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郑耀林,等:顶空气相色谱-串联质谱法测定水产品中三甲胺的含量


                   trimethylamine  and  trimethylamine-n-oxide  in  fish   中三甲胺的含量[J]. 理化检验-化学分册,2023,59(4):
                   extracts  by  capillary  electrophoresis  with  indirect  UV-  394-399.
                   detection[J]. Food Chemistry,2002,76(4):509-518.   [23]  国家市场监督管理总局,中国国家标准化管理委
               [19]  KONOP  M,RYBKA  M,WARAKSA  E,et  al.            员会. 食品安全国家标准  食品中三甲胺的测定:
                   Electrophoretic  determination  of  trimethylamine  GB 5009. 179—2016[S]. 北京:中国标准出版社,2017.
                  (TMA) in  biological  samples  as  a  novel  potential    [24]  潘晓玉, 王宗义,赵逸涵,等. 冷冻脱脂-分散固相萃取/

                   biomarker  of  cardiovascular  diseases  methodological   气相色谱-串联质谱法检测食物植物油中4种多环芳
                   approach[J]. International  Journal  of  Environmental   烃[J]. 分析试验室,2022,41(4):419-423.
                   Research and Public Health,2021,18(23):12318.   [25]  ÖZOGUL F,POLAT A,ÖZOGUL Y. The effects of
               [20]  国家质检总局,中国国家标准化管理委员会. 火腿中三                       modified  atmosphere  packaging  and  vacuum  packaging
                   甲胺氮的测定:GB/T 5009. 179—2003[S]. 北京:中国              on  chemical,sensory  and  microbiological  changes  of
                   标准出版社,2011.                                       sardines (Sardina pilchardus) [J]. Food  Chemistry,

               [21]  陈锦文,崔燕芒,赵燕. 三甲胺、二甲胺及氧化三甲胺                       2004,85(1):49-57.
                   含量测定方法的研究进展[J]. 西北药学杂志,2015,                  [26]  马成林,陈琦昌,李力权,等. 应用三甲胺评价鱼类新
                   30(2):216-219.                                    鲜度与TVBN/TMA比值的研究[J]. 食品科学,1993,
               [22]  胡丽雅. 苏码罐采样-气相色谱-质谱法测定环境空气                       14(11):16-19.


                   Determination of Trimethylamine in Aquatic Products by Headspace-Gas
                                   Chromatography-Tandem Mass Spectrometry



                      ZHENG Yaolin , LU Guiting , LIN Qiufeng , MO Shumei , YANG Le , ZHANG Shuquan   1
                                                             1
                                                1,2
                                    1
                                                                          1
                                                                                    1
                                  (1. Dongguan Institute for Food and Drug Control, Dongguan 523808, China;
                         2. College of Food Science and Technology, Guangdong Ocean University, Zhanjiang 524088, China)
                  Abstract:  The  10  g  of  aquatic  product  sample  was  taken,  and  20  mL  of  5%  (volume  fraction,  the  same  below)
              trichloroacetic acid solution was added. The mixture was homogenized for 1 min, and centrifuged for 5 min. The supernatant was
              passed through the defatted cotton, and the filtrate was collected. The residue was extracted with 15, 10 mL of 5% trichloroacetic
              acid solution, respectively. All the filtrate was combined, and diluted to 50 mL with 5% trichloroacetic acid solution. An aliquot
              (2. 0 mL) was placed into a 20 mL-headspace vial, which was sealed with a cap. Then 5 mL of 10% (mass fraction) sodium
              hydroxide solution was injected from the edge of the cap with a syringe. After equilibrating at 45  ℃ for 40 min, the resulting
              gas was introduced into a gas chromatograph-tandem mass spectrometer. Trimethylamine was separated on HP-INNOWAX
              capillary column under programmed temperature conditions, ionized with an electron bombardment ion source, and scanned in
              multiple reaction monitoring mode. The characteristic ion pairs at mass to charge ratio (m/z) of 58/42 was used for quantitative
              analysis by the external standard method, and m/z 59/43 and m/z 58/30 were used for qualitative analysis. It was shown that
              linear relationship between the peak area of quantitative ion pair and mass concentration of trimethylamine was kept in the range of
                          −1                                 −1                                           −1
              0. 2-50 mg · L  , with detection limit (3S/N) of 0. 3 mg · kg  .  The recovery at the addition level of 5, 25, 100 mg · kg  was
              found in the range of 88. 3%-94. 0%, with RSDs (n=6) of the determined values in the range of 1. 1%-3. 7%. The proposed
              method was used for the analysis of fish meat samples, and trimethylamine was not detected. The above sample was stored at
                                                                               −1
              −18, 4 ℃ for 7 d, giving the detection amounts of trimethylamine of 0. 4, 195 mg · kg  , which might be related to the microbial
              decomposition of fish meat into trimethylamine during storage.
                  Keywords: trimethylamine; headspace-gas chromatography- tandem mass spectrometry; aquatic product












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