Single and multiple daily dose toxicokinetics of fluoride after oral administration of sodium fluoride along with aluminum sulfate in goats

Our previous study suggested that toxicokinetic parameters of fluoride were significantly changed on the 30th day as compared with 1st day, after repeated oral administration of sodium fluoride alone for 30 days in goats. The purpose of this study was to investigate whether aluminum sulfate has ameliorative effect on the toxicokinetics of fluoride. For this, sodium fluoride (20 mg kg^?1 b. wt.) along with aluminum sulfate (150 mg kg^?1 b. wt.) was administered in goats for 30 days to investigate its effect on toxicokinetics of fluoride on days 1 and 30. The fluoride levels against time were adequately described by one compartment open model. The peak plasma level of fluoride was observed at 2 h. The toxicokinetics data revealed a nonsignificant decrease in β (elimination rate constant) and C _max (the maximum plasma concentration) and increase in t _1/2 K _a (absorption half-lives), t _1/2 β (elimination half-lives), area under the plasma (AUC) concentration versus time curve and mean residence time (MRT) was observed for the last dose from their respective first dose values. On the basis of changes in the toxicokinetic parameters, it was concluded that repeated oral administration has cumulative effect on plasma fluoride level and concurrent oral administration of aluminum sulfate has ameliorative action on the toxicokinetics of fluoride in goats.     

Differential effects of UV-B radiation fluence rates on growth,photosynthesis, and phosphate metabolism in two cyanobacteria under copper toxicity

This work was undertaken to ascertain the impact of different fluence rates of ultraviolet-B (UV-B) radiation on two cyanobacterial biofertilizers, Phormidium foveolarum and Nostoc muscorum, growing under copper toxicity. Copper (2 and 5?µmol?L^?1) and high UV-B fluence rate (UV-B_H; 1.0?µmol?m^?2?s^?1) decreased the growth, pigment content, photosynthetic oxygen yield, phosphate uptake, and acid phosphatase activity in both the strains analyzed after 24 and 72?h of experiments, and combined exposure further enhanced the toxic effects. Respiration and alkaline phosphatase activities were stimulated appreciably. The damaging effect was shown on the order on pigments: phycocyanin?>?chlorophyll a?>?carotenoids, and on photosystems: whole chain photosynthetic reaction?>?photosystem II?>?photosystem I. Partial recovery in the photosystem II activity in the presence of artificial electron donors; diphenyl carbazide (DPC), hydroxylamine (NH₂OH), and manganese chloride (MnCl₂) pointed out the interruption of electron flow on the oxidation side of photosystem II. Unlike UV-B_H, low UV-B fluence rate (UV-B_L; 0.1?µmol?m^?2?s^?1), rather than causing damaging effect partially, alleviated the toxic effects of Cu. This study suggests that the cyanobacterium P. foveolarum is less sensitive against UV-B_H and excess Cu (2 and 5?µmol?L^?1), thus P. foveolarum may be used as a biofertilizer for sustainable agriculture.     

Efficient arsenic depollution in water using modified maize powder

This article reports the synthesis of an efficient, low-cost material from maize powder to depollute arsenic-contaminated water. Arsenic is toxic for humans and other organisms even at low concentrations. The most well-known and severe case of arsenic poisoning through drinking water has been found in India and Bangladesh. Numerous inorganic materials have been tested for the removal of arsenic from water bodies over the last two decades. However, all such materials have several disadvantages such as unpredictable arsenic ion removal, high cost and the generation of toxic sludge that is often more difficult to manage. Alternatively, organic material from agricultural waste may be modified to enrich functional groups responsible for As sorption and, in turn, used to depollute contaminated waters. Here, Zea mays cob powder has been modified to remove arsenic species from water. Two modified materials were produced: an aminated maize powder and a thiolated maize powder. Amination was done using epichlorohydrin and dimethylamine. Thiolation was done using thioglycolic acids. Amination increased As (III) sorption from 70 to 75.8 % and As (V) sorption from 85 to 94.42 %, compared with unmodified maize powder. Thiolation increased As (III) sorption from 70 to 81.7 % and As (V) sorption from 85 to 90 %. Amination increased usability cycles from 3 to 5. Thiolation increased usability cycles from 3 to 6. The novel modified maize biosorbent has enough potential for the development of a low-cost technological pre-treatment step, prior to high-tech chemical treatments.     

A performance-based tabular approach for joint systematic improvement of risk control and resilience applied to telecommunication grid,gas network,and ultrasound localization system

Environment Systems and Decisions - Organizational and technical approaches have proven successful in increasing the performance and preventing risks at socio-technical systems at all scales....     

Ggum-poly(Itaconic Acid) Based Superabsorbents Via Two-Step Free-Radical Aqueous Polymerization for Environmental and Antibacterial Applications

Ggum-based conducting hydrogels possessing dye removal and antibacterial property were developed by two-step free-radical aqueous polymerization method. Conductivity was introduced with polyaniline (PANI) chains incorporated within the crosslinked network of Ggum-poly(itaconic acid) superabsorbent. The material properties of the synthesized samples were characterized using FTIR spectroscopy, thermal analysis and scanning electron microscopy techniques. Results showed that synthesized samples exhibited the best antibacterial activity against Gram-positive bacteria. Synthesized samples were found to be effective in removal of toxic methylene blue (MB) dye from the waste water. The adsorption kinetics of superabsorbents has been described by using pseudo first and pseudo second order kinetics models. Furthermore, application of hydrogels to improve the water retention properties of different soils was also studied for agricultural purpose.     

Application of ameliorated wood pulp to recover Cd(II), Pb(II), and Ni(II) from e-waste

In this study, dl-malic acid and hydrogen peroxide were used as leaching agents to remove metals from e-waste (printed-circuit boards) and itaconic acid-grafted poly(vinyl alcohol)-encapsulated wood pulp (IA-g-PVA-en-WP) to uptake metals from leachate with high proficiency [11.63 mg g^?1; 93.03 % for Cd(II), 11.90 mg g^?1; 95.18 % for Pb(II), and 12.14 mg g^?1; 97.08 % for Ni(II)]. Metals were recovered from the loaded biosorbent by desorption studies. The standard analytical techniques, such as elemental analysis, Fourier-transform-infrared spectroscopy, scanning electron microscopy, atomic force microscopy, and thermogravimetric analysis, were used to characterize the recovering agent (biosorbent). At equilibrium, the metal uptake data were fitted to Langmuir and D–R isotherms (R ² > 0.99) significantly, revealing, the homogeneous distribution of active sites on biosorbent’s backbone. The possible mechanism appeared to be ion exchanges of metal ions with H⁺ together with binding over functionalities (COO^?). Dimensionless equilibrium parameter (R _L) showed the favourability of metal uptake at lower concentration, while mean adsorption energy (E) certified the physical binding of metal on functionalities which was further confirmed by sticking probability and activation energy parameters. Reusability studies were also conducted to state the performance of biosorbent.     

Assessment of physicochemical characteristics of Ganga Canal water quality in Uttarakhand

Assessment of physicochemical parameters of Ganga Canal water was carried out during 2012–2013 at Haridwar (Uttarakhand) with two different sites, i.e., Bhimgoda Barrage (site 1—control site) and Bahadrabad (site 2—contaminated site), where canal water flows with loads of pollution from highly commercial and industrial areas. During investigation, maximum turbidity (287.72 ± 56.28 JTU), total solids (1167.60 ± 303.90 mg l^?1), free CO₂ (1.88 ± 0.22 mg l^?1), total hardness (60.14 ± 1.13 mg l^?1), pH (7.1 ± 0.13), nitrate (0.048 ± 0.010), nitrite (0.019 ± 0.001), biochemical oxygen demand (2.866 ± 1.098), chemical oxygen demand (6.8 ± 2.61) and phosphate (0.087 ± 0.015), while minimum velocity (1.71 ± 0.19 ms^?1), transparency (0.12 ± 0.08 m) and dissolved oxygen (7.95 ± 0.44 mg l^?1) were recorded in monsoon season at site 2 in comparison with site 1. The mean values of these parameters were compared with WHO and ISI standards and found significant differences (p < 0.05) in the mean values of turbidity, total solids, pH, dissolved oxygen, free CO₂ and total hardness with sampling sites. The turbidity of both the sites 1 and 2 was recorded above the permissible limit. Turbidity of site 2 is much higher than of site 1, so it is counted as more polluted. The values of the studied parameters were more during monsoon season and summer season at site 2 as compared to site 1. The results indicated that most of the physicochemical parameters from Ganga Canal system were within or at periphery in comparison with permissible limit of ISI and WHO for drinking water and therefore may be suitable for domestic purposes, but it requires perceptible consideration due to intense changes in climate and increase in pollution.     

Optimization of pretreatment conditions for enhanced sugar release

Present investigation was done to evaluate various algal genera found in water bodies of Varanasi city. The potential of any biomass for biofuels (bioalcohols, biohydrogen, etc.) production depends on the quantity of extractable sugar present in it. Acid (H₂SO₄) and alkali (NaOH) pretreatment were performed, and H₂SO₄ was chosen due to its nearly double yield as compared with alkaline pretreatment. Response surface methodology was utilized for the optimization of operating parameters such as treatment temperature, time, and acid concentration. Sugar yield up to 0.33 g/g of dry biomass was obtained using cyanobacterial biomass of Lyngbya limnetica, at 100°C, 59.19 min, and H₂SO₄ concentration of 1.63 M.