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Development of ion trap HPLC-MS detection methods for the determination of prevalent mycotoxins in grain and application to real samples

机译:开发离子阱HpLC-ms检测方法,用于测定谷物中的普遍霉菌毒素,并应用于实际样品

摘要

The prevalent trichothecenes deoxynivalenol, nivalenol and HT-2 as well as zearalenone, zearalenol, ochratoxin A and citrinin are typical widespread mycotoxins in temperate climate zones mainly produced by the genus Fusarium, Aspergillus and Penicillium. Consequently, they co-occur frequently in the same agricultural commodities, especially in grain. Their simultaneous determination is highly desirable for screening method devices, due to the continuous need to protect the health of humans and animals by limiting their exposure to mycotoxins.udA rapid quantitative method for the simultaneous determination of the above mentioned mycotoxins was developed using HPLC coupled to an ion trap mass spectrometer equipped with an atmospheric pressure chemical ionization (APCI) source. It has been specifically developed for the rapid primary screening of cereal samples. The fast HPLC separation and APCI(+) detection which allows to detect mycotoxins of highly different polarity (lipophilic to ionic), make this method suitable for high sample throughput and routine analysis. Additionally, a fast and easy sample cleanup method was developed applying C18 and SAX SPE cartridges for the elution of mycotoxins with a wide range of polarity. Recoveries were in the range of 46-106 % and the limits of detection were between 25 and 125 ppb for different mycotoxins. Wheat and corn was chosen for the analysis of real samples.ududFumonisins belong to a substance class of mycotoxins, which was discovered recently (1988) and consists of long-chain methyl branched amino alcohols. Even nowadays the analysis of fumonisins is a big challenge not only because of the risk of the already known fumonisins in food, but also due to the fact that they form degradation and reaction products during food processing, which are not sufficiently characterized yet.udA method was developed for the quantification of fumonisins in corn based on reversed phase HPLC/MS and multiple MS. This lead for FB1 to a improved LOD of 0.6 ppb and a LOQ of 8 ppb, which is a factor of five better compared to the former fluorescence method. Furthermore, a reduced chromatographic run time of up to 50 % could be applied successfully even for the analysis of real samples. Various corn products were examined for fumonisin contaminations. Products from the Swiss market were all below the tolerance level of 1 ppm.udTo overcome matrix effects and guarantee to a reliable quantification of analytes an adequate ISTD was searched. Several approaches using uncomplicated and easy to perform synthesis was carried out adding protection groups to fumonisins. Unfortunately, the obtained products had either a too low stability under acidic conditions or the synthesis was not complete.udA total of 48 winter wheat samples from 1998 and 2000 were investigated by HPLC-MS for the presence of the trichothecenes nivalenol (NIV), deoxynivalenol (DON), neosolaniol (NEO), fusarenon-X (F-X), diacetoxyscirpenol (DAS), 3-acetyldeoxynivalenol (3-ADON), 15-acetyldeoxynivalenol (15-ADON), HT-2-toxin (HT-2) and T-2-toxin (T-2). Robustness of the applied technique under routine conditions was good and corresponding quality control information is given. The wheat samples were cultivated on a long-term field trial inududSwitzerland with three different farming systems (biodynamic, bioorganic and conventional). DON was detected in 100%, NIV in 67% and HT-2 in 25% of all wheat samples. Only 48% of the detectable DON concentrations were above the limit of quantification (LOQ, 50 μg/kg). The range varied between 10-206 μg/kg. NIV and HT-2 were detected at concentrations around or below their LOQ (NIV: 100 μg/kg; HT-2: 10 μg/kg).udStatistically significant differences between the three farming systems could not be found although there were some indications that wheat from organic farming had lower DON contaminations than that from conventional farming. However, the results indicated that the presence and levels of (selected) trichothecenes may not be suitable as marker to differentiate between the three given farming systems. Furthermore, the results showed that even in years with low or nearly no fungal infection (warm and dry summers) low contaminations of DON in wheat are inevitable.
机译:在温带气候区,流行的曲霉菌脱氧雪腐烯酚,雪腐烯酚和HT-2以及玉米赤霉烯酮,玉米赤霉烯醇,曲霉毒素A和citrinin是典型的分布广泛的霉菌毒素,主要由镰刀菌属,曲霉属和青霉属产生。因此,它们经常同时出现在相同的农产品中,尤其是谷物中。由于持续需要通过限制真菌毒素的暴露来保护人类和动物的健康,因此它们的同时测定对于筛选方法设备是非常需要的。 ud使用HPLC联用开发了一种同时测定上述霉菌毒素的快速定量方法配备了大气压化学电离(APCI)源的离子阱质谱仪。它是专为谷物样品的快速初步筛选而开发的。快速HPLC分离和APCI(+)检测可检测极性高度不同(亲脂性至离子性)的霉菌毒素,使该方法适用于高样品通量和常规分析。此外,使用C18和SAX SPE柱开发了一种快速简便的样品净化方法,用于洗脱极性范围较广的霉菌毒素。回收率在46-106%范围内,不同真菌毒素的检出限在25至125 ppb之间。小麦和玉米被选择用于实际样品的分析。 ud ud富莫尼菌素属于霉菌毒素的一种物质,最近发现(1988年),由长链甲基支链氨基醇组成。即使在当今,对伏马毒素的分析也是一个巨大的挑战,这不仅是因为食品中存在已知的伏马毒素的风险,而且还因为它们在食品加工过程中会形成降解和反应产物,但尚未充分表征。建立了基于反相HPLC / MS和多重MS定量分析玉米中伏马毒素的方法。导致FB1的LOD改善到0.6 ppb,LOQ改善到8 ppb,这比以前的荧光方法提高了五倍。此外,即使对于分析真实样品,也可以成功地将色谱运行时间缩短多达50%。检查了各种玉米产品中伏马毒素的污染。瑞士市场的产品均低于1 ppm的容许水平。 ud为了克服基质效应并保证对分析物进行可靠的定量,已搜索了足够的ISTD。进行了几种使用简单且易于执行的合成的方法,在伏马菌素中添加了保护基。不幸的是,获得的产品在酸性条件下的稳定性太低或合成不完整。 ud通过HPLC-MS调查了1998年和2000年的48个冬小麦样品中是否存在Trichothecenes nivalenol(NIV),脱氧雪茄烯醇(DON),新茄尼醇(NEO),富沙农-X(FX),双乙酰氧基scirpenol(DAS),3-乙酰基脱氧雪茄烯醇(3-ADON),15-乙酰基脱氧雪茄烯醇(15-ADON),HT-2-毒素(HT-2)和T-2-毒素(T-2)。在常规条件下所应用技术的鲁棒性良好,并给出了相应的质量控制信息。小麦样品是在瑞士 ud ud的长期田间试验中种植的,采用三种不同的耕作系统(生物动力,生物有机和常规)。在所有小麦样品中,分别检测到100%的DON,67%的NIV和25%的HT-2。可检测的DON浓度中只有48%超过了定量极限(LOQ,50μg/ kg)。范围在10-206μg/ kg之间。检测到NIV和HT-2的浓度约为或低于其最低检测限(NIV:100μg/ kg; HT-2:10μg/ kg)。 ud尽管存在某些迹象,但未发现三种耕作系统之间的统计学显着差异与常规耕作相比,有机耕作的小麦具有较低的DON污染。但是,结果表明(选定的)单端孢菌烯的存在和水平可能不适合作为区分三种给定耕作制度的标记。此外,结果表明,即使在真菌感染率较低或几乎没有的年份(夏季温暖干燥),小麦中DON的低污染也是不可避免的。

著录项

  • 作者

    Griesshaber Dorrit Suenja;

  • 作者单位
  • 年度 2007
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
  • 中图分类
  • 入库时间 2022-08-20 21:07:25

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