scholarly journals Fabrication of Gelatin-ZnO Nanofibers for Antibacterial Applications

Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 103
Author(s):  
Nataliya Babayevska ◽  
Łucja Przysiecka ◽  
Grzegorz Nowaczyk ◽  
Marcin Jarek ◽  
Martin Järvekülg ◽  
...  

In this study, GNF@ZnO composites (gelatin nanofibers (GNF) with zinc oxide (ZnO) nanoparticles (NPs)) as a novel antibacterial agent were obtained using a wet chemistry approach. The physicochemical characterization of ZnO nanoparticles (NPs) and GNF@ZnO composites, as well as the evaluation of their antibacterial activity toward Gram-positive (Staphyloccocus aureus and Bacillus pumilus) and Gram-negative (Escherichia coli and Pseudomonas fluorescens) bacteria were performed. ZnO NPs were synthesized using a facile sol-gel approach. Gelatin nanofibers (GNF) were obtained by an electrospinning technique. GNF@ZnO composites were obtained by adding previously produced GNF into a Zn2+ methanol solution during ZnO NPs synthesis. Crystal structure, phase, and elemental compositions, morphology, as well as photoluminescent properties of pristine ZnO NPs, pristine GNF, and GNF@ZnO composites were characterized using powder X-ray diffraction (XRD), FTIR analysis, transmission and scanning electron microscopies (TEM/SEM), and photoluminescence spectroscopy. SEM, EDX, as well as FTIR analyses, confirmed the adsorption of ZnO NPs on the GNF surface. The pristine ZnO NPs were highly crystalline and monodispersed with a size of approximately 7 nm and had a high surface area (83 m2/g). The thickness of the pristine gelatin nanofiber was around 1 µm. The antibacterial properties of GNF@ZnO composites were investigated by a disk diffusion assay on agar plates. Results show that both pristine ZnO NPs and their GNF-based composites have the strongest antibacterial properties against Pseudomonas fluorescence and Staphylococcus aureus, with the zone of inhibition above 10 mm. Right behind them is Escherichia coli with slightly less inhibition of bacterial growth. These properties of GNF@ZnO composites suggest their suitability for a range of antimicrobial uses, such as in the food industry or in biomedical applications.

2019 ◽  
Vol 39 (8) ◽  
pp. 752-761
Author(s):  
Ayse Celik Bedeloglu ◽  
Zeynep Islek Cin

Abstract Polymer-based nanofibers are good candidates for medical textiles due to their excellent properties including high surface area, breathability and flexibility. Doping polymer nanofibers with different nanoparticles enhances their existing properties. In this study, electrospun polyamide 6,6 (PA6,6) composite nanofibers containing ZnO nanoparticles (<50 nm) in different amounts (1%, 3% and 5%) were first produced by electrospinning technique; then, these nanofibers were coated with sol-gel ZnO solution (0.5 m) via dip coating method at 1000, 3000 and 5000 μm/s speeds. The sol-gel coating process increased the breaking strength of nanofiber mats, while the incorporation of ZnO nanoparticles into the polymer nanofibers reduced. Compared to pure PA6,6 nanofiber mats, the ZnO sol-gel coated samples and doped nanofibers had lower reflectance values. In addition, the reflection values decreased as the additive and coating speed increased.


2018 ◽  
Vol 4 (5) ◽  
pp. 555-559
Author(s):  
K.V. Divya Lakshmi ◽  
T. Siva Rao

Nickel and sulfur co-doped TiO2 photocatalyst were prepared by using sol-gel method with dopants precursors of nickel nitrate and thiourea. Prepared samples were characterized by XRD, UV-Vis-DRS, TEM, BET, FT-IR and SEM-EDX. These characterization and experimental results revealed that there is a formation of anatase phase, decreased band gap 2.62 eV for NIST-2, small particle size 7.3 nm and high surface area 142.62 m2/g. The FT-IR frequency shift for Ti-O-Ti was observed from 569 cm-1 to 460-560 cm-1 for co-doped TiO2. The efficiency of photocatalytic and antibacterial was evaluated by degradation of Orange-II dye and Escherichia coli (MTCC-443) respectively. The complete degradation of Orange-II was achieved in 120 min at optimum reaction parameters for NIST-2 at pH-3, catalyst dosage-100 mg/L and initial dye concentration at 10 mg/L.


2019 ◽  
Vol 2 (1) ◽  
pp. 42-52
Author(s):  
Abdur Rehman ◽  
Saira Ahmad ◽  
Abdul Mateen ◽  
Huma Qamar ◽  
Mudaber Ahmad Mubashar ◽  
...  

Nanotechnology is the science, engineering and technology conducted at the scale that ranges between 1-100 nanometers. For the bio-application, evolution of nanotechnology is creating the concern of scientists towards the synthesis of nanoparticles. The nanoparticles have unique characteristics as compare to bulk materials. Zinc oxide (ZnO) is a matchless semiconductor and it has been under investigation due to its wide range of applications in various areas like biomedical, electronics, material science and optics. In the present work synthesis of ZnO nanoparticles was carried out by using simple chemical approach, Sol-gel method for being effective and inexpensive, by employing zinc acetate dehydrate Zn (CH3CO2)2.2H2O as a precursor and sodium hydroxide (NaOH) starch as a constant agent. The structural properties of resultant zinc oxide nanoparticles were investigated by X-ray diffraction (XRD) technique. The XRD data confirmed the hexagonal wurtzite structure of ZnO powder confirmed by JCPDS 36-1451 data. Particles size was calculated by Scherrer formula and calculated size was 30.14 nm. These nanoparticles were investigated for inhibition zone of bacterial strain Escherichia coli, a gram-negative microbe, at various concentrations of ZnO nanoparticles. Zinc oxide nanoparticles were very proficient for inhibition of growth of bacterial strain E. coli. The mechanism of ZnO NPs for antibacterial activity is release of reactive oxygen species which not only hydrolyze cell wall but cell membrane and cellular components as well providing a potential bactericidal effect.


2014 ◽  
Vol 354 ◽  
pp. 201-213 ◽  
Author(s):  
Mohamad Sahban Alnarabiji ◽  
Noorhana Yahya ◽  
Sharifah Bee Abdul Hamid ◽  
Khairun Azizi Azizli ◽  
Muhammad Kashif ◽  
...  

Synthesising zinc oxide nanoparticles (ZnO-NPs) to get certain characteristics to be applied in Enhanced Oil Recovery (EOR) is still challenging to date. In this work, the importance of high surface area of ZnO nanoparticles as EOR agent was highlighted. A simulation on density of state (DOS), band structure and adsorption energy of hydrogen and nitrogen gases on the surface of ZnO was carried out; it is observed that from the band structure of the band gap value for ZnO is 0.808ev. For the ZnO, Zn 4s states contribute to conduction band and O 2p states contribute to valence band. ZnO-NPs were synthesised using the sol-gel method by dissolving zinc nitrate hexahydrate in nitric acid and varying the stirring time (1 and 24h) and sintering time (30 and 40 min). A microwave oven was used for annealing ZnO without insulating the samples in any casket. The results show that 30 and 40 min of annealing and stirring for 1 & 24 h influenced the morphology and size of ZnO-NPs. These parameters could be tailored to generate a range of nanoparticle morphology (flask and/with agglomerated nanoparticles in a corn shape) obtained by Field Emission Scanning Electron Microscope (FESEM) and hexagonal crystal, determined by X-ray diffractometer (XRD), with the mean size of 70.5 & 74.9 nm and a main growth at the peak (101). The prepared sample via stirring for 24h and sintering for 40 min was chosen to prepare ZnO nanofluid because it has the highest surface area (BET) among the rest of samples, 0.23 m2/g. 10% of Original Oil In Place (OOIP) was recovered successfully to prove that ZnO is a good candidate to be applied in some chemical reactions. Moreover, it was found that ZnO is a promising catalyst for ammonia synthesis based on the adsorption energy of hydrogen and nitrogen gases (-1.05 and-1.60 kcal/mol respectively).


2020 ◽  
Vol 10 ◽  
pp. 184798042090918
Author(s):  
Ricardo Solano ◽  
David Patiño-Ruiz ◽  
Adriana Herrera

Recently, an increase in the production of intelligent nanomaterials has been reported for the application of solid surface coating. These nanomaterials provide a wide number of functionalities such as anticorrosive, antibacterial, and self-cleaning properties. Hence, titanium dioxide (TiO2) and zinc oxide (ZnO) nanoparticles were synthesized using a green chemistry approach. These nanoparticles were fully characterized by scanning electron microscopy, energy-dispersive X-ray, high-resolution transmission electron microscopy, X-ray diffraction, ultraviolet (UV)–visible spectroscopy, Brunauer–Emmett–Teller test, and nitrogen adsorption–desorption isotherm. Then, a commercial enamel-type paint was modified by using different concentrations (2, 3.5, and 5 w/v%) of nanoparticles. These nanofilled paints were then brushed onto the surface of different types of materials such as carbon steel sheets, wood sheets, and aluminum disks. Anticorrosive, self-cleaning, and antibacterial properties of the nanofilled paints were evaluated, with the aim to determine the capability for this application. According to the characterization results, TiO2 and ZnO nanoparticles exhibited similar physicochemical properties compared to those synthesized using traditional methods. The anticorrosion results revealed that nanofilled paints provide a barrier using low concentrations of nanoparticles, due to the decrease of agglomerates on the surface avoiding the presence of high porosity. In the case of self-cleaning, a proposed mechanism of degradation demonstrated that the presence of both nanoparticles in the paint provided high degradation of methylene blue due to the high surface area offered by the nanoparticles. On the other hand, antibacterial activity under UV light was observed only for ZnO nanoparticles, which may be related to the diffusion of nanoparticles into the cell membrane of the bacteria, affecting the normal function. These results showed to be promising for the modification of paints with TiO2 and ZnO nanoparticles, and the application on solid surfaces for the construction, and even in textile fields.


2021 ◽  
Author(s):  
Lawrence Kioko Munguti ◽  
Francis Birhanu Dejene

Abstract Zeolite Na-A supported ZnO nanocomposites (ZnO/Zeolite Na-A NCs) were synthesized at low temperature (70 ℃) via the sol-gel process and characterized by X-ray diffraction technique (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-visible diffuse reflectance spectroscopy (UV-vis DRS) and Fourier transform infrared (FTIR) spectroscopy for structural, morphological, optical and bonding properties. The textural properties and porosity were obtained by Brunauer-Emmett-Teller (BET) technique. The obtained XRD and microscopy results indicated that the obtained nanopowders were crystalline in nature and no collapse of the structure of zeolite Na-A. In addition, the synthesized ZnO nanoparticles occurred mainly on the surface of the zeolite support. It is clear that the zeolite supported ZnO nanoparticles were more dispersed as compared to the pure ZnO with improved porosity and high surface area. Photocatalytic activity for the ZnO/zeolite Na-A was tremendously increased which was attributed to the synergetic combined effects of both ZnO and zeolite aluminosilicate network such as increased surface area (SBET), high adsorption and restrained charge recombination.


2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Mona Gholami ◽  
Mahdiyeh Esmaeilzadeh ◽  
Zahra Kachoei ◽  
Mojgan Kachoei ◽  
Baharak Divband

White spot lesions (WSLs) are one of the adverse effects of fixed orthodontic treatments. They are the primary sign of caries, which means inhibiting this process by antibacterial agents will reverse the procedure. The current study tested the surface modification of nickel-titanium (NiTi) wires with ZnO nanoparticles (NPs), as antimicrobial agents. As the morphology of NPs is one of the most critical factors for their properties, the antibacterial properties of different morphologies of ZnO nanostructures coated on the NiTi wire were investigated. For the preparation of ZnO nanostructures, five coating methods, including chemical vapor deposition (CVD), chemical precipitation method, polymer composite coating, sol-gel synthesis, and electrospinning process, were used. The antibacterial activity of NPs was assessed against Streptococcus mutans by the colony counting method. The obtained results showed that all the samples had antibacterial effects. The antibacterial properties of ZnO NPs were significantly improved when the specific surface area of particles increased, by the ZnO nanocrystals prepared via the CVD coating method.


2010 ◽  
Vol 93 (12) ◽  
pp. 4047-4052 ◽  
Author(s):  
Padmaja Parameswaran Nampi ◽  
Padmanabhan Moothetty ◽  
Wilfried Wunderlich ◽  
Frank John Berry ◽  
Michael Mortimer ◽  
...  

2018 ◽  
Vol 29 (7) ◽  
pp. 075702 ◽  
Author(s):  
Feng Qingge ◽  
Cai Huidong ◽  
Lin Haiying ◽  
Qin Siying ◽  
Liu Zheng ◽  
...  

2013 ◽  
Vol 284-287 ◽  
pp. 230-234
Author(s):  
Yu Jen Chou ◽  
Chi Jen Shih ◽  
Shao Ju Shih

Recent years mesoporous bioactive glasses (MBGs) have become important biomaterials because of their high surface area and the superior bioactivity. Various studies have reported that when MBGs implanted in a human body, hydroxyl apatite layers, constituting the main inorganic components of human bones, will form on the MBG surfaces to increase the bioactivity. Therefore, MBGs have been widely applied in the fields of tissue regeneration and drug delivery. The sol-gel process has replaced the conventional glasses process for MBG synthesis because of the advantages of low contamination, chemical flexibility and lower calcination temperature. In the sol-gel process, several types of surfactants were mixed with MBG precursor solutions to generate micelle structures. Afterwards, these micelles decompose to form porous structures after calcination. Although calcination is significant for contamination, crystalline and surface area in MBG, to the best of the authors’ knowledge, only few systematic studies related to calcination were reported. This study correlated the calcination parameters and the microstructure of MBGs. Microstructure evaluation was characterized by transmission electron microscopy and nitrogen adsorption/desorption. The experimental results show that the surface area and the pore size of MBGs decreased with the increasing of the calcination temperature, and decreased dramatically at 800°C due to the formation of crystalline phases.


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