ABSTRACT
Reperfusion following cerebral ischemia causes both structural and functional damage to brain tissue and could aggravate a patient's condition; this phenomenon is known as cerebral ischemia-reperfusion injury. Current studies have elucidated the neuroprotective role of the sirtuin protein family (Sirtuins) in modulating cerebral ischemia-reperfusion injury. However, the potential of utilizing it as a novel intervention target to influence the prognosis of cerebral ischemia-reperfusion injury requires additional exploration. In this review, the origin and research progress of Sirtuins are summarized, suggesting the involvement of Sirtuins in diverse mechanisms that affect cerebral ischemia-reperfusion injury, including inflammation, oxidative stress, blood-brain barrier damage, apoptosis, pyroptosis, and autophagy. The therapeutic avenues related to Sirtuins that may improve the prognosis of cerebral ischemia-reperfusion injury were also investigated by modulating Sirtuins expression and affecting representative pathways, such as nuclear factor-kappa B signaling, oxidative stress mediated by adenosine monophosphate-activated protein kinase, and the forkhead box O. This review also summarizes the potential of endogenous substances, such as RNA and hormones, drugs, dietary supplements, and emerging therapies that regulate Sirtuins expression. This review also reveals that regulating Sirtuins mitigates cerebral ischemia-reperfusion injury when combined with other risk factors. While Sirtuins show promise as a potential target for the treatment of cerebral ischemia-reperfusion injury, most recent studies are based on rodent models with circadian rhythms that are distinct from those of humans, potentially influencing the efficacy of Sirtuins-targeting drug therapies. Overall, this review provides new insights into the role of Sirtuins in the pathology and treatment of cerebral ischemia-reperfusion injury.
ABSTRACT
Fluorinated liquid-crystal monomers (FLCMs), a new class of potential persistent, bioaccumulative and toxic (PBT) emerging pollutants, are extensively utilized in the display panel of various electronic devices. These compounds have been found in various environmental matrixes and dietary. Our previous studies have documented their ubiquitous occurrence in high fat foodstuffs. Infants, a vulnerable group, are more susceptible to the impacts of these pollutants compared to adults. Herein, we provided an assessment of the health risks posed by FLCMs to infants, focusing on their exposure through infant formula. The presence of FLCMs was detected in all infant formulas, with median concentration of 16.5 ng/g dry weight (dw) and the 95th percentile concentration of 65.7 ng/g dw. The most prevalent pollutant in these formulas was 2-fluoro-4-[4'-propyl-1,1'-bi(cyclohexyl)-4-yl] phenyl trifluoromethyl ether (FPrBP), with median and a 95th percentile concentration of 12.2 ng/g dw and 23.8 ng/g dw, accounting for 55.2% to the total FLCMs. Infants aged 0-6 months had the highest estimated daily intakes (EDIs) of FLCMs, with the EDImedian of 267 ng/kg bw/day. FPrBP and 4-[trans-4-(trans-4-Propylcyclohexyl) cyclohexyl]-1-trifluoromethoxybenzene (PCTB) together made up 83.3% of the total EDIs in median exposure scenario of 0-6 months infant. The highest EDI value was 1.30 × 103 ng/kg bw/day, 77.1% of which was attributed to a combination of FPrBP, 4â³-ethyl-2'-fluoro-4-propyl-1,1':4',1â³-terphenyl (EFPT), 2-[4'-[difluoro(3,4,5-trifluoro-2-methyl-phenoxy)methyl]-3',5'-difluoro-[1,1'-biphenyl]-4-yl]-5-ethyl-tetrahydro-pyran (DTMPMDP), 4-[Difluoro-(3,4,5-trifluoro-2-methyl-phenoxy)-methyl]-3,5-difluoro-4'-propyl-1,1-biphenyl (DTMPMDB), 2,3-difluoro-1-methyl-4-[(trans, trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]benzene (DMPBB) and PCTB. It's worth noting that FLCMs have higher exposure risk. Based on the threshold of toxicological concern (TTC) method, the EDImedian of FPrBP (183 ng/kg bw/day) and FPCB (3.27 ng/kg bw/day) were beyond their TTC values (2.5 ng/kg bw/day) in 0-6 months infant, implying their prospective health risk.
ABSTRACT
Jarosite [MeFe3(SO4)2(OH)6] is a typical non-ferrous smelting slag produced in the process of iron removal from hydrometallurgical solution, which contains a large number of valuable and toxic metal elements. Treating the complex and hazardous jarosite residue in an economically and environmentally sound way has always been an urgent problem. A novel one-step hydrothermal treatment method was proposed in this paper for recycling of jarosite residues. It can be seen from the XRD and TEM results that jarosite residues could be completely transformed into hematite crystal particles under hydrothermal conditions at temperature above 220â. Meanwhile, other valuable metal components (such as nickel sulfate hexahydrate) entrained in the residue will be dissolved in the aqueous solution, which can be reused in the hydrometallurgical process. Through phase composition analysis of the hydrothermal process, it is concluded that jarosite was firstly pyrolyzed to generate Fe3+. The obtained Fe3+ was then hydrolyzed to Fe (OH)3, which was transformed into Fe2O3 through dehydration condensation and directional arrangement. Further roasting the hematite particles, the obtained product contained 62.57 % of Fe, but only 0.21 % of S and 0.04 % of As, which meets the requirements of raw materials for iron making. In addition, compared with the current international standard ISO 1248:2006 (E), the obtained hematite particles with nanometer size and single crystal structure can be used as iron oxide red pigment. Overall, the one-step hydrothermal treatment of jarosite residues followed by reduction roasting not only realizes the economic recycling of the metal resources, but also solves the stacking problem of those hazardous residues.
Subject(s)
Ferric Compounds , Sulfates , Ferric Compounds/chemistry , Sulfates/chemistry , Iron/chemistry , MetalsABSTRACT
We developed a highly sensitive fluorescent assay to detect okadaic acid (OA), a prevalent aquatic toxin posing serious health risks. Our approach uses a mismatched duplexed aptamer (DA) immobilized on streptavidin-conjugated magnetic beads (SMBs) to create a DA@SMB complex. In the presence of OA, the cDNA unwinds, hybridizes with a G-rich segment pre-encoding circular template (CT), and undergoes rolling circle amplification (RCA) to produce G-quadruplexes, which are detected using the fluorescent dye thioflavine T (ThT). The method has a LOD of 3.1 × 10-3 ng/mL, a linear range of 0.1 â¼ 1.0 × 103 ng/mL, and was successfully applied to shellfish samples with spiked recoveries of 85.9% â¼ 102.2% and RSD less than 13%. Furthermore, instrumental analysis confirmed the accuracy and reliability of this rapid detection method. Overall, this work represents a significant advancement in the field of rapid aquatic toxin detection and has important implications for public health and safety.
Subject(s)
Aptamers, Nucleotide , Biosensing Techniques , Nucleic Acids , Okadaic Acid , Reproducibility of Results , Nucleic Acid Amplification Techniques/methods , Oligonucleotides , Fluorescent Dyes , Biosensing Techniques/methods , Aptamers, Nucleotide/genetics , Limit of DetectionABSTRACT
Background: The estimated global latent tuberculosis infection (LTBI) burden indicates a large reservoir of population at risk of developing active tuberculosis (TB). Previous studies suggested diabetes mellitus (DM) might associate with LTBI, though still controversial. We aimed to systematically assess the association between DM and LTBI. Methods: We searched PubMed, Embase, Cochrane Library and Web of Science. Observational studies reporting the number of LTBI and non-LTBI individuals with and without DM were included. Random-effects or fixed-effects models were used to estimate the pooled effect by risk ratios (RRs) and odds ratios (ORs) and its 95% confidence interval (CI), using the original number of participants involved. Results: 20 studies involving 4,055,082 participants were included. The pooled effect showed a significant association between DM and LTBI (for cohort studies, RR = 1.62, 95% CI: 1.02-2.56; for cross-sectional studies, OR = 1.55, 95% CI: 1.30-1.84). The pooled OR was high in studies with healthcare workers (5.27, 95% CI: 1.52-8.20), refugees (2.88, 95% CI: 1.93-4.29), sample size of 1,000-5,000 (1.99, 95% CI: 1.49-2.66), and male participants accounted for less than 40% (2.28, 95% CI: 1.28-4.06). Prediabetes also associated with LTBI (OR = 1.36, 95% CI: 1.01-1.84). Conclusion: The risk of LTBI was found to be a 60% increase in DM patients, compared with non-DM patients. LTBI screening among DM patients could be of vital importance. More studies are needed to explore appropriate strategies for targeted LTBI screening among DM patients.
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Retarders are important factors controlling the hydration and properties of magnesium potassium phosphate cements (MKPCs). Boric acid and borax are the most commonly used retarders for MKPC which could control the setting time in a wide range upon changing their content. However, with the increase in borax content, the early strength of MKPC can be reduced, and boron compounds are now included in the EU candidate list of substances of very high concern for authorization, due to their reproductive toxicity. Exploring alternative set retarders to boron compounds is, thus, of significance. This work investigated the effects of a candidate retarder, namely, sodium alginate, on the setting time, mechanical properties, hydration products, and microstructures of MKPC. Sodium alginate presented dramatically retarding effects on MKPCs in the range of 0% to 2% (by mass of water). One percent of sodium alginate by mass of water could extend the setting time of MKPCs from 15 min to 35 min, which presented a better retarding effect than borax (a typical retarder for MKPCs) and produced higher early strength of MKPCs. Adding no more than 1% of sodium alginate did not have a notably adverse effect on the formation of hydration product over the long term, but an unfavorable effect could be found regardless of the sodium alginate content, which could reduce the compressive strength of MKPCs.
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About 60 million tons of Fe-rich Cu slag (IRCS) are generated annually worldwide during Cu slag flotation and cause irreversible water and soil pollution. Current research provides an environmentally friendly technology, the preparation of internal electrolysis materials (IEMs) through the carbothermal reduction of IRCS, for the degradation of printing and dyeing wastewater. XRD and SEM-EDS indicated that carbothermal reduction could promote the conversion of fayalite to zero-valent iron (ZVI), and ZVI could effectively form IEM with residual carbon. The degradation capacity of IEM for methylene blue (MB) was remarkably improved compared with raw IRCS after roasting for 60 min at 1100 °C with 35% anthracite dosage. MB degradation efficiency improved by increasing the IEM dosage and reaction temperature and decreasing the MB concentration and solution pH. FTIR, XRD, SEM-EDS, and XPS all detected the formation of Fe oxide or Fe hydroxide. UV-vis and TOC demonstrated that the characteristic groups of MB were destroyed and resulted in the mineralization of MB. MB degradation could be attributed to the Fe2+, [H], and ·OH produced by the galvanic reaction induced by IEM. Overall, this study offers theoretical guidance in the treatment of printing and dyeing wastewater and the reuse of IRCS.
Subject(s)
Wastewater , Water Pollutants, Chemical , Coloring Agents , Electrolysis , Water Pollutants, Chemical/analysisABSTRACT
This work studied the effect of the nano-oxides, such as Nano-Fe2O3 (NF), Nano-Al2O3 (NA), Nano-MgO (NM), and Nano-SiO2 (NS), on the workability and mechanical properties of quick-setting grouting materials serviced in the underground environment. The results show that 2.0% NS could remarkably shorten the setting time of the grouting materials by 29.16%, compared to the control one (without nano-oxides), and the final setting time was shortened by 46.51%. The results also show that 2.0% NS could decrease the initial fluidity of the grouting material by 41.09%, compared to the control one, and the 30 min fluidity was decreased by 48.93%. The XRD results show that NF, NM, and NS contribute to a higher quantity of AFt than that NA. Moreover, grouting material doped with NF, NM, and NS produces more needle-like ettringite, leading to a more compact structure.
ABSTRACT
Sulfur mustard (SM) is a notorious blistering chemical warfare agent. Rapid field screening for trace SM is of vital significance for the detection of antiterrorism and timely treatment. Here, a visual assay for SM was constructed on the basis of its inhibition for the G-quadruplexes/hemin DNAzyme. Specifically, multiple guanine (G)-rich single stranded oligonucleotides (ssODN) named S1 (80% of G in the total bases), i.e., the precursor for G-quadruplex, which could oxide tetramethylbenzidine (TMB) to its green product, were conjugated on the nonfouling polymer brush grafted magnetic beads (MB@P(C-H)). SM could specifically alkylate the N7 and O6 sites of G in the S1; thus, it failed to form the DNAzyme based signal reporter. It was demonstrated that the nonfouling P(C-H) interface on the magnetic bead (MB) could protect the conjugated ssODN from nuclease degradation, thus ensuring its well sensing performance in complex samples. Under the optimized conditions, this method achieved good sensitivity and selectivity with a limit of detection (LOD) as low as 0.26 µmol L-1, and the recoveries ranging from 86% to 117% were obtained for different SM spiked real samples. Above all, this method combining low cost and ready operation could be suited for rapid field SM screening in a wide range of environmental matrices.
Subject(s)
DNA, Catalytic , G-Quadruplexes , Mustard Gas , Hemin , Mustard Gas/toxicity , ResearchABSTRACT
Importance: Asymptomatic infections are potential sources of transmission for COVID-19. Objective: To evaluate the percentage of asymptomatic infections among individuals undergoing testing (tested population) and those with confirmed COVID-19 (confirmed population). Data Sources: PubMed, EMBASE, and ScienceDirect were searched on February 4, 2021. Study Selection: Cross-sectional studies, cohort studies, case series studies, and case series on transmission reporting the number of asymptomatic infections among the tested and confirmed COVID-19 populations that were published in Chinese or English were included. Data Extraction and Synthesis: This meta-analysis was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guideline. Random-effects models were used to estimate the pooled percentage and its 95% CI. Three researchers performed the data extraction independently. Main Outcomes and Measures: The percentage of asymptomatic infections among the tested and confirmed populations. Results: Ninety-five unique eligible studies were included, covering 29â¯776â¯306 individuals undergoing testing. The pooled percentage of asymptomatic infections among the tested population was 0.25% (95% CI, 0.23%-0.27%), which was higher in nursing home residents or staff (4.52% [95% CI, 4.15%-4.89%]), air or cruise travelers (2.02% [95% CI, 1.66%-2.38%]), and pregnant women (2.34% [95% CI, 1.89%-2.78%]). The pooled percentage of asymptomatic infections among the confirmed population was 40.50% (95% CI, 33.50%-47.50%), which was higher in pregnant women (54.11% [95% CI, 39.16%-69.05%]), air or cruise travelers (52.91% [95% CI, 36.08%-69.73%]), and nursing home residents or staff (47.53% [95% CI, 36.36%-58.70%]). Conclusions and Relevance: In this meta-analysis of the percentage of asymptomatic SARS-CoV-2 infections among populations tested for and with confirmed COVID-19, the pooled percentage of asymptomatic infections was 0.25% among the tested population and 40.50% among the confirmed population. The high percentage of asymptomatic infections highlights the potential transmission risk of asymptomatic infections in communities.
Subject(s)
Asymptomatic Infections/epidemiology , COVID-19/epidemiology , SARS-CoV-2 , Adolescent , Adult , Aged , COVID-19/transmission , COVID-19/virology , COVID-19 Testing , Child , Female , Global Health , Humans , Male , Middle Aged , Pregnancy , PrevalenceABSTRACT
The Qinling Mountain is a natural boundary between warm temperate zone and subtropical zone. While the China Forest Biodiversity Monitoring Network (CForBio) have basically covered most of the climate regions in China, few plots were located in the climate transition zone. Following the field protocol of CForBio and the Center for Tropical Forest Science (CTFS), a 25 hm2(500 m×500 m) forest plot was established in Huangguan Nature Reserve in Shaanxi Province, China, in 2019. In this study, we analyzed species composition, flora characteristics, diameter class structure, and spatial distribution patterns of dominant tree species based on the data of all woody species with a diameter at breast height (DBH) ≥1 cm. The results showed that there were 75137 woody individuals with DBH ≥1 cm in the plot (95679 when including branching individuals), belonging to 121 species, 83 genera and 44 families. The flora type at the genera level was mainly temperate, accounting for 71.1% of the total genera, and mixed with some tropical components. The dominant species in the community were obvious, with the number of individuals in the top 5 species exceeding 40% of the total number of individuals, the number of individuals in the top 50 species accounting for 95% of the total number of individuals, and the number of individuals in the remaining 61 species being less than 5% of the total. The diameter distribution of all woody indivi-duals in the plot was inverted 'J' type. Spatial distribution patterns varied across the four most abundant species with importance value >5. The degree of aggregation within species decreased with the increases of scales, while the spatial distribution of different species was affected by environmental heterogeneity. Warm-temperate deciduous broadleaved forest in Qinling Mountains had abundant species, stable community structure and good regeneration, reflecting the typical characteristics of the transition from warm temperate zone to subtropical zone. Environmental heterogeneity might be an important factor affecting the spatial distribution of tree species in the plot.
Subject(s)
Forests , Trees , Biodiversity , China , Humans , WoodABSTRACT
Rapid screening monofluoroacetic acid (FAcOH) is responsible for preventing chemical poisoning and food safety events. Whereas surface enhanced Raman scattering (SERS) spectra is an effective tool for detecting forbidden chemicals, it is difficult to directly detect FAcOH due to its small Raman scattering cross section as well as weak adsorption on SERS substrates. In this work, the metal phenolic supramolecular networks (MPNs, i.e., the tannic acid and Fe3+ complex) were fabricated on the commercial nanoanodic aluminum oxide film (NAAO) for assisting in situ chemical deposition highly uniform Ag nanostructure over large areas (the NAAO@AgNS). The low cost and simple fabrication process made the NAAO@AgNS a single-use consumable. For FAcOH detection, a specific derivative reaction between FAcOH and thiosalicylic acid (TSA) was introduced. By taking TSA as the Raman probe, its SERS signal attenuated constantly with the increasing amount of FAcOH. For improving quantitative accuracy, thiocyanate (SCN-) was introduced on the NAAO@AgNS as an internal standard; thus, the characteristic peak intensity ratios associated with TSA and SCN- (I1035/I2125) were fitted to the concentration of FAcOH. It was demonstrated that the SERS assay achieved good sensitivity and selection toward FAcOH with the limit of quantitation (LOD) as low as 50 nmol L-1. The NAAO@AgNS featured with highly sensitive, uniform, and consistent SERS performances could easily extend to wide SERS applications.
Subject(s)
Nanostructures , Silver , Aluminum Oxide , FluoroacetatesABSTRACT
In the work, we employed a hydrothermal method for modification of red mud using colloidal silica and sodium hydroxide under mild conditions, and applied it into adsorbing Pb(II) ions in aqueous solutions. In the modification, zeolite structure was formed. The adsorption experiments found that the adsorption capacity of the modified red mud for Pb(II) ions was significantly improved, almost 10 times as much as that of the original red mud. Both the pseudo-first-order and pseudo-second-order kinetic equation can describe the adsorption process, indicating it a more complicated interaction. Langmuir and Dubinin-Radushkevich models well fit the adsorption isotherm, indicating that the modified red mud mainly removes lead ions from aqueous solution by monolayer physical adsorption. According to the fitting results, the saturated adsorption capacity of Pb (II) by the modified red mud is 551.11 mg/g, confirming its high efficiency adsorption performance. XRD, FTIR, XPS and SEM-EDS all detected the formation of PbCO3 and Pb3(CO3)2(OH)2. It was speculated that the adsorption mechanism should be attributed to the joint contribution of ion exchange and precipitation. The excellent performance of the modified red mud on Pb(II) ions adsorption makes it a promising candidate for the treatment of wastewater contaminated by heavy metal ions.
ABSTRACT
This paper aims to provide new insight into a method to improve the chloride ion corrosion resistance of steel fiber reinforced concrete. The steel fiber was pretreated by zinc phosphate before the preparation of the fiber reinforced concrete. Interfacial bond strength, micro-hardness and micro-morphology properties were respectively analyzed in the steel fiber reinforced concrete before and after the chloride corrosion cycle test. The results show that the chloride ion corrosion resistance of the steel fiber was enhanced by zinc phosphate treatment. Compared to plain steel fiber reinforced concrete under chloride ion corrosion, the interfacial bond strength of the concrete prepared by steel fiber with phosphating treatment increased by 15.4%. The thickness of the interface layer between the pretreated steel fiber and cement matrix was reduced by 50%. The micro-hardness of the weakest point in the interface area increased by 54.2%. The micro-morphology of the interface area was almost unchanged before and after the corrosion. The steel fiber reinforced concrete modified by zinc phosphate can not only maintain the stability of the microstructure when corroded by chloride ion but also presents good bearing capacity.
ABSTRACT
Three rare-earth orthoborates Ba2MgY2(BO3)4, Ba2CdY2(BO3)4, and Ba2CdSc(BO3)3 were synthesized via a high-temperature solution method and their structures were determined by single crystal X-ray diffraction for the first time. Ba2MgY2(BO3)4 and Ba2CdY2(BO3)4 are isostructural and both crystallize in the monoclinic crystal system, P21/c, while Ba2CdSc(BO3)3 crystallizes in the triclinic crystal system, P1[combining macron]. The structures of Ba2MgY2(BO3)4 and Ba2CdY2(BO3)4 can be described as the three-dimensional (3D) frameworks composed of MO5 (M = Mg, Cd), YOn (n = 6, 7) polyhedra with isolated BO3 and Ba2+ cations residing in the space of the frameworks. The structure of Ba2CdSc(BO3)3 is composed of 2D [CdSc(BO3)3]∞ layers separated by Ba2+ cations. In addition, structural comparisons, thermal behaviors, UV-vis-NIR diffuse reflectance spectra, and infrared spectroscopy results are also reported.
ABSTRACT
Portland cement-silica fume binary cementitious materials are widely used in engineering construction and have been investigated from micro- to macroscopic aspects. However, the theoretical background on the hydration kinetics of the binary system has not been sufficiently covered in the literature. In this study, the hydration dynamic characteristics of the Portland cement-silica fume binary system curing at low temperature were investigated. Hydration kinetics equations were optimized and a hydration model followed by a computer program was developed to calculate the reaction rate constant K and the reaction order n. This model presented that the hydration process of the binary system at low temperature could be divided into three stages, namely, nucleation and growth (NG), interactions at phase boundaries (I), and diffusion (D). The n values for the binary system varied in the range of 1.2 to 1.6, indicating that the hydration of the binary system at low temperature was a complex elementary reaction. Silica fume can reduce the total heat at the later stage of the hydration and the reaction order n, but increase the heat flow at the accelerating stage and the hydration rate constant K. Low temperature prolonged the hydration induction period, decreased and delayed the secondary exothermic peak, as well as reduced the n and K value.
ABSTRACT
Traditional chemical precipitation of phosphates from wastewater is somewhat inefficient because it produces some ultrafine hydroxyapatite particles that are difficult to settle. In this study, magnetic seeds with a core-shell structure were prepared by sulfation roasting for magnetic flocculation of those fine particles. Zeta potential measurements show that the hydroxyapatite particles are positively charged at pHâ¯10, whereas the magnetic seeds are negatively charged. The Derjaguin-Landau-Verwey-Overbeek calculation indicates that the van der Waals force between the magnetic seeds and hydroxyapatite particles is always attractive. Moreover, the electrostatic attraction also contributes to aggregation of the magnetic seeds and hydroxyapatite particles. Orthogonal experiments show that the main factor affecting the magnetic flocculation is the dosage of magnetic seeds, and polymeric ferric sulfate also plays an important role. Under the optimal magnetic flocculation experimental conditions, the turbidity of wastewater after magnetic separation was only 16.388 NTU, contributing to the removal of phosphate contaminants. Therefore, magnetic flocculation and magnetic separation may provide an alternative solution for efficient purification of phosphate-containing wastewater.
ABSTRACT
Core-shell magnetic seeds with certain adsorption capacity that were prepared by sulfated roasting, served as the core of a magnetic separation technology for purification of starch wastewater. XRD and SEM results indicate that magnetite's surface transformed to be porous α-Fe2O3 structure. Compared with magnetite particles, the specific surface area was significantly improved to be 8.361 from 2.591â¯m2/g, with little decrease in specific susceptibility. Zeta potential, FT-IR and XPS experiments indicate that both phosphate and starch adsorbed on the surface of the core-shell magnetic seeds by chemical adsorption, which fits well with the Langmuir adsorption model. The porous surface structure of magnetic seeds significantly contributes to the adsorption of phosphate and starch species, which can be efficiently removed to be 1.51â¯mg/L (phosphate) and 9.51â¯mg/L (starch) using magnetic separation.
Subject(s)
Phosphorus/analysis , Starch/analysis , Waste Disposal, Fluid/methods , Wastewater/chemistry , Water Pollutants, Chemical/analysis , Ferrosoferric Oxide/chemistry , Magnetics , Sulfates/chemistryABSTRACT
Artemisia absinthium L. has pharmaceutical and medicinal effects such as antimicrobial, antiparasitic, hepatoprotective, and antioxidant activities. Here, we prepared A. absinthium ethanol extract (AAEE) and its subfractions including petroleum ether (AAEE-Pe) and ethyl acetate (AAEE-Ea) and investigated their antitumor effect on human hepatoma BEL-7404 cells and mouse hepatoma H22 cells. The cell viability of hepatoma cells was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The apoptosis, cell cycle, mitochondrial membrane potential (Δψm), and reactive oxygen species (ROS) were analyzed by flow cytometry. The levels of proteins in the cell cycle and apoptotic pathways were detected by Western blot. AAEE, AAEE-Pe, and AAEE-Ea exhibited potent cytotoxicity for both BEL-7404 cells and H22 cells through the induction of cell apoptosis and cell cycle arrest. Moreover, AAEE, AAEE-Pe, and AAEE-Ea significantly reduced Δψm, increased the release of cytochrome c, and promoted the cleavage of caspase-3, caspase-9, and poly(ADP-ribose) polymerase (PARP) in BEL-7404 and H22 cells. AAEE, AAEE-Pe, and AAEE-Ea significantly upregulated the levels of ROS and C/EBP-homologous protein (CHOP). Further, AAEE, AAEE-Pe, and AAEE-Ea significantly inhibited tumor growth in the H22 tumor mouse model and improved the survival of tumor mice without side effects. These results suggest that AAEE, AAEE-Pe, and AAEE-Ea inhibited the growth of hepatoma cells through induction of apoptosis, which might be mediated by the endoplasmic reticulum stress and mitochondrial-dependent pathway.
Subject(s)
Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/pharmacology , Apoptosis/drug effects , Artemisia absinthium/chemistry , Endoplasmic Reticulum Stress/drug effects , Plant Extracts/chemistry , Plant Extracts/pharmacology , Animals , Cell Cycle Checkpoints/drug effects , Cell Line, Tumor , Humans , Inhibitory Concentration 50 , Membrane Potential, Mitochondrial/drug effects , Mitochondria/drug effects , Reactive Oxygen Species/metabolism , Signal Transduction/drug effectsABSTRACT
This study introduces the use of a waste by-product from wet limestone flue gas desulfurization as a potential material for fluoride removal. Systematic laboratory-scale experiments were tested to identify the fluoride removal performance and determine the underlying mechanism. Flue gas desulfurization (FGD) gypsum removes 93.31% of fluoride from 109â¯mg/L to 7.3â¯mg/L. Fluoride can be efficiently removed at the optimum pH range of 5-11. Kinetics analysis indicates that the theoretical fluoride capacity at 1â¯g/L FGD gypsum is 96.9â¯mg/g. Equilibrium speciation analysis indicates that the decrease of system pH to lower than 5 is unsuitable for the formation of calcium fluoride, and the increase of system pH to higher than 11 opposes calcium release from FGD gypsum. Thermodynamic analysis confirms the feasibility of converting calcium sulphate into calcium fluoride at pHâ¯>â¯5. FGD gypsum and precipitates were characterized to describe their surface morphology, elemental composition and crystalline phase. Results indicate that FGD gypsum removes fluoride through the combination of calcium with fluoride to generate calcium fluoride.