液相色谱-串联质谱法测定养殖水体中的氯霉素
Determination of Chloramphenicol Level in Aquaculture Water by Liquid Chromatography-Tandem Mass Spectrometry
投稿时间:2015-06-10  修订日期:2015-11-06
DOI:10.15928/j.1674-3075.2015.06.003
中文关键词:氯霉素  养殖水体  液相色谱-串联质谱法
英文关键词:chloramphenicol  aquaculture water  liquid chromatography-tandem mass spectrometry
基金项目:辽宁省地方标准资助项目(2014333)
作者单位E-mail
张秀妍* 大连市水产技术推广总站辽宁 大连 116023 13700zxy@sina.cn 
马琳 大连市水产技术推广总站辽宁 大连 116023  
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中文摘要:
      本文采用回收率较高、较稳定的内标定量法(对养殖水体中氯霉素的检测方法进行了研究, 建立了养殖水体中氯霉素残留的检测方法。应用液相色谱-串联质谱(LC-MS/MS)测定养殖水体中氯霉素的含量,量取250 mL水样,用100 mL乙酸乙酯分2次萃取,萃取液经旋转蒸发仪浓缩近干,以40%的甲醇-水溶液定容至1 mL。氯霉素标准系列溶液浓度为0.25、0.50、1.00、1.25、2.50、5.00 ng/mL,氘代氯霉素的含量均为2.0 ng/mL,上机检测,内标法定量。结果表明,氯霉素为外标,氘代氯霉素为内标,其峰面积比值(y)与浓度比值(x)的曲线方程为:y=1.136512x+0.012050(R2=0.9990);该方法氯霉素的检出限为2 ng/L,定量限为4 ng/L,仪器线性范围为0.25~5.0 ng/mL;加标浓度在2~20 ng/L时,平均回收率在80%~110%,相对标准偏差小于10%。实验证明该方法比较稳定、灵敏度高,适用于检测养殖水体中氯霉素的含量。
英文摘要:
      Chloramphenicol is forbidden as a drug for veterinary use in China because of toxicity and serious side effects to humans. However, chloramphenicol is often determined in routine monitoring for drug residues in water-based products, natural waters and even in the ponds of some restaurants. Thus, it is important to develop a reliable method for determining chloramphenicol in water to support monitoring, control sources of chloramphenicol and improve the detection index of pollution-free water. In this study, a high performance liquid chromatography-tandem mass spectrometric (HPLC-MS/MS) method was developed to determine chloramphenicol levels in aquaculture water. Water samples were obtained from the aquafarm, seedling rearing rooms and storage ponds of restaurants. A 250 mL water sample was extracted with 100 mL of ethyl acetate twice, each for three minutes and the extractant was concentrated to 1 mL prior to analysis. The analysis was carried out in the multi-reaction monitoring (MRM) mode and the internal standard isotope dilution method was used for chloramphenicol quantification. The sensitivity and accuracy of the method was tested using a series of low concentration chloramphenicol standards (0.25, 0.50, 1.00, 1.25, 2.50 and 5.00 ng/mL), all with cekafix as the internal standard at a concentration of 2.0 ng/mL. The calibration curve for chloramphenicol exhibited good linearity over the concentration range from 0.25 ng/mL to 5.0 ng/mL, with detection limit of 2 ng/L and quantification limit of 4 ng/L. When the standard addition concentration was in the range of 2-20 ng/L, the average recovery rate was in the range of 80%-110% and the relative standard deviation (RSD) was less than 10%. The method proved to be accurate, stable and sensitive and meets the requirements for chloramphenicol detection in aquaculture water.
张秀妍,马琳.2015.液相色谱-串联质谱法测定养殖水体中的氯霉素[J].水生态学杂志,36(6):14-18.
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