首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Development and validation of a liquid chromatography-electros-ray tandemmass spectrometry method for mebendazole and its metabolites hydroxymebendazoel and aminomebendazole in sheep liver
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Development and validation of a liquid chromatography-electros-ray tandemmass spectrometry method for mebendazole and its metabolites hydroxymebendazoel and aminomebendazole in sheep liver

机译:羊肝中甲苯苯达唑及其代谢产物羟基苯达唑和氨基苯达唑的液相色谱-电射线坦德姆法的建立与验证

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摘要

A quantitative liquid chromatography-electrospray tandem mass spectrometry method for the determination of mebendazoel and its hydrolysed and reduced metabolites in sheep liver has been developed and validated.The benzimidazole substances were extracted with ethyl acetate after the sample mixture had been made alkaline.The HPLC separation was performed on a reversed-phase C_(18) column with gradient elution using a mobile phase consisting of water containing 0.1% formic acid and acetonitrile.The analytes were detected after atmospheric pressure electrospray ionization on a tandem quadrupole mass spectrometer in MS-MS mode.The components were measured by the MS-MS transitions of the molecular ion to the two most abundant daughter ions.The detection limits are lower than 1 #mu#k KG~(-1).For this application,the validation limit ws set at 50#mu#g kg(-1).The examined validation paameters were in accordance with teh permitted tolerances ranges stipulated in the proposed new European validation criteria for residue surveillance.For the three analytes,the overall recovery was higher than 90%.The RSD for the repeatability ranged from 5 to 11%.The range for the within-laboratory reproducibility was between 2 and 17%.The decison limits for mebendazole,the hydrolysed and the reduced metabolite were 56.6,61.8 and 64.2 #mu#g kg~(-1),respectively.The detection capabilities for these substances were 60.0,86.1 and 90.9 #mu#g kg~(-1),respectively.
机译:建立并验证了定量液相色谱-电喷雾串联质谱法测定羊肝中甲苯达唑及其水解和还原代谢产物的方法,并将混合液碱化后,用乙酸乙酯萃取苯并咪唑类物质。在反相C_(18)色谱柱上进行梯度洗脱,使用的流动相由含有0.1%甲酸和乙腈的水组成。大气压电喷雾电离后,在串联四极杆质谱仪上以MS-MS模式检测分析物通过分子离子到两个最丰富的子离子的MS-MS跃迁测量组分。检测限低于1#mu#k KG〜(-1)。对于此应用,设置验证限重量为50#mu#g kg(-1)。检查的验证参数符合拟议的新欧洲验证书中规定的允许公差范围残留监测的离子标准。三种分析物的总回收率均高于90%。重复性的RSD为5至11%。实验室内重现性的范围为2%至17%。决策极限甲苯苯达唑的水解物和还原代谢物分别为56.6、61.8和64.2#mu#g kg〜(-1)。这些物质的检测能力为60.0、86.1和90.9#mu#g kg〜(-1) ,分别。

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