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.     

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.     

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.     

Polymeric materials for long‐term durability of photovoltaic systems

Photovoltaic (PV) technology has evolved rapidly in the past few decades and now encompasses a large variety of materials and device structures. A key aspect to be taken into account in any PV technology is the operational durability of the systems in outdoor conditions. Clearly, loss of performance during operation represents a significant drawback and limitation in the commercialization of this technology. In this context, the large compositional flexibility of polymeric materials as well as their proven easy processability may be of great help in imparting improved durability to PV systems. In this review, a summary on the state of the art and most recent developments in the field of polymeric materials for improved long‐term durability of PV devices is presented, with particular emphasis on the use of polymers as encapsulation materials and protective coatings in the field of both PV and light‐concentration systems. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43080.     

Gastro‐resistant controlled release of OTC encapsulated in alginate/chitosan matrix coated with acryl‐EZE® MP in fluidized bed

A gastro‐resistant system of acryl‐EZE® MP coated alginate/chitosan microparticles was developed to improve the controlled release of oxytetracycline (OTC). Microparticles were obtained by complex coacervation and, thereafter, were coated using fluidized polymer dispersion with acryl‐EZE® MP solution. OTC distribution inside the microparticles was determined by multiphoton confocal microscopy, demonstrating the efficiency of encapsulation process. In vitro OTC release kinetic was performed in order to obtain the release profile in gastric and intestinal simulated fluids. A fast initial release, or burst effect, was observed with uncoated microparticles loaded with OTC in gastric conditions. When a 50% mass increase in acryl‐EZE® MP coating was achieved, OTC release in acidic medium was greatly reduced, resulting in the expected gastro‐resistant effect. Different mathematical models were applied to describe the drug diffusion across the polymer matrix. The Logistic model was the best tool to interpret the experimental data in most of the systems studied. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40444.     

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.     

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.     

Microstructural characterization of short glass fibre reinforced polyethersulfone composites

To explore the effect of short glass fiber reinforcement (SGFR) on the mechanical properties of polyethersulfone (PES), microstructural characterization has been performed by positron lifetime technique. The free volume distribution of SGFR‐PES composites derived from CONTIN‐PALS2 program exhibits the narrow full width at half maximum (FWHM) indicates the strong interaction between polymeric chains of PES matrix and SGF. The positron lifetime parameters of SGFR‐PES composites are correlated with the mechanical properties viz., Tensile strength (TS), Young's modulus (YM) and elongation at break (EB). The decreased positron lifetime parameters, improved mechanical properties and reduced crystallinity of SGFR‐PES composites are attributed to the improved chemical and physical interaction between the functional groups of both SGF and PES matrix. This is clearly evident from the FTIR (Fourier Transform Infrared Spectrometry) studies. The hydrodynamic interaction parameter (h) show negative values, suggest the improved interaction in SGFR‐PES composites by the generation of excess friction at the interface. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43647.     

Incorporation of chloramphenicol and captopril into poly(GL)‐b‐poly(GL‐co‐TMC‐co‐CL)‐b‐poly(GL) monofilar surgical sutures

Incorporation of chloramphenicol and captopril into coated and uncoated monofilament sutures was evaluated, as well as the derived bactericide and wound healing effects. To this end, a commercially available suture and an amorphous random copolymer constituted by trimethylene carbonate and lactide units were considered. The suture had a segmented architecture based on polyglycolide hard blocks and a soft block constituted by glycolide, trimethylene carbonate and ε‐caprolactone units. Chloramphenicol was better loaded when the coating copolymer was employed due to its protective effect whereas captopril showed an opposite behavior due to partial solubilization during immersion in the coating bath. Interestingly, the release behavior was very different for the two studied drugs since a significant retention of chloramphenicol was always detected, suggesting the establishment of interactions between drug and copolymers. On the other hand, delivery of captopril showed a typical dose dependent behavior. A low in vitro toxicity of the two drugs was determined considering both epithelial‐like and fibroblast‐like cells. Bactericide effect of chloramphenicol against Gram‐negative and Gram‐positive bacteria was demonstrated at a dose that was non‐toxic for all assayed cells. An accelerating wound healing effect of captopril was also demonstrated for early events. In this case, the use of a coating copolymer was fundamental to avoid cytotoxic effects on highly loaded sutures. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44762.     

Production of hyaluronic‐acid‐based cell‐enclosing microparticles and microcapsules via enzymatic reaction using a microfluidic system

This article describes the preparation of cell‐enclosing hyaluronic acid (HA) microparticles with solid core and microcapsules with liquid core through cell‐friendly horseradish peroxidase (HRP)‐catalyzed hydrogelation. The spherical vehicles were made from HA derivative possessing phenolic hydroxyl moieties (HA‐Ph) cross‐linkable through the enzymatic reaction by extruding cell‐suspending HA‐Ph aqueous solution containing HRP from a needle of 180 μm in inner diameter into the ambient coaxial flow of liquid paraffin containing H₂O₂ in a microtubule of 600 μm in diameter. By altering the flow rate of liquid paraffin, the diameters of gelatin and HA‐Ph microparticles were varied in the range of 120–220 μm and 100–300 μm, respectively. The viability of the enclosed human hepatoma HepG2 cells in the HA‐Ph microparticles of 180 μm in diameter was 94.2 ± 2.3%. The growth of the enclosed HepG2 cells was enhanced by decreasing the HRP concentration. The microcapsules of 200 μm in diameter were obtained by extruding HA‐Ph aqueous solution containing thermally liquefiable cell‐enclosing gelatin microparticles of 150 μm in diameter using the same microfluidic system. The enclosed cells grew and filled the cavity within 10 days. Spherical tissues covered with a heterogeneous cell layer were obtained by degrading the microcapsule membrane using hyaluronidase after covering the surface with a heterogeneous cell layer. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43107.     

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.     

Thiocarbohydrazide‐modified chitosan as anticorrosion and metal ion adsorbent

To explore the application of chitosan (CS) derivatives in anticorrosion and adsorption, thiocarbohydrazide‐modified chitosan (TCHECS) derivative was synthesized and characterized. The preliminary electrochemical measurements of the behaviors of 304 steel and Cu sheets in 2% HAc (v/v) containing TCHECS, chitosan (CS), and hydrazine cross‐linked epoxy‐N‐phthaloylchitosan (HECS) had been performed. The short‐term electrochemical tests show that the new compound can act as a mixed‐type metal anticorrosion inhibitor; its inhibition efficiency is 88% when the concentration was 30 mg/L. The preliminary adsorption studies for sorbents TCHECS and HECS on a metal ion mixture aqueous solution were also performed. The results show that TCHECS can absorb As (V), Ni (II), Cu (II), Cd (II), and Pb (II) efficiently at pH 9; the removal of the As (V), Ni (II), Cu (II), Cd (II), and Pb (II) are around 55.6–99.9%. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40671.     

Design of hemocompatible poly(DMAEMA‐co‐PEGMA) hydrogels for controlled release of insulin

This works aims at (i) studying the antiadhesive properties and the hemocompatibility of poly[2‐(dimethylamino)ethyl methacrylate]‐co‐poly[(ethylene glycol)methacrylate] [poly(DMAEMA‐co‐PEGMA)] copolymers and (ii) investigating the insulin delivery kinetics through hydrogels at physiological pH. A series of poly(DMAEMA‐co‐PEGMA) hydrogels have been synthesized, and their controlled composition was confirmed by X‐ray photoelectron spectroscopy. Then, antibiofouling properties of hydrogels—fibrinogen, erythrocytes, and thrombocytes adhesion—are correlated to their molecular compositions through their hydrophilic properties. As DMAEMA/PEGMA ratio of 70/30 (D70) offers the best compromise between pH sensitivity and hemocompatibility, it is selected for investigating the kinetic rate of insulin release at physiological pH, and the diffusion coefficient of insulin in gel is found to be 0.64 × 10^?7 cm² s^?1. Overall, this study unveils that poly(DMAEMA‐co‐PEGMA) copolymers are promising hemocompatible materials for drug delivery systems. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42365.     

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.     

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.     

Fabrication of a tunable hydrogel membrane for constructing indirect cell coculture system

In this study, an improved indirect cell coculture system was constructed by using a polyelectrolyte complex membrane generated by alginate (A) and chitosan (C). Methodologies of characterizing thickness and permeability of flat AC membrane were first established due to the importance of these two parameters in determining intercellular distance and degree of contact between cocultured cells. Compared to reaction time, both alginate concentration and molecular weight (M_w) of chitosan play more dominant roles in determining the membrane thickness and diffusion coefficients. Moreover, cells in the alginate gel and on the AC membrane could maintain high cell viability. Thus, an improved indirect cell coculture system constructed by flat AC membrane was fabricated and characterized, which provides a robust tool to study the effect of intercellular distance and degree of contact between cocultured cells on cell–cell interactions. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43100.     

Effect of stereoisomerism of poly(lactic acid) during neural guide conduit membrane synthesis

Poly(lactic acid) membranes are being developed as biomaterials for several purposes such as artificial implants for peripheral nerve injury, also known as neural guide conduits (NGC). These membranes need to meet standards of mechanical, degradability, and permeability properties, besides dimensional and structural requirements. Among the stereoisomers of polylactides, poly(l ‐lactic acid), and poly(d ,l ‐lactic acid) are the most used as biomaterials, having significant differences in solubility, crystallinity thermal, and mechanical properties. In this work, PLLA and PDLLA were compared for hollow fiber membrane synthesis by liquid induced phase separation. PLLA samples presented 18% of crystallinity, while PDLLA is amorphous. PDLLA and PLLA polymer solutions on N‐methyl‐pyrrolidone presented values of 3428 and 320.2 cP, respectively. In immersion of PLA‐NMP solutions in water, PLLA solution presented instantaneous demixing, while PDLLA showed a 28 s delay on precipitation. The PLLA–NMP–water has a larger demixing region compared to PDLLA–NMP–water system. Hollow fibers of both polymers presented closed external surface with finger‐like macropores morphology in their cross‐sections. PDLLA presented typical liquid–liquid demixing pores while PLLA presented spherulitical crystalline solid–liquid separation structures, which deeply compromised its mechanical properties. PDLLA presented as a good candidate for hollow fiber NGC material, as presented good mechanical resistance in tensile and suture simulating tests. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46190.     

Preparation and characterizations of superparamagnetic iron oxide‐embedded poly(2‐hydroxyethyl methacrylate) nanocarriers

The present study aims at formulating a novel multifunctional biocompatible superparamagnetic nanoparticles carrier system with homogeneously dispersed magnetic material in solid polymer matrix of poly(2‐hydroxyethyl methacrylate) (PHEMA). The nanocomposites were designed by modified suspension polymerization of 2‐hydroxyethyl methacrylate followed by in situ coprecipitation of iron oxide inside the nanoparticle matrix yielding magnetic PHEMA (mPHEMA) nanocomposites. The so prepared nanocomposites were characterized by Fourier transform Infrared spectroscopy, X‐ray diffraction technique, Raman spectroscopy, electron diffraction, and energy‐dispersive X‐ray spectroscopy confirming the presence of Fe₃O₄ inside the PHEMA nanoparticles. The magnetization studies of nanocomposites conducted at room temperature using vibrating sample magnetometer suggested for their superparamagnetic nature having saturation magnetization (Ms) of 20 emu/g at applied magnetic field of 5 kOe. Transmission electron microscopy, field‐emission scanning electron microscopy, and dynamic light scattering/zeta potential measurements were also performed which revealed that size of mPHEMA nanocomposites was lying in the range of 60–300 nm having zeta potential of ?93 mV. The nanocomposites showed no toxicity as revealed by cytotoxicity test performed on L‐929 fibroblast by extract method. The results indicated that the prepared superparamagnetic mPHEMA nanocomposites have enormous potential to provide a possible option for magnetically assisted targeted delivery of anticancer drugs. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40791.     

Mechanical characterization of high‐performance graphene oxide incorporated aligned fibroporous poly(carbonate urethane) membrane for potential biomedical applications

In this article, we report the development of graphene oxide (GO) reinforced electrospun poly(carbonate urethane) (PCU) nanocomposite membranes intended for biomedical applications. In this study, we aimed to improve the mechanical properties of PCU fibroporous electrospun membranes through fiber alignment and GO incorporation. Membranes with 1, 1.5, and 3% loadings of GO were evaluated for their morphology, mechanical properties, crystallinity, biocompatibility, and hemocompatibility. The mechanical properties were assessed under both static and dynamic conditions to explore the tensile characteristics and viscoelastic properties. The results show that GO presented a good dispersion and exfoliation in the PCU matrix, contributing to an increase in the mechanical performance. The static mechanical properties indicated a 55% increase in the tensile strength, a 127% increase in toughness for 1.5 wt % GO loading and the achievement of a maximum strength reinforcement efficiency value at the same loading. Crystallinity changes in membranes were examined by X‐ray diffraction analysis. In vitro cytotoxicity tests with L‐929 fibroblast cells and percentage hemolysis tests with fresh venous blood displayed the membranes to be cytocompatible with acceptable levels of hemolytic characteristics. Accordingly, these results highlight the potential of this mechanically improved composite membrane's application in the biomedical field. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41809.     

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