食品中合成酸性染料中红血素的光度测定

Y. М. Pliashak, S. M. Leschev, A. I. Palianskikh, L. L. Belysheva
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摘要

在白俄罗斯共和国和欧亚经济联盟国家,合成染料e127(红素)被禁止用于生产食品。为了控制该添加剂的含量,需要准确、快速的测定方法。为了建立食品合成染料(e102、e104、e110、e122、e123、e124、e128、e129、e131、e132、e133、e142、e143、e151、e155)中红素含量的测定方法,研究了有机溶剂对染料的萃取方法,并测定了染料的分布系数。根据在上述染料存在下获得的数据,提出了一种不使用昂贵的色谱设备测定e127的方法。该技术基于样品制备,包括使用氯仿从食品基质(pH=2)的水溶液中选择性提取e127。其他合成染料未提取。然后,将提取液蒸发,溶解于pH=9的缓冲溶液中,在527 nm波长处进行光度测定。在食品基质中存在疏水有机染料(胡萝卜素、番茄红素)的情况下,用氯仿从pH=9的水溶液中初步提取;在此条件下,包括e127在内的所有染料均未被提取。液体食品的定量限为0.05 mg/kg,固体食品的定量限为- 0.13 mg/kg,标准偏差为2 ~ 3%。
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PHOTOMETRIC DETERMINATION OF ERYTHROSIN IN THE PRESENCE OF SYNTHETIC ACIDIC DYES IN FOOD PRODUCTS
In Republic of Belarus and the countries of the EACU, the synthetic dye E 127 (erythrosine) is prohibited for the use in the production of food products. To control the content of this additive, accurate and rapid methods of determination are required. In order to develop a methodology for determination of erythrosin in the presence of food synthetic dyes (E 102, E 104, E 110, E 122, E 123, E 124, E 128, E 129, E 131, E 132, E 133, E 142, E 143 , E 151, E 155) the extraction of dyes with organic solvents from aqueous solutions was studied and their distribution coefficients were determined. Based on the data obtained in the presence of the above dyes, a method for determining E 127 without the use of expensive chromatographic equipment was proposed. The technique is based on sample preparation, which consists of the selective extraction of E 127 from an aqueous solution of the food matrix (pH=2) using chloroform. Other synthetic dyes were not extracted. Next, the extract was evaporated, dissolved in a buffer solution at pH=9 and photometrically measured at the wavelength of 527 nm. In the presence of hydrophobic organic dyes (carotene, lycopene) in the food matrix, their preliminary extraction was carried out from the aqueous solution at pH=9 with chloroform; under these conditions all dyes, including E 127, were not extracted. The limit of quantitative determination by the proposed method for liquid food products was 0.05 mg/kg, for solid – 0.13 mg/kg, the standard deviation was 2–3 %.
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