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1.
Environ Pollut ; 218: 66-76, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27552039

ABSTRACT

The antipsychotic drug quetiapine (QUT) has been frequently detected in sewage treatment plants. However, information on the fate of QUT in aquatic environments and its behavior during UV treatment is limited. In this study, QUT is shown not to be readily biodegradable in the Closed Bottle Test and the Manometric Respirometry Test according to OECD guidelines. The main biotransformation product (BTP) formed in the tests, a carboxylic acid derivative, was identified by means of high-resolution mass spectrometry. This BTP is presumably a human metabolite and showed higher detection rates than QUT in a river sampling campaign conducted in northern Germany. UV elimination kinetics of QUT at different initial concentrations (226.5, 45.3, 11.3, and 2.3 µmol L-1) were faster at lower initial concentrations. All seven phototransformation products (PTPs) could be still identified at initial concentration of 11.3 µmol L-1. The photolytic mixture generated after 128 min of photolysis of QUT was not better biodegradable than QUT. Initial UV treatment of QUT led to the formation of several additional BTPs. Four of them were identified. The bacterial cytotoxicity and genotoxicity before and after phototransformation of QUT in a modified luminescent bacteria test (LBT) and the umu-test (ISO/FDIS 13829) showed cytotoxic effects in the LBT for QUT. Furthermore, PTPs had similar cytotoxic effects on luminescent bacteria. The umu-test did not reveal any genotoxic activity for QUT or PTPs. In conclusion, the release of QUT into sewage treatment plants and aquatic environments could result in the formation of a main BTP. Additional UV treatment of QUT would lead to the formation of additional BTPs. Moreover, treatment did not result in lower toxicity to tested organisms. In conclusion, UV treatment of QUT should be considered critically as a potential treatment for QUT in aquatic systems.


Subject(s)
Antipsychotic Agents/analysis , Quetiapine Fumarate/analysis , Ultraviolet Rays , Water Pollutants, Chemical/analysis , Water Purification/methods , Aliivibrio fischeri/drug effects , Antipsychotic Agents/metabolism , Antipsychotic Agents/radiation effects , Antipsychotic Agents/toxicity , Biodegradation, Environmental , Biological Oxygen Demand Analysis , Biotransformation , Germany , Humans , Mass Spectrometry , Microbial Viability , Photolysis , Quetiapine Fumarate/metabolism , Quetiapine Fumarate/radiation effects , Quetiapine Fumarate/toxicity , Rivers/chemistry , Rivers/microbiology , Salmonella typhimurium/drug effects , Salmonella typhimurium/genetics , Toxicity Tests , Water Pollutants, Chemical/metabolism , Water Pollutants, Chemical/radiation effects , Water Pollutants, Chemical/toxicity
2.
Int J Med Microbiol ; 305(8): 957-9, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26560681

ABSTRACT

Corynebacterium (C.) kroppenstedtii is a rarely detected agent of bacterial infections in humans. Here, we describe the first case of prosthetic valve endocarditis caused by C. kroppenstedtii. Application of molecular methods using surgically excised valve tissue was a cornerstone for the establishment of the microbiological diagnosis, which is crucial for targeted antimicrobial treatment.


Subject(s)
Corynebacterium Infections/diagnosis , Corynebacterium Infections/pathology , Corynebacterium/isolation & purification , Endocarditis/diagnosis , Endocarditis/pathology , Prosthesis-Related Infections/diagnosis , Prosthesis-Related Infections/pathology , Anti-Bacterial Agents/pharmacology , Bacteriological Techniques , Corynebacterium/classification , Corynebacterium/genetics , Corynebacterium Infections/surgery , Debridement , Endocarditis/microbiology , Endocarditis/surgery , Heart Valve Prosthesis/microbiology , Humans , Male , Microbial Sensitivity Tests , Microscopy , Middle Aged , Molecular Diagnostic Techniques , Prosthesis-Related Infections/microbiology , Prosthesis-Related Infections/surgery
3.
Environ Int ; 85: 61-76, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26340755

ABSTRACT

Active pharmaceutical ingredients (APIs) have been frequently found in the environment. It is, however, still not quite clear who is mainly responsible for API emissions. Hospitals have been considered to be the main contributing point sources for wastewater (WW) discharge of APIs. However, recent studies have shown that the contribution of hospitals to the input of APIs into the aquatic environment is quite low. Due to demographic change and the increase of psychiatric diseases, health institutions (HIs) such as psychiatric hospitals and nursing homes are likely to be important sources as well, but no data is available in this respect. This study aims to assess the impact of HIs and to provide a methodology to measure their respective contributions. Drawing on pharmaceutical consumption data for the years 2010, 2011, and 2012, this study identified API usage patterns for a psychiatric hospital (146 beds), a nursing home (286 inhabitants), and a general hospital (741 beds), the latter of which comprises three separate locations. All the HIs are located in two sub-regions of a county district with about 400,000 citizens in southwestern Germany. A selection of neurological drugs was quantified in the sewer of these facilities to evaluate the correlation between consumption and emission. The API contribution of HIs was assessed by comparing the specific consumption in the facilities with the consumption in households, expressed as the emission potential (IEP). The study shows that the usage patterns of APIs in the psychiatric hospital and the nursing home were different from the general hospital. Neurological drugs such as anticonvulsants, psycholeptics, and psychoanaleptics were mainly consumed in the psychiatric hospital and the nursing home (74% and 65%, respectively). Predicted and average measured concentrations in the effluent of the investigated HIs differed mostly by less than one order of magnitude. Therefore, the consumption-based approach is a useful method to assess usage patterns of APIs in HIs and to predict their respective contributions to WW. The national contribution of HIs on total WW discharge of APIs compared to households was very low. Only the results for the sedative clomethiazole in general hospitals as well as the antidepressant moclobemide and the antipsychotic quetiapine for the nursing homes were found to deserve some attention. The regional comparison showed that in sub-regions with a comparably higher density of HIs, the allocated facilities could be seen as point sources emitting particular APIs. However, in general, the bulk of the consumed pharmaceuticals to WW discharge has to be attributed to households.


Subject(s)
Drug Utilization , Hospitals , Nursing Homes , Pharmaceutical Preparations/analysis , Wastewater/chemistry , Water Pollutants, Chemical/analysis , Drug Utilization/trends , Germany , Humans
4.
Water Res ; 85: 11-21, 2015 Nov 15.
Article in English | MEDLINE | ID: mdl-26281960

ABSTRACT

The anticonvulsant drug Gabapentin (GAB) is used for the treatment of various diseases (e.g. epilepsy, bipolar disorder, neuropathic pain) and is being consumed in high amounts. As GAB is not metabolized and shows a weak elimination in sewage treatment plants (STPs), it has been detected in surface water and even in raw potable water. Moreover, the confirmed teratogenic effects of GAB indicate the need for further investigations regarding options for the elimination of GAB in the water cycle. Little is known about the behavior of GAB during treatment with UV light, which is normally used for the disinfection of potable water and discussed for advanced wastewater treatment. In this study, GAB was exposed to polychromatic UV irradiation at different initial concentrations in aqueous solution. Afterwards the structures of the resulting phototransformation products (PTPs) were identified and elucidated by means of high-resolution mass spectrometry. GAB and photolytic mixtures were submitted to the Closed Bottle Test (CBT; OECD 301 D) to assess biodegradability. Furthermore, the toxicity of GAB and its photolytic mixtures was initially addressed on screening level using a modified luminescent bacteria test (LBT) and the umu-test (ISO/FDIS 13829). Environmentally realistic concentrations of GAB were disclosed by predicting STP influent concentrations (24.3 and 23.2 µg L(-1)). GAB with initial concentration of 100 mg L(-1) was eliminated by 80% after 128 min of direct UV irradiation, but just 9% of non-purgeable organic carbon (NPOC) was removed indicating the formation of dead-end transformation products (TPs). Structures of different PTPs were elucidated and several identical PTPs could also be identified at lower initial treatment concentrations (20 mg L(-1), 5 mg L(-1), 1 mg L(-1) and 0.1 mg L(-1)). GAB was classified as not readily biodegradable. Moreover, photo treatment did not result in better biodegradable PTPs. With increasing UV treatment duration, photolytic mixtures of GAB showed an increased inhibition of both, the bacterial luminescence emission as well as the growth in the modified LBT. In the umu-test no significant induction of the umuC gene as an indicator of genotoxicity was observed. Our results show that UV irradiation of GAB containing water would lead to the formation of recalcitrant PTPs. Considering that GAB was found in raw drinking water, the formation of toxic PTPs during drinking water treatment with UV light might be possible. Therefore, further studies should be conducted regarding the fate and effects on human health and the environment of GAB and the PTPs identified within this study.


Subject(s)
Amines/radiation effects , Anticonvulsants/radiation effects , Cyclohexanecarboxylic Acids/radiation effects , Photolysis , Water Pollutants, Chemical/radiation effects , gamma-Aminobutyric Acid/radiation effects , Amines/toxicity , Anticonvulsants/toxicity , Bacteria/drug effects , Biodegradation, Environmental , Cyclohexanecarboxylic Acids/toxicity , Gabapentin , Luminescence , Mutagenicity Tests , Toxicity Tests, Acute/methods , Ultraviolet Rays , Water Pollutants, Chemical/toxicity , gamma-Aminobutyric Acid/toxicity
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