Pinte Jérémy, Joly Catherine, Plé Karen, Dole Patrice, Feigenbaum Alexandre
UMR FARE (INRA-URCA), Moulin de la Housse, BP 1039, 51867 Reims Cedex, France.
J Agric Food Chem. 2008 Nov 12;56(21):10003-11. doi: 10.1021/jf802166e. Epub 2008 Oct 18.
The migration of additives from food packaging to food stuffs is kinetically governed by the diffusion coefficient (D) of the additive within the polymer. Food safety authorities have recently allowed the use of mathematical models to predict D, with the additive molecular weight as a single entry parameter. Such models require experimental values to feed the databases, but these values are often scattered. To deal with this issue, a fluorescent chemically homologous series of model additives was synthesized with molecular weights (MW) ranging from 236 g.mol (-1) to 1120 g.mol (-1). This set was then used to collect diffusion coefficients D through confocal fluorescence recovery after photobleaching (FRAP). This microscopic technique allows in situ packaging micro migration tests. The FRAP method was tested against results from the literature before being applied to two different model polystyrenes in a preliminary study to investigate the relationship D = f(MW). Our intermediate objective was to compare various experimental D = f(MW) from our method with predictions from other mathematical or semiempirical models.
食品包装中添加剂向食品的迁移在动力学上受添加剂在聚合物中的扩散系数(D)控制。食品安全当局最近允许使用数学模型来预测D,将添加剂分子量作为唯一输入参数。此类模型需要实验值来填充数据库,但这些值往往分散。为解决此问题,合成了一系列荧光化学同源的模型添加剂,其分子量(MW)范围为236 g·mol⁻¹至1120 g·mol⁻¹。然后使用该系列通过光漂白后共聚焦荧光恢复(FRAP)来收集扩散系数D。这种微观技术可进行原位包装微迁移测试。在将FRAP方法应用于两种不同的模型聚苯乙烯以研究D = f(MW)关系的初步研究之前,先根据文献结果对该方法进行了测试。我们的中间目标是将我们方法得到的各种实验D = f(MW)与其他数学或半经验模型的预测结果进行比较。