Static Magnetic Field Reduces Intracellular ROS Levels and Protects Cells Against Peroxide-Induced Damage: Suggested Roles for Catalase.

A feature in neurodegenerative disorders is the loss of neurons, caused by several factors including oxidative stress induced by reactive oxygen species (ROS). In this work, static magnetic field (SMF) was applied in vitro to evaluate its effect on the viability, proliferation, and migration of human neuroblastoma SH-SY5Y cells, and on the toxicity induced by hydrogen peroxide (H2O2), tert-butyl hydroperoxide (tBHP), H2O2/sodium azide (NaN3) and photosensitized oxidations by photodynamic therapy (PDT) photosensitizers. The SMF increased almost twofold the cell expression of the proliferation biomarker Ki-67 compared to control cells after 7 days of exposure. Exposure to SMF accelerated the wound healing of scratched cell monolayers and significantly reduced the H2O2-induced and the tBHP-induced cell deaths. Interestingly, SMF was able to revert the effects of NaN3 (a catalase inhibitor), suggesting an increased activity of catalase under the influence of the magnetic field. In agreement with this hypothesis, SMF significantly reduced the oxidation of DCF-H2, indicating a lower level of intracellular ROS. When the redox imbalance was triggered through photosensitized oxidation, no protection was observed. This observation aligns with the proposed role of catalase in cellular proctetion under SMF.  Exposition to SMF should be further validated in vitro and in vivo as a potential therapeutic approach for neurodegenerative disorders.

Caffeine Release from Magneto-Responsive Hydrogels Controlled by External Magnetic Field and Calcium Ions and Its Effect on the Viability of Neuronal Cells.

Caffeine (CAF) is a psychostimulant present in many beverages and with rapid bioabsorption. For this reason, matrices that effectuate the sustained release of a low amount of CAF would help reduce the intake frequency and side effects caused by high doses of this stimulant. Thus, in this study, CAF was loaded into magnetic gelatin/alginate (Gel/Alg/MNP) hydrogels at 18.5 mg/ghydrogel. The in vitro release of CAF was evaluated in the absence and presence of an external magnetic field (EMF) and Ca2+. In all cases, the presence of Ca2+ (0.002 M) retarded the release of CAF due to favorable interactions between them. Remarkably, the release of CAF from Gel/Alg/MNP in PBS/CaCl2 (0.002 M) at 37 °C under an EMF was more sustained due to synergic effects. In PBS/CaCl2 (0.002 M) and at 37 °C, the amounts of CAF released after 45 min from Gel/Alg and Gel/Alg/MNP/EMF were 8.3 ± 0.2 mg/ghydrogel and 6.1 ± 0.8 mg/ghydrogel, respectively. The concentration of CAF released from Gel/Alg and Gel/Alg/MNP hydrogels amounted to ~0.35 mM, thereby promoting an increase in cell viability for 48 h. Gel/Alg and Gel/Alg/MNP hydrogels can be applied as reservoirs to release CAF at suitable concentrations, thus forestalling possible side effects and improving the viability of SH-SY5Y cells.

Environmental risk assessment of potentially toxic elements in Doce River watershed after mining sludge dam breakdown in Mariana, MG, Brazil.

Faced with a potential risk of a colossal amount of sludge released into the Doce River basin in the most shocking Brazilian mining disaster, we proposed to assess the environmental risk from a new perspective: Understanding the mobilization of potentially toxic elements (PTE) with the geochemical fractions. Soil and sediment samples were taken in nine sites throughout the basin and characterized. The environmental risk was assessed from the PTE sequential extraction in three fractions: soluble, reducible, and oxidizable, in addition to the pseudo-total concentration. The potential mobile fraction (PMF) showed a considerable PTE mobilization from the soil and sediment samples. Principal component statistical analysis indicated the sludge as the single source of PTE. The risk assessment depended on the fractional distribution and the PTE enrichment degree in the affected samples. The fractional distribution contributed mainly to Mn, Sb, and Pb mobility, with PMF of 96%, 81%, and 100%, respectively. The mobilization of Cd, Co, Ag, Ni, Pb, Zn, and Cu was predominantly related to the degree of enrichment. The risk assessment from the geochemical fractions pointed to the magnitude of the disaster and the dispersion of PTE with severe effects on the affected populations. Therefore, more strongly enforced regulations in the basin are needed, in addition to the urgent use of more secure containment dams. It is also essential to emphasize the transferability of the design of this study to other environmental units in mining disaster conditions.

Vanillin crosslinked chitosan films: The states of water and the effect of carriers on curcumin uptake.

In this work, chitosan chains were crosslinked with different contents of vanillin (Van), characterized and loaded with curcumin (CUR), a hydrophobic drug. Sodium dodecyl sulfate (SDS), Tween 20® (T20) and ß-cyclodextrin (ßCD) were used as curcumin carriers. Films prepared with Van 20 % yielded gel content of 70 %, swelling degree of ~23 gwater/g, bound water and capillary water, as revealed by Time-Domain Nuclear Magnetic Resonance measurements. Films prepared with higher Van contents showed small swelling degree (< 1.6 gwater/g) and hydrophobicity, making them inadequate for drug loading. UV-Vis and fluorescence spectroscopic studies indicated that Van 20 % combined with SDS and SDS/ßCD presented the highest CUR uptake (~3.0 mg/g), favored by electrostatic interactions and hydrophobic interactions. CHI and Van 20 % films did not present any cytotoxicity in human neuroblastoma SH-SY5Y cells. At pH 1.0 the films were completely soluble, pointing to their potential application as gastric delivery systems for hydrophobic drugs. Chemical compounds studied in the manuscript: Chitosan, vanillin, curcumin, ß-cyclodextrin, sodium dodecyl sulfate, polyethylene glycol sorbitan monolaurate.

Crosslinkers for polysaccharides and proteins: Synthesis conditions, mechanisms, and crosslinking efficiency, a review.

Polysaccharides and proteins are important macromolecules for developing hydrogels devoted to biomedical applications. Chemical hydrogels offer chemical, mechanical, and dimensional stability than physical hydrogels due to the chemical bonds among the chains mediated by crosslinkers. There are many crosslinkers to synthesize polysaccharides and proteins based on hydrogels. In this review, we revisited the crosslinking reaction mechanisms between synthetic or natural crosslinkers and polysaccharides or proteins. The selected synthetic crosslinkers were glutaraldehyde, carbodiimide, boric acid, sodium trimetaphosphate, N,N'-methylene bisacrylamide, and polycarboxylic acid, whereas the selected natural crosslinkers included transglutaminase, tyrosinase, horseradish peroxidase, laccase, sortase A, genipin, vanillin, tannic acid, and phytic acid. No less important are the reactions involving click chemistry and the macromolecular crosslinkers for polysaccharides and proteins. Literature examples of polysaccharides or proteins crosslinked by the different strategies were presented along with the corresponding highlights. The general mechanism involved in chemical crosslinking mediated by gamma and UV radiation was discussed, with particular attention to materials commonly used in digital light processing. The evaluation of crosslinking efficiency by gravimetric measurements, rheology, and spectroscopic techniques was presented. Finally, we presented the challenges and opportunities to create safe chemical hydrogels for biomedical applications.

Modeling the kinetics of potentially toxic elements desorption in sediment affected by a dam breakdown disaster in Doce River - Brazil.

On November 5th, 2015, a mining dam spilled a huge plume of mining waste in the Doce River. Even though many studies have reported the environmental impact from the Doce River's tragedy, the transport of potentially toxic elements (PTE) by kinetic modeling to determine how long the basin takes to achieve the natural balance has not been described. Therefore, samples of sludge, sediment, and water were collected along the Doce River basin, to assess the elements' total leaching by kinetic modeling. The elements Fe, Al, Mn, Cu, Ag, Pb, Cd, and As were evaluated. An innovative mobilization factor (FS/D) indicated that Mn2+, Ag+, and Cd2+ can be mobilized about 80, 89, and 57 times more than its initial concentration. Besides, in low pH, the Al and Pb ions can be mobilized. The desorption kinetics showed a lower rate constant (k) and higher initial desorption constant (h) for Mn2+ than Cd2+ and Ag+, suggesting both high- and low-affinity interaction sites for Mn2+. The exponential decay demonstrated that metals can leach for months or years. Thus, the long-lasting release of metals from mining tailing waste in concentrations that endanger the ecosystem and human health makes clear the need for long-term monitoring.

A new approach to evaluate toxic metal transport in a catchment.

Competitive sorption and desorption of Cd2+, Pb2+, and Hg2+ onto riverbank and sediment samples of an area impacted by pyritic residue in a Southern Brazilian catchment were evaluated. Although these ions are considered poorly mobile, a new approach has been proposed to assess their behavior and associated risk. In this sense, factorial design and three-dimensional surface methodology are proposed to describe the competitive sorption behavior of the metal ion in the environmental matrix, as well as an innovative mobilization factor (MF) to describe the desorption rate from the integration of the normalized difference of sorption-desorption fluorescence peaks. Sorption was carried out with a central composite factorial design (23) to estimate simultaneous effects of independent variables. Three-dimensional surface analysis indicated increasing Cd2+ equilibrium concentration (Ceq) with Hg2+ and Pb2+ initial concentration (Ci), showing synergistic effect and low Cd2+ affinity to the solid phase. Statistical analysis presented [Formula: see text] as a significant variable for cadmium and lead dynamics, although [Formula: see text] was also significant for Hg2+ releasing to the liquid phase. After integrating the sorption and desorption fluorescence peaks, the MF for Cd2+, Pb2+, and Hg2+ was around 0.2, 0.5, and 0.1 in riverbank sediment, and 0.3, 0.9, and 0.1 in sediment, respectively. Hence, consistent ion mobilization along the river was observed, with Pb2+ mobilizing 9 and 6 times more than Hg2+ and Cd2+, respectively. The transport of ions such as Pb2+ and Hg2+, usually considered immobile, has indeed occurred, causing contamination through the watershed and increasing environmental risk. Graphical Abstract A new approach to determine toxic metal mobilization factor in a river catchment.