RESUMO
OBJECTIVE: Approximately 3 million Americans served in the armed forces during the Vietnam War. Veterans have a higher incidence rate of lung cancer compared with the general population, which may be related to exposures sustained during service. Agent Orange, one of the tactical herbicides used by the armed forces as a means of destroying crops and clearing vegetation, has been linked to the development of several cancers including non-small cell lung cancer. However, traditional risk models of lung cancer survival and recurrence often do not include such exposures. We aimed to examine the relationship between Agent Orange exposure and overall survival and disease recurrence for surgically treated stage I non-small cell lung cancer. METHODS: We performed a retrospective cohort study using a uniquely compiled dataset of US Veterans with pathologic I non-small cell lung cancer. We included adult patients who served in the Vietnam War and underwent surgical resection between 2010 and 2016. Our 2 comparison groups included those with identified Agent Orange exposure and those who were unexposed. We used multivariable Cox proportional hazards and Fine and Gray competing risk analyses to examine overall survival and disease recurrence for patients with pathologic stage I disease, respectively. RESULTS: A total of 3958 Vietnam Veterans with pathologic stage I disease were identified (994 who had Agent Orange exposure and 2964 who were unexposed). Those who had Agent Orange exposure were more likely to be male, to be White, and to live a further distance from their treatment facility (P < .05). Tumor size distribution, grade, and histology were similar between cohorts. Multivariable Cox proportional hazards modeling identified similar overall survival between cohorts (Agent Orange exposure hazard ratio, 0.97; 95% CI, 0.86-1.09). Patients who had Agent Orange exposure had a 19% increased risk of disease recurrence (hazard ratio, 1.19; 95% CI, 1.02-1.40). CONCLUSIONS: Veterans with known Agent Orange exposure who undergo surgical treatment for stage I non-small cell lung cancer have an approximately 20% increased risk of disease recurrence compared with their nonexposed counterparts. Agent Orange exposure should be taken into consideration when determining treatment and surveillance regimens for Veteran patients.
Assuntos
Carcinoma Pulmonar de Células não Pequenas , Neoplasias Pulmonares , Dibenzodioxinas Policloradas , Veteranos , Adulto , Humanos , Masculino , Estados Unidos/epidemiologia , Feminino , Agente Laranja , Carcinoma Pulmonar de Células não Pequenas/cirurgia , Ácido 2,4-Diclorofenoxiacético/efeitos adversos , Ácido 2,4-Diclorofenoxiacético/análise , Estudos Retrospectivos , Ácido 2,4,5-Triclorofenoxiacético/efeitos adversos , Ácido 2,4,5-Triclorofenoxiacético/análise , Dibenzodioxinas Policloradas/efeitos adversos , Dibenzodioxinas Policloradas/análise , Neoplasias Pulmonares/induzido quimicamente , Neoplasias Pulmonares/cirurgia , Recidiva Local de Neoplasia/epidemiologiaRESUMO
Chromatography combined with mass spectrometry is the most commonly used detection technology, and it offers the advantages of high sensitivity and high selectivity. The quick, easy, inexpensive, effective, rugged, and safe (QuEChERS) method is low-cost, effective, and time efficient. The application of the QuEChERS has now been extended to the analysis of contaminants in food samples. The aim of the study was to identify different concentration levels of multiple harmful drug residues in bean sprouts. In this study, QuEChERS coupled with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was established for the simultaneous determination of 40 plant growth regulators, fungicides, insecticides, and antibiotics in bean sprouts. In the HPLC-MS/MS experiment, gibberellic acid, 4-fluorophenoxyacetic acid, chloramphenicol, N6-(δ2-isopentenyl)-adenine, 6-benzylaminopurine, 4-chlorophenoxyacetic acid, and 2,4-dichlorophenoxyacetic acid (2,4-D) were analyzed by MS/MS with negative electrospray ionization (ESI-). The other 33 target analytes (chlormequat, ronidazole, metronidazole, pymetrozine, dimetridazole, methomyl, carbendazim, enoxacin, levofloxacin, pefloxacin mesylate, norfloxacin, ciprofloxacin, enrofloxacin, thiabendazole, lomefloxacin, chlorpyrifos, sarafloxacin, imidacloprid, etc.) were analyzed by MS/MS with positive electrospray ionization (ESI+). Sensitive MS conditions were realized by optimizing the instrumental parameters such as the desolvent temperature, collision energy, spraying needle position, precursor ions, and product ions. Then, the optimal pretreatment method was determined by comparing the recovery rates of the 40 drugs obtained with different extraction solvents (methanol, acetonitrile, acetonitrile containing 0.1% ammonia, acetonitrile with 1% acetic acid), different extraction methods (ultrasonic extraction, shaking extraction), and purification with primary secondary amine (PSA) and C18. In this study, the bean sprouts samples were extracted twice by 10 mL acetonitrile with 1% acetic acid, and extracted under ultrasonic conditions. Then, the extracting solution was only cleaned with 100 mg C18. The chromatographic separation of the 40 compounds was accomplished on a Waters ACQUITY UPLC BEH C18 column (100 mm×2.1 mm, 1.7 µm) with gradient elution. Methanol and 0.01% formic acid aqueous solution were used as the mobile phases. The 40 compounds were analyzed in the multiple reaction monitoring (MRM) mode. The matrix matching external standard method was used for quantitative determination. The results showed that the 40 compounds could be analyzed within 15 min. Under the optimized conditions, the calibration curves showed good linearities for the 40 compounds, and the coefficients of determination (r2) were greater than 0.99 in the range of 2-200 µg/L. The limits of detection (LODs) and limits of quantification (LOQs) were in the range of 0.1-3 µg/kg and 0.3-9 µg/kg, respectively. Using negative bean sprouts as the substrates, the recovery tests were carried out at three spiked levels of 5, 10, and 50 µg/kg. The average recoveries of the 40 drugs were 78.5% to 115.3%, and the corresponding relative standard deviations (RSDs) were 1.3% to 9.7% (n=6). This method was successfully applied to the analysis of the 40 drug residues in 21 batches of local bean sprouts in Handan city. The results revealed the presence of extensive drug residues in the bean sprouts. The 26 batches were detected to varying degrees, among which 4-chlorophenoxyacetic acid, carbendazim, 6-benzyladenine, 2,4-D, enrofloxacin, and metronidazole were detected at high rates. The detection rates of 4-chlorophenoxyacetic acid, 6-benzyladenine, carbendazim, 2,4-D, gibberellic acid, and enrofloxacin were 28.6%, 19.0%, 9.5%, 9.5%, 4.8%, and 4.8%, respectively. The contents ranged from 37.5-352.4, 32.4-273.1, 28.8-38.7, 316.1-20.2, 19.9 and 13.6 µg/kg, respectively. Given its advantages of simplicity, rapidness, and high sensitivity, the developed method can be used for the rapid and accurate determination of trace levels of the 40 drug residues in large quantities of bean sprouts.
Assuntos
Clorpirifos , Fungicidas Industriais , Inseticidas , Ácido 2,4-Diclorofenoxiacético/análogos & derivados , Ácido 2,4-Diclorofenoxiacético/análise , Acetonitrilas , Adenina , Amônia , Antibacterianos , Benzimidazóis , Compostos de Benzil , Carbamatos , Cloranfenicol/análise , Clormequat , Cromatografia Líquida de Alta Pressão , Ciprofloxacina , Dimetridazol , Enoxacino , Enrofloxacina , Fungicidas Industriais/análise , Giberelinas , Inseticidas/análise , Levofloxacino , Metanol , Metomil , Metronidazol , Norfloxacino , Pefloxacina , Reguladores de Crescimento de Plantas/análise , Purinas , Ronidazole , Solventes , Espectrometria de Massas em Tandem , TiabendazolRESUMO
Surface-enhanced Raman spectroscopy (SERS) has been extensively investigated for rapid and sensitive detection of trace level chemical contaminants in foods. Lack of selectivity to the targeted molecules in food matrices and fairly poor spectral reproducibility remain the main challenges for practical SERS applications. Herein, an ingenious strategy was proposed to hybridize molecularly imprinted polymers (MIPs) with gold nanoparticles as the functional SERS substrate for selective separation and detection of 2,4-dichlorophenoxyacetic acid (2,4-D), a systemic herbicide that has acute toxicity and potential cancer risk. The core-shell AuNPs@MIPs nanoparticles were finely tailored by wrapping an ultrathin layer of MIPs shell on the surface of AuNPs, which allowed selectively separating and enriching 2,4-D to the near surface of AuNPs and ensured the enhancement of Raman scattering signal of the analyte. Embedding an internal standard (i.e., 4-aminothiophenol) inside AuNPs@MIPs for SERS spectral calibration improved the quantification accuracy for 2,4-D. Three-dimensional finite difference time domain (3D-FDTD) simulation demonstrated the maximal electric field enhancement presented in the gap between adjacent AuNPs@MIPs with the theoretical enhancement factor (EF) as high as 5.85 × 106. Chemometric models established using SERS spectra showed accurate differentiation and quantification results for 2,4-D in milk at various contamination levels with a limit of detection (LOD) of 0.011 µg/mL. Our approach to integrate MIPs with noble metallic nanoparticles has great potential for selective and quantitative detection of analytes using SERS for practical agri-food analysis.
Assuntos
Herbicidas , Nanopartículas Metálicas , Ácido 2,4-Diclorofenoxiacético/análise , Animais , Ouro/química , Herbicidas/análise , Nanopartículas Metálicas/química , Leite/química , Reprodutibilidade dos Testes , Análise Espectral Raman/métodosRESUMO
Bark residues of the forest species Cedrela fissilis were physically and chemically modified with zinc chloride (ZnCl2) as an activating agent. The two modified materials were analyzed as adsorbents in removing atrazine and 2,4-D herbicides from effluents. Firstly, the precursor material and the modified ones were characterized by different techniques to identify the structural changes that occurred in the surfaces. Through TGA, it was observed that both modified materials have thermal stability close to each other and are highly superior to the precursor. X-ray diffractions proved that the amorphous structure was not altered, the three materials being highly heterogeneous and irregular. The micrographs showed that the treatments brought new spaces and cavities on the surface, especially for the material carbonized with ZnCl2. The pHPZC of the modified materials was close to 7.5. The physically modified material had a surface area of 47.31 m2 g-1 and pore volume of 0.0095 cm3 g-1, whereas the carbonized material had a surface area of 98.12 m2 g-1 and pore volume of 0.0099 cm3 g-1. Initial tests indicated that none of the adsorbents were efficient in removing 2,4-D. However, they showed good potential for removing atrazine. The Koble-Corrigan isothermal model best fits the experimental data, with a maximum capacity of 3.44 mg g-1 and 2.70 mg g-1 for physically modified and with ZnCl2, respectively. The kinetic studies showed that the system tends to enter into equilibrium after 120 min, presenting good statistical indicators to the linear driving force model (LDF). The surface diffusion coefficients were 2.18×10-9 and 2.37×10-9 cm2 s-1 for atrazine adsorption on the physically and chemically modified materials. These results showed that the application of residues from the processing of cedar bark is promising. However, new future studies must be carried out to improve the porous development of the material and obtain greater adsorption capacities.
Assuntos
Atrazina , Praguicidas , Poluentes Químicos da Água , Ácido 2,4-Diclorofenoxiacético/análise , Adsorção , Atrazina/análise , Carvão Vegetal/química , Cinética , Praguicidas/análise , Casca de Planta/química , Poluentes Químicos da Água/análiseRESUMO
The objective of this study was to evaluate the potential for non-invasive biomonitoring of 2,4-Dichlorophenoxyacetic acid (2,4-D) in saliva. Using an in vitro rat salivary gland epithelial cell (SGEC) system, a collection of experiments investigating chemical protein binding, temporal and directional transport, as well as competitive transport with para-aminohippuric acid (PAH), a substrate for renal organic anion transporters, was conducted to identify cellular transport parameters required to computationally model salivary transport of 2,4-D. Additionally, a physiological protein gradient was implemented to mimic physiologically relevant concentrations of protein in rat plasma and saliva, and under these conditions the transfer of 2,4-D was markedly slower, driven by increased protein binding (i.e. reduced free 2,4-D species available to cross salivary barrier). The rate of transfer was directly proportional to the amount of unbound 2,4-D and demonstrated no indication of active transport. An in vivo assessment of 2,4-D exposure in rats revealed non-linear protein binding in plasma, indicating saturated protein binding and increased levels of unbound 2,4-D species at higher doses. A strong correlation between 2,4-D concentrations in saliva and unbound 2,4-D in plasma was observed (Pearson correlation coefficient = 0.95). Saliva:plasma 2,4-D ratios measured in vivo (0.0079) were consistent within the linear protein binding range and expected 2,4-D levels from occupational exposures but were significantly different than ratios measured in vitro (physiological conditions) (0.034), possibly due to 2,4-D concentrations in saliva not being at equilibrium with 2,4-D concentrations in blood, as well as physiological features absent in in vitro settings (e.g. blood flow). We demonstrated that 2,4-D is consistently transported into saliva using both in vitro and in vivo models, making 2,4-D a potential candidate for human non-invasive salivary biomonitoring. Further work is needed to understand whether current sensor limits of detection are sufficient to measure occupationally relevant exposures.
Assuntos
Ácido 2,4-Diclorofenoxiacético/análise , Monitoramento Ambiental/métodos , Herbicidas/análise , Saliva/química , Ácido 2,4-Diclorofenoxiacético/sangue , Ácido 2,4-Diclorofenoxiacético/farmacocinética , Animais , Polaridade Celular/efeitos dos fármacos , Células Epiteliais , Herbicidas/sangue , Herbicidas/farmacocinética , Masculino , Exposição Ocupacional , Cultura Primária de Células , Ligação Proteica , Ratos , Ratos Sprague-Dawley , Glândulas Salivares/citologia , Glândulas Salivares/metabolismo , Junções Íntimas/efeitos dos fármacosRESUMO
The possible phytoremediation capacity of Plectranthus neochilus (boldo) exposed to the commercial pesticide (Aminol) in soil and water through consecutive extractions (days interval) was evaluated. After the exposure period, tea leaves from the plant were analyzed in terms of the presence of 2,4-D, total antioxidant capacity (DPPH), concentration of total polyphenols and flavonoids for plants exposed to soil and water. In water, 2,4-D remained up to 67% in the 60 days of experiment in the control group, which provided the use of two treatment groups with the plant (one group of plants for 30 days and another group in the remaining 30 days in the same system), thus, a decontamination up to 49% of the 2,4-D was obtained in this system with water. In both experiments (soil and water) the 2,4-D was not detected in tea leaves, the reduction of the antioxidant activity, polyphenols and flavonoids of plants exposed to the herbicide was also observed when compared to the non-exposed plants. In tea - plants in water - it was also possible to quantify the phenolic compounds and it was observed that in the group of plants of the first 30 days there was a decrease in caffeic acid and an increase in coumaric and ferulic acids, compared to the group of plants that were not exposed to 2,4-D. In the remaining 30 days with the new seedlings there was a decrease of the coumaric acid and an increase of the caffeic and ferulic acids.
Assuntos
Ácido 2,4-Diclorofenoxiacético/análise , Antioxidantes/análise , Biodegradação Ambiental , Herbicidas/análise , Folhas de Planta/química , Plectranthus/metabolismo , Ácidos Cafeicos/análise , Ácidos Cumáricos/análise , Tolerância a Medicamentos , Flavonoides/análise , Fenóis/análise , Polifenóis/análiseRESUMO
The Sinos River is one of the most polluted rivers in Brazil. The purpose of this work was to monitor the presence of some pesticides and hydrocarbons as well as the genotoxic and cytotoxic potential on HEp-2 cells from water samples collected at seven sites in the Sinos River Basin (SRB), southern Brazil. Nine samples were taken from the three main rivers in the SRB and used as a solution to dilute the HEp-2 cell culture medium after microfiltration. Twenty-four pesticides and 19 hydrocarbons were measured. Cytotoxicity was assessed by methyl thiazolyl tetrazolium (MTT) and neutral red (NR) assays, in which cells were exposed to different concentrations of the water samples for 24 h. Genotoxicity of the microfiltrated raw water samples was assessed by comet assay after 6 and 24 h of exposure. Among the chemicals analyzed, only the 2,4-D, dichloromethane, tetrachloroethene, chloroform, bromodichloromethane, styrene, and toluene were detected, but they were all lower than the limit established by Brazilian regulations. Twenty samples from a total of 60 had a cytotoxic effect in the MTT assay and 30 in the NR assay. The comet assay indicated the presence of genotoxic substances in the water at the seven locations monitored. Temporal and spatial variation was observed in the cytotoxicity and genotoxicity assays. Results indicated that the water in all stretches of the SRB is contaminated and it can cause harmful effects to humans and to the aquatic biota. This HEp-2 cell-line approach can be an additional tool for environmental monitoring.
Assuntos
Monitoramento Ambiental/métodos , Hidrocarbonetos/toxicidade , Praguicidas/toxicidade , Poluentes Químicos da Água/toxicidade , Ácido 2,4-Diclorofenoxiacético/análise , Ácido 2,4-Diclorofenoxiacético/toxicidade , Brasil , Ensaio Cometa , Hidrocarbonetos/análise , Praguicidas/análise , Rios/química , Poluentes Químicos da Água/análiseRESUMO
With the widespread application of plastic pipes in drinking water distribution system, the effects of various leachable organic chemicals have been investigated and their occurrence in drinking water supplies is monitored. Most studies focus on the odor problems these substances may cause. This study investigates the potential endocrine disrupting effects of the migrating compound 2,4-di-tert-butylphenol (2,4-d-t-BP). The summarized results show that the migration of 2,4-d-t-BP from plastic pipes could result in chronic exposure and the migration levels varied greatly among different plastic pipe materials and manufacturing brands. Based on estrogen equivalent (EEQ), the migrating levels of the leachable compound 2,4-d-t-BP in most plastic pipes were relative low. However, the EEQ levels in drinking water migrating from four out of 15 pipes may pose significant adverse effects. With the increasingly strict requirements on regulation of drinking water quality, these results indicate that some drinking water transported with plastic pipes may not be safe for human consumption due to the occurrence of 2,4-d-t-BP. Moreover, 2,4-d-t-BP is not the only plastic pipe-migrating estrogenic compound, other compounds such as 2-tert-butylphenol (2-t-BP), 4-tert-butylphenol (4-t-BP), and others may also be leachable from plastic pipes.
Assuntos
Água Potável/química , Estrogênios/efeitos adversos , Estrogênios/análise , Plásticos/química , Engenharia Sanitária , Ácido 2,4-Diclorofenoxiacético/análise , Animais , Humanos , Fenóis/análise , Polietileno/química , Qualidade da Água , Abastecimento de ÁguaRESUMO
2,4-Dichlorophenoxyacetic acid (2,4-D) is one of the most applicable herbicides in the world. Therefore, its residue in aquatic environment threatens the human health and ecosystems. In this study, Fe2O3 (hematite) nanoparticles (HNPs) were synthesized, and the characteristics of the obtained HNPs were determined using X-ray powder diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET) technique, and particle size analyzer (PSA). The catalytic activity of HNPs was evaluated for the activation of peroxymonosulfate (PMS) for the degradation of 2,4-D. The effects of the operating parameters were studied for the PMS/HNPs system. The results showed that the acidic condition provided higher efficiency, while overdosing of PMS had a scavenging effect. The PMS/HNPs showed high efficiency in comparison with the homogeneous forms of iron (Fe2+ and Fe3+). Reusability of HNPs was studied in five consequent usages. The presence of the anions (chloride, nitrate, and hydrogen phosphate) reduced the 2,4-D degradation. Moreover, the catalytic activity of HNPs was also investigated in the presence of other oxidants. UV irradiation increased the function of PMS/HNPs and its mechanism was described. The order of 2,4-D removal for the oxidants was PMS > persulfate > H2O2 > percarbonate. A total of 29.7% of 2,4-D chlorine content was released during the destruction of 2,4-D. The quenching study showed that sulfate radical was the major agent in the degradation of 2,4-D.
Assuntos
Ácido 2,4-Diclorofenoxiacético/análise , Compostos Férricos/química , Nanopartículas/química , Peróxidos/química , Poluentes Químicos da Água/análise , Ácido 2,4-Diclorofenoxiacético/efeitos da radiação , Catálise , Modelos Químicos , Oxidantes/química , Oxirredução , Sulfatos/química , Propriedades de Superfície , Raios Ultravioleta , Poluentes Químicos da Água/efeitos da radiaçãoRESUMO
In this study, a fixed bed flow through UVA-LED photoreactor was used to compare the efficiency of ozone, photocatalysis and photocatalysis-ozone degradation, and mineralization of two pure pesticides, 2,4-dichlorophenoxyacetic acid (2,4-D) and 2-methyl-4-chlorophenoxyacetic acid (MCPA), and a commercial one, Killex®. For the degradation of the parent compounds, ozone-based processes were more effective. While for mineralization, photocatalytic processes were more effective. Photocatalytic ozonation was the most efficient process for both the degradation and mineralization of the parent compounds. The degradation rates and mineralization by photocatalytic ozonation were higher than the summation of the corresponding rates by ozonation and photocatalysis, indicating a symbiotic relationship.Overall, the photocatalytic ozonation process with the fixed bed TiO2 reduces the time needed for the degradation and mineralization of the pesticides, reduces the costs of powder catalyst separation and overcomes the reduced efficiency of immobilized catalysts, which makes the process quite attractive for practical applications.
Assuntos
Ozônio/química , Praguicidas/química , Processos Fotoquímicos , Semicondutores , Raios Ultravioleta , Poluentes Químicos da Água/química , Ácido 2,4-Diclorofenoxiacético/análise , Ácido 2,4-Diclorofenoxiacético/química , Ácido 2-Metil-4-clorofenoxiacético/análise , Ácido 2-Metil-4-clorofenoxiacético/química , Catálise , Praguicidas/análise , Titânio/química , Poluentes Químicos da Água/análiseRESUMO
OBJECTIVE: A method for the simultaneous determination of 6 plant growth regulator (PGR) residues in bean sprout was developed by ultra high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). 6-Benzylaminopurine, isopentennyladenine, 4-chlorophenoxyacetic acid, 4-fluorophenoxyacetic acid, indole-3- acetic acid and indole-3-butyric acid were concerned. METHODS: Bean sprout samples were extracted by acetonitrile and QuEChERS extraction kit, purified by C18 powers. After centrifugation, the sample liquids was diluted 10 times by ultrapure water. The chromatographic analysis was carried out on an waters acquity UPLC BEH C18 column( 100 mm x 2.1 mm, 1.7 microm). The analyzer confirmed and quantified by mass spectrum of triple quadrupole in the multiple reaction monitoring (MRM) mode and quantified by matrix-matched external standard method. RESULTS: The calibration curves showed good linearity in each range with correlation coefficients greater than 0.998. 3 levels spiked recoveries were carried out using blank bean sprout extraction as substrate, the recoveries ranged from 84.2% to 107.5%, the relative standard deviations (RSDs) ranged from 3.08% to 12.71%. The qualitative limits of detections (S/N = 3) were 0.03-3.0 microg/kg and the quantitative limits(S/N = 10) were 0.1-10.0 microg/kg for the 6 PGRs. CONSLUSION: The method is simple and easy to operate, with less organic reagent, high sensitivity and good stability. It is suitable for the detection of 6 kinds of plant growth regulators in bean sprouts.
Assuntos
Phaseolus/química , Reguladores de Crescimento de Plantas/análise , Ácido 2,4-Diclorofenoxiacético/análogos & derivados , Ácido 2,4-Diclorofenoxiacético/análise , Compostos de Benzil , Cromatografia Líquida de Alta Pressão , Ácidos Indolacéticos/análise , Indóis/análise , Isopenteniladenosina/análise , Cinetina/análise , Purinas , Espectrometria de Massas em TandemRESUMO
Most studies on the relationship between Agent Orange and prostate cancer have focused on US veterans of the Vietnam War. There have been few studies focusing on the relationship between levels of prostate-specific antigen (PSA) and dioxins or steroid hormones in Vietnamese men. In 2009-2011, we collected blood samples from 97 men who had resided in a "dioxin hotspot" and 85 men from a non-sprayed region in Vietnam. Then levels of PSA, dioxins, and steroid hormones were analyzed. Levels of most dioxins, furans, and non-ortho polychlorinated biphenyls were higher in the hotspot than those in the non-sprayed region. Levels of testosterone, dehydroepiandrosterone, and estradiol differed significantly between the hotspot and the non-sprayed region, but there were no correlations between levels of PSA and steroid hormones and dioxins in either of the two regions. Our findings suggest that PSA levels in Vietnamese men are not associated with levels of dioxin or steroid hormones in these two regions.
Assuntos
Ácido 2,4,5-Triclorofenoxiacético/toxicidade , Ácido 2,4-Diclorofenoxiacético/toxicidade , Poluentes Ambientais/toxicidade , Hormônios Esteroides Gonadais/sangue , Dibenzodioxinas Policloradas/toxicidade , Antígeno Prostático Específico/sangue , Ácido 2,4,5-Triclorofenoxiacético/análise , Ácido 2,4-Diclorofenoxiacético/análise , Idoso , Agente Laranja , Benzofuranos , Dioxinas , Poluentes Ambientais/análise , Furanos/análise , Humanos , Masculino , Pessoa de Meia-Idade , Bifenilos Policlorados/análise , Neoplasias da Próstata , Esteroides , Testosterona , VietnãRESUMO
New immunosensors working in organic solvent mixtures (OPIEs) for the analysis of traces of different pesticides (triazinic, organophosphates and chlorurates) present in hydrophobic matrices such as olive oil were developed and tested. A Clark electrode was used as transducer and peroxidase enzyme as marker. The competitive process took place in a chloroform-hexane 50% (V/V) mixture, while the subsequent enzymatic final measurement was performed in decane and using tert-butylhydroperoxide as substrate of the enzymatic reaction. A linear response of between about 10nM and 5.0µM was usually obtained in the presence of olive oil. Recovery tests were carried out in commercial or artisanal extra virgin olive oil. Traces of pesticides were also checked in the oily matrix, in pomace and mill wastewaters from an industrial oil mill. Immunosensors show good selectivity and satisfactory precision and recovery tests performed in olive oil gave excellent results.
Assuntos
Ácido 2,4,5-Triclorofenoxiacético/análise , Ácido 2,4-Diclorofenoxiacético/análise , Desfolhantes Químicos/análise , Contaminação de Alimentos/análise , Óleos Industriais/análise , Azeite de Oliva/análise , Organofosfatos/análise , Praguicidas/análise , Dibenzodioxinas Policloradas/análise , Triazinas/análise , Agente Laranja , Técnicas Biossensoriais/métodos , Herbicidas/análise , Imunoensaio , Eliminação de Resíduos LíquidosRESUMO
A fully automated on-line system for monitoring the photocatalytic degradation of herbicides was developed using multisyringe flow injection analysis (MSFIA) coupled to a solid phase extraction (SPE) unit with UV detection. The calibration curves were linear in the concentration range of 100-1000 µg L(-1) for 3,6-dichloro-2-methoxybenzoic acid (dicamba) and 500-3000 µg L(-1) for 2,4-dichlorophenoxyacetic acid (2,4-D), while the detection limits were 30 and 135 µg L(-1) for dicamba and 2,4-D, respectively. The monitoring of the photocatalytic degradation (TiO2 anatase/UV 254 nm) of these two herbicides was performed by MSFIA-SPE system using a small sample volume (2 mL) in a fully automated approach. The degradation was assessed in ultrapure and drinking water with initial concentrations of 1000 and 2000 µg L(-1) for dicamba and 2,4-D, respectively. Degradation percentages of approximately 85% were obtained for both herbicides in ultrapure water after 45 min of photocatalytic treatment. A similar degradation efficiency in drinking water was observed for 2,4-D, whereas dicamba exhibited a lower degradation percentage (75%), which could be attributed to the presence of inorganic species in this kind of water.
Assuntos
Ácido 2,4-Diclorofenoxiacético/análise , Dicamba/análise , Monitoramento Ambiental/métodos , Herbicidas/análise , Sistemas On-Line , Poluentes Químicos da Água/análise , Ácido 2,4-Diclorofenoxiacético/química , Dicamba/química , Monitoramento Ambiental/instrumentação , Análise de Injeção de Fluxo/instrumentação , Análise de Injeção de Fluxo/métodos , Herbicidas/química , Sistemas On-Line/instrumentação , Fotólise , Extração em Fase Sólida/instrumentação , Extração em Fase Sólida/métodos , Poluentes Químicos da Água/químicaRESUMO
The detection of pesticides has attracted considerable attention in numerous fields, such as environmental monitoring and food safety. Although traditional sensors for pesticides have been widely explored due to their high sensitivity and specificity, it is still challenging to develop a low-cost, portable, fast, and easy-to-use detection method for the public use at home or in the field. To address these challenges, herein, we report a novel paper-based molecular imprinted polymer (MIP)-grafted multi-disk micro-disk plate (P-MIP-MMP) for sensitive and specific chemiluminescence (CL) detection of pesticides through an indirect competitive assay using 2,4-dichlorophenoxyacetic acid (2,4-D) as a proof-of-concept analyte. The MIP-grafted paper disks were prepared by a simple in situ polymerization of MIP layer on the surface of cellulose fibers in paper. The quantification mechanism of this P-MIP-MMP is based on a competition between free 2,4-D and tobacco peroxidase (TOP) labeled 2,4-D and the enzyme catalyzed CL emission from the luminol-TOP-H2O2 CL system. At optimal conditions, this P-MIP-MMP can detect 2,4-D at the concentration of femtomolar level. This approach provided a powerful protocol for simple, low-cost, rapid, and high-throughput detection of pesticides in real samples with satisfactory results for use in areas such as food inspection and environmental monitoring.
Assuntos
Ácido 2,4-Diclorofenoxiacético/análise , Técnicas Biossensoriais/instrumentação , Medições Luminescentes/instrumentação , Impressão Molecular , Praguicidas/análise , Polímeros/química , Celulose/química , Limite de Detecção , Luminescência , Modelos Moleculares , PapelRESUMO
Electrochemical impedance immunosensor, with its high sensitivity from electrochemical impedance analysis and ideal specificity from the immunoassay, is increasingly used in the detection of a kind of phenoxy acid herbicides which is 2,4-Dichlorophenoxybutyric acid (2,4-DB). In this experiment, synthetic 2,4-DB antibodies were immobilized on the electrode by the crosslinking of L-Cysteine/glutaraldehyde, and 2,4-DB were measured by the increase of electron-transfer resistance when the immune reaction occurred, with Fe(CN)(6)(3-)/Fe(CN)(6)(4-) as the probe. Under optimal conditions, the change of resistance is in a linear relationship with the logarithm of the concentration in the range of 1.0×10(-7)-1.0×10(-3) g/L (R=0.994) with the detection limit of 1.0×10(-7) g/L (0.1 ppb). This method bears such merits as simplicity in operation, high sensitivity, wide linear range, specificity, reproducibility and good stability. The actual soybean samples were analyzed with the recovery of 82.8%-102.3%.
Assuntos
Ácido 2,4-Diclorofenoxiacético/análogos & derivados , Técnicas Biossensoriais , Glycine max/química , Ácido 2,4-Diclorofenoxiacético/análise , Reprodutibilidade dos TestesRESUMO
The present study intended to develop receptor-mediated luciferase reporter gene assays to evaluate and compare the estrogen receptor (ER), androgen receptor (AR) and thyroid hormone receptor (TR) activities of target chemicals. Di-2-ethylhexyl-phthalate (DEHP), chlorpyrifos (CPF), 2,4-dichlorophenoxyacetic acid (2,4-D) and bisphenol A (BPA) are some of the most common contaminants in drinking water and are frequently detected in China and worldwide. The chemicals were tested at concentrations of 0.1, 1, 10 and 100 times their maximum contaminant level in drinking water. The results showed that BPA possessed various activities on ER, AR and TR. DEHP and CPF could suppress 17ß-estradiol or testosterone activity with different potencies, and DEHP possessed weaker anti-thyroid hormone activity. 2,4-D showed no agonist or antagonist activity against these hormone receptors, but it significantly enhanced the activity of testosterone through AR. Furthermore, the mixture of DEHP and CPF exhibited stronger ER and AR antagonist activities than each single component alone, but their combined effects were less than the expected effects based on the additive model. These results implied that the transcription activation mediated by hormone receptors was the potential endocrine-disrupting mechanism of the test chemicals. Our study also provided useful tools for evaluation of their endocrine disrupting activity.
Assuntos
Água Potável/química , Genes Reporter , Poluentes Químicos da Água/toxicidade , Ácido 2,4-Diclorofenoxiacético/análise , Ácido 2,4-Diclorofenoxiacético/toxicidade , Animais , Compostos Benzidrílicos , China , Chlorocebus aethiops , Clorpirifos/análise , Clorpirifos/toxicidade , Dietilexilftalato/análise , Dietilexilftalato/toxicidade , Água Potável/análise , Disruptores Endócrinos/toxicidade , Estradiol/genética , Luciferases/genética , Luciferases/metabolismo , Fenóis/análise , Fenóis/toxicidade , Receptores Androgênicos/genética , Receptores Androgênicos/metabolismo , Receptores de Estrogênio/genética , Receptores de Estrogênio/metabolismo , Receptores dos Hormônios Tireóideos/genética , Receptores dos Hormônios Tireóideos/metabolismo , Testosterona/genética , Testosterona/metabolismo , Células Vero , Poluentes Químicos da Água/análiseRESUMO
The risk assessment of groundwater pollution by pesticides may be based on pesticide sorption and biodegradation kinetic parameters estimated with inverse modeling of datasets from either batch or continuous flow soil column experiments. In the present work, a chemical non-equilibrium and non-linear 2-site sorption model is incorporated into solute transport models to invert the datasets of batch and soil column experiments, and estimate the kinetic sorption parameters for two pesticides: N-phosphonomethyl glycine (glyphosate) and 2,4-dichlorophenoxy-acetic acid (2,4-D). When coupling the 2-site sorption model with the 2-region transport model, except of the kinetic sorption parameters, the soil column datasets enable us to estimate the mass-transfer coefficients associated with solute diffusion between mobile and immobile regions. In order to improve the reliability of models and kinetic parameter values, a stepwise strategy that combines batch and continuous flow tests with adequate true-to-the mechanism analytical of numerical models, and decouples the kinetics of purely reactive steps of sorption from physical mass-transfer processes is required.
Assuntos
Ácido 2,4-Diclorofenoxiacético/química , Glicina/análogos & derivados , Herbicidas/química , Poluentes Químicos da Água/química , Ácido 2,4-Diclorofenoxiacético/análise , Adsorção , Biodegradação Ambiental , Difusão , Monitoramento Ambiental , Glicina/análise , Glicina/química , Água Subterrânea , Herbicidas/análise , Cinética , Modelos Químicos , Dinâmica não Linear , Poluentes do Solo/análise , Poluentes do Solo/química , Movimentos da Água , Poluentes Químicos da Água/análise , GlifosatoRESUMO
Molecularly imprinted polypyrrole (PPy) nanonecklaces were facilely synthesized through a two-step oxidative polymerization route for the amperometric detection of non-electrochemically active herbicide. It has been demonstrated that dissolved oxygen can preoxidize pyrrole to form PPy oligomer bundles, which further self-assemble into necklace-like micelles in the presence of cetyltrimethylammonium bromide. Subsequently, these microstructures were immediately gelled through quick polymerization of residual pyrrole monomers, leading to the formation of PPy nanonecklaces. Meanwhile, herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) was synchronously imprinted into the formed PPy and highly dense imprinted sites were generated in PPy nanonecklaces because the necklace-like structure with microgaps/pores provides the facile and complete removal of templates. The imprinted nanonecklaces exhibit the high capacity and fast kinetics to uptake 2,4-D molecules, and produce a imprinting factor of ~4.2. Importantly, the recognition and binding to 2,4-D significantly amplify the current response by a factor of 8 times in amperometric measurements, providing a sensitive detection of 2,4-D. The molecular imprinting strategy opens a novel avenue to the direct detection of non-electrochemically active species in a more convenient, simpler and cheaper way than the traditional competition-displacing approaches.
Assuntos
Ácido 2,4-Diclorofenoxiacético/análise , Técnicas Eletroquímicas/métodos , Herbicidas/análise , Impressão Molecular/métodos , Polímeros/análise , Pirróis/análise , Cetrimônio , Compostos de Cetrimônio/química , Técnicas Eletroquímicas/instrumentação , Humanos , Impressão Molecular/instrumentação , Nanoestruturas/análise , Nanoestruturas/química , Sensibilidade e EspecificidadeRESUMO
A single-chain variable fragment antibody against herbicide, 2,4-dichlorophenoxyacetic acid (2,4-D-scFv) has been successfully expressed in the hemolymph of silkworm larvae using a rapid Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid DNA system. Variable heavy- and light-chain domains were cloned directly from the cDNA of the hybridoma cell line 2C4 and assembled together with flexible peptide linker (Gly(4)Ser)(3) between two domains. The yield of functional 2,4-D-scFv after purification was 640 µg per 30 ml of hemolymph, which is equivalent to 21.3 mg per liter of hemolymph. The characterization of 2,4-D-scFv using an indirect competitive enzyme-linked immunosorbent assay (icELISA) revealed that it has wide cross-reactivities against 2,4,5-trichlorophenoxyacetic acid (65.5%), 2,4-dichlorophenol (47.9%), and 2,4-dichlorobenzoic acid (26.0%), making it possible to apply 2,4-D-scFv to icELISA for detecting/determining 2,4-D and its metabolites. Judging from its cost and time requirements and its ease of handling, this BmNPV bacmid DNA expression system is more useful for expressing functional scFv than bacterial systems, which frequently require costly and time-consuming refolding.