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Photocatalytic degradation of selected anticancer drugs and identification of their transformation products in water by liquid chromatography-high resolution mass spectrometry

机译:液相色谱-高分辨率质谱法光催化降解所选抗癌药物及其在水中的转化产物鉴定

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摘要

A study on the fate of two antineoplastic drugs, methotrexate and doxorubicin, in the aquatic environment is presented. The investigation involved a study of their decomposition under dark experiments, homogeneous photolysis and heterogeneous photocatalysis using titanium dioxide, the identification of intermediate compounds, as well as the assessment of acute toxicity over time. The analysis were carried out using LC (ESI positive mode) coupled with LTQ-Orbitrap analyser; accurate mass-to-charge ratios of parent ions were reported with inaccuracy below 10mmu, which guarantee the correct assignment of their molecular formula in all cases, while their MS~2 and MS~3 spectra showed several structural-diagnostic ions that allowed to characterize the different transformation products and to discriminate the isobaric species. Fourteen and eight main species were identified subsequently to doxorubicin or methotrexate transformation. The major transformation processes for doxorubicin involved (poli)hydroxylation and/or oxidation of the molecule, or the detachment of the sugar moiety. Methotrexate transformation involved decarboxylation or the molecule cleavage. Acute toxicity measurements showed that not only the two drugs exhibit high toxicity, but also their initial transformation products are highly toxic.
机译:提出了对两种抗肿瘤药甲氨蝶呤和阿霉素在水生环境中的命运的研究。这项研究涉及在黑暗实验中分解它们,使用二氧化钛进行均相光解和非均相光催化,鉴定中间化合物以及评估随时间的急性毒性。使用LC(ESI正模式)结合LTQ-Orbitrap分析仪进行分析。报告了准确的母离子质荷比,其准确度低于10mmu,这在所有情况下均能确保分子式的正确分配,而其MS〜2和MS〜3光谱显示了几种结构可诊断的离子,可以表征不同的转化产物并区分等压物种。阿霉素或甲氨蝶呤转化后鉴定出14个和8个主要物种。阿霉素的主要转化过程涉及分子的(聚)羟基化和/或氧化,或糖部分的脱离。甲氨蝶呤转化涉及脱羧或分子裂解。急性毒性测量结果表明,这两种药物不仅显示出高毒性,而且其最初的转化产物也具有高毒性。

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