Office of Regulatory Science, Center for Food Safety and Applied Nutrition (CFSAN), United States Food and Drug Administration (FDA) , 5001 Campus Drive, College Park, Maryland 20740, United States.
Research and Development, Abbott Nutrition Division, Abbott Laboratories , 3300 Stelzer Road, Columbus, Ohio 43219, United States.
J Agric Food Chem. 2017 Jul 19;65(28):5799-5809. doi: 10.1021/acs.jafc.7b02083. Epub 2017 Jul 6.
The United States Pharmacopeial Convention has led an international collaborative project to develop a toolbox of screening methods and reference standards for the detection of milk powder adulteration. During the development of adulterated milk powder reference standards, blending methods used to combine melamine and milk had unanticipated strong effects on the near-infrared (NIR) spectrum of melamine. The prominent absorbance band at 1468 nm of melamine was retained when it was dry-blended with skim milk powder but disappeared in wet-blended mixtures, where spray-dried milk powder samples were prepared from solution. Analyses using polarized light microscopy, Raman spectroscopy, dielectric relaxation spectroscopy, X-ray diffraction, and mass spectrometry indicated that wet blending promoted reversible and early Maillard reactions with lactose that are responsible for differences in melamine NIR spectra between wet- and dry-blended samples. Targeted detection estimates based solely on dry-blended reference standards are likely to overestimate NIR detection capabilities in wet-blended samples as a result of previously overlooked matrix effects arising from changes in melamine hydrogen-bonding status, covalent complexation with lactose, and the lower but more homogeneous melamine local concentration distribution produced in wet-blended samples. Techniques used to incorporate potential adulterants can determine the suitability of milk reference standards for use with rapid detection methods.
美国药典协会领导了一个国际合作项目,开发了一套用于检测奶粉掺假的筛选方法和参考标准工具包。在掺假奶粉参考标准的开发过程中,用于混合三聚氰胺和牛奶的方法对三聚氰胺的近红外(NIR)光谱产生了意想不到的强烈影响。当三聚氰胺与脱脂奶粉干式混合时,其在 1468nm 处的明显吸收带得以保留,但在湿式混合混合物中消失,其中喷雾干燥的奶粉样品是从溶液中制备的。偏振光显微镜、拉曼光谱、介电弛豫光谱、X 射线衍射和质谱分析表明,湿混促进了与乳糖的可逆和早期美拉德反应,这是导致湿混和干混样品中三聚氰胺近红外光谱差异的原因。仅基于干式混合参考标准进行的靶向检测估计可能会高估湿式混合样品中的 NIR 检测能力,因为之前忽略了由于三聚氰胺氢键状态变化、与乳糖的共价络合以及湿式混合样品中产生的较低但更均匀的三聚氰胺局部浓度分布而产生的基质效应。用于掺入潜在掺杂物的技术可以确定牛奶参考标准是否适合与快速检测方法一起使用。