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超声提取-高效液相色谱法测定食品中碱性橙Ⅱ染料 被引量:16

DETERMINATION OF BASIC ORANGE Ⅱ IN FOODS BY ULTRASONIC EXTRACTION AND HIGH PERFORMANCE LIQUID CHROMATOGRAPHY
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摘要 建立超声提取-高效液相色谱法测定食品中碱性橙Ⅱ染料的方法。样品均质后,正已烷超声除去杂质,再用无水乙醇多次超声至无色,合并提取液浓缩离心,取上清液进行色谱分析。高效液相色谱仪采用C18柱,检测波长为449nm。方法最低检出限为0.10mg/L,回收率超过98.5%,同一色谱条件下日落黄对碱性橙Ⅱ检出无影响。方法精密度分别为5.8%,6.2%及1.1%。 A method for determination of Basic Orange Ⅱ by ultrasonic extraction and High Performance Liquid Chromatography (HPLC) in foods was developed. Samples were homogenized and transacted by ultrasonic with hexane. Then the impurity layers were removed. Basic Orange Ⅱ was extraced using ultrasonic in the remains with ethanol time after time until the extraction became achromatous. The extraction was amalgamated and concentrated by centrifuge, and supernatant was analysed by chromatogram. Analytical separation was performed on C18 column with photodiode-array detection at 449 nm where maximal absorption peak could be obtained. The detection limit was 0.10 mg/L and the recoveries were all above 98.5 %. There was no effect for sunset yellow on determination of Basic Orange Ⅱ. The RSD were 6.2 %, 5.8 % and 1.1%.
出处 《食品研究与开发》 CAS 北大核心 2009年第7期153-155,共3页 Food Research and Development
关键词 食品 碱性橙Ⅱ 超声提取 高效液相色谱 foods basic orange Ⅱ ultrasonic extraction High Performance Liquid Chromatography(HPLC)
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参考文献4

  • 1International Agency for Research on Cancer, World Health Organization. IARC Monographs on the Ealuation of Carcinogenic Risk of Chemicals to Man[J]. Geneva, 1971-1982, 8:91-96.
  • 2NTP Chemical Repository C.I. Basic Orange[M]. National Toxicology Program, 1992.
  • 3铁晓威,黄百芬,任一平.RP-HPLC法测定染色黄鱼中的碱性橙含量[J].中国卫生检验杂志,2004,14(1):59-60. 被引量:39
  • 4任一平,黄百芬,铁晓威,等.LC—MS/MS测定染色海洋杂鱼中的碱性橙的含量[C].第十五次全国色谱学术报告会(下册)[C].郑州.2005.

二级参考文献2

  • 1International Agency for Research on Cancer, World Health Organization. I ARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. International Agency for Research on Cancer. Geneva, 1971 - 1982,8:91~96.
  • 2NTP CHEMICAL REPOSITORY C.I. BASIC ORANGE 2.

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