Cultures of the ligninolytic fungus Irpex lacteus incubated in a nutrient liquid medium degraded more than 70% of the initially applied benz[a]anthracene within 14 days. At the first step of metabolization, benz[a]anthracene was transformed via a typical pathway of ligninolytic fungi to benz[a]anthracene-7,12-dione (BaAQ). The product was further transformed by at least two ways, whereas one is...

Introduction: Anthracene is one of the chemical and persistent pollutants released into the environment and the food chain causing irreparable damage to the immune system. This study aimed at removing anthracene from aqueous solutions using modified magnetic nanoparticles.   Materials & Methods: Initially, Fe3O4 nanoparticles were synthesized with silicon dioxide shell and then modified with ...

Rainbow trout were exposed for 72 h to [ 14C]anthracene alone and [ I4C]anthracene in an oil shale retort water. Tissue levels of [I4C]anthracene were analyzed at 24, 48 and 72 h to determine non-steady-state bicconcentration factors (BCFs), and uptake and depuration rates were calculated from anthracene disappearance in exposure waters and metabolite appearance in depuration waters. Uptake rat...

The abilities of the racemic trans-3,4-, 5,6-, and 8,9-dihydrodiols of 7,12-dimethylbenz(a)anthracene to initiate skin tumors in mice were determined by using a two-stage system of tumorigenesis. The 7,12-dimethylbenz(a)anthracene trans-3,4-dihydrodiol was found to be much more active as a tumor initiator than the parent hydrocarbon. The 7,12-dimethylbenz(a)anthracene trans-5,6- and 8,9-dihydro...

K-region epoxides of dibenz(a,h)anthracene and benz(a)anthracene were more active in producing malignant transforma tion of hamster embryo cells than the corresponding hydrocarbons, K-regions CMand frans-dihydrodiols and phenols. The cytotoxicity exerted by epoxides, relative to the other derivatives, varied among those tested. The 8,9-epoxide (non-K-region) of benz(a)anthracene was less active...

1. 7- and 12-Methylbenz[a]anthracene were converted by rat-liver homogenates into the corresponding hydroxymethyl derivatives, products that are probably the 8,9-dihydro-8,9-dihydroxy and the 5,6-dihydro-5,6-dihydroxy derivatives, and a number of phenolic products. 2. Both hydrocarbons were converted into glutathione conjugates; that from 7-methylbenz[a]anthracene was also formed, together with...

The UV absorption and emission spectra of anthracene in an argon matrix were measured. Three major spectroscopic systems were observed, assignable to anthracene molecules occupying distinct sites. The origins of these systems were red-shifted with respect to the isolated molecule by 535,69 1 and 722 cm-‘. At 17 K all lines were well resolved, with about 8 cm-’ fwhm. Addition of a small amount o...

In this work, centimeter-scale macrocrystals of nonpolar colloidal quantum dots (QDs) incorporated into anthracene were grown for the first time. The exciton transfer from the anthracene host to acceptor QDs was systematically investigated, and anisotropic emission from the isotropic QDs in the anthracene macrocrystals was discovered. Results showed a decreasing photoluminescence lifetime of th...

RNA was isolated by a phenol extraction method from mouse embryo cells treated in culture with either [G-3H]-7-methylbenz(a)anthracene or [G-3H]-7-methylbenz(a)anthracene 5,6-oxide (the K-region epoxide). The RNA was degraded to ribonucleosides, mixed with ultraviolet-absorbing quantities of the epoxide ribonucleoside products isolated from RNA that had reacted with 7-methylbenz(a)anthracene 5,...