Past and future evolution in colloidal drug delivery systems

被引:71
作者
Boyd, Ben J. [1 ]
机构
[1] Monash Univ, Dept Pharmaceut, Victorian Coll Pharm, Parkville, Vic 3052, Australia
关键词
colloidal drug delivery; dendrimer; emulsion; liposome; micelle; nanoparticle;
D O I
10.1517/17425247.5.1.69
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Colloidal drug delivery systems have been providing alternative formulation approaches for problematic drug candidates, and improved delivery for existing compounds for decades. Colloidal systems for drug delivery have all evolved down a similar pathway, almost irrespective of the delivery system, from conception, to the use of safer excipients, PEGylation for passive targeting and attachment of ligands for active targeting. The recent emergence of truly biologically interactive systems represents the latest step forward in colloidal delivery systems. In this article, the maturation pathway and recent advances for the major classes of colloidal delivery systems are reviewed, and the paper poses the question of whether the nanotechnology boom will create a revolution in colloidal delivery, or just the next natural stage in evolution.
引用
收藏
页码:69 / 85
页数:17
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