Design of nanoparticles composed of graft copolymers for oral peptide delivery

被引:152
作者
Sakuma, S
Hayashi, M
Akashi, M
机构
[1] Daiichi Pharmaceut Co Ltd, Pharmaceut Formulat Res Lab, Edogawa Ku, Tokyo 1348630, Japan
[2] Sci Univ Tokyo, Fac Pharmaceut Sci, Shinjuku Ku, Tokyo 1620826, Japan
[3] Kagoshima Univ, Fac Engn, Dept Appl Chem & Chem Engn, Kagoshima 8900065, Japan
关键词
nanoparticles; macromonomer; graft copolymer; absorption enhancement; gastrointestinal tract; peptide; mucoadhesion; stabilization;
D O I
10.1016/S0169-409X(00)00119-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The development of a dosage form that improves the absorption of peptide and protein drugs via the gastrointestinal tract is one of the greatest challenges in the pharmaceutical field. Many researchers have taken up the challenge, using approaches including mucoadhesive drug delivery, colon delivery, particulate drug delivery such as nanoparticles, microcapsules, liposomes, emulsions, micelles, and so on. The objective of this article is to provide the reader with outlines of novel nanoparticle technologies for oral peptide delivery based on polymer chemistry. The physicochemical properties of nanoparticles and their behavior on exposure to physiological media are greatly dominated by their chemical structures and surface characteristics. We will especially focus on the design of nanoparticles composed of novel graft copolymers having a hydrophobic backbone and hydrophilic branches as drug carriers. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:21 / 37
页数:17
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