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Article 2024 · 18 citations

Design and preparation of multifunctional astaxanthin nanoparticles with good acid stability and hepatocyte-targeting ability for alcoholic liver injury alleviation

Hua, Zheng, Zhang, Xuedi, Xing, Shanghua, Li, Jiaxuan, Liang, Duo, Chen, Yannan, Abd El-Aty, A. M., Zhu, Bei-Wei, Liu, Donghong, Tan, Mingqian

Abstract

As a dietary nutrition supplement, astaxanthin (AXT) has attracted much attention in alleviating ethanol-induced liver injury due to its superior antioxidant ability. However, the poor water solubility and pH-vulnerable characteristics of AXT significantly restrict its application in nutrition intervention. In this study, multifunctional astaxanthin nanoparticles (LAD6:1@AXT) with good acid stability and hepatocyte-targeting ability were designed and prepared using 2-hydroxypropyl-beta-cyclodextrin, lactobionic acid, and sodium alginate as raw materials. At pH 2.0, LAD6:1@AXT displayed a double reservation rate of the relative AXT content compared to free AXT. Significant antioxidative activity of LAD6:1@AXT was observed in cellular experiments. Ex vivo experiments revealed that the astaxanthin nanoparticles showed 90 % increased accumulation in the liver after oral administration for 24 h. A strong hepatic-targeting effect was found for LAD6:1@AXT, which could effectively ameliorate alcoholic liver injury. Our data indicated that the developed astaxanthin nanoparticles have the potential of nutrition intervention for alcohol-induced liver impairment.

Keywords
Astaxanthin Novel nanoparticles pH stable Hepatic targeting Gut microbiota modulated Alcoholic liver injury GUT MICROBIOTA MODEL 2-HYDROXYPROPYL-BETA-CYCLODEXTRIN DISEASE
WoS Categories
Nanoscience & Nanotechnology Materials Science, Multidisciplinary
Sustainable Development Goals
Citation
Journal
MATERIALS TODAY NANO
Year
2024
Volume
25
ISSN
2588-8420
DOI
10.1016/j.mtnano.2023.100436
WoS UID
WOS:001126086300001
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