A study on melt spinning of polyethylene terephthalate filament yarns containing various concentrations of synthesized CuO nanoparticles

In this research the CuO nanoparticles were synthesized with four different methods then used to produce polyethylene terephthalate (PET) fibers with antibacterial, antifungal, and photocatalytic properties during the melt spinning process. Nanoparticles were synthesized in different ways using copper acetate salt (Cu(CH₃COO)₂) and sodium hydroxide (NaOH). The synthesis of copper oxide (CuO) nanoparticles was confirmed by field-emission scanning electron microscopy (FE-SEM images), EDX patterns, TGA, FTIR, X-ray diffraction pattern XRD, and UV-vis absorption spectrum. The results showed that synthesized nanoparticles exhibited strong antibacterial activity against gram-positive and gram-negative bacteria. Finally, after examining the fibers with different percentages of nanoparticles), fibers containing 1% of nanoparticles were produced using a 20% nanocopper oxide masterbatch as the optimal sample. The presence of nanoparticles in the fiber structure was confirmed by FE-SEM images, EDX, XRD, and FTIR analysis. Furthermore, the tensile properties, thermal behavior, and photocatalytic properties of the fibers were investigated. Evaluation of the antibacterial and antifungal activity of the produced fibers against gram-positive bacteria Staphylococcus aureus and Candida albicans fungus showed about 90% death of bacteria and fungi.     

Biocompatibility and antibacterial activity of chitosan and hyaluronic acid immobilized polyester fibers

Poly(ethylene terephthalate) (PET) fibers were treated with ⁶⁰Co‐γ‐ray and grafted with acrylic acid. The resulting fibers were further grafted with chitosan (CS) via esterification. Afterward, hyaluronic acid (HA) was immobilized onto CS‐grafting fibers. The antibacterial activity of CS against S. aureus, E. coli, and P. aeruginosa was preserved after HA‐immobilization. After immobilizing HA, the L929 fibroblasts cell proliferation was improved forCS‐grafting PET fiber. The results indicate that by grafting with CS and immobilizing with HA, PET fibers not only exhibit antibacterial activity, but also improve the cell proliferation for fibroblast. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 220–225, 2007     

Preparation and antibacterial activity of C2-benzaldehyde-C6-aniline double Schiff base derivatives of chitosan

C₂-benzaldehyde-C₆-aniline double Schiff base derivatives of chitosan were synthesized with positioning protection method for the first time. The structures and properties of the new synthesized products were characterized by Fourier transform infrared spectroscopy, ¹³C nuclear magnetic resonance, scanning electron microscope image, X-ray diffraction, and elemental analysis. The elemental analysis results indicated that the degrees of substitution of the products were from 39.6% to 48.2%. The synthesized compounds exhibited an excellent solubility in organic solvents. The antibacterial activities of all of the derivatives were tested in the experiment, and the results showed that the prepared chitosan derivatives had significantly improved antibacterial activity of chitosan and C₂-benzaldehyde Schiff bases of chitosan toward Staphylococcus aureus (ATCC 25923) and Escherichia coli (ATCC 35218). Antibacterial activity of the Schiff bases against E. coli differs from the substituent at the same position of different anilines and increases as the sequence aniline?>?p-toluidine?>?o-toluidine, and the antibacterial activity of the Schiff bases against S. aureus increases as the sequence p-toluidine?>?aniline?>?o-toluidine. The I_C50 of the C₂-benzaldehyde-C₆-aniline double Schiff base derivatives of chitosan against E. coli and S. aureus is 0.0035 and 0.0031?mg?L^?1, respectively, much lower than that of chitosan (0.0064?mg?L^?1) and C₂-benzaldehyde Schiff bases of chitosan (0.0054?mg?L^?1). The cytotoxicity test showed that compared with chitosan and C₂-benzaldehyde Schiff bases of chitosan, the prepared chitosan derivatives had lower cytotoxicity against SCG-7901. This paper provided a new method for the synthesis of Schiff bases of chitosan, which was enlightening.     

Quasi-Diamond Platelet-Shaped Zinc Oxide Nanostructures Display Enhanced Antibacterial Activity

The current study compares the antibacterial activity of zinc oxide nanostructures (neZnO). For this purpose, two bacterial strains, Escherichia coli (ATCC 4157) and Staphylococcus aureus (ATCC 29213) were challenged in room light conditions with the aforementioned materials. Colloidal and hydrothermal methods were used to obtain the quasi-round and quasi-diamond platelet-shape nanostructures. Thus, the oxygen vacancy (V_O) effects on the surface of neZnO are also considered to assess its effects on antibacterial activity. The neZnO characterization was achieved by X-ray diffraction (XRD), a selected area electron diffraction (SAED) and Raman spectroscopy. The microstructural effects were monitored by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Furthermore, optical absorption ultraviolet visible spectrophotometry (UV-Vis) and X-ray photoelectron spectroscopy (XPS) analyses complement the physical characterization of these nanostructures; neZnO caused 50 % inhibition (IC₅₀) at concentrations from 0.064 to 0.072 mg/mL for S. aureus and from 0.083 to 0.104 mg/mL for E. coli, indicating an increase in activity against S. aureus compared to E. coli. Consequently, quasi-diamond platelet-shaped nanostructures (average particle size of 377.6±10 nm) showed enhanced antibacterial activity compared to quasi-round agglomerated particles (average size of 442.8±12 nm), regardless of Vo presence or absence.     

Cure behavior and antimicrobial performance of sulfur‐cured natural rubber vulcanizates containing 2‐hydroxypropyl‐3‐piperazinylquinolinecarboxylic acid methacrylate or silver‐substituted zeolite

This work used 2‐hydroxypropyl‐3‐piperazinylquinolinecarboxylic acid methacrylate (HPQM) or silver‐substituted zeolite (SSZ) as antibacterial agents for natural rubber (NR) compounds vulcanized by conventional vulcanization (CV), semi‐efficient vulcanization, and efficient vulcanization (EV) systems. The cure behavior and antibacterial performance of the NR vulcanizates were studied by varying the loadings of HPQM or SSZ, contact times, and vulcanization systems. The antibacterial performance of the rubber compounds was examined by halo test and plate‐count‐agar methods against Escherichia coli (E. coli, ATCC 25922) and Staphylococcus aureus (S. aureus, ATCC 25923) as the testing bacteria. The cure time and crosslink density were dependent on the vulcanization recipe used but were not affected by the addition of HPQM or SSZ. Diphenylguanidine at the level of 1.0 phr (parts by weight per hundred parts of resin) in NR vulcanized by the EV system had the ability to kill the E. coli and S. aureus bacteria. The NR vulcanized by the CV system showed the most pronounced antibacterial performance, as compared with the other two vulcanization systems, via migration and diffusion of HPQM or SSZ onto the NR surfaces, this being identified by the relatively large reduction of contact angle values. The HPQM showed the most preference for NR compounds vulcanized with the CV system with a contact time of 120 min or longer to achieve a bacteria‐killing efficacy of 99.0–99.9%, the efficacy being more pronounced for E. coli bacteria. J. VINYL ADDIT. TECHNOL., 19:123–131, 2013. © 2013 Society of Plastics Engineers     

Radiation-Induced Acrylamide/4-Vinyl Pyridine Biocidal Hydrogels: Synthesis,Characterization, and Antimicrobial Activities

Acrylamide/4-vinyl pyridine hydrogels were synthesized by radiation polymerization technique using a γ-irradiator. The prepared radiation-synthesized acrylamide/4-vinyl pyridine hydrogels were then treated using a modifying agent with aromatic functional group. The modifying agent used in the modification of acrylamide/4-vinyl pyridine hydrogels was the N-aromatic alkyl quaternizing agent of chloromethyl benzene. The functional group on the modified acrylamide/4-vinyl pyridine hydrogels was confirmed with Fourier transform infrared (FTIR) spectrometry. Thermal analysis, surface morphology investigation, and swelling of the modified and unmodified hydrogels were completed. The antibacterial and antifungal activities of the modified and unmodified hydrogels were also tested against gram-positive Staphylococcus aureus (ATCC 25923); two gram-negative Escherichia coli (ATCC 25922), and Pseudomonas aeruginosa (ATCC 27853) human pathogenic bacteria and a fungal strain—Candida albicans (ATCC 10231) for their MBC values. It was found that acrylamide/4-vinyl pyridine hydrogels do not possess biocidal properties, whereas the modified form of acrylamide/4-vinyl pyridine?chloromethyl benzene showed highly bactericidal characteristics.     

Silver‐loaded lyocell fibers modified by tempo‐mediated oxidation

The purpose of this research was to accomplish antimicrobial properties in lyocell fibers by Ag⁺ ions sorption from aqueous silver nitrate solution. Sorption properties of lyocell fibers were improved by the selective TEMPO‐mediated oxidation, i.e. oxidation with sodium hypochlorite and catalytic amount of sodium bromide and 2,2,6,6‐tetramethylpiperidine‐1‐oxy radical (TEMPO). The most suitable experimental conditions for the selective TEMPO‐mediated oxidation were determined by changing oxidation conditions: concentration of sodium hypochlorite, as well as duration of sorption. The obtained results showed that the maximum sorption capacity (0.809 mmol of Ag⁺ ions per gram of fibers) of modified lyocell fibers was obtained for the sample modified with 4.84 mmol NaClO per gram of cellulose, during 1 h. The antifungal activity of the TEMPO‐oxidized lyocell fibers with silver ions against fungi from the Candida family, Candida albicans (ATCC 24433), and antibacterial activity against two strains: Staphylococcus aureus (ATCC 25923) and Escherichia coli (ATCC 25922) were confirmed in vitro. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Surface grafting of polyester fiber with chitosan and the antibacterial activity of pathogenic bacteria

Three polyesters—poly(ethylene terephthalate), poly(2‐methyl‐1,3‐propylene terephthalate‐co‐ethylene terephthalate), and poly(1,4‐cyclohexylene terephthalate‐co‐ethylene terephthalate)—were preirradiated with ⁶⁰Co‐γ‐rays. Then, acrylic acid and N‐vinylformamide were grafted to these irradiated fibers. Fibers grafted with N‐vinylformamide were further hydrolyzed with acid so that the amide groups would convert into amino groups, and they were treated with glutaraldehyde so that aldehyde groups would be introduced. Chitosan or chitooligosaccharide was then grafted to these fibers via either esterification or imine formation. Four pathogenic bacteria—methicillin‐resistant Staphylococcus aureus‐1 (MRSA), Staphylococcus aureus‐2, Escherichid coli, and Pseudomonas aeruginosa—were tested to determine the antibacterial activities of chitosan‐grafted and chitooligosaccharide‐grafted fibers. The results showed that grafting chitosan via imine formation could achieve a higher surface density for amino groups and give higher antibacterial activity to those four bacteria tested. The antibacterial activity for E. coli was the highest and that for MRSA was the lowest among the four bacteria tested. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2977–2983, 2002     

Enhanced functionality of colloidal polyaniline/polyvinyl alcohol nanocomposite as an antibacterial agent

This study describes the preparation of colloidal polyaniline/polyvinyl alcohol (PAn/PVA) nanocomposite by chemical polymerization of aniline (AN) in the presence of ammonium peroxydisulphate (APS) as an oxidant and PVA as a stabilizer. The product was characterized morphologically using a scanning electron microscope (SEM) and transmission electron microscopy (TEM), chemically using Fourier transform infrared (FTIR) and optically UV–visible. The prepared polymer was then tested for the antibacterial properties against gram‐negative bacteria: Escherichia coli (E. coli) and Pseudomonas aeruginosa (P. aeruginosa); and gram‐positive bacteria: Staphylococcus aureus (S. aureus). The antibacterial properties were assessed by disk diffusion, minimum inhibitory concentration (MIC), minimum bactericidal concentrations (MBCs), and the bactericidal effect methods. The results clearly showed that colloidal PAn/PVA nanocomposite strongly inhibits the growth of wild‐type E. coli (19 ± 0.5) mm followed by P. aeruginosa (17 ± 0.5 mm) and S. aureus (17.5 ± 0.5 mm) bacteria. S. aureus was completely killed after exposure for only 15 min, whereas S. aureus and E. coli were completely killed after exposure for 25 min. J. VINYL ADDIT. TECHNOL., 22:267–272, 2016. © 2014 Society of Plastics Engineers     

Study of antibacterial properties of polypropylene filled with surfactant‐coated silver nanoparticles

Medical applications require, in most cases, antibacterial protection. The use of silver (Ag) gives important antibacterial properties since silver is highly toxic for bacteria. In this research work, we have used silver nanoparticles (Ag NPs) with different surfactants, polyvinyl pyrrolidone (PVP) and oleic acid (OA) to facilitate dispersion. PP‐Ag NPs compounds were prepared by melt mixing, and the effects of the processing conditions on nanoparticles' dispersion were investigated by transmission electron microscopy (TEM). The antibacterial efficiency of PP‐Ag NPs compounds against Staphylococcus aureus ATCC 6538 and Escherichia coli ATCC 8379 was evaluated. Results show that good dispersion is obtained with rotating speeds in the 350–500 rpm range. TEM analysis reveals balanced dispersion and presence of some Ag NPs aggregates. Regarding antimicrobial properties, the use of PVP as surfactant leads to “significant” antimicrobial activity of 1.5 against Staphylococcus aureus and Escherichia coli; on other hand, the use of oleic acid (OA) as surfactant leads to strong protection against Staphylococcus aureus (antimicrobial activity between 2.5 and 3.3) but the overall protection against Escherichia coli is very low (lower than 1). Results show that the use of surfactants for Ag NPs has important effects on antibacterial properties of polypropylene filled with coated Ag NPs. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers     

Melt‐electrospinning of poly(ethylene terephthalate) and polyalirate

Rodlike polymer samples were made from three kinds of poly(ethylene terephthalate) (PET) pellets with different intrinsic viscosities (IV), and from polyalirate (Vectra) pellets. PET and Vectra fibers were produced using a melt‐electrospinning system equipped with a CO₂‐laser melting device from these rodlike samples. The effects of IV value and laser output power on the fiber diameter of PET were investigated. Furthermore, the effect of the laser output power on the fiber diameter of Vectra was investigated. The crystal orientation of these produced fibers was also investigated by X‐ray photographs. The following conclusions were reached: (i) the diameter of PET fiber decreases with increasing laser output power; (ii) the minimum average diameter of PET fibers is scarcely influenced by the value of IV; (iii) the electrospun PET fibers show isotropic crystal orientation; (iv) fibers having an average fiber diameter smaller than 1 μm cannot be obtained from PET and Vectra using the system developed; and (v) preferred liquid crystal orientation can be seen in electrospun Vectra fibers. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Preparation of antibacterial biocompatible polycaprolactone/keratin nanofibrous mats by electrospinning

Keratin-based materials are widely used in biomedical applications due to excellent biocompatibility and biodegradability. In this study, keratin was extracted from waste wool fibers and blended with polycaprolactone (PCL) to produce PCL/keratin nanofibrous mats by electrospinning. The electrospun PCL/keratin nanofibrous mats were chlorinated in diluted sodium hypochlorite solution to endow antibacterial properties. The prepared nanofibrous mats were characterized by scanning electron microscopy, X-ray photoelectron, and Fourier infrared spectroscopy. The effect of the chlorination time on the active chlorine loading of the mats was investigated. The chlorinated PCL/keratin nanofibrous mats with 0.78 ± 0.009 wt% active chlorine displayed potent antibacterial activity against Gram-positive Staphylococcus aureus (ATCC 6538) and Gram-negative Escherichia coli O157:H7 (ATCC 43895) with 6.88 and 6.81 log reductions, respectively. It was found that the mats were compatible with mouse fibroblast cells (L929). The chlorinated PCL/keratin nanofibrous mats might find promising applications in the biomedical field.     

Antibacterial activity of modified polyamide fibers

Polyamide fibers were modified for the attainment of antibacterial activity using a graft copolymerization method. The fibers were grafted with monomers containing quaternary ammonium groups using sodium persulfate as initiator. Two monomers were used as vinyl monomers. The first monomer, called METAC, is methacryloyloxyethyl trimethylammonium chloride [H₂C = C(CH₃)‐ CO₂CH₂CH₂N(CH₃)₃Cl]. The second monomer, denoted CATAL, is a methacryloyloxyethyl dimethyldodecylammonium bromide [H₂C = C(CH₃)CONHCH₂CH₂CH₂N‐ (CH₃)₂(C₁₂H₂₅)Br], kindly supplied by Catalyze (France). The graft copolymerization was confirmed by several methods such as elemental analysis and FTIR spectroscopy. The antibacterial activity of modified samples was investigated against Staphylococcus aureus using the antibacterial standard AFNOR test method XP G39–100. Polyamide fibers grafted with the second monomer exhibit high antibacterial activity against S. aureus, but the fibers grafted with the methacryloyloxyethyl trimethylammonium chloride did not. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 997–1000, 2005     

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     

The influence of coating with aminopropyl triethoxysilane and CuO/Cu2O nanoparticles on antimicrobial activity of cotton fabrics under dark conditions

A novel impregnation process for the fabrication of cotton nanocomposite with strong antimicrobial activity against antibiotics-resistant bacteria and yeast was developed. The impregnation process includes the sol–gel treatment of fabric with (3-aminopropyl)triethoxysilane in the first step, and synthesis of the CuO/Cu₂O nanoparticles (NPs) on the fabric surface in the second step. The in situ synthesis of the CuO/Cu₂O NPs was based on the adsorption of Cu²⁺-ions by the introduced amino groups of the sol–gel coating. The adsorbed Cu²⁺-ions are subsequently reduced in the alkaline solution of NaBH₄. X-ray diffraction measurements confirmed the formation of CuO/Cu₂O NPs. Scanning electron microscopy and atomic absorption spectrometry analyses indicate that the particle size, agglomeration, and amounts of synthesized NPs were highly affected by the initial concentration of CuSO₄ solution. The toxicity of nanocomposites to human keratinocytes (HaCaT) and antimicrobial activity against Gram-negative Escherichia coli ATCC 25922, E. coli ATCC BAA 2469, and Klebsiella pneumoniae ATCC BAA 2146, and Gram-positive bacteria Staphylococcus aureus ATCC 25923, S. aureus ATCC 43300 and yeast Candida albicans ATCC 24433 strongly depended on the copper content. In addition to excellent antimicrobial activity, controlled release of Cu²⁺-ions from the fabrics into physiological saline solution was obtained.     

Synthesis of novel pyridinium N‐chloramine precursors and its antimicrobial application on cotton fabrics

To control pathogenic microbial contamination on polymeric material surface, it is pivotal to develop materials with efficacious antimicrobial activity. Two pyridinium N‐chloramine precursors containing a siloxane handle were synthesized, characterized, and grafted onto cotton fabrics. The attenuated total reflectance spectra and scanning electron microscope photo analysis indicated that the cotton fabric surface was successfully modified. The resultant chlorinated fabric samples were challenged against bacteria Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 25923. Results showed that: (1) the surface modified cotton fabrics displayed satisfactory biocidal efficacy; (2) the precursor structure played a major role on surface grafting and antibacterial activity. This work provides two promising pyridinium N‐chloramine precursors which hold potential application for preparing antibacterial textile materials. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45323.     

Preparation,characterization, and antibacterial activity of chitosan/silicone rubber filled zeolite,silver, and copper nanocomposites against Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus

The ongoing emergence of antibiotic-resistant bacteria has become one of the biggest threats to global health and development today. Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus (MRSA) are important antibiotic-resistant bacteria due to their increasing resistance to a broad array of antimicrobial agents. Herein, we developed a novel antibacterial nanocomposite based on chitosan and liquid silicone rubber filled zeolite-A, Ag, and Cu nanoparticles with remarkable antibacterial activity against P. aeruginosa and MRSA. The antibacterial activity of the nanocomposite was studied by disc diffusion and broth culture methods. Besides, the mechanical properties, wetting behavior, and chemical structure of the present nanocomposite were also investigated. The results exhibited that the inhibition zone diameter of the nanocomposite for P. aeruginosa and MRSA were 40 and 27 mm, respectively. It also took approximately 1 h to inhibit the growth of the tested bacteria. The nanocomposite sample with a thickness of around 1 mm showed an elastic elongation of nearly 49% and a contact angle of roughly 120°. Thus, the present nanocomposite was found to be useful in killing and inhibiting the growth of P. aeruginosa and MRSA, and it could also be qualified as a superior elastic and hydrophobic material.     

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     

Design,Synthesis, and Dual Evaluation of Quinoline and Quinolinium Iodide Salt Derivatives as Potential Anticancer and Antibacterial Agents

A series of novel quinoline and quinolinium iodide derivatives were designed and synthesized to discover potential anticancer and antibacterial agents. With regard to anticancer properties, in vitro cytotoxicities against three human cancer cell lines (A-549, HeLa and SGC-7901) were evaluated. The antibacterial properties against two strains, Escherichia coli (ATCC 29213) and Staphylococcus aureus (ATCC 8739), along with minimum inhibitory concentration (MIC) values were evaluated. The target alkyliodine substituted compounds exhibited significant antitumor and antibacterial activity, of which compound 8-((4-(benzyloxy)phenyl)amino)-7-(ethoxycarbonyl)-5-propyl-[1,3]dioxolo[4,5-g]quinolin-5-ium ( 12 ) was found to be the most potent derivative with IC₅₀ values of 4.45±0.88, 4.74±0.42, 14.54±1.96, and 32.12±3.66 against A-549, HeLa, SGC-7901, and L-02 cells, respectively, stronger than the positive controls 5-FU and MTX. Furthermore, compound 12 had the most potent bacterial inhibitory activity. The MIC of this compound against both E. coli and S. aureus was 3.125 nmol ⋅ mL⁻¹, which was smaller than that against the reference agents amoxicillin and ciprofloxacin.     

Optimizing Graphene Oxide Encapsulated TiO2 and Hydroxyapatite; Structure and Biological Response

Nanocomposites based on hydroxyapatite (HAP) are fabricated with/without combining titanium oxide (TiO₂) and graphene oxide. Structure investigation was done for all compositions using X-ray diffraction (XRD), Fourier-transform infrared in addition to X-ray photoelectron to study the chemical compositions of the obtained nanocomposites. The surface morphology investigation was done with the scanning electron microscope and transmission electron microscope. In this regard, TiO₂ nanoparticles were exhibited in spherical shapes, while HAP was detected as nanorods. The dimensions of HAP have been decreased from 53 and 18 to 27 and 10 nm for length and diameter, respectively. The crystallite sizes obtained from XRD data are around 15 and 33 nm for HAP and TiO₂ respectively. Moreover, the diameter of TiO₂ reached 80 nm. Further, the average roughness parameter (R_a) improved from 9.2 to 11.1 nm from HAP to TNC. Besides, the root mean square (R_q), maximum height of the roughness (R_t), and maximum roughness valley depth (R_v) increased to 14.7, 104, and 55.9 nm, respectively. Furthermore, cell viability enhanced from 96.3?±?3 to 102.4?±?3%. Besides, the antibacterial behavior improved to be 15.3?±?1.3 and 14.2?±?0.9 mm for TNC against E. coli and S. aureus respectively.