自愈水凝胶
药物输送
纳米技术
材料科学
生物物理学
化学
药品
脚手架
生物医学工程
透皮
药理学
高分子化学
医学
生物
作者
Wenxu Sun,Heting Jiang,Xin Wu,Zhengyu Xu,Yao Chen,Juan Wang,Meng Qin,Qing Jiang,Wei Wang,Dongquan Shi,Yi Cao
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2018-09-06
卷期号:12 (1): 115-119
被引量:70
标识
DOI:10.1007/s12274-018-2188-4
摘要
Hydrogels that can respond to dynamic forces either from endogenous biological activities or from external mechanical stimuli show great promise as novel drug delivery systems (DDS). However, it remains challenging to engineer hydrogels that specifically respond to externally applied mechanical forces with minimal basal drug leakage under normal stressful physiological conditions. Here we present an ultrasound responsive hydrogel-based DDS with special dual-crosslinked nanoscale network architecture. The covalent crosslinks endow the hydrogel high mechanical stability and greatly suppress deformation-triggered drug release. Meanwhile, the dynamic covalent boronate ester linkages between hydrogel backbone and the anti-inflammation compound, tannic acid (TA), allow effective ultrasound-triggered pulsatile release of TA. As such, the hydrogel shows distinct drug release profiles under compression and ultrasound. A proof-of-principle demonstration of the suppression of inflammation activation of macrophage upon ultrasound-triggered release of TA was also illustrated. We anticipate that this novel hydrogel-based drug delivery system can be used for the treatment of inflammatory diseases on load-bearing tissues, such as muscle and cartilage.
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