Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Polycyclic Compounds”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 811 records · Page 45Linked to original sources
PubMed2002

Formation and decomposition of hazardous chemical components contained in atmospheric aerosol particles.

Air particulate matter contains a wide range of substances, some of which pose a threat to human health. Chemical reactions occurring on aerosol particles in the atmosphere can transform hazardous components and increase or decrease their potential for adverse health effects. Especially organic compounds react readily with atmospheric oxidants, and since fine aerosol particles have a high surface-to-volume ratio, their chemical composition can be efficiently changed by interaction with trace gases such as ozone and nitrogen oxides. In this paper the concepts required to understand and describe the formation and decomposition of hazardous chemical components contained in atmospheric aerosol particles are outlined. The processes at work on a molecular level in the chemical transformation of atmospheric particle components are illustrated for soot and polycyclic aromatic compounds (PACs), in particular for benzo[a]pyrene (BaP) which is one of the most prominent hazardous pollutants in the class of polycyclic aromatic hydrocarbons (PAHs). Recent results on the reaction kinetics and mechanisms of BaP degradation by ozone and nitrogen dioxide are presented. These results indicate faster degradation by atmospheric oxidants than previously estimated, which implies a higher potential for sampling artifacts and underestimation of the actual atmospheric abundance of BaP and other PAHs. Thus human exposure close to the sources of these compounds such as busy roadways may be significantly higher than previously assumed.

Aerosols↗
PubMed2003

Pyrrole-based conductive polymer as the solid-phase extraction medium for the preconcentration of environmental pollutants in water samples followed by gas chromatography with flame ionization and mass spectrometry detection.

A pyrrole-based polymer was synthesized and applied as a new sorbent for solid-phase extraction (SPE) of some environmental pollutants from water samples. Polypyrrole (PPy) was synthesized by chemical oxidation of the monomer in nonaqueous solution. SPE of selected phenols, pesticides, and polyaromatic hydrocarbons (PAHs) from aqueous samples were performed using 200 mg PPy. The determination was subsequently carried out by gas chromatography-flame ionization detection (GC-FID) and gas chromatography-mass spectrometry (GC-MS). The polymer showed much higher recoveries for aromatic compounds than aliphatics. Preconcentration of sample volumes up 11 led to acceptable recoveries for aromatic and other tested polar compounds. The R.S.D. for a river water sample spiked with phenols, pesticides and PAHs at sub-ppb level was lower than 10% (n = 3) and limits of detection for these compounds were between 15 and 120 ng l(-1).

Gas Chromatography-Mass Spectrometry↗
PubMed2001

Simultaneous absorption of vapor phase polycyclic aromatic hydrocarbon and carbon dioxide in anionic surfactant solutions.

The goal of this work was to investigate whether the solubility of vapor phase polycyclic aromatic compounds (PAHs) and CO2 in water could be enhanced by adding anionic surfactant during the absorption process. Naphthalene was the PAH surrogate and sodium dodecyl sulfate (SDS) was the anionic surfactant. A series of batch experiments in an absorption cell were performed at 50 degrees C with the surfactant concentration both lower than and higher than the critical micelle concentration (CMC). The experimental findings indicate that the CMC was not a function of pH at values of 3, 5 and 7. Furthermore, at surfactant concentrations less than the CMC, naphthalene apparent solubility increased slightly. On the other hand, the equilibrium naphthalene or CO2 apparent solubility increased linearly, in proportion to the surfactant concentration at concentrations greater than the CMC. This is due to the solubilization effect of micelles, which were formed by the surfactant at concentrations above the CMC. During simultaneous absorption of the two, the presence of CO2 only slightly decreased naphthalene apparent solubility, while the apparent solubility of CO2 was drastically reduced in the presence of naphthalene. As the magnitude of the micelle solubilization effect was greater than the reduction of the mass transfer coefficient in the presence of the surfactant, the total gas absorption rate increased. When the surfactant concentration was 0.1 M, the enrichment factor (the ratio of the solubility in surfactant solution to that in water) values of naphthalene both with and without CO2 increased to 9.05 and 8.60, respectively. These experimental findings demonstrate that anionic surfactant may be applied to increase the removal efficiency of hydrophobic compounds and CO2 through either a spray or packed tower.

Absorption↗
PubMed1975

Radiation damage in electron microscopy of organic materials: effect of low temperatures.

As measured by the life-time of their electron diffraction patterns, the radiation sensitivity of anthracene and coronene at 500 kV is reduced by a factor of three to four at liquid helium temperature in comparison to room temperature, For l-valine the ratio is about 1-8 but there is a wide variation in the results, possibly due to differences in crystal thickness. The end-dose at 20 degrees K for valine is equivalent to 13 electrons/A2; for anthracene and coronene it is about 600 electrons/A2 at room temperature. The variation of end-dose with temperature shows that at least two mechanisms must be involved in damage to such compounds, possibly concerning the breaking of intermolecular and intramolecular bonds, respectively.

Anthracenes↗
PubMed2005

Multivariate statistical methods for evaluating biodegradation of mineral oil.

Two methods were developed for evaluating natural attenuation and bioremediation of mineral oil after environmental spills and during in vitro experiments. Gas chromatography-mass spectrometry (GC-MS) in selected ion monitoring (SIM) mode was used to obtain compound-specific data. The chromatographic data were then preprocessed either by calculating the first derivative, retention time alignment and normalization or by peak identification, quantification and calculation of diagnostic ratios within homologue series of polycyclic aromatic compounds (PACs). Finally, principal component analysis (PCA) was applied to the preprocessed chromatograms or diagnostic ratios to study the fate of the oil. The methods were applied to data from an in vitro biodegradation experiment with a North Sea crude oil exposed to three mixtures of bacterial strains: R (alkane degraders and surfactant producers), U (PAC degraders) and M (mixture of R- and U-strains) over a 1-year-period with five sampling times. Assessment of variation in degradability within isomer groups of methylfluorenes (m/z 180), methylphenanthrenes (m/z 192) and methyldibenzothiophenes (m/z 198) was used to evaluate the effects of microbial degradation on the composition of the oil. The two evaluation methods gave comparable results. In the objective pattern matching approach, principal component 1 (PC1) described the general changes in the isomer abundances, whereas M samples were separated from U and R samples along PC2. Furthermore, in the diagnostic ratio approach, a third component (PC3) could be extracted; although minor, it separated R samples from U and M samples. These results demonstrated that the two methods were able to differentiate between the effects due to the different bacterial activities, and that bacterial strain mixtures affected the PAC isomer patterns in different ways in accordance with their different metabolic capabilities.

Bacteria↗
PubMed2001

Spectroscopic studies of interaction of chlorobenzylidine with DNA.

Electronic absorbance and fluorescence titrations are used to probe the interaction of chlorobenzylidine with DNA. The binding of chlorobenzylidine to DNA results in hypochromism, a small shift to a longer wavelength in the absorption spectra, and emission quenching in the fluorescence spectra. These spectral characteristics suggest that chlorobenzylidine binds to DNA by an intercalative mode. This conclusion is reinforced by fluorescence polarization measurements. Scatchard plots constructed from fluorescence titration data give a binding constant of 1.3 x 10(5) M(-1) and a binding site size of 10 base pairs. This indicates that chlorobenzylidine has a high affinity with DNA. The intercalative interaction is exothermic with a Van't Hoff enthalpy of -143 kJ/mol. This result is obtained from the temperature dependence of the binding constant. The interaction of chlorobenzylidine with DNA is affected by the pH value of the solution. The binding constant has its maximum at pH 3.0. Upon binding to DNA, the fluorescence from chlorobenzylidine is quenched efficiently by the DNA bases and the fluorescence intensity tends to be constant at high concentrations of DNA when the binding is saturated. The Stern-Volmer quenching constant obtained from the linear quenching plot is 1.6 x 10(4) M(-1) at 25 degrees C. The measurements of the fluorescence lifetime and the dependence of the quenching constant on the temperature indicate that the fluorescence quenching process is static. The fluorescence lifetime of chlorobenzylidine is 1.9 +/- 0.4 ns.

Animals↗
PubMed1993

Regulation of endothelin-1 mRNA by angiotensin II in rat heart endothelial cells.

In a series of experiments carried out in cultured endothelial cells derived from rat hearts (RHE), angiotensin II (AII) is shown to stimulate preproendothelin-1 mRNA in a dose- and time-dependent manner. The induction of preproendothelin-1 mRNA is rapid, reaching a maximal level 1 h after the addition of AII (1 x 10(-8) M). The mRNA levels decline rapidly to basal levels in 4 h. The addition of Losartan (Dup 753; 1 x 10(-6) M), an AII receptor (type I) antagonist, blocks the AII effect. Calphostin C, a potent protein kinase C inhibitor, is able to abolish this effect of AII suggesting that the induction of preproendothelin-1 mRNA is mediated by a protein kinase C-dependent pathway. Since endothelial cells line the inner surface of the myocardium and blood vessels and sense the rise of AII associated with renovascular hypertension at the endothelial surface, these data suggest that endothelin which is produced by RHE cells in response to AII could be an important mediator which may play a role in modulating gene expression in AII-mediated cardiac hypertrophy.

Angiotensin II↗
PubMed2003

Comparison of hormonal activity (estrogen, androgen and progestin) of standardized plant extracts for large scale use in hormone replacement therapy.

Extracts from red clover (Trifolium pratense), soybean (Glycine max.) and black cohosh (Cimicifuga racemosa) are frequently used as alternative compounds for hormone replacement therapy (HRT) to treat menopausal disorders. Fifteen commercially available products made either from red clover, soybean or black cohosh were tested in in vitro assays in this study. The main polycyclic phenolic compounds of soy and red clover products were biochanin A, genistein, daidzein, formononetin, and glycitein. In red clover products glycitein was not abundant. All the compounds showed clear estrogenic activity through estrogen receptor alpha (ERalpha) and estrogen receptor beta (ERbeta) and affinity to progesterone receptor (PR) and androgen receptor (AR), whereas the compounds from black cohosh did not. This was corroborated by synthetic isoflavones such as biochanin A, daidzein, genistein and formononetin. They exerted affinity to PR and AR in the range of 0.39-110 mM. Statistical analysis applying principal component analysis (PCA) revealed that all red clover and soy products are grouped in different clusters. Red clover products showed a higher affinity to AR and PR than soy products, which is explained by the higher amount of isoflavones present. In vitro assays and chemical analysis showed that theoretical estrogenic activity expressed as equivalent E2 concentration is in the same range as recommended for synthetic estrogens. Broader spectrum of action and hypothesized lower side effects by action through ERbeta make them suitable for alternative hormone replacement therapy.

Androgens↗
PubMed2006

8-hydroxydihydrochelerythrine and 8-hydroxydihydrosanguinarine with a potent acetylcholinesterase inhibitory activity from Chelidonium majus L.

Ethanol extract of the aerial portion of Chelidonium majus L. inhibited acetylcholinesterase (AChE) activity without a significant inhibition of butyrylcholinesterase (BuChE). Using mass spectrometry and NMR studies, three active constituents were isolated and identified: 8-hydroxydihydrochelerythrine (1), 8-hydroxydihydrosanguinarine (2), and berberine (3). Compounds 1-3 showed potent inhibitory activity against AChE, with IC50 (microM) values of 0.61-1.85. Compound 1 exhibited competitive and selective inhibition for AChE.

Acetylcholinesterase↗
PubMed2002

An evaluation of the relative potential public health concern for the self-defense spray active ingredients oleoresin capsicum, o-chlorobenzylidene malononitrile, and 2-chloroacetophenone.

In 1996, the New York State Department of Health was charged by the State Legislature to develop regulations regarding the types of self-defense spray devices which could lawfully be purchased, possessed, and used in New York State. Prior to this legislation, sale or possession of self-defense spray devices in New York State was illegal. The Department of Health used existing data to evaluate three commonly used self-defense spray active ingredients (oleoresin capsicum, o-chlorobenzylidene malononitrile, and 2-chloroacetophenone) with respect to their relative toxicity and their involvement in accidental poisonings. Based on the balance of the available information, the Department of Health determined that oleoresin capsicum posed a lower public health concern than o-chlorobenzylidene malononitrile or 2-chloroacetophenone, and developed a rule that specifies oleoresin capsicum as the only active ingredient to be used in self-defense sprays for sale and use in New York State.

Accidents↗
PubMed1983

Mutagenicity of air samples from various combustion sources.

The emission of mutagens from various combustion sources was compared. Flue gas samples from power plants and boilers burning coal, oil and wood were studied. Little or no mutagenic activity was observed in samples from big boilers operated under optimal conditions. The mutagenic activity of emission samples from different boiler systems burning the same fuel varied considerably. This variation was larger than the difference obtained from boilers of comparable size utilizing different fuels. The highest mutagenic activity was observed in samples from a small coal combustion unit, utilizing the fluidized-bed technique. In this case the activity was highest without metabolic activation. Extracts from all samples contained toxic compounds that, in high doses, inhibited mutagenicity.

Air Pollutants↗
PubMed2002

Antimycobacterial activity of 5-arylidene aromatic derivatives of hydantoin.

Various 5-(chlorobenzylidene)-2-isoniazido and 5-(chlorobenzylidene)-2-amino substituted derivatives of imidazoline-4-one were synthesized and evaluated in the primary assay for their antimycobacterial activity against Mycobacterium tuberculosis H37Rv. Eight of them exhibited > 90% inhibition in the primary screening at 12.5 microg/ml. For these primarily selected compounds the actual MIC and IC50 values were determined. Two of the isoniazid derivatives, for which MIC < 3.13 microg/ml and SI > 10, were selected for further screening and investigated for efficacy in vitro in a TB-infected macrophage model. The most promising compound, 5-(3-chlorobenzylidene)-2-(isonicotinoylhydrazino)-imidazoline-4-one, with activity in vitro comparable with rifampin (MIC = 0.8 microg/ml. SI > 78) was tested in vivo in the animal tuberculosis model but exhibited insignificant activity. For several compounds the primary screening of antimycobacterial activity against Mycobacterium avium (ATCC 25291) was conducted as well, but none of them demonstrated satisfactory activity.

Animals↗
PubMed2004

Theoretical (DFT, GIAO-NMR, NICS) study of carbocations (M+H)+, dications (M2+) and dianions (M2-) from dihydro-dicyclopenta[ef,kl]heptalene (dihydro-azupyrene), dihydro-dicyclohepta[ed,gh]pentalene, and related bridged [14]annulenes.

The annulenium ions of protonation, the two-electron oxidation dications, and the two-electron reduction dianions derived from dihydro- and dimethyldihydro derivatives (cis and trans) of dicyclopenta[ef,kl]heptalene (azupyrene) (1) and dicyclohepta[ed,gh]pentalene (2), which are the nonalternant isomers of pyrene, were studied by density functional theory (DFT) at the B3LYP/6-31G(d), 6-31+G(d,p), or 6-31++G(d,p) levels. Charge delocalization modes in the energetically most favored annulenium ions, as well as in the singlet and triplet dications and dianions, were assessed based on gauge-including atomic orbital (GIAO) Deltadelta](13)C values and via changes in natural population analysis (NPA) charges. Relative aromaticity/antiaromaticity in the annulenes were gauged via nucleus-independent chemical shift (NICS) and DeltaNICS. Annulenium ions of monoprotonation, the dications, and dianions derived from bismethano- and propanediylidene [14]annulenes were also studied by DFT for comparison with the cis-dihydro isomers derived from . Computed GIAO NMR data and the optimized geometries were compared with the experimental data when available, and the optimized geometries were compared with the X-ray data if known. A basis-set dependency study of the computed GIAO chemical shifts was also undertaken. The present DFT work represents the first detailed comparative theoretical study of charged annulenes derived from the dihydro derivatives of and .

Anions↗
PubMed1990

DNA adducts in human environmentally exposed to aromatic compounds in an industrial area of Poland.

The effect of environmental pollution on DNA adducts in humans was analysed in a highly industrialized area of Poland. Coded samples of white blood cell DNA were analysed by 32P-postlabelling and immunoassay from three populations: coke workers, exposed occupationally to high levels of polycyclic aromatic hydrocarbons (PAHs); residents of the towns around cokeries (local controls); and residents from rural Poland (countryside controls). Local controls exhibited adduct levels and patterns similar to those of coke workers, while the levels in rural controls were 2-3 times lower. The results, based on coded samples and two different assays, suggest that environmental pollution is likely to contribute to the adduct levels in local controls. Furthermore, the results show that the levels of aromatic adducts in white blood cell DNA do not linearily relate to ambient air levels of PAHs but other sources such as food may be important contributors.

Air Pollutants↗
PubMed2006

Rapid semi-continuous calibration and field test of membrane-enclosed silicone collector as passive water sampler.

The new membrane-enclosed silicone collector (MESCO) was, in two different configurations with respect to the thickness of low-density polyethylene membrane used, subject to serial batch extraction tests to obtain (preliminary) sampling rates for estimating water concentrations of selected chlorinated organic compounds and polycyclic aromatic hydrocarbons. This rapid calibration procedure is simple to implement compared to experiments in a flow-through apparatus and yielded reasonable sampling rates in the range of 50 microL-2 mL per hour for the compounds tested. The new MESCO formats were also exposed for 28 days in the polluted creek to test their field performance. For priority contaminants of special interest, alpha-hexachlorocyclohexane and hexachlorobenzene, the time-weighted average concentrations derived from the freshly calibrated sampling devices agree well with those obtained by conventional water analysis of spot samples.

Calibration↗
PubMed2002

Photodegradation of 1-nitropyrene in solution and in the adsorbed state.

The photodegradation of the 1-nitropyrene (NPy) has been studied using conventional (Xe and medium pressure Hg lamps) and laser sources (XeCl excimer and Nd-YAG UV). Low energy monochromatic light sources were used to study the early stages of degradation (up to 50% conversion). The medium pressure Hg lamp was used for longer periods of irradiation (up to 6h) and for greater degradation of NPy. The results of our work confirm that degradation occurs by radical mechanism. Aromatic hydroxymethyl, methoxy, hydroxy and nitroso derivatives of pyrene (Py) are created by low energy UV irradiation. After a massive UV irradiation, the Py aromatic system is destroyed and more polar low-molecular compounds are generated. The photochemical method described in this paper, based on irradiation by UV lamp, is therefore, suitable for degradation of fused benzene ring(s) and thus should also be effective for degradation of other nitrated polycyclic aromatic compounds.

Adsorption↗