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Biomedical subjects

F Korte

Publications and source records attributed to F Korte.

At least 55 records · Page 3Linked to original sources

Long-term fate of organochlorine xenobiotics in aquatic ecosystems. Distribution, residual behavior, and metabolism of hexachlorobenzene, pentachloronitrobenzene, and 4-chloroaniline in small experimental ponds.

Hexachlorobenzene (HCB), pentachloronitrobenzene (PCNB), and 4-chloroaniline (4-CA) were dosed into the water of small experimental ponds in Southern Germany. The average concentration of the chemicals in the pond water during the application period (4-6 weeks) was about 50 micrograms/liter. Chemical residue concentrations were determined in water, sediment, and flora and fauna species up to 166 weeks after application. The decrease of all chemicals in the water phase follows exponential functions and can be correlated to some extent with the physicochemical properties such as volatility from water and vapor pressure. Although chemically quite different, the residual behavior of the model compounds followed a similar pattern resulting in relatively high initial concentrations in biota and a slow buildup and subsequent decline of concentrations in the sediment. As to some fauna species (backswimmers and libellula larvae) and to sediment (0- to 20-cm layers), even 3 years after application, 14C residues of about 0.1 mg/kg could be found. In all analyzed flora species, however, no more residues could be measured in the new vegetation period after application. The amounts of the chemicals used did not cause detectable symptoms of poisoning over the investigation period. Anisols and azo compounds were found to be conversion products of pentachloronitrobenzene and 4-chloroaniline.

Adsorption

Studies on 3-chloro-4-methyl-(4-14C)-7-hydroxycoumarin in rats.

The distribution, excretion and biotransformation of 3-chloro-4-methyl-(4-14C)-7-hydroxycoumarin [(14C) chlorferron] were studied in the rats after single oral administration. Male and female Wistar rats were given single oral doses of 0.5 and 20.0 mg/kg body weight of (14C) chlorferron and routes and rates of elimination of 14C activity were followed for 7 days. Following administration of 20 mg/kg, 96.74 +/- 3.68% and 94.98 +/- 6.15% of the dose were excreted by male and female rats, respectively. The excretion of total radioactivity after 0.5 mg/kg was significantly (P less than 0.05) higher in male rats (93.77 +/- 2.27%) as compared to female rats (87.23 +/- 1.96%). Approximately 80-90% of the excreted radioactivity was detected in urine. Analysis of urine showed no qualitative difference in the biotransformation pattern of (14C) chlorferron in male and female rats. (14C) chlorferron derived metabolites were excreted in both conjugated and unconjugated forms. After 7 days of dosing, very low concentrations of (14C) chlorferron derived residues were detected in different body tissues. No detectable sex difference in body distribution of radioactivity was observed. These results suggest that (14C) chlorferron is rapidly eliminated from the body and only small amounts are stored in the organs.

Animals

Biotransformation and disposition of the coumaphos metabolite 3-chloro-4-methyl-(4-14C)-7-hydroxycoumarin in rats.

The biotransformation and disposition of 3-chloro-4-methyl-(4-14C)-7-hydroxycoumarin [(14C) chlorferron] were investigated in rats after single oral administration. Following administration of (14C) chlorferron at 0.5 and 20 mg/kg body weight to male rats, greater than 90% of the given dose was eliminated in the urine (77-84%) and faeces (7-15%) within 24 h. Low levels of (14C) chlorferron derived residues were detected in different organs of rats 7 days after dosing. Administration of (14C) chlorferron at 20 mg/kg allowed the isolation of three metabolites in the 24-h urine of male and female rats. Compounds tentatively identified were dechlorinated metabolites of chlorferron besides unchanged chlorferron. The majority of the metabolites were excreted in conjugated forms. The pattern of biotransformation of chlorferron was qualitatively similar in male and female rats. Comparative studies on the elimination and biodistribution of (14C) chlorferron and its parent compound (14C) coumaphos in male rats indicated rapid metabolism and faster elimination of chlorferron and its metabolites from the body than that of the parent compound.

Animals

Elimination pattern and biodistribution of [14C]chlorferron in rats.

Administration of [14C]chlorferron in a single oral dose of 0.5 and 20 mg/kg body weight to female rats resulted in a urinary excretion of greater than 74% of the given dose during the first 24 h. Approx. 8% of the dose was eliminated in faeces within 7 days. 7 days after dosing, very low levels of [14C]chlorferron-derived residues were detected in all analyzed organs. These findings indicated that chlorferron was absorbed from the gastro-intestinal tract in appreciable quantities, but was rapidly excreted mainly via the urine with small amounts only in the faeces.

Animals

Metabolism of beta-hexachlorocyclohexane-14C in rats following low dosing in the daily diet.

beta-Hexachlorocyclohexane-14C (1.5 ppm) was administered in the diet to rats for one week. During the elimination phase three therapeutic agents were fed to enhance the clearance. Renal and fecal excreted radioactive products were collected for 8 weeks and extracted. Although significant differences in the total excreted amount of radioactivity were registered between controls and treated rats, there were no quantitative differences in the extractability of the excreta and no differences in the chemical nature of metabolites found. Radioactivity in urine consisted to 100% of conversion products, about 30% of which were unextractable residues. In the organic soluble fraction the 2,4,6-trichlorophenol was the major metabolite in urine and the only metabolite detected in feces. Minor conversion products of beta-HCH in urine were a trichlorohydroxyme-thoxybenzene, a dichlorophenol and a trace of a tetrachlorocyclohexane-isomer.

Animals

Fate of 14C-allylalcohol herbicide in soils and crop residues.

Residue disappearance and leaching of 14C-allylalcohol from different soils were studied in laboratory experiments. Additionally, the uptake of residues by lettuce and carrots was investigated in the greenhouse. In laboratory experiments, residue disappearance and leaching from soils was correlated negatively to the organic matter content. In greenhouse experiments with a sandy loam soil at an application rate normally used in practice, an average of 12.5% of the applied radioactivity was recovered after an eight day interval between application and sowing. Furthermore, an average of 8% (sum in soil and plants) of the applied radioactivity was recovered after lettuce or carrot growing. Uptake of residues was higher by carrots than by lettuce, and higher by lettuce roots than by lettuce tops. No bioaccumulation was observed. The residues in soils and plants were, to a high percent-age, unextractable and, to a smaller extent, fully water-soluble products. Unchanged allylalcohol could not be detected by the analytical methods used.

1-Propanol

Fingerprint analyses of plant and animal tissues with respect to the occurrence of foreign compounds.

Glass capillary chromatography can be used for the characterization of complex mixtures of plant and animal samples after clean-up by counter-current distribution. For good reproducibility of fingerprint patterns a special splitless injection system is used. This method prevents any loss at injection. In order to determine organochlorine substances also in trace amounts (a few pg) an electroncapture detector (ECD) was used. Each step in the analysis procedure was checked with the aid of radioactively labelled substances, e.g. the polar compound pentachlorophenol and the non-polar compound hexachlorobenzene. With the aid of capillary chromatography-mass spectrometry substances in complex mixtures in a concentration of 10 to 100 ng/microliters can be characterized. Suitable glass capillaries for these investigation were prepared in this laboratory. The results indicate that a standardization of the procedure is practicable.

Animals

Fate of chloroalkylene-9-14C in carrots, sugar beets, and soil under outdoor conditions.

Immediately after application of chloroalkylene-9-14C to soil (1.32 ppm, based on dry weight of soil in the upper layer of 0 to 10 cm) under outdoor conditions, carrots were sown; in the following year, sugar beets were grown. About 80% of the radioactivity applied volatilized within one vegetation period. Most of the remaining radioactivity was still in the upper soil layer; 0.8% had dispersed to a depth of 40 cm, and 3.3% was taken up by the carrot plants. In the second year, no more decreases of soil residues was observed; uptake by sugar beets was 0.1% of the applied radioactivity. In the first year, the residues in the upper soil layer consisted of 41% unchanged chloroalkylene-9, 19% soluble metabolites, and 40% unextractable residues; the amount of unextractable residues rose to 68% in the second year. The following conversion products were characterized in the soil extracts: a monohydroxylated dichlorobiphenyl, a monomethoxylated dichlorobiphenyl, and two isomeric monohydroxylated, monoisopropylated dichlorobiphenyls; in carrot roots, a monomethoxylated dichlorobiphenyl was detected. Conjugates occurring in the soil yielded, after acid hydrolysis, a monohydroxylated dichlorobiphenyl among other compounds.

Hydrolysis

Mass spectrometry and stability of t-butyldimethylsilylethers of some estrogens and androstanes.

In addition to using radioimmunoassays for the determination of estrogens and other steroids, the possibility of using mass fragmentography for analysis was investigated. t-Butyldimethylsilyl chloride was selected as a reagent for derivatisation because it forms rather stable silylethers. In all the mass-spectra obrained from the steroid derivatives, one pronounced peak suitable for mass fragmentography was always present. Some of the spectra of the investigated estrogens, as well as testosterone, 3 alpha-hydroxy-5 alpha-androstan-17-one and 17 alpha-methyl-17 beta-hydroxy-5 alpha-androstan-3-one are discussed. The stability of various t-butyldimethylsilylethers and the rate of enolization of testosterone and progesterone in the presence of the silylation-agent under different conditions were established.

Androstanes