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1.
Int J Hyg Environ Health ; 220(2 Pt A): 254-260, 2017 03.
Artículo en Inglés | MEDLINE | ID: mdl-27939065

RESUMEN

In spite of food safety controls for pesticide residues, a conventional diet still leads to a noticeable exposure of the general population to several pesticides. In a pilot study the response of exposure reduction by organic diet intervention on the urinary levels of pesticide metabolites was investigated. In the study two adult individuals were kept on a conventional diet for 11days and morning urine voids were collected at the last four days of the period. Afterwards, the participants switched to exclusively organic food intake for 18days and likewise morning urine samples were collected at the last four days of this period. In the urine samples six pyrethroid metabolites, six dialkylphosphates, four phenolic parameter for organophosphate pesticides and carbamates, 6-chloronicotinic acid (ClNA) as parameter for neonicotinoid insecticides, seven phenoxy herbicides, glyphosate and its metabolite AMPA were quantified using gas chromatographic mass spectrometric methods. Generally, the comparative analyses revealed greater shares as well as higher levels of the parameters in the samples taken during the common diet period compared to the organic diet period. Considerable decrease of the levels was found for almost all pyrethroid metabolites, dialkyphosphates and phenoxy herbicids, as well as for the phenolic metabolites 4-nitrophenol and 3,5,6-trichloropyridinol. In contrast, higher values were found for the organic diet period for ClNA and the metabolite of coumaphos in one of the volunteers. The present study confirms the results of former studies which indicated that an organic diet intervention results in considerable lower exposure to organophosphate pesticides and pyrethroids. It also verifies the former experience that monitoring of urinary parameters for non-persistent pesticides permits a reliable efficiency control of short-time effects by dietary interventions. Additionally to former studies, the results of the present study highlight the need of an extension of the parameter spectrum to all prominent pesticide groups.


Asunto(s)
Dieta , Exposición a Riesgos Ambientales/análisis , Exposición a Riesgos Ambientales/prevención & control , Contaminantes Ambientales/orina , Contaminación de Alimentos , Alimentos Orgánicos , Plaguicidas/orina , Femenino , Glicina/análogos & derivados , Glicina/orina , Humanos , Masculino , Persona de Mediana Edad , Ácidos Nicotínicos/orina , Organofosfatos/orina , Fenoxiacetatos/orina , Piretrinas/orina , Glifosato
2.
Pharmazie ; 70(4): 219-24, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26012250

RESUMEN

A highly sensitive and rapid liquid chromatography-tandem mass spectrometry method was developed for the determination of clinofibrate in human urine. The analyte and IS were extracted through a simple protein precipitation by the mixture of acetonitrile and 1 mol/L hydrochloric acid (95:5, v/v) and separated on an Inspire C18 (150 mm x 4.6 mm I.D., 5 µm particle size) column using isocratic elution with methanol and water containing 0.1% formic acid and 10 mM ammonium acetate (90:10, v/v). Mass spectrometric detection was performed in electrospray positive ionization MRM mode. The mass transition was m/z 486.3-->175.0 for clinofibrate and m/z 361.1-->233.1 for IS, respectively. The flow rate was 0.6 mL/min and the column oven temperature was set at 35 °C. The total run time was 6.5 min. Good linear relationships were obtained for all analytes over the concentrations ranging of 0.1002-10.02 µg/mL (r2 = 0.9991) and the limit of quantification was 0.1002 µg/mL. The extraction recovery was larger than 87.4% and intra- and inter-batch precision and accuracy with RSD were all less than 6.5%. The total amount of unchanged clinofibrate excreted in urine was less than 0.34%. This method was successfully applied to the pharmacokinetic study of clinofibrate in human urine.


Asunto(s)
Hipolipemiantes/orina , Fenoxiacetatos/orina , Adulto , Cromatografía Líquida de Alta Presión , Femenino , Fenofibrato/farmacocinética , Fenofibrato/orina , Humanos , Hipolipemiantes/farmacocinética , Masculino , Fenoxiacetatos/farmacocinética , Estándares de Referencia , Reproducibilidad de los Resultados , Espectrometría de Masa por Ionización de Electrospray , Espectrometría de Masas en Tándem
3.
Br J Haematol ; 130(1): 138-44, 2005 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-15982356

RESUMEN

Hydroxyurea is increasingly used in the treatment of sickle cell disease (SCD) although there is little evidence on how best to monitor treatment and compliance. It is also not known why 10-50% patients do not benefit from the drug and whether some of this resistance is because of pharmacokinetic factors. We have developed an assay using mass spectrometry (MS) to measure urinary concentrations of hydroxyurea. We have used this assay to study 12 children and six adults with SCD taking hydroxyurea and found that urinary hydroxyurea was present for at least 12 h following tablet ingestion. Thirty-five urine samples were analysed that were expected to contain hydroxyurea, based on the reported timing of the last dose and hydroxyurea was detected in 29 (83%) of these. There were also marked differences in urinary hydroxyurea concentrations, suggesting pharmacokinetic variability may explain some of the differences in response to hydroxyurea. Urine samples were also analysed by MS for penicillin metabolites and 43 of the 57 (75%) contained phenoxyacetate, suggesting the ingestion of penicillin within the last 12 h. These assays are potentially useful to study hydroxyurea metabolism further, develop optimal dosing regimes and monitor compliance with treatment.


Asunto(s)
Anemia de Células Falciformes/orina , Antidrepanocíticos/orina , Hidroxiurea/orina , Adolescente , Anemia de Células Falciformes/tratamiento farmacológico , Antidrepanocíticos/uso terapéutico , Biomarcadores/orina , Niño , Creatinina/orina , Quimioterapia Combinada , Femenino , Humanos , Hidroxiurea/uso terapéutico , Masculino , Cooperación del Paciente , Penicilina V/uso terapéutico , Fenoxiacetatos/orina
4.
Mutagenesis ; 1(4): 241-5, 1986 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-3331666

RESUMEN

The effects of phenoxyacetic acid herbicides were investigated on the induction of chromosome aberrations in human peripheral lymphocyte cultures in vitro and in lymphocytes of exposed workers in vivo. Pure 2,4-dichlorophenoxyacetic acid (2,4-D; 0.125, 0.150, 0.200 and 0.350 mM) did not increase the number of aberrations, whereas the commercial 2,4-D formulation (0.125, 0.250, 0.500, 1.000 and 1.250 mM, with respect to phenoxyacetic acid concentration) significantly increased the number of chromosome aberrations in vitro (without exogenous metabolic activation). The phenoxy acid levels in the breathing zone of the workers varied between 0.3 and 0.4 mg/m3, and the concentrations of phenoxyacetic acids in the urine of the workers after exposure varied from 0.000 to 0.055 mmol/l. There were no increases in chromosome aberrations in peripheral lymphocytes of the exposed subjects.


Asunto(s)
Ácido 2,4-Diclorofenoxiacético/efectos adversos , Aberraciones Cromosómicas , Glicolatos/efectos adversos , Fenoxiacetatos/efectos adversos , Ácido 2-Metil-4-clorofenoxiacético/efectos adversos , Ácido 2-Metil-4-clorofenoxiacético/orina , Agricultura , Humanos , Linfocitos , Masculino , Enfermedades Profesionales/inducido químicamente , Fenoxiacetatos/orina
6.
J Pharm Sci ; 67(8): 1095-8, 1978 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-671244

RESUMEN

A sensitive GLC assay for ticrynafen, a diuretic agent with uricosuric properties, and its two metabolites in urine, serum, and plasma is described. The method employs methylation of carboxylic acid groups and trimethylsilyation of the hydroxyl group on one metabolite that cannot otherwise be separated readily from ticrynafen as a simple methyl ester. Urinary output and serum or plasma levels of ticrynafen and its two metabolites were measured in specimens from human volunteers receiving one 250-mg tablet.


Asunto(s)
Diuréticos/análisis , Glicolatos/análisis , Fenoxiacetatos/análisis , Tiofenos/análisis , Animales , Cromatografía de Gases , Diuréticos/sangre , Diuréticos/orina , Perros , Humanos , Espectrometría de Masas , Métodos , Fenoxiacetatos/sangre , Fenoxiacetatos/orina , Plasma/análisis , Tiofenos/sangre , Tiofenos/orina
7.
Xenobiotica ; 7(8): 457-68, 1977 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-888448

RESUMEN

1. The effect of a carboxyl substituent on the metabolism of aromatic aldehydes has been examined in several species of animals. 2. Phthalaldehydic acid was exclusively reduced to the corresponding alcohol in mice, rats, rabbits, dogs and man. The oxidized metabolite phthalic acid was not detected appreciably in any species. 3. Iso- and terephthalaldehydic acid were oxidized to the corresponding dicarboxylic acids in rats and dogs. The reduced metabolites were not detected. 4. The aldehyde group of o-formylphenoxyacetic acid and o-formylphenoxypropionic acid was largely reduced to the corresponding alcohol in rats, rabbits and dogs. In contrast, oxidation to the carboxylic acid predominant over the reduction in mice. In the former three species, the amount of the minor metabolite carboxylic acid was larger with o-formylphenoxypropionic acid than with o-formylphenoxyacetic acid. 5. 1,8-Naphthaldehydic acid, m- and p-formylphenoxyacetic acid were mainly oxidized to the corresponding carboxylic acids in rats. 6. It was concluded that aromatic aldehydes bearing a carboxyl group in the ortho position, attached either directly or indirectly to the benzene nucleus, tend to be reduced to the corresponding alcohols in animals.


Asunto(s)
Aldehídos/orina , Ácidos Carboxílicos/orina , Adulto , Animales , Cromatografía de Gases , Perros , Humanos , Masculino , Espectrometría de Masas , Ratones , Fenoxiacetatos/orina , Ácidos Ftálicos/orina , Conejos , Ratas , Especificidad de la Especie , Relación Estructura-Actividad
8.
Naunyn Schmiedebergs Arch Pharmacol ; 296(2): 87-9, 1977 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-834318

RESUMEN

It is shown that 4-acetaminophenoxyacetic acid (APOA) is an urinary metabolite of phenacetin. APOA was isolated by means of silica gel TLC in various solvent systems from the urine of rats, dogs, and humans, collected 24 h after p.o. treatment with phenacetin (rats and dogs: 200 mg/kg; humans: three single doses of 0.5 g). Expressed as a percentage of the dose, APOA was detected at levels of 1% in rats, 0.13% in dogs and 0.04% in humans. 4-Acetaminophenoxyacetic acid was identified as its methylester--synthetized in the reaction of APOA and diazomethene--by thin layer chromatography, UV absorbance, melting point, and mass spectroscopy.


Asunto(s)
Glicolatos/orina , Fenacetina/orina , Fenoxiacetatos/orina , Animales , Cromatografía en Capa Delgada , Perros , Femenino , Humanos , Masculino , Ratas
9.
J Chromatogr ; 123(2): 379-84, 1976 Aug 04.
Artículo en Inglés | MEDLINE | ID: mdl-956314

RESUMEN

A gas-liquid chromatographic method is described for the determination of tienilic acid (SKF 62.698), a diuretic with uricosuric properties, in human plasma and urine. The method, which is based on the methylation of the compound, is rapid, specific and sensitive. The lowest level accurately determined is about 50 ng/ml in plasma and 1 mug/ml in urine. The first results from a human volunteer are given.


Asunto(s)
Cromatografía de Gases , Diuréticos/análisis , Glicolatos/análisis , Fenoxiacetatos/análisis , Tiofenos/análisis , Cromatografía Liquida , Diuréticos/sangre , Diuréticos/orina , Humanos , Métodos , Metilación , Fenoxiacetatos/sangre , Fenoxiacetatos/orina , Tiofenos/sangre , Tiofenos/orina , Uricosúricos/sangre , Uricosúricos/orina
10.
Toxicology ; 3(3): 349-59, 1975.
Artículo en Inglés | MEDLINE | ID: mdl-123666

RESUMEN

The herbicieds 2-methyl-4-chlorophenoxy acetic acid (MCPA) and 2-(2-methyl-4-chlorophenoxy) propionic acid (MCPP or mecoprop) were tested for 90 days in rats. The compounds were added to the diet at levels of 0, 50, 400, and 3200 ppm. Growth, food intake, mortality, haematology, blood and liver chemistry, organ weights and histopathology were used as criteria. The main effects of both compounds were growth retardation and elevated relative kidney weights at levels of 400 ppm and more. The 50 ppm dose level can be considered as a no-toxic-effect level in the 90-day study. In subacute dermal studies in rabbits during 3 weeks the dosages were 0, 0.5, 1.0 and 2 g MCPA or MCPP per kg body weight. Therafter followed a recovery period of 2 weeks. Growth, mortality, skin reaction, haematology, organ weights (MCPP) and histopathology were recorded and determined. Both compounds caused slight to moderate erythema at all dose levels, whereas elasticity of the skin was decreased. In both experiments the skin returned to normal during the recovery period. Weight loss was observed at all dose levels. In the MCPA experiment high mortality and histopathological changes in the liver, kidneys, spleen and thymus were recorded at the two highest dose levels. The cause of this could have been either the treatment with MCPA or a dysbacteria infection which developed during the experiment. Oral and intraperitoneal acute toxicity of MCPP for the rat were found to be 1210 and 402 mg/kg, respectively. After a single oral or dermal application of MCPA to the rabbit, the compound was excreted unchanged in the urine.


Asunto(s)
Glicolatos/toxicidad , Herbicidas/toxicidad , Fenoxiacetatos/toxicidad , Propionatos/toxicidad , Administración Oral , Animales , Conducta Animal/efectos de los fármacos , Peso Corporal/efectos de los fármacos , Clorobencenos/toxicidad , Enzimas/sangre , Eritema/inducido químicamente , Conducta Alimentaria/efectos de los fármacos , Femenino , Inyecciones Intraperitoneales , Dosificación Letal Mediana , Masculino , Tamaño de los Órganos , Fenoxiacetatos/sangre , Fenoxiacetatos/orina , Éteres Fenílicos/toxicidad , Propionatos/sangre , Conejos , Ratas , Piel/efectos de los fármacos , Organismos Libres de Patógenos Específicos , Factores de Tiempo , Tolueno/análogos & derivados , Tolueno/toxicidad , Urea/sangre
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