Oral pectin/oligochitosan microspheres for colon-specific controlled release of quercetin to treat inflammatory bowel disease

被引:18
|
作者
Jing, Shisuo [1 ,2 ]
Chen, Huayuan [2 ,3 ]
Liu, Ergang [2 ]
Zhang, Meng [4 ]
Shen, Huan [2 ,6 ]
Zeng, Feng [5 ]
Fang, Yuefei [2 ]
Muhitdinov, Bahtiyor [6 ,7 ]
Huang, Yongzhuo [1 ,2 ,6 ]
机构
[1] Zunyi Med Univ, Sch Pharm, Zunyi 563006, Peoples R China
[2] Chinese Acad Sci, Zhongshan Inst Drug Discovery, Shanghai Inst Mat Med, Zhongshan 528400, Peoples R China
[3] Southern Med Univ, Sch Pharmaceut Sci, Guangzhou 510515, Peoples R China
[4] Zhejiang Univ, Womens Hosp, Dept Pharm, Sch Med, Hangzhou 310006, Peoples R China
[5] Guangzhou Univ Chinese Med, Artemisinin Res Ctr, Guangzhou 510450, Peoples R China
[6] Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
[7] Uzbek Acad Sci, Inst Bioorgan Chem, Tashkent 100125, Uzbekistan
基金
中国国家自然科学基金;
关键词
Inflammatory bowel disease; Quercetin; colon-targeted delivery; Pectin microsphere; Oligochitosan; Immune microenvironment; SWELLING BEHAVIOR; DELIVERY-SYSTEMS; DRUG-DELIVERY; RAT INTESTINE; NOTCH; PECTIN; CHITOSAN; CELLS; PHARMACOKINETICS; POLYSACCHARIDES;
D O I
10.1016/j.carbpol.2023.121025
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Inflammatory bowel disease (IBD) is a chronic, life quality-reducing disease with no cures available yet. To develop an effective medication suitable for long-term use is an urgent but unmet need. Quercetin (QT) is a natural dietary flavonoid with good safety and multifaceted pharmacological activities against inflammation. However, orally administrated quercetin yields unproductive outcomes for IBD treatment because of its poor solubility and extensive metabolism in the gastrointestinal tract. In this work, a colon-targeted QT delivery system (termed COS-CaP-QT) was developed, of which the pectin (PEC)/Ca2+ microspheres were prepared and then crosslinked by oligochitosan (COS). The drug release profile of COS-CaP-QT was pH-dependent and colon microenvironment-responsive, and COS-CaP-QT showed preferential distribution in the colon. The mechanism study showed that QT triggered the Notch pathway to regulate the proliferation of T helper 2 (Th2) cells and group 3 innate lymphoid cells (ILC3s) and the inflammatory microenvironment was remodeled. The in vivo therapeutic results revealed that COS-CaP-QT could relieve the colitis symptoms and maintain the colon length and intestinal barrier integrity.
引用
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页数:15
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