Acute oral toxicity and liver oxidant/antioxidant stress of halogenated benzene, phenol, and diphenyl ether in mice: a comparative and mechanism exploration

The lethal doses (LD₅₀s) of fluorinated, chlorinated, brominated, and iodinated benzene, phenol, and diphenyl ether in mice were ascertained respectively under the consistent condition. The acute toxicity of four benzenes orders in fluorobenzene (FB)?<?iodobenzene?<?chlorobenzene≈bromobenzene, that of four phenols orders in 4-iodophenol≈4-bromophenol?<?4-chlorophenol (4-MCP)?<?4-fluorophenol (4-MFP), and that of four diphenyl ethers orders in 4,4′-iododiphenyl ether?<?4,4′-difluorodiphenyl ether?<?4,4′-dichlorodiphenyl ether≈4,4′-dibromodiphenyl ether. General behavior adverse effects were observed, and poisoned mouse were dissected to observe visceral lesions. FB, 4-MCP, and 4-MFP produced toxic faster than other halogenated benzenes and phenols, as they had lower octanol–water partition coefficients. Pathological changes in liver and liver/kidney weight changes were also observed. Hepatic superoxide dismutase, catalase activities, and malondialdehyde level were tested after a 28-day exposure, which reflects a toxicity order basically consistent with that reflected by the LD₅₀s. By theoretical calculation and building models, the toxicity of benzene, phenol, and diphenyl ether were influenced by different structural properties.