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过一硫酸盐和 TiO2 光催化氧化协同作用有效去除天然水中抗 HIV 药物马拉维若:动力学研究及转化产物分析。

Efficient removal of anti-HIV drug - maraviroc from natural water by peroxymonosulfate and TiO photocatalytic oxidation: Kinetic studies and identification of transformation products.

机构信息

Department of Medicinal Chemistry, Faculty of Pharmacy, Medical University of Lublin, Jaczewskiego 4, 20-090, Lublin, Poland.

Department of Medicinal Chemistry, Faculty of Pharmacy, Medical University of Lublin, Jaczewskiego 4, 20-090, Lublin, Poland.

出版信息

J Environ Manage. 2022 Oct 1;319:115735. doi: 10.1016/j.jenvman.2022.115735. Epub 2022 Jul 18.

DOI:10.1016/j.jenvman.2022.115735
PMID:35863307
Abstract

In this study photochemical transformation of the antiretroviral pharmaceutical maraviroc under the simulated UV-Vis radiation was presented. The drug was shown to be extremely photo-resistant, with a half-life over 250 h, which is particularly significant, considering its presence in the aquatic environments. Addition of the natural river water matrix substantially increased the degradation rate, albeit the process led to formation of numerous phototransformation products. Due to high photostability and presumable environmental persistence of maraviroc, a photocatalytic method of its elimination was proposed. Although titanium dioxide alone presented acceptable results, its combination with peroxymonosulfate enormously accelerated the degradation process, increasing it over 67 000 times in comparison with the direct photolysis. Substitution of ultrapure water with river water resulted in inhibition of the PMS-driven processes, however the decomposition efficiency was still very high. Noteworthy, majority of the identified photoproducts were still present after termination of irradiation in all the experiments, which may indicate necessity of ecotoxicological assessment of those compounds.

摘要

本研究提出了模拟紫外可见辐射下抗逆转录病毒药物马拉维若的光化学转化。该药物具有极强的耐光性,半衰期超过 250 小时,考虑到其存在于水环境中,这一点尤为重要。天然河水基质的添加大大提高了降解速率,尽管该过程导致形成了许多光转化产物。由于马拉维若具有高稳定性和假定的环境持久性,因此提出了一种光催化消除方法。尽管单独的二氧化钛表现出可接受的结果,但它与过一硫酸盐的结合极大地加速了降解过程,与直接光解相比,将其提高了 67000 多倍。用河水替代超纯水会抑制 PMS 驱动的过程,但分解效率仍然非常高。值得注意的是,在所有实验中,照射终止后仍有大部分鉴定出的光产物存在,这可能表明需要对这些化合物进行生态毒理学评估。

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