化学
药物输送
壳聚糖
微粒
炎症性肠病
体内
卡拉胶
柠檬酸
共聚物
微流控
控制释放
纳米技术
生物医学工程
材料科学
化学工程
聚合物
生物化学
有机化学
生物技术
病理
工程类
生物
医学
疾病
作者
Shima Ostovar,Mohammad Amin Zaker,Mohammad Akrami,Amirhossein Heidari,Yekta Ghane,Nazila Heidari,Homayoun Pishraft-sabet,Parastou Gorovanchi,Zeinab Salehi,Vahid Bazargan,Seyed Mohsen Ahmadi Tafti,Marco Marengo
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2025-07-25
卷期号:26 (9): 5791-5806
标识
DOI:10.1021/acs.biomac.5c00663
摘要
Mesalamine (Mes) is a first-line anti-inflammatory agent extensively used to treat inflammatory bowel disease (IBD). Mes can be locally delivered using alginate-based microparticles as a pH-sensitive drug delivery system. In this study, we enhanced Alg microparticles by synthesizing an Alg-Kappa-carrageenan block copolymer using a biocompatible method with citric acid. The Alg-CA-κCar microparticles were fabricated on microfluidic chips and coated with chitosan (CS) to improve the encapsulation of Mes. FE-SEM images confirmed spherical microparticles with a narrow size distribution. TGA analysis showed better thermal stability for Alg-CA-κCar/CS microparticles compared with Alg microparticles. Alg-CA-κCar/CS microparticles achieved 73.8% drug encapsulation and demonstrated a pH-sensitive release profile with protection at pH 2 and increased release at pH 7.4. In vivo studies showed reduced pro-inflammatory factors such as TNF-α, MPO, and IL-6 levels in treated rats. Overall, Alg-CA-κCar/CS microparticles provide a more controlled carrier for Mes, demonstrating potential in effectively treating and managing the IBD.
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