In vivo assessment of the toxic impact of exposure to magnetic iron oxide nanoparticles (IONPs) using Drosophila melanogaster.

Iron oxide nanoparticles (IONPs) have useful properties, such as strong magnetism and compatibility with living organisms which is preferable for medical applications such as drug delivery and imaging. However, increasing use of these materials, especially in medicine, has raised concerns regarding potential risks to human health. In this study, IONPs were coated with silicon dioxide (SiO2), citric acid (CA), and polyethylenimine (PEI) to enhance their dispersion and biocompatibility. Both coated and uncoated IONPs were assessed for genotoxic effects on Drosophila melanogaster. Results showed that uncoated IONPs induced genotoxic effects, including mutations and recombinations, while the coated IONPs demonstrated reduced or negligible genotoxicity. Additionally, bioinformatic analyses highlighted potential implications of induced recombination in various cancer types, underscoring the importance of understanding nanoparticle-induced genomic instability. This study highlights the importance of nanoparticle coatings in reducing potential genotoxic effects and emphasizes the necessity for comprehensive toxicity assessments in nanomaterial research.

Enhancement of enzyme activity by laser-induced energy propulsion of upconverting nanoparticles under near-infrared light: A comprehensive methodology for in vitro and in vivo applications.

If the appropriate immobilization method and carrier support are not selected, partial decreases in the activity of enzymes may occur after immobilization. Herein, to overcome this challenge, an excitation mechanism that enables energy transfer was proposed. Modified upconverting nanoparticles (UCNPs) were constructed and the important role of near-infrared (NIR) excitation in enhancing the catalytic activity of the enzyme was demonstrated. For this purpose, UCNPs were first synthesized via the hydrothermal method, functionalized with isocyanate groups, and then, PEG-L-ASNase was immobilized via covalent binding. UCNPs with and without PEG-L-ASNase were extensively characterized by different methods. These supports had immobilization yield and activity efficiency of >96 % and 78 %, respectively. Moreover, immobilized enzymes exhibited improved pH, thermal, and storage stability. In addition, they retained >65 % of their initial activity even after 20 catalytic cycles. Biochemical and histological findings did not indicate a trend of toxicity in rats due to UCNPs. Most importantly, PEG-L-ASNase activity was triggered approximately 5- and 2-fold under in vitro and in vivo conditions, respectively. Overall, it is anticipated that this pioneering work will shed new light on the realistic and promising usage of NIR-excited UCNPs for the immobilization of enzymes in expensive and extensive applications.

Three-Dimensional Nano-Morphology of Carbon Nanotube/Epoxy Filled Poly(methyl methacrylate) Microcapsules.

The three-dimensional nano-morphology of poly(methyl methacrylate; PMMA) microcapsules filled with carbon nanotubes (CNTs) and epoxy resin were investigated by various microscopy methods, including a novel, laser scanning confocal microscopy (LSCM) method. Initially, PMMA microcapsules containing various amounts of CNTs were synthesized by a solvent evaporation method. Scanning electron microscopy analysis showed that pore-free, smooth-surface microcapsules formed with various types of core-shell morphologies. The average size of CNT/epoxy/PMMA microcapsules was shown to decrease from ~52 µm to ~15 µm when mixing speed during synthesis increased from 300 rpm to 1000 rpm. In general, the presence of CNTs resulted in slightly larger microcapsules and higher variations in size. Moreover, three-dimensional scans obtained from confocal microscopy revealed that higher CNT content increased the occurrence and size of CNT aggregates inside the microcapsules. Entrapped submicron air bubbles were also observed inside most microcapsules, particularly within those with higher CNT content.

Photocatalytic degradation of azo dye using core@shell nano-TiO2 particles to reduce toxicity.

Clean and safe water is fundamental for human and environmental health. Traditional remediation of textile dye-polluted water with chemical, physical, and biological processes has many disadvantages. Due to this, nano-engineered materials are drawing more attention to this area. However, the widespread use of nano-particles for this purpose may lead to photocatalytic degradation of xenobiotics, while increasing the risk of nano-particle-induced ecotoxicity. Therefore, we comparatively evaluated the toxicity of novel synthesized core@shell TiO2 and SiO2 nano-particles to embryonic stages of Danio rerio and Xenopus laevis. The ability of photocatalytic destruction of the synthesized nano-particles was tested using toxic azo dye, disperse red 65, and the effects of reducing the toxicity were evaluated. The reflux process was used to synthesize catalysts in the study. The samples were characterized by scanning electron microscopy, X-ray fluorescence spectroscopy, X-ray diffractometry, BET surface area, and UV-vis-diffuse reflectance spectra. It was determined that the synthesized nano-particles had no significant toxic effect on D. rerio and X. laevis embryos. On the other hand, photocatalytic degradation of the dye significantly reduced lethal effects on embryonic stages of the organisms. Therefore, we suggest that specific nano-particles may be useful for water remediation to prevent human health and environmental impact. However, further risk assessment should be conducted for the ecotoxicological risks of nano-particles spilled in aquatic environments and the relationship of photocatalytic interaction with nano-particles and xenobiotics.

Toxicological aspects of photocatalytic degradation of selected xenobiotics with nano-sized Mn-doped TiO2.

The toxic effects of two selected xenobiotics, bisphenol A (BPA) and atrazine (ATZ), were evaluated after photocatalytic degradation using nano-sized, Mn-doped TiO2. Undoped and Mn-doped TiO2 nanoparticles were synthesized. The samples were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), UV-vis-diffuse reflectance spectra (DRS), X-ray fluorescence spectroscopy (XRF), and BET surface area. The photocatalytic efficiency of the undoped and Mn-doped TiO2 was evaluated for BPA and ATZ. The toxicity of the synthesized photocatalysts and photocatalytic by-products of BPA and ATZ was determined using frog embryos and tadpoles, zebrafish embryos, and bioluminescent bacteria. Possible toxic effects were also evaluated using selected enzyme biomarkers. The results showed that Mn-doped TiO2 nanoparticles did not cause significant lethality in Xenopus laevis embryos and tadpoles, but nonfiltered samples caused lethality in zebrafish. Furthermore, Mn-doping of TiO2 increased the photocatalytic degradation capability of nanoparticles, and it successfully degraded BPA and AZT, but degradation of AZT caused an increase of the lethal effects on both tadpoles and fish embryos. Degradation of BPA caused a significant reduction of lethal effects, especially after 2-4h of degradation. However, biochemical assays showed that both Mn-doped TiO2 and the degradation by-products caused a significant change of selected biomarkers on X. laevis tadpoles; thus, the ecological risks of Mn-doped TiO2 should be considered due to nanomaterial applications and for spilled nanoparticles in an aquatic ecosystem. Also, the risk of nanoparticles should be considered using indicator reference biochemical markers to verify the environmental health impacts.

Effects of coating with different ceromers on the impact strength, transverse strength and elastic modulus of polymethyl methacrylate.

The aim of this study was to evaluate the mechanical properties of polymethyl methacrylate (PMMA) after coating with different ceromers. For transverse strength and modulus of elasticity tests, specimens of 65×10×2.5 mm dimensions were prepared (5 groups, n=10). For impact strength test, specimens of 60×7.5×4 mm dimensions were prepared (5 groups, n=10). Test group specimens were coated with one of four different types of ceromers, and specimens in the control group were not coated. After specimens were tested for transverse and impact strengths, the data were analyzed with Kruskal-Wallis and Conover post hoc tests (p<0.05). GLYMOTEOS-TiO2 and A174-TEOS significantly increased the transverse strength of PMMA. All ceromers caused a statistically significant increase in the elastic modulus of PMMA. While GLYMO-TEOS-ZrO2 significantly decreased the impact strength, the other ceromers did not cause any statistically significant difference in impact strength. Coating with ceromers substantially improved the mechanical properties of PMMA.

Photocatalytic antibacterial performance of Sn(4+)-doped TiO(2) thin films on glass substrate.

Pure anatase, nanosized and Sn(4+) ion doped titanium dioxide (TiO(2)) particulates (TiO(2)-Sn(4+)) were synthesized by hydrothermal process. TiO(2)-Sn(4+) was used to coat glass surfaces to investigate the photocatalytic antibacterial effect of Sn(4+) doping to TiO(2) against gram negative Escherichia coli (E. coli) and gram positive Staphylococcus aureus (S. aureus). Relationship between solid ratio of TiO(2)-Sn(4+) in coatings and antibacterial activity was reported. The particulates and the films were characterized using particle size analyzer, zeta potential analyzer, Brunauer-Emmett-Teller (BET), X-ray diffractometer (XRD), SEM, AAS and UV/VIS/NIR techniques. The results showed that TiO(2)-Sn(4+) is fully anatase crystalline form and easily dispersed in water. Increasing the solid ratio of TiO(2)-Sn(4+) from 10 to 50% in the coating solution increased antibacterial effect.

Photocatalytic degradation of Congo Red by hydrothermally synthesized nanocrystalline TiO2 and identification of degradation products by LC-MS.

Degradation of Congo Red (CR) dye in aqueous solutions was investigated by means of photocatalysis of TiO2 which was hydrothermally synthesized at 200 degrees C in 2 h, in anatase phase with 8 nm crystallite size. Efficiency of TiO2 in photocatalytic degradation under visible irradiation was studied by investigating the effects of amount of TiO2, irradiation time, initial CR concentration and pH. It was found that complete decolorization is achieved within 30 min of irradiation. Effects of nitrate and sulphate ions and humic acid on the degradation were also tested. The results were compared with Degussa P-25 TiO2 at the same degradation conditions. Degradation products were detected using LC-MS technique. The probable pathways for the formation of degradation products were proposed.

Characterization of the hydrothermally synthesized nano-TiO2 crystallite and the photocatalytic degradation of Rhodamine B.

Pure anatase-TiO2 nanoparticles with 8 nm average crystallite size was synthesized hydrothermally at 200 degrees C in 2 h. The structural and physico-chemical properties of nano-TiO2 were determined by powder XRD, FT-IR, BET and SEM analyses. The behavior of anatase nano-TiO2 in catalytic degradation of Rhodamine B (RB) dye in transparent nano-TiO2 sol under UV-light was examined as a function of irradiation power of UV-light, irradiation time, amount of nano-TiO2 and initial RB concentration in the sol. Rhodamine B was fully degraded with the catalysis of the nano-TiO2 in a short time as low as 60 min. Photocatalytic activity of the nano-TiO2 for degradation of RB was compared with Degussa P-25 at optimum catalysis conditions determined for the nano-TiO2. It was found that, when compared to Degussa P-25, the nano-TiO2 could be repeatedly used with increasing photocatalytic activity. It was found that the photodegradation obeys the pseudo first-order reaction kinetics with the rate constant of 0.0658 min(-1), and the half period t1/2 was 10.53 min.