Engineering Biodegradable Nanoparticles for Drug and Gene Delivery

被引:0
|
作者
Zhang, Junwei [2 ]
Saltzman, W. Mark [1 ]
机构
[1] Yale Univ, New Haven, CT 06520 USA
[2] Yale Univ, Dept Chem & Environm Engn, New Haven, CT 06520 USA
关键词
DESIGN; COPOLYMERS; CONJUGATE; ACID;
D O I
暂无
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Engineered nanoparticles (NP) can deliver therapeutic agents to specifically targeted cells and then release those agents in a controlled manner. NPs can significantly improve the pharacokinetic properties of encapsulated agents. Fragile biological agents, such as DNA, can be protected against premature degradation. The stability of hydrophobic drugs in the bloodstream can be significantly increased. Coating NPs with PEG can increase the circulation time of the drug-loaded NP, which is crucial for sustained release and controlled biodistribution. One goal in designing NPs for drug/gene delivery is to reduce the toxicity of the therapeutic agent. This can be done by controlling the pattern of its release from the NPs, either temporally or spatially. It is essential to understand the physicochemical forces that determine the properties of NPs, as well as the molecular interactions that govern how NPs interact with cells and tissues.
引用
收藏
页码:25 / 30
页数:6
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