Indoor air is typically a mixture of many chemicals at low concentrations without any adverse health effects alone, but in mixtures they may cause toxicity and risks to human health. The aim of this study was by using new approach methods to assess the potential toxicity of indoor air condensates. In specific, different in vitro test methods including cyto-and immunotoxicity, skin sensitization and endocrine disruption were applied. In addition to biological effects, the indoor air samples were subjected to targeted analysis of 25 volatile organic compounds (VOCs) and Genapol X-80 (a nonionic emulsifier) suspected to be present in the samples, and to a non-targeted "total chemical scan" to find out whether the chemical composition of the samples is associated with the biological effects. The results confirm that assessing health risks of indoor air by analysing individual chemicals is not an adequate approach: We were not able to detect the VOCs and Genapol X-80 in the indoor air samples, yet, several types of toxicity, namely, cytotoxicity, immunotoxicity, skin sensitization and endocrine disruption were detected. In the non-targeted total chemical scan of the indoor air samples, a larger number of compounds were found in the cytotoxic samples than in the non-cytotoxic samples supporting the biological findings. If only one biological method would be selected for the screening of indoor air quality, THP-1 macrophage/WST-1 assay would best fit for the purpose as it is sensitive and serves as a good representative for different sub-toxic end points, including immunotoxicity, (skin) sensitization and endocrine disruption.
- Publikační typ
- časopisecké články MeSH
Health care facilities and hospitals generate significant amounts of wastewater which are released into the sewage system, either after a preliminary treatment or without any further treatment. Hospital wastewater may contain large amounts of hazardous chemicals and pharmaceuticals, some of which cannot be eliminated entirely by wastewater treatment plants. Moreover, hospital effluents may be loaded with a plethora of pathogenic microorganisms or other microbiota and microbiome residues. The need to monitor hospital effluents for their genotoxic hazard is of high importance, as detailed information is scarce. DNA-based information can be acquired directly from samples through the application of various molecular methods, while cell-based biomonitoring assays can provide important information about impaired cellular pathways or mechanisms of toxicity without prior knowledge of the identity of each toxicant. In our study, we evaluated samples of chlorinated hospital wastewater discharged into the sewage system after this disinfection process. The assessment of cytotoxicity, genotoxicity and mutagenicity of the hospital effluents was performed in vitro by using a broad battery of biomonitoring assays that are relevant for human health effects. All the tested hospital wastewater samples could be classified as potentially genotoxic, and it is concluded that the microbiota present in hospital wastewater might contribute to this genotoxic potential.
- MeSH
- chemické látky znečišťující vodu * analýza toxicita MeSH
- lidé MeSH
- nemocnice MeSH
- odpadní voda * toxicita MeSH
- poškození DNA MeSH
- testy genotoxicity MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Medical devices must be tested before marketing in accordance with ISO EN 10993-10 in order to avoid skin sensitization. This standard predominantly refers to the in vivo test but does not exclude the use of in vitro methods that have been sufficiently technically and scientifically validated for medical device testing. It is foreseen that, due to the complexity of the sensitization endpoint, a combination of several methods will be needed to address all key events occurring in the sensitization process. The objective of this pilot study was to evaluate the sensitization potential of selected medical devices using a combination of in chemico (DPRA, OECD TG 442C) and in vitro (LuSens, OECD TG 442D) methods in comparison with the in vivo (LLNA DA, OECD TG 442A) method and to suggest a possible testing strategy for the safety assessment of medical device extracts. Overall, one of the 42 tested samples exhibited positive results in all employed test methods, while 33 samples were predicted as non-sensitizing in all three performed methods. This study demonstrated good agreement between in vitro and in vivo results regarding non-sensitizing samples; however, some discrepancies in positive classification were recorded. A testing strategy is suggested in which negative results are accepted and any positive results in the in chemico or in vitro tests are followed up with a third in vitro test and evaluated in accordance with the “2 out of 3 approach”. This strategy may reduce and replace animal use for testing the sensitization potential of medical devices.
- MeSH
- alergická kontaktní dermatitida * MeSH
- alternativy testů na zvířatech * MeSH
- biotest MeSH
- kůže MeSH
- pilotní projekty MeSH
- techniky in vitro MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
The aim of the study was toxicological testing of an innovative and efficient antimicrobial agent based on photoactive phthalocyanine (Pc) derivative. A promising Aluminium phthalocyanine (AlPc) with efficient and stable antimicrobial effects was subjected to a battery of toxicological tests to avoid local and systemic toxicity hazard. In compliance with the current European legislation restricting the use of experimental animals, the methods comprised exclusively in vitro procedures based on cellular and tissue models of human origin or mimicking human tissues. The battery of toxicological tests to identify local toxicity included skin corrosion/irritation, eye irritation, and phototoxicity. The basic systemic toxicity tests included acute toxicity, skin sensitization, genotoxicity, and endocrine disruption. The results showed that AlPc induced skin and eye irritation, exhibited borderline sensitization potential and mutagenic potential in one test strain of the Ames test, which was not confirmed in the chromosome aberration test. The AlPc was found to be phototoxic. The results from the cytotoxicity test designed for acute oral toxicity estimation were not conclusive, the acute toxicity potential has to be determined by conventional tests in vivo. Regarding endocrine disruption, no agonistic activity of the AlPc on human estrogen receptor α, nor human androgen receptor was observed. The skin penetration/absorption test revealed that the AlPc has not penetrated into the dermis and receptor fluid, confirming no risk of systemic exposure via the bloodstream.
- MeSH
- alfa receptor estrogenů metabolismus MeSH
- androgenní receptory metabolismus MeSH
- antiinfekční látky farmakokinetika toxicita MeSH
- chorioalantoická membrána krevní zásobení účinky léků MeSH
- dráždivé látky farmakokinetika toxicita MeSH
- fotochemické procesy MeSH
- indoly farmakokinetika toxicita MeSH
- kožní absorpce MeSH
- kultivované buňky MeSH
- kuřecí embryo MeSH
- kůže účinky léků metabolismus MeSH
- lidé MeSH
- lymfocyty účinky léků MeSH
- myši inbrední BALB C MeSH
- oči účinky léků MeSH
- poškození DNA MeSH
- prasata MeSH
- testy toxicity MeSH
- zvířata MeSH
- Check Tag
- kuřecí embryo MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Klíčová slova
- photodynamická terapie,
- MeSH
- cévy fyziologie růst a vývoj sekrece účinky léků MeSH
- exprese genu účinky léků MeSH
- fibroblastové růstové faktory MeSH
- fotochemoterapie využití MeSH
- fotosenzibilizující látky MeSH
- inhibitory angiogeneze * aplikace a dávkování terapeutické užití MeSH
- kyselina salicylová aplikace a dávkování MeSH
- látky indukující angiogenezi MeSH
- lidé MeSH
- nádory * terapie MeSH
- prospektivní studie MeSH
- TNF-alfa toxicita MeSH
- vaskulární endoteliální růstové faktory sekrece MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- grafy a diagramy MeSH
- práce podpořená grantem MeSH
- Klíčová slova
- hASC+HUVEC co-kultura,
- MeSH
- antiinfekční látky terapeutické užití MeSH
- fotochemoterapie využití MeSH
- fotosenzibilizující látky aplikace a dávkování terapeutické užití MeSH
- inhibitory angiogeneze * fyziologie MeSH
- kyselina salicylová * aplikace a dávkování terapeutické užití MeSH
- lidé MeSH
- nádory terapie MeSH
- prospektivní studie MeSH
- techniky in vitro MeSH
- vaskulární endoteliální růstové faktory MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- práce podpořená grantem MeSH
