Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo 11562, Egypt; The Institute of Education in Healthcare and Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresthill, Aberdeen, AB25 2ZD, United Kingdom.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo 11562, Egypt; Translational and Clinical Research Institute, Level 4 Leech, Newcastle University, Newcastle Upon Tyne, NE2 4HH, United Kingdom.
Chemosphere. 2024 Sep;363:142827. doi: 10.1016/j.chemosphere.2024.142827. Epub 2024 Jul 15.
A class of chemical with a potentially important perceived future contribution to the net zero carbon goal (as "green" solvents) is the methylimidazolium ionic liquids (MILs). These solvents are used in industrial processes such as biofuel production yet little is known about their environmental stability or toxicity in man although one MIL - 1-octyl-3-methylimidazolium (M8OI) - has been shown to activate the human estrogen receptor alpha (ERα). The stabilities of the chloride unsubstituted methylimidazolium (MI) and MILs possessing increasing alkyl chain lengths (2C, 1-ethyl-3-methylimidazolium (EMI); 4C, 1-butyl-3-methylimidazolium (BMI); 6C; 1-hexyl-3-methylimidazolium (HMI), 8C, M8OI; 10C, 1-decyl-3-methylimidazolium (DMI)) were examined in river water and a human liver model system. The MILs were also screened for their abilities to activate the human ERα in vitro and induce uterine growth in pre-pubertal rats in vivo. Short chain MILs (EMI, BMI and HMI) underwent negligible metabolism and mineralisation in river water; were not metabolised in a model of human liver metabolism; activated the human ERα in vitro and were estrogenic in vivo in rats. A structure-based computational approach predicted short chain MIL binding to both the estrogen binding site and an additional site on the human estrogen receptor alpha. Longer chain MILs (M8OI and DMI) were metabolised in river water and partially mineralised. Based on structure-activity considerations, some of these environmentally-derived metabolites may however, remain a hazard to the population. MILs therefore have the potential to become forever chemicals with adverse effects to both man, other animals and the environment in general.
一类具有潜在重要贡献的化学物质,有望实现净零碳目标(即“绿色”溶剂),是甲基咪唑鎓离子液体(MILs)。这些溶剂用于生物燃料生产等工业过程,但人们对其在环境中的稳定性或毒性知之甚少,尽管有一种 MIL - 1-辛基-3-甲基咪唑鎓(M8OI)已被证明能激活人类雌激素受体 alpha(ERα)。氯化未取代的甲基咪唑鎓(MI)和具有增加的烷基链长度的 MILs(2C,1-乙基-3-甲基咪唑鎓(EMI);4C,1-丁基-3-甲基咪唑鎓(BMI);6C;1-己基-3-甲基咪唑鎓(HMI),8C,M8OI;10C,1-癸基-3-甲基咪唑鎓(DMI))在河水中和人类肝脏模型系统中的稳定性进行了研究。还筛选了这些 MILs 在体外激活人类 ERα 的能力,并在体内诱导未成年大鼠子宫生长的能力。短链 MILs(EMI、BMI 和 HMI)在河水中几乎没有发生代谢和矿化;在人类肝脏代谢模型中没有发生代谢;在体外激活人类 ERα,并在体内对大鼠具有雌激素活性。基于结构的计算方法预测,短链 MIL 结合到人类雌激素受体 alpha 的雌激素结合部位和另外一个部位。较长链的 MILs(M8OI 和 DMI)在河水中发生代谢,并部分矿化。基于结构活性考虑,这些环境衍生的代谢物中的一些可能仍然对人群构成危害。因此,MILs 有可能成为对人类、其他动物和环境都有不利影响的永久性化学物质。