# Improving in vitro Gastrointestinal Stability of Phlorotannins From Food Grade Fucus vesiculosus Extracts Using Cyclodextrins

**Authors:** Sofia F. Reis, Marcelo D. Catarino, Susana S. Braga, Manuel A. Coimbra, Artur M. S. Silva, Susana M. Cardoso

PMC · DOI: 10.1111/1750-3841.70830 · 2026-01-13

## TL;DR

This study shows that using β-cyclodextrin during microwave extraction improves the survival of phlorotannins through the digestive system, boosting their potential health benefits.

## Contribution

The study introduces β-cyclodextrin-assisted microwave extraction as a novel method to enhance phlorotannin gastrointestinal stability.

## Key findings

- Higher cyclodextrin concentrations improved phlorotannin stability during digestion.
- β-cyclodextrin-assisted extraction retained 35% of phlorotannins after the intestinal phase.
- Microwave-assisted extraction with β-cyclodextrin outperformed post-extraction addition.

## Abstract

Phlorotannins have gained significant attention for their potential bioactive and functional properties. However, these compounds are highly sensitive to gastrointestinal digestion, which limits their bioavailability and consequently the in vivo efficacy.

To address this limitation, this study explored the use of various concentrations of γ‐ and β‐cyclodextrins in the aqueous microwave‐assisted extraction of phlorotannins from Fucus vesiculosus and submitted the resulting extracts to an in vitro gastrointestinal digestion protocol.

While higher cyclodextrin concentrations resulted in an increase in extraction yields (from 47% to approximately 55% for both cyclodextrins), the opposite was observed for the total phlorotannin content. Notably, higher cyclodextrin concentrations markedly improved phlorotannin stability across the different stages of gastrointestinal digestion. Specifically, β‐cyclodextrin exhibited the highest protective effect, preventing phlorotannin degradation almost completely in both oral and gastric phases, and retaining approximately 35% (approximately 1.0 mg/g extract) of the initial content (approximately 3.0 mg/g extract) after the intestinal phase, thereby enhancing the compounds’ resistance and residence time in the intestinal lumen. A comparison between the addition of β‐cyclodextrin during extraction and post‐extraction revealed that, although both approaches reduce the phlorotannin loss throughout the gastrointestinal tract, the β‐cyclodextrin‐assisted extraction showed better efficacy. This indicates that strong guest‐host interactions are formed between phlorotannins and cyclodextrins during the extraction, possibly due to the increased enthalpy generated by microwave heating.

Overall, this study highlights β‐cyclodextrin‐microwave‐assisted extraction as a promising approach to enhance the stability of phlorotannins in their transit through the gastrointestinal tract, ensuring their delivery to the intestinal lumen, where they can be released and available for absorption.

## Linked entities

- **Species:** Fucus vesiculosus (taxon 49266)

## Full-text entities

- **Diseases:** macular degeneration (MESH:D008268), Gastrointestinal Digestion (MESH:D004828), inflammation (MESH:D007249)
- **Chemicals:** O2 (MESH:D013481), anthocyanin (MESH:D000872), phloroglucinol (MESH:D010696), nitrogen (MESH:D009584), NO (MESH:D009614), sodium borohydride (MESH:C025364), D-glucose (MESH:D005947), beta-CD (MESH:D047392), thymol (MESH:D013943), sugar (MESH:D000073893), HCl (MESH:D006851), Sodium nitroprusside (MESH:D009599), KBr (MESH:C039004), catechins (MESH:D002392), Sodium di-hydrogen phosphate (MESH:C018279), Fuc-fucose (-), nitric oxide (MESH:D009569), galacturonic acid (MESH:C007819), CDs (MESH:D002104), tannins (MESH:D013634), polyphenol (MESH:D059808), Ascorbic acid (MESH:D001205), alginic acid (MESH:D000077322), fucoidans (MESH:C007789), oligosaccharides (MESH:D009844), gamma-CD (MESH:D047408), metal (MESH:D008670), 2-deoxyglucose (MESH:D003847), xylitol (MESH:D014993), essential oils (MESH:D009822), mannitol (MESH:D008353), sulfanilamide (MESH:D000077145), gamma-cyclodextrin (MESH:C023792), EtOH (MESH:D000431), NaHCO3 (MESH:D017693), acetone (MESH:D000096), Hexuronic acids (MESH:D006603), potassium di-hydrogen phosphate (MESH:C013216), beta-cyclodextrin (MESH:C031215), Calcium chloride (MESH:D002122), guluronic acid (MESH:C007896), 2,4-dimethoxybenzaldehyde (MESH:C071066), terpenes (MESH:D013729), carbohydrates (MESH:D002241), glucuronic acid (MESH:D020723), alpha-CD (MESH:D047391), starch (MESH:D013213), acetic acid (MESH:D019342), fucose (MESH:D005643), chrysin (MESH:C043561), mannuronic acid (MESH:C008324), NADH (MESH:D009243), 1-methylimidazole (MESH:C018100), piceatannol (MESH:C041525), bile salts (MESH:D001647), 3-phenylphenol (MESH:C059903), phenazine methosulfate (MESH:D008773), chitosan-tripolyphosphate (MESH:C000623170), alginates (MESH:D000464), gallic acid (MESH:D005707)
- **Species:** Fucus vesiculosus (species) [taxon 49266], PX clade (clade) [taxon 569578], Sargassum ilicifolium (species) [taxon 246892], Homo sapiens (human, species) [taxon 9606], Ascophyllum nodosum (species) [taxon 52969]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12797003/full.md

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Source: https://tomesphere.com/paper/PMC12797003