Breast Milk Metabolome Characterization in a Single-Phase Extraction, Multiplatform Analytical Approach

被引:69
|
作者
Villasenor, Alma [1 ]
Garcia-Perez, Isabel [2 ,3 ]
Garcia, Antonia [1 ]
Posma, Joram M. [2 ]
Fernandez-Lopez, Mariano [4 ]
Nicholas, Andreas J. [5 ]
Modi, Neena [5 ]
Holmes, Elaine [2 ]
Barbas, Coral [1 ]
机构
[1] Univ San Pablo CEU, Fac Pharm, Ctr Metabol & Bioanal CEMBIO, Madrid 28668, Spain
[2] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Surg & Canc, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Endocrinol & Metab, Nutr & Dietet Res Grp, London W12 0NN, England
[4] Univ San Pablo CEU, Escuela Politecn Super, Madrid 28668, Spain
[5] Imperial Coll Sch Med, Dept Med, Sect Neonatal Med, London SW10 9NH, England
关键词
FATTY-ACID-COMPOSITION; TERT-BUTYL ETHER; MASS-SPECTROMETRY; TRIACYLGLYCEROL COMPOSITION; GAS-CHROMATOGRAPHY; PLASMA; MOTHERS; TISSUE; NMR; QUANTIFICATION;
D O I
10.1021/ac501853d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Breast milk (BM) is a biofluid that has a fundamental role in early life nutrition and has direct impact on growth, neurodevelopment, and health. Global metabolic profiling is increasingly being utilized to characterize complex metabolic changes in biological samples. However, in order to achieve broad metabolite coverage, it is necessary to employ more than one analytical platform, typically requiring multiple sample preparation protocols. In an effort to improve analytical efficiency and retain comprehensive coverage of the metabolome, a new extraction methodology was developed that successfully retains metabolites from BM in a single-phase using an optimized methyl-tert-butyl ether solvent system. We conducted this single-phase extraction procedure on a representative pool of BM, and characterized the metabolic composition using LC-QTOF-MS and GC-Q-MS for polar and lipidic metabolites. To ensure that the extraction method was reproducible and fit-for-purpose, the analytical procedure was evaluated on both platforms using 18 metabolites selected to cover a range of chromatographic retention times and biochemical classes. Having validated the method, the metabolic signature of BM composition was mapped as a metabolic reaction network highlighting interconnected biological pathways and showing that the LC-MS and GC-MS platforms targeted largely different domains of the network. Subsequently, the same protocol was applied to ascertain compositional differences between BM at week 1 (n = 10) and 4 weeks (n = 9) post-partum. This single-phase approach is more efficient in terms of time, simplicity, cost, and sample volume than the existing two-phase methods and will be suited to high-throughput metabolic profiling studies of BM.
引用
收藏
页码:8245 / 8252
页数:8
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