Chemical, ecotoxicological, cytotoxic, and mutagenic evaluation of gelling agents used in the production of 70% alcohol gel.

With COVID-19, there has been an increase in the use of gelling agents for hand sanitizer production, and as a result, the release of this product into wastewater could induce impacts and adverse reactions in living organisms. Thus, ecotoxicological and cytotoxicological assessments of gelling agents with test organisms from different trophic levels are necessary to assess their environmental safety. For this, seven cellulose-based gelling agents and a polyacrylic acid derivative (C940) were selected for tests with Artemia salina. The most toxic agent was tested on Allium cepa to assess cytotoxicity. The volatile compounds of the gelling agents were analyzed. Cellulose-based gelling agents were not considered toxic according to their LC50, but C940 presented moderate toxicity to A. salina and cytotoxicity to Allium cepa, but without mutagenicity. In addition, C940 contained cyclohexane as a volatile compound. Thus, cellulose-based gelling agents are better environmental options than carbomer for 70% alcohol gel sanitizer.

Cancer evaluation in dogs using cerumen as a source for volatile biomarker prospection.

Cancer is one of the deadliest diseases in humans and dogs. Nevertheless, most tumor types spread faster in canines, and early cancer detection methods are necessary to enhance animal survival. Here, cerumen (earwax) was tested as a source of potential biomarkers for cancer evaluation in dogs. Earwax samples from dogs were collected from tumor-bearing and clinically healthy dogs, followed by Headspace/Gas Chromatography-Mass Spectrometry (HS/GC-MS) analyses and multivariate statistical workflow. An evolutionary-based multivariate algorithm selected 18 out of 128 volatile metabolites as a potential cancer biomarker panel in dogs. The candidate biomarkers showed a full discrimination pattern between tumor-bearing dogs and cancer-free canines with high accuracy in the test dataset: an accuracy of 95.0% (75.1-99.9), and sensitivity and specificity of 100.0% and 92.9%, respectively. In summary, this work raises a new perspective on cancer diagnosis in dogs, being carried out painlessly and non-invasive, facilitating sample collection and periodic application in a veterinary routine.

Genotoxic effect of heavy metals on Astyanax lacustris in an urban stream.

Uncontrolled urbanization growth contributes to the pollution of aquatic environments. Heavy metals released by domestic and industrial effluents can negatively affect aquatic organisms. This study aimed to evaluate the effect of environmental pollutants, such as metals, on fish DNA damage, in stretches of an urban stream. Specimens of the Neotropical fish, Astyanax lacustris, were exposed in situ for 96 h along the Antas stream, a Brazilian aquatic system deteriorated by anthropogenic factors. Water and sediment samples were collected simultaneously for physicochemical and heavy metal analyses. The comet assay was performed as a biomarker of genotoxicity. Fish located downstream had a higher frequency of DNA damage than in the reference site. We found concentrations of Cr and Ni above acceptable levels in sediment samples. Generally, Ba, Mn, Mg, Zn, Cr, and Ni were the elements most associated with genotoxic damage. Water and sediment of the Antas stream showed genotoxic potential in A. lacustris according to the urbanization gradient, demonstrating the importance to prevent the release of environmental pollutants, especially heavy metals in urban areas.

Potential use of a thermal water cyanobacterium as raw material to produce biodiesel and pigments.

Global energy demand is increasing every day and most is still derived from non-renewable sources. Therefore, sustainable alternatives are sought to produce biofuels, such as biodiesel. Several studies have demonstrated the potential of microalgae and cyanobacteria to produce biodiesel and pigments. These pigments, such as lutein and astaxanthin, have a high commercial value and can economically support the production of biodiesel. However, few studies have explored the potential of cyanobacteria collected in thermal water. In these microorganisms, both biomass and metabolites production can be altered by the culture form. Thus, a cosmopolitan filamentous cyanobacterium (Geitlerinema amphibium) from thermal water was collected and isolated to evaluate its potential to produce fatty acids, biodiesel, and pigments in two culture media. G. amphibium was cultured in WC (Wright's Cryptophyte) and BBM (Bold's Basal Medium) media. Thermal stress (40 °C for 48 h) was applied to the medium, which generated higher productivity of the biomass in BBM. The cyanobacterium contained higher biodiesel content in the WC medium and higher pigment content in the BBM medium. Thermal stress increased the biodiesel content by 350%, but decreased pigment content. Two pigments with high commercial value (astaxanthin and lutein) were identified. G. amphibium produced up to 2.74 mg g-1 of astaxanthin and 5.49 mg g-1 of lutein, which is seven times more lutein than Marigold, currently the main raw material used commercially. Therefore, G. amphibium has the potential to produce biodiesel, astaxanthin, and lutein concomitantly.

Analysis of major carotenoids and fatty acid composition of freshwater microalgae.

Considering the nutraceutical properties, the high commercial value from pigments and essential lipids and the environmental sustainability, the purposes of this study were to assess the major carotenoids and fatty acids composition of nine microalgae species as a source of nutraceutical compounds and as fatty raw material for biodiesel production. The carotenoid and fatty acid content were analyzed by high performance liquid chromatography tandem mass spectrometry detection method with atmospheric pressure chemical ionization mode (HPLC/APCI-MS/MS) and by high resolution gas chromatography with flame ionization detector (GC-FID). For the carotenoid analysis, the developed method presented a rapid response, a good chromatographic separation, higher sensitivity and can provides more compounds information due the mass spectrum. Among the microalgae evaluated, Desmodesmus protuberans (10.3 mg g-1), Desmodesmus denticulatus var. linearis (8.43 mg g-1) and Chlamydomonas planctogloea (7.4 mg g-1) are good lutein sources. Coelastrum sphaericum (15.29 mg g-1) and Parachlorella kessleri (22.96 mg g-1) showed high astaxanthin content; the others microalgae species presents low carotenoid content. In addition, Chlorella zofingiensis provides high quantities of γ-linolenic acid (4.3%). Eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) levels were lower than 1.1 %. Regarding for biodiesel production, the promising strains are Coelastrum sphaericum and Parachlorella kessleri.

Biosorption of hexavalent chromium by Pleurotus ostreatus.

The existing techniques for the removal of heavy metals are expensive and frequently inefficient. Thus the application of biosorbents has arisen as an alternative, this being emergent technology that must be studied and explored, with the aim of promoting better environmental and human life quality. The objective of this study was to verify the capacity of active and inactive Pleurotus ostreatus fungal biomass in removing Cr(VI) ions by biosorption from synthetic aqueous solutions of these ions at concentrations of 10, 25, 50, 75, 100, 125 and 150 mg L-1. When using active biomass, the kinetic studies showed that 100% of biosorption was reached from the 25 mg L-1Cr(VI) solution in 360 hours, equivalent to the removal of 169.84 mg g-1 of total Cr. On the other hand the inactive biomass reached 100% of its saturation capacity in 22 minutes for a concentration of 50 mg L-1 of Cr(VI), equivalent to the removal of 368.21 mg g-1 of total Cr. The kinetic study was shown to be highly effective, presenting an efficiencies of times 500 and 750 for the active and inactive P. ostreatus biomasses, respectively, when compared to the limit of 0.1 mg L-1 of Cr(VI) for industrial effluents described in CONAMA resolution n° 430/2011.

Avaliação química, ecotoxicológica e genotoxicológica de águas de cavas de mineração a céu aberto / Chemical, ecotoxicological and genotoxicological evaluation of waters of open pit mine lakes

RESUMO Lagos artificiais formados em áreas de mineração a céu aberto são unidades complexas e se constituem em passivos ambientais emergentes advindos da indústria da mineração. Embora estejam aumentando em número em várias partes do globo, são um problema ambiental recente e ainda pouco estudado, especialmente no tocante à qualidade e à toxicidade de suas águas, que podem apresentar riscos ambientais preocupantes, dado seu potencial de contaminação. O presente trabalho descreve os resultados da análise sazonal de aspectos químicos, ecotoxicológicos e genotoxicológicos das águas de três cavas de mineração de ouro desativadas localizadas em Mara Rosa, Goiás, Brasil. Amostras de água foram coletadas em perfil em duas estações climáticas distintas - inverno e verão - e foram analisadas quimicamente para determinação de metais e ânions. Também foram desenvolvidos testes ecotoxicológicos e ensaios cometa com peixes da espécie Danio rerio. Os resultados indicaram que as concentrações das espécies químicas analisadas se mostraram predominantemente crescentes no sentido da superfície ao fundo e mais elevadas durante a estação seca. As águas do Lago Azul demonstram estar quimicamente comprometidas, pois são ácidas e ricas em analitos potencialmente tóxicos, como alumínio, cádmio, chumbo, cobre, manganês, níquel e zinco. Não foram identificadas alterações ecotoxicológicas significativas para nenhuma das amostras analisadas, todavia, em termos genotoxicológicos, o Lago Azul apresentou danos ao DNA a partir da concentração de 25% na estação seca e de 50% na estação chuvosa.

ABSTRACT Artificial lakes formed in open pit mining areas are complex units and constitute emerging environmental liabilities arising from the mining industry. Although they are increasing in number in several parts of the world, they still form a recent and little studied environmental problem, especially regarding the quality and toxicity of its waters, which may represent worrying environmental risks. This study describes the results of the seasonal analysis of chemical, ecotoxicological and genotoxicological aspects of the waters of three disused gold mining pit lakes located in Mara Rosa, Goiás, Brazil. Samples were collected in profile in two different climatic seasons, winter and summer, and were chemically analyzed to determine their load of metals and anions. Ecotoxicological Tests and Comet Assays were also developed with fish of the Danio rerio species. The results indicated that the concentrations of the chemical species analyzed were predominantly increased in the surface-bottom direction and higher during the dry season. Lago Azul waters have been shown to be chemically more compromised as they are acidic and rich in potentially toxic analytes such as aluminum, cadmium, lead, copper, manganese, nickel, and zinc. No significant ecotoxicological alterations were identified for any of the analyzed samples, although, in genotoxicological terms, Lago Azul presented DNA damage from concentrations of 25% in the dry season and 50% in the wet season.

Earwax metabolomics: An innovative pilot metabolic profiling study for assessing metabolic changes in ewes during periparturition period.

Important metabolic changes occur during transition period of late pregnancy and early lactation to meet increasing energy demands of the growing fetus and for milk production. The aim of this investigation is to present an innovative and non-invasive tool using ewe earwax sample analysis to assess the metabolic profile in ewes during late pregnancy and early lactation. In this work, earwax samples were collected from 28 healthy Brazilian Santa Inês ewes divided into 3 sub-groups: 9 non-pregnant ewes, 6 pregnant ewes in the last 30 days of gestation, and 13 lactating ewes ≤ 30 days postpartum. Then, a range of metabolites including volatile organic compounds (VOC), amino acids (AA), and minerals were profiled and quantified in the samples by applying headspace gas chromatography/mass spectrometry, high performance liquid chromatography/tandem mass spectrometry, and inductively coupled plasma-optical emission spectrometry, respectively. As evident in our results, significant changes were observed in the metabolite profile of earwax between the studied groups where a remarkable elevation was detected in the levels of non-esterified fatty acids, alcohols, ketones, and hydroxy urea in the VOC profile of samples obtained from pregnant and lactating ewes. Meanwhile, a significant decrease was detected in the levels of 9 minerals and 14 AA including essential AA (leucine, phenyl alanine, lysine, isoleucine, threonine, valine), conditionally essential AA (arginine, glycine, tyrosine, proline, serine), and a non-essential AA (alanine). Multivariate analysis using robust principal component analysis and hierarchical cluster analysis was successfully applied to discriminate the three study groups using the variations of metabolites in the two stress states (pregnancy and lactation) from the healthy non-stress condition. The innovative developed method was successful in evaluating pre- and post-parturient metabolic changes using earwax and can in the future be applied to recognize markers for diagnosis, prevention, and intervention of pregnancy complications in ewes.

Earwax: A clue to discover fluoroacetate intoxication in cattle.

An innovative method was developed to detect fluoroacetate poisoning in cattle by headspace/gas chromatographic analysis of earwax samples of intoxicated cattle. Samples were collected from 2 groups of cattle subjected to induced fluoroacetate intoxication, each group receiving a different dose of acetamide (antidote). Monofluoroacetic acid was detected in samples of intoxicated cattle in concentrations inversely proportional to the dose of acetamide. Thus, earwax analysis represents a successful approach for detection and monitoring of fluoroacetate poisoning.

Heavy metals in hair of wild canids from the Brazilian Cerrado.

In this study, we aimed to assess whether free-ranging wild canids are exposed to heavy metals in one of the most developed and populated regions of Brazil. Hair of 26 wild canids (maned wolves Chrysocyon brachyurus, crab-eating foxes Cerdocyon thous, and hoary foxes Lycalopex vetulus) from the Cerrado biome in Southeast Brazil were analyzed by spectrophotometry to detect cadmium, chromium, and lead, and also the essential copper, iron, manganese, and zinc traces. All samples showed traces of copper, iron, manganese, and zinc. Non-essential lead was detected in 57% (2.35 ± 0.99 mg/kg), and chromium in 88% (2.98 ± 1.56 mg/kg) of samples. Cadmium traces (detection limit 0.8 mg/kg) were not found. Crab-eating foxes had more copper, iron, and manganese in hair than maned wolves. Correlations among element levels differed between maned wolves and crab-eating foxes. Concentrations of chromium and lead were outstandingly higher than in wild canids from other areas. Addressing the causes of such levels and the impacts of the heavy metal pollution in Neotropical ecosystems is urgent for animal health and conservation purposes. We argue that heavy metal pollution should be considered as dangerous threats to wildlife health in Brazil and recommend hair sampling as a biomonitoring tool for heavy metals in Neotropical terrestrial mammals.

Use of feathers of feral pigeons (Columba livia) as a technique for metal quantification and environmental monitoring.

This study quantifies metal concentrations in washed and unwashed feathers of feral pigeons (Columba livia). The material was collected in two different sites: Goiânia (capital of Goiás State), with high anthropic activities, and Jataí (a city in Goiás), with low anthropic activities. Results revealed that metals such as Pb, Cr, and Cd were deposited in the feathers originating from air and soil (exogenous process). Other metals such as Cu, Fe, Mn, and Zn, which are part of the tissue constitution of a living being, were absorbed through the pigeons' diet (endogenous process). There was a statistically significant difference between mean values of Cd, Pb, and Cr in the three collection sites. The order of metal concentrations were Civic Square > Zoo > Jataí, which shows highest levels of metal contamination in anthropic environments. Significant differences between Cd, Pb, and Cr in washed and unwashed feathers suggest that metal concentrations are directly related to exposure time due to exogenous sources. We concluded that it is possible to quantify and monitor metal levels in the environment by analyzing the feathers of urban feral pigeons. Furthermore, unwashed feathers were especially efficient to investigate endogenous and exogenous absorption of the metals in our study.

Sorption, solubility and residual monomers of a dental adhesive cured by different light-curing units.

The aim of this study was to assess polymerization ability of three light-curing units by evaluating the influence of the light source, curing regimen and permeant (water or ethanol) on sorption, solubility and amount of residual monomers of a dental adhesive. Specimens of Adper Single Bond 2 were fabricated using a stainless steel circular matrix (8 mm x 1 mm). One quartz-tungsten-halogen (QTH) lamp and two light-emitting diode (LED) device at three different curing regimes (L1 = 12 J; L2 = 24 J; L3 = 24 J) were used to cure the specimens. Specimens were stored in two types of permeants - deionized water or 75% ethanol - for two storage times (G1 =7 days; G2 = 30 days). The specimens underwent water sorption and solubility tests, according to ISO 4049:2000 standard. After storage, residual monomers were identified and quantified by high performance liquid chromatography (HPLC). For sorption, L1 showed the highest values and QTH, the lowest. For solubility, in ethanol-stored groups, L1 had also the highest values, and QTH, the lowest, and findings were significantly different from the other curing regimens. L1 leached significantly more monomers than the others, and QTH had the lowest results. In conclusion, the type of light source, the curing regimen and the permeant affected sorption, solubility and amount of residual monomers of the adhesive under study.

Sorption, solubility and residual monomers of a dental adhesive cured by different light-curing units

The aim of this study was to assess polymerization ability of three light-curing units by evaluating the influence of the light source, curing regimen and permeant (water or ethanol) on sorption, solubility and amount of residual monomers of a dental adhesive. Specimens of Adper Single Bond 2 were fabricated using a stainless steel circular matrix (8 mm x 1 mm). One quartz-tungsten-halogen (QTH) lamp and two light-emitting diode (LED) device at three different curing regimes (L1 = 12 J; L2 = 24 J; L3 = 24 J) were used to cure the specimens. Specimens were stored in two types of permeants - deionized water or 75 percent ethanol - for two storage times (G1 =7 days; G2 = 30 days). The specimens underwent water sorption and solubility tests, according to ISO 4049:2000 standard. After storage, residual monomers were identified and quantified by high performance liquid chromatography (HPLC). For sorption, L1 showed the highest values and QTH, the lowest. For solubility, in ethanol-stored groups, L1 had also the highest values, and QTH, the lowest, and findings were significantly different from the other curing regimens. L1 leached significantly more monomers than the others, and QTH had the lowest results. In conclusion, the type of light source, the curing regimen and the permeant affected sorption, solubility and amount of residual monomers of the adhesive under study.

O objetivo deste estudo foi avaliar a capacidade de polimerização de três unidades fotopolimerizadoras por meio da análise da influência das fontes de luz, regimes de cura (QTH, L1, L2 e L3) e diferentes permeantes (água e etanol) na sorção, solubilidade e quantidade de monômeros residuais de um adesivo dentário. Espécimes de AdperTM Single Bond 2 foram feitos utilizando uma matriz circular de aço inoxidável (8 mm x 1 mm). Três fontes de luz, uma a base de luz halógena (QTH) e duas a base de diodos emissores de luz (LED), em três diferentes regimes de cura (L1 = 12J; L2 = 24J; L3 = 24J) foram usados para fotoativar os espécimes. Os espécimes foram armazenados em dois tipos de permeantes (água deionizada ou etanol a 75 por cento), por dois diferentes períodos de armazenamento (G1 =7 dias; G2 = 30 dias). Os espécimes foram submetidos a testes de sorção e solubilidade de acordo com a ISO 4049:2000. Após o período de armazenamento, os monômeros residuais foram identificados e quantificados por cromatografia líquida de alta eficiência (HPLC). Para sorção, L1 apresentou os maiores valores significantes e QTH os menores. Para solubilidade, nos grupos do etanol, L1 apresentou os maiores valores e QTH os menores e os achados foram estatisticamente diferentes dos outros regimes de cura. L1 extraiu significantemente mais monômeros do que os outros regimes e QTH teve os menores resultados. As fontes de luz, os regimes de polimerização e os diferentes permeantes influenciaram na sorção, solubilidade e quantidade de monômeros residuais extraídos do adesivo em estudo.

Isotretinoína: perfis farmacológico, farmacocinético e analítico / Isotretinoin: pharmacological, pharmacokinetic and analytical profiles

A isotretinoína quimicamente conhecida como ácido-13-cis-retinóico, faz parte do amplo grupo de compostos relacionados à vitamina A. É empregada particularmente no tratamento da acne cística e nodular e como inibidor da proliferação de células neoplásicas, por exercer efeito regulador sobre a diferenciação celular. Os efeitos adversos envolvendo o uso de isotretinoína estãrelacionados à pele e membranas mucosas, sistemas nervoso, músculo esquelético, linfático, gastrintestinal, cardiorespiratório e geniturinário. A isotretinoína é um composto termo e fotossensível e, por assim se apresentar, desperta o interesse pelo estudo de sua estabilidade...