王 博,吴剑平,张 婧,徐 汀,严 凤.液相色谱串联四极杆质谱法测定猪浓缩饲料中25-羟基维生素D3含量[J].食品安全质量检测学报,2020,11(2):567-573
液相色谱串联四极杆质谱法测定猪浓缩饲料中25-羟基维生素D3含量
Determination of 25-hydroxyvitamin D3 in pig concentrated feed by liquid chromatography-tandem mass spectrometry
投稿时间:2019-10-29  修订日期:2019-12-19
DOI:
中文关键词:  液相色谱-串联质谱法  猪浓缩饲料  25-羟基维生素D3
英文关键词:liquid chromatography-tandem mass spectrometry  pig concentrated feed  25-hydroxyvitamin D3
基金项目:
作者单位
王 博 上海市兽药饲料检测所 
吴剑平 上海市兽药饲料检测所 
张 婧 上海市兽药饲料检测所 
徐 汀 上海市兽药饲料检测所 
严 凤 上海市兽药饲料检测所 
AuthorInstitution
WANG Bo Shanghai Municipal Supervisory Institute Veterinary Drugs and Feedstaff 
WU Jian-Ping Shanghai Municipal Supervisory Institute Veterinary Drugs and Feedstaff 
ZHANG Jing Shanghai Municipal Supervisory Institute Veterinary Drugs and Feedstaff 
XU Ting Shanghai Municipal Supervisory Institute Veterinary Drugs and Feedstaff 
YAN Feng Shanghai Municipal Supervisory Institute Veterinary Drugs and Feedstaff 
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中文摘要:
      目的 建立液相色谱-串联四极杆质谱法(liquid chromatography-tandem mass spectrometry, LC-MS/MS)测定猪浓缩饲料中25-羟基维生素D3的分析方法。方法 取适量猪浓缩饲料样品于离心管中, 加水后置于振荡器上振荡破除环糊精包囊, 再加入叔丁基甲醚振荡对目标物进行提取, 在9000 r/min条件下离心5 min, 氮气吹干后用2.00 mL流动相溶解, 过滤膜后上机测定。实验使用反相色谱柱进行分离, 流动相为甲醇(0.1%甲酸)和0.1%甲酸, 采用梯度程序洗脱, 三重四极杆质谱进行定量定性分析, 采用内标法进行计算。结果 该方法的检测限为5 μg/kg, 定量限为10 μg/kg, 在2~500 μg/L范围内线性良好(r≥0.999), 加标回收率在77.85%~90.22%之间, 相对标准偏差(relative standard deviation, RSD)≤8.8%。结论 本方法具有良好的准确度与精密度, 具有较好的实用性和专属性。
英文摘要:
      Objective To establish a method for the determination of 25-hydroxyvitamin D3 in pig concentrated feed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Methods A suitable amount of pig feed sample was taken in the centrifugal tube. The water was chosen to get rid of cyclodextrin by oscillating, and the tert butyl methyl ether was chosen to extract 25-hydroxyvitamin D3 by oscillating. After 9000 r/min centrifugation for 5 min, nitrogen blowed to dry and dissolved in 2.00 mL mobile phase, then the solution was filtered by 0.22 μm film and then injected. The targets were separated by the gradient elution with a reverse phase column as the stationary phase and 0.1% formic acid with methanol as the mobile phase. The qualification and quantification were achieved by a tandem mass spectrometry and internal standard method was used for calculation. Results The results showed that the limit of detection (LOD) was 5 μg/kg, limits of quantification (LOQ) was 10 μg/kg. The linearity of the method was good in the range of 2~500 μg/L and the liner correlations were all above 0.999, the recovery rate was between 77.85%~90.22%, and the RSD(relative standard deviation) was lower than 8.8%. Conclusion This method has good accuracy and precision, and has good practicability and specificity.
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