Smart Nanoscale Drug Delivery Platforms from Stimuli-Responsive Polymers and Liposomes

被引:102
|
作者
Lee, Sang-Min [1 ,2 ,3 ]
Nguyen, SonBinh T. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Ctr Canc Nanotechnol Excellence, Evanston, IL 60208 USA
[3] Catholic Univ Korea, Dept Chem, Puchon 420743, Gyeonggi Do, South Korea
关键词
PH-SENSITIVE LIPOSOMES; CAGED NANOBINS; TRIGGERED RELEASE; POLY(ETHYLENE GLYCOL); INTERBILAYER TRANSFER; PHASE-TRANSITIONS; MODEL MEMBRANES; CANCER; HYDROGELS; THERAPEUTICS;
D O I
10.1021/ma401529w
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Since the 1960s, stimuli-responsive polymers have been utilized as functional soft materials for biological applications such as the triggered-release delivery of biologically active cargos. Over the same period, liposomes have been explored as an alternative drug delivery system with potentials to decrease the toxic side effects often associated with conventional small-molecule drugs. However, the lack of drug-release triggers and the instability of bare liposomes often limit their practical applications, causing short circulation time and low therapeutic efficacy. This Perspective highlights recent work in integrating liposomes and stimuli-responsive polymers together to achieve a targetable, triggerable nanoscale platform that fulfills all the characteristics of a near-ideal drug delivery system. Through a drop-in, post-synthesis modification strategy, a network of stimuli-responsive polymers can be integrated onto the surface of liposomes to form polymer-caged nanobins, a multifunctional nanoscale delivery platform that allows for multidrug loading, targeted delivery, triggered drug release, and theranostic capabilities.
引用
收藏
页码:9169 / 9180
页数:12
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