Oral Nanotherapeutics of Andrographolide/Carbon Monoxide Donor for Synergistically Anti-inflammatory and Pro-resolving Treatment of Ulcerative Colitis

被引:21
|
作者
Zhou, Ying [1 ,2 ]
Yang, Mei [3 ]
Yan, Xiangji [4 ]
Zhang, Lingmin [5 ]
Lu, Ning [6 ]
Ma, Yana [4 ]
Zhang, Yuanyuan [4 ]
Cui, Manli [6 ]
Zhang, Mingzhen [4 ]
Zhang, Mingxin [6 ]
机构
[1] Shaanxi Univ Chinese Med, Clin Med Coll 2, Xianyang 712046, Shaanxi, Peoples R China
[2] Air Force Med Univ, Tangdu Hosp, Dept Pediat, Xian 710032, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Thorac Surg, Xian 710061, Peoples R China
[4] Xi An Jiao Tong Univ, Hlth Sci Ctr, Sch Basic Med Sci, Xian 710061, Shaanxi, Peoples R China
[5] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Anesthesiol, Xian 710061, Shaanxi, Peoples R China
[6] Xian Med Univ, Affiliated Hosp 1, Dept Gastroenterol, Xian 710077, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
ulcerative colitis(UC); anti-inflammation; pro-resolution; oral nanotherapeutics; andrographolide(AG); carbon monoxide (CO); DRUG-DELIVERY; NITRIC-OXIDE; GUT MICROBIOTA; COLON-CANCER; INFLAMMATION; RESOLUTION; PATHOGENESIS; OXYGENASE-1; ACTIVATION; MOLECULES;
D O I
10.1021/acsami.3c09342
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ulcerativecolitis (UC) is a chronic inflammatory boweldiseaseof unknown etiology affecting the colon and rectum. Current therapeuticsare focused on suppressing inflammation but are ineffective. Combininganti-inflammatory therapeutic approaches with pro-resolution mightbe a superior strategy for UC treatment. Andrographolide (AG), anactive compound from the plant Andrographis paniculata, presented anti-inflammatory effects in various inflammatory diseases.Gaseous mediators, such as carbon monoxide (CO), have a role in inflammatoryresolution. Herein, we developed a dextran-functionalized PLGA nanocarrierfor efficient delivery of AG and a carbon monoxide donor (CORM-2)for synergistically anti-inflammatory/pro-resolving treatment of UC(AG/CORM-2@NP-Dex) based on PLGA with good biocompatibility, slowdrug release, efficient targeting, and biodegradability. The resultingnanocarrier had a nano-scaled diameter of & SIM;200 nm and a sphericalshape. After being coated with dextran (Dex), the resulting AG/CORM-2@NP-Dexcould be efficiently internalized by Colon-26 and Raw 264.7 cells in vitro and preferentially localized to the inflamed colonwith chitosan/alginate hydrogel protection by gavage. AG/CORM-2@NP-Dexperformed anti-inflammatory effects by eliminating the over-productionof pro-inflammatory mediator, nitric oxide (NO), and down-regulatingthe expression of pro-inflammatory cytokines (TNF-& alpha;, IL-1 & beta;and IL-6), while it showed pro-resolving function by acceleratingM1 to M2 macrophage conversion and up-regulating resolution-relatedgenes (IL-10, TGF-& beta;, and HO-1). In the colitis model, oral administrationof AG/CORM-2@NP-Dex in a chitosan/alginate hydrogel also showed synergisticallyanti-inflammatory/pro-resolving effects, therefore relieving UC effectively.Without appreciable systemic toxicity, this bifunctional nanocarrierrepresents a novel therapeutic approach for UC and is expected toachieve long-term inflammatory remission.
引用
收藏
页码:36061 / 36075
页数:15
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