite polymer electrolyte (PE, NCPE) membranes with different MgAl₂O₄ filler content is evaluated in Li/celgard 2320, PE, NCPE/LiCoO₂ CR 2032 coin cells at current density 0.1 C-rate. The NCPE with 5 wt.% of MgAl₂O₄ delivers an initial discharge capacity of 158 mAhg⁻¹ and stable cycle performance compared with the other cells containing celgard 2320 separator and pure membrane.     

Controlling drug delivery from polymer microspheres by exploiting the complex interrelationship of excipient and drug crystallization

Semicrystalline polymers are often used as macromolecular excipients in active pharmaceutical ingredient (API)-delivery systems. In such systems, the morphological structure and crystalline characteristics of the excipient have a direct impact upon the drug-delivery rate. In this study, polycaprolactone (PCL)-based microspheres prepared via melt-printing were loaded with 10, 30, and 50% ibuprofen (IBU). In vitro release studies showed that, for a constant amount of IBU, the API was released fastest from the 30%-loaded microspheres, followed by the 50%- and 10%-loaded microspheres. The discrepancy in these release rates was investigated using scanning electron microscopy, differential scanning calorimetry, X-ray diffraction, and thermodynamic analyses, revealing the complex morphological and crystalline interrelationships of PCL and IBU. Although it is generally accepted that the degree of crystallinity of the excipient is the main factor controlling the release of the API, we found that the crystallite size of the small-molecule API is of primary importance. Moreover, these factors, which are controllable via the parameters used in melt-based preparation, can be exploited to tune drug-release rates. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47227.     

Fabrication and characterization of silver nanoparticle-incorporated bilayer electrospun–melt-blown micro/nanofibrous membrane

In this study, we fabricated an antifouling bilayered fibrous filter media having micro-nonwoven by melt blowing and nano-nonwoven by electrospinning process. Silver nanoparticle-incorporated polyurethane nanofibers were electrospun on the meltblown fiber of polypropylene. Silver nanoparticles were synthesized in situ in the polyurethane electrospun nanofibers through reduction of silver nitrate. The filter media were characterized by field emission scanning electron microscope, transmission electron microscopy, and X-ray diffraction and energy-dispersive X-ray spectroscopy analyses. The composite membrane showed that a thin layer of electrospun nanofibers improved the filtration efficiency without substantial increase in pressure drop. In situ synthesis of Ag NPs imparted the antibacterial and antifouling characteristics to the membrane.     

Biodegradable Electrospun Poly(lactic acid) Nanofibers for Effective PM 2.5 Removal

In addition to the rapid urbanization and industrialization around the world, air pollution due to particulate matter is a substantial threat to human health. A considerable research effort has been devoted to the development of electrospun polymer nanofibers for air filter applications. Among these new technologies, electrostatic charge‐assisted air filtration is a promising technology for removing small particulate matter (PM). In this investigation, biodegradable electrospun poly(l ‐lactic acid) (PLLA) polymer nanofibers are employed for air filter applications. Electrostatic charges generated from the PLLA nanofiber can significantly enhance air filter applications. Compared with a 3M commercial respirator filter, electrospun PLLA fibrous filters exhibit a high efficiency of 99.3%. Even after 6 h of filtration time, the PLLA filtration membrane still exhibits a 15% improvement in quality factor for PM 2.5 particles than the 3M respirator. This is mainly attributed to the electrostatic force generated from the electrospun PLLA nanofibers, which significantly benefit submicron particle absorption. Due to their biodegradability, ease of fabrication, and relatively high efficiency, electrospun PLLA nanofibers show great promise in applications such as air cleaning systems and personal air purifier applications.     

Evaluation of the Structural Modification of Ibuprofen on the Penetration Release of Ibuprofen from a Drug-in-Adhesive Matrix Type Transdermal Patch

This study aimed to evaluate the effect of chemical modifications of the structure of active compounds on the skin permeation and accumulation of ibuprofen [IBU] from the acrylic pressure-sensitive adhesive used as a drug-in-adhesives matrix type transdermal patch. The active substances tested were ibuprofen salts obtained by pairing the ibuprofen anion with organic cations, such as amino acid isopropyl esters. The structural modification of ibuprofen tested were Ibuprofen sodium salt, [GlyOiPr][IBU], [AlaOiPr][IBU], [ValOiPr][IBU], [SerOiPr][IBU], [ThrOiPr][IBU], [(AspOiPr)₂][IBU], [LysOiPr][IBU], [LysOiPr][IBU]₂, [PheOiPr][IBU], and [ProOiPr][IBU]. For comparison, the penetration of unmodified ibuprofen and commercially available patches was also investigated. Thus, twelve transdermal patches with new drug modifications have been developed whose adhesive carrier is an acrylate copolymer. The obtained patches were characterized for their adhesive properties and tested for permeability of the active substance. Our results show that the obtained ibuprofen patches demonstrate similar permeability to commercial patches compared to those with structural modifications of ibuprofen. However, these modified patches show an increased drug permeability of 2.3 to even 6.4 times greater than unmodified ibuprofen. Increasing the permeability of the active substance and properties such as adhesion, cohesion, and tack make the obtained patches an excellent alternative to commercial patches containing ibuprofen.     

Transdermal Delivery Systems for Ibuprofen and Ibuprofen Modified with Amino Acids Alkyl Esters Based on Bacterial Cellulose

The potential of bacterial cellulose as a carrier for the transport of ibuprofen (a typical example of non-steroidal anti-inflammatory drugs) through the skin was investigated. Ibuprofen and its amino acid ester salts-loaded BC membranes were prepared through a simple methodology and characterized in terms of structure and morphology. Two salts of amino acid isopropyl esters were used in the research, namely L-valine isopropyl ester ibuprofenate ([ValOiPr][IBU]) and L-leucine isopropyl ester ibuprofenate ([LeuOiPr][IBU]). [LeuOiPr][IBU] is a new compound; therefore, it has been fully characterized and its identity confirmed. For all membranes obtained the surface morphology, tensile mechanical properties, active compound dissolution assays, and permeation and skin accumulation studies of API (active pharmaceutical ingredient) were determined. The obtained membranes were very homogeneous. In vitro diffusion studies with Franz cells were conducted using pig epidermal membranes, and showed that the incorporation of ibuprofen in BC membranes provided lower permeation rates to those obtained with amino acids ester salts of ibuprofen. This release profile together with the ease of application and the simple preparation and assembly of the drug-loaded membranes indicates the enormous potentialities of using BC membranes for transdermal application of ibuprofen in the form of amino acid ester salts.     

Effect of hot‐press on electrospun poly(vinylidene fluoride) membranes

Poly(vinylidene fluoride) (PVDF) was electrospun into ultrafine fibrous membranes from its solutions in a mixture of N,N‐dimethylformamide and acetone (9:1, v/v). The electrospun membranes were subsequently treated by continuous hot‐press at elevated temperatures up to 155°C. Changes of morphology, crystallinity, porosity, liquid absorption, and mechanical properties of the membranes after hot‐press were investigated. Results of scanning electron microscopy showed that there were no significant changes in fibrous membrane morphology when the hot‐press temperature varied from room temperature to 130°C, but larger pores were formed because of fibers melting and bonding under higher temperatures. Analyses of X‐ray diffraction and differential scanning calorimeter exhibited that the crystalline form of PVDF could transfer from β‐type to α‐type during hot‐press at temperatures higher than 65°C. Tensile tests suggested that the mechanical properties of the electrospun PVDF membranes were remarkably enhanced from 25 to 130°C, whereas the porosity and the liquid absorption decreased. The hot‐press at 130°C was optimal for the electrospun PVDF membranes. The continuous hot‐press post‐treatment could be a feasible method to produce electrospun membranes, not limited to PVDF, with suitable mechanical properties as well as good porosity and liquid absorption for their applications in high‐quality filtrations or battery separators. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers     

Characterization and cell response of electrospun Rana chensinensis skin collagen/poly(l‐lactide) scaffolds with different fiber orientations

Collagen was extracted from Rana chensinensis skin supplied from byproducts via an acid enzymatic extraction method. The R. chensinensis skin collagen (RCSC) and poly(l ‐lactide) (PLLA) were blended at a 3:7 ratio in 1,1,1,3,3,3‐hexafluoroisopropanol (HFIP) at a concentration of 10% (g/mL) and electrospun to produce nanofibers in an aligned and random orientation. For comparison, pure PLLA nanofibrous membranes with aligned and random nanofiber orientations were also produced. The secondary structure of the RCSC nanofibers was investigated by circular dichroism to confirm that the extracted substance was collagen. The presence of collagen in the blend nanofiber was verified by LSCM. The blended nanofibers showed uniform, smooth, and bead‐free morphologies and presented a smaller fiber diameter (278 and and 259 nm) than the pure the ones of PLLA (559 and and 439 nm) nanofibers. It was found that the addition of RCSC and the modification of the nanofiber's orientation affected the fiber's diameter and the crystallization of PLLA. The cell viability studies with human fibroblast cells demonstrated that the RCSC/PLLA nanofibrous membranes formed by electrospinning exhibited good biocompatibility and that the aligned scaffolds could regulate the cell morphology by inducing cell orientation. The empirical results in this study indicated that the aligned RCSC/PLLA nanofibrous membrane is a potential wound dressing candidate for skin regeneration. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45109.     

Fabrication of hollow and porous polystyrene fibrous membranes by electrospinning combined with freeze-drying for oil removal from water

A novel method was proposed to fabricate hollow and surface porous polystyrene (PS) fibrous membranes for the removal of oil from water. Spinning solutions were prepared by using camphene and tetraethoxysilane (TEOS) as pore-forming agents, and hollow PS fibers with 100–400 nm pores on the surface were fabricated by electrospinning and freeze-drying. The distribution and volatilization of camphene and TEOS, as well as the drying behavior of solvents in high relative humidity, were important factors in forming the porous structure of PS fibers. The specific surface area of obtained PS fibrous membranes was twice that of conventional electrospun PS fibrous membranes and displayed superhydrophobic properties. Moreover, the large adsorption storage space was formed due to the hollow structure and porous surface of PS fibers. The maximum oil adsorption capacity of the porous PS fibrous membrane was 105.4 g g⁻¹, and was larger than that of the conventional PS fibrous membrane after repeated five times, thus making it a promising tool for oil spill cleanups. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47262.