Yang Yue, Zhou Biao, Zheng Chenyang
International Healthcare Center, First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310003, China.
Institute of Nutrition and Food Safety, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China.
Molecules. 2024 Apr 15;29(8):1795. doi: 10.3390/molecules29081795.
This study presents a new technique for determining vitamin B12 in milk powder using high-performance liquid chromatography-inductively coupled plasma mass spectrometry (HPLC-ICP-MS). We used ultrasonics with potassium ferrocyanide and zinc acetate solutions to extract the samples. Co was employed as the analytical target for cyanocobalamin. It was separated using a Phenomenex Luna 5 μm C18 (250 × 4.6 mm) chromatographic column with a mobile phase consisting of 1.6 mmol/L EDTA and 0.4 mmol/L KHPO in a 60% / methanol solution (pH = 4.0). The sample has an excellent separating degree for free cobalt and cyanocobalamin, and isocratic elution can be finished within 4.0 min. To eliminate the matrix interference due to the presence of milk powder, we applied collision mode (KED). The linear range of cyanocobalamine ranged from 1.0 μg/L to 20 μg/L, with correlation coefficients (r) of 0.9994. The limit of detection (LOD) was 0.63 μg/kg, and the limit of quantitation (LOQ) was 2.11 μg/kg. The mean recoveries were in the range of 87.4-103.6%. The accuracy and precision of the developed method are well suited for the fast quantification of the trace vitamin B12 in milk powder.
本研究提出了一种使用高效液相色谱 - 电感耦合等离子体质谱法(HPLC - ICP - MS)测定奶粉中维生素B12的新技术。我们使用超声波结合亚铁氰化钾和醋酸锌溶液来提取样品。采用钴作为钴胺素的分析目标物。使用Phenomenex Luna 5μm C18(250×4.6mm)色谱柱进行分离,流动相由1.6mmol/L乙二胺四乙酸(EDTA)和0.4mmol/L磷酸二氢钾(KHPO)的60%甲醇溶液(pH = 4.0)组成。该样品对游离钴和钴胺素具有出色的分离度,等度洗脱可在4.0分钟内完成。为消除奶粉存在所导致的基质干扰,我们采用了碰撞模式(KED)。钴胺素的线性范围为1.0μg/L至20μg/L,相关系数(r)为0.9994。检测限(LOD)为0.63μg/kg,定量限(LOQ)为2.11μg/kg。平均回收率在87.4 - 103.6%范围内。所建立方法的准确度和精密度非常适合奶粉中痕量维生素B12的快速定量分析。