Stereoselective analysis of thioridazine-2-sulfoxide and thioridazine-5-sulfoxide:: An investigation of rac-thioridazine biotransformation by some endophytic fungi

被引:37
作者
Borges, Keyller Bastos [1 ]
Borges, Warley De Souza [2 ]
Pupo, Monica Tallarico [2 ]
Bonato, Pierina Sueli [1 ]
机构
[1] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Quim & Fis, BR-14040903 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Ciencias Farmaceut, BR-14040903 Ribeirao Preto, Brazil
基金
巴西圣保罗研究基金会;
关键词
thioridazine; thioridazine-2-sulfoxide; thioridazine-5-sulfoxide; biotransformation; endophytic fungi;
D O I
10.1016/j.jpba.2007.05.018
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
The purpose of this study was to develop a method for the stereoselective analysis of thioridazine-2-sulfoxide (THD-2-SO) and thioridazine-5-sulfoxide (THD-5-SO) in culture medium and to study the biotransformation of rac-thioridazine (THD) by some endophytic fungi. The simultaneous resolution of THD-2-SO and THD-5-SO diastereoisomers was performed on a CHIRALPAK(R) AS column using a mobile phase of hexane: ethanol: methanol (92:6:2, v/v/v) + 0.5% diethylamine; UV detection was carried out at 262 nm. Diethyl ether was used as extractor solvent. The validated method was used to evaluate the biotransformation of THD by 12 endophytic fungi isolated from Tithonia diversifolia, Viguiera arenaria and Viguiera robusta. Among the 12 fungi evaluated, 4 of them deserve prominence for presenting an evidenced stereoselective biotransformation potential: Phomopsis sp. (TD2) presented greater mono-2-sulfoxidation to the form (S)-(SE) (12.1%); Glomerella cingulata (VA1) presented greater mono-5-sulfoxidation to the forms (S)-(SE) + (R)-(FE) (10.5%); Diaporthe phaseolorum (VR4) presented greater mono-2-sulfoxidation to the forms (S)-(SE) and (R)-(FE) (84.4% and 82.5%, respectively) and Aspergillus fumigatus (VR12) presented greater mono-2-sulfoxidation to the forms (S)-(SE) and (R)-(SE) (31.5% and 34.4%, respectively). (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:945 / 952
页数:8
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