Emerging nanomedicine and prodrug delivery strategies for the treatment of inflammatory bowel disease

被引:22
|
作者
Sun, Mengchi [1 ]
Ban, Weiyue [1 ]
Ling, Hao [1 ]
Yu, Xiang [2 ]
He, Zhonggui [1 ]
Jiang, Qikun [1 ]
Sun, Jin [1 ]
机构
[1] Shenyang Pharmaceut Univ, Wuya Coll Innovat, Shenyang 110016, Peoples R China
[2] Huzhou Univ, Huzhou Cent Hosp, Affiliated Huzhou Hosp, Zhejiang Univ,Sch Med,Affiliated Cent Hosp, Huzhou 110016, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金; 国家重点研发计划;
关键词
Inflammatory bowel disease (IBD); Nanotechnology-based nanomedicines (NMs); Prodrug strategy; Pathophysiological microenvirnoment; Passive targeted and active targeted NMs; COLON-SPECIFIC DELIVERY; IN-VIVO EVALUATION; DRUG-DELIVERY; SALICYLIC-ACID; GASTROINTESTINAL TRANSIT; OPHIOPOGON-JAPONICUS; COMBINATION THERAPY; ULCERATIVE-COLITIS; POTENTIAL PRODRUGS; REDOX NANOPARTICLE;
D O I
10.1016/j.cclet.2022.03.061
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inflammatory bowel disease (IBD) is a chronic and recurrent disease of the gastrointestinal tract, mainly including Crohn's disease (CD) and ulcerative colitis (UC). However, current approaches against IBD do not precisely deliver drugs to the inflammatory site, which leads to life-long medication and serious side effects that can adversely impact patients' adherence. It is necessary to construct optimal drug delivery systems (DDSs) that can target drugs to the region of inflammation, thereby improve therapeutic efficacy and reduce side effects. With the burgeoning development of nanotechnology-based nanomedicines (NMs) and prodrug strategy, remarkable progresses in the treatment of IBD have been made in recent years. Herein, the latest advances are outlined at the intersection of IBD treatment and nanotherapeutics as well as prodrug therapy. First, the pathophysiological microenvironment of inflammatory sites of IBD is introduced in order to rationally design potential NMs and prodrugs. Second, the necessity of NMs for the IBD therapy is elaborated, and the representative nanotherapeutics via passive targeted and active targeted NMs developed to treat the IBD are overviewed. Furthermore, the emerging prodrug-based therapeutics are summarized, including 5-aminosalicylic acid-, amino acid-, and carbohydrate-conjugated prodrugs. Finally, the design considerations and perspectives of these NMs and prodrugs-driven IBD therapeutics in the clinical translation are spotlighted. (C) 2022 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页码:4449 / 4460
页数:12
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