Evidence map›Paper›PMID 41445830›Full record

ArticleFrontiers in nutrition2025

"Hot" alkaline hydrolysis of UiO-66 to enhance quercetin loading,

Ruimiao Chang, Huichun Wang, Shumian Liu, Shuai Jia, Jingjing Wang, Ying Song, Xiaolu Ji, Qingqing Li

Abstract read
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Article in Frontiers in nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ruimiao ChangDepartment of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, China.
Huichun WangDepartment of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, China.
Shumian LiuDepartment of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, China.
Shuai JiaDepartment of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, China.
Jingjing WangDepartment of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, China.
Ying SongDepartment of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Xiaolu JiDepartment of Pharmacy, Shanxi Medical University, Taiyuan, Shanxi, China.
Qingqing LiThird Hospital of Shanxi Medical University, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Taiyuan, Shanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Food and Drug Administration (FDA) classifies quercetin (QU) as a generally recognized as safe (GRAS) substance and exhibits striking antioxidant and anti-inflammatory activities. However, its extremely low solubility in water limits its application in the fields of food and nutrition. Nanomaterials such as UiO-66 (University of Oslo 66) have been widely used in the field of nutrient delivery. Methods: In this study, terephthalic acid ligands were stripped from small-sized UiO-66 via a thermal alkaline hydrolysis method, resulting in a new drug-loaded material, UiO-66-BH-100 (UiO-66 blended and heated, with a size of 100 nm). The obtained UiO-66-BH-100 showed significantly increased porosity and good thermal stability. UiO-66-BH-100, which is rich in hydroxyl groups (1.7 × 1019/m Results: The QU-loaded drug carrier UiO-66-BH-100@QU has good biocompatibility and could significantly improve the in vitro release behavior of QU. Notably, the capacity of UiO-66-BH-100@QU to scavenge diphenyl-2-picrylhydrazyl (DPPH) and 22'-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS), as well as its ability to inhibit NO secretion, was almost comparable to that of QU, demonstrating promising antioxidant and anti-inflammatory potential. Conclusion: This study provides a simple and effective new approach for delivering natural active ingredients with excellent bioavailability in the field of functional foods.

Indexed as

adsorption capacityin vitro releasequercetinsmall sizethermal alkaline hydrolysis

Identifiers

PMID41445830
PMCPMC12723612

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