王 婵,赵永拓,彭心婷,孙兴权,刘慧颖,张 彧,曹际娟.QuEChERS法联合高效液相色谱法快速检测扇贝中的软骨藻酸[J].食品安全质量检测学报,2015,6(1):72-77
QuEChERS法联合高效液相色谱法快速检测扇贝中的软骨藻酸
Rapid detection of domoic acid in scallops by QuEChERS method coupled with high performance liquid chromatography
投稿时间:2014-11-12  修订日期:2015-01-17
DOI:
中文关键词:  软骨藻酸  QuEChERS样品制备法  高效液相色谱法  快速检测
英文关键词:domoic acid  QuEChERS extration  high performance liquid chromatography  rapid detection
基金项目:质检公益性行业科研专项(No.201310141)
作者单位
王 婵 大连工业大学, 辽宁出入境检验检疫局 
赵永拓 鲅鱼圈出入境检验检疫局 
彭心婷 塔城出入境检验检疫局 
孙兴权 辽宁出入境检验检疫局 
刘慧颖 辽宁出入境检验检疫局 
张 彧 大连工业大学 
曹际娟 辽宁出入境检验检疫局 
AuthorInstitution
WANG Chan Dalian Polytechnic University, Liaoning Entry-Exit Inspection and Quarantine Bureau 
ZHAO Yong-Tuo Bayuquan Entry-Exit Inspection and Quarantine Bureau 
PENG Xin-Ting Tacheng Entry-Exit Inspection and Quarantine Bureau 
SUN Xing-Quan Liaoning Entry-Exit Inspection and Quarantine Bureau 
LIU Hui-Ying Liaoning Entry-Exit Inspection and Quarantine Bureau 
ZHANG Yu Dalian Polytechnic University 
CAO Ji-Juan Liaoning Entry-Exit Inspection and Quarantine Bureau 
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中文摘要:
      目的 利用QuEChERS样品制备结合高效液相色谱法建立测定扇贝中记忆缺失性贝类毒素—软骨藻酸(domoic acid, DA)残留的检测方法。方法 QuEChERS样品制备法进行样品前处理, 即样品经甲醇:乙腈:水=6:3:1(v:v:v)提取, C18粉末净化, 反相高效液相色谱分离, 242 nm波长下检测, 基质匹配校准曲线外标法定量。结果 方法的检测低限(limit of quantitation, LOQ)为1.8 μg/g, DA在0.72~30.00 μg/mL浓度范围内线性良好(相关系数r=0.9998), 在1.8~6.0 μg/g添加浓度范围内, 平均回收率为90%左右, 相对标准偏差(relative standard deviation, RSD)小于5%。结论 本实验建方法检测低限完全满足DA 20 μg/g的限量要求, 且步骤简单、可操作性强、节省时间、试剂用量少、准确度高、精密度好, 具有快速高效的特点。
英文摘要:
      Objective To established a method to detect domoic acid residues in scallops by the sample processing method of QuEChERS in combination with high performance liquid chromatography (HPLC). Methods Samples were cleaned up by QuEChERS with extracting by methanol : acetonitrile : water = 6:3:1 (v:v:v), and purified by C18 powder, separated by reversed phase high performance liquid chromatography and detected at wave length of 242 nm, and quantified by the matrix matching calibration curve external standard method of matrix matching calibration curve at last. Results The limit of quantitative was 1.8 μg/g, working curve correlation coefficient was 0.9998 at the linear range of 0.72~30.00 μg/mL, the recovery rate was higher than 90% at the spiking concentration range of 1.8~6.0 μg/g, and relative standard deviation (RSD) was less than 5%. Conclusion This method with a fast speed and a high sensitivity and exactitude can satisfy the limit of detection of DA 20 μg/g.
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