Self synthesize of silver nanoparticles in/on polyurethane nanofibers: Nano‐biotechnological approach

In this study, we are introducing a new class of Polyurethane (PU) nanofibers containing silver nanoparticles (NPs) by electrospinning. A simple method not depending on the addition of foreign chemicals has been used to self‐synthesize of silver NPs in/on PU nanofibers. Typically, a sol?gel consisting of AgNO₃/PU/N,N‐dimethylformamide (DMF) has been electrospun and aged for a week, so silver NPs have been created in/on PU nanofibers. Syntheses of silver NPs were carried out by exploiting the reduction ability of the DMF solvent which is the main constituent to obtain PU electrospun nanofibers in decomposition of silver nitrate precursor into silver NPs. Physiochemical characterizations confirmed well oriented nanofibers and good dispersing of pure silver NPs. Various parameters affecting utilizing of the prepared nanofibers on various nano‐biotechnological fields have been studied. For instance, the obtained nanofiber mats were checked for mechanical properties which showed the improvement of the tensile strength upon increase in silver NPs content. Moreover, the nanofibers were subjected to 10 times successive washing experiments with using solid to liquid ratio of 3 : 5000 for 25 h, UV spectroscopy analysis reveals no losses of silver NPs from the PU nanofibers. 3T3‐L1 fibroblasts were cultured in presence of the designed nanofibers. The morphological features of the cells attached on nanofibers were examined by BIO‐SEM, which showed well attachment of cells to fibrous mats. The cytotoxicity results indicated absence of toxic effect on the 3T3‐L1 cells after cell culturing. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Studies on the synthesis of electrospun PAN‐Ag composite nanofibers for antibacterial application

We have successfully synthesized polyacrylonitrile (PAN) nanofibers impregnated with Ag nanoparticles by electrospinning method at room temperature. Briefly, the PAN‐Ag composite nanofibers were prepared by electrospinning PAN (10% w/v) in dimethyl formamide (DMF) solvent containing silver nitrate (AgNO₃) in the amounts of 8% by weight of PAN. The silver ions were reduced into silver particles in three different methods i.e., by refluxing the solution before electrospinning, treating with sodium borohydride (NaBH₄), as reducing agent, and heating the prepared composite nanofibers at 160°C. The prepared PAN nanofibers functionalized with Ag nanoparticles were characterized by field emission scanning electron microscopy (FESEM), SEM elemental detection X‐ray analysis (SEM‐EDAX), transmission electron microscopy (TEM), and ultraviolet‐visible spectroscopy (UV‐VIS) analytical techniques. UV‐VIS spectra analysis showed distinct absorption band at 410 nm, suggesting the formation of Ag nanoparticles. TEM micrographs confirmed homogeneous dispersion of Ag nanoparticles on the surface of PAN nanofibers, and particle diameter was found to be 5–15 nm. It was found that all the three electrospun PAN‐Ag composite nanofibers showed strong antibacterial activity toward both gram positive and gram negative bacteria. However, the antibacterial activity of PAN‐Ag composite nanofibers membrane prepared by refluxed method was most prominent against S. aureus bacteria. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Preparation and Characterization of Gelatin Nanofibers Containing Silver Nanoparticles

Ag nanoparticles (NPs) were synthesized in formic acid aqueous solutions through chemical reduction. Formic acid was used for a reducing agent of Ag precursor and solvent of gelatin. Silver acetate, silver tetrafluoroborate, silver nitrate, and silver phosphate were used as Ag precursors. Ag⁺ ions were reduced into Ag NPs by formic acid. The formation of Ag NPs was characterized by a UV-Vis spectrophotometer. Ag NPs were quickly generated within a few minutes in silver nitrate (AgNO₃)/formic acid solution. As the water content of formic acid aqueous solution increased, more Ag NPs were generated, at a higher rate and with greater size. When gelatin was added to the AgNO₃/formic acid solution, the Ag NPs were stabilized, resulting in smaller particles. Moreover, gelatin limits further aggregation of Ag NPs, which were effectively dispersed in solution. The amount of Ag NPs formed increased with increasing concentration of AgNO₃ and aging time. Gelatin nanofibers containing Ag NPs were fabricated by electrospinning. The average diameters of gelatin nanofibers were 166.52 ± 32.72 nm, but these decreased with the addition of AgNO₃. The average diameters of the Ag NPs in gelatin nanofibers ranged between 13 and 25 nm, which was confirmed by transmission electron microscopy (TEM).     

Antibacterial Ag containing core-shell polyvinyl alcohol-poly (lactic acid) nanofibers for biomedical applications

Core-shell-structured polyvinyl alcohol (PVA)-poly (lactic acid) (PLA) nanofibers combining the hydrophilic trait of PVA and the biocompatibility of PLA were produced using coaxial electrospinning. This allowed the incorporation of AgNO₃ in the PVA core of the distinct fibers as shown through transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR). Scanning electron microscopy (SEM) showed relatively uniform and bead-free fibers with smooth surfaces. Ag-containing fibers show significantly decreased diameters compared with Ag-free samples as a result of the increased conductivity of the spinning solutions with increasing amounts of AgNO₃. In a postsynthetic treatment, the AgNO₃ was reduced forming silver nanoparticles (Ag NPs). Ag NPs of 45 to 90 nm size were located in the PVA core but also on the surface of the core-shell fibers and as individual, agglomerated, and polymer-coated particles of 100-200 nm. Powder X-ray diffraction (PXRD), energy dispersive X-ray spectroscopy (EDX), and UV-vis absorption spectroscopy confirmed the increasing amounts of Ag in the core-shell fibers when using increasing amounts of AgNO₃ in the spinning solutions. The antibacterial activity of the nanofiber mats against two prokaryotes Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) increased with increasing amounts of Ag, as expected and produces inhibition zones of 1 to 2 mm.     

Antibacterial polycaprolactone electrospun fiber mats prepared by soluble eggshell membrane protein–assisted adsorption of silver nanoparticles

Antibacterial polycaprolactone (PCL) electrospun fiber mats were prepared by coelectrospinning PCL with soluble eggshell membrane protein (SEP) in 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP), followed by adsorption of silver nanoparticles (Ag NPs) through hydrogen‐bonding interaction between the amide groups of SEP and the carboxylic acid groups capped on the surfaces of Ag NPs. The PCL/SEP fiber mat was characterized by X‐ray photoelectron spectroscopy, indicating the presence of some SEP on the fiber surface. The adsorption of Ag NPs was confirmed by transmission electron microscopy and quantitatively characterized by thermogravimetric analysis. The pH value of the silver sol used for adsorption is very important in view of the amount and dispersion state of Ag NPs adsorbed on the fibers. The Ag NP–decorated PCL/SEP fiber mats prepared at pH 3–5 exhibit strong antibacterial activity against both gram‐negative Escherichia coli and gram‐positive Bacillus subtilis. Antibacterial PCL fiber mats were also obtained similarly with the assistance of collagen (another protein) instead of SEP, showing that protein‐assisted adsorption of Ag NPs is a versatile method to prepare antibacterial electrospun fiber mats. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43850.     

Electrospun antibacterial nylon nanofibers through in situ synthesis of nanosilver: preparation and characteristics

A new method for production of nylon nanofibers with antibacterial properties containing silver nanoparticles (nylon nanofibers/Ag NPs) is introduced via in situ synthesis of nano-silver by reduction of silver nitrate in the polymer solution prior to electrospinning. The properties of the electrospinning solutions and the structures of the electrospun fibers were studied using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDAX), UV?Cvis spectrophotometer and reflection spectrophotometer. Further, the antibacterial properties of the nanofibers were investigated against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) bacteria. Interestingly, an antibacterial properties has been found on nylon 6 nanofibers while the nylon nanofibers/Ag NPs showed excellent antibacterial activities against both tested bacteria. The produced nylon nanofibers/Ag NPs can be a good candidate for biomedical applications, water and air filtration.     

Improvements on electrical conductivity of the electrospun microfibers using the silver nanoparticles

Conductive electrospun polymer fibers have attracted a great deal of interest in recent years. This study describes the preparation of electrically conductive microfibers composed of polyethersulfone/polydopamine/silver nanoparticles (PES/PDA/Ag NPs). Ag NPs acted as conductive centers, while hydroxyl- and amino-rich functional groups and excellent adhesion properties of PDA served to connect the Ag NPs and PES microfibers. Fourier transform infrared spectroscopy and scanning electron microscopy (SEM) showed that PDA was firmly adhered to PES microfibers. PES/PDA microfibers absorbed considerable amounts of silver ion from AgNO₃ solution, resulting in Ag NPs. X-ray diffraction, X-ray photoelectron spectroscopy, and SEM data represented the successful formation of PES/PDA/Ag NPs microfibers. Microfibers with optimal conductivity were obtained using a solution of 2% AgNO₃ at pH 9 at 50 °C for 45 min. The electrical resistivity of our PES/PDA/Ag NPs microfibers was only 202 Ω/cm, much lower than that of regular PES microfibers (2.1 × 10⁹ Ω/cm). These results show that the PES/PDA/Ag NPs microfibers are suitable for use as conductive polymer fibers in electromagnetic shielding, and conductivity-sensing applications, and in flexible electronic devices and biosensors. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48788.     

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.     

Ultrasmall Ag nanocrystals supported on chitosan/PVA nanofiber mats with bifunctional properties

Bifunctional nanofiber mats consisting of chitosan (CS), poly(vinyl alcohol) (PVA), and silver nanocrystals (Ag NCs) have been fabricated by a facile electrospinning method. The formation and presence of Ag NCs supported on CS/PVA nanofibers are confirmed by ultraviolet‐visible spectroscopy and X‐ray diffraction. The morphology of the samples is characterized by transmission electron microscopy and scanning electron microscopy. The prepared Ag NCs/CS/PVA nanofiber mats show pronounced antibacterial activity against Escherichia coli and excellent filtration property for suspended particulate matter (SPM) particles. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46504.     

A promising technique of Aegle marmelos leaf extract mediated self‐assembly for silver nanoprism formation

The Aegle marmelos leaf extract (LE) mediated synthesis of prismatic and spherical Ag nanoparticles (NPs) has been studied. The formation of prismatic structures from spherical NPs was observed microscopically using scanning electron microscope, transmission electron microscope, and atomic force microscope. The shape transformation from spherical NPs to prismatic nanostructures was studied by simply changing LE concentration, keeping constant AgNO₃ concentration (1 mM). The role of pH toward prism formation and the effect of sonication on the formed structures were also investigated. The antimicrobial activity of the synthesized Ag spherical/prismatic NPs was evaluated against gram negative bacteria (Escherichia coli, Pseudomonas aeruginosa) and on a phytopathogen Fusarium solani. This green synthesis approach for the synthesis of prismatic Ag nanostructures may be useful for surface‐enhanced Raman spectroscopy application for the detection of low concentration organic molecules, apart from the studied antimicrobial activity. © 2017 American Institute of Chemical Engineers AIChE J, 63: 3670–3680, 2017     

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.     

Antimicrobial properties of silver nanoparticles synthesized by bioaffinity adsorption coupled with TiO2 photocatalysis

BACKGROUND: On the basis of effective bioaffinity adsorption of Ag⁺, silver nanoparticles (Ag NPs) were synthesized on the surface of chitosan‐TiO₂ adsorbent (CTA) by TiO₂ photocatalysis for crystal growth. RESULTS: Among the microstructure characterizations of the resulting silver nanoparticles‐ loaded chitosan‐TiO₂ adsorbent (Ag‐CTA), X‐ray diffraction (XRD) and scanning electron microscopy (SEM) equipped with energy dispersive X‐ray (EDX) revealed the formation of metallic Ag on the CTA, which was further confirmed by the surface plasmon resonance of Ag NPs in the UV‐visible absorption spectrum. The underlying mechanism behind the formation of Ag NPs on the CTA by TiO₂ photoreduction was studied by Fourier transform infrared (FTIR) spectroscopy. The distinctive feature of Ag‐CTA after adsorption was the highly efficient antimicrobial activity in inactivating different test strains. In the case of Escherichia coli, 1.50 mg 1.67 wt% Ag‐CTA could totally inhibit 1.0–1.2 × 10⁷ colony forming units (CFU) in 100 mL nutrient medium, which was superior to that previously reported. CONCLUSIONS: CTA effectively adsorbed the precious metal ion Ag⁺ onto active imprinting sites on the adsorbent and then exerted efficient antimicrobial effects against diverse microbes. This research will be useful for designing a novel CTA‐based wastewater treatment for multi‐functional performance. Copyright © 2010 Society of Chemical Industry     

Preparation and antibacterial activity of PET/chitosan nanofibrous mats using an electrospinning technique

The nanofiber deposition method, by electrospinning, was employed to introduce antibacterial activity and biocompatibility to the surface of poly (ethylene terephthalate) (PET) textiles. The polymer blends of PET and chitosan were electrospun on to the PET micro‐nonwoven mats for biomedical applications. The PET/chitosan nanofibers were evenly deposited on to the surface, and the diameter of the nanofibers was in the range between 500 and 800 nm. The surface of the nanofibers was characterized using SEM, ESCA, AFM, and ATR‐FTIR. The wettability of the PET nanofibers was significantly enhanced by the incorporation of chitosan. The antibacterial activity of the samples was evaluated utilizing the colony counting method against Staphylococcus aureus and Klebsiella pneumoniae. The results indicated that the PET/chitosan nanofiber mats showed a significantly higher growth inhibition rate compared with the PET nanofiber control. In addition, the fibroblast cells adhered better to the PET/chitosan nanofibers than to the PET nanofibers mats, suggesting better tissue compatibility. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Preparation and properties of silver‐containing nylon 6 nanofibers formed by electrospinning

Nylon 6 nanofibers containing silver nanoparticles (nylon 6/silver) were successfully prepared by electrospinning. The structure and properties of the electrospun fibers were studied with the aid of scanning electron microscopy, transmission electron microscopy, energy‐dispersive spectroscopy, and X‐ray diffraction. The structural analysis indicated that the fibers electrospun at maximum conditions were straight and that silver nanoparticles were distributed in the fibers. Finally, the antibacterial activities of the nylon 6/silver nanofiber mats were investigated in a broth dilution test against Staphylococcus aureus (Gram‐positive) and Klebsiella pneumoniae (Gram‐negative) bacteria. It was revealed that nylon 6/silver possessed excellent antibacterial properties and an inhibitory effect on the growth of S. aureus and K. pneumoniae. On the contrary, nylon 6 fibers without silver nanoparticles did not show any such antibacterial activity. Therefore, electrospun nylon 6/silver nanocomposites could be used in water filters, wound dressings, or antiadhesion membranes. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Preparation and antibacterial activity of polyvinyl alcohol/regenerated silk fibroin composite fibers containing Ag nanoparticles

Polyvinyl alcohol (PVA)/regenerated silk fibroin (SF)/AgNO₃ composite nanofibers were prepared by electrospinning. A large number of nanoparticles containing silver were generated in situ and well‐dispersed nanoparticles were confirmed by transmission electron microscopy (TEM) intuitionally. Ultraviolet (UV)‐visible spectroscopy and X‐ray diffraction (XRD) patterns indicated that nanoparticles containing Ag were present both in blend solution and in composite nanofibers after heat treatment and after subsequent UV irradiation. By annealing the nanofibers, Ag⁺ therein was reduced so as to produce nanoparticles containing silver. By combining heat treatment with UV irradiation, Ag⁺ was transformed into Ag clusters and further oxidized into Ag₃O₄ and Ag₂O₂. Especially size of the nanoparticles increased with heat treatment and subsequent UV irradiation. This indicated that the nanoparticles containing silver could be regulated by heat treatment and UV irradiation. The antimicrobial activity of heat‐treated composite nanofibers was evaluated by Halo test method and the resultant nanofibers showed very strong antimicrobial activity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

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

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

Preparation and characterization of poly(vinyl alcohol) cryogel‐silver nanocomposites and evaluation of blood compatibility,cytotoxicity, and antimicrobial behaviors

In this investigation, cryogels composed of poly(vinyl alcohol) (PVA) were prepared by repeated freeze‐thaw method. The prepared cryogels served as templates for producing highly stable and uniformly distributed silver nanoparticles via in situ reduction of silver nitrate (AgNO₃) using alkaline formaldehyde solution as reducing agent. The structure of the PVA/Ag cryogel nanocomposites was characterized by a Fourier transform infrared and Raman spectroscopy. The morphologies of pure PVA cryogels and PVA/Ag nanocomposites were observed by a scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. The SEM analysis suggested that cryogels show a well defined porous morphology whereas TEM micrographs revealed the presence of nearly spherical and well separated Ag nanoparticles with diameter about 100 nm. XRD results showed all relevant Bragg's reflections for crystal structure of silver nanoparticles. The amount of silver in cryogel nanocomposites and thermal stability were determined by inductively coupled plasma atomic emission spectrometry (ICP‐AES) and thermogravimetric analysis measurements. Mechanical properties of nanocomposites were observed in terms of tensile strength. The antibacterial studies of the synthesized nanosilver containing cryogels showed good antibacterial activity against both gram‐negative and gram‐positive bacteria. The prepared PVA/Ag nanocomposites were also investigated for swelling and deswelling behaviors. The results reveal that both the swelling and deswelling process depends on the chemical composition of the cryogel silver nanocomposites, number of freeze‐Thaw cycles and pH and temperature of the swelling medium. The biocompatibility of the prepared nanocomposites was judged by in vitro methods of percent hemolysis and protein (BSA) adsorption. POLYM. COMPOS., 36:1983–1997, 2015. © 2014 Society of Plastics Engineer     

Oxidative solution polymerization of aniline hydrochloride onto electrospun nanofibers mats of polylactic acid: Preparation method and characterization

In this work, we present the preparation of polylactic acid (PLLA)/polyaniline (PANI) conductive composite nanofibers mats. They are prepared by bulk oxidative solution polymerization of PANI onto electrospun non‐woven fibers mats of PLLA. The PANI ratio in the composite is about 70%w/w. Scanning electron microscopy (SEM) shows that PLLA nanofibers are randomly oriented, beads free with diameters of 186 ± 85 nm, The PLLA/PANI composite nanofibers diameter values are 518 ± 128 nm with a good adherence between PANI and PLLA nanofibers. DSC and XRD measurements reveal an amorphous structure of the electrospun PLLA fibers due to the rapid evaporization of the solvent. FTIR and UV–vis spectra reflect good mutual interactions between PANI and PLLA chains. The DC‐conductivities ( ) far better than other published ones for similar composites prepared by bulk oxidative solution polymerization of PANI onto other electrospun nanofiber mats or with electrospun nanofibers from a solution mixture of PLLA and PANI. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41618.     

Preparation and properties of electrospun poly(vinyl alcohol)/silver fiber web as wound dressings

A novel wound dressing material was prepared by electrospinning poly(vinyl alcohol) (PVA)/AgNO₃ aqueous solution into nonwoven webs and then treating the webs by heat or UV radiation. Through SEM, TEM, and XPS analyses, it was observed that the silver (Ag) nanoparticles were generated and existed in the near surface of the electrospun nanofibers. It was found that heat treatment as well as UV radiation reduced the Ag⁺⁺⁺ ions in the electrospun PVA/AgNO₃ fiber web into the Ag nanoparticles. Also the heat treatment improved the crystallinity of the electrospun PVA fiber web and so it made the web unsolved in moisture environment. Therefore, it was concluded that the only heat treated electrospun PVA/AgNO₃ fiber web was a good material as wound dressings because it had structural stability in moisture environment as well as excellent antimicrobial ability and, quick and continuous release of the effectiveness. POLYM. ENG. SCI., 47:43–49, 2007. © 2006 Society of Plastics Engineers     

Antibacterial activities of novel nanocomposite biofilms of chitosan/phosphoramide/Ag NPs

Novel nanocomposite films of chitosan/phosphoramide/Ag NPs were prepared containing 1–5% of silver nanoparticles. The Ag NPs were synthesized according to the citrate reduction method. The XRD and SEM analysis of Ag NPs, chitosan (CS), phosphoramide (Ph), CS/Ph, CS/Ag NPs films and the nanocomposite films 1–5 containing CS/Ph/1–5% Ag NPs were investigated. The in vitro antibacterial activities were evaluated against four bacteria including two Gram‐positive Staphylococcus aureus (S. aureus), Bacillus cereus (B. cereus) and two Gram‐negative Escherchia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa) bacteria. Results revealed greater antibacterial effects of the films against Gram‐positive bacteria. Also, nanocomposite films containing higher percent of Ag NPs showed more antibacterial activities. POLYM. COMPOS. 36:454–466, 2015. © 2014 Society of Plastics Engineers