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dichloromethane/hypoxia
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Combining transcriptomics and PBPK modeling indicates a primary role of hypoxia and altered circadian signaling in dichloromethane carcinogenicity in mouse lung and liver.
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Dichloromethane (DCM) is a lung and liver carcinogen in mice at inhalation exposures≥2000ppm. The modes of action (MOA) of these responses have been attributed to formation of genotoxic, reactive metabolite(s). Here, we examined gene expression in lung and liver from female B6C3F1 mice exposed to 0,
Determination of a new hypoxia selective agent from 2-quinoxalinecarbonitrile 1,4-di-N-oxides in plasma by high performance liquid chromatography.
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A high performance liquid chromatography (HPLC) method was developed and validated for the determination of 7-chloro-3-[[(N,N-dimethylamino)propyl]amino]-2-quinaxolinecarbonitri le 1,4-di-N-oxide (Q-85), a new hypoxia-selective agent, in plasma. The assay involves extraction into
The neurotoxicity of dichloromethane.
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Dichloromethane (DCM) is a clear, waterwhite, non-inflammable liquid of high volatility and sweet aromatic odor. It is widely used as an industrial solvent. In considering its neurotoxicity the CNS-depressant effects of both narcotic and hypoxic action must be taken into account, hypoxia being
An introduction to the clinical toxicology of volatile substances.
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Acute poisoning with organic solvents and other volatile compounds now usually follows deliberate inhalation (volatile substance abuse) or ingestion of these compounds. Solvents from adhesives, typewriter correction and dry cleaning fluids, cigarette lighter refills (butane) and aerosol propellants
A simple phototheranostics strategy to continuously deliver singlet oxygen in dark and hypoxic tumor microenvironment.
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Continuous irradiation during photodynamic therapy (PDT) process inevitably induces tumor hypoxia, thereby weakening the PDT effect. In the PDT induced temporary hypoxia, sustainably providing singlet oxygen from stored chemical energy may enhance the cell killing effect and boost the
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