王杏,周小倩,刘超,黄容,邓樱花.高效液相色谱法同时测定果蔬中6种植物激素的残留[J].食品安全质量检测学报,2018,9(20):5376-5380
高效液相色谱法同时测定果蔬中6种植物激素的残留
Determination of 6 kinds of plant hormones residues in fruits and vegetables by high performance liquid chromatography
投稿时间:2018-08-23  修订日期:2018-09-23
DOI:
中文关键词:  植物激素  高效液相色谱法  残留  果蔬
英文关键词:plant hormones  high performance liquid chromatography  residues  fruits and vegetables
基金项目:湖北省高等学校优秀中青年科技创新团队计划项目(T201718)
作者单位
王杏 湖北第二师范学院化学与生命科学学院 
周小倩 湖北第二师范学院化学与生命科学学院 
刘超 湖北第二师范学院化学与生命科学学院 
黄容 湖北第二师范学院化学与生命科学学院 
邓樱花 湖北第二师范学院化学与生命科学学院 
AuthorInstitution
WANG Xing Department of Chemistry and Life Science,Hubei university of Education 
ZHOU Xiao-Qian Department of Chemistry and Life Science,Hubei university of Education 
LIU Chao Department of Chemistry and Life Science,Hubei university of Education 
HUANG Rong Department of Chemistry and Life Science,Hubei university of Education 
DENG Ying-Hua Department of Chemistry and Life Science,Hubei university of Education 
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中文摘要:
      目的 建立一种可同时测定水果蔬菜中的6种植物激素 (玉米素、吲哚乙酸、6-苄基腺嘌呤、脱落酸、吲哚丁酸和α-萘乙酸) 残留的高效液相色谱方法。方法 将果蔬样品中的植物激素用80%甲醇提取, 对变波长高效液相色谱法的检测条件进行优化, 优化的色谱条件为: Agilent ZORBAX Eclipse Plus C18 (150 mm×4.6 mm, 5 μm)反相色谱柱, 流动相A为甲醇, 流动相B为磷酸-氢氧化钠缓冲溶液(0.1 mol/L, pH=3.0), 流速为1.0 mL/min, 等度洗脱、变波长检测。采用该方法进行精密度和加标回收率实验。结果 对4种果蔬样品进行了精密度和加标实验, 6种植物激素的相对标准偏差(relative standard deviation, RSD)为0.21%~8.90%, 回收率为73.84%~128.40%, 最低检出限为1.4 ng/mL。结论 该方法操作简单、精确可靠、重复性好, 适合测定果蔬中6种植物激素的残留。
英文摘要:
      Objective To establish a method for simultaneous determination of 6 kinds of plant hormones (including zeatin, indole acetic acid , 6-benzyl adenine, abscisic acid, indole butyric acid and α-naphthyl acetic acid) residues in fruits and vegetables by high performance liquid chromatography (HPLC). Methods The plant hormones in fruit and vegetable samples were extracted with 80% methanol solution. The detection conditions of the HPLC method with variable wavelength detector were optimized. The reversed phase column was Agilent ZORBAX Eclipse Plus C18 (150 mm×4.6 mm, 5 μm). The mobile phase consisted of solution A was methanol and solution B was phosphate-sodium hydroxide buffer (0.1 mol/L, pH 3.0) with isocratic elution and variable wavelength detection. The flow rate was 1.0 mL/min. The recoveries of standard addition and the precision were also tested. Results Precision and recoveries experiments were conducted on 4 fruit and vegetable samples. The relative standard deviations (RSDs) of 6 kinds of plant hormones were 0.21%-8.90%, and the average recoveries 73.84%~128.40%. The limits of detection for the 6 kinds of plant hormones were 1.4 ng/mL. Conclusion This method is easy, accurate, reliable and reproducible, which is suitable for detecting the plant hormones residues in fruits and vegetables samples.
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