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采用液相色谱-高分辨质谱法对水中选定的抗癌药物进行光催化降解,并鉴定其转化产物。

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

机构信息

Department of Chemistry, University of Turin, Via P. Giuria 5, 10125 Torino, Italy.

Department of Molecular Biotechnology and Health Sciences, University of Turin, Via P. Giuria 5, 10125 Torino, Italy.

出版信息

J Chromatogr A. 2014 Oct 3;1362:135-44. doi: 10.1016/j.chroma.2014.08.035. Epub 2014 Aug 16.

Abstract

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.

摘要

本研究考察了两种抗肿瘤药物(甲氨蝶呤和阿霉素)在水生态环境中的命运。实验分别采用黑暗实验、均相光解和 TiO2 多相光催化的方法对它们的分解情况进行了研究,对中间化合物进行了鉴定,并评估了它们在不同时间的急性毒性。分析采用 LC(ESI 正模式)与 LTQ-Orbitrap 分析仪联用的方法;母离子的精确质量与质荷比的偏差低于 10mmu,保证了所有情况下分子公式的正确赋值,而它们的 MS(2) 和 MS(3) 谱图显示出几个结构诊断离子,可以对不同的转化产物进行特征化,并区分出等质异位体。随后,阿霉素或甲氨蝶呤转化产物鉴定出 14 种和 8 种主要物质。阿霉素的主要转化过程包括(多)羟基化和/或分子氧化,或糖部分的脱落。甲氨蝶呤的转化涉及脱羧或分子裂解。急性毒性测量表明,不仅这两种药物具有高毒性,而且它们的初始转化产物也具有高毒性。

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