The aim of study was evaluation of the concentration of dermally applied (14)C DDT in the organs of rats, and evaluation of histological and ultrastructural changes after the dermal application of unlabelled DDT standard in the organs of rats, in which the presence of this pesticide was determined by the radio-isotopic method. (14)C DDT of radiochemical purity of 97% was applied in the study. The activity of the preparation per 1 cm(2) of the tail skin was 22.2 KBq--(175.38 microg DDT). The material for the study was taken directly after single exposure and 6 h, 8 h, 10 h, 12 h, 14 h, 18 h and 20 h after exposure. The following organs were taken for the determination of radioactivity of tissues: brain, heart, lung, liver, kidney, skin at the site of exposure. Unlabelled chemically pure, DDT (99.7%) was used to evaluate histological and ultrastructural changes after dermal application. Experimental animals received an oil emulsion of DDT (10 mg/9 cm(2)), applied to the skin of the tail for 4 weeks. The time of exposure was 4h daily. The animals of the control group were dermally exposed to the emulsion at the same time and under the same conditions. 4 h after dermal exposure it was observed that the preparation applied on the surface of 9 cm(2) in the amount of 1.578 microg was present in the skin in the amount of 1 microg/9 cm(2) (0.11 microg/cm(2)), i.e. 0.063% of (14)C DDT applied dose. Directly after dermal application lasting 4 h the greatest amount of (14)C DDT was noted in the liver--0.285 microg, i.e. 0.033 micrcog/g. Histopatological and ultrastructural changes were observed in the liver, kidney, lungs and heart.
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Chem Res Toxicol
January 2015
Biology and Biotechnology Research Division, and ¶the Center for Accelerator Mass Spectrometry, Lawrence Livermore National Laboratory , Livermore, California 94550, United States.
Dibenzo(def,p)chrysene (DBC), (also known as dibenzo[a,l]pyrene), is a high molecular weight polycyclic aromatic hydrocarbon (PAH) found in the environment, including food, produced by the incomplete combustion of hydrocarbons. DBC, classified by IARC as a 2A probable human carcinogen, has a relative potency factor (RPF) in animal cancer models 30-fold higher than benzo[a]pyrene. No data are available describing the disposition of high molecular weight (>4 rings) PAHs in humans to compare to animal studies.
View Article and Find Full Text PDFMar Pollut Bull
December 2012
Marine Biology and Ecology Research Centre, School of Marine Science and Engineering, Plymouth University, Drake Circus, Plymouth, Devon PL4 8AA, United Kingdom.
Plastics are known to sorb persistent organic pollutants from seawater. However, studies to quantify sorption rates have only considered the affinity of chemicals in isolation, unlike the conditions in the environment where contaminants are present as complex mixtures. Here we examine whether phenanthrene and 4,4'-DDT, in a mixture, compete for sorption sites onto PVC with no added additives (unplasticised PVC or uPVC) and Ultra-High Molecular Weight polyethylene.
View Article and Find Full Text PDFChemosphere
August 2009
Department of Environmental Chemistry, Stockholm University, SE-10691 Stockholm, Sweden.
For the first time, a pathway for synthesis of 2-(4-chlorophenyl)-2-(4-chloro-3-thiophenol)-1,1-dichloroethene (3-SH-DDE), is presented. The compound is of particular interest as a precursor for synthesis of alkylsulfonyl-DDE containing different alkyl groups to discover structural activity relationships, and to promote synthesis of radiolabeled methylsulfonyl-DDE. 2-Chloro-5-methylphenol was first methylated and further oxidized to the corresponding benzoic acid.
View Article and Find Full Text PDFEnviron Res
October 2008
Department of Environmental and Occupational medicine, Unit of Cellular and Molecular Toxicology, Institute of Public Health, University of Aarhus, Aarhus, Vennelyst Boulevard 6, Bygn 1260, 8000 Aarhus C, DK, Denmark.
There are a number of interactions related to the transport of lipophilic xenobiotic compounds in the blood stream of mammals. This paper will focus on the interactions between lipoproteins and persistent organic pollutants (POPs) and how these particles are taken up by cells. A number of POPs including the pesticide p,p'-dichlorodiphenyltrichloroethane (DDT), and especially its metabolite p,p'-dichlorodiphenyldichloroethene (DDE), interacts with nuclear hormone receptors causing these to malfunction, which in turn results in a range of deleterious health effects in humans.
View Article and Find Full Text PDFJ Chromatogr A
April 2007
State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China.
Aqueous solutions of (14)C-labeled analogs of seven hydrophobic organic chemicals (HOCs) were subject to solid-phase microextraction (SPME) under static conditions to assess their multi-compartment distribution and to compare poly(dimethyl)siloxane (PDMS)-water partition coefficients (K(f) values) with previously reported values. To accomplish this, a protocol for quantitative desorption of radiolabelled HOCs from SPME fibers using hexane was developed. Time series extractions indicated that loading of SPME fibers had reached steady-state by day 8 for PCBs 52, 77 and 153, phenanthrene, benzo[a]pyrene, p,p'-DDT and p,p'-DDE.
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