Affiliations 

  • 1 Centre for Biospectroscopy, School of Chemistry, Faculty of Science, Monash University, Clayton, Victoria 3800, Australia and Department of Food Industry, Faculty of Bioresource and Food Industry, Universiti Sultan Zainal Abidin, 22200 Terengganu, Malaysia and CSIRO Agriculture & Food, Werribee, Victoria 3030, Australia. maryann.augustin@csiro.au
  • 2 Centre for Biospectroscopy, School of Chemistry, Faculty of Science, Monash University, Clayton, Victoria 3800, Australia
  • 3 CSIRO Agriculture & Food, Werribee, Victoria 3030, Australia. maryann.augustin@csiro.au
Food Funct, 2017 Sep 18.
PMID: 28920995 DOI: 10.1039/c7fo01012e

Abstract

Varying the β-carotene (0.1-0.3 g kg(-1)) and whey protein isolate (WPI) (2-20 g kg(-1)) concentrations in an oil-in-water (O/W) emulsion influenced the partitioning and stability of β-carotene upon 30 d storage at 25 and 40 °C. The total β-carotene in the emulsion was extracted with a solvent and quantified using UV/visible spectroscopy. The β-carotene in oil phase was obtained using in situ Raman micro-spectroscopy. The β-carotene in the aqueous phase was obtained by difference. Increasing β-carotene concentration resulted in increased partitioning of β-carotene into the aqueous phase whereas increasing WPI concentration had the opposite effect. With all freshly made emulsions, there was a higher proportion of β-carotene found in the oil phase. At the end of the storage period, the higher proportion and concentration of β-carotene was in the aqueous phase. This suggested that oxidation of β-carotene occurred faster in the oil phase and that WPI in the aqueous phase protected β-carotene against oxidation. This work informs the formulation of protein-based emulsions for the delivery of β-carotene.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.