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采用超高效液相色谱/电喷雾串联质谱法测定婴儿配方食品和乳清蛋白浓缩物中的二唾液酸神经节苷脂 GD3 和单唾液酸神经节苷脂 GM3。

Determination of disialoganglioside GD3 and monosialoganglioside GM3 in infant formulas and whey protein concentrates by ultra-performance liquid chromatography/electrospray ionization tandem mass spectrometry.

机构信息

Department of Food Science and Nutrition, College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou, Zhejiang, P R China.

出版信息

J Sep Sci. 2012 Apr;35(8):937-46. doi: 10.1002/jssc.201101039.

Abstract

A method of ultra-performance liquid chromatography combined with electrospray ionization triple quadrupole tandem mass spectrometry (UPLC-ESI-MS/MS) has been established for simultaneous determination of major disialoganglioside 3 (GD3) and monosialoganglioside 3 (GM3) in infant formulas and whey protein concentrates. Gangliosides were extracted by using the technique of Svennerholm and Fredman and then cleaned up with OASIS HLB solid-phase extraction (SPE) cartridges. The various molecular species of gangliosides were separated on an Acquity UPLC BEH C8 column and analyzed under the negative ion mode. GD3 and GM3 were rapidly quantified using internal standard (IS) method. The developed method was further validated by determining the linearity, average recovery, sensitivity (limit of quantification), and precision. The results presented high correlation coefficients (R(2) > 0.993) of the selected 16 gangliosides molecular species and provided the respective linear ranges. The limit of quantification was 0.325-0.734 mg/100 g for eight molecular species of GD3 and 0.008-0.312 mg/100 g for eight molecular species of GM3, respectively. The reasonable average recoveries (81-95%) and precision (relative standard deviation [RSD] ≤15%) were also demonstrated in three different spiked levels. This new method would be very useful in the quantitative determination of gangliosides in infant formulas and whey protein concentrates.

摘要

建立了一种超高效液相色谱-电喷雾电离三重四极杆串联质谱法(UPLC-ESI-MS/MS),用于同时测定婴儿配方食品和乳清蛋白浓缩物中主要二唾液酸神经节苷脂 3(GD3)和单唾液酸神经节苷脂 3(GM3)。采用 Svennerholm 和 Fredman 的技术提取神经节苷脂,然后用 Oasis HLB 固相萃取(SPE)小柱进行净化。各种神经节苷脂分子在 Acquity UPLC BEH C8 柱上分离,并在负离子模式下分析。使用内标(IS)法快速定量 GD3 和 GM3。通过测定线性、平均回收率、灵敏度(定量限)和精密度,对所建立的方法进行了进一步验证。结果表明,所选 16 种神经节苷脂分子的相关系数(R²>0.993)均较高,并提供了各自的线性范围。八种 GD3 分子的定量限为 0.325-0.734mg/100g,八种 GM3 分子的定量限为 0.008-0.312mg/100g。在三个不同的加标水平下,还证明了合理的平均回收率(81-95%)和精密度(相对标准偏差[RSD]≤15%)。该新方法将非常有助于婴儿配方食品和乳清蛋白浓缩物中神经节苷脂的定量测定。

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