3D lithographically fabricated nanoliter containers for drug delivery

被引:71
|
作者
Randall, Christina L. [2 ]
Leong, Timothy G. [1 ]
Bassik, Noy [1 ]
Gracias, David H. [1 ,3 ]
机构
[1] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
基金
美国国家卫生研究院;
关键词
drug delivery; lithography; cell encapsulation; on-demand release; self-assembly; containers;
D O I
10.1016/j.addr.2007.08.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lithographic patterning offers the possibility for precise structuring of drug delivery devices. The fabrication process can also facilitate the incorporation of advanced functionality for imaging, sensing, telemetry and actuation. However, a major limitation of present day lithographic fabrication is the inherent two-dimensionality of the patterning process. We review a new approach to construct three dimensional (3D) patterned containers by lithographically patterning two dimensional (2D) templates with liquefiable hinges that spontaneously fold upon heating into hollow polyhedral containers. The containers have finite encapsulation volumes, can be made small enough to pass through a hypodermic needle, and the 3D profile of the containers facilitates enhanced diffusion with the surrounding medium as compared to reservoir systems fabricated in planar substrates. We compare the features of the containers to those of present day drug delivery systems. These features include ease of manufacture, versatility in size and shape, monodisperse porosity, ability for spatial manipulation and remote triggering to release drugs on-demand, the incorporation of electronic modules, cell encapsulation, biocompatibility and stability. We also review possible applications in drug delivery and cell encapsulation therapy (CET). The results summarized in this review suggest a new strategy to enable construction of "smart", three dimensional drug delivery systems using lithography. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1547 / 1561
页数:15
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