Thermally activated reversible shape switch of polymer particles

被引:71
|
作者
Gong, Tao [1 ]
Zhao, Kun [1 ]
Wang, Wenxi [1 ]
Chen, Hongmei [1 ]
Wang, Lin [1 ]
Zhou, Shaobing [1 ]
机构
[1] Southwest Jiaotong Univ, Sch Mat Sci & Engn, Minist Educ, Key Lab Adv Technol Mat, Chengdu 610031, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
EPSILON-CAPROLACTONE; MEMORY POLYMERS; CELLULAR INTERNALIZATION; MECHANICAL-PROPERTIES; TEMPERATURE MEMORY; DRUG CARRIERS; DESIGN; DELIVERY; NANOCOMPOSITES; COMPOSITES;
D O I
10.1039/c4tb01155d
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
The particles that can reversibly switch shape in response to an environmental stimulus are preferable for controlling the performance of drug carriers. In this work, we present a facile strategy towards the design and fabrication of polymer particles that can reversibly switch their shape on the basis of a biocompatible and biodegradable polymer network containing well-defined six-arm poly(ethylene glycol)-poly(epsilon-caprolactone) (6A PEG-PCL). These polymer particles have a capacity of reversibly changing shape from spherical to elliptical either extracellularly or intracellularly with the cyclic heating and cooling between 43 degrees C and 0 degrees C under a stress-free condition via a reversible two-way shape memory effect (2W-SME) of a polymer matrix. This study of the shape-switching particles opens up exciting possibilities for engineering dynamically shape-switching drug delivery carriers to either avoid or promote phagocytosis.
引用
收藏
页码:6855 / 6866
页数:12
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