Multifunctional nanoparticles for drug/gene delivery in nanomedicine

被引:3
作者
Seale, Mary-Margaret [1 ]
Zemlyanov, Dimitry [4 ]
Cooper, Christy L. [2 ]
Haglund, Emily [1 ]
Prow, Tarl W. [5 ]
Reece, Lisa M. [2 ]
Leary, James F. [1 ,2 ,3 ,4 ]
机构
[1] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
[2] Purdue Univ, Sch Vet Med, Dept Basic Med Sci, W Lafayette, IN 47907 USA
[3] Purdue Univ, Bindley Biosci Ctr, W Lafayette, IN 47907 USA
[4] Purdue Univ, Birck Nanotechnol Ctr, W Lafayette, IN 47907 USA
[5] Johns Hopkins Univ, Wilmer Ophthalmol Inst, Sch Med, Dept Ophthalmol, Baltimore, MD 21218 USA
来源
NANOSCALE IMAGING, SPECTROSCOPY, SENSING, AND ACTUATION FOR BIOMEDICAL APPLICATIONS IV | 2007年 / 6447卷
关键词
nanomedicine; nanoparticles; drug delivery; gene delivery; therapeutic genes; SPIO;
D O I
10.1117/12.701645
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Multifunctional nanoparticles hold great promise for drug/gene delivery. Multilayered nanoparticles can act as nanomedical systems with on-board "molecular programming" to accomplish complex multi-step tasks. For example, the targeting process has only begun when the nanosystem has found the correct diseased cell of interest. Then it must pass the cell membrane and avoid enzymatic destruction within the endosomes of the cell. Since the nanosystem is only about one millionth the volume of a human cell, for it to have therapeutic efficacy with its contained package, it must deliver that drug or gene to the appropriate site within the living cell. The successive delayering of these nanosystems in a controlled fashion allows the system to accomplish operations that would be difficult or impossible to do with even complex single molecules. In addition, portions of the nanosystem may be protected from premature degradation or mistargeting to non-diseased cells. All of these problems remain major obstacles to successful drug deliver), with a minimum of deleterious side effects to the patient. This paper describes some of the many components involved in the design of a general platform technology for nanomedical systems. The feasibility of most of these components has been demonstrated by our group and others. But the integration of these interacting sub-components remains a challenge. We highlight four components of this process as examples. Each subcomponent has its own sublevels of complexity. But good nanomedical systems have to be designed/engineered as a full inanomedical system, recognizing the need for the other components.
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页数:9
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