Biological identity of nanomaterials: Opportunities and challenges

被引:24
作者
Deng Jun [1 ]
Yu DaHai [1 ]
Gao ChangYou [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
nanoparticles; carriers; cellular uptake; protein corona; MULTIFUNCTIONAL MAGNETIC NANOPARTICLES; DRUG-DELIVERY; CELLULAR UPTAKE; BIOMEDICAL APPLICATIONS; PROTEIN CORONA; SEMICONDUCTOR CLUSTERS; SILICA NANOPARTICLES; MACROPHAGE UPTAKE; ANTICANCER DRUG; PLGA PARTICLES;
D O I
10.1007/s11426-013-4972-z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The emergence of nanoparticles (NPs) has attracted tremendous interest of the scientific community for decades due to their unique properties and potential applications in diverse areas, including drug delivery and therapy. Many novel NPs have been synthesized and used to reduce drug toxicity, improve bio-availability, prolong circulation time, control drug release, and actively target to desired cells or tissues. However, clinical translation of NPs with the goal of treating particularly challenging diseases, such as cancer, will require a thorough understanding of how the NP properties influence their fate in biological systems, especially in vivo. Many efforts have been paid to studying the interactions and mechanisms of NPs and cells. Unless deliberately designed, the NPs in contact with biological fluids are rapidly covered by a selected group of biomolecules especially proteins to form a corona that interacts with biological systems. In this view, the recent development of NPs in drug delivery and the interactions of NPs with cells and proteins are summarized. By understanding the protein-NP interactions, some guidelines for safety design of NPs, challenges and future perspectives are discussed.
引用
收藏
页码:1533 / 1541
页数:9
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