Chemical profiles of cannabis sativa medicinal oil using different extraction and concentration methods.

The present study shows the variability in chemical profiles of three different varieties of Cannabis sativa extracts used in medicinal cannabis oil when using two different extraction and evaporation methods. Procedures were compared by analyzing rate of total terpenoids to the principal cannabinoids, tetrahydrocannabinol (THC) and cannabidiol (CBD), using gas chromatography coupled to mass spectrometry (GC-MS). The extraction of inflorescences using soxhlet method showed the highest mass of final extract. Also, the use of heating and the presence of oxygen when evaporating the solvents, greatly modified the final profiles due to evaporation or chemical reactions. These variations in chemical profiles must be carefully taken into account and standardized in the elaboration of medicinal oils.

Occurrence and Gas-Particle Partitioning of Organic UV-Filters in Urban Air.

A retrospective analysis of a comprehensive series of high-volume air samples (n = 70) collected during 2010-2011 in Toronto (Canada) was performed. Seven UV compounds were analyzed by gas chromatography-tandem mass spectrometry (GC-MS/MS) with sum of concentrations (gas + particle phase) ranging from 80 to 2030 pg/m3. Homosalate (HMS) was the most prevalent organic UV-filter in air (47% of the total concentration), followed by 2-ethylhexyl salicylate (EHS, ∼29%), E- and Z-2-ethylhexyl 4-methoxycinnamate (EHMC, ∼17%). Ambient air (gas + particle phase) concentrations of organic UV-filters showed a strong seasonality, with peak levels during the summer. An analysis of Clausius-Clapeyron slopes indicated that much of the ambient burden of organic UV-filters are explained by volatilization from terrestrial and aquatic surfaces and supplemented with human activities and use of lotions and sunscreens, containing organic UV-filters, in addition to its use in plastics, textiles, paints, and pesticides. The results showed that organic UV-filters exist mainly in the gas phase with some exceptions, for instance, octocrylene (OCR), which was associated with both gas and particle phases, and avobenzone (AVB), which was predominantly in the particle phase. Lastly, this study revealed the need for basic physical chemical property data for organic UV-filters, including information on transformation rates and products, for better evaluating their environmental fate and effects.

Occurrence of persistent organic pollutants in air at different sites in the province of Córdoba, Argentina.

The occurrence of persistent organic pollutants (POPs) and polycyclic aromatic hydrocarbons (PAHs) in the atmosphere of six sites with different emission sources in the province of Córdoba, Argentina, was analyzed. The sites included urban, industrial, agricultural, and mountain areas. Samples were collected using passive air samplers (PAS) consisting of polyurethane foam disks (PUF). Samples were analyzed for 12 PAHs, 31 polychlorinated biphenyls (PCBs), 12 organochlorine pesticides (OCPs), and 11 polybrominated diphenyl ethers (PBDEs). The concentrations of PAHs in the atmosphere were elevated at urban sites and were even higher at the industrial site. With respect to OCPs, it was observed that the concentrations of endosulfan were greater at the agricultural site (AGR) (416 ± 4 pg m-3). For hexachlorocyclohexanes (HCHs), only the alpha isomer was detected and there were minimal differences between the different sampling sites (5.9-13.3 pg m-3). In the case of dieldrin, the highest concentrations (33.6 pg m-3) were found at the mountain site, which may have been due to its use for insect control. Although heptachlor epoxide was not detected, the concentration of heptachlor was significantly higher at the agricultural and downtown sites (∼ 3.6 pg m-3). Regarding DDTs, the isomers p,p'-DDT and p,p'-DDE showed the highest concentrations at the mountain site (ΣDDT 120 ± 12 pg m-3) and downtown site (ΣDDT 157 ± 62 pg m-3). The relationship between the isomers suggested that at the downtown site, the contribution of this pesticide to the environment was recent, probably for the control of diseases vectors. The congener pattern of PBDEs was dominated by BDE-47, and BDE-99 at all sites, with the downtown site having the highest concentrations of compound esters (ΣPBDEs 118 ± 38 pg m-3). Finally, high concentrations of PCBs were found at the industrial site (ΣPCBs 1677 ± 134 pg m-3), and the predominating homologs were 5-Cl and 6-Cl, in contrast to the other sites where PCBs were dominated by 3-Cl and 4-Cl. This is the first study of POPs carried out in the province of Córdoba.

Assessing levels of POPs in air over the South Atlantic Ocean off the coast of South America.

The occurrence of persistent organic pollutants (POPs) in the atmosphere of the near-coast South Atlantic Ocean was studied. Air samples were collected using a high-volume air sampler (filter and polyurethane foam) on board the Argentinean research cruise R/V Puerto Deseado (CONICET). Samples were analyzed for 50 polychlorinated biphenyl (PCBs), 22 organochlorine pesticides (OCPs) and 14 polybrominated diphenyl ethers (PBDEs). These POPs classes showed a trend of decreasing levels from near-shore to open ocean sites. OCPs and PCBs were in the same order of magnitude (2.71-87.1pg/m(3) and 9.56-130pg/m(3), respectively) while PBDEs levels were significantly lower (0.69-2.58pg/m(3)). Dichlorodiphenyltrichloroethanes (DDTs), endosulfans, chlordanes, hexachlorocyclohexanes (HCHs) and heptachlors were between 0.20 and 17.8pg/m(3), while drines and hexachlorobenzene (HCB) were at lower levels (0.28-3.71pg/m(3)). The most frequently detected PCBs were congeners 32, 28, 44, 52, 95, representing >50% of the total. The PBDEs congener pattern was dominated by congener 209 (70%), followed by 47 and 99 (16% and 7%, respectively). Air parcel back trajectories for the study period provided few insights as trajectories mainly stemmed from the open ocean with limited inputs from continental sources. These results indicate that the concentration of POPs (namely PCBs, OCPs, and PBDEs) in air remain elevated in the near-shore environment and then drop-off substantially beyond a distance of about 400km. This has implications for the loading of POPs and delivery to the marine environment in the near coastal zone.

Measurements of octanol-air partition coefficients, vapor pressures and vaporization enthalpies of the (E) and (Z) isomers of the 2-ethylhexyl 4-methoxycinnamate as parameters of environmental impact assessment.

2-Ethylhexyl 4-methoxycinnamate is one of the UVB blocking agents more widely used in a variety of industrial fields. There are more than one hundred industrial suppliers worldwide. Given the enormous annual consumption of octinoxate, problems that arise due to the accumulation of this compound in nature should be taken into consideration. The GC-RT was used in this work with the aim of determining the vapor pressure, enthalpies of vaporization and octanol-air partition coefficient, for the BBP, DOP, E- and Z-EHMC esters. The results showed that Z-EHMC is almost five times more volatile than E-EHMC. Moreover, BBP, Z-EHMC and E-EHMC can be classified as substances with a relatively low mobility since they lie within the range of 810 and log(PL/Pa)<-4, therefore, a low mobility can be expected. From these parameters, their particle-bound fraction and gas-particle partition coefficient were also derived.

Role of ruthenium oxidation states in ligand-to-ligand charge transfer processes.

We describe in this paper the properties of [Ru(II/III)(bpy)(2)ClL](+1/+2) and [Ru(II/III)(bpy)(2)L(2)](+2/+3). L = ditolyl-3-pyridylamine (dt3pya) is a redox active ligand related to triarylamines, which is very similar to 3-aminopyridine except for the reversible redox behavior. The monosubstituted complex shows a metal-to-ligand charge-transfer (MLCT) at 502 nm, and reversible waves in acetonitrile at E(0)(Ru(III/II)) = 1.07 V, E(0)(L(+/0)) = 1.46 V (NHE). The disubstituted complex shows an MLCT at 461 nm, a photorelease of dt3pya with quantum yield of 0.11 at 473 nm, and two reversible one-electron overlapped waves at 1.39 V associated with one of the ligands (1.37 V) and Ru(III/II) (1.41 V). Further oxidation of the second ligand at 1.80 V forms a 2,2'-bipiridine derivative, in an irreversible reaction similar to dimerization of triphenylamine to yield tetraphenylbenzidine. In the dioxidized state, the spectroelectrochemistry of the disubstituted complex shows a ligand-to-ligand charge transfer at 1425 nm, with a transition moment of 1.25 Å and an effective two-state coupling of 1200 cm(-1). No charge transfer between ligands was observed when Ru was in a 2+ oxidation state. We propose that a superexchange process would be involved in ligand-metal-ligand charge transfer, when ligands and metals are engaged in complementary π interactions, as in metal-ligand-metal complexes. Best orbital matching occurs when metallic donor fragments are combined with acceptor ligands and vice versa. In our case, Ru(III) bridge (an acceptor) and two dt3pya (donors, one of them being oxidized) made the complex a Robin-Day Class II system, while the Ru(II) bridge (a donor, reduced) was not able to couple two dt3pya (also donors, one oxidized).