Natural Ellagic Acid-Polyphenol ″Sandwich Biscuit″ Self-Assembled Solubilizing System for Formation Mechanism and Antibacterial Synergia

Ellagic acid (EA) has limited utility due to its extremely low solubility. Inspired by the naturally high content of EA in <i>Triphala</i>, the research group discovered that there might be noncovalent self-assembled nanoaggregates centered on EA in natural polyphenols that could significantly improve EA's solubility and enhance its antibacterial activity. Therefore, seven polyphenols that we found were potentially involved in EA self-assembly were separated and identified from <i>Triphala</i>, and 18 binary, ternary, and quaternary self-assembly systems were constructed by combining them with EA. Finally, a ternary self-assembled solubilizing system centered on ellagic acid-gallic acid-catechin (EA-GA-CA) was established. The system could improve the solubility of EA from 0.95 to 171.345 μg·mL<sup>-1</sup>, leading to a notable 180-fold increase, and the stability of EA in water was increased 3 times compared with the mixture of EA, GA, and CA, which is currently the most effective carrier-free hydrotropic solubilizing method of EA. The in vitro release rate reached about 61%, which was about 60 times higher than that of EA. Exploring the formation mechanism of the self-assembled complex revealed that EA, GA, and CA were induced by hydrogen bonding and π-π stacking to form a solubilizing structure resembling a sandwich biscuit. In addition, in vitro antibacterial experiments, biofilm clearance experiments, and infected wound healing experiments demonstrated that the EA-GA-CA complex has a better inhibitory effect on <i>Staphylococcus aureus</i> (<i>S. aureus</i>) and methicillin-resistant <i>S. aureus</i> (MRSA) than EA, GA, CA, benzylpenicillin potassium, and the mixture of EA, GA, and CA (MIC = 12.5 mM). The inhibition rate of the EA-GA-CA complex against S. aureus reaches 82.68%, and it can rapidly promote the healing of infected wounds caused by <i>S. aureus</i> within 4-6 days (the healing rate increased from 15 to 75%). This study aims to provide new ideas for EA's natural small molecule carrier-free self-assembly solubilization and synergistic applications.

Authors

Institutions

Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-03-25
DOI
https://doi.org/10.1021/acsami.5c00683
Citations
12
Primary Topic
Pomegranate: compositions and health benefits
Type
article
Field-Weighted Citation Impact
12.32

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Natural Ellagic Acid-Polyphenol ″Sandwich Biscuit″ Self-Assembled Solubilizing System for Formation Mechanism and Antibacterial Synergia

Yurou Jiang, Tianchun Ye, Tian Yin, Xinqi Yang et al.
12 citations
ACS Applied Materials & Interfaces
Pomegranate: compositions and health benefits
12.32
article

Natural Ellagic Acid-Polyphenol ″Sandwich Biscuit″ Self-Assembled Solubilizing System for Formation Mechanism and Antibacterial Synergia

Yurou Jiang, Tianchun Ye, Tian Yin, Xinqi Yang, Sanhu Fan, Haozhou Huang, Dingkun Zhang, Li Han, Chunli Ge, Mengqi Li, Junzhi Lin, Xiaorong Wei, Yingbi Xu
article en
12 citations

Abstract

Ellagic acid (EA) has limited utility due to its extremely low solubility. Inspired by the naturally high content of EA in <i>Triphala</i>, the research group discovered that there might be noncovalent self-assembled nanoaggregates centered on EA in natural polyphenols that could significantly improve EA's solubility and enhance its antibacterial activity. Therefore, seven polyphenols that we found were potentially involved in EA self-assembly were separated and identified from <i>Triphala</i>, and 18 binary, ternary, and quaternary self-assembly systems were constructed by combining them with EA. Finally, a ternary self-assembled solubilizing system centered on ellagic acid-gallic acid-catechin (EA-GA-CA) was established. The system could improve the solubility of EA from 0.95 to 171.345 μg·mL<sup>-1</sup>, leading to a notable 180-fold increase, and the stability of EA in water was increased 3 times compared with the mixture of EA, GA, and CA, which is currently the most effective carrier-free hydrotropic solubilizing method of EA. The in vitro release rate reached about 61%, which was about 60 times higher than that of EA. Exploring the formation mechanism of the self-assembled complex revealed that EA, GA, and CA were induced by hydrogen bonding and π-π stacking to form a solubilizing structure resembling a sandwich biscuit. In addition, in vitro antibacterial experiments, biofilm clearance experiments, and infected wound healing experiments demonstrated that the EA-GA-CA complex has a better inhibitory effect on <i>Staphylococcus aureus</i> (<i>S. aureus</i>) and methicillin-resistant <i>S. aureus</i> (MRSA) than EA, GA, CA, benzylpenicillin potassium, and the mixture of EA, GA, and CA (MIC = 12.5 mM). The inhibition rate of the EA-GA-CA complex against S. aureus reaches 82.68%, and it can rapidly promote the healing of infected wounds caused by <i>S. aureus</i> within 4-6 days (the healing rate increased from 15 to 75%). This study aims to provide new ideas for EA's natural small molecule carrier-free self-assembly solubilization and synergistic applications.

ACS Applied Materials & InterfacesVol. 17(19)
Second Affiliated Hospital of Chengdu University of Traditional Chinese (CN), Chengdu University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation
Zero hunger
Openalex Percentile: Top 1%
Pomegranate: compositions and health benefits
12.32
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.