Tumor-Targeted Drug Delivery with Aptamers

被引:94
作者
Zhang, Y. [2 ]
Hong, H. [1 ]
Cai, W. [1 ,2 ,3 ]
机构
[1] Univ Wisconsin, Dept Radiol, Sch Med & Publ Hlth, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Med Phys, Sch Med & Publ Hlth, Madison, WI 53705 USA
[3] Univ Wisconsin Carbone Canc Ctr, Madison, WI USA
关键词
Aptamers; drug delivery; cancer; nanomedicine; theranostics; RNA interference; siRNA; ASPARTYL CHLORIN E(6); PROSTATE-CANCER CELLS; IN-VIVO; QUANTUM DOTS; CHEMICAL BIOLOGY; RNA MOLECULES; HIGH-AFFINITY; DOXORUBICIN; GROWTH; SIRNA;
D O I
10.2174/092986711797189547
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
Cancer is one of the leading causes of death around the world. Tumor-targeted drug delivery is one of the major areas in cancer research. Aptamers exhibit many desirable properties for tumor-targeted drug delivery, such as ease of selection and synthesis, high binding affinity and specificity, low immunogenicity, and versatile synthetic accessibility. Over the last several years, aptamers have quickly become a new class of targeting ligands for drug delivery applications. In this review, we will discuss in detail about aptamer-based delivery of chemotherapy drugs (e. g. doxorubicin, docetaxel, daunorubicin, and cisplatin), toxins (e. g. gelonin and various photodynamic therapy agents), and a variety of small interfering RNAs. Although the results are promising which warrants enthusiasm for aptamer-based drug delivery, tumor homing of aptamer-based conjugates after systemic injection has only been achieved in one report. Much remains to be done before aptamer-based drug delivery can reach clinical trials and eventually the day-to-day management of cancer patients. Therefore, future directions and challenges in aptamer-based drug delivery are also discussed.
引用
收藏
页码:4185 / 4194
页数:10
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