Preparation of bioactive glycosylated glial cell‐line derived neurotrophic factor‐loaded microspheres for medical applications

Poly (lactic‐co‐glycolic acid) (PLGA)‐coated gelatin microspheres containing glial cell‐line derived neurotrophic factor (GDNF) were developed by thermal gelation through a water‐in‐oil emulsion technique. Gelatin types (A and B) at four different pH levels were investigated for their influences on the morphology, the microsphere size, the zeta potential, and the swelling ability. The encapsulation of GDNF and the release characteristics of GDNF were also determined using enzyme‐linked immunosorbent assay (ELISA). The maximum cumulative released amounts of GDNF from the microspheres were increased from 50 to 90% after 4 d (based on the actual amount of the GDNF). Thus, the release of the GDNF contents in the microspheres depends on the amount of GDNF. Trigeminal ganglion cells (TGCs) were used to study the bioactivity of GDNF released from the microspheres, which was proven to retain its bioactivity in promoting the TGCs' neurite outgrowth. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40167.     

Effects of copolymer microstructure on the properties of electrospun poly(l‐lactide‐co‐ε‐caprolactone) absorbable nerve guide tubes

The main objective of this work has been to study the effects of copolymer microstructure, both chemical and physical, on the microporosity, in vitro hydrolytic degradability and biocompatibility of electrospun poly(l ‐lactide‐co‐ε‐caprolactone), PLC, copolymer tubes for potential use as absorbable nerve guides. PLC copolymers with L : C compositions of 50 : 50 and 67 : 33 mol % were synthesized via the ring‐opening copolymerization of l ‐lactide (L) and ε‐caprolactone (C) at 120°C for 72 h using stannous octoate (tin(II) 2‐ethylhexanoate) and n‐hexanol as the initiating system. Electrospinning was carried out from solution in a dichloromethane/dimethylformamide (7 : 3 v/v) mixed solvent at room temperature. The in vitro hydrolytic degradation of the electrospun PLC tubes was studied in phosphate buffer saline over a period of 36 weeks. The microporous tubes were found to be gradually degradable by a simple hydrolysis mechanism leading to random chain scission. At the end of the degradation period, the % weight retentions of the PLC 50 : 50 and 67 : 33 tubes were 15.6% and 70.2%, respectively. Pore stability during storage as well as cell attachment and proliferation of mouse fibroblast cells (L929) showed the greater potential of the PLC 67 : 33 tubes for use as temporary scaffolds in reconstructive nerve surgery. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 4357–4366, 2013     

In vivo bioactivity of herbal‐drug‐incorporated nanofibrous matrixes

Aloe‐vera‐incorporated polycaprolactone nanofibrous matrixes were prepared by an electrospinning method. These developed matrixes were evaluated for their water absorption capacity, water vapor permeability, and contact angle, and, in an in vivo animal model, wound‐healing ability. The incorporation of the herbal drug made the matrixes hydrophilic with improved water retention and permeability properties. The in vivo studies were carried out in a rat model and showed improved results with respect to healing. Thus, this study confirmed that the developed matrixes could be used for wound‐healing applications. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42178.     

pH‐sensitive keratin‐based polymer hydrogel and its controllable drug‐release behavior

Using feather keratin as biocompatible and inexpensive natural biopolymer and methacrylic acid as a functional monomer, we prepared a pH‐sensitive feather‐keratin‐based polymer hydrogel (FKPGel) with grafted copolymerization. The obtained FKPGel was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy. The swelling behavior and pH sensitivity of the FKPGel were investigated. When the small molecule (rhodamine B) and macromolecule (bovine serum albumin) were used as model drug molecules, the FKPGel exhibited controllable release behavior in vitro, and the hydrogels had pH sensitivity. For a small molecular drug, the cumulative release rate was 97% in 24 h at pH 8.4. For macromolecular drug, the cumulative release rate reached 89% at pH 7.4. Its release behavior could be controlled by the pH value. In summary, a simple method was found to reuse disused feathers. It is a kind of pH‐sensitive hydrogels to be applied in drug‐delivery systems. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41572.     

Chitosan‐finished Antheraea mylitta silk fibroin nonwoven composite films for wound dressing

In this study, we aimed to produce nonwoven wound‐dressing films made of Antheraea mylitta (tasar) silk fibroin by a solution‐casting method. These nonwoven films were finished with chitosan solutions of different concentrations ranging from 0.75 to 2% w/v with a pad–dry method to fabricate nonwoven composite films. Chitosan‐finished tasar fibroin nonwoven composite films (CMTFFs) showed higher mechanical and dynamic mechanical properties as compared to nonwoven tasar fibroin. The physical, structural, and thermal properties of the films were investigated. The hemocompatibility, cytocompatibility, and biodegradation tests showed that the CMTFF was a promising material for use as a wound dressing. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44341.     

Preparation of polylactide microcapsules at a high throughput with a packed‐bed premix emulsification system

Core–shell polymer microcapsules are well known for their biomedical applications as drug carriers when they are filled with drugs and gas‐filled microcapsules that can be used as ultrasound contrast agents. The properties of microcapsules are strongly dependent on their size (distribution); therefore, equipment that allows the preparation of small and well‐defined microcapsules is of great practical relevance. In this study, we made polylactide microcapsules with a packed‐bed premix emulsification system that previously gave good results for regular emulsions. Here, we tested it for applicability to a system in which droplets shrank and solidified to obtain capsules. The packed‐bed column was loaded with glass beads of different sizes (30–90 µm) at various bed heights (2–20 mm), and coarse emulsions consisting of the polymer, a solvent, and a nonsolvent were pushed repeatedly through this system at selected applied pressures (1–4 bar). The obtained transmembrane fluxes (100–1000 m³ m^?2 h^?1) were much higher than those recorded for other membrane emulsification techniques. The average size of the obtained microcapsules ranged between 2 and 8 µm, with an average span of about 1; interestingly, the capsules were 2–10 times smaller than the interstitial voids of the beds. The droplets were larger when we used thicker beds and larger glass beads, and these effect correlated with the pore Reynolds number (Re_p). Two breakup mechanisms were identified: spontaneous droplet snap‐off dominated the system at low Re_ps, and localized shear forces dominated the system at higher Re_p. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43536.     

Design and in vivo assessment of polyester copolymers based on trimethylene carbonate and ε‐caprolactone

Poly(trimethylene carbonate‐co‐caprolactone) (PTCL) copolymers with various trimethylene carbonate ratios were synthesized by ring‐opening polymerization and were used to prepare implants for an in vivo experiment. Medical silicone rubber was used as the control. Implants were prepared by compression molding with a laboratory instrument. The properties of these copolymer implants were investigated. PTCL implants and silicone rubbers were implanted subcutaneously in the dorsal region of New Zealand white rabbits. The assessment was performed 1, 2, 3, 4, 5, 6, 7, and 8 months postoperatively by the determination of the weight loss, water uptake, thermal behavior, molecular weight of the explanted implants, and histological examination. During the 8‐month implantation, the value of maximum weight loss was found to be 25%. A continuous decrease in the molecular weight occurred. No remarkable tissue reactions were observed during degradation, and foreign‐body reactions were similar to those of silicone rubbers, which are commercially available materials. In this study, we aimed to indicate the likely clinical behavior but good biodegradable properties of PTCL copolymers compared to those of silicone rubber. This may open a new avenue of application for them in the drug industry. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41815.     

Silver nanoparticle incorporated poly(l‐lactide‐co‐glycolide) nanofibers: Evaluation of their biocompatibility and antibacterial properties

The objective of this work is the fabrication of poly(l ‐lactide‐co‐glycolide) or PLGA (with LA/GA ratios of 50/50 and 75/25) nanofibers containing silver nanoparticles (AgNPs) by the method of electrospinning. The incorporation of AgNPs in PLGA was carried out in three different concentrations (1, 3, 6 w/w %).The electrospun nanofibers were evaluated for their morphology by scanning electron microscopy and their fiber diameters ranged between 487 and 781 nm. Integration of AgNPs within the fibers was verified by spectroscopy studies, while the mechanical properties of the developed fibers were found comparable to the mechanical properties of the human skin. Proliferation of human dermal fibroblasts (HDF) demonstrated minimal cytotoxicity on fibers containing 1 wt % and 3 wt % of AgNPs, while 6 wt % of AgNPs inhibited cell proliferation. Antimicrobial activity was studied using three different strains of Gram‐positive and Gram‐negative bacteria. Results of the HDF proliferation and antimicrobial studies showed that the electrospun PLGA75/25 containing 3 wt % AgNP can function as a suitable substrate for wound dressing, compared to the other scaffolds of this study. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42686.     

Synergistic effect and drug‐resistance relief of paclitaxel and cisplatin caused by Co‐delivery using polymeric micelles

Combination therapy of paclitaxel (PTX) and cisplatin has been used to treat several cancers in clinic practice, but often causes serious systemic toxicity. Co‐delivery of PTX and cisplatin by means of polymeric micelles can reduce the systemic toxicity, but often needs two carrier polymers because of the solubility difference between them. Therefore, a strategy is developed to co‐deliver both PTX and cisplatin with only one carrier polymer by encapsulating PTX in the core of a polymeric micelle and cross‐linking the micelle with cisplatin. The PTX and Pt contents in the micellar formulation M(PTX/Pt) were 10 and 14 wt %, respectively. In vitro cytotoxicity of M(PTX/Pt) was evaluated via 3‐(4,5‐dimethylthiazol‐2‐yl)?2,5‐diphenyltetrazolium bromide assay in comparison with PTX and its micelle M(PTX), cisplatin and its micelle M(Pt), and PTX/cisplatin combination towards human hepatocarcinoma (SMMC‐7721) cells and chemoresistant SMMC‐7721(SMMC‐7721R) cells. The M(PTX/Pt) exhibited a high synergistic effect in the inhibition of cell growth and proliferation of both SMMC‐7721 and SMMC‐7721R cells and showed reasonable drug‐resistance relief. The synergistic effect and resistance relief were further supported or explained by intracellular uptake measurement of dye‐labeled micelles and by the confocal laser scanning microscopy observation of SMMC‐7721 and SMMC‐7721R cells treated with various formulations. Therefore, M(PTX/Pt) micelles were expected to find potential application in cancer chemotherapy. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41440.     

Polyphosphoester‐based paclitaxel complexes

We demonstrated a feasible approach for the preparation of a biodegradable, water soluble polyphosphoester based paclitaxel complex. Applying poly(hydroxyoxyethylene phosphate) which contains both a strong proton accepting P?O group and a proton donating P? OH group, paclitaxel has been physically immobilized onto the polymer via H‐bonding. The water soluble complex contained 16.7 wt % paclitaxel and more than 4000 times increased drug solubility was achieved. The polymer‐drug complex formed nanosized aggregates that were characterized by dynamic light scattering. Intravenous injection of poly(hydroxyoxyethylene phosphate) in rats at a dose of 1000 mg/kg did not induce any clinical signs or body weight gain reduction. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42772.     

Poly(2‐hydroxyethyl methacrylate)/boric acid composite hydrogel as soft contact lens material: Thermal,optical, rheological,and enhanced antibacterial properties

The present work proposes to fabricate a composite hydrogel material that well characterized, transparent, biocompatible, and self‐antibacterial as potential soft contact lens material. For this purpose, poly(2‐hydroxyethyl methacrylate) (PHEMA)/boric acid (BA) composite hydrogels were successfully prepared by chemical crosslinking with BA through in situ polymerization using different BA ratios between 1 and 10% w/w. Afterward, the compositions, thermal stability, transparence, oxygen permeability, water uptake capacity, swelling ratio as well as morphological and rheological properties, in vitro degradability, in vitro cytotoxicity, and antibacterial properties of the all prepared materials were analyzed using a series of different techniques. The thermal stability, hydrophilicity, water uptake, oxygen permeability gradually increased depending ratio of BA, which is desirable for biomaterial. While the transparence and refractive index decreased, the composite hydrogels, except for BA content of 10 wt %, maintained enough transparency to be used for contact lens. In addition, PHEMA/BA composite hydrogels exhibited good cytocompatibility (PHEMA‐1%BA and PHEMA‐3%BA) and excellent antibacterial activity against Gram‐positive (Staphylococcus aureus and Enterococcus faecium) and Gram‐negative (Escherichia coli and Pseudomonas aeruginosa) bacteria. Overall, the results demonstrated that the obtained PHEMA/BA composite hydrogels could be considered as self‐antibacterial contact lens and a potential composite biomaterial for other applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46575.     

Water‐resistant plant protein‐based nanofiber membranes

Developing green and sustainable alternative materials to replace petroleum based ones is the need of the day. Such green materials are becoming popular because they can be composted once their useful life is over. In the current research, protein‐based nanofibers were fabricated without the use of any toxic cross‐linking agent. Defatted soy flour was purified using an acid‐wash process to obtain material with higher protein content, blended with gluten, and successfully electrospun into nanofibers with the help of polyvinyl alcohol. Oxidation of sucrose with hydrogen peroxide (H₂O₂) was carried out to synthesize oxidized sugar‐containing aldehyde (—CHO) groups and used as green cross‐linker. The cross‐linking quality of protein‐based nanofibers modified by oxidized sugar was found to be similar to nanofibers cross‐linked using toxic glyoxal and show good resistance to water. These novel green protein‐based nanofibers can be useful in fabricating inexpensive products with very high specific surface area and highly porous structure. © 2015 The Authors Journal of Applied Polymer Science Published by Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41852.     

Formulation of silver chloride/poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (AgCl/PHBV) films for potential use in bone tissue engineering

Orthopedic implant failure due to bacterial infection has been a concern in bone tissue engineering. Here, we have formulated a composite made of biodegradable polymer, i.e., poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV), and silver chloride. Ag⁺ ions released from the AgCl/PHBV film can promote an aseptic environment by promoting inhibition of bacterial growth while maintaining bone cell growth, depending on AgCl loading. The objective of this study is to formulate AgCl/PHBV film(s) of varying composition so as to evaluate the dependence of AgCl loading in the film on antimicrobial activity and cytotoxicity. The release kinetics of silver ions from AgCl/PHBV film in aqueous and Dulbecco's Modified Eagle Medium showed similarity in the initial burst of ions during the first day of desorption followed by a gradual release of ions over extended time period. The antibacterial efficacy of AgCl/PHBV film against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa was evaluated by microbiological assay, while cytotoxicity of the film toward MC3T3‐E1 cells was determined by MTT assay. For all compositions studied, a clear zone of inhibition around AgCl/PHBV film was noticed on a modified Kirby‐Bauer disk diffusion assay. We established that MC3T3‐E1 cell attachment on AgCl/PHBV film is strongly related to loading of AgCl in the film. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45162.     

Evaluation of bioresorbable polymers as potential stent material—In vivo degradation behavior and histocompatibility

A PLLA‐TMC‐GA terpolymer of 90/5/5 molar ratio was synthesized by ring‐opening polymerization of l ‐lactide (LLA), trimethylene carbonate (TMC), and glycolide (GA), using stannous octoate as initiator. In vivo degradation of the obtained terpolymer and a composite made up of the terpolymer matrix reinforced by PLLA‐GA fibers was realized by subcutaneous implantation in rats for 9 months, in comparison with PLLA homopolymer and PLLA‐TMC copolymer of 95/5 molar ratio. The terpolymer shows ideal degradation profile because it is expected to maintain relatively high radial support for 3 months and lose its mechanical properties in 3 to 6 months inferred from molar mass changes. Increase of crystallinity and LLA content in the terpolymer and composite is observed during degradation. According to the gross observation and H&E staining appearance, all samples present good tissue compatibility. These results suggest that the terpolymer is promising for uses as fully biodegradable vascular scaffold. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44355.     

Comparison of the antibacterial activity of modified‐cotton with magainin I and LL‐37 with potential as wound‐dressings

Wounds are the ideal setting for the development of micro‐organisms, so it is often necessary to apply a dressing to control bacterial colonization. Cotton is commonly used in dressings, as it exhibits important hydrophilic characteristics such as high moisture and fluid retention properties, but it may provide a sustainable media for the development of micro‐organisms. In this way, the development of new strategies to provide cotton materials with lasting and effective antimicrobial properties is of the utmost importance. Consequently, here we described two processes to develop cotton‐dressings functionalized with antimicrobial peptides (AMPs) magainin I (MagI) and LL‐37, in order to give cotton‐dressings an antibacterial effect. The AMPs showed no cytotoxic effect against human fibroblasts so they are safe to contact with skin. In addition, the functionalized materials with either LL‐37 or MagI present an antimicrobial effect exhibiting inhibition ratios of 89% against Klebsiella pneumoniae and 58% against Staphylococcus aureus, respectively. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40997.     

Development of shape memory polyurethane based on polyethylene glycol and liquefied 4,4′‐diphenylmethane diisocyanate using a bulk method for biomedical applications

In this study, a series of shape memory polyurethanes (SMPUs) were synthesized successfully by the bulk polymerization method from liquefied 4,4′‐diphenylmethane diisocyanate (L‐MDI), 1,4‐butanediol (BDO) and polyethylene glycol (PEG). The influence of the hard segment content (HSC) on the structure, morphology, properties and biocompatibility of PEG based SMPUs (PEGSMPUs) was carefully investigated. The results show that a microphase separation structure composed of a semicrystalline soft phase and an amorphous hard phase is formed in the PEG6000/L‐MDI/BDO system. Crystallization of the PEG soft segment is influenced by the hard segments. The PEG semicrystalline soft phase serves as a reversible phase while the L‐MDI?BDO hard segment acts as physical netpoints. Finally, a cyclic tensile test shows that all PEGSMPUs have good shape recovery (e.g. above 80%), whereas good shape fixity can only be achieved when the HSC is less than 35 wt%. The Cell Counting Kit 8 assay also demonstrates that only PEGSMPUs containing less than 40 wt% HSC have low cytotoxicity. It is thus concluded that PEGSMPUs bearing both good shape memory effects and good biocompatibility can be used as shape memory materials for biomedical applications when the HSC is less than 35 wt%. © 2014 Society of Chemical Industry     

Measurement of the nonlinear mechanical properties of a poly(vinyl alcohol) sponge under longitudinal and circumferential loading

Poly(vinyl alcohol) sponges (P‐sponges) have been used as a potential implant material for the replacement and repair of soft tissues, including cartilage, liver, and kidney. However, the application of P‐sponges as tissue replacement materials is almost entirely bounded because of a lack of sufficient mechanical properties. In this study, we characterized the mechanical properties of a fabricated poly(vinyl alcohol) sponge (P‐sponge) under a series of longitudinal and circumferential uniaxial loadings. The nonlinear mechanical behavior of the P‐sponge was also computationally investigated with hyperelastic strain energy density functions, that is, the Ogden, Yeoh, Mooney–Rivlin, and Neo‐Hookean models. A hyperelastic constitutive model was selected to best fit the axial behavior of the sponge. The results reveal that the Young's modulus and maximum stress of the P‐sponge in the longitudinal direction were 16 and 17% greater than that in the circumferential direction, respectively. The Yeoh model, in addition, was selected to represent the nonlinear behavior of the poly(vinyl alcohol) material and could be used in future biomechanical simulations of the soft tissues. These results can be used to understand the mechanical properties of spongy materials in different loading directions. In addition, they have implications for ophthalmic and plastic surgeries and wound healing and tissue engineering purposes. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40257.     

Characterization and use of ultraviolet‐reactive low‐molecular‐weight polyhydroxybutyrate to prepare biodegradable acrylates

The characterizations of prepared low‐molecular‐weight polyhydroxybutyrate (LMWPHB) and the properties of LMWPHB photopolymerized with hydrophilic and hydrophobic acrylic monomers were studied with ¹H‐NMR spectroscopy, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy, Instron tensile testing, and biodegradation tests. The results of ¹H‐NMR and FTIR spectroscopy confirmed that the prepared LMWPHB had transformed unsaturated ends that were photoreactive under UV light. The tensile strengths of the LMWPHB/acrylates decreased with increasing content of the added biodegradable LMWPHB because of the relatively long chains and large equivalent molar weights of LMWPHB. However, the flexibility of LMWPHB/acrylates changed differently with the type of acrylic monomer used. The LMWPHB/hydrophilic acrylate had a much more rapid biodegradation rate than the LMWPHB/hydrophobic acrylate because of the fast penetration of microorganisms. We demonstrated that the prepared LMWPHB could be used to control the biodegradation properties of acrylates and then could potentially be applied in biomedical fields. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39501.     

Permeability and blood compatibility of nanoporous parylene film‐coated polyethersulfone membrane under long‐term blood diffusion

Nanoporous polyethersulfone (PES) membranes are widely used in dialysis systems due to their permeability and diffusion characteristics. However, PES membranes lack blood compatibility, which influences their permeability performance when employed in blood contact devices. Parylene film was deposited on a PES membrane surface and the membrane permeability and blood compatibility were investigated by long‐term blood diffusion testing. After 28 days of testing, 90% of a bare PES membrane was covered with platelets, while the parylene film coated PES membrane had improved biocompatibility with a platelet coverage of only 20–30%. The permeability of the bare PES membrane significantly declined during the first 7 days of the blood diffusion and became stable after 8 days. In contrast, the permeability of the parylene film coated PES membrane exhibited more consistent performance during the entire test. Thus, parylene film coating on PES membrane has potential for application in hemodialysis systems. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 40024.     

Core–shell PVA/gelatin nanofibrous scaffolds using co‐solvent,aqueous electrospinning: Toward a green approach

Electrospinning (ES) of gelatin often requires cytotoxic organic solvents or acidic environments, which deteriorate cell recognition sites. In this study, aqueous, non‐toxic, co‐solvent ES was performed to obtain core–shell poly(vinyl alcohol) (PVA)/gelatin nanofiber scaffolds. Effects of the core/shell feed rate ratio (FRR) were investigated on a morphological and mechanical basis. PVA:gelatin ratio of 1:4 was the limiting ratio for specific voltage and electrode distance parameters to obtain uniform fibers. Core–shell bead‐free structures were obtained at 8% PVA and gelatin aqueous solutions. A mean diameter of 280 nm was obtained for 1:1 FRR at 15 kV and 15 cm of electrode distance. Crosslinking resulted in slight improvement in tensile strengths and severe decrease in ductility. Fourier transform infrared spectra revealed retention and improvement of stable secondary structures of gelatin after ES. The scaffolds almost degraded more than 60% in 14 days. Based on the results, present scaffolds hold great promise as suitable candidates for biomedical applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46582.