Targeted nanoparticles in mitochondrial medicine

被引:125
作者
Pathak, Rakesh K. [1 ]
Kolishetti, Nagesh [1 ,2 ]
Dhar, Shanta [1 ]
机构
[1] Univ Georgia, Dept Chem, NanoTherapeut Res Lab, Athens, GA 30602 USA
[2] PartiKula LLC, Hollywood, FL USA
基金
美国国家卫生研究院;
关键词
DRUG-DELIVERY; IN-VITRO; SUPEROXIDE-DISMUTASE; OXIDATIVE STRESS; DEGENERATIVE DISEASES; ISCHEMIA-REPERFUSION; HYBRID NANOPARTICLES; MODIFIED LIPOSOMES; DNA-DAMAGE; DYSFUNCTION;
D O I
10.1002/wnan.1305
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Mitochondria, the so-called energy factory of cells' not only produce energy but also contribute immensely in cellular mortality management. Mitochondrial dysfunctions result in various diseases including but not limited to cancer, atherosclerosis, and neurodegenerative diseases. In the recent years, targeting mitochondria emerged as an attractive strategy to control mitochondrial dysfunction-related diseases. Despite the desire to direct therapeutics to the mitochondria, the actual task is more difficult due to the highly complex nature of the mitochondria. The potential benefits of integrating nanomaterials with properties such as biodegradability, magnetization, and fluorescence into a single object of nanoscale dimensions can lead to the development of hybrid nanomedical platforms for targeting therapeutics to the mitochondria. Only a handful of nanoparticles based on metal oxides, gold nanoparticles, dendrons, carbon nanotubes, and liposomes were recently engineered to target mitochondria. Most of these materials face tremendous challenges when administered in vivo due to their limited biocompatibility. Biodegradable polymeric nanoparticles emerged as eminent candidates for effective drug delivery. In this review, we highlight the current advancements in the development of biodegradable nanoparticle platforms as effective targeting tools for mitochondrial medicine. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:315 / 329
页数:15
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