Application of chitosan/alginate nanoparticle in oral drug delivery systems: prospects and challenges

被引:82
|
作者
Li Shangyong [1 ,2 ]
Zhang Hui [1 ]
Chen Kaiwei [1 ]
Jin Mengfei [1 ]
Vu Son Hai [2 ,3 ]
Jung, Samil [2 ]
He Ningning [1 ]
Zheng Zhou [4 ]
Lee, Myeong-Sok [2 ]
机构
[1] Qingdao Univ, Qingdao Med Coll, Sch Basic Med, Qingdao, Peoples R China
[2] Sookmyung Womens Univ, Cellular Heterogene Res Ctr, Dept Biosyst, Mol Canc Biol Lab, Seoul, South Korea
[3] Ho Chi Minh City Univ Technol HUTECH, Inst Appl Sci, Ho Chi Minh City, Vietnam
[4] Minist Nat Resource, Inst Oceanog 1, Key Lab Marine Ecoenvironm Sci & Technol, Qingdao, Peoples R China
基金
新加坡国家研究基金会;
关键词
Oral drug delivery; chitosan; alginate nanoparticle; insulin; ulcerative colitis; colon cancer; POLYELECTROLYTE COMPLEXES; POLYMERIC NANOPARTICLES; CHITOSAN NANOPARTICLES; PARTICLE-SIZE; ALGINATE; MICROSPHERES; OPTIMIZATION; FORMULATION; EFFICIENT; CARRIERS;
D O I
10.1080/10717544.2022.2058646
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oral drug delivery systems (ODDSs) have various advantages of simple operation and few side effects. ODDSs are highly desirable for colon-targeted therapy (e.g. ulcerative colitis and colorectal cancer), as they improve therapeutic efficiency and reduce systemic toxicity. Chitosan/alginate nanoparticles (CANPs) show strong electrostatic interaction between the carboxyl group of alginates and the amino group of chitosan which leads to shrinkage and gel formation at low pH, thereby protecting the drugs from the gastrointestinal tract (GIT) and aggressive gastric environment. Meanwhile, CANPs as biocompatible polymer, show intestinal mucosal adhesion, which could extend the retention time of drugs on inflammatory sites. Recently, CANPs have attracted increasing interest as colon-targeted oral drug delivery system for intestinal diseases. The purpose of this review is to summarize the application and treatment of CANPs in intestinal diseases and insulin delivery. And then provide a future perspective of the potential and development direction of CANPs as colon-targeted ODDSs.
引用
收藏
页码:1142 / 1149
页数:8
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