Release Of Hydrogen Sulfide Research Articles

Catalase-templated nanozyme-loaded microneedles integrated with polymyxin B for immunoregulation and antibacterial activity in diabetic wounds

Diabetic wounds are characterized by chronic trauma, with long-term non-healing attributed to persistent inflammation and recurrent bacterial infections. Exacerbation of the inflammatory response is largely due to increased levels of reactive oxygen species (ROS). In this study, catalase (CAT) was used as a biological template to synthesize nanozyme-supported natural enzymes (CAT-Mn(SH)x) using a biomimetic mineralization method. Subsequently, polymyxin B (CAT-Mn(SH)x@PMB) was immobilized on its surface through electrostatic assembly. CAT-Mn(SH)x@PMB demonstrates the ability for slow and sustained release of hydrogen sulfide (H2S). Finally, CAT-Mn(SH)x@PMB loaded microneedles (MNs) substrate were synthesized using polyvinyl alcohol (PVA) and hydroxyethyl methacrylate (HEMA), and named CAT-(MnSH)x@PMB-MNs. It exhibited enhanced enzyme and antioxidant activities, along with effective antibacterial properties. Validation findings indicate that it can up-regulate the level of M2 macrophages and reduce the level of pro-inflammatory cytokine tumor necrosis factor-α (TNF-α). Additionally, it promotes angiogenesis and rapid nerve regeneration, thereby facilitating wound healing through its dual anti-inflammatory and antibacterial effects. Hence,this study introduces a time–space tissue-penetrating and soluble microneedle patch with dual anti-inflammatory and antibacterial effects for the treatment of diabetic wounds.

Infection Microenvironment-Responsive Coating on Titanium Surfaces for On-Demand Release of Therapeutic Gas and Antibiotic.

Aseptic loosening and bacterial infection pose significant challenges in the clinical application of titanium (Ti) orthopedic implants, which are primarily caused by insufficient osseointegration and bacterial contamination. To address these issues, a responsive coating on Ti surface is constructed, which achieves enhanced osseointegration and infection elimination by on-demand release of therapeutic gas hydrogen sulfide (H2S) and antibiotic. TiO2 nanotubes (TNT) are anodized on the Ti surface to enhance its bioactivity and serve as reservoirs for the antibiotic. An infection microenvironment-responsive macromolecular H2S donor layer is coated on top of TNT to inhibit premature leakage of antibiotic. This layer exhibits a sustained release of low-dosage H2S, which is capable of promoting the osteogenic differentiation and migration of cells. Moreover, the compactness of the macromolecular H2S donor layer could be broken by bacterial invasion, leading to rapid antibiotic release thus preventing infection. In vitro antibacterial experiments validates significant antibacterial activity of the coating against both Gram-negative (Escherichia coli) and Gram-positive bacteria (Staphylococcus aureus). Crucially, this coating effectively suppresses implant-associated infection with 98.7% antibacterial efficiency in a rat femoral bone defect model, mitigates inflammation at the defect site and promotes osseointegration of the Ti orthopedic implant.

Safeguarding ecosystems using innovative approaches to manage animal wastes

Animal wastes (AWs) are excreta or discarded materials associated with animal production industries. It could be in solid, liquid, or gaseous form, such as animal dung or droppings, discarded feed, feathers, fur, decayed bodies of dead animals, blood waste, effluent from animal farms, milk wastes, urine, and fart. Animal wastes are generated in high quantity, even beyond the control of animal farmers, due to the increase in animal production globally. These wastes pollute the ecosystem. They release greenhouse gases (GHGs) such as methane (CH4), carbon dioxide (CO2), and nitrous oxide (N2O) into the atmosphere through anaerobic fermentation which deplete ozone layer. Nitrogen and phosphorus constituents of Aws alter soil texture and pollute water bodies through run-off and direct disposal into water systems. The resultant effects of the pollution include climate change, degradation of soil and burning of crops, death of aquatic biota, release of offensive odour, especially ammonia (NH3) and hydrogen sulphide (H2S), and cause diseases of public health concern to human beings and animals. These consequences are due to the emission of harmful gases and compounds and the presence of pathogens in the waste. Animal wastes are potential sources of income and resources, and their environmental consequences could be reduced if farmers could use innovative approaches such as vermicomposting, production of biogas using wastes, membrane filtration, liquid – solid separation, thermal treatment and chemical treatment approaches to manage animal wastes. Government regulation and policies against indiscriminate disposal and application of animal wastes, coupled with the sensitization of people to the benefits and dangers associated with animal waste, could also prevent environmental challenges.

Assessment of the danger of the release of deep hydrogen sulfide from the Black Sea to the surface

The relevance of this study is due to the fact that the Black Sea is the largest body of water with a hydrogen sulfide zone. The proven reserves of hydrogen sulfide in the water column of the Black Sea amount to five billion tons. In terms of volume, this corresponds to 3.5 trillion cubic meters. At the same time, a mixture of hydrogen sulfide with air is explosive starting with a concentration of hydrogen sulfide in the air of 50 g/ m3. In addition, hydrogen sulfide is toxic, since it is a nerve gas, deadly already at 1 g/ m3. It is of interest to assess the possibility of the release of hydrogen sulfide waters of the sea to the surface with their subsequent degassing, as well as the consequences of increasing the concentration of hydrogen sulfide in surface waters and in the air for coastal areas. The distribution of hydrogen sulfide in the Black Sea is well studied. Especially a lot of measurement data was obtained for the top layer at a depth of 1000 m. Data on the concentration of hydrogen sulfide at depths from 1000 m to 2000 m is significantly less for technical reasons. The maximum concentration of hydrogen sulfide in the sea is reached at depths above 1500 m. A numerical assessment of the consequences of the release of deep waters to the surface has been obtained. It is shown that the concentration of hydrogen sulfide in the air will not exceed 1 g/m3, which is almost two orders of magnitude less than the explosive concentration. The balance estimates of oxygen and hydrogen sulfide fluxes in the Black Sea are considered in connection with forecasts of a rise in the boundary of the hydrogen sulfide zone. It is shown that the rise of the boundary is a consequence of the imbalance of these flows, however, the amount of net hydrogen sulfide production cannot be estimated accurately enough. With an accuracy of estimates of the fluxes themselves of 20-30%, the resulting increase in the amount of hydrogen sulfide per year is a statistically insignificant amount. The release of hydrogen sulfide to the surface in the foreseeable future is possible if the stratification of waters is disrupted by mechanical intervention.

An injectable hydrogel dressing for controlled release of hydrogen sulfide pleiotropically mediates the wound microenvironment.

The healing of scalded wounds faces many challenges such as chronic inflammation, oxidative stress, wound infection, and difficulties in vascular and nerve regeneration. Treating a single problem cannot effectively coordinate the complex regenerative microenvironment of scalded wounds, limiting the healing and functional recovery of the skin. Therefore, there is a need to develop a multi-effect treatment plan that can adaptively address the issues at each stage of wound healing. In this study, we propose a scheme for on-demand release of hydrogen sulfide (H2S) based on the concentration of reactive oxygen species (ROS) in the wound microenvironment. This is achieved by encapsulating peroxythiocarbamate (PTCM) in the ROS-responsive polymer poly(ethylene glycol)-poly(L-methionine) (PMet) to form nanoparticles, which are loaded into a thermosensitive injectable hydrogel, F127-poly(L-aspartic acid-N-hydroxysuccinimide) (F127-P(Asp-NHS)), to create a scald dressing. The H2S released by the hydrogel dressing on demand regulates the wound microenvironment by alleviating infection, reducing oxidative stress, and remodeling inflammation, thereby accelerating the healing of full-thickness scalded wounds. This hydrogel dressing for the adaptive release of H2S has great potential in addressing complex scalded wounds associated with infection and chronic inflammation.

H2S serves as the immunoregulatory essence of apoptotic cell death

Apoptosis supports tissue homeostasis and prevents immune disorders by removing damaged and functionally aberrant cells. Here, Ou etal. utilized genetic, pharmacological, and proteomic approaches focused on sulfur amino acid catabolism to discover that hydrogen sulfide (H2S) release during apoptosis suppresses Th17 cell differentiation, thus providing therapeutic targets for autoimmune diseases.

Hydrosulphide-methaemoglobin-albumin cluster: a hydrogen sulphide donor.

Methaemoglobin (metHb) possesses inherent characteristics that facilitate reversible binding to hydrogen sulphide. Exogenous hydrogen sulphide supplementation imparts beneficial bioactive effects, including antioxidant and anti-inflammatory; hence, we hypothesized that the metHb-hydrogen sulphide complex could act as a hydrogen sulphide donor for medication. In this study, we prepared a hydrosulphide-metHb-albumin (H2S-metHb-albumin) cluster and examined its applicability as a hydrogen sulphide donor in the mice model of hepatic ischemia-reperfusion injury. Structural analysis revealed that the H2S-metHb-albumin cluster exhibited a nanostructure wherein one metHb was wrapped by an average of three albumins, and hydrogen sulphide was bound to the haem. Additionally, the H2S-metHb-albumin cluster exhibited low-pH responsiveness, leading to sustained release of hydrogen sulphide. Owing to these structural and pharmaceutical characteristics, the severity of hepatic ischemia-reperfusion injury was alleviated via antioxidant and anti-inflammatory effects of the H2S-metHb-albumin cluster treatment. The protective effects were more potent in the H2S-metHb-albumin cluster compared to that in a conventional hydrogen sulphide donor (sodium hydrogen sulphide). No abnormal signs of toxic and biological responses were observed after the H2S-metHb-albumin cluster administration, confirming high biological compatibility. These results successfully establish the proof of concept that the H2S-metHb-albumin cluster is a promising hydrogen sulphide donor. To the best of our knowledge, this is the first report demonstrating the remarkable potential of metHb as a biomaterial for hydrogen sulphide donors.

A small-diameter vascular graft promotes rapid and benign remodeling of the neointima through dual release of nitric oxide and hydrogen sulfide

Coronary artery bypass grafting often requires autologous veins as alternatives. The limited source and problem of over-expansion are major obstacles for vein grafts, which could be solved by small-diameter artificial vascular graft. However, their clinical application is limited by thrombosis and restenosis caused by incomplete endothelialization and abnormal smooth muscle cells (SMCs) proliferation. Nitric oxide (NO) and hydrogen sulfide (H2S) are crucial signaling molecules in the cardiovascular system, known to regulate endothelial cells(ECs) and SMCs proliferation, migration, reduce oxidative stress, and inhibit inflammation to prevent intimal hyperplasia. In this study, we developed a new method to prepare a keratin based H2S donor(KAT) complexed with copper ions and electrospun it with PCL to prepare PCL/KAT-Cu small-diameter tissue-engineered vascular graft, which is capable of dual release of NO and H2S. We investigated the effects of NO and H2S release on human umbilical vein endothelial cells (HUVECs) and human umbilical arterial smooth muscle cells(HUASMCs) proliferation and migration, evaluated the graft's selectivity for HUVECs, and assessed its effects on macrophage phenotypic transitions and its protective effect on HUVECs under reactive oxygen species (ROS) conditions. Additionally, we tested the graft's ability to rapidly endothelialize under shear force using an in vitro 3D-perfusion system. After one month of in situ transplantation in rat abdominal aorta, the PCL/KAT-Cu small-diameter tissue-engineered vascular grafts demonstrated satisfactory intimal remodeling, comparable to natural blood vessels. In conclusion, our study presents a promising new strategy for remodeling small-diameter vascular grafts.

Erucin Exerts Cardioprotective Effects on Ischemia/Reperfusion Injury through the Modulation of mitoKATP Channels.

Modulation of mitochondrial K channels represents a pharmacological strategy to promote cardioprotective effects. Isothiocyanates emerge as molecules capable of releasing hydrogen sulfide (H2S), an endogenous pleiotropic gasotransmitter responsible for anti-ischemic cardioprotective effects also through the involvement of mitoK channels. Erucin (ERU) is a natural isothiocyanate resulting from the enzymatic hydrolysis of glucosinolates (GSLs) present in Eruca sativa Mill. seeds, an edible plant of the Brassicaceae family. In this experimental work, the specific involvement of mitoKATP channels in the cardioprotective effect induced by ERU was evaluated in detail. An in vivo preclinical model of acute myocardial infarction was reproduced in rats to evaluate the cardioprotective effect of ERU. Diazoxide was used as a reference compound for the modulation of potassium fluxes and 5-hydroxydecanoic acid (5HD) as a selective blocker of KATP channels. Specific investigations on isolated cardiac mitochondria were carried out to evaluate the involvement of mitoKATP channels. The results obtained showed ERU cardioprotective effects against ischemia/reperfusion (I/R) damage through the involvement of mitoKATP channels and the consequent depolarizing effect, which in turn reduced calcium entry and preserved mitochondrial integrity.

Sulfate reduction behavior in response to landfill dynamic pressure changes

During the long-term stabilization process of landfills, the pressure field undergoes constant changes. This study constructed dynamic pressure changes scenarios of high-pressure differentials (0.6 MPa) and low-pressure differentials (0.2 MPa) in the landfill pressure field at 25 °C and 50 °C, and investigated the sulfate reduction behavior in response to landfill dynamic pressure changes. The results showed that the pressurization or depressurization of high-pressure differentials caused more significant differences in sulfate reduction behavior than that of low-pressure differentials. The lowest hydrogen sulfide (H2S) release peak concentration under pressurization was only 29.67% of that under initial pressure condition; under depressurization, the highest peak concentration of H2S was up to 21,828 mg m−3, posing a serious risk of H2S pollution. Microbial community and correlation analysis showed that pressure had a negative impact on the sulfate-reducing bacteria (SRB) community, and the SRB community adjusted its structure to adapt to pressure changes. Specific SRBs were further enriched with pressure changes. Differential H2S release behavior under pressure changes in the 25 °C pressure environments were mediated by Desulfofarcimen (ASV343) and Desulfosporosinus (ASV1336), while Candidatus Desulforudis (ASV24) and Desulfohalotomaculum (ASV94) played a key role at 50 °C. This study is helpful in the formulation of control strategies for the source of odor pollution in landfills.

Hydrogen sulfide releasing and carboxybetaine modified vascular graft with enhanced anticoagulant, anticalcification, and pro-endothelialization properties

In the cardiovascular system, hydrogen sulfide(H2S) gasotransmitter regulates physiological processes involved in vasorelaxation, cardioprotection, anti-inflammation, and anti-oxidation. In this study, H2S releasing and carboxybetaine modified vascular graft with enhanced anticoagulant, anticalcification, and pro-endothelialization properties was designed and fabricated to meet the demand for small-diameter vascular grafts. Initially, a keratin-based bio-macromolecular donor of H2S was synthesized and then coelectrospun with polycaprolactone(PCL) to afford nanofibrous mats. Next, zwitterionic carboxybetaine was immobilized through dopamine self-polymerization to prolong the release of H2S, improve blood compatibility, and reduce calcification effectively. The biocomposite mats performed cell selectivity by promoting the adhesion and migration of HUVECs while inhibiting the proliferation of HUASMCs. Furthermore, the mats showed an excellent ability to resist oxidative stress. The results of the 3D perfusion culture proved that the grafts could promote endothelium formation under shear force. In vivo implantation results suggested that these grafts were capable of facilitating rapid endothelialization and reducing calcification.

Case study of hydrogen sulfide release in the sulfate-rich sewage drop structure

Abstract H2S is one of the principal odor gases released from sewer networks and understanding the rate of H2S release into sewer air space and ventilation to the atmosphere is crucial for preventing or minimizing odor and corrosion issues in sewer systems. TOXCHEM model was used to simulate the fate of H2S gas in roads for this study. The model was calibrated for the spring and summer seasons and validated for the remainder of the seasons. The predicted behavior showed good correlation to measurements on real samples following statistical analysis, with R2, R, and RMSE results between (0.93–0.97), (0.8–0.82), and (0.000438–0.000838), respectively. A sensitivity study was performed to assess the effect of various pH values, drop heights, tailwater depths, stream widths, and sewer ventilation rate levels. The results showed that the emissions concentrations for winter, spring, summer, and autumn reached 3500, 5044, 6425, and 4045 ppm respectively. All the emissions levels from this DS can be considered hazardous, and this was particularly evident during the summer months. This study has helped to clarify the fate and emission of hydrogen sulfide gas at the DS by simulation using a TOXCHEM model.

Insights into effects of thermotolerant nitrifying and sulfur-oxidizing inoculants on nitrogen-sulfur co-metabolism in sewage sludge composting

In this study, high temperature thermotolerant nitrifying bacteria (TNB) and high temperature thermotolerant sulfide oxidizing bacteria (TSOB) were obtained from compost samples and inoculated into sewage sludge (SS) compost. The effects of inoculation on physical and chemical parameters, ammonia and hydrogen sulfide release, nitrogen form and sulfur compound content change and physical-chemical properties during nitrogen and sulfur conversion were studied. The results showed that inoculation of TNB and TSOB increased the temperature, pH, OM degradation, C/N ratio and germination index (GI) of compost. Compared with the control treatment (CK), the addition of inoculants reduced the release of NH3 and H2S, and transformed them into nitrogen and sulfur compounds, the hydrolysis of polymeric ferrous sulfate was promoted, resulting in relatively high content of sulfite and sulfate. At the same time, the physical and chemical properties of SS have a strong correlation with nitrogen and sulfur compounds.

Cyanobacterial water blooms as an environmental hazard to waters

The article describes and analyzes the problem of cyanotoxin contamination of water bodies in Ukraine and other countries of the world. Eutrophication of water bodies, which is caused by human activity, climate change lead to uncontrolled development of cyanobacteria, and thus to ecological danger in hydrosphere objects. Anthropogenic eutrophication (increasing the content of nutrients in water due to their introduction into water bodies during pollution of water bodies by flood and municipal runoff, fish farming use of water bodies), temperature rise, increase in carbon dioxide content in the atmosphere, as a result of the transformation of introduced organic matter in water, contribute to increasing the dominance of cyanobacteria in water ecosystems. Bloomforming cyanobacteria produce various neurotoxins, hepatotoxins, and dermatotoxins that can be fatal to birds and mammals (including waterfowl, cattle, and dogs) and threaten the use of water bodies for public water supply, recreation, irrigation, and fishing. Among the toxins of blue-green algae, nodularin, saxitoxin, microcystin, domoic acid, guanitoxin, anatoxins and others were found. Exceeding the critical mass of algae and their metabolites activates the selfdecomposition process. This leads to the removal of oxygen from the water, and instead the release of methane, hydrogen sulfide, ammonia, and other toxic substances. The result of this is not only the death of fish. Cyanobacteria are capable of natural genetic transformation — genetic change of the cell as a result of direct absorption and inclusion of exogenous DNA from its environment. A sufficiently effective solution to the issue of controlling the activity of cyanobacteria is the use of humic preparations. it was established that humic substances (humic acids, fulvic acids) in certain concentrations negatively affect the growth, development and activity of cyanobacteria. Humic substances, as a component of organic matter and a reserve of organic carbon in its global cycle, have a negative effect on hydrobionts by increasing their concentration in water bodies. However, humic substances are able to regulate the activity of phytoplankton. The introduction of humic substances at a concentration of 2-5 mg/l of reservoir water significantly affects the activity of phytoplankton (suppresses phytoplankton vegetation, reduces the slime formation of cyanobacteria, and, from the beginning, inactivates the synthesis of cyanotoxins). This effect is provided by the alkaline pH of humates, high content of iron and copper.

Bioactive Vanadium Disulfide Nanostructure with "Dual" Antitumor Effects of Vanadate and Gas for Immune-Checkpoint Blockade-Enhanced Cancer Immunotherapy.

Bioactive inorganic nanomaterials and the biological effects of metal ions have attracted extensive attention in tumor therapy in recent years. Vanadium (V), as a typical bioactive metal element, regulates a variety of biological functions. However, its role in antitumor therapy remains to be revealed. Herein, biodegradable vanadium disulfide (VS2) nanosheets (NSs) were prepared as a responsive gas donor and bioactive V source for activating cancer immunotherapy in combination with immune-checkpoint blockade therapy. After PEGylation, VS2-PEG exhibited efficient glutathione (GSH) depletion and GSH-activated hydrogen sulfide (H2S) release. Exogenous H2S caused lysosome escape and reduced adenosine triphosphate (ATP) synthesis in tumor cells by interfering with the mitochondrial membrane potential and inducing acidosis. In addition, VS2-PEG degraded into high-valent vanadate, leading to Na+/K+ ATPase inhibition, potassium efflux, and interleukin (IL)-1β production. Together with further induction of ferroptosis and immunogenic cell death, a strong antitumor immune response was stimulated by reversing the immunosuppressive tumor microenvironment. Moreover, the combined treatment of VS2-PEG and α-PD-1 amplified antitumor therapy, significantly suppressed tumor growth, and further elicited robust immunity to effectively defeat tumors. This work highlights the biological effects of vanadium for application in cancer treatment.

Hydrogen Sulfide-Releasing Indomethacin-Derivative (ATB-344) Prevents the Development of Oxidative Gastric Mucosal Injuries.

Hydrogen sulfide (H2S) emerged recently as an anti-oxidative signaling molecule that contributes to gastrointestinal (GI) mucosal defense and repair. Indomethacin belongs to the class of non-steroidal anti-inflammatory drugs (NSAIDs) and is used as an effective intervention in the treatment of gout- or osteoarthritis-related inflammation. However, its clinical use is strongly limited since indomethacin inhibits gastric mucosal prostaglandin (PG) biosynthesis, predisposing to or even inducing ulcerogenesis. The H2S moiety was shown to decrease the GI toxicity of some NSAIDs. However, the GI safety and anti-oxidative effect of a novel H2S-releasing indomethacin derivative (ATB-344) remain unexplored. Thus, we aimed here to compare the impact of ATB-344 and classic indomethacin on gastric mucosal integrity and their ability to counteract the development of oxidative gastric mucosal injuries. Wistar rats were pretreated intragastrically (i.g.) with vehicle, ATB-344 (7-28 mg/kg i.g.), or indomethacin (5-20 mg/kg i.g.). Next, animals were exposed to microsurgical gastric ischemia-reperfusion (I/R). Gastric damage was assessed micro- and macroscopically. The volatile H2S level was assessed in the gastric mucosa using the modified methylene blue method. Serum and gastric mucosal PGE2 and 8-hydroxyguanozine (8-OHG) concentrations were evaluated by ELISA. Molecular alterations for gastric mucosal barrier-specific targets such as cyclooxygenase-1 (COX)-1, COX-2, heme oxygenase-1 (HMOX)-1, HMOX-2, superoxide dismutase-1 (SOD)-1, SOD-2, hypoxia inducible factor (HIF)-1α, xanthine oxidase (XDH), suppressor of cytokine signaling 3 (SOCS3), CCAAT enhancer binding protein (C/EBP), annexin A1 (ANXA1), interleukin 1 beta (IL-1β), interleukin 1 receptor type I (IL-1R1), interleukin 1 receptor type II (IL-1R2), inducible nitric oxide synthase (iNOS), tumor necrosis factor receptor 2 (TNFR2), or H2S-producing enzymes, cystathionine γ-lyase (CTH), cystathionine β-synthase (CBS), or 3-mercaptopyruvate sulfur transferase (MPST), were assessed at the mRNA level by real-time PCR. ATB-344 (7 mg/kg i.g.) reduced the area of gastric I/R injuries in contrast to an equimolar dose of indomethacin. ATB-344 increased gastric H2S production, did not affect gastric mucosal PGE2 content, prevented RNA oxidation, and maintained or enhanced the expression of oxidation-sensitive HMOX-1 and SOD-2 in line with decreased IL-1β and XDH. We conclude that due to the H2S-releasing ability, i.g., treatment with ATB-344 not only exerts dose-dependent GI safety but even enhances gastric mucosal barrier capacity to counteract acute oxidative injury development when applied at a low dose of 7 mg/kg, in contrast to classic indomethacin. ATB-344 (7 mg/kg) inhibited COX activity on a systemic level but did not affect cytoprotective PGE2 content in the gastric mucosa and, as a result, evoked gastroprotection against oxidative damage.

GYY4137, a hydrogen sulfide donor, protects against endothelial dysfunction in porcine coronary arteries exposed to myeloperoxidase and hypochlorous acid

Background and aimsMyeloperoxidase (MPO) and its principal reaction product hypochlorous acid (HOCl) are part of the innate immune response but are also associated with endothelial dysfunction, thought to involve a reduction in nitric oxide (NO) bioavailability. We aimed to investigate the effect of MPO and HOCl on vasorelaxation of coronary arteries and to assess directly the involvement of NO. In addition, we hypothesised that the slow release hydrogen sulfide (H2S) donor GYY4137 would salvage coronary artery endothelial function in the presence of MPO and HOCl. Methods and resultsContractility of porcine coronary artery segments was measured using isometric tension recording. Incubation with MPO (50 ng/ml) plus hydrogen peroxide (H2O2) (30 μM; substrate for MPO) impaired endothelium-dependent vasorelaxation to bradykinin in coronary arteries. HOCl (10–500 μM) also impaired endothelium-dependent relaxations. There was no effect of MPO plus H2O2, or HOCl, on endothelium-independent relaxations to 5′-N-ethylcarboxamidoadenosine and sodium nitroprusside. L-NAME (300 μM), a NO synthase inhibitor, attenuated bradykinin relaxations, leaving L-NAME-resistant relaxations to bradykinin mediated by endothelium-dependent hyperpolarization. In the presence of L-NAME, MPO plus H2O2 largely failed to impair endothelium-dependent relaxations to bradykinin. Similarly, HOCl failed to inhibit endothelium-dependent relaxations to bradykinin in the presence of L-NAME. GYY4137 (1–100 μM) protected endothelium-dependent relaxations to bradykinin from dysfunction caused by MPO plus H2O2, and HOCl, with no effect alone on bradykinin relaxation responses. The specific MPO inhibitor aminobenzoic acid hydrazide (ABAH) (1 and 10 μM) also protected against MPO plus H2O2-induced endothelial dysfunction (at 10 μM ABAH), but was less potent than GYY4137. ConclusionsMPO plus H2O2, and HOCl, impair coronary artery endothelium-dependent vasorelaxation via inhibition of NO. GYY4137 protects against endothelial dysfunction in arteries exposed to MPO plus H2O2, and HOCl. H2S donors such as GYY4137 are possible therapeutic options to control excessive MPO activity in cardiovascular diseases.

Glucose Oxidase Driven Hydrogen Sulfide-Releasing Nanocascade for Diabetic Infection Treatment.

Diabetic ulcers have received much attention in recent years due to their high incidence and mortality, motivating the scientific community to develop various strategies for such chronic disease treatments. However, the therapeutic outcome of these approaches is highly compromised by invasive bacteria and a severe inflammatory microenvironment. To overcome these dilemmas, microenvironment-responsive self-delivery glucose oxidase@manganese sulfide (GOx@MnS) nanoparticles (NPs) are developed by one-step biomineralization. When they encounter the high glucose level in the ulcer site, GOx particles catalyze glucose to decrease the local pH and trigger the steady release of both manganese ions (Mn2+) and hydrogen sulfide (H2S). Mn2+ reacts with hydrogen peroxide to generate hydroxyl radicals for the elimination of bacterial infection; meanwhile, H2S is able to suppress the inflammatory response and accelerate diabetic wound healing through macrophage polarization. The excellent biocompatibility, strong bactericidal activity, and considerable immunomodulatory effect promise GOx@MnS NPs have great therapeutic potential for diabetic wound treatment.

Deep Processing of Dump Slag from the Copper-Nickel Industry

This work proposes an environmentally safe and economically feasible method of waste copper-nickel production slag utilization (Kola Mining-Metallurgical Company, Nornickel, Kola Peninsula, Russia). This process involves the decomposition of slag by diluted solutions of sulfuric acid (7–10 wt.% H2SO4) with a transfer in a solution of more than 70% silicon, 77% iron and 78% magnesium, and a concentration of non-ferrous metals in the residue (~70%). Copper ions were used in the leaching stage to prevent the release of hydrogen sulfide into the working atmosphere. Dehydration of the solution, followed by washing of water-soluble sulphates from silica, was carried out to separate silica from the leaching solution. The dehydration temperature effect on the silica structural characteristics was determined. The possibility of recovering non-ferrous metals from solutions after silica extraction by precipitation, in the form of copper cementite, and the sum of nickel and cobalt sulfides, was evaluated. Pigment-grade iron dioxide, magnesium sulphate and aluminium hydroxide were obtained by dehydration of the solution after extraction of base metals, calcination and other operations. Sulfuric acid leaching resulted in the disclosure of sulfide grains encapsulated in ferrosilicate, which is a favorable factor for flotation. The depleted residue can be successfully used in the construction industry.

New application for Micromax in aqueous drilling fluids as a hydrogen sulfide scavenger

The release of hydrogen sulfide (H2S) during drilling operations endangers workers' health and safety while also causing corrosion-related equipment damage. Various H2S scavengers have been used, but researchers are still looking for an optimal and feasible scavenger. Micromax (manganese tetroxide, Mn3O4), which has high oxidation and absorption capabilities with a high manganese oxide content, may effectively scavenge H2S. This study aimed to address the potential of using Micromax as a scavenger for H2S in aqueous drilling fluid. The study investigated the impact of Micromax addition on the drilling fluid rheology, filtering behavior, alkalinity, and corrosion propensity. The experiments were performed for a base drilling fluid without scavengers and with two commercial scavengers (i.e., triazine and SourScav®), which serve as benchmarking references. The findings showed that Micromax increased the scavenging capacity of the fluid by 706.6%, which was about 4 and 5 times higher than those of triazine and SourScav, respectively. Micromax and commercial scavengers did not impair the drilling fluid's rheology, but they slightly increased the formed filter cake thickness. Micromax and triazine maintained the pH of drilling fluids at a safe level above 10, which is required in a sour environment, unlike SourScav, which reduced the pH to a critical value of 7.9. Micromax and the other two commercial scavengers demonstrated noncorrosive characteristics with nearly zero corrosion rate. For the first time, the present work demonstrated the potential application of Micromax as a low-cost H2S scavenger with competent mud properties for effective and safe drilling operations.