Dual pH-Responsive Hydrogel Actuator for Lipophilic Drug Delivery

被引:192
|
作者
Han, Zilong [1 ,2 ]
Wang, Peng [1 ,2 ]
Mao, Guoyong [1 ,2 ]
Yin, Tenghao [1 ,2 ]
Zhong, Danming [1 ,2 ]
Yiming, Burebi [1 ,2 ]
Hu, Xiaocheng [1 ,2 ]
Jia, Zheng [1 ,2 ]
Nian, Guodong [1 ,2 ]
Qu, Shaoxing [1 ,2 ]
Yang, Wei [1 ]
机构
[1] Zhejiang Univ, Ctr X Mech, Key Lab Soft Machines & Smart Devices Zhejiang Pr, State Key Lab Fluid Power & Mechatron Syst, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ, Dept Engn Mech, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
capsule switch; actuator control; drug release; dual pH-responsive hydrogel;
D O I
10.1021/acsami.9b21713
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
As one of the most promising drug delivery carriers, hydrogels have received considerable attention in recent years. Many previous efforts have focused on diffusion-controlled release, which allows hydrogels to load and release drugs in vitro and/or in vivo. However, it hardly applies to lipophilic drug delivery due to their poor compatibility with hydrogels. Herein, we propose a novel method for lipophilic drug release based on a dual pH-responsive hydrogel actuator. Specifically, the drug is encapsulated and can be released by a dual pH-controlled capsule switch. Inspired by the deformation mechanism of Drosera leaves, we fabricate the capsule switch with a double-layer structure that is made of two kinds of pH-responsive hydrogels. Two layers are covalently bonded together through silane coupling agents. They can bend collaboratively in a basic or acidic environment to achieve the "turn on" motion of the capsule switch. By incorporating an array of parallel elastomer stripes on one side of the hydrogel bilayer, various motions (e.g., bending, twisting, and rolling) of the hydrogel bilayer actuator were achieved. We conducted an in vitro lipophilic drug release test. The feasibility of this new drug release method is verified. We believe this dual pH-responsive actuatorcontrolled drug release method may shed light on the possibilities of various drug delivery systems.
引用
收藏
页码:12010 / 12017
页数:8
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