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P-31 NMR Quantification of Phospholipids and Lysophospholipids in Food Emulsions

机译:P-31 NMR定量磷脂和食品乳液中的溶血磷脂

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摘要

For food emulsions containing enzymatically modified egg yolk, the conventional Folch extraction does not fully recover the polar lysophospholipids. This can be overcome by repeated methanol extractions. After solvent evaporation, the extracted (lyso)phospholipids are solubilized into mixed micelles with cholate as a detergent. The solubilized (lyso)phospholipids can be accurately quantified by P-31 NMR with recoveries ranging between 96% and 108%. Detection at a high (16.4 T) relative to a mainstream (9.4 T) magnetic field strength did not offer a significant advantage since the slow molecular tumbling of the mixed micelles increased line widths. This was due to field-strength-dependent chemical shift anisotropy relaxation. Method precision is similar at 9.4 and 16.4 T, with within-laboratory reproducibilities of 7-22% and 12-25%, respectively. The method can be implemented as a routine analytical procedure at 9.4 T (400 MHz NMR spectrometer), and the limits of detection and quantification are adequate for the verification of the standard of identity of a mayonnaise prepared with enzymatically modified egg yolk.
机译:对于含有酶改性蛋黄的食物乳液,常规叶片提取不完全回收极性溶血磷脂。这可以通过重复的甲醇提取来克服。在溶剂蒸发后,将萃取的(LySO)磷脂溶解成用胆晶作为洗涤剂的混合胶束。溶解(LySO)磷脂可以通过P-31 NMR精确定量,回收率在96%和108%之间。相对于主流(9.4T)的高(16.4T)检测磁场强度没有提供显着的优势,因为混合胶束的慢分子滚动增加了线宽。这是由于场强依赖的化学变化各向异性弛豫。方法精度在9.4和16.4吨中相似,实验室内的实验室再现,分别为7-22%和12-25%。该方法可以作为9.4T(400MHz NMR光谱仪)的常规分析过程来实现,并且检测和定量的极限是足以验证用酶促改性蛋黄制备的蛋黄酱的标准。

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