Enzyme-responsive nanomaterials for controlled drug delivery

被引:480
作者
Hu, Quanyin [1 ,2 ,3 ,4 ]
Katti, Prateek S. [5 ]
Gu, Zhen [1 ,2 ,3 ,4 ]
机构
[1] Univ N Carolina, Joint Dept Biomed Engn, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Raleigh, NC 27695 USA
[3] Univ N Carolina, Ctr Nanotechnol Drug Delivery, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Div Mol Pharmaceut, UNC Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, UNC Sch Med, UNC MD PhD Program, Chapel Hill, NC 27599 USA
关键词
CONTROLLED-RELEASE; CO-DELIVERY; PHOSPHOLIPASE-A(2) EXPRESSION; GALACTOSYLATED LIPOSOMES; CANCER NANOTECHNOLOGY; GOLD NANOPARTICLES; PEPTIDE; SYSTEMS; NANOMEDICINE; NANOCARRIERS;
D O I
10.1039/c4nr04249b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enzymes underpin physiological function and exhibit dysregulation in many disease-associated micro-environments and aberrant cell processes. Exploiting altered enzyme activity and expression for diagnostics, drug targeting, and drug release is tremendously promising. When combined with booming research in nanobiotechnology, enzyme-responsive nanomaterials used for controlled drug release have achieved significant development and have been studied as an important class of drug delivery strategies in nano-medicine. In this review, we describe enzymes such as proteases, phospholipases and oxidoreductases that serve as delivery triggers. Subsequently, we explore recently developed enzyme-responsive nanomaterials with versatile applications for extracellular and intracellular drug delivery. We conclude by discussing future opportunities and challenges in this area.
引用
收藏
页码:12273 / 12286
页数:14
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