化学
色谱法
微粒体
CYP3A4型
质谱法
双酚
新陈代谢
代谢途径
药物代谢
串联质谱法
细胞色素P450
CYP1A2
液相色谱-质谱法
碎片(计算)
体外
生物化学
有机化学
生物
环氧树脂
生态学
作者
Ons Ousji,Leanne Ohlund,Lekha Sleno
标识
DOI:10.1021/acs.chemrestox.0c00042
摘要
Bisphenol A (BPA) metabolism has been investigated using several in vitro models, including human and rat liver microsomes and subcellular (S9) fractions, as well as human-recombinant cytochrome P450 3A4 (CYP3A4) expressed in Supersomes, for a comprehensive look at all possible metabolic pathways. By an untargeted approach using liquid chromatography coupled to a high-resolution quadrupole-time-of-flight mass spectrometer, we were able to detect a large number of known Phase I and Phase II metabolites of BPA, as well as several previously uncharacterized ones. A detailed fragmentation study of BPA and its detected metabolites was crucial to confirm structures. Isotope-labeled BPA analogs were highly useful for the structural elucidation of many metabolites. These results contribute to a better understanding of BPA metabolism, including pathways that may introduce additional toxicity, as well as help with the assessment of BPA exposure in different biological matrices.
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