首页|期刊导航|中国渔业质量与标准|液相色谱串联质谱法快速检测水产品中孔雀石绿残留物

液相色谱串联质谱法快速检测水产品中孔雀石绿残留物OA

Rapid detection of malachite green residue in aquatic products by liquid chromatography tandem mass spectrometry

中文摘要英文摘要

建立液相色谱串联质谱法快速测定水产品中的孔雀石绿(MG)和隐色孔雀石绿(LMG).以乙腈和乙酸铵为溶剂,对样品进行快速提取,提取液经 Thermo Hypersil GOLD C18 柱(100.0 mm×2.1 mm,1.9 μm)分离,以乙腈-5 mmol/L乙酸铵溶液(含体积分数为 0.1%的甲酸)为流动相,梯度洗脱,采用电喷雾正离子扫描,以多反应监测(MRM)模式测定,内标法定量.MG和LMG的质量浓度在0.125~2.500 μg/L内,与色谱峰面积线性关系良好,相关系数均大于0.999,方法检出限均为0.25 μg/kg,定量限均为1.00 μg/kg,样品加标回收率为80.9%~98.9%,相对标准偏差为0.9%~5.2%(n=6).该方法满足现行标准的检测要求,检测效率高,可作为大批量水产品中MG和LMG残留量的快速定量分析方法.[中国渔业质量与标准,2025,15(2):15-21]。

A liquid chromatography-tandem mass spectrometry(LC-MS/MS)method was developed for the rapid quantification of malachite green(MG)and leucomalachite green(LMG)in aquatic products.Samples were rapidly extracted with acetonitrile and ammonium acetate as solvents.The extract was separated on a Thermo Hypersil GOLD C18 column(100 mm×2.1 mm,1.9 μm).A mobile phase of acetonitrile and 5 mmol/L ammonium acetate(0.1%formic acid,v/v)was employed in gradient elution.Detection was by electrospray ionization in positive mode with multiple reaction monitoring(MRM),and quantification used an internal standard.MG and LMG exhibited linear re-sponses over 0.125~2.500 μg/L,with correlation coefficients(R2)greater than 0.999.The limits of detection(LOD)and quantification(LOQ)were 0.25 μg/kg and 1.00 μg/kg,respectively.The recovery rates of sample ranged from 80.9%to 98.9%,with relative standard deviations(RSDs)of 0.9%to 5.2%(n=6).This method complied with current standards and demonstrated high throughput.It was suitable for rapid quantitative of MG and LMG residues in large-scale aquatic products screening.[Chinese Fishery Quality and Standards,2025,15(2):15-21].

黄鸾玉

广西壮族自治区水产科学研究院,广西 南宁 530021

农业科技

孔雀石绿液相色谱串联质谱法水产品药物残留

Malachite greenliquid chromatography tandem mass spectrometryaquatic productsdrug residues

《中国渔业质量与标准》 2025 (2)

15-21,7

广西重点研发计划(桂科AB23026007)广西农业科技自筹经费项目(Z2023041Z2023042)

10.3969/j.issn.2095-1833.2025.02.002

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