Nanoimprint lithography based fabrication of shape-specific, enzymatically-triggered smart nanoparticles

被引:174
作者
Glangchai, Luz Cristal [1 ]
Caldorera-Moore, Mary [1 ]
Shi, Li [2 ,3 ,4 ]
Roy, Krishnendu [1 ,3 ,4 ]
机构
[1] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Mech Engn, Austin, TX 78712 USA
[3] Univ Texas Austin, Ctr Nano & Mol Sci & Technol, Austin, TX 78712 USA
[4] Univ Texas Austin, Texas Med Inst, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
nano fabrication; nanoparticles; drug delivery; stimuli-responsive; nanoimprint;
D O I
10.1016/j.jconrel.2007.10.021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Our ability to precisely manipulate size, shape and composition of nanoscale carriers is essential for controlling their in-vivo transport, bio-distribution and drug release mechanism. Shape-specific, "smart" nanoparticles that deliver drugs or imaging agents to target tissues primarily in response to disease-specific or physiological signals could significantly improve therapeutic care of complex diseases. Current methods in nanoparticle synthesis do not allow such simultaneous control over particle size, shape and environmentally-triggered drug release, especially at the sub 100 nm range. We report here a high-throughput nanofabrication technique using synthetic and biological macromers (peptides) to produce highly monodisperse, enzymatically-triggered nanoparticles of precise sizes and shapes. Particles as small as 50 nm were fabricated on silicon wafers and harvested directly into aqueous buffers using a biocompatible, one-step release technique. We further demonstrate successful encapsulation and precisely controlled enzyme-triggered release of antibodies and nucleic acids from these nanoparticles, thus providing a potential means for disease-controlled delivery of biomolecules. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:263 / 272
页数:10
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