In vitro and in vivo models for the study of oral delivery of nanoparticles

被引:252
作者
Gamboa, Jennifer M. [1 ]
Leong, Kam W. [1 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
关键词
Nanoparticles; Oral delivery; Simulated intestinal fluid; Transwell (R); Closed loop; Gut-on-a-chip; CaCo-2; Epithelium; Oral delivery barriers; CELL-CULTURE MODEL; TRANSEPITHELIAL ELECTRICAL-RESISTANCE; FOLLICLE-ASSOCIATED EPITHELIUM; CHITOSAN-DNA NANOPARTICLES; NONVIRAL GENE DELIVERY; HEMOPHILIA-A MICE; CACO-2; CELLS; GAMMA-SCINTIGRAPHY; TIGHT JUNCTION; DRUG-DELIVERY;
D O I
10.1016/j.addr.2013.01.003
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Oral delivery is an attractive route to deliver therapeutics via nanoparticles due to its ease of administration and patient compliance. This review discusses laboratory techniques for studying oral delivery of nanoparticles, which offer protection of cargo through the gastrointestinal tract. Some of the difficulties in modeling oral delivery include the harsh acidic environment, variable pH, and the tight monolayer of endothelial cells present throughout the gastrointestinal tract. The use of in vitro techniques including the Transwell (R) system, simulated gastric/intestinal fluid, and diffusion chambers addresses these challenges. When studying effects after oral delivery in vivo, bioimaging of nanoparticle biodistribution using radioactive markers has been popular. Functional assays such as immune response and systemic protein concentration analysis can further define the merits of the oral delivery systems. As biologics become increasingly more important in chronic therapies, nanoparticle-mediated oral delivery will assume greater prominence, and more sophisticated in vitro and in vivo models will be required. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:800 / 810
页数:11
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