Smart linkers in polymer-drug conjugates for tumor-targeted delivery

被引:72
作者
Chang, Minglu [1 ]
Zhang, Fang [1 ]
Wei, Ting [1 ]
Zuo, Tiantian [1 ]
Guan, Yuanyuan [1 ]
Lin, Guimei [1 ]
Shao, Wei [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Jinan 250012, Peoples R China
基金
中国国家自然科学基金;
关键词
Chemotherapy; controlled release; delivery system; nanomedicine; stimulus-sensitive; IN-VITRO EVALUATION; ENHANCED ANTICANCER ACTIVITY; CATHEPSIN-B; COMBINATION THERAPY; INTRACELLULAR DRUG; PROSTATE-CANCER; DOXORUBICIN CONJUGATE; ANTITUMOR EFFICACY; COPOLYMER PACLITAXEL; GOLD NANOPARTICLES;
D O I
10.3109/1061186X.2015.1108324
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To achieve effective chemotherapy, many types of drug delivery systems have been developed for the specific environments in tumor tissues. Polymer-drug conjugates are increasingly used in tumor therapy due to several significant advantages over traditional delivery systems. In the fabrication of polymer-drug conjugates, a smart linker is an important component that joins two fragments or molecules together and can be cleared by a specific stimulus, which results in targeted drug delivery and controlled release. By regulating the conjugation between the drug and the nanocarriers, stimulus-sensitive systems based on smart linkers can offer high payloads, certified stability, controlled release and targeted delivery. In this review, we summarize the current state of smart linkers (e.g. disulfide, hydrazone, peptide, azo) used recently in various polymer-drug conjugate-based delivery systems with a primary focus on their sophisticated design principles and drug delivery mechanisms as well as in vivo processes.
引用
收藏
页码:475 / 491
页数:17
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