食品科学 ›› 2026, Vol. 47 ›› Issue (19): 322-329.doi: 10.7506/spkx1002-6630-20260330-232

• 安全检测 • 上一篇    

乳品中香兰素溯源与定量检测方法的建立及应用

李文君,许秀丽,尹睿杰,韩晓旭,裴晓燕,廉洁,聂雪梅,沈正超,王秀娟   

  1. (1.中国质量检验检测科学研究院,北京 100176;2.中国人民公安大学侦查学院,北京 100038;3.国家乳业技术创新中心,内蒙古 呼和浩特 010000)
  • 发布日期:2026-10-22
  • 基金资助:
    国家乳业技术创新中心项目(2024-KFKT-004)

Establishment and Application of Methods for Traceability and Quantitative Detection of Vanillin in Dairy Products

LI Wenjun, XU Xiuli, YIN Ruijie, HAN Xiaoxu, PEI Xiaoyan, LIAN Jie, NIE Xuemei, SHEN Zhengchao, WANG Xiujuan   

  1. (1. Chinese Academy of Quality and Inspection & Testing, Beijing 100176, China; 2. School of Criminal Investigation, People’s Public Security University of China, Beijing 100038, China; 3. National Technology Innovation Center for Dairy, Hohhot 010000, China)
  • Published:2026-10-22

摘要: 建立一种基于超高效液相色谱-三重四极杆串联质谱(ultra-high performance liquid chromatography-triple quadrupole tandem mass spectrometry,UPLC-MS/MS)的分析方法,用于乳品中香兰素的准确定量;同时建立气相色谱-燃烧-同位素比值质谱(gas chromatography-combustion-isotope ratio mass spectrometry,GC-C-IRMS)方法,对香兰素进行溯源鉴别。对样品前处理条件及UPLC-MS/MS相关参数进行优化,并完成系统的方法学验证。结果表明,该方法检出限为0.3 μg/kg,定量限为1.0 μg/kg,在不同加标水平下的回收率为97.30%~100.80%,证明该UPLC-MS/MS检测方法具有良好的灵敏度与准确性。基质效应验证表明,前处理过程未引起显著的同位素分馏,GC-C-IRMS方法稳定可靠。将所建立的方法应用于26 份实际乳品样品分析,结果表明UPLC-MS/MS可实现痕量香兰素的准确定量,阳性样品主要分布在调制乳((87.47±0.91)mg/kg)中;GC-C-IRMS溯源结果证实,高含量阳性样品中检出的香兰素均为合成香兰素。UPLC-MS/MS能够实现香兰素的高灵敏度定量检测,但无法区分其来源;而两种技术的优势互补,充分表明了“精准定量”与“同位素溯源”相结合在乳品中香兰素天然与合成属性鉴别领域具有重要的应用意义。本研究实现了乳品香兰素定量与溯源的深度整合,可为科学判定乳品中香兰素的来源归属提供严谨的技术手段。

关键词: 香兰素;乳品;超高效液相色谱-三重四极杆串联质谱;气相色谱-燃烧-同位素比值质谱;来源鉴别

Abstract: An accurate analytical method based on ultra-high performance liquid chromatography-triple quadrupole tandem mass spectrometry (UPLC-MS/MS) was established for the quantification of vanillin in dairy products. Additionally, a gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS) method was developed for the traceability and identification of vanillin. The sample pretreatment conditions and the UPLC-MS/MS parameters were optimized, and the methods were validated systematically. The UPLC-MS/MS method showed a limit of detection (LOD) of 0.3 μg/kg and a limit of quantification (LOQ) of 1.0 μg/kg, with recoveries at different spiked levels ranging from 97.30% to 100.80%, demonstrating excellent sensitivity and accuracy. Matrix effect verification indicated that the pretreatment process did not induce significant isotope fractionation, confirming that the GC-C-IRMS method was stable and reliable. The established methods were applied to the analysis of 26 commercial dairy samples. The UPLC-MS/MS method enabled accurate quantification of trace vanillin, with positive results primarily found in formula milk ((87.47 ± 0.91) mg/kg). Traceability analysis by GC-C-IRMS confirmed that the vanillin detected in the positive samples with high vanillin content was synthetic. While UPLC-MS/MS provided high-sensitivity quantification, it could not distinguish the sources of the analyte. The complementarity of these two techniques highlights the significance of combining “precise quantification” with “stable isotope traceability” in differentiating between natural and synthetic vanillin in dairy products. This study achieves the deep integration of vanillin quantification and traceability, providing a rigorous technical tool for the scientific determination of vanillin sources.

Key words: vanillin; dairy products; ultra-high performance liquid chromatography-triple quadrupole tandem mass spectrometry; gas chromatography-combustion-isotope ratio mass spectrometry; source identification

中图分类号: