气相色谱-串联质谱法检测水产品中氯霉素残留量  被引量:15

Determination of chloramphenicol residues in aquatic products by gas chromatography-tandem mass spectrometry

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作  者:宋宏娟 

机构地区:[1]新疆维吾尔自治区水环境监测中心,乌鲁木齐830000

出  处:《食品安全质量检测学报》2015年第6期2373-2378,共6页Journal of Food Safety and Quality

摘  要:目的建立检测分析水产品中氯霉素残留量的气相色谱-串联质谱联用(GC-MS/MS)的方法。方法样品采用乙酸乙酯提取、经过C<sub>18</sub>固相萃取柱净化,用硅烷化试剂衍生化,采用GC-MS/MS分析时,氯霉素在15min内流出。结果对样品添加两种浓度的加标质控,回收率在80%以上,相对标准偏差(RSD)在6.2%以内。在0.5<sup>1</sup>0 mg/L质量浓度范围内呈线性关系,相关系数大于0.99。结论该方法可用于氯霉素残留的准确定量分析,灵敏度、精密度和准确度均能满足渔药残留检测分析要求。ABSTRACT:Objective To establish a determination method of chloramphenicol (CAP) in aquatic products by gas chromatography-tandem mass spectrometry (GC-MS/MS). Methods The samples were extracted by ethyl acetate, cleaned up by C18 SPE column, and derived with silanization reagent, then the extracts were determined by MS/MS detector based on SCAN and MRM mode. Results CAP was well separated within 15 min. This method showed that the spiked average recoveries above 80%, the RSD ranged within 6.2%, and the calibration of those pesticides were linearity within the range of 0.5~10 mg/L (r2>0.99). Conclusion The method is accurate and sensitive, it is suitable for analysis of CAP residues in aquatic products.

关 键 词:氯霉素 气相色谱-串联质谱法 药物残留 水产品 

分 类 号:O657.63[理学—分析化学] TS254.7[理学—化学]

 

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