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首页> 外文期刊>Journal of separation science. >Chromatography column comparison and rapid pretreatment for the simultaneous analysis of amantadine, rimantadine, acyclovir, ribavirin, and moroxydine in chicken muscle by ultra high performance liquid chromatography and tandem mass spectrometry
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Chromatography column comparison and rapid pretreatment for the simultaneous analysis of amantadine, rimantadine, acyclovir, ribavirin, and moroxydine in chicken muscle by ultra high performance liquid chromatography and tandem mass spectrometry

机译:超高效液相色谱-串联质谱法同时分析鸡肉中金刚烷胺,金刚乙胺,阿昔洛韦,利巴韦林和吗啉的色谱柱比较和快速预处理

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In this work, a chromatography column comparison and rapid pretreatment development were carried out. A multi-class method was built based on the quick, easy, cheap, effective, rugged, and safe pretreatment method with hydrophilic interaction ultra high performance liquid chromatography and tandem mass spectrometry for the high-throughput analysis of five antivirals in chickenmuscle. TheHSS T3 column, BEH HILIC column and BEH Amide column were studied, and their chemical functionalities and chromatographic separation effectiveness were compared. The BEH Amide column was selected to perform the mass spectrometry analysis under the hydrophilic interaction chromatography mode. First, a different strategy without adding MgSO4 and NaCl into the muscle samples was considered. Then, different concentrations of formic acid, acetic acid, and ammonia in acetonitrile were compared for better extraction efficiency. Nine sorbents (C-18, PSA, NH2, Florisil, Alumina-B, Alumina-N, PestiCarb, NANO, and NANO-NH2) were studied. The optimized procedure consisted of the use of 10% acetic acid in acetonitrile for the extraction solvent and NANO-NH2 for clean-up. NANO-NH2 had not been applied in other matrix and pollutants so far. The developed method provided favorable trueness, precision, and acceptable matrix effect. Meanwhile, the method was sensitive, the limits of detection of amantadine, rimantadine, acyclovir, ribavirin, and moroxydine achieved were 0.56, 0.50, 0.30, 2.22, and 0.51 mu g/kg, respectively, and were successfully applied for the routine detection of antivirals in the chicken samples.
机译:在这项工作中,进行了色谱柱比较和快速预处理开发。建立了一种基于亲水相互作用超高效液相色谱和串联质谱的快速,简便,廉价,有效,坚固和安全的预处理方法的多类方法,用于高通量分析鸡肌肉中的五种抗病毒剂。研究了HSS T3色谱柱,BEH HILIC色谱柱和BEH Amide色谱柱,并比较了它们的化学功能和色谱分离效果。选择BEH Amide柱在亲水相互作用色谱模式下进行质谱分析。首先,考虑了不向肌肉样品中添加MgSO4和NaCl的另一种策略。然后,比较乙腈中不同浓度的甲酸,乙酸和氨,以提高提取效率。研究了九种吸附剂(C-18,PSA,NH2,Florisil,Alumina-B,Alumina-N,PestiCarb,NANO和NANO-NH2)。优化的程序包括在乙腈中使用10%的乙酸作为萃取溶剂,并使用NANO-NH2进行净化。到目前为止,NANO-NH2尚未用于其他基质和污染物中。所开发的方法提供了良好的真实性,精度和可接受的矩阵效果。同时,该方法灵敏,金刚烷胺,金刚烷胺,阿昔洛韦,利巴韦林和莫拉西定的检出限分别为0.56、0.50、0.30、2.22和0.51μg/ kg,并成功地应用于常规检测。鸡样品中的抗病毒药。

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