食品科学 ›› 2025, Vol. 46 ›› Issue (23): 311-320.doi: 10.7506/spkx1002-6630-20250630-211

• 安全检测 • 上一篇    

液相色谱及离子色谱法测定婴幼儿配方食品中母乳低聚糖的对比分析

刘爽,陈刚,张影,董立雅,陈家伦,姚斐,张旭光,田芳   

  1. (1.内蒙古蒙牛乳业(集团)股份有限公司,内蒙古 呼和浩特 011500;2.虹摹生物科技(上海)有限公司,北京 102209)
  • 发布日期:2025-12-26

Comparative Study of Liquid Chromatography and Ion Chromatography for the Determination of Human Milk Oligosaccharides in Infant Formula

LIU Shuang, CHEN Gang, ZHANG Ying, DONG Liya, CHEN Jialun, YAO Fei, ZHANG Xuguang, TIAN Fang   

  1. (1. Inner Mongolia Mengniu Dairy (Group) Co. Ltd., Hohhot 011500, China;2. Synaura Biotechnology (Shanghai) Co. Ltd., Beijing 102209, China)
  • Published:2025-12-26

摘要: 通过在液相色谱法中引入双内标定量策略,在离子色谱法中优化梯度洗脱程序以及特异性酶解体系测定婴幼儿配方食品中7 种母乳低聚糖(human milk oligosaccharides,HMOs),并系统对比两种方法的技术性能和实用性。在技术性能方面,两种方法均表现出良好的特异性,7 种HMOs在较宽质量浓度范围内呈现良好的线性关系(R2>0.999)。液相色谱法中,7 种HMOs在固态样品中的定量限为1.8~3.6 mg/100 g,液态样品为0.2~0.4 mg/100 g,定量限加标的回收率为81.1%~118.8%;测定范围加标的加标回收率为91.3%~108.0%,相对标准偏差为1.8%~2.8%。离子色谱法中,7 种HMOs在固态样品中的定量限为18~36 mg/100 g,液态样品为2~4 mg/100 g,定量限加标的回收率为80.7%~118.5%;测定范围加标的加标回收率为90.9%~109.4%,相对标准偏差为1.7%~3.7%。验证结果表明两种方法均适用于婴幼儿配方食品中7 种HMOs的测定。本研究进一步分析了两种方法的应用场景,液相色谱法因其定量限较低更适用于检测乳粉中HMOs本底含量,而离子色谱法因其预处理方法较简便更适用于羊乳基配方食品中HMOs的测定。在实用性方面,离子色谱法在操作便捷性及分析时效性方面更具优势。本研究填补了液相色谱和离子色谱法在HMOs检测中系统对比的研究空白,为不同应用场景下的方法选择提供了实验依据,为实际食品安全工作中相关标准制定提供了重要参考。

关键词: 母乳低聚糖;液相色谱法;离子色谱法;婴幼儿配方食品;对比分析

Abstract: In this study, a comprehensive comparison of the technical performance and practical applicability of liquid chromatography (LC) and ion chromatography (IC) was conducted in the determination of seven human milk oligosaccharides (HMOs) in infant formula. We introduced a dual-internal standard quantification strategy into LC. In IC, we optimized the gradient elution program and established a specific enzymatic hydrolysis system. Both methods demonstrated good specificity, and all seven HMOs showed excellent linearity (R2 > 0.999) over a wide concentration range. The limit of quantification (LOQ) of LC ranged from 1.8 to 3.6 mg/100 g for solid samples and from 0.2 to 0.4 mg/100 g for liquid samples. The spiked recoveries at the LOQ level were between 81.1% and 118.8%, and those within the determination range were 91.3%−108.0%, with relative standard deviations (RSDs) of 1.8%−2.8%. The LOQs of IC ranged from 18 to 36 mg/100 g for solid samples and from 2 to 4 mg/100 g for liquid samples. The spiked recoveries at the LOQ level were 80.7%−118.5%, and those within the determination range were 90.9%−109.4%, with RSDs of 1.7%−3.7%. The validation results confirmed that both methods were suitable for the determination of the seven HMOs in infant formula. This study further clarified the applicable scenario of each method. Due to its lower LOQ, LC was more suitable for detecting endogenous HMOs in milk powder, whereas IC, with simpler pretreatment, was more applicable for the determination of goat milk-based formula. In terms of practicality, IC offered advantages in ease of operation and analytical timeliness. This research fills a gap in the systematic comparison between LC and IC for HMO detection, provides experimental support for method selection in different application contexts, and offers a valuable reference for the establishment of relevant food safety standards.

Key words: human milk oligosaccharides; liquid chromatography; ion chromatography; infant formula; comparative study

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