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.     

Fabrication of PLA/PEG/MWCNT electrospun nanofibrous scaffolds for anticancer drug delivery

In the present study, polylactic acid (PLA)/polyethylene glycol (PEG)/multiwalled carbon nanotube (MWCNT) electrospun nanofibrous scaffolds were prepared via electrospinning process and their applications for the anticancer drug delivery system were investigated. A response surface methodology based on Box–Behnken design (BBD) was used to evaluate the effect of key parameters of electrospinning process including solution concentration, feeding rate, tip–collector distance (TCD) and applied voltage on the morphology of PLA/PEG/MWCNT nanofibrous scaffolds. In optimum conditions (concentration of 8.15%, feeding rate of 0.2 mL/h, voltage of 18.50 kV and TCD of 13.0 cm), the minimum experimental fiber diameter was found to be 225 nm which was in good agreement with the predicted value by the BBD analysis (228 nm). In vitro drug release study of doxorubicin (DOX)‐loaded nanofibrous scaffolds, higher drug content induced an extended release of drug. Also, drug release rate was not dependent on drug/polymer ratio in different electrospun nanofibrous formulations. The equation of M_t = c₀ + kt^0.5was used to describe the kinetic data of DOX release from electrospun nanofibers. The cell viability of DOX‐loaded nanofibrous scaffolds was evaluated using 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide, a tetrazole assay on lung cancer A549 cell lines. We propose that DOX‐incorporated PLA/PEG/MWCNT nanofibrous scaffold could be used as a superior candidate for antitumor drug delivery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41286.     

Three‐layered electrospun PVA/PCL/PVA nanofibrous mats containing tetracycline hydrochloride and phenytoin sodium: A case study on sustained control release,antibacterial, and cell culture properties

The main objective of this work was to prepare a tailor‐made electrospun nanofibrous samples based on poly(?‐caprolactone) (PCL) containing tetracycline hydrochloride (TC‐HCl) as a middle layer and poly(vinyl alcohol) (PVA) including phenytoin sodium (PHT‐Na) as lateral layers. The characterizations of the three‐layered electrospun samples were carried out by using SEM, ATR‐FTIR spectroscopy along with swelling/weight loss, UV–vis spectrophotometry as well as HPLC, antibacterial and MTT tests. The SEM micrograph images showed that the average diameter of PCL nanofibers was decreased from 243 ± 7 nm to 181 ± 5 nm by adding TC‐HCl. The hydrolytic degradation of PVA nanofibers in the exposure of phosphate buffer solution (PBS) was confirmed by ATR‐FTIR results in which a change at the intensity of the characteristic peak located at 3333 cm^?1 corresponding to hydroxyl groups (? OH) was observed. The UV–vis outcomes revealed a sustained control release of TC‐HCl from the three‐layered nanofibrous samples (PVA/PCL/PVA) with an amount of about 43% compared to the PCL nanofibers which had an ultimate release of the drug about 79%. Furthermore, the HPLC chromatograms showed the released PHT‐Na from PVA nanofibers about 87%. Finally, the MTT assay along with the antibacterial evaluation exhibited that the surfaces of these electrospun three‐layered nanofibrous samples have no cytotoxicity as well as the controlled release of TC‐HCl from them enabled their prolonged use for preventing the bacterium growth such as S. aureus during 24‐h treatment time. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43309.     

5-Fluorouracil-loaded poly(vinyl alcohol)/chitosan blend nanofibers: morphology,drug release and cell culture studies

Electrospun polymeric nanofibers as carriers for anticancer drugs have received a great deal of attention to treat tumor cells. This work was aimed to prepare an optimized nanofibrous sample based on poly(vinyl alcohol) (PVA)/chitosan (CS) blend, and then evaluate it containing 5-fluorouracil (5-FU) in terms of morphology, drug release, and cell culture. The electrospinning conditions to produce PVA/CS (50/50) blend nanofibers with an average diameter of approximately 150.8 nm were adjusted as follows: applied voltage 17 kV, needle tip to collector distance 60 cm, and flow rate 0.1 mL/h. The obtained results from Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) showed that there were no chemical interactions between the polymers and drug during the electrospinning process and the uniform morphology without beads. Moreover, to prolong 5-FU release from the blend nanofibers, three layered samples consisting of PVA/CS blend and poly (ε-caprolactone) (PCL) [PVA/CS-PCL 3-layers] were electrospun. On the other hand, by adding PCL in the PVA/CS blend nanofibers, the samples showed more hydrophobic property. Eventually, thiazolyl blue (MTT) assay along with NIH 3T3 cells culture proved that the sample could kill more than 80% of the cells. This formulation could be a promising candidate for cancer therapy potentially.

     

Electrospun biocompatible poly (ε-caprolactonediol)-based polyurethane core/shell nanofibrous scaffold for controlled release of temozolomide

The electrospun biocompatible poly (ε-caprolactonediol)-based polyurethane (PCL-Diol-b-PU) core/shell nanofibrous scaffolds were prepared via the coaxial electrospinning process. Temozolomide (TMZ) as an anticancer drug was loaded into the core of fibers to control the release of TMZ for the treatment of glioblastoma. The properties of nanofibers were characterized using XRD, FTIR, SEM, and TEM analysis. The sustained delivery of TMZ without initial burst release was achieved from all prepared core–shell nanofibrous samples over 30 days. The cytotoxicity results revealed that the TMZ-loaded PCL-Diol-b-PU core–shell nanofibers could be used as a drug delivery implant to deliver TMZ against glioblastoma tumors.     

Protein encapsulated in electrospun nanofibrous scaffolds for tissue engineering applications

The main purpose of tissue engineering is the preparation of fibrous scaffolds with similar structural and biochemical cues to the extracellular matrix in order to provide a substrate to support the cells. Controlled release of bioactive agents such as growth factors from the fibrous scaffolds improves cell behavior on the scaffolds and accelerates tissue regeneration. In this study, nanofibrous scaffolds were fabricated from biocompatible and biodegradable poly(lactic‐co‐glycolic acid) through the electrospinning technique. Nanofibers with a core–sheath structure encapsulating bovine serum albumin (BSA) as a model protein for hydrophilic bioactive agents were prepared through emulsion electrospinning. The morphology of the nanofibers was evaluated by field‐emission scanning electron microscopy and the core–sheath structure of the emulsion electrospun nanofibers was observed by transmission electron microscopy. The results of the mechanical properties and X‐ray diffraction are reported. The scaffolds demonstrated a sustained release profile of BSA. Biocompatibility of the scaffolds was evaluated using the MTT (3(4,5‐ dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide) assay for NIH‐3T3 fibroblast cells. The results indicated desirable biocompatibility of the scaffolds with the capability of encapsulation and controlled release of the protein, which can serve as tissue engineering scaffolds. © 2013 Society of Chemical Industry     

Stabilized electrospinning of heat stimuli/in situ crosslinkable nanofibers and their self‐same nanocomposites

We present a strategy for stabilizing the morphological integrity of electrospun polymeric nanofibers by heat stimuli in situ crosslinking. Amorphous polymer nanofibers, such as polystyrene (PS) and its co‐polymers tend to lose their fiber morphology during processing at temperatures above their glass transition temperature (T_g) typically bound to happen in nanocomposite/structural composite applications. As an answer to this problem, incorporation of the crosslinking agents, phthalic anhydride (PA) and tributylamine (TBA), into the electrospinning polymer solution functionalized by glycidylmethacrylate (GMA) copolymerization, namely P(St‐co‐GMA), is demonstrated. Despite the presence of the crosslinker molecules, the electrospinning polymer solution is stable and its viscosity remains unaffected below 60 °C. Crosslinking reaction stands‐by and can be thermally stimulated during post‐processing of the electrospun P(St‐co‐GMA)/PA‐TBA fiber mat at intermediate temperatures (below the T_g). This strategy enables the preservation of the nanofiber morphology during subsequent high temperature processing. The crosslinking event leads to an increase in T_g of the base polymer by 30 °C depending on degree of crosslinking. Crosslinked nanofibers are able to maintain their nanofibrous morphology above the T_g and upon exposure to organic solvents. In situ crosslinking in epoxy matrix is also reported as an example of high temperature demanding application/processing. Finally, a self‐same fibrous nanocomposite is demonstrated by dual electrospinning of P(St‐co‐GMA) and stabilized P(St‐co‐GMA)/PA‐TBA, forming an intermingled nanofibrous mat, followed by a heating cycle. The product is a composite of crosslinked P(St‐co‐GMA)/PA‐TBA fibers fused by P(St‐co‐GMA) matrix. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44090.     

Electrospun silk fibroin/β-cyclodextrin citrate nanofibers as a novel biomaterial for application in controlled drug release

Abstract

A novel β-cyclodextrin-grafted silk fibroin (SF) nanofibers was successfully fabricated. The morphology and diameter of the electrospun nanofibers were characterized. FE-SEM images showed that the morphology and diameter of the nanofibers were mainly affected by weight ratio of the blend. FTIR, ¹H-NMR, DSC and TGA confirmed the crosslinking reaction between β-cyclodextrin and SF. The release rate of Ciprofloxacin was measured and observed that the SF-g-CD nanofibrous mat provided slower release of the entrapped drug when compared with SF nanofibrous mat. A mathematical analysis of the drug release data suggested that the Higuchi model was the best fitted model.     

Effect of the cross-linking degree on the morphology of poly(NIPAAm-co-AAc) hydrogels

Hydrogels of poly(N-isopropylacrylamide) co-polymerized with acrylic acid [P(NIPAAm-co-AAc)] were synthesized with cross-linking degrees of 2-7% using (N,N′-methylenebisacrylamide). SEM micrographs revealed that the morphology of dry hydrogels changes from interconnected spherical pores to channel-like pores, with the change in the cross-linking degrees from 3 to 5%. The change in morphology is associated with a significant change in the swelling ratio. It was found that the diffusion rates and permeabilities of methylene blue (MB) through the hydrogel with channel-like pores are significantly higher if the main axes of the pores are oriented parallel to the flow of MB molecules, than if it is oriented perpendicularly. These results show that different morphologies can be obtained by controlling the cross-linking degree of P(NIPAAm-co-AAc) hydrogels in a narrow range around 5% and by performing the polymerization reaction in moulds placed in horizontal and vertical positions, opening a new perspective for modulating their properties in applications as matrices for controlled release of drugs or as membranes for separation processes.     

Synthesis,antimicrobial activity,and release of tetracycline hydrochloride loaded poly(vinyl alcohol)/soybean protein isolate/zirconium dioxide nanofibrous membranes

Tetracycline hydrochloride loaded poly(vinyl alcohol)/soybean protein isolate/zirconium (Tet–PVA/SPI/ZrO₂) nanofibrous membranes were fabricated via an electrospinning technique. The average diameter of the PVA/soybean protein isolate (SPI)/ZrO₂ nanofibers used as drug carriers increased with increasing ZrO₂ content, and the nanofibers were uneven and tended to stick together when the ZrO₂ content was above 15 wt %. The Tet–PVA/SPI/ZrO₂ nanofibers were similar in morphology when the loading dosage of the model drug tetracycline hydrochloride was below 6 wt %. The PVA, SPI, and ZrO₂ units were linked by hydrogen bonds in the hybrid networks, and the addition of ZrO₂ improved the thermostability of the polymer matrix. The Tet–PVA/SPI/ZrO₂ nanofibrous membranes exhibited good controlled drug‐release properties and antimicrobial activity against Staphylococcus aureus. The results of this study suggest that those nanofibrous membranes were suitable for drug delivery and wound dressing. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40903.     

Nanofibrous scaffold prepared by electrospinning of poly(vinyl alcohol)/gelatin aqueous solutions

A series of nanofibrous scaffolds were prepared by electrospinning of poly(vinyl alcohol) (PVA)/gelatin aqueous solution. PVA and gelatin was dissolved in pure water and blended in full range, then being electrospun to prepared nanofibers, followed by being crosslinked with glutaraldehyde vapor and heat treatment to form nanofibrous scaffold. Field emission scanning electron microscope (FESEM) images of the nanofibers manifested that the fiber average diameters decreased from 290 to 90 nm with the increasing of gelatin. In vitro degradation rates of the nanofibers were also correlated with the composition and physical properties of electrospinning solutions. Cytocompatibility of the scaffolds was evaluated by cells morphology and MTT assay. The FESEM images revealed that NIH 3T3 fibroblasts spread and elongated actively on the scaffolds with spindle‐like and star‐type shape. The results of cell attachment and proliferation on the nanofibrous scaffolds suggested that the cytotoxicity of all samples are grade 1 or grade 0, indicating that the material had sound biosafety as biomaterials. Compared with pure PVA and gelatin scaffolds, the hybrid ones possess improved biocompatibility and controllability. These results indicate that the PVA/gelatin nanofibrous have potential as skin scaffolds or wound dressing. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Preparation, characterization, and encapsulation/release studies of a composite nanofiber mat electrospun from an emulsion containing poly(lactic-co-glycolic acid)

The aim of this study was to investigate the preparation, characterization, and encapsulation/release performance of an electrospun composite nanofiber mat. The hypothesis was that the composite nanofiber mat with nano-scaled drug particles impregnated in biocompatible and biodegradable polymer nanofibers can serve as an innovative type of tissue engineering scaffold with desired and controllable drug encapsulation/release properties. To test the hypothesis, the composite nanofiber mat electrospun from an emulsion consisting of poly(lactic-co-glycolic acid) (PLGA) Rhodamine B (a model compound to simulate drugs), sorbitan monooleate (Span-80, a non-ionic emulsifier/surfactant that is presumably non-toxic/safe for cell-growth), chloroform, DMF, and distilled water was prepared and characterized; and the Rhodamine B encapsulation/release profile in phosphate buffered saline (pH = 7.4) was recorded and analyzed. For comparison purposes, two additional nanofiber mats electrospun from (1) a solution containing PLGA and Rhodamine B, and (2) a solution containing PLGA, Rhodamine B, and Span-80 were also prepared and assessed as the control samples. The results indicated that the composite nanofiber mat electrospun from the emulsion had the most desired and controllable Rhodamine B encapsulation/release profile and the excellent morphological sustainability; thus, it could be utilized as both a drug encapsulation/release vehicle and a tissue engineering scaffold.     

Poly(l-lactide-co-?-caprolactone) electrospun nanofibers for encapsulating and sustained releasing proteins

The aim of this study was to investigate coaxial electrospun poly(l-lactide-co-?-caprolactone) [PLLACL] nanofibers for the application in nerve tissue engineering. The hypothesis was that the nanofibrous mats fabricated by coaxial electrospun PLLACL could be effective scaffolds for releasing proteins, such as Bovine Serum Albumin (BSA) or/and Nerve Growth Factor (NGF), in a sustained manner. To test the hypothesis, the coaxial electrospun nanofibers with PLLACL as the shell and BSA/NGF as the core were characterized. Morphologies and mechanical properties of nanofibrous mats were examined. BSA released behavior was studied. The results demonstrated that BSA could be sustainedly released from coaxial electrospun PLLACL nanofibers, however, BSA released from mix electrospun nanofibers present the burst release behavior. Bioactivity of released NGF from coaxial electrospun nanofibers was verified by testing the differentiation of rat pheochromocytoma cells (PC12).     

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.     

Effect of Pluronic F127 on the 3D pore morphology of poly(N-isopropylacrylamide-co-acrylic acid) hydrogels and their nitric oxide release from S-nitrosoglutathione

Changing the pore morphology of hydrogels can be an effective strategy to modulate their drug release profiles. Herein, Pluronic F127 was used to change the three-dimensional pore morphology of crosslinked poly(N-isopropylacrylamide-co-acrylic acid) (P[NIPAm-co-AAc]) hydrogels. F127 reduced the pore diameters from 20 ± 4 to 2.9 ± 0.4 μm and from 11 ± 1 to 1.4 ± 0.4 μm in hydrogels synthesized at 8 and 30°C, respectively. Small-angle X-ray scattering indicates that the segregation of the F127 during the polymerization process induces F127 phase transitions from unimers (at 8°C) or cubic-packed micelles (at 30°C) to a lamellar structure. P(NIPAm-co-AAc) hydrogels charged with S-nitrosoglutathione (GSNO), released nitric oxide (NO) spontaneously during hydration. The decrease in the pore diameter led to a twofold to threefold increase in the rate of water absorption and a fourfold to sixfold increase in the rate of NO release of the hydrogels. F127 can be used to change the pore morphology of P(NIPAm-co-AAc) hydrogels, with concomitant changes in their rate of hydration and NO release from GSNO, opening a new perspective for their use in topical NO delivery.     

Co‐electrospun nanofibers of PVA‐SbQ and Zein for wound healing

In this study, electrospun biocompatible nanofibers with random orientation were prepared by physically blending poly(vinyl alcohol)‐stilbazol quaternized (PVA‐SbQ) with zein in acetic acid solution for wound healing. PVA‐SbQ was used as the foundation polymer as well as crosslinking agent, blended with zein to achieve desirable properties such as improved tensile strength, surface wettability, and in vitro degradable properties. Moreover, vaccarin drug was incorporated in situ into electrospun nanofibrous membranes for cell viability and cell attachment. The addition of vaccarin showed great effects on the morphology of nanofiber and enhanced cell viability and proliferation in comparison with composite nanofibers without drug. The presence of PVA‐SbQ, zein, and vaccarin drug in the nanofibrous membranes exhibited good compatibility, hydrophilicity, and biocompatibility and created a moist environment to have potential application for wound healing. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42565.     

Effect of solution properties on nanofibrous structure of electrospun poly(lactic‐co‐glycolic acid)

Electrospinning of poly(lactic‐co‐glycolic acid) (PLGA) in chloroform or 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP) was investigated, focusing on its solution parameters, to develop nonwoven biodegradable nanofibrous structures for tissue engineering. PLGA nanofibers were obtained by electrospinning of 15 wt % PLGA solution and the resulting average fiber diameters were varied with the range of 270–760 nm, depending on solution property. When small amounts of benzyl triethylammonium chloride (BTEAC) was added to the PLGA/chloroform solution, the average diameter was decreased from 760 to 450 nm and the fibers were densely amounted in a straight shape. In addition, the average fiber diameter (270 nm) of nanofibers electrospun from polar HFIP solvent was much smaller than that (760 nm) of nanofibers electrospun from nonpolar chloroform solvent. Therefore, it could be concluded that conductivity or dielectric constant of the PLGA solution was a major parameter affecting the morphology and diameter of the electrospun PLGA fibers. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1214–1221, 2006     

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.     

Modification of PCL Electrospun Nanofibrous Mat With Calendula officinalis Extract for Improved Interaction With Cells

Nanofibers have improved the performance of biomaterials, and could be considered effective. In this study, poly(?-caprolactone) (PCL)/Calendula officinalis nanofibers were well designed by different analyses. FTIR structural analysis showed the presence of functional groups on the nanofibrous surfaces. The SEM images showed the average size of nanofibers increased with increase in Calendula concentration. The 100° difference was obtained in the contact angle analysis with changes in Calendula concentration; however, tensile strength decreased for the Poly(?-caprolactone)/Calendula officinalis nanofibrous mat compared those unmodified ones. Cellular investigation showed better adhesion, proliferation, and tenocyte cells growth on poly(?-caprolactone)/Calendula officinalis nanofibrous samples than pure PCL nanofibrous mat. The bioavailability of PCL fibers with Calendula officinalis extract was found to be identical to that of PCL fibers, indicating that Calendula officinalis extract is a suitable material for enhancing the biocompatibility of tissue engineering scaffolds.     

Fabrication of althea officinalis loaded electrospun nanofibrous scaffold for potential application of skin tissue engineering

The Althea Officinalis (AO) extract is well known as a traditional herbal drug for its wound healing ability owing to the anti-inflammatory and antimicrobial properties. Furthermore, its mucilaginous properties provide moisturizing and nutritional effects on skin cell proliferation. Therefore, AO extract can be applied in the temporary skin substitute for the ability to expedite the therapy duration. In this study, different concentrations of AO extract (0, 5, 10, 15, and 20 wt %) were incorporated into the nanofibrous scaffolds to study their potential for the skin tissue repairing. The desired scaffolds were prepared by electrospinning the blend of poly(ε -caprolactone) and gelatin as a synthesized and natural polymer. The electrospun nanofibers were characterized by SEM, FTIR, DSC, TGA, tensile, AO extract release, and cellular culture tests. This study proposed incorporating the AO extract into the nanofibrous scaffolds for accelerating the skin tissue repairing and the optimized amount of AO extract as about 15% was introduced for offering the most desirable electrospun scaffolds for this application. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48587.