resumo
The bioaccessibility and bioavailability of phenolic compounds (PC) influence directly their role in disease prevention/control. Studies have evaluated this ability through complex plant and food matrices, which may reflect more a synergistic effect of the matrix than the ability of the PCs, hindering their individual exploitation in nutraceutical or pharmaceutical applications. In the present study ten pure PCs representing major classes were evaluated for their bioaccessibility and intestinal absorption in an in vitro simulated gastrointestinal digestion (SGD). This is the first study concerning the bioaccessibility evaluation of pure phloretin, phloroglucinol, naringin, naringenin and daidzein, while no in vitro SGD has been performed before for the other compounds considered here. PCs were analyzed through ultra -high-performance liquid chromatography coupled with diode -array detection and tandem mass spectrometry (UHPLC-DAD-MS n ). Most of the compounds remained present along the gastrointestinal tract, and the bioaccessibility was in general higher than 50%, except for quercetin, epigallocatechin gallate, and ellagic acid. All compounds were highly absorbed in the intestine, with phloretin showing the lowest percentage at about 82%. The study findings provide new knowledge on the bioaccessibility and intestinal absorption of different PCs classes.
palavras-chave
POLYPHENOLS; QUERCETIN; TRANSPORT; BIOAVAILABILITY; ANTIOXIDANT; METABOLISM; MECHANISMS; MICROBIOTA; FLAVANONE; IMPACT
categoria
Science & Technology - Other Topics
autores
Pais, ACS; Coscueta, ER; Pintado, MM; Silvestre, AJD; Santos, SAO
nossos autores
Projectos
CICECO - Aveiro Institute of Materials (UIDB/50011/2020)
CICECO - Aveiro Institute of Materials (UIDP/50011/2020)
Associated Laboratory CICECO-Aveiro Institute of Materials (LA/P/0006/2020)
agradecimentos
This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020, UIDP/50011/2020 & LA/P/0006/2020, financed by national funds through the FCT/MCTES (PIDDAC) . Thank the CBQF for its institutional support through the FCT project UIDB/50016/2020. Acknowledgments are also due to FCT/MCTES for the PhD grant to Adriana C.S. Pais (SFRH/BD/143348/2019) and for the research contract under Scientific Employment Stimulus to Sonia A.O. Santos (2021.03348. CEECIND) .

