首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Identification and determination of deoxynivalenol (DON) and deepoxydeoxynivalenol (DOM-1) in pig colostrum and serum using liquid chromatography in combination with high resolution mass spectrometry (LC-MS/MS (HR))
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Identification and determination of deoxynivalenol (DON) and deepoxydeoxynivalenol (DOM-1) in pig colostrum and serum using liquid chromatography in combination with high resolution mass spectrometry (LC-MS/MS (HR))

机译:使用液相色谱法与高分辨率质谱(LC-MS / MS(HR)组合使用液相色谱法鉴定和测定猪初乳和血清中的猪初乳和血清中的血清醇和血清

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Deoxynivalenol (DON) is one of the most common mycotoxins produced by field fungi (especially Fusarium). Contamination of livestock feed is a significant risk factor, especially for pigs that are highly susceptible to the toxic effects of deoxynivalenol. In this study, validated ultra-high performance liquid chromatography (U-HPLC) combined with a HR-Orbitrap-MS analysis method is described for the identification and quantitative determination of the mycotoxin compounds (DON and deepoxy-deoxynivalenol (DOM-1)) in pig colostrum (milk) and serum. Pre-treatment of the samples involved a deproteinisation step with methanol followed by a purification step by solid phase extraction (HLB cartridges). The chromatographic separation was performed on a C18 column with 1.7 μm-particle size using a water-methanol mobile phase. Detection of analytes was achieved on the tandem hybrid mass spectrometer Q Exactive, with a heated electrospray ionisation probe measured in positive mode (H-ESI+). For the confirmation of identification, a mass spectrometer was utilized in the full scan mode with resolving power (PR)=140,000 (FWHM) and for quantification analysis, it was utilized in the parallel reaction monitoring mode (PRM). The method has been fully validated according to the requirements of Commission Decision 2002/657/EC for confirmatory analyses, plus the addition of a mass accuracy (MA) parameter. For the confirmation of the presence of these analytes in pig colostrum and serum, matching of the retention time with mass accuracy for the precursor ion from MS and product ions from MS/MS was used. A deuterium isotopically labelled internal standard and a matrix-matched calibration curve were employed for quantification. The linear range of quantification was 0.5-20 μg L~(?1) and the correlation coefficient (R~2) was>0.999 for all calibrations. The limit of detection for DON and DOM-1 in colostrum was 0.48 μg L~(?1) and 0.54 μg L~(?1), respectively, and in serum 0.24 μg L~(?1) a
机译:脱氧性苯酚(Don)是由田间真菌(尤其是镰刀菌)产生的最常见的霉菌毒素之一。牲畜饲料的污染是一种显着的风险因素,特别是对于高易受脱氧酚苯酚的毒性作用的猪的猪。在该研究中,验证的超高效液相色谱(U-HPLC)与HR-orbitrap-MS分析方法组合用于鉴定和定量测定霉菌毒素化合物(DON和Exedoxy-exoxynolenol(Dom-1))在猪初乳(牛奶)和血清中。样品的预处理涉及用甲醇的脱蛋白步骤,然后通过固相萃取(HLB盒)纯化步骤。使用水 - 甲醇流动相对1.7μm粒径的C18柱进行色谱分离。在串联杂交质谱仪Q上实现了分析物的检测,其在阳性模式(H-ESI +)中测得的加热电喷雾电离探针。为了确认识别,在全扫描模式下使用质谱仪,通过解决功率(PR)= 140,000(FWHM)和定量分析,其在并联反应监测模式(PRM)中使用。该方法已根据委员会决定2002/657 / EC进行确认分析的要求完全验证,加上了质量准确度(MA)参数。为了确认猪初乳和血清中这些分析物的存在,使用与来自MS / MS的MS和产物离子的预体离子的保留时间与来自MS / MS的产物离子的质量准确匹配。采用氘表发氘标记的内标和基质匹配的校准曲线进行量化。线性定量范围为0.5-20μgL〜(α1),所有校准的相关系数(R〜2)> 0.999。在初乳中的DON和DOM-1的检测极限分别为0.48μg1-(α1)和0.54μgL〜(α1),血清0.24μgL〜(α1)a

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