Control of organic contaminants in groundwater by passive sampling and multivariate statistical analysis.

Organic contaminants in groundwater are among the most challenging chemical compound contaminants today, particularly when it comes to understanding their occurrence, origin, and relations in groundwater, as well as the transport processes, fate, and environmental impacts involved. This paper presents the use of active carbon fibre (AFC) passive sampling and multivariate statistical processing of the results to predict the possible occurrence of organic compounds (OCs) in groundwater and to determine the origin of various anthropogenic activity. This study aims to deepen our knowledge on the control of OCs in groundwater by introducing a multi-analytical and multi-elemental holistic approach, using the Dravsko polje aquifer, the largest intergranular aquifer in Slovenia, as an example. The occurrence of OCs in groundwater was determined by means of ACFs and compared against the characteristics of the recharge area and the type of compounds detected. We combined hierarchical cluster analysis (HCA) and principal component analysis (PCA) to identify the relationship between different OCs in groundwater. The relationships between their occurrence, environmental setting and type of compound were determined using multiple linear regression (MLR). From the total of 343 organic compounds detected using passive sampling, 47 were included in further statistical analysis. MLR shows that the environmental setting is one of the most important factors affecting the different types of pollutants in groundwater. MLR models were calculated for different sources of pollution (agricultural, urban, and industrial) based on the environmental setting, land use, agglomeration, infrastructure networks, and hydrogeological characteristics of the aquifer. By means of HCA and PCA, we identified the relationships between different OCs in groundwater. As expected, the strongest correlations were found between primary compounds and their degradation products (e.g. atrazine and desethylatrazine) and compounds of similar use (e.g. atrazine and propazine, also desethylatrazine and propazine, atrazine and simazine). Some of them were also found to have a similar molecular structure (e.g. palmitic and stearic acid, 5-methoxygramine and 5-methoxytryptamine). The use of the same substances in different environments (agricultural/urban) makes them markers of both (different) origins. Therefore, it is particularly important to determine the combination of markers of different origin using multivariate statistical methods, especially in the case of mixed land use. This study identifies the main factors influencing the distribution of groundwater OCs and thus contributes to a more comprehensive understanding of the vulnerability of shallow groundwater to surface-derived contamination in similar environments.

Emerging organic compounds in European groundwater.

In Europe, emerging organic compounds (EOCs) in groundwater is a growing research area. Prioritisation for monitoring EOCs in Europe was formalised in 2019 through the development of the first voluntary groundwater watch list (GWWL). Despite this, groundwater occurrence data in the peer reviewed literature for Europe has not been reviewed to date. Questions surrounding the effect, toxicity, movement in the subsurface and unsaturated zone make the process of regulating EOC use difficult. The aim in Europe is to develop a unified strategy for the classification, and prioritisation of EOCs to be monitored in groundwater. This paper compiles evidence from the recent published studies from across Europe, since 2012, when the last major literature global review of EOCs in groundwater took place. A total of 39 studies were identified for review based on specific selection criteria (geography, publication date, sample size>10, inclusion of EOCs data). Data on specific compounds, and associated meta-data, are compiled and reviewed. The two most frequently detected EOCs, carbamazepine and caffeine, occurred in groundwater at concentrations of up to 2.3 and 14.8 µg/L, respectively. The most frequently reported category of compounds were 'Pharmaceuticals'; a highly studied group with 135 compounds identified within 31 of the 39 studies. In Europe, the majority of reviewed studies (23) were at a regional scale, looking specifically at EOCs in a specific city or aquifer. The use of analytical methods is not uniform across Europe, and this inevitably influences the current assessment of EOCs in groundwater. A correlation between the number of compounds analysed for, and the number detected in groundwater highlights the need for further studies, especially larger-scale studies throughout Europe. For the development of EU and national regulation, further work is required to understand the occurrence and impacts of EOCs in groundwater throughout Europe and elsewhere.

Pharmacokinetics of isoniazid in Indian children with tuberculosis on daily treatment.

OBJECTIVE: To assess the pharmacokinetics of isoniazid (INH) at 10 mg/kg/day among Indian children. METHODS: INH levels were estimated using liquid chromatography-tandem mass spectroscopy in 35 children aged 1-15 years on daily anti-tuberculosis treatment. Blood samples were collected 0, 1, 2, 3, 6 and 24 h after INH administration. The maximum concentration (Cmax) and area under the curve (AUC0-24) were determined. The normal therapeutic range for Cmax is 3-5 µg/ml. An AUC of <10.52 µg•h/ml for INH is low. RESULTS: The mean Cmax was 8.3 ± 4.28 µg/ml and was attained in 1.22 ± 0.5 h, with a median time to Cmax (Tmax) of 1 h. The mean AUC for INH was 46.23 ± 34.82 µg•h/ml. Children aged 1-4.9 years, 5-10 years and >10 years had a mean Cmax of respectively 9.87 ± 5.75 µg/ml, 7.62 ± 3.37 µg/ml and 7.21 ± 2.50 µg/ml (P = 0.08) and a mean AUC of respectively 60.97 ± 49.90 µg•h/ml, 38.95 ± 22.28 µg•h/ml and 36.09 ± 13.56 µg•h/ml (P = 0.29). The mean Cmax in children taking fixed-drug combinations and individual drugs was respectively 9.07 ± 4.67 µg/ml and 7.43 ± 3.71 µg/ml (P = 0.26); the mean AUC was respectively 50.48 ± 38.38 µg•h/ml and 41.20 ± 30.52 µg•h/ml (P = 0.44). Two children had hepatitis. CONCLUSION: Most Indian children had higher than normal INH AUC and Cmax values. It is necessary to determine the ideal dose of INH in Indian children using the genotypic acetylator status of the patients and pharmacokinetic toxicity analysis.

Passive sampling as a tool for identifying micro-organic compounds in groundwater.

The paper presents the use of a simple and cost efficient passive sampling device with integrated active carbon with which to test the possibility of determining the presence of micro-organic compounds (MOs) in groundwater and identifying the potential source of pollution as well as the seasonal variability of contamination. Advantage of the passive sampler is to cover a long sampling period by integrating the pollutant concentration over time, and the consequently analytical costs over the monitoring period can be reduced substantially. Passive samplers were installed in 15 boreholes in the Maribor City area in Slovenia, with two sampling campaigns covered a period about one year. At all sampling sites in the first series a total of 103 compounds were detected, and 144 in the second series. Of all detected compounds the 53 most frequently detected were selected for further analysis. These were classified into eight groups based on the type of their source: Pesticides, Halogenated solvents, Non-halogenated solvents, Domestic and personal, Plasticizers and additives, Other industrial, Sterols and Natural compounds. The most frequently detected MO compounds in groundwater were tetrachloroethene and trichloroethene from the Halogenated solvents group. The most frequently detected among the compound's groups were pesticides. Analysis of frequency also showed significant differences between the two sampling series, with less frequent detections in the summer series. For the analysis to determine the origin of contamination three groups of compounds were determined according to type of use: agriculture, urban and industry. Frequency of detection indicates mixed land use in the recharge areas of sampling sites, which makes it difficult to specify the dominant origin of the compound. Passive sampling has proved to be useful tool with which to identify MOs in groundwater and for assessing groundwater quality.

Determination of micro-organic contaminants in groundwater (Maribor, Slovenia).

Micro-organic (MO) contaminants in groundwater can have adverse effects on both the environment and on human health. They enter the natural environment as a result of various processes, their presence in groundwater is the result of current anthropogenic activity and pollution loads from the past. A study on the occurrence and concentrations levels of selected contaminants in water was performed in the city of Maribor, Slovenia. A total of 56 groundwater and 4 surface water samples were collected in together four rounds in different hydrogeological periods (dry and wet seasons), and a total of 13 selected contaminants were analysed in this study. Carbamazepine, propyphenazone, caffeine, 2-methyl-2H-benzotriazole (2-MBT) and 2.4-dimethyl-2H-benzotriazole (2.4-DMBT) were determined as indicators of urban pollution, while pesticides and their metabolites (atrazine, desethylatrazine, deisopropylatrazine, terbuthylazine, desethylterbuthylazine, metolachlor, simazine, propazine) were mainly defined as indicators of crop production. All of the selected MO contaminants were detected both in the aquifer and Drava River. The most frequently detected MO compounds in groundwater were desethylatrazine (frequency of detection 98.2%; max. concentration 103.0ngL(-1)), atrazine (94.6%; 229ngL(-1)), 2.4-DMBT (92.9%; 273ngL(-1)), carbamazepine (80.4%; 88.00ngL(-1)), desethylterbuthylazine (76.8%; 7.0ngL(-1)) and simazine (76.8%; 29.6ngL(-1)), whereas propyphenazone (14.3%; 10.7ngL(-1)) was the least frequently detected. Detected MO concentrations in the study were compared with results published elsewhere around the world. Concentrations in groundwater indicate specific land use in their recharge areas. On the basis of correlations and the spatial distribution of selected MOs, groundwater origin for every sampling point was determined. Sampling sites were divided into three different groups for which indicative groundwater quality properties were defined.

Novel glutathione conjugates of phenyl isocyanate identified by ultra-performance liquid chromatography/electrospray ionization mass spectrometry and nuclear magnetic resonance.

Phenyl isocyanate is a highly reactive compound that is used as a reagent in organic synthesis and in the production of polyurethanes. The potential for extensive occupational exposure to this compound makes it important to elucidate its reactivity towards different nucleophiles and potential targets in the body. In vitro reactions between glutathione and phenyl isocyanate were studied. Three adducts of glutathione with phenyl isocyanate were identified using ultra-performance liquid chromatography/electrospray ionization mass spectrometry and nuclear magnetic resonance (NMR). Mass spectrometric data for these adducts have not previously been reported. Nucleophilic attack on phenyl isocyanate occurred via either the cysteinyl thiol group or the glutamic acid α-amino group of glutathione. In addition, a double adduct was formed by the reaction of both these moieties. NMR analysis confirmed the proposed structure of the double adduct, which has not previously been described. These results suggest that phenyl isocyanate may react with free cysteines, the α-amino group and also with lysine residues whose side chain contains a primary amine.

P450-catalyzed vs. electrochemical oxidation of haloperidol studied by ultra-performance liquid chromatography/electrospray ionization mass spectrometry.

The metabolites formed via the major metabolic pathways of haloperidol in liver microsomes, N-dealkylation and ring oxidation to the pyridinium species, were produced by electrochemical oxidation and characterized by ultra-performance liquid chromatography/electrospray ionization mass spectrometry (UPLC/ESI-MS). Liver microsomal incubations and electrochemical oxidation in the presence of potassium cyanide (KCN) resulted in two diastereomeric cyano adducts, proposed to be generated from trapping of the endocyclic iminium species of haloperidol. Electrochemical oxidation of haloperidol in the presence of KCN gave a third isomeric cyano adduct, resulting from trapping of the exocyclic iminium species of haloperidol. In the electrochemical experiments, addition of KCN almost completely blocked the formation of the major oxidation products, namely the N-dealkylated products, the pyridinium species and a putative lactam. This major shift in product formation by electrochemical oxidation was not observed for the liver microsomal incubations where the N-dealkylation and the pyridinium species were the major metabolites also in the presence of KCN. The previously not observed dihydropyridinium species of haloperidol was detected in the samples, both from electrochemical oxidation and the liver microsomal incubations, in the presence of KCN. The presence of the dihydropyridinium species and the absence of the corresponding cyano adduct lead to the speculation that an unstable cyano adduct was formed, but that cyanide was eliminated to regenerate the stable conjugated system. The formation of the exocyclic cyano adduct in the electrochemical experiments but not in the liver microsomal incubations suggests that the exocyclic iminium intermediate, obligatory in the electrochemically mediated N-dealkylation, may not be formed in the P450-catalyzed reaction.