Receptor-targeted nanocarriers for therapeutic delivery to cancer

被引:287
作者
Yu, Bo [2 ,3 ]
Tai, Heng Chiat [1 ]
Xue, Weiming [2 ,4 ]
Lee, L. James [2 ,3 ]
Lee, Robert J. [1 ,3 ]
机构
[1] Ohio State Univ, Coll Pharm, Div Pharmaceut, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Chem & Biomol Engn, Columbus, OH 43210 USA
[3] Ohio State Univ, NSF, NSEC, Columbus, OH 43210 USA
[4] Northwest Univ, Sch Chem Engn, Xian, Peoples R China
关键词
Drug delivery; nanocarriers; drug targeting; DENSITY-LIPOPROTEIN NANOPARTICLES; SENSITIVE FUSOGENIC PEPTIDE; LIPOSOMAL ANTICANCER DRUGS; POLYMER-BOUND DOXORUBICIN; CELLS IN-VITRO; BREAST-CANCER; MONOCLONAL-ANTIBODY; GENE DELIVERY; PHARMACEUTICAL NANOCARRIERS; ANTI-HER2; IMMUNOLIPOSOMES;
D O I
10.3109/09687688.2010.521200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Efficient and site-specific delivery of therapeutic drugs is a critical challenge in clinical treatment of cancer. Nano-sized carriers such as liposomes, micelles, and polymeric nanoparticles have been investigated for improving bioavailability and pharmacokinetic properties of therapeutics via various mechanisms, for example, the enhanced permeability and retention (EPR) effect. Further improvement can potentially be achieved by conjugation of targeting ligands onto nanocarriers to achieve selective delivery to the tumour cell or the tumour vasculature. Indeed, receptor-targeted nanocarrier delivery has been shown to improve therapeutic responses both in vitro and in vivo. A variety of ligands have been investigated including folate, transferrin, antibodies, peptides and aptamers. Multiple functionalities can be incorporated into the design of nanoparticles, e.g., to enable imaging and triggered intracellular drug release. In this review, we mainly focus on recent advances on the development of targeted nanocarriers and will introduce novel concepts such as multi-targeting and multi-functional nanoparticles.
引用
收藏
页码:286 / 298
页数:13
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