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

被引:51
作者
Calza, P. [1 ]
Medana, C. [2 ]
Sarro, M. [1 ]
Rosato, V. [1 ]
Aigotti, R. [2 ]
Baiocchi, C. [2 ]
Minero, C. [1 ]
机构
[1] Univ Turin, Dept Chem, I-10125 Turin, Italy
[2] Univ Turin, Dept Mol Biotechnol & Hlth Sci, I-10125 Turin, Italy
关键词
HRMS; TiO2; Doxorubicin; Methotrexate; Emerging pollutants; Toxicity; WASTE-WATER; PHARMACEUTICALS; FATE; METABOLITES; CYTOSTATICS; EXTRACTION; CHALLENGE; MOLECULES; BEHAVIOR; SLUDGE;
D O I
10.1016/j.chroma.2014.08.035
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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 overtime. 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 10 mmu, which guarantee the correct assignment of their molecular formula in all cases, while their MS2 and MS3 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. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 144
页数:10
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