PEGylated zinc oxide nanoparticles induce apoptosis in pancreatic cancer cells through reactive oxygen species

In this study, the authors have successfully prepared the polyethylene glycol (PEG)‐coated zinc oxide nanoparticles (ZNPs) and studied its effect in pancreatic cancer cells. The authors have observed a nanosized particle with spherical shape. In this study, the authors have demonstrated the cytotoxic effect of ZNP and PZNP in PANC1 cells. To be specific, PZNP was more cytotoxic compared to that of ZNP in PANC1 cancer cells. The authors have further showed that apoptosis is the main mode of cytotoxic activity. It is worth noting that PEGylation of ZNP did not decrease the cell killing activity of zinc particles, whereas it further increases its anticancer effect in the pancreatic cancer cells. The authors have observed a significant upregulation of proapoptotic BAX while expression of antiapoptotic Bcl‐2 was significantly downregulated indicating the potent anticancer effect of zinc nanoparticles. Overall, PEGylation of ZNP could be an effective strategy to improve the stability, while at the same time, its anticancer activity could be enhanced for better therapeutic response.Inspec keywords: biomedical materials, drug delivery systems, tumours, toxicology, nanoparticles, cellular biophysics, drugs, nanomedicine, cancer, nanofabrication, zinc compounds, II‐VI semiconductorsOther keywords: pancreatic cancer cells, reactive oxygen species, polyethylene glycol‐coated zinc oxide nanoparticles, cytotoxic effect, cytotoxic activity, PEGylation, anticancer effect, PEGylated zinc oxide nanoparticle induce apoptosis, proapoptotic BAX upregulation, ZnO     

In vitro germination and biochemical profiling of Brassica napus in response to biosynthesised zinc nanoparticles

With the progression of nanotechnology, the use of nanoparticles (NPs) in consumer products has increased dramatically and green synthesis is one of the cheapest and eco‐friendly methods to obtain non‐hazardous NPs. In the current research zinc (Zn) NPs synthesis was carried out by using the fresh and healthy leaves of Mentha arvensis L. followed by characterisation through ultraviolet (UV)–visible spectroscopy, X‐ray diffraction (XRD) and scanning electron microscopy (SEM). UV–visible spectroscopy confirmed the green synthesis of ZnNPs, while XRD confirmed the size of NPs, which was 30–70 nm. SEM shows that the shape of ZnNPs was irregular. The effects of green synthesised NPs on two different varieties of Brassica napus were evaluated. Exposure to ZnNPs (5, 15, and 25 mg/l⁻¹) caused a significant increase in root and shoot length of B. napus. The application of NPs significantly improved plant germination and triggered the production of secondary metabolite and antioxidant enzymes. ZnNPs showed a significant increase in chlorophyll, superoxide dismutase, total flavonoid content (TFC) and antioxidant enzymes while total phenolic content was decreased when TFC increased. Thus, it has been concluded from the current study that ZnNPs may possibly trigger the production of antioxidant enzymes and various biochemical compounds.Inspec keywords: zinc, nanoparticles, nanofabrication, ultraviolet spectra, visible spectra, X‐ray diffraction, scanning electron microscopy, particle size, enzymes, molecular biophysics, biochemistry, nanobiotechnology, botanyOther keywords: biochemical profiling, Brassica napus, biosynthesised zinc nanoparticles, nanotechnology, Mentha arvensis L, ultraviolet‐visible spectroscopy, X‐ray diffraction, Zn, biochemical compounds, total phenolic content, total flavonoid content, superoxide dismutase, chlorophyll, antioxidant enzymes, secondary metabolite, plant germination, green synthesis, SEM, scanning electron microscopy, XRD     

5 Fluorouracil‐loaded biosynthesised gold nanoparticles for the in vitro treatment of human pancreatic cancer cell

In this study, green synthesis of gold nanoparticles (AuNPs) was performed by a sunlight irradiation method using the Borassus flabellifer fruit extract as a reducing agent. 5‐Fluorouracil (5‐FU)‐loaded GG capped AuNPs (5FU‐G‐AuNPs) was prepared. The nanoparticles was further characterised by UV‐visible spectra, particle size analysis, zeta potential, SAED, HRTEM, and XRD. The MTT assay results showed the suitability 5‐FU‐G‐AuNPs. In this study, 5‐FU‐G‐AuNPs exhibited potential cytotoxic and apoptotic effects on (MiaPaCa‐2) cell line.Inspec keywords: gold, biochemistry, X‐ray diffraction, nanofabrication, biomedical materials, transmission electron microscopy, toxicology, electrokinetic effects, particle size, nanoparticles, cancer, visible spectra, cellular biophysics, ultraviolet spectra, nanomedicine, patient treatment, organic compoundsOther keywords: 5FU‐G‐AuNPs, suitability 5‐FU‐G‐AuNPs, human pancreatic cancer cell, green synthesis, sunlight irradiation method, 5‐Fluorouracil‐loaded GG, in vitro treatment, 5 fluorouracil‐loaded biosynthesised gold nanoparticles, borassus flabellifer fruit extract, reducing agent, UV‐visible spectra, particle size analysis, zeta potential, SAED, HRTEM, XRD, MTT assay, apoptotic effects, cytotoxic effects, MiaPaCa‐2 cell line, Au     

Cytogenetic and genotoxic effects of zinc oxide nanoparticles on root cells of Allium cepa

Increasing use of zinc oxide nanoparticles (ZnO NP) in consumer products may enhance its release into the environment. Phytotoxicity study is important to understand its possible environmental impact. Allium cepa (Onion bulb) is the best model organism to study genetic toxicology of nanoparticles. Here we have reported cytogenetic and genotoxic effects of ZnO NPs on the root cells of A. cepa. The effects of ZnO NPs on the mitotic index (MI), micronuclei index (MN index), chromosomal aberration index, and lipid peroxidation were determined through the hydroponic culturing of A. cepa. A. cepa roots were treated with the dispersions of ZnO NPs at four different concentrations (25, 50, 75, and 100 μg ml(-1)). With the increasing concentrations of ZnO NPs MI decreased with the increase of pycnotic cells, on the other hand MN and chromosomal aberration index increased. The frequency of micronucleated cells was higher in ZnO NPs treated cells as compared to control (deionized distilled water). The number of cells in each mitotic phase changed upon ZnO NPs treatment. The effect of ZnO NPs on lipid peroxidation as examined by measuring TBARS concentration was evident at all the concentrations compared to bulk ZnO. The TEM image showed internalization of ZnO NPs like particles. SEM image of treated A. cepa demonstrated that the internalized nanoparticles agglomerated depending on the physico-chemical environment inside the cell. Our results demonstrated that ZnO NPs can be a clastogenic/genotoxic and cytotoxic agent. In conclusion, the A. cepa cytogenetic test can be used for the genotoxicity monitoring of novel nanomaterials like ZnO NPs, which is used in many consumer products.     

Acute toxicity of ferric oxide and zinc oxide nanoparticles in rats

We investigated the toxic effects of inhalation exposure to ferric oxide (Fe2O3) and zinc oxide (ZnO) nanoparticles in rats. Male Wistar rats were consecutively treated with Fe22O3 at 8.5 mg/kg body weight and ZnO nanoparticles at 2.5 mg/kg body weight, twice daily for 3 days. Content of Fe2O3 and ZnO in tissues, biochemical parameters in serum, and hispathological examinations were analyzed at 12 h and 36 h after the 3 day treatment. In the Fe2O3-treated group, iron (Fe) content in liver and lung tissues was significantly increased at 36 h. In the ZnO-treated group, zinc (Zn) content in liver tissues was significantly increased at 12 h and further increased at 36 h. The levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total protein (TP), creatine kinase (CK), and lactate dehydrogenase (LDH) in both nanoparticle-exposed groups were significantly decreased compared to the unexposed controls. Histopathological examination showed that both types of nanoparticles caused severe damage in liver and lung tissues. Although this damage progressed in both liver and lung throughout the postexposure period, no significant elevation of serum enzyme activities was observed in response to either nanoparticle type.     

Cytotoxicity of zinc oxide nanoparticles: importance of microenvironment

While ZnO particles are widely used in many fields, including personal care products, the high toxicity of ZnO nanoparticles has been reported and aroused great health concerns. In this study, the cytotoxicity of ZnO nanoparticles was evaluated and, in particular, the role of microenvironment in their toxicity was investigated. Our results show that ZnO nanoparticles are highly toxic to NIH/3T3 cells, inducing viability loss, membrane leakage and morphology changes. The microenviroment, here the CO2 atmosphere under cell culture condition, promoted the solubilization of ZnO nanoparticles. Then the released Zn from ZnO nanoparticles induces the cytotoxicity. The importance of microenvironment on the ZnO nanotoxicity is presented and the implications to future nanotoxicology studies are discussed.     

Synthesis of zinc and zinc oxide nanoparticles from zinc electrode using plasma in liquid

Nanoparticles are synthesized efficiently from zinc electrode by microwave plasma in liquid. The nanoparticles synthesized from alcohol resulted in pure zinc particles in the shape of spheres or hexagonal cylinders with a production rate of 3.3 g/h, and energy consumption of 267 J/mg for 1 mg. Whereas the nanoparticles synthesized in pure water are composed of Zn and ZnO. The Zn reacts with water through heat or the passage of time to become ZnO, releasing hydrogen gas. An upper disk placed 1 mm away from the electrode along with the bubbles generated simultaneously with the plasma ignition plays a key role in the synthesis of nanoparticles.     

Nephron ultrastructural alterations induced by zinc oxide nanoparticles: an electron microscopic study

Due to their unique properties, zinc oxide nanoparticles (ZnO NPs) are invested in many industries, commercial products, and nanomedicine with potential risk for human health and the environment. The present study aims to focus on alterations that might be induced by ZnO NPs in the nephron ultrastructure. Male Wister Albino rats were subjected to ZnO NPs at a daily dose of 2 mg/kg for 21 days. Kidney biopsies were processed to transmission electron microscopy (TEM) and ultrastructural pathology examinations. Exposure to ZnO NPs‐induced ultrastructural alterations in the proximal convoluted tubules (PCTs) and to lesser extent in the distal ones (DCTs), while the loops of Henle were almost not affected. The glomeruli demonstrated dilatation, partial mesangial cells loss, matrix ballooning, slits filtration widening, and basement membrane thickening. Moreover, PCT revealed cytoplasmic necrosis, vacuolation, erosion, and disorganisation of the apical microvilli together with mitochondrial swelling and cristae destruction. The nuclei of the renal cells exhibited nuclear deformity, heterochromatin accumulation, and apoptotic activities. The findings indicate that ZnO nanomaterial have the potential to affect the nephron ultrastructure suggesting alteration in the kidney functions. More work is needed for better understanding the toxicity and pathogenesis of ZnO oxide nanomaterial.Inspec keywords: electron microscopy, zinc compounds, transmission electron microscopy, nanomedicine, biochemistry, diseases, cellular biophysics, biomembranes, kidney, nanofabrication, molecular biophysics, nanoparticles, II‐VI semiconductors, biomedical optical imagingOther keywords: electron microscopic study, unique properties, zinc oxide nanoparticles, ZnO NPs, nephron ultrastructure, Male Wister Albino rats, ultrastructural pathology examinations, NPs‐induced ultrastructural alterations, partial mesangial cells loss, ZnO nonmaterial, ZnO oxide nonmaterial, nephron ultrastructural alterations, kidney biopsies, time 21.0 d, ZnO     

Microwave‐mediated synthesis of zinc oxide nanoparticles: a therapeutic approach against Malassezia species

A successful protocol was developed to aid in the reduction in dandruff‐causing fungi, namely Malassezia globasa and Malassezia furfur. Both the species were isolated from volunteers aged between 20 and 22 suffering from dandruff, cultured ex vivo, and tested against the presence of synthesised zinc oxide nanoparticles (ZnNP). Direct microscopy, scanning electron microscopy (SEM), and biochemical assays specific to Malassezia species were conducted to identify dandruff‐causing fungal species. Microwave‐mediated synthesis of ZnNP was performed and characterised by UV–vis, X‐ray diffraction, and SEM. The nanoparticles were tested against both Malassezia species and proved highly effective in inhibiting these fungi, although M. furfur was more susceptible than M. globosa. An optimum amount of 100 ppm was found to be sufficient to work as an antifungal agent. Synergistic effects of ZnNP with commercial shampoos were tested, and the result showed enhanced antifungal effects. To mimic the natural biofilm formed by these species on human skin, the formation of fungal biofilm was allowed on polystyrene coverslips. ZnNP was effective in eradication biofilm. Since zinc is an essential mineral for all living organism and is considered as biocompatible, the synthesised nanomaterials can be used in the formulation of antidandruff shampoos.Inspec keywords: skin, X‐ray diffraction, antibacterial activity, scanning electron microscopy, biochemistry, biomedical materials, nanoparticles, nanofabrication, visible spectra, zinc compounds, microorganisms, ultraviolet spectra, nanomedicineOther keywords: Malassezia furfur, Malassezia species, fungal species, microwave‐mediated synthesis, Malassezia globasa, zinc oxide nanoparticles, dandruff‐causing fungi, scanning electron microscopy, direct microscopy, biochemical assays, UV–visible spectroscopy, X‐ray diffraction, antifungal agent, natural biofilm, eradication biofilm, antidandruff shampoos, human skin, ZnO     

Cytotoxicity,leishmanicidal, and antioxidant activity of biosynthesised zinc sulphide nanoparticles using Phoenix dactylifera

The synthesis of zinc sulphide nanoparticles (ZnS NPs) using a green approach was explored. The resulting nanoparticles (NPs) were characterised by UV–vis spectroscopy, scanning and transmission electron microscopy, X‐ray diffraction and Fourier transform infrared spectroscopy. The leishmanicidal, cytotoxic and antioxidant activity of the resulting synthesised ZnS NPs (<70 nm) were evaluated against Leishmania major (L. major) promastigotes and amastigotes by MTT assay and using a macrophage model. The ZnS NPs were able to counteract the effects of oxidative metabolites as demonstrated by the oxidant activity. The IC₅₀ value of butylated hydroxyanisole was 26.04 µg/ml as compared with the IC₅₀ for ZnS NPs (90.95 µg/ml). The NPs displayed no cytotoxicity for the murine macrophaghes as the selectivity index (SI) fell into the safety range (SI ≥ 10). These nanomaterials exhibited good antileishmanial activity against the L. major stages that were comparable to that of Glucantime, the drug of choice. The IC₅₀ values of ZnS NPs and Glucantime against amastigotes were 11.59 ± 2.51 and 4.95 ± 2.51 μg/ml, respectively. The IC₅₀ values for ZnS NPs and Glucantime versus promastigote were 29.81 ± 3.15 and 14.75 ± 4.05 μg/ml, respectively. Further investigation is essential to explore the biological effects of ZnS NPs on animal and/or clinical models.Inspec keywords: nanoparticles, nanofabrication, microorganisms, antibacterial activity, ultraviolet spectra, visible spectra, nanobiotechnology, X‐ray diffraction, Fourier transform infrared spectra, zinc compoundsOther keywords: cytotoxicity, leishmanicidal activity, antioxidant activity, biosynthesised zinc sulphide nanoparticles, Phoenix dactylifera, green approach, UV–vis spectroscopy, scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, Leishmania major promastigotes, Leishmania major amastigotes, MTT assay, macrophage model, oxidative metabolites, butylated hydroxyanisole, murine macrophaghes, selectivity index, glucantime, ZnS     

Mass imaging of iron oxide nanoparticles inside cells for in vitro cytotoxicity

Time-of-flight secondary ion mass spectrometry (ToF-SIMS) imaging analysis was performed on murine macrophage cells treated with various concentrations of iron oxide (Fe3O4) nanoparticles, which are used as MRI contrast agents. First, murine macrophage cells were seeded on a slide glass for 24 hrs and treated with varying concentrations of Fe3O4 nanoparticles for 24 hrs. To expose a cross section of each cell and obtain a distribution of the nanoparticles inside the cells, the cells were sputtered using Bi ions after which the cross section of each cell was scanned and imaged using the focused cluster ion beam with a spatial resolution of 300 nm. Fe3O4 nanoparticles were found mainly in the cytoplasm region of the cells, not in the nucleus region of cells, suggesting that the uptake of the Fe3O4 nanoparticles were into the cytoplasm of cell, not into the nucleus of cell. Based on these observations, our protocol using mass imaging analysis would be a useful addition to the study of in vitro nanoparticle cytotoxicity.     

Optical and electrical properties of aluminum-doped zinc oxide nanoparticles

Aluminum-doped zinc oxide nanopowders were prepared using a surfactant assisted complex sol–gel method, and were characterized using inductively coupled plasma, X-ray diffraction, scanning electron microscopy/energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and UV–Vis spectroscopy. Al was effectively doped into the ZnO matrix with concentrations up to 6.00 atomic ratio percents (at.%). X-ray diffraction results revealed that all of the nanoparticles had a pure hexagonal wurtzite structure free of any impurities when annealing temperature was below 1273 K. The optical band gap of the nanopowders, which was affected by the Al-doping concentration, reached a maximum of 3.43 eV when ZnO was doped with 4.00 at.% Al. The effect of post-annealing temperature and vacuum conditions on the resistivities of the Al-doped ZnO nanoparticles was also investigated. And the lowest volume resistivity (1.2 Ω cm) was achieved by annealing the Al-doped ZnO nanoparticles in a vacuum at 1173 K for 2 h.     

In vitro cytotoxicity of transparent yellow iron oxide nanoparticles on human glioma cells

With rapid development of nanotechnology, concerns about the possible adverse health effects on human beings by using nanomaterials have been raised. Transparent yellow iron oxide (alpha-FeOOH) nanoparticles have been widely used in paints, plastic, rubber, building materials, papermaking, food products and pharmaceutical industry, thus the potential health implications by the exposure should be considered. The purpose of this study is to assess the cytotoxicity of transparent yellow iron oxide nanoparticles on U251 human glioma cells. The alpha-FeOOH nanoparticles are in clubbed shapes with 9 nm in diameter and 43 nm long. The specific surface area is 115.3 m2/g. After physicochemical characterization of the nanoparticles, U251 cells were exposed to a-FeOOH at the doses of 0, 3.75, 15, 60 and 120 microg/mL. The results showed that the alpha-FeOOH nanoparticles reduced the cell viability and induced necrosis and apoptosis in U251 cells. In addition, nanoparticle exposure significantly increased the levels of superoxide anion and nitric oxide in a dose-dependent fashion in the cells. Our results suggest that exposure to alpha-FeOOH nanoparticles induce significant free radical formation and cytotoxic effects. The large surface area that induced high surface reactivity may play an important role in the cytotoxic effect of alpha-FeOOH nanoparticles.     

Effect of film thickness in hybrid polymer/polymer solar cells with zinc oxide nanoparticles

We briefly report the effect of film thickness on the performance of hybrid polymer/polymer solar cells that were made using poly(3-hexylthiophene), poly(9,9-dioctylfluorene-co-benzothiadiazole) (F8BT), and zinc oxide (ZnO) nanoparticles. The ZnO nanoparticles were introduced to improve the electron transport property of P3HT/F8BT blend films. Results showed that the open circuit voltage (V(OC)) was remarkably decreased by adding only approximately 0.5 wt% ZnO nanoparticles though the optical absorption spectra were not much changed due to the small amount of ZnO nanoparticles in the ternary blend films (approximately 1.9%). In contrast, the fill factor (FF) of devices was improved for the ternary blend devices with the ZnO nanoparticles due to the improved electron transport as evidenced by the reduced series resistance. The short circuit current density of devices was not much changed because of the enhanced charge transport. However, the addition of ZnO nanoparticles decreased the power conversion efficiency of devices owing to the larger influence of V(OC) compared to the FF improvement.     

In vitro evaluation of antimicrobial and antibiofilm potentials of silver nanoparticles biosynthesised by Streptomyces griseorubens

This study was performed to determine the antimicrobial and antibiofilm activities of silver nanoparticles (AgNPs) biosynthesised using Streptomyces griseorubens AU2 isolated from soil. The antimicrobial activity of the AgNPs was determined by agar well diffusion, disc diffusion and broth microdilution methods. Diameters of the zone of inhibition results clearly displayed that the microbially biosynthesised AgNPs have potent antimicrobial activity against Candida albicans, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus. The minimum inhibitory concentration (MIC) and minimum lethal concentration (MLC) of the nanoparticles that had been determined by broth microdilution method were found to be 20 and 50 µg/ml for C. albicans, B. subtilis and S. aureus; 10 and 20 µg/ml for E. coli and P. aeruginosa, respectively. For determining the effect of AgNPs on biofilm formation under in vitro conditions, MIC and subMICs were studied on P. aeruginosa and S. aureus biofilms by using microplate biofilm assay. Treatment of the AgNPs resulted in a decrease in the biofilm formation of S. aureus and P. aeruginosa as 26.52 and 25.50%, respectively. As a result of this study, it can be suggested that actinobacterially synthesised AgNPs have an effective potential to be used for pharmaceutical applications against multi‐resistant microorganisms.Inspec keywords: silver, nanoparticles, nanomedicine, antibacterial activity, biomedical materials, microorganismsOther keywords: antimicrobial potentials, antibiofilm potentials, silver nanoparticles, antimicrobial activity, antibiofilm activity, Streptomyces griseorubens AU2, disc diffusion, microdilution method, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, nanoparticle minimum inhibitory concentration, nanoparticle minimum lethal concentration, biofilm formation, in vitro conditions, microplate biofilm assay, pharmaceutical applications, multiresistant microorganisms, Ag     

Synthesis and anti-ultraviolet properties of monodisperse BSA-conjugated zinc oxide nanoparticles

A three-step process was designed to fabricate bovine serum albumin (BSA)-conjugated zinc oxide nanoparticles (BZnOs) by using BSA as the structure directing agent. The morphology and crystal phase of BZnOs were characterized by transmission electron microscopy (TEM) and powder X-ray diffraction (XRD). The composition and BSA content of BZnOs were measured by Fourier transform infrared spectrograph (FTIR) and thermogravimetry (TG) analysis. The ultraviolet-visible absorption property and ultraviolet blocking effects of BZnOs were also studied. The results indicated that the monodisperse BZnOs with 20.5 ± 3.5 nm in diameter had better anti-ultraviolet activities and exhibited the potential as the sunscreen.     

Formation of zinc oxide nanoparticles during electric discharge in water

A method for obtaining nanodimensional structures of zinc oxide (ZnO) by means of electric discharge in water is described. Data on the phase composition and luminescent properties of the synthesized ZnO powder deposited from a colloidal solution onto single crystal silicon surface are presented. It is shown that the partial concentrations of zinc in the oxide and metallic phases in the colloidal solution depend on the supply of oxygen to the zone of the chemical reaction. Optimum conditions for the discharge synthesis of nanodimensional powder with an almost 100% ZnO content have been found.     

Controllable preparation and sterilization activity of zinc aluminium oxide nanoparticles

The zinc aluminium oxide (ZAO) NPs with homogeneous dispersion and crystal stability were prepared through synergistic reaction with ultrasonic-microwave and different dispersants. The products were characterized by X-ray diffraction analysis, transmission electron microscopy and UV–vis absorption spectra. The ZAO NPs of 45, 30, 25 and 20 nm in diameter could be controllably obtained under the same reaction conditions. These ZAO NPs were high crystalline and with wurtzite crystal structure. Specially, the sterilization activity of ZAO NPs was investigated firstly. Our bacteriological study showed the enhanced sterilization activity of ZAO NPs compared with ZnO NPs. This demonstrated that the bactericidal efficacy of ZAO NPs increases with decreasing particle size.