Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Mol Nutr Food Res ; 55(4): 509-21, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21351250

RESUMO

Fatty acid esters of 3-chloropropane-1,2-diol (3-MCPD) and glycidol are a newly identified class of food process contaminants. They are widespread in refined vegetable oils and fats and have been detected in vegetable fat-containing products, including infant formulas. There are no toxicological data available yet on the 3-MCPD and glycidol esters, and the primary toxicological concern is based on the potential release of 3-MCPD or glycidol from the parent esters by lipase-catalyzed hydrolysis in the gastrointestinal tract. Although 3-MCPD is assessed as a nongenotoxic carcinogen with a tolerable daily intake (TDI) of 2 µg/kg body weight (bw), glycidol is a known genotoxic carcinogen, which induces tumors in numerous organs of rodents. The initial exposure estimates, conducted by Federal Institute for Risk Assessment (BfR) under the assumption that 100% of the 3-MPCD and glycidol are released from their esters, revealed especially that infants being fed commercial infant formula could ingest harmful amounts of 3-MCPD and glycidol. However, the real oral bioavailability may be lower. As this gives rise for toxicological concern, the currently available toxicological data of 3-MCPD and glycidol and their esters are summarized in this review and discussed with regard to data gaps and further research needs.


Assuntos
Carcinógenos/toxicidade , Compostos de Epóxi/toxicidade , Ésteres/toxicidade , Ácidos Graxos/química , Contaminação de Alimentos , Mutagênicos/toxicidade , Propanóis/toxicidade , alfa-Cloridrina/toxicidade , Animais , Biotransformação , Carcinógenos/administração & dosagem , Carcinógenos/química , Carcinógenos/farmacocinética , Compostos de Epóxi/administração & dosagem , Compostos de Epóxi/química , Compostos de Epóxi/farmacocinética , Ésteres/administração & dosagem , Ésteres/química , Ésteres/farmacocinética , Feminino , Humanos , Infertilidade Masculina/induzido quimicamente , Masculino , Mutagênicos/administração & dosagem , Mutagênicos/química , Mutagênicos/farmacocinética , Neoplasias/induzido quimicamente , Óleos de Plantas/efeitos adversos , Óleos de Plantas/química , Propanóis/administração & dosagem , Propanóis/química , Propanóis/farmacocinética , Insuficiência Renal/induzido quimicamente , Medição de Risco , alfa-Cloridrina/administração & dosagem , alfa-Cloridrina/análise , alfa-Cloridrina/farmacocinética
2.
Mutat Res ; 394(1-3): 59-68, 1997 Nov 27.
Artigo em Inglês | MEDLINE | ID: mdl-9434844

RESUMO

In this study, the vicinal chloroalcohols 1,3-dichloro-2-propanol (DC2P), 3-chloro-1,2-propanediol (3CPD) and 2-chloro-1,3-propanediol (2CPD) were investigated for genotoxicity in the wing spot test of Drosophila. DC2P is an important starting material in many processes of synthesis in chemical industry. 3CPD as well as some related glycerol chlorohydrins were identified in protein hydrolysates industrially used for the production of food items such as seasonings, sauces and soups. The wing spot test is a somatic mutation and recombination test (SMART) and is a sensitive in vivo assay for the detection of mutagens and promutagens. The test was applied here in its standard version with normal bioactivation and in a variant with increased cytochrome P450-dependent bioactivation capacity. All three compounds were clearly non-genotoxic in these in vivo assays. The results are in agreement with recent findings which strongly suggest that positive genotoxicity results in in vitro testing of vicinal chloroalcohols such as DC2P are due to directly acting genotoxic intermediates arising from a chemical reaction with the culture medium rather than from enzymatic biotransformation.


Assuntos
Drosophila melanogaster/efeitos dos fármacos , Mutagênicos/toxicidade , Asas de Animais/efeitos dos fármacos , alfa-Cloridrina/análogos & derivados , alfa-Cloridrina/toxicidade , Animais , Biotransformação , Mutagênicos/farmacocinética , alfa-Cloridrina/farmacocinética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA