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Application of core-shell technology for determination of retinol and alpha-tocopherol in breast milk
J. Plíšek, M. Kašparová, D. Solichová, L. Krčmová, B. Kučerová, L. Sobotka, P. Solich,
Language English Country Netherlands
Document type Journal Article, Research Support, Non-U.S. Gov't, Validation Study
- MeSH
- alpha-Tocopherol analysis MeSH
- Time Factors MeSH
- Humans MeSH
- Limit of Detection MeSH
- Milk, Human chemistry MeSH
- Reproducibility of Results MeSH
- Vitamin A analysis MeSH
- Vitamins analysis MeSH
- Chromatography, High Pressure Liquid economics instrumentation MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Validation Study MeSH
Breast milk is a main source of fat-soluble vitamins for newborns and it is needful to monitor the nutritional status prior to its application. In this work a novel, high-throughput and low-cost method for monitoring of retinol and alpha-tocopherol in breast milk was developed, validated and compared with reference method using monolithic column. For this purpose five various porous shell and monolithic columns were tested on the basis of relationship between HETP and linear mobile phase velocity, analysis time and consumption of solvents. Finally the core-shell analytical column Kinetex C18 (2.6 μm, 100 Å, 100×4.6 mm) was chosen as the best and optimal values of flow rate, injection volume and temperature of analysis were established. The detection of retinol and alpha-tocopherol was carried out at 325 and 295 nm, respectively by diode array detector. The LOD 0.004 μmol/L and 0.078 μmol/L, the LOQ 0.012 μmol/L and 0.182 μmol/L for retinol and alpha-tocopherol, respectively were calculated. The validation data showed good linearity, repeatability of retention time with RSD 0.22% and 0.12%, repeatability of peak area with RSD 6.94% and 1.75%, recovery 114.1-116.3% and 99.0-108.6% for retinol and alpha-tocopherol, respectively. Moreover, the newly developed method substantially decreased the solvent consumption by about 263 mL per 100 samples with the total time of analysis 1.75 min in comparison with analysis time 1.80 of the reference method.
References provided by Crossref.org
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