Intestinal delivery of non-viral gene therapeutics: physiological barriers and preclinical models

被引:88
作者
O'Neill, Martin J. [1 ]
Bourre, Ludovic [1 ]
Melgar, Silvia [2 ]
O'Driscoll, Caitriona M. [1 ]
机构
[1] Univ Coll Cork, Sch Pharm, Pharmacodelivery Grp, Cork, Ireland
[2] Univ Coll Cork, Alimentary Pharmabiot Ctr, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
INFLAMMATORY-BOWEL-DISEASE; POLYPOSIS-COLI GENE; IN-VITRO MODEL; FOLLICLE-ASSOCIATED EPITHELIUM; CELL-CULTURE MODELS; ATTENUATED SALMONELLA-TYPHIMURIUM; CHITOSAN-DNA NANOPARTICLES; PROTEIN-KINASE-A; ORAL DELIVERY; DRUG ABSORPTION;
D O I
10.1016/j.drudis.2011.01.003
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The future of nucleic acid-based therapeutics is dependent on achieving successful delivery. Recently, there has been an increasing interest in delivery via the gastrointestinal tract. Gene therapy via this route has many advantages, including non-invasive access and the versatility to treat local diseases, such as inflammatory bowel disease, as well as systemic diseases, such as haemophilia. However, the intestine presents several distinct barriers and, therefore, the design of robust non-viral delivery systems is key to future success. Several non-viral delivery strategies have provided evidence of activity in vivo. To facilitate the design of more efficient and safe gene medicines, more physiologically relevant models, at both the in vitro and in vivo levels, are essential.
引用
收藏
页码:203 / 218
页数:16
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