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  • 标题:Determination of Vitamin C in Commercial non-Alcoholic Beverages
  • 本地全文:下载
  • 作者:Akihiko NAKAMA ; Koichi Yamada
  • 期刊名称:生活衛生
  • 印刷版ISSN:0582-4176
  • 电子版ISSN:1883-6631
  • 出版年度:1997
  • 卷号:41
  • 期号:5
  • 页码:183-188
  • DOI:10.11468/seikatsueisei1957.41.183
  • 出版社:Osaka Urban Living and Health Association
  • 摘要:We determined the amount of ascorbic acid (AsA) in 31 commercial non-alcoholic beverages sold in Osaka City, Japan. AsA was analyzed by high performance liquid chromatography (HPLC) using a LiCrosorb 100 NH2 column and 3mM ammonium phosphate/acetonitrile (30:70) as mobile phase. Concentrated-restored fruit juices contained 210-470μg/ml AsA, more than natural fruit juices (110-140μg/ml). The content of AsA in tea drinks was similar to that in concentrated-restored fruit juices at 290-360μg/ml. Furthermore, beverages prepared from natural materials such as orange juices or green tea showed differing AsA content between different product lots. To estimate the difference between AsA analytical methods, we used 5 AsA analytical methods, HPLC, the indophenol titrimetric method, the dinitrophenylhydrazine method, the fluorometric method, and the enzymic method. In green tea, the enzymic method showed the minimum reading, which was 80% of that found using the indophenol titrimetric method, which showed the maximum. The AsA content of concentrated-restored fruit juices varied widely according to method. The dinitrophenylhydrazine and enzymic methods showed significant difference from other methods; in particular, the enzymic method showed 1.8-2.9 -fold higher AsA content than HPLC. The AsA content of natural fruit juices showed no appreciable difference between methods. These findings suggest that the enzymic method cannot determine accurately the AsA content of concentrated-restored fruit juices. Whether a fruit juice is concentrated-restored or natural can probably be distinguished by the difference in AsA content using the enzymic and HPLC methods.
  • 关键词:Vitamin C;Ascorbic acid;non-Alcoholic beverages;HPLC;Enzymic analysis
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