Advances in Receptor-Mediated, Tumor-Targeted Drug Delivery

被引:134
作者
Large, Danielle E. [1 ]
Soucy, Jonathan R. [1 ]
Hebert, Jacob [1 ]
Auguste, Debra T. [1 ]
机构
[1] Northeastern Univ, Dept Chem Engn, 360 Huntington Ave, Boston, MA 02115 USA
关键词
cancer; receptor targeting; targeted drug delivery; therapeutic; tumor accumulation; BREAST-CANCER CELLS; FREE CLICK-CHEMISTRY; IN-VIVO; GOLD NANOPARTICLES; PROSTATE-CANCER; INTERLEUKIN-4; RECEPTOR; LIPOSOMAL DOXORUBICIN; TRANSFERRIN RECEPTOR; CELLULAR UPTAKE; BIOLOGICAL EVALUATION;
D O I
10.1002/adtp.201800091
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Receptor-mediated drug delivery presents an opportunity to enhance therapeutic efficiency by accumulating drug within the tissue of interest and reducing undesired, off-target effects. In cancer, receptor overexpression is a platform for binding and inhibiting pathways that shape biodistribution, toxicity, cell binding and uptake, and therapeutic function. This review will identify tumor-targeted drug delivery vehicles and receptors that show promise for clinical translation based on quantitative in vitro and in vivo data. The authors describe the rationale to engineer a targeted drug delivery vehicle based on the ligand, chemical conjugation method, and type of drug delivery vehicle. Recent advances in multivalent targeting and ligand organization on tumor accumulation are discussed. Revolutionizing receptor-mediated drug delivery may be leveraged in the therapeutic delivery of chemotherapy, gene editing tools, and epigenetic drugs.
引用
收藏
页数:27
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