XIA Ri-yao, Liang Qi, DU Lian-duo, ZHANG Jian-jun, LUO Qiu-shui, DU Juan, XIONG Jian-hua. Simultaneous Determination of Nine N-nitrosamine in Pickling Dried Fish by GC-FID[J]. Science and Technology of Food Industry, 2020, 41(10): 213-218,223. DOI: 10.13386/j.issn1002-0306.2020.10.035
Citation: XIA Ri-yao, Liang Qi, DU Lian-duo, ZHANG Jian-jun, LUO Qiu-shui, DU Juan, XIONG Jian-hua. Simultaneous Determination of Nine N-nitrosamine in Pickling Dried Fish by GC-FID[J]. Science and Technology of Food Industry, 2020, 41(10): 213-218,223. DOI: 10.13386/j.issn1002-0306.2020.10.035

Simultaneous Determination of Nine N-nitrosamine in Pickling Dried Fish by GC-FID

  • A method for the simultaneous determination of nine N-nitrosamine in pickling dried fish was developed by gas chromatography-hydrogen flame detector(GC-FID)with by lye heating treatment combined with dichloromethane extraction. The filtrate was purified by coconut shell activated carbon,and concentrated by C18 SPE columns;the chromatographic separation were carried with a DB-WAXETR polar column(30 m×0.25 mm,0.25 μm). The column temperature was programmed to rise. Results showed that:The Nine nitrosamines had good linearity in the range of 0.05~5 μg/mL(R2>0. 999);The detection limits and quantitation limits were ranged from 0.05 to 0.29 μg/mL and 0.18 to 0.95 μg/mL. The recoveries and RSD were 76.8%~129.5% and 2.29%~15.5%. The actual sample detection result in 50 kinds of pickled dried fish showed that the detection rates of NDEA,NDIP and NPYR were 20%,20% and 24%. Only one sample exceeded the national standard limit(NDMA<4 μg/kg).
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