Oral chitosan-cyclodextrin "shell-core" nanoparticles co-loaded Rhein and chlorogenic acid for ulcerative colitis treatment.

IF 7.7 1区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY International Journal of Biological Macromolecules Pub Date : 2025-02-01 Epub Date: 2024-12-06 DOI:10.1016/j.ijbiomac.2024.138493
Wenbiao Nie, Wenzhen Zhong, Lin Qian, Huiyun Zhong, Yusen Hou, Haiting Xu, Shanshan Qi, Linxin Dai, Xiaoqin Han, Xinyue Yang, Runchun Xu, Yao He, Dasheng Lin, Fei Gao
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Abstract

The food-derived ingredients Rhein (RH) and chlorogenic acid (CGA) have DEMONSTRATED a potential synergistic effect in the treatment of ulcerative colitis (UC) through their anti-inflammatory and antioxidant properties. However, the oral co-delivery of RH and CGA faces challenges such as differences in hydrophilicity and hydrophobicity, gastrointestinal instability, and inadequate colonic targeting. To address these issues, shell-core nanoparticles were developed for the co-encapsulation of RH and CGA (CP@CGA-FA/TA@RH NPs). These nanoparticles utilize cyclodextrin-based polymers and folate-amantadine polymers to form a supramolecular core that targets macrophages for anti-inflammatory action with RH, while chitosan cross-link to CGA in the outer shell provides microenvironment-sensitive antioxidant release. The results indicate that CP@CGA-FA/TA@RH NPs could effectively inhibit the classical TLR4/MyD88/NF-κB-mediated anti-inflammatory pathway and activate the Nrf2/HO-1-mediated antioxidant pathway, offering a novel approach to UC treatment. Q-value analysis confirms the substantial co-medication effect between RH and CGA. This study is the first to develop a nano-system combining two food-derived ingredients for the integrated treatment of UC.

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口服壳聚糖-环糊精“壳核”纳米颗粒共载大黄酸和绿原酸治疗溃疡性结肠炎。
食品来源的成分Rhein (RH)和绿原酸(CGA)通过其抗炎和抗氧化特性在治疗溃疡性结肠炎(UC)中显示出潜在的协同作用。然而,RH和CGA的口服共给药面临着诸如亲疏水性差异、胃肠道不稳定和结肠靶向性不足等挑战。为了解决这些问题,开发了壳核纳米颗粒用于RH和CGA的共包封(CP@CGA-FA/TA@RH NPs)。这些纳米颗粒利用环糊精聚合物和叶酸-金刚烷胺聚合物形成一个超分子核心,针对巨噬细胞发挥RH的抗炎作用,而壳聚糖与外壳中的CGA交联提供微环境敏感的抗氧化剂释放。结果表明,CP@CGA-FA/TA@RH NPs可有效抑制TLR4/MyD88/NF-κ b介导的经典抗炎途径,激活Nrf2/ ho -1介导的抗氧化途径,为UC治疗提供了新的途径。q值分析证实了RH与CGA之间存在实质性的共用药效应。这项研究首次开发了一种结合两种食物来源成分的纳米系统,用于UC的综合治疗。
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麦克林
TA
麦克林
pectin
麦克林
pectin
麦克林
TA
阿拉丁
TPGS
阿拉丁
TPGS
Sigma
4-dimethylaminopyridine (DMAP)
Sigma
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC)
Sigma
N-hydroxysuccinimide (NHS)
Sigma
Triethanolamine (TEA)
Sigma
N-hydroxysuccinimide (NHS)
Sigma
Triethanolamine (TEA)
Sigma
4-dimethylaminopyridine (DMAP)
来源期刊
International Journal of Biological Macromolecules
International Journal of Biological Macromolecules 生物-生化与分子生物学
CiteScore
13.70
自引率
9.80%
发文量
2728
审稿时长
64 days
期刊介绍: The International Journal of Biological Macromolecules is a well-established international journal dedicated to research on the chemical and biological aspects of natural macromolecules. Focusing on proteins, macromolecular carbohydrates, glycoproteins, proteoglycans, lignins, biological poly-acids, and nucleic acids, the journal presents the latest findings in molecular structure, properties, biological activities, interactions, modifications, and functional properties. Papers must offer new and novel insights, encompassing related model systems, structural conformational studies, theoretical developments, and analytical techniques. Each paper is required to primarily focus on at least one named biological macromolecule, reflected in the title, abstract, and text.
期刊最新文献
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