. . . "Environmental Science & Technology" . "P(GA525/08/1590), Z(MZE0002716202)" . "Ciganek, Miroslav" . "Vondr\u00E1\u010Dek, Jan" . "14"^^ . . "6"^^ . . "45" . . . . "6" . "P\u00E1lkov\u00E1, Lenka" . "Polar Compounds Dominate in Vitro Effects of Sediment Extracts"@en . . . . "L\u00FCbcke-von Varel, U." . . . "Polar Compounds Dominate in Vitro Effects of Sediment Extracts" . . . "JUNCTIONAL INTERCELLULAR COMMUNICATION; RECEPTOR-MEDIATED LUCIFERASE; BROMINATED FLAME RETARDANTS; EFFECT-DIRECTED ANALYSIS; POLYCHLORINATED NAPHTHALENES; RECOMBINANT TRANSTHYRETIN; FRACTIONATION PROCEDURE; COMPLEX-MIXTURES"@en . "[A29DB424C6F5]" . "6"^^ . . "Polar Compounds Dominate in Vitro Effects of Sediment Extracts"@en . . . . . "Ne\u010Da, Ji\u0159\u00ED" . "Polar Compounds Dominate in Vitro Effects of Sediment Extracts" . . . "RIV/00027162:_____/11:#0000784!RIV12-MZE-00027162" . . "Sediment extracts from three polluted sites of the river Elbe basin,were fractionated using a novel online fractionation procedure. Resulting fractions were screened for mutagenic, aryl hydrocarbon receptor (AhR)-mediated, transthyretin (TTR)-binding, and estrogenic. activities and their potency to inhibit gap junctional intercellular communication (GJIC) to compare toxicity patterns and identify priority fractions. Additionally, more than 200 compounds and compound classes were identified using GC-MS/MS, LC-MS/MS, and HPL,C-DAD methods. For all investigated end, points, major activities were found in polar fractions, which are defined here as fractions containing dominantly compounds with atleast one polar functional group. Nonpolar PAR fractions contributed to mutagenic,andAhR-mediated activities while inhibitior of GJIC and estrogenic and TTR-binding activities were exclusively observed in the polar fractions. Known mutagens in polar fractions included nitro and dinitro-PAHs, azaarenes, and keto-PAHs, while parent and monomethylated PAHs such as benzo[a]pyrene and benzofluoranthenes were identified in nonpolar fractions. Additionally, for one sample, high AhR-mediated activities Were determined in one fraction characterized by PCDD/Fs, PCBs, and PCNs. Estrone, 17 beta -estradiol, 9H-benz[de]anthracen-7-one, and 4-nonylphenol were identified as possible estrogenic and TTR-binding compounds. Thus, not only nonpolar compounds such as PCBs, and PCDD/Fs but also the less characterized and investigated more polar substances should be considered as Potent mutagenic, estrogenic, AhR-inducing, TTR-binding, and GJIC-inhibiting components for future studies."@en . "Machala, Miroslav" . "0013-936X" . . "P\u011Bn\u010D\u00EDkov\u00E1, Kate\u0159ina" . . . . "221056" . "Sediment extracts from three polluted sites of the river Elbe basin,were fractionated using a novel online fractionation procedure. Resulting fractions were screened for mutagenic, aryl hydrocarbon receptor (AhR)-mediated, transthyretin (TTR)-binding, and estrogenic. activities and their potency to inhibit gap junctional intercellular communication (GJIC) to compare toxicity patterns and identify priority fractions. Additionally, more than 200 compounds and compound classes were identified using GC-MS/MS, LC-MS/MS, and HPL,C-DAD methods. For all investigated end, points, major activities were found in polar fractions, which are defined here as fractions containing dominantly compounds with atleast one polar functional group. Nonpolar PAR fractions contributed to mutagenic,andAhR-mediated activities while inhibitior of GJIC and estrogenic and TTR-binding activities were exclusively observed in the polar fractions. Known mutagens in polar fractions included nitro and dinitro-PAHs, azaarenes, and keto-PAHs, while parent and monomethylated PAHs such as benzo[a]pyrene and benzofluoranthenes were identified in nonpolar fractions. Additionally, for one sample, high AhR-mediated activities Were determined in one fraction characterized by PCDD/Fs, PCBs, and PCNs. Estrone, 17 beta -estradiol, 9H-benz[de]anthracen-7-one, and 4-nonylphenol were identified as possible estrogenic and TTR-binding compounds. Thus, not only nonpolar compounds such as PCBs, and PCDD/Fs but also the less characterized and investigated more polar substances should be considered as Potent mutagenic, estrogenic, AhR-inducing, TTR-binding, and GJIC-inhibiting components for future studies." . . "RIV/00027162:_____/11:#0000784" . "US - Spojen\u00E9 st\u00E1ty americk\u00E9" .