Cell membrane nanomaterials composed of phospholipids and glycoproteins for drug delivery in inflammatory bowel disease: A review

被引:11
|
作者
Lei, Pengyu [1 ]
Yu, Haiyang [1 ]
Ma, Jiahui [1 ]
Du, Jiao [1 ]
Fang, Yimeng [1 ]
Yang, Qinsi [2 ]
Zhang, Kun [3 ]
Luo, Li [4 ]
Jin, Libo [1 ]
Wu, Wei [3 ]
Sun, Da [1 ]
机构
[1] Wenzhou Univ, Inst Life Sci & Biomed, Collaborat Innovat Ctr Zhejiang Prov, Wenzhou 325035, Peoples R China
[2] Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325000, Peoples R China
[3] Chongqing Univ, Key Lab Biorheol Sci & Technol, State & Local Joint Engn Lab Vasc Implants, Bioengn Coll,Minist Educ, Chongqing 400044, Peoples R China
[4] Southern Med Univ, Affiliated Dongguan Hosp, Dongguan 523059, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Cell membranes; Biological macromolecules; Inflammatory bowel disease; Nanoparticles; Probiotics; Targeted delivery; ERYTHROCYTES-MEDIATED DELIVERY; LONG-TERM INTAKE; ULCERATIVE-COLITIS; CROHNS-DISEASE; GUT MICROBIOTA; IN-VITRO; ADHESION MOLECULE-1; RISK-FACTORS; NANOPARTICLES; IBD;
D O I
10.1016/j.ijbiomac.2023.126000
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inflammatory bowel disease (IBD) is a serious chronic intestinal disorder with an increasing global incidence. However, current treatment strategies, such as anti-inflammatory drugs and probiotics, have limitations in terms of safety, stability, and effectiveness. The emergence of targeted nanoparticles has revolutionized IBD treatment by enhancing the biological properties of drugs and promoting efficiency and safety. Unlike synthetic nanoparticles, cell membrane nanomaterials (CMNs) consist primarily of biological macromolecules, including phospholipids, proteins, and sugars. CMNs include red blood cell membranes, macrophage membranes, and leukocyte membranes, which possess abundant glycoprotein receptors and ligands on their surfaces, allowing for the formation of cell-to-cell connections with other biological macromolecules. Consequently, they exhibit superior cell affinity, evade immune responses, and target inflammation effectively, making them ideal material for targeted delivery of IBD therapies. This review explores various CMNs delivery systems for IBD treatment. However, due to the complexity and harsh nature of the intestinal microenvironment, the lack of flexibility or loss of selectivity poses challenges in designing single CMNs delivery strategies. Therefore, we propose a hierarchically programmed delivery modality that combines CMNs with pH, charge, ROS and ligand-modified responsive nanoparticles. This approach significantly improves delivery efficiency and points the way for future research in this area.
引用
收藏
页数:25
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