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[高效液相色谱法同时测定食品中的7种防腐剂和糖精,并采用液相色谱-串联质谱法进行鉴定]

[Simultaneous determination of 7 kinds of preservatives and saccharin in foods with HPLC, and identification with LC/MS/MS].

作者信息

Ujiie Aiko, Hasebe Hiroshi, Chiba Yoshiko, Yanagita Noriaki

机构信息

Miyagi Prefectual Institute of Public Health and Environment, 4-7-2 Saiwai-cho, Miyagino-ku, Sendai 983-8666, Japan.

出版信息

Shokuhin Eiseigaku Zasshi. 2007 Dec;48(6):163-9. doi: 10.3358/shokueishi.48.163.

Abstract

A simultaneous determination method of saccharin (SA), sorbic acid (SOA), benzoic acid (BA), p-hydroxybenzoic acid ethyl (PHBA-Et), p-hydroxybenzoic acid isopropyl (PHBA-isoPr), p-hydroxybenzoic acid propyl (PHBA-Pr), p-hydroxybenzoic acid isobutyl (PHBA-isoBu) and p-hydroxybenzoic acid butyl (PHBA-Bu) in foods by HPLC was examined. A mixture of acetonitrile-water (1:1) was used to extract these additives from foods excluding liquid foods, while acetonitrile was used to extract them from liquid foods. HPLC was performed using a TSKgel ODS80Ts (4.6 mm i.d. x 150 mm) column with a mobile phase of 0.01% formic acid solution containing 2 mmol/L-di-n-butyl (or amyl) ammonium acetate (A) and acetonitrile (B) under the following conditions: A/B = 8: 2 (0-8 min) --> 6: 4 (15-32 min). Recoveries of these additives spiked in foods were 78-120%. The determination limits were 10 microg/g. As the identification method, examination by liquid chromatography with electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS) was used. Unknown compounds were identified by detection of product ions from their precursor ions in the negative mode with multiple reaction monitoring, m/z 182 > 106 for SA, m/z 121 > 77 for BA, m/z 111 > 67 for SOA and m/z 165 > 92 for PHBA-Et. Ratios of intensity of m/z 179 > 137 to m/z 179 > 92 were used for identification of isomers PHBA-isoPr and PHBA-Pr, and the ratios of intensity of m/z 193 > 137 to m/z 193 > 92 were used for isomers PHBA-isoBu and PHBA-Bu, because these isomers have very similar (Received December 12, 2006)

摘要

考察了一种采用高效液相色谱法同时测定食品中糖精(SA)、山梨酸(SOA)、苯甲酸(BA)、对羟基苯甲酸乙酯(PHBA-Et)、对羟基苯甲酸异丙酯(PHBA-isoPr)、对羟基苯甲酸丙酯(PHBA-Pr)、对羟基苯甲酸异丁酯(PHBA-isoBu)和对羟基苯甲酸丁酯(PHBA-Bu)的方法。对于非液态食品,使用乙腈-水(1:1)混合溶液从食品中提取这些添加剂;对于液态食品,则使用乙腈进行提取。高效液相色谱分析采用TSKgel ODS80Ts(内径4.6 mm×150 mm)色谱柱,流动相为含2 mmol/L - 二正丁基(或戊基)乙酸铵(A)和乙腈(B)的0.01%甲酸溶液,条件如下:A/B = 8:2(0 - 8分钟)→6:4(15 - 32分钟)。这些添加剂在食品中的加标回收率为78% - 120%。测定限为10 μg/g。作为鉴定方法,采用电喷雾电离串联质谱液相色谱法(LC/ESI-MS/MS)进行检测。通过在负离子模式下采用多反应监测检测前体离子的产物离子来鉴定未知化合物,SA的m/z 182 > 106,BA的m/z 121 > 77,SOA的m/z 111 > 67,PHBA-Et的m/z 165 > 92。m/z 179 > 137与m/z 179 > 92的强度比用于鉴定异构体PHBA-isoPr和PHBA-Pr,m/z 193 > 137与m/z 193 > 92的强度比用于鉴定异构体PHBA-isoBu和PHBA-Bu,因为这些异构体非常相似(2006年12月12日收到)

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