首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >LC-MS/MS characterization of the urinary excretion profile of the mycotoxin deoxynivalenol in human and rat
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LC-MS/MS characterization of the urinary excretion profile of the mycotoxin deoxynivalenol in human and rat

机译:LC-MS / MS表征人和大鼠中霉菌毒素脱氧雪腐酚的尿排泄曲线

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The understanding of mycotoxins transfer to biological fluids is challenged by the difficulties in performing and replicating in vivo experiments as well as the lack of suitable methods of analysis to detect simultaneously a range of chemically different metabolites at trace levels. LC-MS/MS has been used herein to study the urinary excretion profile of the mycotoxin deoxynivalenol in human and Wistar rat. Deoxynivalenol and deoxynivalenol glucuronide were found in both human and rat urines, whereas de-epoxydeoxynivalenol and its glucuronide conjugate were only detected in rat urine. The presence of two deoxynivalenol glucuronide isomers in Wistar rat urine has been shown for the first time. Structure confirmation of the detected metabolites was provided by the analysis of fragmentation patterns. A solid phase extraction clean up procedure allowing recoveries in the range 72-102% for deoxynivalenol, de-epoxydeoxynivalenol, and their glucuronide conjugates was optimized. A multiple reaction monitoring method for the simultaneous determination of all investigated metabolites was elaborated allowing the direct detection of deoxynivalenol metabolites without the hydrolysis step. Deoxynivalenol urinary levels in the range 0.003-0.008. μg/ml were detected in healthy human subjects, whereas deoxynivalenol and de-epoxynivalenol levels between 1.9-4.9. μg/ml and 1.6-5.9. μg/ml, respectively were found in administered rat urine. These findings emphasize the relevance of the highly selective and sensitive LC-MS/MS technique for the direct detection and characterization of deoxynivalenol metabolites in complex biological matrices.
机译:进行体内实验和复制的困难以及缺乏同时检测痕量水平的化学不同代谢物的合适分析方法的挑战,对霉菌毒素向生物体液转移的理解提出了挑战。 LC-MS / MS已在本文中用于研究人和Wistar大鼠中霉菌毒素脱氧雪腐酚的尿排泄曲线。在人和大鼠的尿液中都发现了脱氧雪腐烯醇和脱氧雪腐烯醇葡糖醛酸,而仅在大鼠尿液中检测到了脱氧脱氧雪腐烯醇及其葡糖醛酸苷结合物。首次证明Wistar大鼠尿液中存在两种脱氧雪腐烯醇葡糖醛酸苷异构体。通过片段化模式的分析提供了对检测到的代谢物的结构确认。固相萃取净化程序可优化脱氧雪茄烯醇,脱环氧脱氧雪茄烯醇及其葡糖醛酸化物结合物的回收率,范围为72-102%。阐述了一种用于同时测定所有研究代谢物的多反应监测方法,可直接检测脱氧雪茄烯醇代谢物而无需进行水解步骤。脱氧雪腐酚尿水平在0.003-0.008的范围内。在健康人类受试者中检测到μg/ ml,而脱氧雪茄烯醇和脱环氧雪茄烯醇的水平在1.9-4.9之间。微克/毫升和1.6-5.9。在大鼠尿液中分别发现微克/毫升。这些发现强调了高度选择性和灵敏的LC-MS / MS技术与直接检测和表征复杂生物基质中脱氧雪腐烯代谢产物的相关性。

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