Anion exchange polymeric sorbent coupled to high-performance liquid chromatography with UV diode array detection for the determination of ten N-nitrosamines in meat products: a validated approach

被引:17
作者
Iammarino, Marco [1 ]
Mangiacotti, Michele [1 ]
Chiaravalle, Antonio E. [1 ]
机构
[1] Ist Zooprofilatt Sperimentale Puglia & Basilicata, Via Manfredonia 20, I-71121 Foggia, Italy
关键词
Anion exchange sorbent; carcinogenic compounds; diode array detection; food safety; high-performance liquid chromatography; meat; nitrosamines; processed meats; solid-phase extraction; validation; PROCESSED MEAT; GAS-CHROMATOGRAPHY; BIOGENIC-AMINES; VOLATILE; NITRITE; EXTRACTION; SAUSAGES; RED;
D O I
10.1111/ijfs.14410
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Among mechanisms and molecules presumably involved in the carcinogenicity induced by meat consumption, the N-nitrosamines (N-NAs) are a class of compounds characteristic of processed meats. In this work, an analytical method for the determination of ten N-nitrosamines (N-nitrosomorpholine, N-nitrosomethylethylamine, N-nitrosopyrrolidine, N-nitrosodiethylamine, N-nitrosopiperidine, N-nitrosodipropylamine, N-nitrosodimethylaniline, N-nitrosodibutylamine, N-nitrosodiphenylamine and N-nitrosodibenzylamine) in fresh meats and meat products was developed, optimised and validated. The method is based on optimised sample purification by solid-phase extraction (anion exchange polymeric sorbent) and separation/detection by high-performance liquid chromatography coupled to UV diode array detection. The validation procedure allowed to ascertaining good analytical performances in terms of sensitivity, selectivity towards interfering compounds, accuracy and robustness. The values obtained for precision (range: 4.3-14.4%) and recovery percentages (range: 80.8-95.1%) were compared to reference values indicated in the Decision No. 657/2002/EC, resulting as compliant. The measurement uncertainty (lower than 14.6%) was satisfactory for each N-NA as well.
引用
收藏
页码:1097 / 1109
页数:13
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