Principles of nanoparticle design for overcoming biological barriers to drug delivery

被引:5089
|
作者
Blanco, Elvin [1 ]
Shen, Haifa [1 ,2 ]
Ferrari, Mauro [1 ,3 ]
机构
[1] Houston Methodist Res Inst, Dept Nanomed, Houston, TX 77030 USA
[2] Weill Cornell Med Coll, Dept Cell & Dev Biol, New York, NY USA
[3] Weill Cornell Med Coll, Dept Med, New York, NY USA
基金
美国国家卫生研究院;
关键词
ALBUMIN-BOUND PACLITAXEL; PHASE-III TRIAL; MULTIDRUG-RESISTANCE; SURFACE-CHARGE; BREAST-CANCER; GENE-THERAPY; IN-VIVO; MACROMOLECULAR THERAPEUTICS; TUMORITROPIC ACCUMULATION; SILICON MICROPARTICLES;
D O I
10.1038/nbt.3330
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
Biological barriers to drug transport prevent successful accumulation of nanotherapeutics specifically at diseased sites, limiting efficacious responses in disease processes ranging from cancer to inflammation. Although substantial research efforts have aimed to incorporate multiple functionalities and moieties within the overall nanoparticle design, many of these strategies fail to adequately address these barriers. Obstacles, such as nonspecific distribution and inadequate accumulation of therapeutics, remain formidable challenges to drug developers. A reimagining of conventional nanoparticles is needed to successfully negotiate these impediments to drug delivery. Site-specific delivery of therapeutics will remain a distant reality unless nanocarrier design takes into account the majority, if not all, of the biological barriers that a particle encounters upon intravenous administration. By successively addressing each of these barriers, innovative design features can be rationally incorporated that will create a new generation of nanotherapeutics, realizing a paradigmatic shift in nanoparticle-based drug delivery.
引用
收藏
页码:941 / 951
页数:11
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