Research Article
A Novel Methodology for the Quantification of B-Vitamers in Breast Milk
Karine Meisser Redeuil*, Sylvie B脙茠脗漏net, Michael Affolter, Sagar Thakkar K and Esther Campos-Gim脙茠脗漏nezNestl脙茠脗漏 Research Center, Nestec Ltd., Lausanne, Switzerland
- *Corresponding Author:
- Karine Meisser Redeuil
Nestl脙茠脗漏 Research Center
Verschez-les-Blanc, PO Box 44
1000 Lausanne 26, Switzerland
Tel: +41217859229
Fax: +41217859486
E-mail: Karine.Meisser@rdls.nestle.com
Received date: February 24, 2017; Accepted date: February 27, 2017; Published date: March 02,2017
Citation: Redeuil KM, B脙茠脗漏net S, Affolter M, Thakkar SK, Campos-Gim脙茠脗漏nez E (2017) A Novel Methodology for the Quantification of B-Vitamers in Breast Milk. J Anal Bioanal Tech 8:352. doi: 10.4172/2155-9872.1000352
Copyright: © 2017 Redeuil KM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
With this report we present development, validation and application of an analytical methodology for the quantification of 18 water soluble vitamers and secreted or biological forms in breast milk. On a relatively low amount of breast milk (200 µL), we applied isotope dilution-based sample preparation based on a combination of enzymatic treatment and protein precipitation using acidic methanol enriched with stable isotope labelled internal standards. Compounds separation was achieved by reversed-phase liquid chromatography and detection performed by tandem mass spectrometry in positive electrospray ionization mode. To perform the quantification of 18 water soluble vitamers, procured pooled breast milk was used to build matrixmatched calibration curves, as labelled internal standards were not available for each vitamer. The analytical approach has been validated according to the EMA guidelines. The overall performance of the method was considered adequate, with 0.3- 28.3% and 0.9-32.6% intra and inter-day precision respectively and averaged accuracy reaching 92.2-107.5%. In addition, performed freeze/thaw stability studies showed the potential degradation of some vitamers. We therefore recommend particular attention in sample collection with rather having dedicated aliquots with small volumes. The feasibility of this analytical approach has been evaluated by quantifying various breast milk samples that were procured from an external supplier. The main forms found in breast milk were thiamine monophosphate for B1, flavin adenine nucleotide for B2, nicotinamide for B3, pyridoxal for B6 and 5-methyl tetrahydrofolic acid for B9. In addition, we newly reported nudifloramide as B3 form present in breast milk. With this analytical approach, it will give more confidence to provide a comprehensive assessment of the presence of water soluble vitamins in breast milk. This will enable the accurate evaluation of the nutritional requirements of infants.