Biomimetic strategies for targeted nanoparticle delivery

被引:125
作者
Dehaini, Diana
Fang, Ronnie H.
Zhang, Liangfang [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
IRON-OXIDE NANOPARTICLES; MESENCHYMAL STEM-CELLS; VIRUS-LIKE PARTICLES; CONJUGATED PLGA NANOPARTICLES; DRUG-DELIVERY; BREAST-CANCER; IN-VITRO; TRANSFERRIN RECEPTOR; MEMBRANE-VESICLES; MULTIFUNCTIONAL NANOPARTICLES;
D O I
10.1002/btm2.10004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nanoparticle-based drug delivery and imaging platforms have become increasingly popular over the past several decades. Among different design parameters that can affect their performance, the incorporation of targeting functionality onto nanoparticle surfaces has been a widely studied subject. Targeted formulations have the ability to improve efficacy and function by positively modulating tissue localization. Many methods exist for creating targeted nanoformulations, including the use of custom biomolecules such as antibodies or aptamers. More recently, a great amount of focus has been placed on biomimetic targeting strategies that leverage targeting interactions found directly in nature. Such strategies, which have been painstakingly selected over time by the process of evolution to maximize functionality, oftentimes enable scientists to forgo the specialized discovery processes associated with many traditional ligands and help to accelerate development of novel nanoparticle formulations. In this review, we categorize and discuss in-depth recentworks in this growing field of bioinspired research.
引用
收藏
页码:30 / 46
页数:17
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