Stimuli-responsive dendrimers in drug delivery

被引:163
|
作者
Wang, Hui [1 ,2 ]
Huang, Quan [2 ]
Chang, Hong [1 ]
Xiao, Jianru [2 ]
Cheng, Yiyun [1 ]
机构
[1] E China Normal Univ, Sch Life Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China
[2] Second Mil Med Univ, Changzheng Hosp, Dept Orthoped Oncol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
SELF-IMMOLATIVE DENDRIMERS; SUPERPARAMAGNETIC IRON-OXIDE; OFF-ON RELEASE; GENE DELIVERY; POLY(AMIDOAMINE) DENDRIMERS; PAMAM DENDRIMERS; THERMOSENSITIVE PROPERTIES; DENDRITIC ORGANOGELS; DISULFIDE LINKAGES; PEPTIDE DENDRIMER;
D O I
10.1039/c5bm00532a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Dendrimers have shown great promise as carriers in drug delivery due to their unique structures and superior properties. However, the precise control of payload release from a dendrimer matrix still presents a great challenge. Stimuli-responsive dendrimers that release payloads in response to a specific trigger could offer distinct clinical advantages over those dendrimers that release payloads passively. These smart polymers are designed to specifically release their payloads at targeted regions or at constant release profiles for specific therapies. They represent an attractive alternative to targeted dendrimers and enable dendrimer-based therapeutics to be more effective, more convenient, and much safer. The wide range of stimuli, either endogenous( acid, enzyme, and redox potentials) or exogenous ( light, ultrasound, and temperature change), allows great flexibility in the design of stimuli-responsive dendrimers. In this review article, we will highlight recent advances and opportunities in the development of stimuli-responsive dendrimers for the treatment of various diseases, with emphasis on cancer. Specifically, the applications of stimuli-responsive dendrimers in drug delivery as well as their mechanisms are intensively reviewed.
引用
收藏
页码:375 / 390
页数:16
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