Sonia C. N. Queiroz

Application of new high-performance liquid chromatography and solid-phase extraction materials to the analysis of pesticides in human urine

A method for the simultaneous determination of diuron and linuron pesticides in human urine was developed, using both solid-phase extraction (SPE) and high-performance liquid chromatography (HPLC) phases made in our own laboratory. These materials were prepared by sorption of polysiloxanes onto a silica surface, followed by immobilization. The HPLC columns were prepared from poly(methyloctylsiloxane), PMOS, immobilized onto silica with microwave radiation while the SPE cartridges where made with poly(methyloctadecylsiloxane), immobilized thermally. Method validation was performed for diuron and linuron for three fortification levels. The recoveries obtained were 85-103%, the inter- and intra-assay precisions were less than 1.6 and 1.8%, respectively. The limits of quantitation and detection for diuron were 2.4 and 8.0 microg/l and for linuron were 5.0 and 12 microg/l, respectively.

Studies on degradation of glyphosate by several oxidative chemical processes: Ozonation, photolysis and heterogeneous photocatalysis

Several different Advanced Oxidation Processes (AOPs) including ozonation at pH 6.5 and 10, photolysis and heterogeneous photocatalysis using TiO2 as semiconductor and dissolved oxygen as electron acceptor were applied to study the degradation of glyphosate (N-phosphonomethyl glycine) in water. The degree of glyphosate degradation, the reactions kinetic and the formation of the major metabolite, aminomethyl phosphonic acid (AMPA), were evaluated. Ozonation at pH 10 resulted in the maximum mineralization of glyphosate. It was observed that under the experimental conditions used in this study the degradation of glyphosate followed the first-order kinetics. The half-life obtained for glyphosate degradation in the O3/pH 10 process was 1.8 minutes.

Comportamento do herbicida hexazinone em área de recarga do aqüífero Guarani cultivada com cana-de-açúcar

Sao Paulo state (Brazil) has an important area of sugarcane production, mainly for obtaining alcohol and sugar, where there is an intensive use of pesticides. An important recharge zone of Guarani aquifer, with supplies water for the local population, is located at Ribeirao Preto city, so the local behavior of pesticides must be investigated. The GUS index was obtained by using the paramenters Koc and half-life for hezazinone herbicide, determinated in representative soil of this region. This study has demonstrated that there is potential risks of hexazinone leaching to ground water, indicating that this herbicide must be monitored in ground water.

Leaching and half-life of the herbicide tebuthiuron on a recharge area of Guarany aquifer in sugarcane fields in Brazil

This study was undertaken to evaluate the degradation and mobility of the herbicide tebuthiuron (N-[5-(1,1-dimethylethyl)-1,3,4-thiadiazol-2-yl]-N,N′-dimethylurea) in soil under field conditions, and its potential for leaching and groundwater contamination. A watershed, Espraiado, located over a recharge area in Brazil, was chosen for soil and water studies. At Espraiado, water samples were collected from seven wells at intervals of three months from March 2004 to June 2006 and analyzed for tebuthiuron. Other samples were taken from city wells located outside of the recharge area. To assess the potential movement to the aquifer, tebuthiuron was also applied to trial plots at the recommended label rate of 1.0 kg/ha a.i. in May of 2004, with and without sugarcane coverage, on sandy soil. Soil samples were collected during the years of 2004 and 2005, at depths intervals of 20 cm from soil surface down to 120 cm and analyzed for tebuthiuron at zero, 3, 30, 60, 90, 120, 150, 180, 240, and 300 days after application. There was no clear effect of sugarcane coverage on the tebuthiuron degradation in soils, but it moved faster into the soil where there was no cover. After 180 days there were no measurable residues in the soil, and tebuthiuron was not found below 40 cm depth in any time. Tebuthiuron had a half-life of 20 days under those conditions. No tebuthiuron residue was found in ground water samples at any sampling time.

Bioassay-directed isolation and identification of phytotoxic and fungitoxic acetylenes from Conyza canadensis.

Conyza canadensis (L.) Cronquist syn. (horseweed) is a problematic and invasive weed with reported allelopathic properties. To identify the phytotoxic constituents of the aerial parts, a systematic bioactivity-guided fractionation of the dichloromethane extract was performed. Three active enyne derivatives, (2Z,8Z)-matricaria acid methyl ester, (4Z,8Z)-matricaria lactone, and (4Z)-lachnophyllum lactone, were identified. The lactones inhibited growth of the monocot Agrostis stolonifera (bentgrass) and the dicot Lactuca sativa (lettuce) at 1 mg mL(-1), while the (2Z,8Z)-matricaria acid methyl ester was less active. In a dose-response screening of the lactones for growth inhibitory activity against Lemna paucicostata , (4Z)-lachnophyllum lactone was the most active with an IC50 of 104 μM, while the (4Z,8Z)-matricaria lactone was less active (IC50 of 220 μM). In a fungal direct bioautography assay, the two lactones at 10 and 100 μg/spot inhibited growth of the plant pathogenic fungi Colletotrichum acutatum , Colletotrichum fragariae , and Colletotrichum gloeosporioides . In a dose-response screening of the lactones against six different plant pathogenic fungi, (4Z,8Z)-matricaria lactone was more active than the commercial fungicide azoxystrobin on Col. acutatum , Col. fragariae , and Col. gloeosporioides at 30 μM and about as active as the commercial fungicide captan against Col. gloeosporioides , while (4Z)-lachnophyllum lactone was less active.

Bioconcentration factor estimates of polycyclic aromatic hydrocarbons in grains of corn plants cultivated in soils treated with sewage sludge

This study presents a model to simulate the organic substance concentrations in corn grains assuming that the substances in soil solution are absorbed via the transpiration stream by plants growing in soils fertilized with sewage sludge (SS). The model was applied and validated using soil and corn grain samples from a long-term field experiment with six successive yearly applications of SS to the soil. The following polycyclic aromatic hydrocarbons (PAHs) were simulated and evaluated in soil and grain samples: acenaphthene, acenaphthylene, anthracene, benz(a)anthracene, benz(a)pyrene, benz(b)fluoranthene, benz(g,h,i)perylene, benz(k)fluoranthene, chrysene, dibenz(a,h)anthracene, fluoranthene, fluorene, indeno(1,2,3-c,d)pyrene, naphthalene, phenanthrene and pyrene. The PAH bioconcentration factors (BCF) in corn grains ranged from 1.57 to 10.97 L kg(-1). Polycyclic aromatic hydrocarbons with low soil distribution coefficients and high values of transpiration stream concentration factors (TSCF) are more likely to be absorbed by corn plants and accumulated in grains. It was possible to estimate and observe that highly lipophilic PAH molecules (heavy PAHs) show lower accumulative potential in corn grains than the less lipophilic ones (light PAHs). Sewage sludges containing significant concentrations of light PAHs with two, three or four benzene rings should be avoided as fertilizers in alimentary field crops.

Antibacterial Compounds from Marine Bacteria, 2010–2015

This review summarizes the reports on antibacterial compounds that have been obtained from marine-derived bacteria during the period 2010-2015. Over 50 active compounds were isolated during this period, most of which (69%) were obtained from Actinobacteria. Several compounds were already known, such as etamycin A (11) and nosiheptide (65), and new experiments with them showed some previously undetected antibacterial activities, highlighting the fact that known natural products may be an important source of new antibacterial leads. New broad-spectrum antibacterial compounds were reported with activity against antibiotic resistant Gram-positive and Gram-negative bacteria. Anthracimycin (33), kocurin (66), gageotetrins A-C (72-74), and gageomacrolactins 1-3 (86-88) are examples of compounds that display promising properties and could be leads to new antibiotics. A number of microbes produced mixtures of metabolites sharing similar chemical scaffolds, and structure-activity relationships are discussed.

Validação de método multirresíduo para determinação de pesticidas em alimentos empregando QuEChERS E UPLC-MS/MS

This paper presents a practical and rapid method which was validated for simultaneous quantification and confirmation of 29 pesticides in fruits and vegetables using ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The samples were extracted following the method known as QuEChERS. Using the developed chromatographic conditions, the pesticides can be separated in less than 9 min. Two multiple reaction monitoring (MRM) assays were used for each pesticide. Four representative matrices (lettuce, tomato, apple and grapes) were selected to investigate the effect in recoveries and precision. Typical recoveries ranged from 70-120%, with relative standard deviation (RSDs) lower than 20%.

Risk simulation of soil contamination by polycyclic aromatic hydrocarbons from sewage sludge used as fertilizers

Este trabalho investigou a presenca de 16 hidrocarbonetos policiclicos aromaticos (HPAs) em lodo de esgoto e em solo com aplicacao de lodo como fertilizante agricola e simulou o risco de contaminacao por HPAs a longo prazo. As amostras foram extraidas usando diclorometano e em seguida com n-hexano em banho ultrassonico. A limpeza do extrato foi feita em coluna de alumina. As quantificacoes dos HPAs foram obtidas por cromatografia gasosa acoplada a um espectrometro de massas (GC-MS/MS ion trap). Os resultados evidenciaram que HPAs encontrados em lodos de esgoto podem apresentar risco de contaminacao de solos. As simulacoes das concentracoes dos HPAs no solo por meio de modelos matematicos foram utilizadas para indicar uma ordem de prioridade para monitoramento da qualidade do solo: fenantreno > criseno > benzo(k)fluoranteno > benzo(a)pireno > pireno > benzo(b)fluoranteno > benzo(g,h,i)perileno > indeno(1,2,3-c,d)pireno > fluoranteno > benzo(a)antraceno > dibenzo(a,h)antraceno > fluoreno > antraceno > naftaleno > acenafteno > acenaftileno. This work investigated the presence of PAH in sewage sludge and in soil with sewage sludge applied as agricultural fertilizer and simulated a long-term risk of soil contamination by PAH. The samples were extracted using dichloromethane and then with n-hexane in ultrasonic bath. The clean-up of the extract was done on a column containing alumina. The residual PAH were obtained using a gas chromatograph coupled to a mass spectrometer (ion trap GC-MS/MS). The results evidenced that PAH concentration levels found in sewage sludge might raise potential contamination risks to the soil. Simulations of the concentrations of PAHs in soil, by mathematical modeling, allowed to indicate a priority order for monitoring soil quality in terms of these contaminants: phenanthrene > chrysene > benzo(k)fluoranthene > benzo(a)pyrene > pyrene > benzo(b)fluoranthene > benzo(g,h,i)perylene > indeno(1,2,3-c,d)pyrene > fluoranthene > benzo(a)anthracene > dibenzo(a,h)anthracene > fluorene > anthracene > naphthalene > acenaphthene > acenaphthylene.

Método para a determinação de hexazinone e tebutiuron em água

METHOD FOR DETERMINATION OF HEXAZINONE AND TEBUTHIURON IN WATER. This work presents an alternative method for determination of the herbicides tebuthiuron and hexazinone in ground water. The extraction was made with dichloromethane and the analyses by high performance liquid chromatography (HPLC), using reversed-phase column, C-18, mobile phase methanol/water 50:50, v/v, detection and quantification at 247 nm. The following validation parameters were obtained: limit of detection of method 0.02 and 0.03 µg L -1 , limit of quantification of method 0.07 and 0.09 µg L -1 ; linear range limit of quantification of instrument – 300 µg L -1 (r 2 ≥ 0.998); recoveries from 90.3 to 108.2% and 90.3 to 101.6%; intermediary precision (%RSD) < 8 and < 6%, for hexazinone and tebuthiuron, respectively. The method showed to be efficient and reliable for determination of the herbicides in ground water.