Windemann H, Meier P, Baumgartner E
Z Lebensm Unters Forsch. 1986 Jul;183(1):26-32. doi: 10.1007/BF01027590.
To recognize and determine the wheat gliadins in unheated gluten-free food for coeliac patients the immunological methods such as ELISA can be used. In heated food (above 80 degrees-90 degrees C) these methods fail wholly or in part to achieve the quantitative determination of wheat gliadin. The changes in protein patterns after heat treatment are also revealed by the RP-HPLC of wheat gliadins and some peaks appear, which are characteristic for heat treated wheat flour. Using these peaks, about 2% admixture of wheat flour (T. aestivum, T. durum) as well as of rye flour can be detected. In foods which contain more than 50% skim milk the addition of only at least 5% of these flours can be detected. The ethanolic extracts of foods were concentrated by freeze-drying prior to analysis by HPLC. The ethanol-soluble non-dialysable food components affect the quantitative determination of wheat or rye proteins by means of peak areas. Selective enrichment is a possibility. The RP-HPLC-analysis of ethanol-soluble proteins makes it possible to detect heated flours of wheat and rye (cooked, roller-dried, extrusion-cooked) in glutenfree food.
为了识别和测定未加热的无麸质食品中对乳糜泻患者有害的小麦醇溶蛋白,可以使用酶联免疫吸附测定法(ELISA)等免疫学方法。对于加热食品(80摄氏度至90摄氏度以上),这些方法完全或部分无法实现对小麦醇溶蛋白的定量测定。小麦醇溶蛋白的反相高效液相色谱法(RP-HPLC)也揭示了热处理后蛋白质图谱的变化,并出现了一些峰,这些峰是热处理小麦粉的特征峰。利用这些峰,可以检测出约2%的小麦粉(普通小麦、硬粒小麦)以及黑麦粉的掺假情况。在含有超过50%脱脂牛奶的食品中,仅添加至少5%的这些面粉就可以被检测出来。食品的乙醇提取物在通过HPLC分析之前通过冷冻干燥进行浓缩。乙醇可溶且不可透析的食品成分会通过峰面积影响小麦或黑麦蛋白的定量测定。选择性富集是一种可行的方法。对乙醇可溶蛋白进行RP-HPLC分析,可以检测无麸质食品中小麦和黑麦的加热面粉(煮熟、滚筒干燥、挤压熟化)。