Fabrication of resveratrol-loaded soy protein isolate-glycyrrhizin nanocomplex for improving bioavailability via pH-responsive hydrogel properties.

Glycyrrhizin Soy protein isolate pH-responsive hydrogel

Journal

International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578

Informations de publication

Date de publication:
22 Dec 2023
Historique:
received: 13 08 2023
revised: 03 12 2023
accepted: 19 12 2023
medline: 25 12 2023
pubmed: 25 12 2023
entrez: 24 12 2023
Statut: aheadofprint

Résumé

Resveratrol (RES) is a functional polyphenol that suffers from low water solubility and poor bioavailability. A novel RES-loaded soy protein isolate-dipotassium glycyrrhizinate (SPI-DG) nanocomplex (RES@SPI-DG) was designed and evaluated in this study. RES@SPI-DG was prepared using a simple but novel self-assembly ultrasonic-assisted pH-driven method. The interactions between RES and SPI-DG were non-covalent bonds, including hydrophobic interactions, hydrogen bonds, and van der Waals interactions. RES@SPI-DG exhibited high encapsulation efficiency (97.60 ± 0.38 %) and loading capacity (8.74 ± 0.03 %) of RES with a uniform small size (68.39 ± 1.10 nm). RES in RES@SPI-DG was in an amorphous state and demonstrated a 24-h apparent solubility 482.53-fold higher than bare RES. RES@SPI-DG also showed strong in vitro antioxidant properties. The pH-responsive hydrogel character of SPI-DG makes it an effective intestine-targeted delivery system that could retard the release of RES in a simulated stomach and accelerate it in a simulated intestine. In animal experiments, the bioavailability of RES@SPI-DG was 5.17 times higher than that of bare RES, and the biodistribution was also significantly improved. RES@SPI-DG demonstrated a strong hepatoprotective effect against overdose acetaminophen-induced liver injury. The SPI-DG complex might be a promising nano-platform for enhancing the bioavailability and efficacy of hydrophobic polyphenols such as RES.

Identifiants

pubmed: 38143068
pii: S0141-8130(23)05849-X
doi: 10.1016/j.ijbiomac.2023.128950
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

128950

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Qingchen Cui (Q)

College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, China; Affiliated Qingdao Third People's Hospital, Qingdao University, Qingdao 266021, China.

Xiaoying Song (X)

Qingdao Hospital, University of Health and Rehabilitation Sciences (Qingdao Municipal Hospital), Qingdao, China.

Liping Zhou (L)

Qingdao Hospital, University of Health and Rehabilitation Sciences (Qingdao Municipal Hospital), Qingdao, China.

Junjie Dong (J)

College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, China.

Yanjun Wei (Y)

College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, China; Viwit Pharmaceutical Co., Ltd., Zaozhuang, Shandong, China.

Zongtao Liu (Z)

College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, China; Affiliated Qingdao Third People's Hospital, Qingdao University, Qingdao 266021, China. Electronic address: liutao009@163.com.

Xianggen Wu (X)

College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, China. Electronic address: wuxianggen@126.com.

Classifications MeSH