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基于柠檬酸托法替布配位的双响应/清除纳米平台调节结肠炎症微环境以缓解结肠炎

Tofacitinib Citrate Coordination-Based Dual-Responsive/Scavenge Nanoplatform Toward Regulate Colonic Inflammatory Microenvironment for Relieving Colitis.

作者信息

Zou Jiafeng, Jiang Kun, Chen You, Ma Ying, Xia Chuanhe, Ding Wenxing, Yao Min, Lin Yiting, Chen Yanzuo, Zhao Yuzheng, Gao Feng

机构信息

Shanghai Frontier Science Center of Optogenetic Techniques for Cell Metabolism, School of Pharmacy, East China University of Science and Technology, Shanghai, 200237, China.

Optogenetics and Synthetic Biology Interdisciplinary Research Center, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China.

出版信息

Adv Healthc Mater. 2024 Dec;13(30):e2401869. doi: 10.1002/adhm.202401869. Epub 2024 Aug 23.

DOI:10.1002/adhm.202401869
PMID:39180276
Abstract

Ulcerative colitis is an inflammation of the colon characterized by immune dysregulation and intestinal inflammation. Developing safe oral nanomedicines that suppress intestinal inflammation, while modulating colonic inflammatory microenvironment by scavenging reactive oxygen species (ROS) and hydrogen sulfide (HS) is crucial for the effective treatment of colitis. Here, the tofacitinib citrate and copper coordination-based nanoparticle (TF-Cu nanoparticle, T-C) to dual-scavenge ROS and HS by coordination competition is synthesized. Moreover, the coordination of T-C using computer simulation is explored. To enhance the acid stability and inflammatory targeting of T-C, it is encapsulated with hyaluronic acid-modified chitosan, along with a calcium pectinate coating (T-C@HP). Owing to the dual pH/pectinase-responsive characteristics of T-C@HP, the nanoplatform can target inflamed colonic lesions, inhibiting phosphorylated Janus kinase 1. Furthermore, T-C@HP scavenges ROS and HS, as well as increases NADPH levels, which is investigated by combining biosensor (HyPer7 and iNap1/c) and chemical probes. T-C@HP also alleviates colitis by regulating the colonic inflammatory microenvironment through multiple processes, including the modulation of apoptosis, macrophage polarization, tight junction, mucus layer, and intestinal flora. Complemented by satisfactory anti-inflammatory and biosafety results, this nanoplatform represents a promising, effective, and safe treatment option for colitis patients.

摘要

溃疡性结肠炎是一种以免疫失调和肠道炎症为特征的结肠炎症。开发安全的口服纳米药物,既能抑制肠道炎症,又能通过清除活性氧(ROS)和硫化氢(HS)来调节结肠炎症微环境,对于结肠炎的有效治疗至关重要。在此,合成了基于枸橼酸托法替布和铜配位的纳米颗粒(TF-Cu纳米颗粒,T-C),通过配位竞争双重清除ROS和HS。此外,还利用计算机模拟探索了T-C的配位情况。为了提高T-C的酸稳定性和炎症靶向性,用透明质酸修饰的壳聚糖对其进行包封,并包覆果胶酸钙涂层(T-C@HP)。由于T-C@HP具有双pH/果胶酶响应特性,该纳米平台能够靶向炎症性结肠病变,抑制磷酸化的Janus激酶1。此外,通过结合生物传感器(HyPer7和iNap1/c)和化学探针研究发现,T-C@HP能清除ROS和HS,并提高NADPH水平。T-C@HP还通过多种过程调节结肠炎症微环境,包括调节细胞凋亡、巨噬细胞极化、紧密连接、黏液层和肠道菌群,从而减轻结肠炎。该纳米平台具有令人满意的抗炎和生物安全性结果,为结肠炎患者提供了一种有前景、有效且安全的治疗选择。

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