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Fat concentration and high-pressure homogenization affect chlorogenic acid bioaccessibility and α-glucosidase inhibitory capacity of milk-based coffee beverages

Alongi, Marilisa
•
Calligaris, Sonia
•
Anese, Monica
2019
  • journal article

Periodico
JOURNAL OF FUNCTIONAL FOODS
Abstract
This study aimed at investigating the effect of coffee formulation and high-pressure homogenization (HPH) on chlorogenic acid bioaccessibility and alpha-glucosidase inhibition. Coffee was added with milk (1:1) containing 0.1, 3.6 or 7.1% fat, homogenized at increasing pressure (0-150 MPa) and in vitro digested. Using milk with the highest fat concentration (7.1%) promoted the formation of smaller particles after HPH treatment, as well as upon digestion. Digested samples with the highest fat content also presented lower zeta-potential, suggesting higher stability. Chlorogenic acids (CGAs) bioaccessibility and alpha-glucosidase inhibition were evaluated upon in vitro digestion. CGAs bioaccessibility increased from nearly 25% to > 50% by adding milk and using HPH. These could promote CGAs micellarization, reducing their susceptibility to degradation during digestion. Properly combined milk and HPH also improved alpha-glucosidase inhibitory effect. No correlation was found between CGAs bioaccessibility and alpha-glucosidase inhibition, suggesting that other components may govern antidiabetic properties of coffee.
DOI
10.1016/j.jff.2019.04.057
WOS
WOS:000471208500015
Archivio
http://hdl.handle.net/11390/1149728
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85064957431
http://www.elsevier.com/wps/find/journaldescription.cws_home/717426/description#description
Diritti
open access
Soggetti
  • Coffee

  • Fat concentration

  • High pressure homogen...

  • In vitro digestion

  • Milk

  • α-glucosidase inhibit...

  • Food Science

  • Medicine (miscellaneo...

  • Nutrition and Dieteti...

Scopus© citazioni
11
Data di acquisizione
Jun 15, 2022
Vedi dettagli
Web of Science© citazioni
13
Data di acquisizione
Mar 27, 2024
Visualizzazioni
4
Data di acquisizione
Apr 19, 2024
Vedi dettagli
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