ABSTRACT
Naphthenic acids, NAs, are a major contaminant of concern and a focus of much research around remediation of oil sand process affected waters, OSPW. Using activated carbon adsorbents are an attractive option given their low cost of fabrication and implementation. A deeper evaluation of the effect NA structural differences have on uptake affinity is warranted. Here we provide an in-depth exploration of NA adsorption including many more model NA species than have been assessed previously with evaluation of adsorption kinetics and isotherms at the relevant alkaline pH of OSPW using several different carbon adsorbents with pH buffering to simulate the behaviour of real OSPW. Uptake for the NA varied considerably regardless of the activated carbon used, ranging from 350 mg/g to near zero highlighting recalcitrant NAs. The equilibrium data was explored to identify structural features of these species and key physiochemical properties that influence adsorption. We found that certain NA will be resistant to adsorption when hydrophobic adsorbents are used. Adsorption isotherm modelling helped explore interactions occurring at the interface between NA and adsorbent surfaces. We identified the importance of NA hydrophobicity for activated carbon uptake. Evidence is also presented that indicates favorable hydrogen bonding between certain NA and surface site hydroxyl groups, demonstrating the importance of adsorbent surface functionality for NA uptake. This research highlights the challenges associated with removing NAs from OSPW through adsorption and also identifies how adsorbent surface chemistry modification can be used to increase the removal efficiency of recalcitrant NA species.
Subject(s)
Carboxylic Acids , Water Pollutants, Chemical , Adsorption , Carboxylic Acids/chemistry , Water Pollutants, Chemical/chemistry , Charcoal/chemistry , Models, Chemical , Kinetics , Hydrogen-Ion ConcentrationABSTRACT
Thermodynamic modeling is still the most widely used method to characterize aerosol acidity, a critical physicochemical property of atmospheric aerosols. However, it remains unclear whether gas-aerosol partitioning should be incorporated when thermodynamic models are employed to estimate the acidity of coarse particles. In this work, field measurements were conducted at a coastal city in northern China across three seasons, and covered wide ranges of temperature, relative humidity and NH3 concentrations. We examined the performance of different modes of ISORROPIA-II (a widely used aerosol thermodynamic model) in estimating aerosol acidity of coarse and fine particles. The M0 mode, which incorporates gas-phase data and runs the model in the forward mode, provided reasonable estimation of aerosol acidity for coarse and fine particles. Compared to M0, the M1 mode, which runs the model in the forward mode but does not include gas-phase data, may capture the general trend of aerosol acidity but underestimates pH for both coarse and fine particles; M2, which runs the model in the reverse mode, results in large errors in estimated aerosol pH for both coarse and fine particles and should not be used for aerosol acidity calculations. However, M1 significantly underestimates liquid water contents for both fine and coarse particles, while M2 provides reliable estimation of liquid water contents. In summary, our work highlights the importance of incorporating gas-aerosol partitioning when estimating coarse particle acidity, and thus may help improve our understanding of acidity of coarse particles.
Subject(s)
Aerosols , Air Pollutants , Models, Chemical , Thermodynamics , Aerosols/analysis , Aerosols/chemistry , Air Pollutants/chemistry , Air Pollutants/analysis , China , Environmental Monitoring/methods , Particulate Matter/chemistry , Particulate Matter/analysis , Hydrogen-Ion Concentration , Particle SizeABSTRACT
The anaerobic acid production experiments were conducted with the pretreated kitchen waste under pH adjustment. The results showed that pH 8 was considered to be the most suitable condition for acid production, especially for the formation of acetic acid and propionic acid. The average value of total volatile fatty acid at pH 8 was 8814 mg COD/L, 1.5 times of that under blank condition. The average yield of acetic acid and propionic acid was 3302 mg COD/L and 2891 mg COD/L, respectively. The activities of key functional enzymes such as phosphotransacetylase, acetokinase, oxaloacetate transcarboxylase and succinyl-coA transferase were all enhanced. To further explore the regulatory mechanisms within the system, the distribution of microorganisms at different levels in the fermentation system was obtained by microbial sequencing, results indicating that the relative abundances of Clostridiales, Bacteroidales, Chloroflexi, Clostridium, Bacteroidetes and Propionibacteriales, which were great contributors for the hydrolysis and acidification, increased rapidly at pH 8 compared with the blank group. Besides, the proportion of genes encoding key enzymes was generally increased, which further verified the mechanism of hydrolytic acidification and acetic acid production of organic matter under pH regulation.
Subject(s)
Fatty Acids, Volatile , Hydrogen-Ion Concentration , Fatty Acids, Volatile/metabolism , Fermentation , Acetic Acid/metabolism , BioreactorsABSTRACT
This (in vitro) investigation was conducted to evaluate PH value and antibacterial effect of Alkasite restorative materials against important oral pathogens Streptococcus mutans and lactobacillus plantarum. MATERIAL AND METHODS: Four groups were made of three different type ion releasing materials Cention N= group 1, Primer free Cention Forte=group 2, Primer applied Cention Forte=group 3 and Fuji IX= group 4. A total number of 72 discs in form samples (2 mm height and 5mm diameter) were constructed in polyethylene mold divided according to the evaluating parameters. 32 specimens for PH measurements (n=8) and 40 specimens were utilized for antibacterial effect (n=5) for each bacterial species. The antibacterial properties of groups were assessed by direct contact test. An adjusted diluted broth culture of each bacterium (Streptococcus mutans) and (Lactobacillus plantarum) were prepared. RESULTS: At all intervals of time both Cention N and Primer free Cention Forte has significantly higher PH value in comparison with Fuji IX. Primer applied Cention Forte. There was no significant difference between Cention N, Primer free Cention and Fuji IX in terms of their effect in reducing viable colony count in both bacterial species. CONCLUSION: Along period of (28day) Alkasite material groups (Cention N and Primer free Cention Forte) showed the ability to increase the storage solution PH value. Also, both groups have antibacterial effect against (Streptococcus mutans) and (Lactobacillus plantarum) by inhibiting their numbers. Applying Cention primer showed negative effect on both PH value and the antibacterial effect of the material.
Subject(s)
Anti-Bacterial Agents , Lactobacillus plantarum , Streptococcus mutans , Hydrogen-Ion Concentration , Streptococcus mutans/drug effects , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Humans , Glass Ionomer Cements/pharmacology , Glass Ionomer Cements/chemistry , Dental Materials/pharmacology , Dental Materials/chemistryABSTRACT
Antibiotic residues persist in the environment and represent serious health hazards; thus, it is important to develop sensitive and effective detection techniques. This paper presents a bio-inspired way to make water-soluble fluorescent polymer carbon dots (PCDs@PVA) by heating biomass precursors and polyvinyl alcohol (PVA) together. For example, the synthesized PCDs@PVA are very stable with enhanced emission intensity. This property was observed in a wide range of environmental conditions, including those with changing temperatures, pH levels, UV light, and ionic strength. PCDs@PVA detected the antibiotic chlortetracycline (CTCs) with great selectivity against structurally related compounds and a low detection limit of 20 nM, demonstrating outstanding sensitivity and specificity. We confirmed the sensor's practical application through real sample analysis, yielding recovery rates of 98%-99% in samples of milk, honey, and river water. The synthesized PCDs@PVA fluorescence sensor was successfully used for CTCs detection in real samples.
Subject(s)
Carbon , Chlortetracycline , Fluorescent Dyes , Polyvinyl Alcohol , Quantum Dots , Chlortetracycline/analysis , Polyvinyl Alcohol/chemistry , Carbon/chemistry , Fluorescent Dyes/chemistry , Fluorescent Dyes/chemical synthesis , Quantum Dots/chemistry , Animals , Milk/chemistry , Anti-Bacterial Agents/analysis , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/chemical synthesis , Limit of Detection , Honey/analysis , Polymers/chemistry , Polymers/chemical synthesis , Water Pollutants, Chemical/analysis , Rivers/chemistry , Spectrometry, Fluorescence , Hydrogen-Ion ConcentrationABSTRACT
This study investigated the capability of electromembrane extraction (EME) as a general technique for peptides, by extracting complex pools of peptides comprising in total of 5953 different substances, varying in size from seven to 16 amino acids. Electromembrane extraction was conducted from a sample adjusted to pH 3.0 and utilized a liquid membrane consisting of 2-nitrophenyl octyl ether and carvacrol (1:1 w/w), containing 2% (w/w) di(2-ethylhexyl) phosphate. The acceptor phase was 50 mM phosphoric acid (pH 1.8), the extraction time was 45 min, and 10 V was used. High extraction efficiency, defined as a higher peptide signal in the acceptor than the sample after extraction, was achieved for 3706 different peptides. Extraction efficiencies were predominantly influenced by the hydrophobicity of the peptides and their net charge in the sample. Hydrophobic peptides were extracted with a net charge of +1, while hydrophilic peptides were extracted when the net charge was +2 or higher. A computational model based on machine learning was developed to predict the extractability of peptides based on peptide descriptors, including the grand average of hydropathy index and net charge at pH 3.0 (sample pH). This research shows that EME has general applicability for peptides and represents the first steps toward in silico prediction of extraction efficiency.
Subject(s)
Hydrophobic and Hydrophilic Interactions , Peptides , Peptides/chemistry , Peptides/isolation & purification , Membranes, Artificial , Electrochemical Techniques , Particle Size , Hydrogen-Ion Concentration , Ethers , OrganophosphatesABSTRACT
Groundwater is the main source of water for more than 2 billion people worldwide. In southern Brazil, the Crystalline Basement Aquifer System is composed of strategic groundwater reservoirs. Groundwater is mostly taken from shallow wells, and it is often used without any treatment, which poses a risk to public health. The present study aims to evaluate shallow groundwater quality and the geochemistry of shallow and deep groundwater located in the municipality of Canguçu, southern Brazil. The physicochemical and microbiological parameters of groundwater samples collected from shallow wells were monitored and analyzed using ANOVA variance analysis and water quality index (CCME WQI) approaches. Also, the results were compared with secondary data from deep wells. The monitored shallow wells had thermotolerant coliforms, Escherichia coli, pH, potassium, manganese, iron, and nitrate in disagreement with the guidelines of the World Health Organization. Moreover, variance analysis showed that the parameters temperature, dissolved oxygen, pH, chloride, and magnesium were the most influenced by seasonal variations. According to the CCME WQI, most samples had good quality (60%), 28% had fair quality, and 12% had poor quality. In addition, the field campaigns with higher precipitation rates also presented fair quality. Therefore, most of the shallow groundwater quality is affected by surface pollutants from the urban area, aggravated in rainy periods. Whereas deep groundwater is influenced by geochemistry mechanisms. The results revealed the risk of water consumption for public health and the urgent need for better maintenance of these wells and water treatment implementation.
Subject(s)
Environmental Monitoring , Groundwater , Water Quality , Groundwater/chemistry , Brazil , Environmental Monitoring/methods , Water Pollutants, Chemical/analysis , Hydrogen-Ion Concentration , Water Microbiology , Seasons , Water Wells , Nitrates/analysisABSTRACT
This study assessed the physicochemical and antibiofilm properties of white mineral trioxide aggregate (MTA) associated with 1 or 2% of farnesol. Setting time was evaluated based on ISO 6876/2012. Radiopacity was evaluated by radiographic analysis. pH was assessed after time intervals of 1, 3, 7, 14, 21, and 28 days. Solubility (% mass loss) and volumetric change (by micro-CT) of the cements were evaluated after immersion in distilled water. The presence of voids inside the materials was assessed by using micro-CT. Antibiofilm activity against Enterococcus faecalis was evaluated by crystal violet assay and the modified direct contact test performed with biofilm previously formed on bovine root dentin for 14 days. Data were submitted to ANOVA/Tukey tests with 5% significance level. The incorporation of farnesol into MTA increased its setting time, but decreased its solubility at 30 days and its volumetric loss in all periods (p < 0.05). Radiopacity and solubility after 7 days were similar among the materials (p > 0.05). The association of farnesol showed the highest pH value after 1 and 3 days (p < 0.05). The association of farnesol with MTA promoted a decrease in the presence of voids, and increased the antimicrobial activity on biofilm biomass of E. faecalis (p < 0.05). In conclusion, the addition of farnesol can be suggested to improve the antimicrobial properties and the consistency of MTA.
Subject(s)
Aluminum Compounds , Biofilms , Calcium Compounds , Drug Combinations , Enterococcus faecalis , Farnesol , Materials Testing , Oxides , Root Canal Filling Materials , Silicates , Solubility , Silicates/pharmacology , Silicates/chemistry , Oxides/pharmacology , Oxides/chemistry , Biofilms/drug effects , Calcium Compounds/pharmacology , Calcium Compounds/chemistry , Enterococcus faecalis/drug effects , Aluminum Compounds/pharmacology , Aluminum Compounds/chemistry , Farnesol/pharmacology , Farnesol/chemistry , Hydrogen-Ion Concentration , Time Factors , Cattle , Root Canal Filling Materials/pharmacology , Root Canal Filling Materials/chemistry , Animals , Analysis of Variance , Reproducibility of Results , Dentin/drug effects , Reference Values , Surface Properties/drug effectsABSTRACT
Signal processing by intracellular kinases controls near all biological processes but how signal pathway functions evolve with changed cellular context is poorly understood. Functional specificity of c-Jun N-terminal Kinases (JNK) are partly encoded by signal strength. Here we reveal that intracellular pH (pHi) is a significant component of the JNK network and defines signal response to specific stimuli. We show pHi regulates JNK activity in response to cell stress, with the relationship between pHi and JNK activity dependent on specific stimuli and upstream kinases activated. Using the optogenetic clustering tag CRY2, we show that an increase in pHi promotes the light-induced phase transition of ASK1 to augment JNK activation. While increased pHi similarly promoted CRY2-tagged JNK2 to form light-induced condensates, this attenuated JNK activity. Mathematical modelling of feedback signalling incorporating pHi and differential contributions by ASK1 and JNK2 condensates was sufficient to delineate signal responses to specific stimuli. Taking pHi and ASK1/JNK2 signal contributions into consideration may delineate oncogenic versus tumour suppressive JNK functions and cancer cell drug responses.
Subject(s)
MAP Kinase Kinase Kinase 5 , Hydrogen-Ion Concentration , MAP Kinase Kinase Kinase 5/metabolism , MAP Kinase Kinase Kinase 5/genetics , Humans , Mitogen-Activated Protein Kinase 9/metabolism , Mitogen-Activated Protein Kinase 9/genetics , Stress, Physiological , Signal Transduction , Animals , Optogenetics , MAP Kinase Signaling SystemABSTRACT
In a national park in Northeast Thailand, agricultural land has been converted from natural forest by small-scale farmers for cassava agriculture. We hypothesise that long-termed cassava monoculture leads to the degradation of soil properties. To test the hypothesis, we conducted a five-year (2016-2020) study on the physical and chemical properties of soil in cassava farmland, and also examined the soil properties of its adjacent natural forests, as a control. The examined cassava farmland was converted from the natural forest during the five years from 2011 to 2015. The significant decrease in organic carbon and the increases in exchangeable potassium and bulk density were found in 2016, indicating that these soil properties varied quickly following the farmland conversion. On the other hand, the significant increase in soil nitrogen and the decrease in pH were found later in 2020, indicating that these soil properties were gradually altered by repeated agricultural activities, such as fertilizer application and trampling. In contrast, there were no significant differences in available phosphate, electrical conductivity, cation exchange capacity, and the soil texture (the fractions of sand, silt, and clay) among the forest and farmland soils. The cation exchange capacity was positively correlated to the fraction of clay, the organic carbon, and pH. The use of glyphosate and paraquat herbicides is prohibited within national parks in Thailand. However, in 2020, glyphosate was detected in farmland soil (up to 5.0 mg kg-1) during both the rainy and dry seasons, and glyphosate (up to 2.5 mg l-1) was detected in stream water from the farmland during the dry season at least in 2020. Soil degradation and herbicide pollution may carry a high risk of causing irreversible changes in terrestrial ecosystems. We discuss the root causes of this issue from perspectives of agricultural production, economy, and the environmental impact, and propose effective policy measures.
Subject(s)
Agriculture , Herbicides , Manihot , Soil , Thailand , Manihot/chemistry , Manihot/growth & development , Soil/chemistry , Herbicides/analysis , Soil Pollutants/analysis , Glycine/analogs & derivatives , Glycine/analysis , Farms , Conservation of Natural Resources , Forests , Hydrogen-Ion ConcentrationABSTRACT
Mitochondria-targeted Keima (mt-Keima) is a pH-sensitive, acid-stable fluorescent protein used for the quantification of mitophagy. Mt-Keima contains a mitochondrial matrix targeting sequence and has bimodal excitation with peaks at 440 nM in neutral environments and 586 nM in acidic environments. From this bimodal excitation, a ratiometric signal may be calculated to quantify mitophagy in live cells. This chapter describes procedures for measuring mitophagy by flow cytometry and live cell confocal microscopy with mt-Keima.
Subject(s)
Flow Cytometry , Microscopy, Confocal , Mitochondria , Mitophagy , Humans , Mitochondria/metabolism , Microscopy, Confocal/methods , Flow Cytometry/methods , Luminescent Proteins/metabolism , Luminescent Proteins/genetics , HeLa Cells , Hydrogen-Ion ConcentrationABSTRACT
To increase the efficiency of phytoremediation to clean up heavy metals in soil, assisted with alternating current (AC) electric field technology is a promising choice. Our experiments utilized the hyperaccumulator Sedum alfredii Hance and the fast-growing, high-biomass willow (Salix sp.). We investigated the efficiency of AC field combined with S. alfredii-willow intercropping for removing Cd from soils with different pH values. In the AC electric field treatment with S. alfredii-willow intercropping, the available Cd content in acidic soil increased by 50.00% compared to the control, and in alkaline soil, the increase was 100.00%. Furthermore, AC electric field promoted Cd uptake by plants in both acidic and alkaline soils, with Cd accumulation in the aboveground increased by 20.52% (P < 0.05) and 11.73%, respectively. In conclusion, the integration of AC electric fields with phytoremediation demonstrates significant favorable effectiveness.
Subject(s)
Biodegradation, Environmental , Cadmium , Electricity , Sedum , Soil Pollutants , Soil , Cadmium/metabolism , Soil Pollutants/metabolism , Hydrogen-Ion Concentration , Sedum/metabolism , Sedum/growth & development , Soil/chemistry , Salix/metabolismABSTRACT
Information on the physical compatibility of intravenous (IV) medications is vital for patient care and safety in acute care settings. Drug information resources list ondansetron and nafcillin as IV compatible, however, bolus concentrations of ondansetron are not reported. This study investigated the in vitro physical compatibility of bolus and infusion concentrations of ondansetron hydrochloride with nafcillin sodium. Two admixtures were prepared: 1) ondansetron hydrochloride 2 mg/mL and nafcillin sodium 20 mg/mL, and 2) ondansetron hydrochloride 0.16 mg/mL and nafcillin sodium 20 mg/mL. The admixtures were prepared in triplicate using aseptic technique according to manufacturer guidance and stored at room temperature (22-23 °C) for up to 24 hours. Admixtures were examined for visual precipitation, turbidity, and pH at baseline and at 1, 5, 8, and 24 hours. Admixture 1 developed a haze immediately after mixing, which was sustained over 24 hours. There was a demonstrative change in absorbance after 1 hour, but pH remained stable until hour 24. Admixture 2 developed a haze at 5 hours, but the absorbance and pH remained stable until hour 24; a decrease in the pH was observed in all samples at hour 24. This in vitro study revealed that ondansetron hydrochloride 2 mg/mL and nafcillin sodium 20 mg/mL are not physically compatible when administered through the same IV line. No demonstrative change was observed with ondansetron hydrochloride 0.16 mg/mL and nafcillin sodium 20 mg/mL; however, concurrent administration of these medications is questionable when delivered through an IV line for periods of five hours or longer.
Subject(s)
Drug Incompatibility , Nafcillin , Ondansetron , Ondansetron/administration & dosage , Ondansetron/chemistry , Nafcillin/administration & dosage , Nafcillin/chemistry , Infusions, Intravenous , Administration, Intravenous , Drug Stability , Hydrogen-Ion Concentration , Antiemetics/administration & dosage , Antiemetics/chemistry , Injections, IntravenousABSTRACT
A novel Pseudochrobactrum saccharolyticum strain NBRI-CRB 13, isolated from tannery sludge, was studied to grow up to 500 mgL-1 of Cr(VI) and showed Cr(VI) detoxification by reducing > 90% of Cr(VI) at different concentrations 25, 50 and 100 mgL-1. Kinetic studies showed that first-order models were fitted (R2 = 0.998) to the time-dependent Cr(VI) reduction with degradation rate constant (k) (1.03-0.429 h-1). Cr(VI) detoxification was primarily related to the extracellular fraction of microbial cells, which showed a maximum extracellular reductase enzyme activity led to 94.6% reduction of Cr(VI). Moreover, the strain showed maximum extracellular polymeric substances (EPS) production at 100 mgL-1 Cr(VI), which is presumably the reason for Cr(VI) removal as EPS serves as the metal binding site for Cr(VI) ions. Further, an optimization study using Box-Behnken design was conducted considering parameters viz., pH, temperature, and initial concentration of Cr(VI). The maximum percent reduction of Cr(VI) was obtained at pH 6.5, temperature 30 °C with 62.5 mgL-1Cr(VI) concentration. Further, the Cr(VI) reduction and adsorption ability of strain P. saccharolyticum NBRI-CRB13 were confirmed by SEM-EDS, FTIR, and XRD analyses. FTIR analysis confirmed the presence of functional groups (-OH, -COOH, -PO4) on bacterial cell walls, which were more likely to interact with positively charged chromium ions. The study elucidated the reduction of Cr(VI) by the novel bacterium within 24 h using the response surface methodology approach and advocated its application in real-time situations.
Subject(s)
Biodegradation, Environmental , Chromium , Sewage , Chromium/metabolism , Kinetics , Sewage/microbiology , Hydrogen-Ion Concentration , Temperature , Extracellular Polymeric Substance Matrix/metabolism , Burkholderiaceae/metabolism , Burkholderiaceae/isolation & purification , Burkholderiaceae/genetics , Oxidation-ReductionABSTRACT
Oligomeric species arising during the aggregation of α-synuclein are implicated as a major source of toxicity in Parkinson's disease, and thus a major potential drug target. However, both their mechanism of formation and role in aggregation are largely unresolved. Here we show that, at physiological pH and in the absence of lipid membranes, α-synuclein aggregates form by secondary nucleation, rather than simple primary nucleation, and that this process is enhanced by agitation. Moreover, using a combination of single molecule and bulk level techniques, we identify secondary nucleation on the surfaces of existing fibrils, rather than formation directly from monomers, as the dominant source of oligomers. Our results highlight secondary nucleation as not only the key source of oligomers, but also the main mechanism of aggregate formation, and show that these processes take place under conditions which recapitulate the neutral pH and ionic strength of the cytosol.
Subject(s)
alpha-Synuclein , alpha-Synuclein/chemistry , alpha-Synuclein/metabolism , Hydrogen-Ion Concentration , Humans , Protein Multimerization , Protein Aggregates , Osmolar Concentration , Parkinson Disease/metabolismABSTRACT
Dental caries is a worldwide public healthcare concern, and is closely related to the acidic environment that caused by bacterial decomposition of food. In this study, a two-step ion exchange liquid-phase stripping method was applied to strip out vermiculite (VMT) nanosheets, then amorphous calcium phosphate (ACP) and dextran were inserted between the VMT nanosheets interlayer to obtain a composite two-dimension nanosheets (VMT/ACP/Dextran). VMT/ACP/Dextran composite nanosheets exhibited excellent biocompatibility and could provide exogenous Ca2+and PO43- from ACP, provide SiO44-, Mg2+, Fe2+ and obtain buffering pH and antibacterial properties from VMT, as well as improve suspension stability and targeting Streptococcus mutans through glucan. The in vitro study showed that the composite materials could promote the mineralization and sealing of dentin tubules by releasing active ions, buffer pH 4.5 (a value close to the pH in the dental plaque environment) to pH 6.6-7.1 (values close to the pH in human saliva) through ion exchange, and exert antibacterial effects by targeting Streptococcus mutans and exerting oxidase like and peroxidase like activities to produce reactive oxygen species (ROS). The in vivo animal study showed that daily cleaning teeth using VMT/ACP/Dextran composite nanosheets could effectively reduce the incidence rate and severity of dental caries in rats. Taking together, the developed VMT/ACP/Dextran composite nanosheets, which integrated the excellent properties of VMT, ACP and dextran, can effectively prevent dental caries through a combination of factors such as buffering acids, antibacterial properties, and promoting calcification, and may be used as an active ingredient for daily oral hygiene or filling materials to prevent and treat dental caries.
Subject(s)
Anti-Bacterial Agents , Calcium Phosphates , Dental Caries , Dentin , Dextrans , Streptococcus mutans , Dental Caries/prevention & control , Dental Caries/microbiology , Dextrans/chemistry , Dextrans/pharmacology , Animals , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Hydrogen-Ion Concentration , Calcium Phosphates/chemistry , Calcium Phosphates/pharmacology , Streptococcus mutans/drug effects , Dentin/chemistry , Dentin/drug effects , Rats , Nanostructures/chemistry , Humans , Male , Rats, Sprague-Dawley , Reactive Oxygen Species/metabolismABSTRACT
A modified carbon paste sensor based on N,N'-(((ethane-1,2-diylbis(oxy))bis(2,1-phenylene))bis(methanylylidene))bis(pyridine-2-amine; BPA Schiff base as Cr(III) selective carrier was fabricated and studied in this work. The proposed sensor homogenization and mechanism of action was studied by infra-red (IR) and scanning electron microscope (SEM) with energy dispersive X-ray (EDX) tools. The sensor covered 1.0 × 10-7-1.0 × 10-1 mol L-1 linear range and a detection limit of 7.22 × 10-8 mol L-1 for Cr(III) with 20.17 ± 0.13 mV decade-1 Nernstian slope. 5 s was the response time of the prepared sensor and it was reproducible and stable for 3 months. The working pH range was 3.3-6.0 and it also works well to determine Cr(III) ion in presence of water miscible solvents up to 12.5% content of the methanol and 17.5% of ethanol. The electrode's selectivity was studied using separate and mixed solution methods for selectivity coefficients determination and the sensor showed good selectivity relative to a variety of metal ions (selectivity coefficients = 1.01 × 10-5-8.57 × 10-3). In addition, the practical analysis value of the sensor was demonstrated by measurement of Cr(III) quantitatively in mineral water, supplement and also as an indicator electrode in Cr(III) against EDTA potentiometric titration with good reproducibility (RSDs of 0.91-2.15%).
Subject(s)
Carbon , Chromium , Chromium/analysis , Chromium/chemistry , Carbon/chemistry , Water/chemistry , Dietary Supplements/analysis , Schiff Bases/chemistry , Limit of Detection , Hydrogen-Ion Concentration , Water Pollutants, Chemical/analysis , Electrodes , Reproducibility of Results , Ions/analysis , Electrochemical Techniques/methodsABSTRACT
OBJECTIVE: To evaluate the impact of diaper change frequency, clinical characteristics, and skin health metrics on development of the skin microbiota in preterm infants. DESIGN: A randomized controlled parallel design was used. METHODS: Medically stable preterm infants born <33 weeks' gestation were randomized to receive diaper changes at a frequency of every 3-hours or every 6-hours. Skin swabs were collected longitudinally from the diapered skin (buttocks) and chest. Skin pH and transepidermal water loss were measured with each sample collection. Stool samples were collected from the diaper. The microbiome at each site was characterized by 16S rRNA gene sequencing. Associations between microbiome features, diaper change frequency, and other covariates were examined using mixed effect models and redundancy analysis. RESULTS: A total of 1179 samples were collected from 46 preterm infants, beginning at a median postnatal age of 44 days and continuing through hospital discharge. Alpha-diversity of the skin microbiota increased over time, but did not differ significantly between 3-hour (n = 20) and 6-hour (n = 26) diaper change groups. Alpha-diversity of the skin microbiota was inversely correlated with skin pH, but not transepidermal water loss. Microbiota community structure differed significantly between body sites (buttocks, chest, and stool) and between individuals. Among samples collected from the diapered skin, diaper change frequency, infant diet, antibiotic exposure, and delivery mode accounted for minor proportions of the variation in microbiota community structure between samples. Relative abundances of multiple genera differed between 3- and 6-hour diaper change groups over time. DISCUSSION/CONCLUSION: The diversity and composition of the diapered skin microbiota is dynamic over time and differs from other body sites. Multiple factors including interindividual effects, diaper change frequency, diet, and antibiotics contribute to variation in the diapered skin microbiota.
Subject(s)
Diapers, Infant , Infant, Premature , Microbiota , Skin , Humans , Infant, Newborn , Skin/microbiology , Female , Male , Feces/microbiology , Hydrogen-Ion Concentration , RNA, Ribosomal, 16S/genetics , Water Loss, InsensibleABSTRACT
BACKGROUND: Disruptions in intracellular pH (pHi) homeostasis, causing deviations from the physiological range, can damage renal epithelial cells. However, the existence of an adaptive mechanism to restore pHi to normalcy remains unclear. Early research identified H+ as a critical mediator of ischemic preconditioning (IPC), leading to the concept of acidic preconditioning (AP). This concept proposes that short-term, repetitive acidic stimulation can enhance a cell's capacity to withstand subsequent adverse stress. While AP has demonstrated protective effects in various ischemia-reperfusion (I/R) injury models, its application in kidney injury remains largely unexplored. METHODS: An AP model was established in human kidney (HK2) cells by treating them with an acidic medium for 12 h, followed by a recovery period with a normal medium for 6 h. To induce hypoxia/reoxygenation (H/R) injury, HK2 cells were subjected to hypoxia for 24 h and reoxygenation for 1 h. In vivo, a mouse model of IPC was established by clamping the bilateral renal pedicles for 15 min, followed by reperfusion for 4 days. Conversely, the I/R model involved clamping the bilateral renal pedicles for 35 min and reperfusion for 24 h. Western blotting was employed to evaluate the expression levels of cleaved caspase 3, cleaved caspase 9, NHE1, KIM1, FAK, and NOX4. A pH-sensitive fluorescent probe was used to measure pHi, while a Hemin/CNF microelectrode monitored kidney tissue pH. Immunofluorescence staining was performed to visualize the localization of NHE1, NOX4, and FAK, along with the actin cytoskeleton structure in HK2 cells. Cell adhesion and scratch assays were conducted to assess cell motility. RESULTS: Our findings demonstrated that AP could effectively mitigate H/R injury in HK2 cells. This protective effect and the maintenance of pHi homeostasis by AP involved the upregulation of Na+/H+ exchanger 1 (NHE1) expression and activity. The activity of NHE1 was regulated by dynamic changes in pHi-dependent phosphorylation of Focal Adhesion Kinase (FAK) at Y397. This process was associated with NOX4-mediated reactive oxygen species (ROS) production. Furthermore, AP induced the co-localization of FAK, NOX4, and NHE1 in focal adhesions, promoting cytoskeletal remodeling and enhancing cell adhesion and migration capabilities. CONCLUSIONS: This study provides compelling evidence that AP maintains pHi homeostasis and promotes cytoskeletal remodeling through FAK/NOX4/NHE1 signaling. This signaling pathway ultimately contributes to alleviated H/R injury in HK2 cells.
Subject(s)
Reperfusion Injury , Sodium-Hydrogen Exchanger 1 , Humans , Animals , Sodium-Hydrogen Exchanger 1/metabolism , Sodium-Hydrogen Exchanger 1/genetics , Phosphorylation , Hydrogen-Ion Concentration , Reperfusion Injury/metabolism , Reperfusion Injury/pathology , Mice , Male , Ischemic Preconditioning , Cell Line , Kidney/metabolism , Kidney/pathology , Mice, Inbred C57BL , Focal Adhesion Protein-Tyrosine Kinases/metabolism , Acids/metabolism , NADPH Oxidase 4/metabolism , NADPH Oxidase 4/genetics , Reactive Oxygen Species/metabolismABSTRACT
Fluoroquinolone antibiotics have been extensively used in clinical treatments for human and animal diseases. However, their long-term presence in the environment increases the risk of producing resistance genes and creates a potential threat to ecosystems and the health of humans and animals. Batch equilibrium experiments were utilized to investigate the adsorption and retention behavior and mechanism of the quinolone antibiotic enrofloxacin (ENR) in farmland soil in North China. The adsorption and desorption kinetics of ENR in soil were best fitted by pseudo-second-order model (R2 > 0.999). Both the adsorption and desorption processes of ENR in soil reached equilibrium in 1 h. The desorption amounts of ENR were significantly lower than the adsorption amounts, with the hysteresis coefficient (HI) being less than 0.7. The adsorption thermodynamic process of ENR followed the Linear and Freundlich models (0.965 < R2 < 0.985). Hydrophobic distribution and heterogeneous multimolecular layer adsorption were identified as critical factors in the adsorption process. The adsorption amount of ENR gradually decreased with increasing temperature and the initial concentration of ENR. The adsorption rate of ENR was above 80%, while the desorption rate remained below 15%, indicating strong retention ability. The adsorption rate of ENR in soil decreased with increasing pH, the adsorption rate reached 98.3% at pH 3.0 but only 31.5% at pH 11. The influence of coexisting ions on adsorption primarily depended on their properties, such as ion radius, ionic strength, and hydrolysis properties, and the inhibition of adsorption increased with increasing ionic strength. These findings contribute to understanding the fate and risk of veterinary antibiotics in loess soil in North China.